阅读说明：本技术 苯磺酰胺化合物作为mPGES-2抑制剂及药物的用途 (Application of benzenesulfonamide compound as mPGES-2 inhibitor and medicine ) 是由 孙莹 高航 权玲玲 张茹梦 万志康 贾占军 钟丹丹 于 2020-05-18 设计创作，主要内容包括：本发明公开了一种苯磺酰胺化合物作为mPGES-2抑制剂及药物的用途。式(I)所示的苯磺酰胺化合物、其异构体或其药学上可接受的衍生物在制备mPGES-2抑制剂、预防和/或治疗糖尿病的药物或mPGES-2靶点产生的预防和/或治疗糖尿病制剂药物中的用途,所述药物至少能够抑制胰岛细胞PGE<Sub>2</Sub>的生成及促进胰岛素分泌；<Image he="278" wi="414" file="DDA0002495854930000011.GIF" imgContent="drawing" imgFormat="GIF" orientation="portrait" inline="no"></Image>本发明通过提供的苯磺酰胺化合物、其异构体或其药学上可接受的衍生物制备得到了mPGES-2抑制剂,通过实验证明,该类化合物及mPGES-2抑制剂可用在糖尿病的改善和治疗中,且可明显证明对改善和治疗糖尿病的作用,其可通过可接受载体制成药物,用于防治糖尿病。(The invention discloses application of a benzenesulfonamide compound as an mPGES-2 inhibitor and a medicament. Application of benzenesulfonamide compound shown as formula (I), isomer or pharmaceutically acceptable derivative thereof in preparation of mPGES-2 inhibitor, medicament for preventing and/or treating diabetes or medicament for preventing and/or treating diabetes by mPGES-2 target generation, wherein the medicament at least can inhibit islet cell PGE 2 To promote insulin secretion; the mPGES-2 inhibitor is prepared by the provided benzenesulfonamide compound, the isomer thereof or the pharmaceutically acceptable derivative thereof, experiments prove that the compound and the mPGES-2 inhibitor can be used in the improvement and treatment of diabetes, and can obviously prove the effect on the improvement and treatment of diabetes, and the compounds can be prepared into medicaments through acceptable carriers for preventing and treating diabetes.)

1. Application of benzenesulfonamide compound shown as formula (I), isomer or pharmaceutically acceptable derivative thereof in preparation of mPGES-2 inhibitor, medicament for preventing and/or treating diabetes or medicament for preventing and/or treating diabetes by mPGES-2 target generationCan inhibit islet cell PGE₂To promote insulin secretion;

wherein R is₁Is selected from C₁-C₁₀Alkyl of (C)₁-C₆Hydroxyalkyl of (C)₁-C₄Alkyl alkoxy of C₁-C₄Aminoalkyl of (C)₁-C₄Halogenoalkyl of, C₁-C₄Is optionally substituted at a carbon atom with one or more substituents selected from hydroxy, nitro, carboxy, cyano, amino, halogen, C₁-C₄Alkyl of (C)₁-C₄Alkoxy group of (a);

R₂is selected from C₁-C₄The alkyl, phenyl, substituted phenyl, quinolyl, substituted quinolyl, naphthyl, substituted naphthyl, thienyl, substituted thienyl, benzyl, substituted benzyl, biphenyl, furyl, pyrrolyl, pyridyl, thiazolyl, piperidinyl, morpholinyl or indolyl of (a) which may be optionally substituted at the carbon atom by one or more substituents selected from hydroxy, nitro, carboxy, cyano, amino, halogen, C₁-C₄Alkyl or C₁-C₄Alkoxy group of (a);

wherein the pharmaceutically acceptable derivative is selected from at least one of a pharmaceutically acceptable salt, polymorph, co-crystal, radiolabeled form, and combinations thereof.

2. Use according to claim 1, characterized in that: the R is₁Is selected from C₁-C₈Alkyl of (C)₁-C₄Hydroxyalkyl of (C)₁-C₄Alkyl alkoxy, phenyl, substituted phenyl, benzyl or substituted benzyl of (A), said substituted phenyl or substituted benzylThe radicals being optionally substituted at the carbon atom by one or more substituents selected from the group consisting of hydroxy, fluoro, bromo, C₁-C₄Alkyl or C₁-C₄Alkoxy group of (a);

preferably, said R is₁Is selected from C₁-C₈Alkyl, 4-hydroxybutyl, 3-hydroxypropyl, 2-hydroxyethyl, 2-methoxyethyl, 2-ethoxyethyl, 3-methoxypropyl, phenyl, benzyl, substituted phenyl or substituted benzyl which may be optionally substituted at a carbon atom by one or more substituents selected from the group consisting of hydroxy, fluoro, bromo, methyl, ethyl, methoxy, ethoxy;

particularly preferably, R is₁Is selected from C₁-C₈Alkyl, 4-hydroxybutyl, 3-hydroxypropyl, 2-hydroxyethyl, 2-methoxyethyl, phenyl or benzyl.

3. Use according to claim 1, characterized in that: the R is₂Selected from phenyl, substituted phenyl, quinolyl, substituted quinolyl, naphthyl, substituted naphthyl, thienyl, substituted thienyl, furyl, pyrrolyl, pyridyl, thiazolyl, piperidyl, morpholinyl or indolyl, wherein the substituted phenyl, substituted quinolyl, substituted naphthyl or substituted thienyl may be optionally substituted at a carbon atom by more than one substituent selected from hydroxyl, amino, halogen, C₁-C₄Alkyl or C₁-C₄Alkoxy group of (a);

preferably, said R is₂Selected from phenyl, substituted phenyl, naphthyl, quinolinyl, thienyl, furyl, pyrrolyl, pyridyl, thiazolyl, piperidinyl, morpholinyl, or indolyl, said substituted phenyl being optionally substituted at a carbon atom with one or more substituents selected from hydroxy, amino, fluoro, bromo, methyl, ethyl, propyl, tert-butyl, methoxy, or ethoxy;

particularly preferably, R is₂Selected from phenyl, substituted phenyl, naphthyl, quinolyl or thienyl, wherein the substituted phenyl can be optionally substituted at carbon atom by more than one substituent selected fromHydroxy, amino, fluoro, bromo, methyl, ethyl, propyl, tert-butyl, methoxy or ethoxy.

4. Use according to claim 1, characterized in that the benzenesulfonamide compound is selected from any one of the following compounds:

5. an mPGES-2 inhibitor, comprising: a benzenesulfonamide compound represented by formula (I), an isomer thereof or a pharmaceutically acceptable derivative thereof, and a pharmaceutically acceptable carrier and/or excipient;

wherein R is₁Is selected from C₁-C₁₀Alkyl of (C)₁-C₆Hydroxyalkyl of (C)₁-C₄Alkyl alkoxy of C₁-C₄Aminoalkyl of (C)₁-C₄Halogenoalkyl of, C₁-C₄Is optionally substituted at a carbon atom with one or more substituents selected from hydroxy, nitro, carboxy, cyano, amino, halogen, C₁-C₄Alkyl of (C)₁-C₄Alkoxy group of (a);

R₂is selected from C₁-C₄Alkyl, phenyl, substituted phenyl, quinolyl and substituted quinoline ofAryl, naphthyl, substituted naphthyl, thienyl, substituted thienyl, benzyl, substituted benzyl, biphenyl, furyl, pyrrolyl, pyridyl, thiazolyl, piperidinyl, morpholinyl, or indolyl, wherein the substituted phenyl, substituted quinolyl, substituted naphthyl, substituted thienyl, or substituted benzyl may be optionally substituted at a carbon atom with one or more substituents selected from the group consisting of hydroxy, nitro, carboxy, cyano, amino, halogen, C₁-C₄Alkyl or C₁-C₄Alkoxy group of (a);

wherein the pharmaceutically acceptable derivative is selected from at least one of a pharmaceutically acceptable salt, polymorph, co-crystal, radiolabeled form, and combinations thereof.

6. A medicament for the treatment and/or prevention of diabetes characterized in that it comprises the mPGES-2 inhibitor of claim 5.

7. The medicament of claim 6, wherein: the medicament further comprises a pharmaceutically acceptable carrier and/or excipient.

8. The medicament of claim 6, wherein: the drug can inhibit islet cell PGE₂And (4) generating.

9. The medicament of claim 6, wherein: the medicine can promote insulin secretion.

10. The medicament of claim 6, wherein: the dosage form of the medicine comprises injection, oral liquid, capsules, tablets or granules; and/or, the mode of administration of the medicament comprises subcutaneous administration, oral administration, intramuscular administration or intraperitoneal administration; and/or, the diabetes is type 1 diabetes and type 2 diabetes.

Technical Field

The invention relates to application of a benzene sulfonamide compound, in particular to application of the benzene sulfonamide compound, pharmaceutically acceptable salts of the benzene sulfonamide compound and a pharmaceutical composition containing the benzene sulfonamide compound as an mPGES-2 inhibitor, and application of the mPGES-2 inhibitor as a medicine for treating and/or preventing diabetes, and belongs to the technical field of medicines.

Background

According to the latest data of the international diabetes union, about 4.25 hundred million adults suffer from diabetes in 2017 globally. Wherein, China is the country with the most sick people, and the sick people in 2017 year reach 1.14 hundred million. Diabetes mellitus (diabetes mellitus) is a metabolic disease characterized by chronic hyperglycemia due to various etiologies, most commonly type 1 diabetes mellitus and type 2 diabetes mellitus. The basic pathophysiology of the medicine is absolute or relative metabolic disorder caused by insufficient insulin secretion and high glucagon activity, including sugar, protein, fat, water, electrolyte and the like, which can cause abnormal acid-base balance in severe cases and cause various complications for a long time.

Prostaglandin E₂The synthetase (PGES) is prostaglandin E₂(PGE₂) Terminal synthetases in the synthetic pathway, at least 3 PGES species have been found: cytosolic PGE synthetase (cPGES), microsomal PGE synthetase 1(mPGES-1) and microsomal PGE synthetase 2 (mPGES-2). mPGES-2 is a Glutathione (GSH) -dependent prostaglandin E₂Synthetase expressed in various cells and tissues and capable of converting prostaglandin H₂(PGH₂) Conversion to PGE₂. Known PGE₂Is the most common prostanoid produced by a variety of cells and tissues and has a wide range of biological activities.

At present, the clinical research on the mechanism of diabetes is always in the exploration stage, most of the diabetes is treated by adopting insulin injection and oral hypoglycemic drugs, but adverse reactions such as hypoglycemia, digestive tract symptoms, allergy, metabolism and nutrition disorder are often accompanied. Therefore, there is a need to develop a new drug for treating diabetes with significant effect and less side effects.

Disclosure of Invention

The invention mainly aims to provide application of a benzenesulfonamide compound shown in formula (I), an isomer thereof or a pharmaceutically acceptable derivative thereof in preparing a medicament for treating and/or preventing diabetes, so as to overcome the defects of the prior art.

It is another object of the present invention to provide a composition.

Another object of the present invention is to provide a medicament for treating and/or preventing diabetes.

In order to achieve the purpose, the technical scheme adopted by the invention comprises the following steps:

the embodiment of the invention provides a benzene sulfonamide compound shown in a formula (I), an isomer thereof or pharmaceutically acceptable salts thereofUse of the accepted derivatives for the preparation of mPGES-2 inhibitors, drugs for the prevention and/or treatment of diabetes or drugs for the prevention and/or treatment of diabetes formulation for the generation of mPGES-2 targets, said drugs being capable of inhibiting at least islet cell PGE₂To promote insulin secretion;

wherein R is₁Is selected from C₁-C₁₀Alkyl of (C)₁-C₆Hydroxyalkyl of (C)₁-C₄Alkyl alkoxy of C₁-C₄Aminoalkyl of (C)₁-C₄Halogenoalkyl of, C₁-C₄Is optionally substituted at a carbon atom with one or more substituents selected from hydroxy, nitro, carboxy, cyano, amino, halogen, C₁-C₄Alkyl of (C)₁-C₄Alkoxy group of (a);

R₂is selected from C₁-C₄The alkyl, phenyl, substituted phenyl, quinolyl, substituted quinolyl, naphthyl, substituted naphthyl, thienyl, substituted thienyl, benzyl, substituted benzyl, biphenyl, furyl, pyrrolyl, pyridyl, thiazolyl, piperidinyl, morpholinyl or indolyl of (a) which may be optionally substituted at the carbon atom by one or more substituents selected from hydroxy, nitro, carboxy, cyano, amino, halogen, C₁-C₄Alkyl or C₁-C₄Alkoxy group of (a);

wherein the pharmaceutically acceptable derivative is selected from at least one of a pharmaceutically acceptable salt, polymorph, co-crystal, radiolabeled form, and combinations thereof.

The embodiment of the invention also provides an mPGES-2 inhibitor, which comprises the following components in part by weight: the aforementioned benzenesulfonamide compounds, isomers thereof or pharmaceutically acceptable derivatives thereof, and a pharmaceutically acceptable carrier and/or excipient;

wherein the pharmaceutically acceptable derivative is selected from at least one of a pharmaceutically acceptable salt, polymorph, co-crystal, radiolabeled form, and combinations thereof.

Embodiments of the present invention also provide a medicament for the treatment and/or prevention of diabetes comprising the aforementioned benzenesulfonamide compound, its isomer or a pharmaceutically acceptable derivative thereof selected from at least one of pharmaceutically acceptable salts, polymorphs, co-crystals, radiolabeled forms, and combinations thereof, or the aforementioned mPGES-2 inhibitor.

Compared with the prior art, the invention has the beneficial effects that:

the mPGES-2 inhibitor is prepared by the provided benzenesulfonamide compound, the isomer thereof or the pharmaceutically acceptable derivative thereof, experiments prove that the compound and the mPGES-2 inhibitor can be used in the improvement and treatment of diabetes, and can obviously prove the effect on the improvement and treatment of diabetes, and the compounds can be prepared into medicaments through acceptable carriers for preventing and treating diabetes.

Drawings

In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings used in the description of the embodiments or the prior art will be briefly described below, it is obvious that the drawings in the following description are only some embodiments described in the present invention, and for those skilled in the art, other drawings can be obtained according to the drawings without creative efforts.

FIG. 1 is a graph showing the inhibition of mPGES-2 enzyme activity by compound SZ0232 in an exemplary embodiment of the invention;

FIG. 2 is a graph showing the results of the inhibition of mPGES-2 activity by compound SZ0232 in an exemplary embodiment of the invention;

FIG. 3 is a graph showing a comparison of the insulin secretion effect of compound SZ0232 on mPGES-2KO and WT mouse islet cells under high sugar (16.7 mMol/L) conditions in an exemplary embodiment of the invention, wherein the concentration of compound SZ0232 is 10. mu. Mol/L;

FIG. 4 is a graph showing the effect of SZ0232 and six other compounds (SZ0206, SZ0218, SZ0231, SZ0240, SZ0247 and SZ0264) on insulin secretion in an exemplary embodiment of the invention, wherein the concentrations of SZ0232 and six other compounds are 10. mu. Mol/L;

FIG. 5 shows the production of PGE by mPGES-2 inhibitor (SZ0232) in control and HepG2 cells overexpressing mPGES-2 in an exemplary embodiment of the invention₂Wherein the concentration of the mPGES-2(SZ0232) inhibitor is 10 mu Mol/L;

FIG. 6 is a schematic diagram of an example of sugar-stimulated insulin secretion (GSIS) experiment performed on isolated islet cells under high sugar stimulation to detect the amount of insulin secretion when mPGES-2 inhibitor (SZ0232) is administered, wherein the concentration of mPGES-2 inhibitor (SZ0232) is 10 μ Mol/L;

FIG. 7 is a graph showing PGE synthesis for COX-2 by a graded concentration of mPGES-2 inhibitor (SZ0232) in an exemplary embodiment of the invention₂A graph of activity inhibition of;

FIG. 8 is a graph showing the PGE synthesis from mPGES-1 by a gradient of mPGES-2 inhibitor (SZ0232) versus mPGES-1 in an exemplary embodiment of the invention₂A graph of activity inhibition of;

FIG. 9 is a graph showing the toxic effect of mPGES-2 inhibitor (SZ0232) on MIN6 cells as measured by the CCK-8 method in an exemplary embodiment of the invention, wherein the control is lysis medium containing cells, the same concentration of compound, culture medium, CCK-8;

FIG. 10 is a graph showing a comparison of insulin secretion by treatment of isolated pancreatic islet cells with graded concentrations of mPGES-2 inhibitor (SZ0232) under conditions of low carbohydrate (3 mMol/L) and high carbohydrate (16.7 mMol/L) in an exemplary embodiment of the invention;

FIG. 11 is a graph showing a comparison of prostaglandin E receptor 3(EP3) antagonists L-798106 and the agonist sulprostone alone and in combination with the mPGES-2 inhibitor (SZ0232) at a concentration of 10 μ Mol/L for the prostaglandin E receptor 3(EP3) and 10 μ Mol/L-798106 for the sulprostone/L for the prostaglandin E receptor 3(EP3) under conditions of low sugar (3 mMol/L) and high sugar (16.7 mMol/L) in an exemplary embodiment of the invention;

FIG. 12 is a graph showing a comparison of the results of Glibenclamide (Glibenclamide) and mPGES-2 inhibitor (SZ0232) alone and in combination with Glibenclamide (Glibenclamide) at a concentration of 10 μ Mol/L and 1 μ Mol/L under conditions of low carbohydrate (3 mMol/L) and high carbohydrate (16.7 mMol/L) in an exemplary embodiment of the invention;

FIG. 13 is a graph showing a comparison of the results of exenatide (Exendin-4) and mPGES-2 inhibitor (SZ0232) alone and in combination with a lower sugar (3 mMol/L) and a higher sugar (16.7 mMol/L) for insulin secretion in an exemplary embodiment of the invention, wherein the concentration of mPGES-2 inhibitor (SZ0232) is 10. mu. Mol/L and the concentration of Exendin-4 is 100 nMol/L.

Detailed Description

In view of the defects in the prior art, the inventor of the present invention provides a technical scheme of the invention through long-term research and a large amount of practice, and mainly provides a benzene sulfonamide compound and an available salt thereof in preparation of an mPGES-2 inhibitor, and an experimental method and application for improving and treating diabetes mellitus. Experiments prove that the mPGES-2 inhibitor has the effect of improving and treating diabetes, can be prepared into a medicament through an acceptable carrier, and is used for preventing and treating diabetes.

The technical solution, its implementation and principles, etc. will be further explained as follows.

One aspect of the embodiment of the invention provides application of a benzenesulfonamide compound represented by formula (I), an isomer thereof or a pharmaceutically acceptable derivative thereof in preparing an mPGES-2 inhibitor, a medicament for preventing and/or treating diabetes or a medicament for preventing and/or treating diabetes by mPGES-2 target generation, wherein the medicament is capable of at least inhibiting islet cell PGE₂To promote the production of insulinSecretion;

wherein R is₁Is selected from C₁-C₁₀Alkyl of (C)₁-C₆Hydroxyalkyl of (C)₁-C₄Alkyl alkoxy of C₁-C₄Aminoalkyl of (C)₁-C₄Halogenoalkyl of, C₁-C₄The substituted phenyl or substituted benzyl group may be optionally substituted at a carbon atom with one or more substituents (i.e., may be optionally mono-or polysubstituted with a substituent selected from the group consisting of hydroxy, nitro, carboxy, cyano, amino, halogen, C)₁-C₄Alkyl of (C)₁-C₄Alkoxy group of (a);

R₂is selected from C₁-C₄The alkyl, phenyl, substituted phenyl, quinolyl, substituted quinolyl, naphthyl, substituted naphthyl, thienyl, substituted thienyl, benzyl, substituted benzyl, biphenyl, furyl, pyrrolyl, pyridyl, thiazolyl, piperidyl, morpholinyl or indolyl of (a) is optionally substituted at a carbon atom with one or more substituents (i.e. optionally mono-or polysubstituted with substituents selected from hydroxy, nitro, carboxy, cyano, amino, halogen, C)₁-C₄Alkyl or C₁-C₄Alkoxy group of (a);

wherein the pharmaceutically acceptable derivative is selected from at least one of a pharmaceutically acceptable salt, polymorph, co-crystal, radiolabeled form, and combinations thereof.

In some preferred embodiments, said R is₁Is selected from C₁-C₈Alkyl of (C)₁-C₄Hydroxyalkyl of (C)₁-C₄Alkyl alkoxy, phenyl, substituted phenyl, benzyl or substituted benzyl of (a), which may be substituted by more than one carbon atomThe substituents are optionally substituted (i.e., optionally mono-or polysubstituted with substituents selected from the group consisting of hydroxy, fluoro, bromo, C₁-C₄Alkyl or C₁-C₄Alkoxy group of (2), and the like, but are not limited thereto.

In some more preferred embodiments, R is₁Is selected from C₁-C₈Alkyl, 4-hydroxybutyl, 3-hydroxypropyl, 2-hydroxyethyl, 2-methoxyethyl, 2-ethoxyethyl, 3-methoxypropyl, phenyl, benzyl, substituted phenyl or substituted benzyl which may be optionally substituted at a carbon atom with one or more substituents (i.e. which may be optionally mono-or polysubstituted with substituents selected from the group consisting of hydroxy, fluoro, bromo, methyl, ethyl, methoxy, ethoxy and the like, but is not limited thereto.

Further, in a particularly preferred embodiment, R is₁Is selected from C₁-C₈Alkyl, 4-hydroxybutyl, 3-hydroxypropyl, 2-hydroxyethyl, 2-methoxyethyl, phenyl or benzyl, etc., but are not limited thereto.

In some preferred embodiments, said R is₂Selected from phenyl, substituted phenyl, quinolyl, substituted quinolyl, naphthyl, substituted naphthyl, thienyl, substituted thienyl, furyl, pyrrolyl, pyridyl, thiazolyl, piperidyl, morpholinyl or indolyl, wherein the substituted phenyl, substituted quinolyl, substituted naphthyl or substituted thienyl can be optionally substituted (i.e., optionally mono-or polysubstituted by) at a carbon atom by more than one substituent selected from hydroxyl, amino, halogen, C₁-C₄Alkyl or C₁-C₄Alkoxy group of (2), and the like, but are not limited thereto.

In some more preferred embodiments, R is₂Is selected from phenyl, substituted phenyl, naphthyl, quinolyl, thienyl, furyl, pyrrolyl, pyridyl, thiazolyl, piperidyl, morpholinyl or indolyl, the substituted phenyl can be optionally substituted (namely optionally mono-substituted or multi-substituted) by more than one substituent at the carbon atom, and the substituent is selected from hydroxyl, amino, fluorineBromine, methyl, ethyl, propyl, tert-butyl, methoxy or ethoxy, and the like, but is not limited thereto.

Further, in a particularly preferred embodiment, R is₂Selected from phenyl, substituted phenyl, naphthyl, quinolyl or thienyl, wherein the substituted phenyl is optionally substituted (i.e. optionally mono-or polysubstituted by substituents selected from hydroxy, amino, fluoro, bromo, methyl, ethyl, propyl, tert-butyl, methoxy or ethoxy) at a carbon atom.

In some more specific embodiments, the structure of the benzenesulfonamide compound in the compound of formula (I), an isomer, or a pharmaceutically acceptable salt thereof, may be selected from the following compounds:

the nomenclature of the above compounds provided by the present invention is as follows:

SZ0206 compound designation: n- ((5- (bis (5-methylfuran-2-yl) methyl) furan-2-yl) methyl) -4-methylbenzenesulfonamide, queried by the Reaxyz database, with PubChem ID of 16762256;

SZ0207 compound designation: 4-methoxy-N- ((3- (4-methoxyphenyl) isoxazol-5-yl) methyl) benzenesulfonamide, queried by the Reaxys database, with a PubChem ID of 8033490;

SZ0209 compound designation: the N- (4-ethoxyphenyl) -4-isopropylbenzenesulfonamide is inquired by a Reaxyz database, and the ID of PubPhem is 4812206;

SZ0218 compound name: 5- ((4-isopropylphenyl) sulfonamide) -2-methylbenzofuran-3-carboxylic acid ethyl ester, queried by the Reaxys database, PubChem ID is 7718538;

SZ0221 compound designation: (E) -N- (3- (2- (pyridin-4-yl) vinyl) phenyl) naphthalene-2-sulfonamide queried by the Reaxys database with PubChem ID of 5305353;

compound designation SZ 0222: (E) -N- (3- (2- (pyridin-4-yl) vinyl) phenyl) naphthalene-2-sulfonamide queried by the Reaxys database with PubChem ID of 5305522;

compound name SZ 0231: n- (3-chloro-4- (pyridin-2-ylsulfanyl) phenyl) -9H-fluorene-2-sulfonamide queried by the Reaxys database with a PubChem ID of 5312255;

compound name SZ 0232: n, N' - ((4- ((4- (2-oxopyrrolidin-1-yl) phenyl) sulfonamido) -1, 2-phenylene) bis (oxy)) bis (ethane-2, 1-diyl)) bisamide, referred to the Reaxys database, PubChem ID 16762323;

SZ0240 compound designation: n- (4-hydroxy-3- ((4-methoxyphenyl) thio) naphthalen-1-yl) -4-methoxybenzenesulfonamide, queried by the Reaxys database, with a PubChem ID of 30438834;

SZ0247 compound designation: 3- (4- ((4- (2-oxopyrrolidin-1-yl) phenyl) sulfonamido) phenyl) propanoic acid, queried by the Reaxys database, PubChem ID 16762287;

SZ0254 compound designation: (1s, 3s) -adamantan-1-yl) methyl 4- (9H-fluorene-2-sulfonamide) benzoate, queried by the Reaxyz database, PubChem ID at 5305297;

SZ0255 compound designation: 4- (2- ((4- (2-oxopyrrolidin-1-yl) phenyl) sulfonamido) ethoxy) benzoic acid, queried by the Reaxys database, PubChem ID 8033773;

SZ0258 compound designation: methyl (4, 5-dimethoxy-2- ((4- (2-oxopyrrolidin-1-yl) phenyl) sulfonamide) phenethyl) carbamate, queried by the Reaxys database, PubChem ID 16762298;

compound designation SZ 0264: 4- ((4- (5-methylfuran-2-yl) thiazol-2-yl) amino) -N- (5-methylisoxazol-3-yl) benzenesulfonamide, queried by the Reaxyz database, PubChem ID of 5303639;

SZ0275 compound nomenclature: 5- ((4-ethoxyphenyl) sulfonamide) -2-methylbenzofuran-3-carboxylic acid, queried by the Reaxys database, PubChem ID is 8028187;

SZ0279 compound nomenclature: n- (2- (dibenzo [ b, d ] furan-3-yl) ethyl) -4- (2-oxopyrrolidin-1-yl) benzenesulfonamide, queried by the Reaxyz database, PubChem ID is 16761772.

The following definitions apply to the compounds relevant to the present invention.

As used herein, the term "halo" or "halogen" refers to fluoro (fluoro), chloro (chloro), bromo (bromo) and iodo (iodo).

Herein, the term "C_1-10Alkyl "whether used alone or in compound terms, refers to a monovalent straight or branched chain hydrocarbon radical having 1 to 10 carbon atoms. As one skilled in the art will appreciate, for example, the term "C_1-10Alkyl "refers to an alkyl chain having 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 carbon atoms or a series including any two alkyl chains containing integers from 1 to 2, 1 to 3, 1 to 4, 1 to 5, 1 to 6, 1 to 7, 1 to 8, 1 to 9, 1 to 10. Suitable alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, pentyl, neopentyl and hexyl. The C is_1-10The alkyl group may be optionally substituted with one or more substituents. The substituents may be at any position of the carbon chain.

Herein, the term "C_1-8Alkyl "whether used alone or in compound terms, refers to a monovalent straight or branched chain hydrocarbon radical having 1 to 8 carbon atoms. As one skilled in the art will appreciate, for example, the term "C_1-8Alkyl "refers to an alkyl chain having 1, 2, 3, 4, 5, 6, 7, or 8 carbon atoms or a series of alkyl chains including any two integers from 1 to 2, 1 to 3, 1 to 4, 1 to 5, 1 to 6, 1 to 7, 1 to 8. Suitable alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, pentyl, neopentyl and hexyl. The C is_1-8The alkyl group may be optionally substituted with one or more substituents. The substituents may be at any position of the carbon chain.

Herein, the term "C_1-6Alkyl "whether used alone or in compound terms, refers to a monovalent straight or branched chain hydrocarbon radical having 1 to 6 carbon atoms.As one skilled in the art will appreciate, for example, the term "C_1-8Alkyl "refers to an alkyl chain having 1, 2, 3, 4, 5, or 6 carbon atoms or a series of alkyl chains including any two integers from 1 to 2, 1 to 3, 1 to 4, 1 to 5, 1 to 6. Suitable alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, pentyl, neopentyl and hexyl. The C is_1-6The alkyl group may be optionally substituted with one or more substituents. The substituents may be at any position of the carbon chain.

The compounds of the present invention include those outlined above and are further illustrated by the classes, subclasses, and species disclosed herein. The following definitions as used herein shall apply unless otherwise indicated. For the purposes of the present invention, chemical Elements are identified according to the Periodic Table of the Elements (chemical abstracts edition, handbook of Chemistry and Physics, 75 th edition). In addition, the general principles of Organic Chemistry are described in "Organic Chemistry" (Thomas Sorrell, university Natural science Books, Sossally (Sausaltio): 1999) and "March Advanced Organic Chemistry" (5 th edition, ed.: Smith (Smith, M.B.) and March (March, J.), John Wiley & Sons, New York (NewYork): 2001), the entire contents of which are incorporated herein by reference.

The term "pharmaceutically acceptable salts" as used herein is intended to refer to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio. Pharmaceutically acceptable salts are well known in the art. For example, pharmaceutically acceptable salts are described in detail in J.pharmaceutical Sciences, 1977, 66, 1-19, by SMBERGE et al, the contents of which are incorporated herein by reference. Pharmaceutically acceptable salts of the compounds of the present invention include those derived from suitable inorganic and organic acids and bases. Examples of pharmaceutically acceptable non-toxic acid addition salts are salts of amino groups formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid, or with organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid, or by using other methods in the art such as ion exchange. Other pharmaceutically acceptable salts include adipates, alginates, ascorbates, aspartates, benzenesulfonates, benzoates, bisulfates, borates, butyrates, camphorates, camphorsulfonates, citrates, cyclopentylpropionates, gluconates, dodecylsulfates, ethanesulfonates, formates, fumarates, glucoheptonates, glycerophosphates, gluconates, hemisulfates, heptanoates, hydroiodides, 2-hydroxyethanesulfonates, lactates, laurates, laurylsulfates, malates, maleates, malonates, methanesulfonates, 2-naphthalenesulfonates, nicotinates, nitrates, oleates, oxalates, palmitates, embonates, pectinates, persulfates, 3-phenylpropionates, phosphates, pivaloates, propionates, stearates, succinates, salts, Sulfates, tartrates, thiocyanates, p-toluenesulfonates, undecanoates, pentanoates, and the like.

Salts derived from suitable bases include alkali metal, alkaline earth metal, ammonium and N + (C1-4 alkyl) 4 salts. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Other pharmaceutically acceptable salts include suitable non-toxic ammonium salts formed using such salts as halides, hydroxides, carboxylates, sulfates, phosphates, nitrates, lower alkyl sulfonates and aryl sulfonates, quaternary ammonium salts and amine cations.

As used herein, "pharmaceutically acceptable salt" refers to a form of the disclosed compound in which the parent compound is modified by making acid or base salts thereof. Examples of pharmaceutically acceptable salts include, but are not limited to, inorganic or organic acid salts of basic residues such as amines; for example, alkali metal or organic salts of acidic residues such as carboxylic acids. Pharmaceutically acceptable salts include the conventional non-toxic salts or the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids. Such conventional non-toxic salts include those derived from inorganic acids such as hydrochloric acid.

The pharmaceutically acceptable salts of the present invention can be synthesized from the parent compound, which contains a basic or acidic moiety, by conventional chemical methods. Generally, such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid, in water or an organic solvent, or a mixture of the two; generally, a nonaqueous medium such as diethyl ether, ethyl acetate, ethanol, isopropanol or acetonitrile is used.

The term "pharmaceutically acceptable derivative" includes any pharmaceutically acceptable salt, hydrate or prodrug, or any other compound that, when administered to a subject, provides (directly or indirectly) a compound of formula (I) or a metabolite or residue having antibacterial activity.

Salts of the compounds of formula (I) are preferably pharmaceutically acceptable, but non-pharmaceutically acceptable salts should also fall within the scope of the invention as such are useful intermediates in the preparation of pharmaceutically acceptable salts.

Suitable pharmaceutically acceptable salts include, but are not limited to, pharmaceutically acceptable inorganic acids such as hydrochloric, sulfuric, phosphoric, nitric, carbonic, boric, sulfamic and hydrobromic acids, or pharmaceutically acceptable organic acids thereof such as hydrochloric, propionic, butyric, tartaric, maleic, hydroxy, fumaric, malic, citric, lactic, mucic, gluconic, benzoic, succinic, oxalic, phenylacetic, methanesulfonic, toluenesulfonic, benzenesulfonic, salicylic, p-amino, aspartic, glutamic, edetic, stearic, palmitic, oleic, lauric, pantothenic, tannic, ascorbic and valeric acids.

Corresponding base salts include, but are not limited to, those formed with pharmaceutically acceptable cations such as sodium, potassium, lithium, calcium, magnesium, zinc, ammonium, alkylammonium, for example, salts formed with triethylamine, alkoxyamines such as those formed with ethanolamine, and salts formed from ethylenediamine, choline or amino acids such as arginine, lysine or histidine. Pharmaceutically acceptable salts and their formation and general information are well known to those skilled in the art, as described in general textbooks such as "salts for handbook pharmacy" PHStahl, CGWermuth, 1 st edition, 2002, willi-VCH.

Unless otherwise indicated, structures described herein are also meant to include all isomeric forms of the structure (e.g., enantiomers, diastereomers, and geometric (or conformational) isomers); for example, the R and S configurations, Z and E double bond isomers, and Z and E conformational isomers of each asymmetric center. Thus, individual stereochemical isomers as well as mixtures of enantiomers, diastereomers, and geometric (or conformational) isomers of mixtures of the compounds of the present invention are within the scope of the present invention. Unless otherwise indicated, all tautomeric forms of the compounds of the invention are within the scope of the invention.

The present invention contemplates that all such compounds, including tautomers, R-and S-enantiomers, diastereomers, (D) -isomers, (L) -isomers, racemic mixtures thereof, and other mixtures thereof, are encompassed within the scope of the present invention.

As used herein, "tautomer" refers to other structural isomers that exist in equilibrium due to migration of hydrogen atoms. For example, in the case where the resulting compound has both properties of a ketone and an unsaturated alcohol, keto-enol tautomerism occurs.

As used herein, the phrase "compound or pharmaceutically acceptable salt" includes hydrates and solvates thereof.

In addition, unless otherwise indicated, the structures described herein include such compounds: which differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the structure of the present invention include replacement of hydrogen by deuterium or tritium, or replacement of carbon by a 13C-or 14C-enriched carbon, all within the scope of the present invention. In some embodiments, a group contains one or more deuterium atoms.

The compounds of formula (I) should also include isotopically labelled forms thereof. Isotopically-labelled forms of compounds having the general formula (I) differ from the compounds only in that one or more atoms of the compound are replaced by one or more atoms having an atomic mass or mass number different from the atomic mass or mass number of the atom usually found in nature. Examples of isotopes which are readily commercially available and which can be incorporated into compounds of formula (I) by known methods include hydrogen, carbon, nitrogen, oxygen, phosphorus, fluorine and chlorine, for example 2H, 3H, 13C, 14C, 15N, 18O, 17O, 31P, 32P, 35S, 18F and 36CI, respectively. Compounds of general formula (I) containing one or more of the above isotopes and/or other isotopes of other atoms, prodrugs thereof or pharmaceutically acceptable salts of any of them are understood to be part of this invention. Isotopically labelled compounds of general formula (I) can be used in a number of advantageous ways. For example, isotopically labeled compounds of formula (I) incorporating a radioisotope, such as 3H or 14C, are useful in drug and/or substrate tissue distribution assays. These two radioactive isotopes, tritium (3H) and carbon-14 (14C), are particularly preferred due to their simplicity of preparation and good detectability. Incorporation of such isotopically labelled compounds into compounds of general formula (I) is therapeutically beneficial due to the higher metabolic stability of heavier isotopes such as deuterium (2H). Higher metabolic stability directly leads to an increased in vivo half-life or a reduced dose, which in most cases represents a preferred embodiment of the invention. Isotopically labeled compounds of general formula (I) can generally be prepared by carrying out the procedures disclosed in the synthetic schemes and associated descriptions in the examples section and preparations section of this document, substituting readily available isotopically labeled reactants for non-isotopically labeled reactants.

The compounds of the present disclosure provided herein also include all polymorphs and pseudopolymorphs of the compounds of formula (I). "polymorphs" are known in the art (see, e.g., J.thermal anal.Cal.64: 37-60(2001)) and are believed to be where the compound of formula (I) is capable of different crystalline phases. The crystalline phases may have different molecular arrangements ("packing polymorphism") and/or conformations ("conformational polymorphism") in the lattice. For example, in two different polymorphs of a compound of formula (I), each polymorph may have the molecules arranged in a different basic crystal system-triclinic, monoclinic, orthorhombic, tetragonal, trigonal, hexagonal or cubic. The term "anhydrate" as used herein is any crystalline form of the compound of formula (I) in which the water molecules are the non-convergent part of the crystal. The anhydrate of the compound of formula (I) can be prepared, for example, by crystallization from a substantially water-free solvent. In one embodiment, the compound of formula (I) is an anhydrate, i.e., as a free base, in which the crystal lattice is substantially free of water molecules and any water molecules present are present as "surface water" (e.g., loosely bound to the surface of the crystal), as those skilled in the art are distinguishable and distinguishable from the water molecules (e.g., hydrates) that are an integral part of the crystal by, for example, thermogravimetric analysis (TGA) and/or Differential Scanning Calorimetry (DSC). In one embodiment, the anhydrate of the compound of formula (I) has less than about 0.2 moles of water, in another embodiment less than about 0.15 moles of water, in another embodiment about 0.12 moles of water, in another embodiment less than about 0.1 moles of water, in another embodiment less than about 0.085 moles of water, in another embodiment less than about 0.075 moles of water, in another embodiment less than about 0.06 moles of water, in another embodiment less than about 0.057 moles of water, in another embodiment less than about 0.05 moles of water, in another embodiment less than about 0.025 moles of water, in another embodiment less than about 0.02 moles of water, in another embodiment less than about 0.01 moles of water, in another embodiment less than about 0.005 moles of water, in another embodiment less than about 0.03 moles of water, and in another embodiment less than about 0.001 moles of water, the presence of surface water is taken into account in each embodiment and each of the embodiments described is based on every 1 mole of compound of formula (I).

The compounds of the present disclosure provided herein also include all solvates of the compounds of formula (I). "solvates" are known in the art and are considered to be the combination, physical association and/or solvation of the compound of formula (I) with solvent molecules. The physical association may comprise varying degrees of ionic and covalent bonding, including hydrogen bonding. When the solvate is in stoichiometric form, there is a fixed ratio of solvent molecules to compound of formula (I), for example when the solvent molecules: the molar ratio of the compounds of formula (I) is 2: 1. 1: 1 or 1: 2, there are a di-solvate, mono-solvate or semi-solvate. In other embodiments, the solvate is in a non-stoichiometric form. For example, crystals of the compound of formula (I) may contain solvent molecules within the structural pores (e.g., channels) of the crystal lattice. In particular examples, the solvate may be isolated, for example, when one or more solvent molecules are incorporated into the crystal lattice of the crystalline solid. Thus "solvate" as used herein includes both solution phase and isolatable solvates. When the crystalline form of the solvate may also be referred to as a "pseudo-polymorph", then the compounds of the present disclosure provided herein also include all pseudo-polymorphs of the compound of formula (I). The compounds of formula (I) of the present disclosure may also exist in solvated forms and with pharmaceutically acceptable solvents such as water, methanol, ethanol and the like, and it is intended that the present disclosure include both solvated and unsolvated forms of the compounds of formula (I). When "hydrate" is associated with a particular subgroup of solvates, i.e. where the solvent molecule is water, then hydrates are included in the solvates of the present invention. In one embodiment, the compounds of formula (I) are present as the monohydrate, i.e. the free base, wherein water: the molar ratio of the compounds of formula (I) is about 1: 1, for example from 0.91 in one embodiment: 1 to 1.09: 1, in another embodiment from 0.94: 1 to 1.06: 1, in another embodiment from 0.97: 1 to 1.03: 1, and in another embodiment from 0.985: 1 to 1.015: each embodiment does not consider any surface water, if any, that may be present. [1013] The preparation of solvates is known in the art. For example j.pharmaceut.sci., 93 (3): 601-611(2004) describes the preparation of solvates of fluconazole (fluconazole) with ethyl acetate and with water. Similar preparations of solvates, hemisolvates, hydrates, etc. are described in aapspharm. Article 12(2004) and chem. comm., pp.603-604 (2001). In one embodiment, a non-limiting method involves dissolving a compound of formula (I) in a desired amount of a desired solvent (organic solvent, water or mixtures thereof) at a temperature of about 20 ℃ to about 25 ℃, cooling the solution at a rate sufficient to form crystals, and isolating the crystals by known methods (e.g., filtration.

The compounds of the present disclosure provided herein also include all co-crystals of the compounds of formula (I). "eutectic" is known in the art and is considered to be a structurally homogeneous crystalline material comprising two or more neutral building blocks in a well-defined stoichiometric amount, e.g., a compound of formula (I) and a coform material. Pharmaceutical 4 (3): 317-322(2007). As used herein, "co-crystal" includes all polymorphs of the co-crystal, i.e., all different crystalline phases of the co-crystal. The main difference between solvates and co-crystals is the physical state of the isolated pure substance. For example, for a two-component system, if one component is a liquid at a temperature of about 25 ℃, crystals containing both components are designated as solvates, and if both components are solids at that temperature, crystals containing both components are designated as co-crystals. Sekhon "Pharmaceutical Co-crystals-AReview," ars. pharm.50 (3): 99-117(2009). In addition, co-crystals and salts may be considered "extrema" on the scale of possible multicomponent structures. Salts are formed by ionization, e.g., by an acid-base reaction or proton donation occurring between the active pharmaceutical ingredient and an acidic or basic substance. Conversely, when the active pharmaceutical ingredient lacks ionizable sites capable of salt formation, the co-crystal may form, for example, hydrogen bonds, π - π or van der Waals interactions between the components through non-ionization. Structural differences between co-crystals, salts and hydrates are exemplified in Crystal Growth & Design9 (6): 2950-2967(2009) are incorporated by reference herein in figures 1 and 2. The preparation of the co-crystals is known in the art, for example as described in the above-cited references and U.S. patent nos. 7452555B2 and 7935817B 2.

In one embodiment, the crystals of the compound of formula (I) comprise hydrochloric acid, tartaric acid, benzenesulfonic acid, toluenesulfonic acid, succinic acid, fumaric acid, citric acid, oxalic acid, benzoic acid, or any mixture thereof in another embodiment, the crystals of the compound of formula (I) comprise hydrochloric acid, benzenesulfonic acid, toluenesulfonic acid, L-tartaric acid, fumaric acid, or any mixture thereof in another embodiment, the co-crystals comprise the compound of formula (I) and hydrochloric acid in another embodiment, the co-crystals comprise the compound of formula (I) and benzenesulfonic acid in another embodiment, the co-crystals comprise the compound of formula (I) and toluenesulfonic acid in another embodiment, the co-crystals comprise the compound of formula (I) and L-tartaric acid in another embodiment, the co-crystals comprise the compound of formula (I) and fumaric acid in another embodiment, the co-crystals comprise about 1 equivalent of the compound of formula (I) and about 0.5 equivalents of fumaric acid in another embodiment, for example, from about 0.3 to about 0.7 equivalents of the co-crystals in one embodiment, the co-crystals comprise about 0.5 equivalents of the compound of formula (I) and about 0.5.5 equivalents of the co-crystals can be determined using differential thermal analysis, from the presence or absence of a spectrum of the co-crystal in another embodiment, from about 0.3 to about 0.7 equivalents of the presence of a single crystal under the condition of a XRD, XPS-X equivalent of a crystalline, XPS-X equivalent of a crystalline, XPS, a crystalline, a.

However, the art recognizes that "the exact classification of compounds as salts or co-crystals is sometimes somewhat ambiguous. "Aakeroy et al, p 321. E.g., aakey, etc. A study is described in which x-ray and neutron diffraction are used to study the hydrogen bonding between urotropine N-oxide and formic acid as a function of temperature, where the exact position of the proton is found to vary with temperature under certain conditions, and the system shows partial proton transfer to the N-oxide group, i.e. the system has intermediate properties between salt and co-crystal. (same as above). In addition, Pop et al describe tiotropium bromide (tiotropium) fumarate as a salt and co-crystal thereof, having 2: 1: 1 stoichiometric cation: anion: co-molding the product. Pop et al "Tiotropium Fumarate: interesting Pharmaceutical Co-crystal, "J.Pharma.Sci.98 (5): 1820-1834(2009). The structure determined by X-ray diffraction is described as "consisting of two monovalent tiotropium bromide cations in combination with a divalent fumarate anion to make a salt, plus non-ionized free fumarate moieties to make a co-crystal" (same as above). Thus, in connection with no undisputable clear distinction between salt and co-crystal, it is to be understood that when the phrase "and combinations thereof" is used in the context of salt and/or co-crystal, it means that a feature attributed to salt and another feature attributed to co-crystal are both present in one embodiment; in another embodiment, there is an intermediate feature between the feature due to the salt and the feature due to the co-crystal.

The compounds disclosed herein also include all Prodrugs of the compounds of formula (I), "Prodrugs" are known in the art and although not necessarily having any pharmaceutical activity per se, are considered to be any covalently bonded carriers that release the active parent Drug in vivo. typically, such Prodrugs are functional derivatives of the compounds of formula (I) which can be readily converted in vivo by, for example, metabolism into the desired compounds of formula (I). conventional procedures for selecting and preparing suitable prodrug derivatives are described, for example, in Drug and Enzyme targets G, Part A, "Method Enzym 112, Academic Press (1985)," diagnosis application of primers, "A Text book of Drug and Development details Chapter No. 5 to No. 191," Krogsga-L sensor and company chemistry (1988), edited by company chemistry, 2. 7. about. D.7. the publication No. 2. the publication No. 7. about. 7. about. polysaccharide-2. about. polysaccharide-7. about. polysaccharide-2. about. polysaccharide-amino acids, 2. about. environmental derivatives.

The invention also includes pharmaceutical compositions comprising prodrugs of compounds of formula (I). Compounds of formula (I) containing free amino, amido, hydroxy or carboxy groups may be converted into prodrugs.

The benzene sulfonamide compound provided by the invention can obviously inhibit islet cell PGE₂The action of promoting the secretion of insulin can be used for preparing the medicaments related to diabetes.

Yet another aspect of an embodiment of the present invention provides a formulation comprising the aforementioned benzenesulfonamide compound, an isomer thereof, or a pharmaceutically acceptable derivative thereof; the pharmaceutically acceptable derivative is selected from the group consisting of pharmaceutically acceptable salts, polymorphs, co-crystals, radiolabeled forms, and combinations thereof.

In another aspect of an embodiment of the present invention there is also provided the use of the aforementioned formulation in the preparation of an mPGES-2 inhibitor.

Yet another aspect of an embodiment of the present invention provides an mPGES-2 inhibitor, comprising: the aforementioned benzenesulfonamide compounds, isomers thereof or pharmaceutically acceptable derivatives thereof, and a pharmaceutically acceptable carrier and/or excipient;

wherein the pharmaceutically acceptable derivative is selected from at least one of a pharmaceutically acceptable salt, polymorph, co-crystal, radiolabeled form, and combinations thereof.

Yet another aspect of an embodiment of the present invention provides the use of the aforementioned benzenesulfonamide compound, an isomer thereof or a pharmaceutically acceptable derivative thereof selected from the group consisting of pharmaceutically acceptable salts, polymorphs, co-crystals, radiolabeled forms and combinations thereof, or the aforementioned mPGES-2 inhibitor, for the manufacture of a medicament for the prevention and/or treatment of diabetes; said drug is capable of inhibiting at least islet cell PGE₂To promote the production and insulin secretion.

In another aspect of the embodiments of the present invention, there is provided a use of the aforementioned benzenesulfonamide compound, its isomer or a pharmaceutically acceptable derivative thereof selected from at least one of pharmaceutically acceptable salts, polymorphs, co-crystals, radiolabeled forms and combinations thereof, or the aforementioned mPGES-2 inhibitor for the preparation of a medicament for the prevention and/or treatment of mPGES-2 target generation.

Yet another aspect of an embodiment of the present invention provides a medicament comprising the aforementioned benzenesulfonamide compound, its isomer, or a pharmaceutically acceptable derivative thereof selected from the group consisting of pharmaceutically acceptable salts, polymorphs, co-crystals, radiolabeled forms, and combinations thereof, or the aforementioned mPGES-2 inhibitor, for use in the treatment and/or prevention of diabetes.

Further, the medicament also comprises a pharmaceutically acceptable carrier and/or excipient. The carrier and/or excipient may be any pharmaceutically acceptable carrier and excipient known to those skilled in the art to be suitable for such use. The term "pharmaceutically acceptable carrier" as used herein has a meaning well known to those skilled in the art and can include any and all solvents, dispersion media, coatings, surfactants, antioxidants, preservatives (e.g., antibacterial agents, antifungal agents), isotonic agents, absorption delaying agents, salts, preservatives, drugs, drug stabilizers, gels, binders, excipients, disintegrants, lubricants, sweeteners, flavoring agents, dyes, the like, and combinations thereof.

Further, the drug is capable of inhibiting islet cell PGE₂And (4) generating.

Further, the drug is capable of promoting insulin secretion.

Furthermore, the dosage form of the medicine comprises injection, oral liquid, capsules, tablets or granules.

Further, the drug of the present invention may be in any form suitable for administration to a patient, for example, the mode of administration of the drug includes subcutaneous administration, oral administration, intramuscular administration, intraperitoneal administration, or the like, but is not limited thereto.

The optimum dose and frequency of administration will depend on the particular condition being treated and its severity; the age, sex, size and weight, diet and general physical condition of the particular patient; other medications that the patient may take; the route of administration; preparing a formula; as well as various other factors known to physicians and others skilled in the art.

Further, the diabetes is type 1 diabetes and type 2 diabetes.

The other aspect of the embodiment of the invention also provides an experimental method and application of the mPGES-2 inhibitor for improving and treating diabetes, and experimental comparison proves that the mPGES-2 inhibitor has the effect of improving and treating diabetes, can be prepared into a medicament through an acceptable carrier, and is used for preventing and treating diabetes.

Specifically, an experimental method for improving and treating diabetes by using an mPGES-2 inhibitor comprises the following steps:

step A, in-vitro enzyme activity experiment:

a1) screening out the effective compound to obtain the compound,

a2) investigating the influence of the compound on the upstream pathway factor cyclooxygenase;

step B, cell assay:

b1) treating mammalian cells with different concentrations of said compound,

b2) culturing said mammalian cells with buffer solutions containing sugars at different concentrations,

b3) culturing mammalian cells using different drugs, alone and in combination with said compounds,

b4) detecting prostaglandin E release from said mammalian cells₂The level of insulin,

b5) subjecting said mammalian cells to prostaglandin E₂Insulin levels and prostaglandin E in mammalian cells not supplemented with the compound₂Insulin levels were compared.

Further, the mammalian cells are islet cells and/or hepatocytes. The mammal is selected from non-primate animal and primate animal.

According to the technical scheme, the mPGES-2 inhibitor is prepared from the provided benzenesulfonamide compound, the isomer of the benzenesulfonamide compound or the pharmaceutically acceptable derivative of the benzenesulfonamide compound, and experiments prove that the benzenesulfonamide compound and the mPGES-2 inhibitor can be used for improving and treating diabetes, and can obviously prove the effect on improving and treating diabetes, and the benzenesulfonamide compound can be prepared into a medicament through an acceptable carrier for preventing and treating diabetes.

In silico screening of Compounds of the invention

Virtual screening of inhibitors of mPGES-2 based on the protein structure of mPGES-2, since the three-dimensional crystal structure of mPGES-2 of human origin has not been reported so far, the crystal structure of mPGES-2 of Cynomolgus monkey (Cynomolgus monkey) is known (PDB ID:1Z9H), and both have an amino acid sequence homology as high as 99.0%. Therefore, the crystal structure of the mPGES-2 of human origin is homologously modeled by using Modeller software with the crystal structure of mPGES-2 of cynomolgus monkey as a template. The process of homologous modeling comprises sequence comparison, determination of a structure conservation area, establishment of a model, optimization, evaluation and the like.

The method comprises the steps of utilizing a Surflex molecule docking module of a Sybyl-X2.1 drug design platform to carry out virtual screening, selecting a Chemdiv small molecule database (which is 100 ten thousand compounds), and utilizing a Compound filtration module to carry out first round screening of 'drug-like rules' on compounds in Chemdiv. Then, an indometacin binding site in the crystal structure of mPGES-2 is selected as an active cavity for virtual screening, and small molecule compounds with a molecular score of 1% of top are screened. Finally, the Surflex molecular docking parameters were restored to default values based on the second round of screening results. And selecting compounds in the target of top500 for manual screening and rechecking, and finally confirming that less than 100 compounds in the target come out.

It will also be appreciated by those skilled in the art that the compounds of the invention may be obtained by methods known to those skilled in the art or by analogous methods. It will also be appreciated that a person skilled in the art will be able to prepare further compounds of the invention, not explicitly specified hereinafter, in a manner analogous to that described hereinafter, by using the appropriate starting components and modifying the synthesis parameters as required.

It will also be appreciated that in the following description, combinations of substituents and/or variables of the general formulae described are permissible only if such combinations result in stable compounds.

It will also be appreciated by those skilled in the art that although these protected derivatives of the compounds of the invention may not be pharmacologically active themselves, they may be administered to a mammal and subsequently metabolized in vivo to form the compounds of the invention which are pharmacologically active. Such derivatives may therefore be referred to as "prodrugs". All prodrugs of the compounds of the present invention are included within the scope of the present invention.

In order to make the objects, technical solutions and advantages of the present invention more apparent, the technical solutions of the present invention are described in further detail below with reference to the accompanying drawings and several preferred embodiments, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all embodiments. All other embodiments, which can be obtained by a person skilled in the art without any inventive step based on the embodiments of the present invention, are within the scope of the present invention. The test methods in the following examples are carried out under conventional conditions without specifying the specific conditions. In addition, the technical features involved in the embodiments of the present invention described below may be combined with each other as long as they do not conflict with each other.