HRP20241378T1 - Karboksi derivati s protuupalnim svojstvima - Google Patents
Karboksi derivati s protuupalnim svojstvima Download PDFInfo
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- HRP20241378T1 HRP20241378T1 HRP20241378TT HRP20241378T HRP20241378T1 HR P20241378 T1 HRP20241378 T1 HR P20241378T1 HR P20241378T T HRP20241378T T HR P20241378TT HR P20241378 T HRP20241378 T HR P20241378T HR P20241378 T1 HRP20241378 T1 HR P20241378T1
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- Croatia
- Prior art keywords
- methyl
- acrylic acid
- oxadiazol
- phenyl
- cyclopropyl
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- 230000003110 anti-inflammatory effect Effects 0.000 title 1
- 125000003178 carboxy group Chemical class [H]OC(*)=O 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 32
- 150000003839 salts Chemical class 0.000 claims 31
- 239000012453 solvate Substances 0.000 claims 20
- 125000005843 halogen group Chemical group 0.000 claims 11
- 239000008194 pharmaceutical composition Substances 0.000 claims 10
- 239000003795 chemical substances by application Substances 0.000 claims 9
- 239000003112 inhibitor Substances 0.000 claims 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- 208000022993 cryopyrin-associated periodic syndrome Diseases 0.000 claims 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 208000011580 syndromic disease Diseases 0.000 claims 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 5
- 230000001363 autoimmune Effects 0.000 claims 5
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 5
- 238000002560 therapeutic procedure Methods 0.000 claims 5
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 4
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 4
- RJKFOVLPORLFTN-LEKSSAKUSA-N Progesterone Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 claims 4
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- 230000001684 chronic effect Effects 0.000 claims 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims 4
- 208000035475 disorder Diseases 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- -1 2-((4-octylpyridin-2-yl)methyl)acrylic acid trifluoroacetic acid salt Chemical compound 0.000 claims 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 3
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- 230000001154 acute effect Effects 0.000 claims 3
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- 201000002215 juvenile rheumatoid arthritis Diseases 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- 108020003175 receptors Proteins 0.000 claims 3
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- 230000008685 targeting Effects 0.000 claims 3
- RUDATBOHQWOJDD-UHFFFAOYSA-N (3beta,5beta,7alpha)-3,7-Dihydroxycholan-24-oic acid Natural products OC1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(O)=O)C)C1(C)CC2 RUDATBOHQWOJDD-UHFFFAOYSA-N 0.000 claims 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 2
- IAKHMKGGTNLKSZ-INIZCTEOSA-N (S)-colchicine Chemical compound C1([C@@H](NC(C)=O)CC2)=CC(=O)C(OC)=CC=C1C1=C2C=C(OC)C(OC)=C1OC IAKHMKGGTNLKSZ-INIZCTEOSA-N 0.000 claims 2
- KSCMHTKJFWCRHJ-UHFFFAOYSA-N 2-[[3-(4-butoxyphenyl)-1,2,4-oxadiazol-5-yl]methyl]prop-2-enoic acid Chemical compound C(CCC)OC1=CC=C(C=C1)C1=NOC(=N1)CC(C(=O)O)=C KSCMHTKJFWCRHJ-UHFFFAOYSA-N 0.000 claims 2
- IPOUXAUBCPEGIH-UHFFFAOYSA-N 2-[[3-[(4-butylphenyl)methyl]-1,2,4-oxadiazol-5-yl]methyl]prop-2-enoic acid Chemical compound C(CCC)C1=CC=C(CC2=NOC(=N2)CC(C(=O)O)=C)C=C1 IPOUXAUBCPEGIH-UHFFFAOYSA-N 0.000 claims 2
- MXXULZUUXSJBAN-UHFFFAOYSA-N 2-[[3-[1-(4-bromophenyl)cyclopropyl]-1,2,4-oxadiazol-5-yl]methyl]prop-2-enoic acid Chemical compound BrC1=CC=C(C=C1)C1(CC1)C1=NOC(=N1)CC(C(=O)O)=C MXXULZUUXSJBAN-UHFFFAOYSA-N 0.000 claims 2
- ANDQEQFQFGKZHR-UHFFFAOYSA-N 2-[[3-[1-[4-(pentafluoro-lambda6-sulfanyl)phenyl]cyclopropyl]-1,2,4-oxadiazol-5-yl]methyl]prop-2-enoic acid Chemical compound FS(C1=CC=C(C=C1)C1(CC1)C1=NOC(=N1)CC(C(=O)O)=C)(F)(F)(F)F ANDQEQFQFGKZHR-UHFFFAOYSA-N 0.000 claims 2
- XBAYZCYLMGAAOC-UHFFFAOYSA-N 2-[[3-[1-[4-(trifluoromethylsulfanyl)phenyl]cyclopropyl]-1,2,4-oxadiazol-5-yl]methyl]prop-2-enoic acid Chemical compound FC(SC1=CC=C(C=C1)C1(CC1)C1=NOC(=N1)CC(C(=O)O)=C)(F)F XBAYZCYLMGAAOC-UHFFFAOYSA-N 0.000 claims 2
- QCHGAHDZXDQDCP-UHFFFAOYSA-N 2-[[3-[4-(pentafluoro-lambda6-sulfanyl)phenyl]-1,2,4-oxadiazol-5-yl]methyl]prop-2-enoic acid Chemical compound FS(C1=CC=C(C=C1)C1=NOC(=N1)CC(C(=O)O)=C)(F)(F)(F)F QCHGAHDZXDQDCP-UHFFFAOYSA-N 0.000 claims 2
- XKFOEZLFLIDKMU-UHFFFAOYSA-N 2-[[5-[(4-chlorophenyl)-difluoromethyl]-1,2,4-oxadiazol-3-yl]methyl]prop-2-enoic acid Chemical compound ClC1=CC=C(C=C1)C(C1=NC(=NO1)CC(C(=O)O)=C)(F)F XKFOEZLFLIDKMU-UHFFFAOYSA-N 0.000 claims 2
- MSYGAHOHLUJIKV-UHFFFAOYSA-N 3,5-dimethyl-1-(3-nitrophenyl)-1h-pyrazole-4-carboxylic acid ethyl ester Chemical compound CC1=C(C(=O)OCC)C(C)=NN1C1=CC=CC([N+]([O-])=O)=C1 MSYGAHOHLUJIKV-UHFFFAOYSA-N 0.000 claims 2
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- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 2
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- 208000018208 Hyperimmunoglobulinemia D with periodic fever Diseases 0.000 claims 2
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- 102000015617 Janus Kinases Human genes 0.000 claims 2
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- 102000002233 Myelin-Oligodendrocyte Glycoprotein Human genes 0.000 claims 2
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- 208000009525 Myocarditis Diseases 0.000 claims 2
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- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 2
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- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 claims 2
- 102000003390 tumor necrosis factor Human genes 0.000 claims 2
- RUDATBOHQWOJDD-UZVSRGJWSA-N ursodeoxycholic acid Chemical compound C([C@H]1C[C@@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)CC1 RUDATBOHQWOJDD-UZVSRGJWSA-N 0.000 claims 2
- 229960001661 ursodiol Drugs 0.000 claims 2
- YLOCGHYTXIINAI-XKUOMLDTSA-N (2s)-2-amino-3-(4-hydroxyphenyl)propanoic acid;(2s)-2-aminopentanedioic acid;(2s)-2-aminopropanoic acid;(2s)-2,6-diaminohexanoic acid Chemical compound C[C@H](N)C(O)=O.NCCCC[C@H](N)C(O)=O.OC(=O)[C@@H](N)CCC(O)=O.OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 YLOCGHYTXIINAI-XKUOMLDTSA-N 0.000 claims 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
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- WHTVZRBIWZFKQO-AWEZNQCLSA-N (S)-chloroquine Chemical compound ClC1=CC=C2C(N[C@@H](C)CCCN(CC)CC)=CC=NC2=C1 WHTVZRBIWZFKQO-AWEZNQCLSA-N 0.000 claims 1
- BBVIDBNAYOIXOE-UHFFFAOYSA-N 1,2,4-oxadiazole Chemical compound C=1N=CON=1 BBVIDBNAYOIXOE-UHFFFAOYSA-N 0.000 claims 1
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- YJWKQZKHPRCDCS-UHFFFAOYSA-N 2-[(3-cycloheptyl-1,2,4-oxadiazol-5-yl)methyl]prop-2-enoic acid Chemical compound C1(CCCCCC1)C1=NOC(=N1)CC(C(=O)O)=C YJWKQZKHPRCDCS-UHFFFAOYSA-N 0.000 claims 1
- DMEDLJNQDIWYHB-UHFFFAOYSA-N 2-[(3-cyclohexyl-1,2,4-oxadiazol-5-yl)methyl]prop-2-enoic acid Chemical compound C1(CCCCC1)C1=NOC(=N1)CC(C(=O)O)=C DMEDLJNQDIWYHB-UHFFFAOYSA-N 0.000 claims 1
- WWKFRXPVBBUVMY-UHFFFAOYSA-N 2-[(3-cyclooctyl-1,2,4-oxadiazol-5-yl)methyl]prop-2-enoic acid Chemical compound C1(CCCCCCC1)C1=NOC(=N1)CC(C(=O)O)=C WWKFRXPVBBUVMY-UHFFFAOYSA-N 0.000 claims 1
- GDVQXNIGPNNLRD-UHFFFAOYSA-N 2-[(3-nonyl-1,2,4-oxadiazol-5-yl)methyl]prop-2-enoic acid Chemical compound C(CCCCCCCC)C1=NOC(=N1)CC(C(=O)O)=C GDVQXNIGPNNLRD-UHFFFAOYSA-N 0.000 claims 1
- XHGHQGWWJGBTOW-UHFFFAOYSA-N 2-[(3-oct-3-ynyl-1,2,4-oxadiazol-5-yl)methyl]prop-2-enoic acid Chemical compound C(CC#CCCCC)C1=NOC(=N1)CC(C(=O)O)=C XHGHQGWWJGBTOW-UHFFFAOYSA-N 0.000 claims 1
- AYCVWQFTTHGTBH-UHFFFAOYSA-N 2-[(3-oct-7-ynyl-1,2,4-oxadiazol-5-yl)methyl]prop-2-enoic acid Chemical compound C(CCCCCC#C)C1=NOC(=N1)CC(C(=O)O)=C AYCVWQFTTHGTBH-UHFFFAOYSA-N 0.000 claims 1
- JFQVEGQTUVGKSY-UHFFFAOYSA-N 2-[(3-octan-2-yl-1,2,4-oxadiazol-5-yl)methyl]prop-2-enoic acid Chemical compound CC(CCCCCC)C1=NOC(=N1)CC(C(=O)O)=C JFQVEGQTUVGKSY-UHFFFAOYSA-N 0.000 claims 1
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- HQNIYWZYASCJCL-UHFFFAOYSA-N 2-[(3-undecyl-1,2,4-oxadiazol-5-yl)methyl]prop-2-enoic acid Chemical compound C(CCCCCCCCCC)C1=NOC(=N1)CC(C(=O)O)=C HQNIYWZYASCJCL-UHFFFAOYSA-N 0.000 claims 1
- MDCSOFJAPKZXTB-UHFFFAOYSA-N 2-[(4,5-dibutyl-1,3-oxazol-2-yl)methyl]prop-2-enoic acid Chemical compound C(CCC)C=1N=C(OC=1CCCC)CC(C(=O)O)=C MDCSOFJAPKZXTB-UHFFFAOYSA-N 0.000 claims 1
- CVMWJOARFZVMTB-UHFFFAOYSA-N 2-[(4-octyl-1,3-oxazol-2-yl)methyl]prop-2-enoic acid Chemical compound C(CCCCCCC)C=1N=C(OC=1)CC(C(=O)O)=C CVMWJOARFZVMTB-UHFFFAOYSA-N 0.000 claims 1
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- IECGQSROBXYODT-UHFFFAOYSA-N 2-[(5-octyl-1,2-oxazol-3-yl)methyl]prop-2-enoic acid Chemical compound C(CCCCCCC)C1=CC(=NO1)CC(C(=O)O)=C IECGQSROBXYODT-UHFFFAOYSA-N 0.000 claims 1
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- NYGMBNIJQOPMIR-UHFFFAOYSA-N 2-[1-[3-[1-[4-(trifluoromethyl)phenyl]cyclopropyl]-1,2,4-oxadiazol-5-yl]cyclopropyl]prop-2-enoic acid Chemical compound FC(C1=CC=C(C=C1)C1(CC1)C1=NOC(=N1)C1(CC1)C(C(=O)O)=C)(F)F NYGMBNIJQOPMIR-UHFFFAOYSA-N 0.000 claims 1
- HRRKMHFHSHTDBZ-UHFFFAOYSA-N 2-[1-[3-[difluoro-[4-(trifluoromethyl)phenyl]methyl]-1,2,4-oxadiazol-5-yl]cyclopropyl]prop-2-enoic acid Chemical compound FC(C1=NOC(=N1)C1(CC1)C(C(=O)O)=C)(C1=CC=C(C=C1)C(F)(F)F)F HRRKMHFHSHTDBZ-UHFFFAOYSA-N 0.000 claims 1
- ZUKFBHPVYIOEEG-RORPREDISA-N 2-[[3-(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecadeuteriooctyl)-1,2,4-oxadiazol-5-yl]methyl]prop-2-enoic acid Chemical compound C(C(C(C(C(C(C(C([2H])([2H])[2H])([2H])[2H])([2H])[2H])([2H])[2H])([2H])[2H])([2H])[2H])([2H])[2H])(C1=NOC(=N1)CC(C(=O)O)=C)([2H])[2H] ZUKFBHPVYIOEEG-RORPREDISA-N 0.000 claims 1
- ORYDFCWSCHWSKL-UHFFFAOYSA-N 2-[[3-(2-methylheptan-2-yl)-1,2,4-oxadiazol-5-yl]methyl]prop-2-enoic acid Chemical compound CC(C)(CCCCC)C1=NOC(=N1)CC(C(=O)O)=C ORYDFCWSCHWSKL-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4245—Oxadiazoles
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/24—Radicals substituted by oxygen atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
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| EP20205768 | 2020-11-04 | ||
| EP20830293.5A EP4081511B3 (en) | 2019-12-23 | 2020-12-23 | Carboxy derivatives with antiinflammatory properties |
| PCT/GB2020/053357 WO2021130492A1 (en) | 2019-12-23 | 2020-12-23 | Carboxy derivatives with antiinflammatory properties |
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| HRP20241378T1 true HRP20241378T1 (hr) | 2025-01-03 |
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| MX2021013299A (es) | 2019-04-30 | 2022-01-31 | Sitryx Therapeutics Ltd | Derivados de acido itaconico y usos de estos en el tratamiento de una enfermedad inflamatoria asociada con una respuesta inmunitaria indeseable. |
| WO2020232247A1 (en) | 2019-05-14 | 2020-11-19 | Provention Bio, Inc. | Methods and compositions for preventing type 1 diabetes |
| IL298999A (en) | 2020-06-11 | 2023-02-01 | Provention Bio Inc | Methods and compositions for the prevention of type 1 diabetes |
| EP4192821A1 (en) | 2020-08-05 | 2023-06-14 | Sitryx Therapeutics Limited | Alpha,beta unsaturated methacrylic esters with anti-inflammatory properties |
| EP4330231A1 (en) * | 2021-04-26 | 2024-03-06 | Sitryx Therapeutics Limited | 2-methylene-4-oxo-butanoic acid drivatives for the treatment of inflammation |
| JP2024520444A (ja) | 2021-05-24 | 2024-05-24 | プロヴェンション・バイオ・インコーポレイテッド | 1型糖尿病を治療するための方法 |
| EP4359390A1 (en) * | 2021-06-22 | 2024-05-01 | Sitryx Therapeutics Limited | Acrylamide derivatives useful as anti-inflammatory agents |
| CN113499453B (zh) * | 2021-07-20 | 2022-10-21 | 徐州医科大学 | 自噬抑制及抗炎联合温合光热诊疗剂及其制备方法与应用 |
| US20240360067A1 (en) | 2021-08-11 | 2024-10-31 | Sitryx Therapeutics Limited | Derivatives of itaconic acid and their use as anti-inflammatory agents |
| AU2023287566A1 (en) | 2022-06-22 | 2025-01-16 | Sitryx Therapeutics Limited | Oxadiazole derivatives, preparation process thereof and their use in treating inflammatory diseases |
| WO2024089421A1 (en) | 2022-10-25 | 2024-05-02 | Sitryx Therapeutics Limited | Tetrazole derivatives |
| CN120712258A (zh) | 2022-12-15 | 2025-09-26 | 西特瑞治疗有限公司 | 用于治疗或预防炎性疾病或与不良免疫反应相关的疾病的取代吡啶类化合物 |
| KR102864655B1 (ko) * | 2023-01-19 | 2025-09-29 | 대한민국 | 뎅기바이러스 감염에 의한 질환의 예방 또는 치료용 약학적 조성물 |
| CN115819186B (zh) * | 2023-02-14 | 2023-05-16 | 广东银珠医药科技有限公司 | 一种3,5-二氯苯甲醇的新型制备方法 |
| CN117205194A (zh) * | 2023-05-10 | 2023-12-12 | 苏州大学 | 衣康酸或其衍生物在制备预防或治疗急性移植物抗宿主病药物中的应用 |
| CN116725998A (zh) * | 2023-07-20 | 2023-09-12 | 中国科学技术大学 | 特立氟胺在抑制nlrp3炎症小体活化中的应用 |
| CN119792264B (zh) * | 2025-03-14 | 2025-06-10 | 华中科技大学同济医学院附属同济医院 | 丁酰肼在制备预防或治疗copd的药物中的应用 |
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| WO1995011235A1 (en) * | 1993-10-20 | 1995-04-27 | The Upjohn Company | Pyrimidinones as antiarthritic and anti-inflammatories |
| US6566384B1 (en) * | 1996-08-07 | 2003-05-20 | Darwin Discovery Ltd. | Hydroxamic and carboxylic acid derivatives having MMP and TNF inhibitory activity |
| TW201206429A (en) * | 2010-07-08 | 2012-02-16 | Merck Serono Sa | Substituted oxadiazole derivatives |
| KR101861883B1 (ko) * | 2010-12-06 | 2018-05-28 | 글락소 그룹 리미티드 | Lp-PLA₂에 의해 매개되는 질환 또는 상태의 치료에 사용하기 위한 피리미디논 화합물 |
| KR102085557B1 (ko) | 2013-03-14 | 2020-03-06 | 엘커메스 파마 아일랜드 리미티드 | 푸마레이트의 프로드럭 및 다양한 질환을 치료하는데 있어서의 이들의 용도 |
| WO2014152263A1 (en) * | 2013-03-15 | 2014-09-25 | Karyopharm Therapeutics Inc. | Exo olefin-containing nuclear transport modulators and uses thereof |
| AU2014290368B2 (en) * | 2013-07-18 | 2019-07-11 | Baylor College Of Medicine | Methods and compositions for treatment of muscle wasting, muscle weakness, and/or cachexia |
| CN103923105B (zh) * | 2014-04-17 | 2016-08-24 | 北京大学 | 2-中氮茚甲酰胺类化合物及其制备和用途 |
| EP3416634A4 (en) | 2016-02-15 | 2019-10-09 | Artyomov, Maxim | IMMUNOMODULATORY AGENTS AND METHOD FOR USE THEREOF |
| WO2019036509A1 (en) | 2017-08-14 | 2019-02-21 | Washington University | METHODS AND COMPOSITIONS FOR TREATING DISEASES ASSOCIATED WITH CANCER, INFLAMMATION OR IMMUNE RESPONSE |
| CN110731955B (zh) | 2019-10-28 | 2023-05-02 | 中山大学 | 衣康酸二甲酯在预防和治疗溃疡性结肠炎及其癌变中的应用 |
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