CA2599470A1 - Anti-inflammatory compounds - Google Patents
Anti-inflammatory compounds Download PDFInfo
- Publication number
- CA2599470A1 CA2599470A1 CA002599470A CA2599470A CA2599470A1 CA 2599470 A1 CA2599470 A1 CA 2599470A1 CA 002599470 A CA002599470 A CA 002599470A CA 2599470 A CA2599470 A CA 2599470A CA 2599470 A1 CA2599470 A1 CA 2599470A1
- Authority
- CA
- Canada
- Prior art keywords
- substituted
- nmr
- formula
- compound
- broad
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- 150000001875 compounds Chemical class 0.000 title claims description 161
- 230000003110 anti-inflammatory effect Effects 0.000 title description 7
- 229940123142 Steroid sulfatase inhibitor Drugs 0.000 claims abstract description 60
- 238000011282 treatment Methods 0.000 claims abstract description 26
- 208000027866 inflammatory disease Diseases 0.000 claims abstract description 8
- 239000003814 drug Substances 0.000 claims abstract description 3
- 238000002360 preparation method Methods 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 41
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 6
- 229940121363 anti-inflammatory agent Drugs 0.000 claims description 3
- 239000002260 anti-inflammatory agent Substances 0.000 claims description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 164
- 239000000203 mixture Substances 0.000 description 117
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 116
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 72
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 69
- 239000002904 solvent Substances 0.000 description 68
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 65
- 239000000243 solution Substances 0.000 description 65
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- 125000000753 cycloalkyl group Chemical group 0.000 description 56
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 54
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- 229910052799 carbon Inorganic materials 0.000 description 44
- 125000004432 carbon atom Chemical group C* 0.000 description 44
- 238000001704 evaporation Methods 0.000 description 43
- 230000008020 evaporation Effects 0.000 description 43
- 238000005160 1H NMR spectroscopy Methods 0.000 description 41
- 125000000217 alkyl group Chemical group 0.000 description 39
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- 229910052739 hydrogen Inorganic materials 0.000 description 33
- -1 substituted - thienyl Chemical group 0.000 description 31
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- 125000003118 aryl group Chemical group 0.000 description 11
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 10
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 10
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide Chemical compound CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 9
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- 125000003545 alkoxy group Chemical group 0.000 description 8
- 206010068168 androgenetic alopecia Diseases 0.000 description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 8
- 239000012074 organic phase Substances 0.000 description 8
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 8
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 8
- 235000017557 sodium bicarbonate Nutrition 0.000 description 8
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- 125000001544 thienyl group Chemical group 0.000 description 8
- 210000001519 tissue Anatomy 0.000 description 8
- UQRLSJLFAHCJBF-UHFFFAOYSA-N 3,5-bis(trifluoromethyl)benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 UQRLSJLFAHCJBF-UHFFFAOYSA-N 0.000 description 7
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- 230000001419 dependent effect Effects 0.000 description 7
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- 150000003840 hydrochlorides Chemical class 0.000 description 7
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- 125000003386 piperidinyl group Chemical group 0.000 description 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 6
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- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
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- 239000013543 active substance Substances 0.000 description 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 6
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
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- 206010039792 Seborrhoea Diseases 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 5
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 description 5
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 description 5
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
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- DNXHEGUUPJUMQT-UHFFFAOYSA-N (+)-estrone Natural products OC1=CC=C2C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 DNXHEGUUPJUMQT-UHFFFAOYSA-N 0.000 description 4
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Emergency Medicine (AREA)
- Transplantation (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Steroid Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0505541.3 | 2005-03-17 | ||
| GBGB0505541.3A GB0505541D0 (en) | 2005-03-17 | 2005-03-17 | Organic compounds |
| PCT/EP2006/002382 WO2006097292A1 (en) | 2005-03-17 | 2006-03-15 | Anti-inflammatory compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2599470A1 true CA2599470A1 (en) | 2006-09-21 |
Family
ID=34531452
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002599470A Abandoned CA2599470A1 (en) | 2005-03-17 | 2006-03-15 | Anti-inflammatory compounds |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20090227620A1 (enExample) |
| EP (1) | EP1861098A1 (enExample) |
| JP (1) | JP2008533079A (enExample) |
| KR (1) | KR20070113226A (enExample) |
| CN (1) | CN101137375A (enExample) |
| AU (1) | AU2006224796A1 (enExample) |
| BR (1) | BRPI0607795A2 (enExample) |
| CA (1) | CA2599470A1 (enExample) |
| GB (1) | GB0505541D0 (enExample) |
| MX (1) | MX2007011320A (enExample) |
| RU (1) | RU2007138263A (enExample) |
| WO (1) | WO2006097292A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EA200900960A1 (ru) * | 2007-01-31 | 2010-02-26 | Новартис Аг | Производные пиперидинацетамида для лечения воспалительных или аллергических заболеваний |
| CA2698814A1 (en) | 2007-09-17 | 2009-03-26 | Preglem S.A. | Treatment of oestrogen dependant conditions in pre-menopausal women |
| TW200936136A (en) * | 2008-01-28 | 2009-09-01 | Sanofi Aventis | Tetrahydroquinoxaline urea derivatives, their preparation and their therapeutic application |
| ES2555260T3 (es) | 2010-06-15 | 2015-12-30 | Bayer Intellectual Property Gmbh | Derivados de diamida de ácido antranílico |
| CN102657642B (zh) * | 2012-04-24 | 2014-01-15 | 广东省农业科学院兽医研究所 | Irosustat在制备抗柔嫩艾美耳球虫药物中的应用 |
| CA2874621A1 (en) | 2012-05-22 | 2013-11-28 | Genentech, Inc. | N-substituted benzamides and their use in the treatment of pain |
| CN107417601A (zh) * | 2017-04-06 | 2017-12-01 | 成都弥贝生物科技有限公司 | 具有抗菌活性的取代2‑酰胺磺酰基‑4,6‑芳基吡啶 |
| KR102458689B1 (ko) * | 2020-07-08 | 2022-10-25 | 원광대학교산학협력단 | 피페리딘 화합물 및 이의 제조 방법 |
| WO2025079965A1 (ko) * | 2023-10-10 | 2025-04-17 | 주식회사 넥시온바이오텍 | 치주 질환의 예방 또는 치료용 조성물 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9807779D0 (en) * | 1998-04-09 | 1998-06-10 | Ciba Geigy Ag | Organic compounds |
| GB0020498D0 (en) * | 2000-08-18 | 2000-10-11 | Sterix Ltd | Compound |
| US6986938B2 (en) * | 2001-10-03 | 2006-01-17 | A & A Manufacturing Co., Inc. | Bellows with molded panels |
| AR037097A1 (es) * | 2001-10-05 | 2004-10-20 | Novartis Ag | Compuestos acilsulfonamidas, composiciones farmaceuticas y el uso de dichos compuestos para la preparacion de un medicamento |
| AR039156A1 (es) * | 2002-03-28 | 2005-02-09 | Novartis Ag | Amidas del acido piperidinilamino sulfamico o piperazinil sulfamico y su uso para la manufactura de un medicamento en enfermedades mediadas por la accion de la sulfatasa esteroide |
| AR041952A1 (es) * | 2002-11-14 | 2005-06-01 | Novartis Ag | N-sulfonilaminotiazol |
-
2005
- 2005-03-17 GB GBGB0505541.3A patent/GB0505541D0/en not_active Ceased
-
2006
- 2006-03-15 JP JP2008501223A patent/JP2008533079A/ja active Pending
- 2006-03-15 EP EP06707567A patent/EP1861098A1/en not_active Withdrawn
- 2006-03-15 CA CA002599470A patent/CA2599470A1/en not_active Abandoned
- 2006-03-15 AU AU2006224796A patent/AU2006224796A1/en not_active Abandoned
- 2006-03-15 CN CNA2006800080245A patent/CN101137375A/zh active Pending
- 2006-03-15 US US11/908,895 patent/US20090227620A1/en not_active Abandoned
- 2006-03-15 RU RU2007138263/15A patent/RU2007138263A/ru not_active Application Discontinuation
- 2006-03-15 BR BRPI0607795-1A patent/BRPI0607795A2/pt not_active IP Right Cessation
- 2006-03-15 KR KR1020077021073A patent/KR20070113226A/ko not_active Withdrawn
- 2006-03-15 MX MX2007011320A patent/MX2007011320A/es not_active Application Discontinuation
- 2006-03-15 WO PCT/EP2006/002382 patent/WO2006097292A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0607795A2 (pt) | 2009-06-13 |
| MX2007011320A (es) | 2007-11-08 |
| US20090227620A1 (en) | 2009-09-10 |
| AU2006224796A1 (en) | 2006-09-21 |
| JP2008533079A (ja) | 2008-08-21 |
| CN101137375A (zh) | 2008-03-05 |
| KR20070113226A (ko) | 2007-11-28 |
| WO2006097292A1 (en) | 2006-09-21 |
| EP1861098A1 (en) | 2007-12-05 |
| GB0505541D0 (en) | 2005-04-27 |
| RU2007138263A (ru) | 2009-04-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |