NO323136B1 - 3-metylen steroid derivater, anvendelse derav og farmasoytisk preparat. - Google Patents
3-metylen steroid derivater, anvendelse derav og farmasoytisk preparat. Download PDFInfo
- Publication number
- NO323136B1 NO323136B1 NO20022521A NO20022521A NO323136B1 NO 323136 B1 NO323136 B1 NO 323136B1 NO 20022521 A NO20022521 A NO 20022521A NO 20022521 A NO20022521 A NO 20022521A NO 323136 B1 NO323136 B1 NO 323136B1
- Authority
- NO
- Norway
- Prior art keywords
- methylene
- methyl
- alkyl
- norpregn
- double bond
- Prior art date
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- 125000000217 alkyl group Chemical group 0.000 claims abstract description 19
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- 230000002401 inhibitory effect Effects 0.000 description 1
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- PBGKTOXHQIOBKM-FHFVDXKLSA-N insulin (human) Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@H]1CSSC[C@H]2C(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@H](C(=O)N[C@H](C(N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=3C=CC(O)=CC=3)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC=3C=CC(O)=CC=3)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=3C=CC(O)=CC=3)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=3NC=NC=3)NC(=O)[C@H](CO)NC(=O)CNC1=O)C(=O)NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(O)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O)=O)CSSC[C@@H](C(N2)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C(C)C)NC(=O)[C@@H](NC(=O)CN)[C@@H](C)CC)[C@@H](C)CC)[C@@H](C)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)CC=1C=CC=CC=1)C(C)C)C1=CN=CN1 PBGKTOXHQIOBKM-FHFVDXKLSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 210000004153 islets of langerhan Anatomy 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
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- 239000008101 lactose Substances 0.000 description 1
- 210000000265 leukocyte Anatomy 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 1
- 239000007922 nasal spray Substances 0.000 description 1
- 229940097496 nasal spray Drugs 0.000 description 1
- 238000003305 oral gavage Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000757 progestagenic effect Effects 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 210000003079 salivary gland Anatomy 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 208000001050 sialadenitis Diseases 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Chemical class 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 229940037128 systemic glucocorticoids Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229960000814 tetanus toxoid Drugs 0.000 description 1
- WZDGZWOAQTVYBX-XOINTXKNSA-N tibolone Chemical compound C([C@@H]12)C[C@]3(C)[C@@](C#C)(O)CC[C@H]3[C@@H]1[C@H](C)CC1=C2CCC(=O)C1 WZDGZWOAQTVYBX-XOINTXKNSA-N 0.000 description 1
- 229960001023 tibolone Drugs 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 210000001364 upper extremity Anatomy 0.000 description 1
- 230000002485 urinary effect Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
- C07J71/0005—Oxygen-containing hetero ring
- C07J71/001—Oxiranes
-
- 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
-
- 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
-
- 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]
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0051—Estrane derivatives
- C07J1/0066—Estrane derivatives substituted in position 17 beta not substituted in position 17 alfa
- C07J1/007—Estrane derivatives substituted in position 17 beta not substituted in position 17 alfa the substituent being an OH group free esterified or etherified
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0051—Estrane derivatives
- C07J1/0081—Substituted in position 17 alfa and 17 beta
- C07J1/0088—Substituted in position 17 alfa and 17 beta the substituent in position 17 alfa being an unsaturated hydrocarbon group
- C07J1/0096—Alkynyl derivatives
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99204000 | 1999-11-29 | ||
| PCT/EP2000/011787 WO2001040253A2 (en) | 1999-11-29 | 2000-11-23 | 3-methylene steroid derivative for the treatment of autoimmune diseases |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20022521D0 NO20022521D0 (no) | 2002-05-28 |
| NO20022521L NO20022521L (no) | 2002-05-28 |
| NO323136B1 true NO323136B1 (no) | 2007-01-08 |
Family
ID=8240918
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20022521A NO323136B1 (no) | 1999-11-29 | 2002-05-28 | 3-metylen steroid derivater, anvendelse derav og farmasoytisk preparat. |
Country Status (30)
| Country | Link |
|---|---|
| US (2) | US6579864B1 (ru) |
| EP (1) | EP1240179B1 (ru) |
| JP (1) | JP2003517472A (ru) |
| KR (1) | KR100720326B1 (ru) |
| CN (1) | CN1254479C (ru) |
| AR (1) | AR033503A1 (ru) |
| AT (1) | ATE319732T1 (ru) |
| AU (1) | AU778773B2 (ru) |
| BR (1) | BR0015950A (ru) |
| CA (1) | CA2391096A1 (ru) |
| CO (1) | CO5251432A1 (ru) |
| CY (1) | CY1106088T1 (ru) |
| CZ (1) | CZ20021837A3 (ru) |
| DE (1) | DE60026608T2 (ru) |
| DK (1) | DK1240179T3 (ru) |
| ES (1) | ES2259624T3 (ru) |
| HK (1) | HK1047595B (ru) |
| HU (1) | HUP0203596A3 (ru) |
| IL (2) | IL149412A0 (ru) |
| MX (1) | MXPA02005334A (ru) |
| NO (1) | NO323136B1 (ru) |
| NZ (1) | NZ518756A (ru) |
| PE (1) | PE20010980A1 (ru) |
| PL (1) | PL355968A1 (ru) |
| PT (1) | PT1240179E (ru) |
| RU (1) | RU2248358C2 (ru) |
| SK (1) | SK285398B6 (ru) |
| TW (1) | TWI265167B (ru) |
| WO (1) | WO2001040253A2 (ru) |
| ZA (1) | ZA200203455B (ru) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI265167B (en) * | 1999-11-29 | 2006-11-01 | Akzo Nobel Nv | 3-methylene steroid derivatives |
| WO2005117968A2 (en) | 2004-04-14 | 2005-12-15 | Genentech, Inc. | Compositions and methods comprising an egfl7 antagonist for modulating vascular development |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1085035A (en) * | 1913-05-01 | 1914-01-20 | George H Greimann | Ditch-digging machine. |
| US1171221A (en) * | 1915-12-13 | 1916-02-08 | Charles Ephriam Marion | Combination-tool. |
| US3213117A (en) * | 1963-07-03 | 1965-10-19 | Syntex Corp | Process for preparation of delta1(10)-5alpha-estren-17beta-ol-2-one and derivatives thereof |
| NL299654A (ru) * | 1963-10-23 | |||
| US4701450A (en) * | 1984-03-21 | 1987-10-20 | Akzo N.V. | Steroids for use as immunomodulators |
| DE3560449D1 (en) | 1984-03-29 | 1987-09-17 | Ciba Geigy Ag | Substituted 1-propanoles, process for their production, chloroformic-acid esters ad their use |
| GB8513723D0 (en) * | 1985-05-31 | 1985-07-03 | Erba Farmitalia | 11-beta substituted steroids |
| IE63051B1 (en) | 1989-03-18 | 1995-03-22 | Akzo Nv | Pharmaceutical composition which contains a pharmaceutically suitable carrier and the compound having the structure (7alpha, 17alpha)-17-Hydroxy-7-methyl-19-nor-17-pregn-5(10)-en-20-yn- 3-one |
| TWI265167B (en) * | 1999-11-29 | 2006-11-01 | Akzo Nobel Nv | 3-methylene steroid derivatives |
-
2000
- 2000-11-14 TW TW089124108A patent/TWI265167B/zh not_active IP Right Cessation
- 2000-11-23 PL PL00355968A patent/PL355968A1/xx not_active Application Discontinuation
- 2000-11-23 WO PCT/EP2000/011787 patent/WO2001040253A2/en active IP Right Grant
- 2000-11-23 KR KR1020027006843A patent/KR100720326B1/ko not_active IP Right Cessation
- 2000-11-23 EP EP00988758A patent/EP1240179B1/en not_active Expired - Lifetime
- 2000-11-23 MX MXPA02005334A patent/MXPA02005334A/es active IP Right Grant
- 2000-11-23 CA CA002391096A patent/CA2391096A1/en not_active Abandoned
- 2000-11-23 SK SK727-2002A patent/SK285398B6/sk unknown
- 2000-11-23 IL IL14941200A patent/IL149412A0/xx active IP Right Grant
- 2000-11-23 CZ CZ20021837A patent/CZ20021837A3/cs unknown
- 2000-11-23 PT PT00988758T patent/PT1240179E/pt unknown
- 2000-11-23 RU RU2002117297/04A patent/RU2248358C2/ru not_active IP Right Cessation
- 2000-11-23 AT AT00988758T patent/ATE319732T1/de not_active IP Right Cessation
- 2000-11-23 US US10/148,247 patent/US6579864B1/en not_active Expired - Fee Related
- 2000-11-23 DK DK00988758T patent/DK1240179T3/da active
- 2000-11-23 NZ NZ518756A patent/NZ518756A/en unknown
- 2000-11-23 ES ES00988758T patent/ES2259624T3/es not_active Expired - Lifetime
- 2000-11-23 DE DE60026608T patent/DE60026608T2/de not_active Expired - Fee Related
- 2000-11-23 BR BR0015950-6A patent/BR0015950A/pt not_active Application Discontinuation
- 2000-11-23 HU HU0203596A patent/HUP0203596A3/hu unknown
- 2000-11-23 JP JP2001541008A patent/JP2003517472A/ja active Pending
- 2000-11-23 AU AU25087/01A patent/AU778773B2/en not_active Ceased
- 2000-11-23 CN CNB008163561A patent/CN1254479C/zh not_active Expired - Fee Related
- 2000-11-28 AR ARP000106246A patent/AR033503A1/es unknown
- 2000-11-28 CO CO00090980A patent/CO5251432A1/es not_active Application Discontinuation
- 2000-11-29 PE PE2000001274A patent/PE20010980A1/es not_active Application Discontinuation
-
2002
- 2002-04-30 IL IL149412A patent/IL149412A/en not_active IP Right Cessation
- 2002-04-30 ZA ZA200203455A patent/ZA200203455B/xx unknown
- 2002-05-28 NO NO20022521A patent/NO323136B1/no unknown
- 2002-12-18 HK HK02109166.7A patent/HK1047595B/zh not_active IP Right Cessation
-
2003
- 2003-04-28 US US10/424,399 patent/US20040043972A1/en not_active Abandoned
-
2006
- 2006-05-16 CY CY20061100629T patent/CY1106088T1/el unknown
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