http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EA-000829-B1
Outgoing Links
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|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d202e9e866984fe229f6facc38f1d740 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P13-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P15-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P5-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P5-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-505 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-506 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4545 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4709 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-495 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-496 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5395 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P13-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P15-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4375 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4427 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4439 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-445 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4178 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4184 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-403 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4045 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-404 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-41 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P5-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P5-24 |
| filingDate | 1996-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_67a62217d325a7d5902e89ac87daf077 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3e4130115804946d77cfa589dabd50cb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_56673beaf696abadb2871f718b98fc00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_efe63c03652e56e1c5738f594d4e8318 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da8e9095539a6fda6525b721fcb5716d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_409c19b25b481028306447cd97a0d225 |
| publicationDate | 2000-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EA-000829-B1 |
| titleOfInvention | Antagonists gonadotropin-releasing factor |
| abstract | 1. A compound of the formula wherein A is C1-C6 alkyl, substituted C1-C6 alkyl C3-C7 cycloalkyl, substituted C3-C7 cycloalkyl, C3-C6 alkenyl, substituted C3-C6 alkenyl, C3-C6 alkynyl, substituted C3-C6 alkynyl, C1-C6 alkoxy, or C0-C5 alkyl-S(O)n-C0-C5 alkyl, C0-C5 alkyl-O-C0-C5 alkyl, C0-C5 alkyl-NR18- C0-C5 alkyl where R18 and the C0-C5 alkyl can be joined to form a ring, or a single bond. R0 is hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, wherein the substituents are as defined below; aryl, substituted aryl, aralkyl or substituted aralkyl, wherein the substituents are as defined for R3, R4 and R5; R1 is R2 is hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, aralkyl, substituted aralkyl, aryl, substituted aryl, alkyl-OR11, C1-C6(NR11R12), C1-C6(CONR11R12) or C(NR11R12)NH; R2 and A taken together form a ring of 5-7 atoms; ; R3, R4 and R5 are independently hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, CN, nitro, C1-C3 perfluoroalkyl, C1-C3 perfluoroalkoxy, aryl, substituted aryl, aralkyl, substituted aralkyl, R11O(CH2)p-, R11C(O)O(CH2)p-, R11OC(O)(CH2)p-, -(CH2)pS(O)nR17-, -(CH2)pC(O)NR11R12 or halogen; wherein R17 is hydrogen, C1-C6 alkyl, C1-C3 perfluoroalkyl, aryl or substituted aryl; R3 and R4 taken together form a carbocyclic ring of 3-7 carbon atoms or a heterocyclic ring containing 1-3 heteroatoms selected from N, O and S; R6 is hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, aryl, substituted aryl, C1-C3 perfluoroalkyl, CN, NO2, halogen, R11O(CH2)p-, NR12C(O)R11, NR12C(O)NR11R12 or SOnR11; R7 is hydrogen, C1-C6 alkyl, or substituted C1-C6 alkyl, unless X is hydrogen or halogen, then R7 is absent; ; R8 is C(O)OR9, C(O)N R11R12, N R11R12, C(O) R11, NR12C(O)R11, NR12C(O)N R11R12, NR12 S(O)2R11, NR12S(O)2N R11R12, OC(O)R11, OC(O)N R11R12, OR11, SOnR11, S(O)nN R11R12, C1-C6 alkyl or substituted C1-C6 alkyl; or R7 and R8 taken together form a heterocyclic ring containing one or more heteroatoms selected from N, O or S which can be optionally substituted by R3, R4 and R5, unless X is hydrogen or halogen, then R8 is absent; R9 and R9a are independently hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl; aryl or substituted aryl, aralkyl or substituted aralkyl when m#0; or R9 and R9a taken together form a carbocyclic ring of 3-7 atoms or when m#0 R9 and A taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms when m#0; or R10 and R10a are independently hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, aryl, substituted aryl, aralkyl or substituted aralkyl; or R10 and R10a taken together form a carbocyclic ring of 3-7 atoms or R9 and R10 taken together form a carbocyclic ring of 3-7 carbon atoms or a heterocyclic ring containing one or more heteroatoms when m#0; or R9 and R2 taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms when m#0; or R10 and R2 taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms; R10 and A taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms; or R11 and R12 are independently hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, aryl, substituted aryl, aralkyl, substituted aralkyl, a carbocyclic ring of 3-7 atoms or a substituted carbocyclic ring containing 3-7 atoms; R11 and R12 taken together can form an optionally substituted ring of 3 7 atoms; R13 is hydrogen, OH, NR7R8, NR11SO2(C1-C6 alkyl), NR11SO2 (substituted C1-C6 alkyl), NR11SO2(aryl), NR11SO2(substituted aryl), NR11SO2(C1-C3 perfluoroalkyl); SO2NR11(C1-C6 alkyl), SO2NR11 (substituted C1-C6 alkyl), SO2NR11(aryl), SO2NR11(substituted aryl), SO2NR11(C1-C3 perfluoroalkyl); SO2NR11(C(O) C1-C6 alkyl); SO2NR11(C(O)-substituted C1-C6 alkyl); SO2NR11(C(O) aryl); SO2NR11(C(O)-substituted aryl); S(O)n(C1-C6 alkyl); S(O)n ( substituted C1-C6 alkyl), S(O)n(aryl), S(O)n(substituted aryl), C1-C3 perfluoroalkyl, C1-C3 perfluoroalkoxy, C1-C6 alkoxy, substituted C1-C6 alkoxy, COOH, halogen, NO2 or CN; R14 and R15 are independently hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, CN, nitro, C1-C3 perfluoroalkyl, C1-C3 perfluoroalkoxy, aryl, substituted aryl, aralkyl, substituted aralkyl, R11O(CH2)p-,R11C(O)O(CH2)p-, R11OC(O)(CH2)p-, -(CH2)pS(O)nR17, -(CH2)pC(O)NR11R12 or halogen; wherein R17 is hydrogen, C1-C6 alkyl, C1-C3 perfluoroalkyl, aryl or substituted aryl; R16 is hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, or N(R11R12); R18 is hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, C(O)OR9, C(O)NR11R12, C(O)R11, S(O)nR11; R19 is either the definition of R13 or R14; X is hydrogen, halogen, N, O, S(O)n. C(O), (C R11R12)p; C2-C6 alkenyl, substituted C2-C6 alkenyl, C2-C6 alkynyl, or substituted C2-C6 alkynyl; when X is hydrogen or halogen, R7 and R8 are absent; when X is O, S(O)n, C(O), orC R11R12 only R7 or R is possible; Zis O, S, or NR11; m is 0-3; n is 0-2; p is 0-4; and wherein the alkyl, alkenyl and alkynyl substituents are selected from C1-C6 alkyl, C3-C7 cycloalkyl, aryl, substituted aryl, aralkyl, substituted aralkyl, hydroxy, oxo, cyano, C1-C6 alkoxy, fluoro, C(O)OR11, aryl C1-C3 alkoxy, substituted aryl C1-C3 alkoxy, and the aryl substituents are as defined for R3, R4 and R5; or a pharmaceutically acceptable addition salt and/or hydrate thereof, or where applicable, a geometric or optical isomer or racemic mixture thereof. 2. The compound according to claim 1 of the formula: wherein R1, R3, R4, R5 and A are as indicated in the table below: 3. The compound according to claim 1 of the formula: wherein R1, R3, R4, R5 and A are as indicated in the table below: 4. The compound according to claim 1 of the formula: wherein R1, R3, R4, R5 and X-R7,R8 are as indicated in the table below: 5. The compound according to claim 1 of the formula: wherein A, R1, R6 and X-R7,R8 are as indicated in the table below: 6. The compound according to claim 1 of the formula: wherein R1, R7,R8 are as indicated in the table below: 7. The compound according to claim 1 of the formula: wherein R1 and A are as indicated in the table below: 8. The compound according to claim 1 of the formula: wherein R1 and X-R7,R8 are as indicated in the table below: 9. The compound according to claim 1 of the formula: wherein R1, R2 and A are as indicated in the table below: 10. The compound according to claim 1 of the formula: wherein A, R1, R2 and X-R7,R8 are as indicated in the table below: 11. The compound according to claim 1 of the formula: wherein R1, X-R7,R8, R9, R9a, R10 and R1oa are as indicated in the table below: 12. The compound according to claim 1 of the formula wherein R1 and X-R7,R8 are as indicated in the table below: 13. The compound according to claim i of the formula: wherein X-R7,R8 is as indicated in the table below: 14. The compound according to claim 1 of the formula wherein A, R1, R2, X-R7,R8, R9, R9a, R10 and R1o are as indicated in the table below: 15. The compound as defined in claim 1 which is a) 1-[2-[2-(3,4-dimethoxyphenyl)-lH-indol-3-yl]ethylamino]-3-(pyridin-4-yloxy)propan-2-ol; b) [2-[2-C3,5-dimethylphenyl)-5-methanesulfonyl-lH-indol-3-yl]ethyl|-(4-pyridin-4-yl-butyl)amine; and c) 3-[2-(3,5-dimethylphenyl)-3-[2-(5-pyridin-4-yl-pentylamino)-ethyl]-1H-indol-5-yl]-1,1-dimethylurea. 16. A pharmaceutical composition which comprises an effective amount of a compound as defined in claim 1 and a pharmaceutically acceptable carrier therefor. 17. A method for antagonizing gonadotropin-re leasing hormone in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in claim 1 to a subject suffering from a gonadotropin-releasing hormone derived disorder. 18. A method according to claim 17 wherein the gonadotropin-releasing hormone derived disorder is a sex-hormone related condition. 19. A method according to claim 17 wherein the gonadotropin-releasing hormone derived disorder is a sex hormone dependent cancer, benign prostatic hypenropy or myoma of the uterus. 20. A method according to claim 19 wherein the sex hormone dependent cancer is selected from the group consisting of prostatic cancer, uterine cancer, breast cancer and pituitary gonadotrophe adenomas. 21. A method according to claim 18 wherein the sex hormone dependent condition is selected from the group consisting of endometriosis, polycystic ovarian disease, uterine fibroids and precocious puberty. 22. A method for preventing pregnancy in a subject in need thereof which comprises administering an effective amount of a compound as defined in claim 1. 23. A method for treating lupus erythematosis in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in claim 1. 24. A method for treating irritable bowel syndrome in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in claim 1. 25. A method for treating premenstrual syndrome in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in claim 1. 26. A method for treating hirsutism in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in claim 1. 27. A method for treating short stature or a growth hormone deficiency in a subject in need thereof which comprises administering to said subject an effective amount of a compound which stimulates the endogenous production or release of growth hormone and an effective amount of a compound as defined in claim 1. 28. A method for treating sleep disorders such as sleep apnea in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in claim 1. 29. A pharmaceutical composition which comprises an ine |
| priorityDate | 1995-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 608.