RU99127433A - ERGOLINE DERIVATIVES AND THEIR APPLICATION AS ANTAGONISTS OF SOMATOSTATIN RECEPTORS - Google Patents
ERGOLINE DERIVATIVES AND THEIR APPLICATION AS ANTAGONISTS OF SOMATOSTATIN RECEPTORSInfo
- Publication number
- RU99127433A RU99127433A RU99127433/04A RU99127433A RU99127433A RU 99127433 A RU99127433 A RU 99127433A RU 99127433/04 A RU99127433/04 A RU 99127433/04A RU 99127433 A RU99127433 A RU 99127433A RU 99127433 A RU99127433 A RU 99127433A
- Authority
- RU
- Russia
- Prior art keywords
- formula
- free base
- denotes
- compound
- pharmaceutically acceptable
- Prior art date
Links
- AWFDCTXCTHGORH-HGHGUNKESA-N 6-[4-[(6ar,9r,10ar)-5-bromo-7-methyl-6,6a,8,9,10,10a-hexahydro-4h-indolo[4,3-fg]quinoline-9-carbonyl]piperazin-1-yl]-1-methylpyridin-2-one Chemical class O=C([C@H]1CN([C@H]2[C@@H](C=3C=CC=C4NC(Br)=C(C=34)C2)C1)C)N(CC1)CCN1C1=CC=CC(=O)N1C AWFDCTXCTHGORH-HGHGUNKESA-N 0.000 title 1
- 108050001286 Somatostatin Receptor Proteins 0.000 title 1
- 102000011096 Somatostatin receptor Human genes 0.000 title 1
- 239000005557 antagonist Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 13
- 150000003839 salts Chemical class 0.000 claims 11
- 239000002253 acid Substances 0.000 claims 10
- 239000012458 free base Substances 0.000 claims 10
- 208000019901 Anxiety disease Diseases 0.000 claims 4
- 208000020925 Bipolar disease Diseases 0.000 claims 4
- 239000000654 additive Substances 0.000 claims 4
- 230000000996 additive effect Effects 0.000 claims 4
- 230000036506 anxiety Effects 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- 208000020401 Depressive disease Diseases 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 239000000460 chlorine Substances 0.000 claims 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 208000035475 disorder Diseases 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 208000013403 hyperactivity Diseases 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 229940126601 medicinal product Drugs 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000008024 pharmaceutical diluent Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 0 CC1*NC2C(C)=CC3=NCC=C3C2C1 Chemical compound CC1*NC2C(C)=CC3=NCC=C3C2C1 0.000 description 1
Claims (10)
где R1 обозначает водород, C1-C4алкил или группу формулы
в которой n равно 1-4 и R7 обозначает фтор, хлор, гидрокси, C1-C4алкил или C1-C4алкокси;
R2 обозначает водород, хлор, бром, йод, С1-C4алкил или C1-C4алкилтио,
R3 обозначает водород или C1-C4алкил;
R4 обозначает (I) группу формулы
или
где R8 обозначает фтор, хлор, нитро или пиано, и R11 обозначает C1-C4алкил или С2-С8алкенил, или (II) группу формулы
или
где радикалы Х независимо друг от друга обозначают О или S, и R5 и R6 каждый обозначает водород или вместе образуют дополнительную связь
между двумя атомами углерода, к которым они присоединены, в форме свободного основания или в форме кислотно-аддитивной соли.1. The compound of formula I
where R 1 denotes hydrogen, C 1 -C 4 alkyl or a group of the formula
in which n is 1-4 and R 7 denotes fluorine, chlorine, hydroxy, C 1 -C 4 alkyl or C 1 -C 4 alkoxy;
R 2 denotes hydrogen, chlorine, bromine, iodine, C 1 -C 4 alkyl or C 1 -C 4 alkylthio,
R 3 is hydrogen or C 1 -C 4 alkyl;
R 4 means (I) a group of the formula
or
where R 8 denotes fluorine, chlorine, nitro or piano, and R 11 denotes C 1 -C 4 alkyl or C 2 -C 8 alkenyl, or (II) a group of the formula
or
where the radicals X independently of one another denote O or S, and R 5 and R 6 each denotes hydrogen or together form an additional bond
between the two carbon atoms to which they are attached, in the form of a free base or in the form of an acid addition salt.
где R1, R2, R3, R5 и R6 имеют значения, указанные в п.1, а М обозначает Н или щелочной металл, с соединением формулы III
где R4 имеет значения, указанные в п.1, и восстановление полученного таким путем соединения формулы I в форме свободного основания или в форме кислотно-аддитивной соли.4. The method of obtaining the compounds of formula I according to claim 1 or its salt, which includes the interaction of the compounds of formula II
where R 1 , R 2 , R 3 , R 5 and R 6 have the meanings indicated in paragraph 1, and M denotes H or an alkali metal, with a compound of formula III
where R 4 has the meanings indicated in claim 1 and the reduction of the compound of formula I thus obtained in the form of the free base or in the form of an acid addition salt.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9711043.1 | 1997-05-29 | ||
| GBGB9711043.1A GB9711043D0 (en) | 1997-05-29 | 1997-05-29 | Organic compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU99127433A true RU99127433A (en) | 2001-09-10 |
| RU2191776C2 RU2191776C2 (en) | 2002-10-27 |
Family
ID=10813201
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU99127433/04A RU2191776C2 (en) | 1997-05-29 | 1998-05-27 | Ergoline derivatives, method of their synthesis, pharmaceutical composition |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US6221870B1 (en) |
| EP (1) | EP0986558A2 (en) |
| JP (1) | JP2001527580A (en) |
| KR (1) | KR20010013103A (en) |
| CN (1) | CN1259946A (en) |
| AR (1) | AR012870A1 (en) |
| AU (1) | AU727841B2 (en) |
| BR (1) | BR9809491A (en) |
| CA (1) | CA2288810A1 (en) |
| CO (1) | CO4950561A1 (en) |
| CZ (1) | CZ289466B6 (en) |
| GB (1) | GB9711043D0 (en) |
| HU (1) | HUP0002311A3 (en) |
| ID (1) | ID22916A (en) |
| IL (1) | IL132571A0 (en) |
| NO (1) | NO995482L (en) |
| NZ (1) | NZ500386A (en) |
| PE (1) | PE74899A1 (en) |
| PL (1) | PL336502A1 (en) |
| RU (1) | RU2191776C2 (en) |
| SK (1) | SK160899A3 (en) |
| TR (1) | TR199902848T2 (en) |
| WO (1) | WO1998054183A2 (en) |
| ZA (1) | ZA984560B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2329273C2 (en) * | 2003-04-11 | 2008-07-20 | Сосьете Де Консей Де Решерш Э Д`Аппликасьон Сьентифик С.А.С. | Chimeric equivalents of ligans of somatostatin and dopermine receptors, pharmaceutical compositions based on them and modalties of somatostatin and/dopermine receptors |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10053397A1 (en) * | 2000-10-20 | 2002-05-02 | Schering Ag | Use of a dopaminergic active ingredient for the treatment of dopaminerg treatable diseases |
| DE10066158B4 (en) * | 2000-08-24 | 2007-08-09 | Neurobiotec Gmbh | Use of a transdermal therapeutic system for the treatment of Restless Legs Syndrome |
| DE10341317B4 (en) * | 2003-09-03 | 2008-10-23 | Axxonis Pharma Ag | Transdermal therapeutic system (TTS) for administration of ergoline compounds except pergolide |
| US20070243240A9 (en) * | 2000-08-24 | 2007-10-18 | Fred Windt-Hanke | Transdermal therapeutic system |
| CN1514843A (en) * | 2001-06-08 | 2004-07-21 | �о���Ӧ�ÿ�ѧЭ��ɷ�����˾ | somatostatin-dopamine chimeric analog |
| FI20031454A0 (en) | 2003-10-06 | 2003-10-06 | Juvantia Pharma Ltd Oy | Selective somatostatin receptor 1 and / or 4 agonists and antagonists |
| KR101000923B1 (en) * | 2004-01-08 | 2010-12-13 | 삼성전자주식회사 | Apparatus and method for setting a macro of a remote controller |
| CA2609161A1 (en) * | 2005-05-18 | 2006-11-23 | Siegfried Wurster | Peptidomimetics selective for the somatostatin receptor subtypes 1 and/or 4 |
| JP2007067096A (en) * | 2005-08-30 | 2007-03-15 | Fujitsu Ltd | Semiconductor device |
| SG181896A1 (en) * | 2009-12-23 | 2012-07-30 | Map Pharmaceuticals Inc | Novel ergoline analogs |
| CN103827113A (en) | 2011-06-23 | 2014-05-28 | Map药物公司 | Novel fluoroergoline analogs |
| EP2793580A4 (en) | 2011-12-19 | 2015-05-20 | Map Pharmaceuticals Inc | Novel iso-ergoline derivatives |
| US8946420B2 (en) | 2011-12-21 | 2015-02-03 | Map Pharmaceuticals, Inc. | Neuromodulatory compounds |
| US9012640B2 (en) | 2012-06-22 | 2015-04-21 | Map Pharmaceuticals, Inc. | Cabergoline derivatives |
| EP2914276A4 (en) | 2012-11-01 | 2016-07-13 | Ipsen Pharma Sas | Somatostatin analogs and dimers thereof |
| TWI523863B (en) | 2012-11-01 | 2016-03-01 | 艾普森藥品公司 | Somatostatin-dopamine chimeric analogs |
| CA2974113A1 (en) | 2015-01-20 | 2016-07-28 | Xoc Pharmaceuticals, Inc. | Isoergoline compounds and uses thereof |
| BR112017015487A2 (en) | 2015-01-20 | 2018-01-30 | Xoc Pharmaceuticals Inc | COMPOUND; COMPOSITION; METHOD OF TREATMENT AND / OR PREVENTION OF MIGRAINE, ALS, ALZHEIMER'S DISEASE, PARKINSON'S DISEASE, EXTRAPYRIMIDAL DISORDERS, DEPRESSION, NAUSEA, AEMESIS, SYNDROME OF THE WASTE LEGS, INSOMENESS, HYGERNESS, AGING , ANXIETY, DRUG DEPENDENCIES, DYSTONIA, PARASSONIA OR HYPERLACTINEMIA IN AN INDIVIDUAL; AGONIZATION METHODS OF D2, 5-HT1D, 5-HT1A AND 5-HT2C RECEPTORS, IN AN INDIVIDUAL; ANTAGONIZATION METHOD OF THE D3 RECEPTOR IN AN INDIVIDUAL; METHODS OF SELECTIVE AGONIZATION OF RECEPTORS 5 -HT1D, AND 5-HT2C, METHOD OF PROVIDING FUNCTIONAL ANTAGONIST ACTIVITY IN RECEPTOR 5 -HT2B OR IN RECEIVER 5-HT7, OR IN BOTH, IN AN INDIVIDUAL; METHOD OF PROVIDING FUNCTIONAL ANTAGONIST ACTIVITY IN ADRENERGIC RECEPTORS IN AN INDIVIDUAL |
| CA3064274A1 (en) | 2017-06-01 | 2018-12-06 | Xoc Pharmaceuticals, Inc. | Ergoline derivatives for use in medicine |
| JP7099717B2 (en) | 2019-09-30 | 2022-07-12 | 株式会社理研バイオ | Somatostatin receptor |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1695682U (en) * | 1955-01-13 | 1955-03-31 | Otto Berning & Co | ADJUSTABLE COLLAR STICK. |
| US3592816A (en) | 1966-02-08 | 1971-07-13 | Sandoz Ltd | N-substituted piperazides of lysergic acid |
| CH475252A (en) * | 1966-02-08 | 1969-07-15 | Sandoz Ag | Process for the production of new lysergic acid derivatives |
| GB1188197A (en) | 1967-10-11 | 1970-04-15 | Sandoz Ltd | Lysergic Acid Derivatives |
| NL6818658A (en) * | 1968-01-18 | 1969-07-22 | ||
| GB1580448A (en) * | 1976-12-06 | 1980-12-03 | Farmaceutici Italia | 8 -acetyl-6-methyl-ergoline i derivatives |
| GB8501078D0 (en) * | 1985-01-16 | 1985-02-20 | Erba Farmitalia | Piperazin-1-yl-ergo-line derivatives |
| TW357143B (en) | 1995-07-07 | 1999-05-01 | Novartis Ag | Benzo[g]quinoline derivatives |
-
1997
- 1997-05-29 GB GBGB9711043.1A patent/GB9711043D0/en active Pending
-
1998
- 1998-05-27 EP EP98932090A patent/EP0986558A2/en not_active Withdrawn
- 1998-05-27 KR KR19997011082A patent/KR20010013103A/en not_active Abandoned
- 1998-05-27 NZ NZ500386A patent/NZ500386A/en unknown
- 1998-05-27 SK SK1608-99A patent/SK160899A3/en unknown
- 1998-05-27 WO PCT/EP1998/003125 patent/WO1998054183A2/en not_active Ceased
- 1998-05-27 IL IL13257198A patent/IL132571A0/en unknown
- 1998-05-27 AU AU82108/98A patent/AU727841B2/en not_active Ceased
- 1998-05-27 PE PE1998000425A patent/PE74899A1/en not_active Application Discontinuation
- 1998-05-27 CA CA002288810A patent/CA2288810A1/en not_active Abandoned
- 1998-05-27 US US09/424,377 patent/US6221870B1/en not_active Expired - Fee Related
- 1998-05-27 HU HU0002311A patent/HUP0002311A3/en unknown
- 1998-05-27 CZ CZ19994245A patent/CZ289466B6/en not_active IP Right Cessation
- 1998-05-27 AR ARP980102461A patent/AR012870A1/en unknown
- 1998-05-27 BR BR9809491-2A patent/BR9809491A/en not_active IP Right Cessation
- 1998-05-27 PL PL98336502A patent/PL336502A1/en unknown
- 1998-05-27 JP JP50023799A patent/JP2001527580A/en active Pending
- 1998-05-27 RU RU99127433/04A patent/RU2191776C2/en active
- 1998-05-27 TR TR1999/02848T patent/TR199902848T2/en unknown
- 1998-05-27 CN CN98805488A patent/CN1259946A/en active Pending
- 1998-05-27 ID IDW991445A patent/ID22916A/en unknown
- 1998-05-28 ZA ZA984560A patent/ZA984560B/en unknown
- 1998-05-28 CO CO98030085A patent/CO4950561A1/en unknown
-
1999
- 1999-11-09 NO NO995482A patent/NO995482L/en not_active Application Discontinuation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2329273C2 (en) * | 2003-04-11 | 2008-07-20 | Сосьете Де Консей Де Решерш Э Д`Аппликасьон Сьентифик С.А.С. | Chimeric equivalents of ligans of somatostatin and dopermine receptors, pharmaceutical compositions based on them and modalties of somatostatin and/dopermine receptors |
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