LT3971B - Luteinizing hormone releasing hormone antagonists - Google Patents
Luteinizing hormone releasing hormone antagonists Download PDFInfo
- Publication number
- LT3971B LT3971B LTIP1513A LTIP1513A LT3971B LT 3971 B LT3971 B LT 3971B LT IP1513 A LTIP1513 A LT IP1513A LT IP1513 A LTIP1513 A LT IP1513A LT 3971 B LT3971 B LT 3971B
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- arg
- d3pal
- leu
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- ser
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- 239000000579 Gonadotropin-Releasing Hormone Substances 0.000 title 1
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- 108010087924 alanylproline Proteins 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 108010068380 arginylarginine Proteins 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- CIHWJRSPVJBHGT-UHFFFAOYSA-N benzhydrylazanium;chloride Chemical compound Cl.C=1C=CC=CC=1C(N)C1=CC=CC=C1 CIHWJRSPVJBHGT-UHFFFAOYSA-N 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011365 complex material Substances 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- DEZRYPDIMOWBDS-UHFFFAOYSA-N dcm dichloromethane Chemical compound ClCCl.ClCCl DEZRYPDIMOWBDS-UHFFFAOYSA-N 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 231100000673 dose–response relationship Toxicity 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003037 female contraceptive agent Substances 0.000 description 1
- 229940124566 female contraceptive agent Drugs 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000002523 gelfiltration Methods 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 239000002622 gonadotropin Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 229960002897 heparin Drugs 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- PPZMYIBUHIPZOS-UHFFFAOYSA-N histamine dihydrochloride Chemical compound Cl.Cl.NCCC1=CN=CN1 PPZMYIBUHIPZOS-UHFFFAOYSA-N 0.000 description 1
- 229960000645 histamine hydrochloride Drugs 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000002267 hypothalamic effect Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000010255 intramuscular injection Methods 0.000 description 1
- 239000007927 intramuscular injection Substances 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229940040129 luteinizing hormone Drugs 0.000 description 1
- 239000008176 lyophilized powder Substances 0.000 description 1
- 239000002583 male contraceptive agent Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- CWWARWOPSKGELM-SARDKLJWSA-N methyl (2s)-2-[[(2s)-2-[[2-[[(2s)-2-[[(2s)-2-[[(2s)-5-amino-2-[[(2s)-5-amino-2-[[(2s)-1-[(2s)-6-amino-2-[[(2s)-1-[(2s)-2-amino-5-(diaminomethylideneamino)pentanoyl]pyrrolidine-2-carbonyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-5-oxopentanoyl]amino]-5 Chemical compound C([C@@H](C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)OC)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H]1N(CCC1)C(=O)[C@@H](N)CCCN=C(N)N)C1=CC=CC=C1 CWWARWOPSKGELM-SARDKLJWSA-N 0.000 description 1
- 210000003101 oviduct Anatomy 0.000 description 1
- 230000027758 ovulation cycle Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000006965 reversible inhibition Effects 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 230000035938 sexual maturation Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- ADNPLDHMAVUMIW-CUZNLEPHSA-N substance P Chemical compound C([C@@H](C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(N)=O)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H]1N(CCC1)C(=O)[C@@H](N)CCCN=C(N)N)C1=CC=CC=C1 ADNPLDHMAVUMIW-CUZNLEPHSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 231100000041 toxicology testing Toxicity 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/23—Luteinising hormone-releasing hormone [LHRH]; Related peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Endocrinology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
- Medicinal Preparation (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN90108955A CN1036343C (zh) | 1990-11-10 | 1990-11-10 | 新促黄体生成素释放激素拮抗类似物的制备方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| LTIP1513A LTIP1513A (en) | 1995-06-26 |
| LT3971B true LT3971B (en) | 1996-05-27 |
Family
ID=4881223
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LTIP1513A LT3971B (en) | 1990-11-10 | 1993-12-03 | Luteinizing hormone releasing hormone antagonists |
Country Status (29)
| Country | Link |
|---|---|
| EP (1) | EP0564466B1 (cs) |
| KR (1) | KR100244624B1 (cs) |
| CN (1) | CN1036343C (cs) |
| AT (1) | ATE149520T1 (cs) |
| AU (1) | AU662496B2 (cs) |
| CA (1) | CA2095932C (cs) |
| CZ (1) | CZ284168B6 (cs) |
| DE (1) | DE69125024T2 (cs) |
| DK (1) | DK0564466T3 (cs) |
| EE (1) | EE03141B1 (cs) |
| ES (1) | ES2100965T3 (cs) |
| FI (1) | FI933156A0 (cs) |
| GR (1) | GR3023389T3 (cs) |
| HR (1) | HRP920585B1 (cs) |
| IE (1) | IE913915A1 (cs) |
| LT (1) | LT3971B (cs) |
| LV (1) | LV10106B (cs) |
| NO (1) | NO931697L (cs) |
| NZ (1) | NZ240505A (cs) |
| PH (1) | PH31178A (cs) |
| PL (1) | PL170564B1 (cs) |
| PT (1) | PT99458B (cs) |
| RU (1) | RU2123499C1 (cs) |
| SI (1) | SI9111779B (cs) |
| SK (1) | SK281319B6 (cs) |
| UA (1) | UA41300C2 (cs) |
| WO (1) | WO1992008733A1 (cs) |
| YU (1) | YU48831B (cs) |
| ZA (1) | ZA918847B (cs) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2136079A1 (en) * | 1992-12-18 | 1994-07-07 | Fortuna Haviv | Lhrh antagonists having modified aminoacyl residues at positions 5 and 6 |
| US6828415B2 (en) | 1993-02-19 | 2004-12-07 | Zentaris Gmbh | Oligopeptide lyophilisate, their preparation and use |
| DE4305225A1 (de) * | 1993-02-19 | 1994-08-25 | Asta Medica Ag | Neues Herstellverfahren für Cetrorelix Lyophilisat |
| DE4338015A1 (de) * | 1993-11-08 | 1995-05-11 | Asta Medica Ag | Verwendung von D-glucopyranuronsäuren und deren Derivaten zum Einbau in pharmakologisch wirksame Peptide und deren Salze |
| US5843901A (en) * | 1995-06-07 | 1998-12-01 | Advanced Research & Technology Institute | LHRH antagonist peptides |
| DE19544212A1 (de) * | 1995-11-28 | 1997-06-05 | Asta Medica Ag | Neue LH-RH-Antagonisten mit verbesserter Wirkung |
| US5968547A (en) | 1997-02-24 | 1999-10-19 | Euro-Celtique, S.A. | Method of providing sustained analgesia with buprenorphine |
| DE19911771B4 (de) * | 1999-03-17 | 2006-03-30 | Zentaris Gmbh | LHRH-Antagonist, Verfahren zu seiner Herstellung und seiner Verwendung |
| CN101037472B (zh) * | 2006-03-14 | 2013-03-27 | 中国人民解放军军事医学科学院毒物药物研究所 | 具有低组胺释放作用的促黄体生成素释放激素拮抗剂 |
| CN102675418B (zh) * | 2011-03-15 | 2016-04-20 | 中国人民解放军军事医学科学院毒物药物研究所 | Lhrh拮抗剂衍生物、其制备方法及用途 |
| CN103524599B (zh) * | 2012-07-05 | 2016-04-20 | 中国人民解放军军事医学科学院毒物药物研究所 | 环肽lhrh拮抗剂衍生物及其药物用途 |
| CN104418936B (zh) * | 2013-08-20 | 2018-06-05 | 中国人民解放军军事医学科学院毒物药物研究所 | Lhrh拮抗剂衍生物及其药物用途 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4801577A (en) * | 1987-02-05 | 1989-01-31 | Syntex (U.S.A.) Inc. | Nonapeptide and decapeptide analogs of LHRH useful as LHRH antagonists |
| US4851385A (en) * | 1987-07-15 | 1989-07-25 | Indiana University Foundation | LHRH antagonist analogs having low histamine-release activity |
-
1990
- 1990-11-10 CN CN90108955A patent/CN1036343C/zh not_active Expired - Lifetime
-
1991
- 1991-11-07 NZ NZ240505A patent/NZ240505A/xx not_active IP Right Cessation
- 1991-11-07 ZA ZA918847A patent/ZA918847B/xx unknown
- 1991-11-08 DE DE69125024T patent/DE69125024T2/de not_active Expired - Lifetime
- 1991-11-08 AT AT91919435T patent/ATE149520T1/de not_active IP Right Cessation
- 1991-11-08 DK DK91919435.7T patent/DK0564466T3/da active
- 1991-11-08 IE IE391591A patent/IE913915A1/en not_active Application Discontinuation
- 1991-11-08 PH PH43428A patent/PH31178A/en unknown
- 1991-11-08 SI SI9111779A patent/SI9111779B/sl not_active IP Right Cessation
- 1991-11-08 UA UA94030668A patent/UA41300C2/uk unknown
- 1991-11-08 KR KR1019930701418A patent/KR100244624B1/ko not_active Expired - Fee Related
- 1991-11-08 EP EP91919435A patent/EP0564466B1/en not_active Expired - Lifetime
- 1991-11-08 SK SK453-93A patent/SK281319B6/sk unknown
- 1991-11-08 AU AU88612/91A patent/AU662496B2/en not_active Ceased
- 1991-11-08 RU RU93004994A patent/RU2123499C1/ru not_active IP Right Cessation
- 1991-11-08 PT PT99458A patent/PT99458B/pt not_active IP Right Cessation
- 1991-11-08 YU YU177991A patent/YU48831B/sh unknown
- 1991-11-08 WO PCT/EP1991/002110 patent/WO1992008733A1/en active IP Right Grant
- 1991-11-08 CA CA002095932A patent/CA2095932C/en not_active Expired - Lifetime
- 1991-11-08 CZ CZ93848A patent/CZ284168B6/cs not_active IP Right Cessation
- 1991-11-08 ES ES91919435T patent/ES2100965T3/es not_active Expired - Lifetime
-
1992
- 1992-09-29 HR HR920585A patent/HRP920585B1/xx not_active IP Right Cessation
- 1992-10-27 LV LVP-92-175A patent/LV10106B/en unknown
-
1993
- 1993-05-10 NO NO93931697A patent/NO931697L/no not_active Application Discontinuation
- 1993-05-10 PL PL91295427A patent/PL170564B1/pl unknown
- 1993-07-09 FI FI933156A patent/FI933156A0/fi not_active Application Discontinuation
- 1993-12-03 LT LTIP1513A patent/LT3971B/lt not_active IP Right Cessation
-
1994
- 1994-10-25 EE EE9400178A patent/EE03141B1/xx not_active IP Right Cessation
-
1997
- 1997-05-09 GR GR970401042T patent/GR3023389T3/el unknown
Non-Patent Citations (1)
| Title |
|---|
| KELIANG LIU ET AL.: "Antagonists of luteinizing hormone releasing hormone with novel unnatural amino acids at position six", INTERNATIONAL JOURNAL OF PEPTIDE AND PROTEIN RESEARCH, 1990, pages 157 - 160, XP000085135 |
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| PC9A | Transfer of patents |
Free format text: TIANJIN MUNICIPAL RESEARCH INSTITUTE FOR FAMILY PLANNING, 10 YINGSHUI ROAD, NANKAI DIST. 300191 TIANJIN, CN,001123 |
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| MM9A | Lapsed patents |
Effective date: 20081203 |