UA72208C2 - Antitumour compounds from spisula polynyma extracts - Google Patents
Antitumour compounds from spisula polynyma extracts Download PDFInfo
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- UA72208C2 UA72208C2 UA2000105675A UA2000105675A UA72208C2 UA 72208 C2 UA72208 C2 UA 72208C2 UA 2000105675 A UA2000105675 A UA 2000105675A UA 2000105675 A UA2000105675 A UA 2000105675A UA 72208 C2 UA72208 C2 UA 72208C2
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- 150000004702 methyl esters Chemical class 0.000 description 1
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- 231100001083 no cytotoxicity Toxicity 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 231100001160 nonlethal Toxicity 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229960002700 octreotide Drugs 0.000 description 1
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- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
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- NXJCBFBQEVOTOW-UHFFFAOYSA-L palladium(2+);dihydroxide Chemical compound O[Pd]O NXJCBFBQEVOTOW-UHFFFAOYSA-L 0.000 description 1
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- FPVKHBSQESCIEP-JQCXWYLXSA-N pentostatin Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(N=CNC[C@H]2O)=C2N=C1 FPVKHBSQESCIEP-JQCXWYLXSA-N 0.000 description 1
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- PHEDXBVPIONUQT-RGYGYFBISA-N phorbol 13-acetate 12-myristate Chemical compound C([C@]1(O)C(=O)C(C)=C[C@H]1[C@@]1(O)[C@H](C)[C@H]2OC(=O)CCCCCCCCCCCCC)C(CO)=C[C@H]1[C@H]1[C@]2(OC(C)=O)C1(C)C PHEDXBVPIONUQT-RGYGYFBISA-N 0.000 description 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical group ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
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- 239000002798 polar solvent Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
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- 230000003389 potentiating effect Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
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- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
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- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- OTKJDMGTUTTYMP-ZWKOTPCHSA-N sphinganine Chemical compound CCCCCCCCCCCCCCC[C@@H](O)[C@@H](N)CO OTKJDMGTUTTYMP-ZWKOTPCHSA-N 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 229960001603 tamoxifen Drugs 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- DKPFODGZWDEEBT-QFIAKTPHSA-N taxane Chemical class C([C@]1(C)CCC[C@@H](C)[C@H]1C1)C[C@H]2[C@H](C)CC[C@@H]1C2(C)C DKPFODGZWDEEBT-QFIAKTPHSA-N 0.000 description 1
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 1
- 229940063683 taxotere Drugs 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 231100001274 therapeutic index Toxicity 0.000 description 1
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- 239000003744 tubulin modulator Substances 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
- 210000003932 urinary bladder Anatomy 0.000 description 1
- 210000003501 vero cell Anatomy 0.000 description 1
- 229960003048 vinblastine Drugs 0.000 description 1
- JXLYSJRDGCGARV-XQKSVPLYSA-N vincaleukoblastine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 JXLYSJRDGCGARV-XQKSVPLYSA-N 0.000 description 1
- OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 description 1
- 229960004528 vincristine Drugs 0.000 description 1
- OGWKCGZFUXNPDA-UHFFFAOYSA-N vincristine Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(OC(C)=O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000001262 western blot Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/133—Amines having hydroxy groups, e.g. sphingosine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
- C07C215/08—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic with only one hydroxy group and one amino group bound to the carbon skeleton
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/56—Materials from animals other than mammals
- A61K35/618—Molluscs, e.g. fresh-water molluscs, oysters, clams, squids, octopus, cuttlefish, snails or slugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Marine Sciences & Fisheries (AREA)
- Zoology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Farming Of Fish And Shellfish (AREA)
- Fodder In General (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/058,456 US6107520A (en) | 1997-04-15 | 1998-04-10 | Spisulosine compounds |
| PCT/GB1999/001091 WO1999052521A1 (en) | 1998-04-10 | 1999-04-09 | Spisulosine compounds having antitumour activity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA72208C2 true UA72208C2 (en) | 2005-02-15 |
Family
ID=22016916
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2000105675A UA72208C2 (en) | 1998-04-10 | 1999-09-04 | Antitumour compounds from spisula polynyma extracts |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US6107520A (da) |
| EP (1) | EP1069894B1 (da) |
| JP (1) | JP2002511410A (da) |
| KR (1) | KR100568964B1 (da) |
| CN (1) | CN1335770A (da) |
| AT (1) | ATE303139T1 (da) |
| AU (1) | AU763981B2 (da) |
| BG (1) | BG64970B1 (da) |
| BR (1) | BR9910120A (da) |
| CA (1) | CA2328126A1 (da) |
| DE (1) | DE69927007T2 (da) |
| DK (1) | DK1069894T3 (da) |
| ES (1) | ES2248995T3 (da) |
| HK (1) | HK1042048A1 (da) |
| HU (1) | HUP0105443A3 (da) |
| IL (1) | IL138886A0 (da) |
| MX (1) | MXPA00009930A (da) |
| NO (1) | NO20005052L (da) |
| PL (1) | PL343381A1 (da) |
| RU (1) | RU2225710C2 (da) |
| SK (1) | SK15082000A3 (da) |
| TR (1) | TR200002955T2 (da) |
| UA (1) | UA72208C2 (da) |
| WO (1) | WO1999052521A1 (da) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6306911B1 (en) * | 2000-02-07 | 2001-10-23 | Ortho-Mcneil Pharmaceutical, Inc. | Substituted amino acids as neutral sphingomyelinase inhibitors |
| ATE316524T1 (de) * | 2000-02-16 | 2006-02-15 | Pharma Mar Sa | Oxy- und aminosubstituierte tetrahydrofurylderivate mit antitumoraktivität |
| JP2003535868A (ja) * | 2000-06-06 | 2003-12-02 | ファルマ・マール・ソシエダード・アノニマ | 抗腫瘍化合物 |
| FR2811556B1 (fr) * | 2000-07-11 | 2002-09-06 | Oreal | Composition comprenant un precurseur de ceramides, utilisation pour ameliorer l'epiderme naturel ou reconstruit , equivalent de peau obtenu |
| US7563810B2 (en) | 2002-11-06 | 2009-07-21 | Celgene Corporation | Methods of using 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myeloproliferative diseases |
| US8034831B2 (en) | 2002-11-06 | 2011-10-11 | Celgene Corporation | Methods for the treatment and management of myeloproliferative diseases using 4-(amino)-2-(2,6-Dioxo(3-piperidyl)-isoindoline-1,3-dione in combination with other therapies |
| WO2004064713A2 (en) * | 2003-01-20 | 2004-08-05 | Vib Vzw | The use of yop preoteins or rho gtpase inhibitors as caspase-1 inhibitors |
| CN100360515C (zh) * | 2004-04-09 | 2008-01-09 | 中国科学院上海药物研究所 | 抗肿瘤活性成份陵水醇、制备方法和用途 |
| WO2006034849A1 (en) * | 2004-09-27 | 2006-04-06 | Pharma Mar, S.A., Sociedad Unipersonal | Antitumoral pharmaceutical compositions comprising a spisulosine and a cyclodextrin |
| KR20100038377A (ko) * | 2007-06-19 | 2010-04-14 | 다케다 야쿠힌 고교 가부시키가이샤 | 암의 예방／치료제 |
| CN102206163B (zh) * | 2011-05-06 | 2013-07-10 | 中国海洋大学 | 一种长链碱的分离制备方法 |
| WO2014118556A2 (en) * | 2013-01-31 | 2014-08-07 | Research Foundation Of The City University Of New York | Selective inhibitors and allosteric activators of sphingosine kinase |
| CN104758275A (zh) * | 2015-03-05 | 2015-07-08 | 青岛申达高新技术开发有限公司 | 一种治疗结肠癌的药物组合物及其应用 |
| JOP20190254A1 (ar) | 2017-04-27 | 2019-10-27 | Pharma Mar Sa | مركبات مضادة للأورام |
| CN112063606A (zh) * | 2020-08-25 | 2020-12-11 | 山东省科学院生物研究所 | 一种快速提取贝类消化内源酶的方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU325756A1 (ru) * | 1966-12-19 | 1983-01-15 | Всесоюзный научно-исследовательский химико-фармацевтический институт им.Серго Орджоникидзе | Лекарственный препарат |
| SU677293A1 (ru) * | 1977-12-07 | 1992-04-23 | Ленинградский Технологический Институт Им.Ленсовета | Актиноцил-бис-( @ -диметиламинопропил)-амин, обладающий противоопухолевой активностью |
| US4816450A (en) * | 1986-09-15 | 1989-03-28 | Duke University | Inhibition of protein kinase C by long-chain bases |
| US5190876A (en) * | 1988-12-27 | 1993-03-02 | Emory University | Method of modifying cellular differentiation and function and compositions therefor |
| US5583160A (en) * | 1989-02-03 | 1996-12-10 | The Biomembrane Institute | Methylsphingosine used to treat apoptosis |
| CA2007507C (en) * | 1989-02-03 | 1998-05-19 | Yasuyuki Igarashi | Sphingosine and n-methyl-sphingosine as inhibitor of cell growth |
| US5426228A (en) * | 1994-06-27 | 1995-06-20 | Koskinen; Ari | General method for preparation of sphingosine bases and their analogues |
| EP0821068A3 (en) * | 1996-03-29 | 1999-06-02 | Rohm And Haas Company | Novel sphingolipids and a process thereto |
-
1998
- 1998-04-10 US US09/058,456 patent/US6107520A/en not_active Ceased
-
1999
- 1999-04-09 EP EP99915898A patent/EP1069894B1/en not_active Expired - Lifetime
- 1999-04-09 KR KR1020007011292A patent/KR100568964B1/ko not_active Expired - Fee Related
- 1999-04-09 MX MXPA00009930A patent/MXPA00009930A/es active IP Right Grant
- 1999-04-09 AU AU34321/99A patent/AU763981B2/en not_active Ceased
- 1999-04-09 IL IL13888699A patent/IL138886A0/xx unknown
- 1999-04-09 CA CA002328126A patent/CA2328126A1/en not_active Abandoned
- 1999-04-09 ES ES99915898T patent/ES2248995T3/es not_active Expired - Lifetime
- 1999-04-09 PL PL99343381A patent/PL343381A1/xx not_active IP Right Cessation
- 1999-04-09 TR TR2000/02955T patent/TR200002955T2/xx unknown
- 1999-04-09 DE DE69927007T patent/DE69927007T2/de not_active Expired - Fee Related
- 1999-04-09 SK SK1508-2000A patent/SK15082000A3/sk unknown
- 1999-04-09 RU RU2000128037/15A patent/RU2225710C2/ru not_active IP Right Cessation
- 1999-04-09 HU HU0105443A patent/HUP0105443A3/hu unknown
- 1999-04-09 DK DK99915898T patent/DK1069894T3/da active
- 1999-04-09 WO PCT/GB1999/001091 patent/WO1999052521A1/en not_active Ceased
- 1999-04-09 AT AT99915898T patent/ATE303139T1/de not_active IP Right Cessation
- 1999-04-09 JP JP2000543131A patent/JP2002511410A/ja not_active Abandoned
- 1999-04-09 HK HK02103875.2A patent/HK1042048A1/zh unknown
- 1999-04-09 BR BR9910120-3A patent/BR9910120A/pt not_active Application Discontinuation
- 1999-04-09 CN CN99807084A patent/CN1335770A/zh active Pending
- 1999-09-04 UA UA2000105675A patent/UA72208C2/uk unknown
-
2000
- 2000-10-06 NO NO20005052A patent/NO20005052L/no not_active Application Discontinuation
- 2000-11-09 BG BG104935A patent/BG64970B1/bg unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL138886A0 (en) | 2001-11-25 |
| JP2002511410A (ja) | 2002-04-16 |
| DK1069894T3 (da) | 2006-01-09 |
| CN1335770A (zh) | 2002-02-13 |
| KR20010074483A (ko) | 2001-08-04 |
| CA2328126A1 (en) | 1999-10-21 |
| HUP0105443A1 (hu) | 2002-07-29 |
| NO20005052D0 (no) | 2000-10-06 |
| ES2248995T3 (es) | 2006-03-16 |
| BG64970B1 (bg) | 2006-11-30 |
| DE69927007T2 (de) | 2006-06-29 |
| DE69927007D1 (de) | 2005-10-06 |
| WO1999052521A1 (en) | 1999-10-21 |
| HUP0105443A3 (en) | 2005-07-28 |
| PL343381A1 (en) | 2001-08-13 |
| EP1069894A1 (en) | 2001-01-24 |
| ATE303139T1 (de) | 2005-09-15 |
| TR200002955T2 (tr) | 2001-01-22 |
| RU2225710C2 (ru) | 2004-03-20 |
| EP1069894B1 (en) | 2005-08-31 |
| MXPA00009930A (es) | 2002-04-24 |
| SK15082000A3 (sk) | 2001-08-06 |
| US6107520A (en) | 2000-08-22 |
| AU763981B2 (en) | 2003-08-07 |
| HK1042048A1 (zh) | 2002-08-02 |
| BG104935A (en) | 2001-07-31 |
| KR100568964B1 (ko) | 2006-04-07 |
| NO20005052L (no) | 2000-12-07 |
| BR9910120A (pt) | 2000-12-26 |
| AU3432199A (en) | 1999-11-01 |
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