JP2003522169A5 - - Google Patents
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- Publication number
- JP2003522169A5 JP2003522169A5 JP2001557861A JP2001557861A JP2003522169A5 JP 2003522169 A5 JP2003522169 A5 JP 2003522169A5 JP 2001557861 A JP2001557861 A JP 2001557861A JP 2001557861 A JP2001557861 A JP 2001557861A JP 2003522169 A5 JP2003522169 A5 JP 2003522169A5
- Authority
- JP
- Japan
- Prior art keywords
- furyl
- taxane
- thienyl
- pyridyl
- phenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- -1 hydroxy, oxy Chemical group 0.000 description 16
- 229940123237 Taxane Drugs 0.000 description 15
- 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 15
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 8
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 6
- 125000002496 methyl group Chemical class [H]C([H])([H])* 0.000 description 5
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 3
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 description 3
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 3
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 description 3
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 3
- 125000004423 acyloxy group Chemical group 0.000 description 3
- 125000000304 alkynyl group Chemical group 0.000 description 3
- 125000004104 aryloxy group Chemical group 0.000 description 3
- 239000003937 drug carrier Substances 0.000 description 3
- 125000002541 furyl group Chemical group 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 125000001544 thienyl group Chemical group 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- GOPDFXUMARJJEA-UHFFFAOYSA-N amino(nitro)azanide Chemical compound N[N-][N+]([O-])=O GOPDFXUMARJJEA-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- UOCJDOLVGGIYIQ-PBFPGSCMSA-N cefatrizine Chemical group S([C@@H]1[C@@H](C(N1C=1C(O)=O)=O)NC(=O)[C@H](N)C=2C=CC(O)=CC=2)CC=1CSC=1C=NNN=1 UOCJDOLVGGIYIQ-PBFPGSCMSA-N 0.000 description 1
- 230000002401 inhibitory effect Effects 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
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17967200P | 2000-02-02 | 2000-02-02 | |
| US60/179,672 | 2000-02-02 | ||
| PCT/US2001/003600 WO2001057029A1 (en) | 2000-02-02 | 2001-02-02 | C7 heterosubstituted acetate taxanes as antitumor agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003522169A JP2003522169A (ja) | 2003-07-22 |
| JP2003522169A5 true JP2003522169A5 (enExample) | 2007-03-08 |
Family
ID=22657505
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001557861A Withdrawn JP2003522169A (ja) | 2000-02-02 | 2001-02-02 | 抗腫瘍剤としてのｃ７ヘテロ置換アセテートタキサン |
Country Status (20)
| Country | Link |
|---|---|
| US (3) | US6673833B2 (enExample) |
| EP (1) | EP1200424B1 (enExample) |
| JP (1) | JP2003522169A (enExample) |
| KR (1) | KR20010112393A (enExample) |
| CN (1) | CN1362957A (enExample) |
| AT (1) | ATE413397T1 (enExample) |
| AU (1) | AU776765B2 (enExample) |
| BR (1) | BR0104353A (enExample) |
| CA (1) | CA2368534A1 (enExample) |
| CZ (1) | CZ20013519A3 (enExample) |
| DE (1) | DE60136430D1 (enExample) |
| HK (1) | HK1047935A1 (enExample) |
| HU (1) | HUP0200651A3 (enExample) |
| IL (1) | IL145642A0 (enExample) |
| MX (1) | MXPA01009922A (enExample) |
| NO (1) | NO20014758L (enExample) |
| NZ (1) | NZ514411A (enExample) |
| PL (1) | PL350328A1 (enExample) |
| WO (1) | WO2001057029A1 (enExample) |
| ZA (1) | ZA200108063B (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003522169A (ja) * | 2000-02-02 | 2003-07-22 | フロリダ・ステイト・ユニバーシティ・リサーチ・ファウンデイション・インコーポレイテッド | 抗腫瘍剤としてのｃ７ヘテロ置換アセテートタキサン |
| US20040210289A1 (en) * | 2002-03-04 | 2004-10-21 | Xingwu Wang | Novel nanomagnetic particles |
| EP1534674A4 (en) | 2002-08-02 | 2007-11-28 | Immunogen Inc | CYTOTOXIC AGENTS CONTAINING NEW, EFFECTIVE TAXANES AND THEIR THERAPEUTIC USE |
| US7390898B2 (en) | 2002-08-02 | 2008-06-24 | Immunogen Inc. | Cytotoxic agents containing novel potent taxanes and their therapeutic use |
| US20070149496A1 (en) * | 2003-10-31 | 2007-06-28 | Jack Tuszynski | Water-soluble compound |
| CN1960721A (zh) * | 2004-03-05 | 2007-05-09 | 佛罗里达州立大学研究基金有限公司 | C7乳酰氧基取代的紫杉烷类 |
| US20050249667A1 (en) * | 2004-03-24 | 2005-11-10 | Tuszynski Jack A | Process for treating a biological organism |
| CN1712399B (zh) * | 2004-06-24 | 2010-08-11 | 中国医学科学院药物研究所 | 紫杉醇和免疫增强剂胞壁酰二肽共轭物的制备及用途 |
| US20080081067A1 (en) * | 2006-10-03 | 2008-04-03 | Gupta Manishkumar | Sustained release pharmaceutical compositions of venlafaxine and process for preparation thereof |
| WO2011147330A1 (zh) | 2010-05-27 | 2011-12-01 | 中国医学科学院药物研究所 | 双功能共缀物的化学合成及抗肿瘤与抗肿瘤转移作用 |
Family Cites Families (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4879929A (en) * | 1988-06-06 | 1989-11-14 | Roth Alfred C | Tapper/threader assembly |
| US4950790A (en) * | 1988-11-14 | 1990-08-21 | Air Products And Chemicals, Inc. | Volatile fluorinated β-ketoimines and associated metal complexes |
| US4960790A (en) | 1989-03-09 | 1990-10-02 | University Of Kansas | Derivatives of taxol, pharmaceutical compositions thereof and methods for the preparation thereof |
| US5175315A (en) | 1989-05-31 | 1992-12-29 | Florida State University | Method for preparation of taxol using β-lactam |
| US5243253A (en) * | 1991-07-30 | 1993-09-07 | Thomson Consumer Electronics, Inc. | Color picture tube having shadow mask with improved tie bar grading |
| US5250683A (en) * | 1991-09-23 | 1993-10-05 | Florida State University | Certain substituted taxanes and pharmaceutical compositions containing them |
| US5283253A (en) | 1991-09-23 | 1994-02-01 | Florida State University | Furyl or thienyl carbonyl substituted taxanes and pharmaceutical compositions containing them |
| US5227400A (en) | 1991-09-23 | 1993-07-13 | Florida State University | Furyl and thienyl substituted taxanes and pharmaceutical compositions containing them |
| US5714513A (en) | 1991-09-23 | 1998-02-03 | Florida State University | C10 taxane derivatives and pharmaceutical compositions |
| US5430160A (en) | 1991-09-23 | 1995-07-04 | Florida State University | Preparation of substituted isoserine esters using β-lactams and metal or ammonium alkoxides |
| US5350866A (en) | 1991-09-23 | 1994-09-27 | Bristol-Myers Squibb Company | 10-desacetoxytaxol derivatives |
| US5721268A (en) | 1991-09-23 | 1998-02-24 | Florida State University | C7 taxane derivatives and pharmaceutical compositions containing them |
| US5243045A (en) | 1991-09-23 | 1993-09-07 | Florida State University | Certain alkoxy substituted taxanes and pharmaceutical compositions containing them |
| ES2230790T3 (es) | 1992-01-15 | 2005-05-01 | E.R. SQUIBB & SONS, INC. | Procedimientos enzimaticos para la resolucion de mezclas enantiomericas de compuestos utiles como intermedios en la preparacion de taxanos. |
| DE4302686C2 (de) | 1992-02-05 | 1994-12-15 | Bierther Hans Dietmar | Hochleistungsventil |
| FR2687150B1 (fr) | 1992-02-07 | 1995-04-28 | Rhone Poulenc Rorer Sa | Procede de preparation de derives du taxane. |
| US5272171A (en) | 1992-02-13 | 1993-12-21 | Bristol-Myers Squibb Company | Phosphonooxy and carbonate derivatives of taxol |
| US5939561A (en) | 1992-03-10 | 1999-08-17 | Rhone-Poulence Rorer S.A. | Process for the preparation of β-phenylisoserine and β-lactam and their analogues |
| US5200534A (en) | 1992-03-13 | 1993-04-06 | University Of Florida | Process for the preparation of taxol and 10-deacetyltaxol |
| IL108443A0 (en) * | 1993-01-29 | 1994-04-12 | Univ Florida State | C7 taxane derivatives and pharmaceutical compositions containing them |
| US5703247A (en) | 1993-03-11 | 1997-12-30 | Virginia Tech Intellectual Properties, Inc. | 2-Debenzoyl-2-acyl taxol derivatives and methods for making same |
| DK1227093T3 (da) * | 1993-03-22 | 2005-08-29 | Univ Florida State | Beta-lactamer, der kan anvendes til fremstilling af taxaner med en furyl- eller thienylsubstitueret sidekæde |
| US5350253A (en) * | 1993-03-24 | 1994-09-27 | John Cunningham | Method for supporting distribution means |
| IL109926A (en) | 1993-06-15 | 2000-02-29 | Bristol Myers Squibb Co | Methods for the preparation of taxanes and microorganisms and enzymes utilized therein |
| TW397866B (en) | 1993-07-14 | 2000-07-11 | Bristol Myers Squibb Co | Enzymatic processes for the resolution of enantiomeric mixtures of compounds useful as intermediates in the preparation of taxanes |
| WO1996013495A1 (en) * | 1994-10-28 | 1996-05-09 | The Research Foundation Of State University Of New York | Taxoid derivatives, their preparation and their use as antitumor agents |
| US5780653A (en) | 1995-06-07 | 1998-07-14 | Vivorx Pharmaceuticals, Inc. | Nitrophenyl, 10-deacetylated substituted taxol derivatives as dual functional cytotoxic/radiosensitizers |
| CA2231837A1 (en) | 1995-09-13 | 1997-03-20 | Florida State University | Radiosensitizing taxanes and their pharmaceutical preparations |
| US5767297A (en) * | 1997-02-05 | 1998-06-16 | Ensuiko Sugar Refining Co., Ltd. | Taxoid derivative and method of producing thereof |
| JP3786462B2 (ja) * | 1996-03-07 | 2006-06-14 | 塩水港精糖株式会社 | タキソイドの配糖化誘導体およびその製造方法 |
| IL126856A0 (en) | 1996-05-06 | 1999-09-22 | Univ Florida State | 1-Deoxy baccatin iii 1-deoxy taxol and 1-deoxy taxol analogs and method for the preparation thereof |
| US5780683A (en) * | 1996-09-11 | 1998-07-14 | Abb Lummus Global Inc. | Cyclohexane oxidation |
| US5811452A (en) | 1997-01-08 | 1998-09-22 | The Research Foundation Of State University Of New York | Taxoid reversal agents for drug-resistance in cancer chemotherapy and pharmaceutical compositions thereof |
| US5912264A (en) | 1997-03-03 | 1999-06-15 | Bristol-Myers Squibb Company | 6-halo-or nitrate-substituted paclitaxels |
| HU224589B1 (hu) | 1997-06-03 | 2005-11-28 | Ensuiko Sugar Refining Co., Ltd. | Taxoidszármazékok és eljárás előállításukra |
| US7288665B1 (en) | 1997-08-18 | 2007-10-30 | Florida State University | Process for selective derivatization of taxanes |
| US6136988A (en) | 1998-04-10 | 2000-10-24 | Hauser, Inc. | 7-hexanoyltaxol and methods for preparing the same |
| JP2003522169A (ja) * | 2000-02-02 | 2003-07-22 | フロリダ・ステイト・ユニバーシティ・リサーチ・ファウンデイション・インコーポレイテッド | 抗腫瘍剤としてのｃ７ヘテロ置換アセテートタキサン |
| EP1175414A1 (en) | 2000-02-02 | 2002-01-30 | Florida State University Research Foundation, Inc. | Taxane formulations having improved solubility |
-
2001
- 2001-02-02 JP JP2001557861A patent/JP2003522169A/ja not_active Withdrawn
- 2001-02-02 KR KR1020017012589A patent/KR20010112393A/ko not_active Abandoned
- 2001-02-02 IL IL14564201A patent/IL145642A0/xx unknown
- 2001-02-02 CA CA002368534A patent/CA2368534A1/en not_active Withdrawn
- 2001-02-02 CN CN01800318A patent/CN1362957A/zh active Pending
- 2001-02-02 MX MXPA01009922A patent/MXPA01009922A/es active IP Right Grant
- 2001-02-02 US US09/776,393 patent/US6673833B2/en not_active Expired - Fee Related
- 2001-02-02 CZ CZ20013519A patent/CZ20013519A3/cs unknown
- 2001-02-02 HK HK03100169.2A patent/HK1047935A1/zh unknown
- 2001-02-02 AT AT01906965T patent/ATE413397T1/de not_active IP Right Cessation
- 2001-02-02 WO PCT/US2001/003600 patent/WO2001057029A1/en not_active Ceased
- 2001-02-02 BR BR0104353-6A patent/BR0104353A/pt not_active IP Right Cessation
- 2001-02-02 DE DE60136430T patent/DE60136430D1/de not_active Expired - Fee Related
- 2001-02-02 PL PL01350328A patent/PL350328A1/xx not_active Application Discontinuation
- 2001-02-02 HU HU0200651A patent/HUP0200651A3/hu unknown
- 2001-02-02 EP EP01906965A patent/EP1200424B1/en not_active Expired - Lifetime
- 2001-02-02 NZ NZ514411A patent/NZ514411A/en unknown
- 2001-02-02 AU AU34804/01A patent/AU776765B2/en not_active Ceased
- 2001-10-01 ZA ZA200108063A patent/ZA200108063B/en unknown
- 2001-10-01 NO NO20014758A patent/NO20014758L/no not_active Application Discontinuation
-
2003
- 2003-11-24 US US10/720,826 patent/US6861446B2/en not_active Expired - Fee Related
-
2005
- 2005-02-23 US US11/063,626 patent/US7183312B2/en not_active Expired - Fee Related
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