CZ284818B6 - Nový způsob esterifikace baccatinu III a 10-desacetylbaccatinu - Google Patents
Nový způsob esterifikace baccatinu III a 10-desacetylbaccatinuInfo
- Publication number
- CZ284818B6 CZ284818B6 CZ95839A CZ83995A CZ284818B6 CZ 284818 B6 CZ284818 B6 CZ 284818B6 CZ 95839 A CZ95839 A CZ 95839A CZ 83995 A CZ83995 A CZ 83995A CZ 284818 B6 CZ284818 B6 CZ 284818B6
- Authority
- CZ
- Czechia
- Prior art keywords
- iii
- sub
- deacetylbaccatin
- baccatin
- hydroxy
- Prior art date
Links
- OVMSOCFBDVBLFW-VHLOTGQHSA-N 5beta,20-epoxy-1,7beta,13alpha-trihydroxy-9-oxotax-11-ene-2alpha,4alpha,10beta-triyl 4,10-diacetate 2-benzoate Chemical compound O([C@@H]1[C@@]2(C[C@H](O)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)O)C(=O)C1=CC=CC=C1 OVMSOCFBDVBLFW-VHLOTGQHSA-N 0.000 title abstract 6
- YWLXLRUDGLRYDR-ZHPRIASZSA-N 5beta,20-epoxy-1,7beta,10beta,13alpha-tetrahydroxy-9-oxotax-11-ene-2alpha,4alpha-diyl 4-acetate 2-benzoate Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](O)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 YWLXLRUDGLRYDR-ZHPRIASZSA-N 0.000 title abstract 5
- 150000002148 esters Chemical class 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 2
- -1 10-deacetylbaccatin iii ester Chemical class 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 229930014667 baccatin III Natural products 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- YWLXLRUDGLRYDR-SKXCCXORSA-N 10-dab iii Chemical compound O([C@H]1C2[C@@](C([C@H](O)C3=C(C)[C@@H](O)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 YWLXLRUDGLRYDR-SKXCCXORSA-N 0.000 abstract 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 230000000719 anti-leukaemic effect Effects 0.000 abstract 1
- 230000000259 anti-tumor effect Effects 0.000 abstract 1
- 125000003435 aroyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001602 bicycloalkyls Chemical group 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000005017 substituted alkenyl group Chemical group 0.000 abstract 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 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D305/00—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms
- C07D305/14—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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)
- Epoxy Compounds (AREA)
- Peptides Or Proteins (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Způsob přípravy esterů baccatinu III nebo 10-desacetylbaccatinu III obecného vzorce I spočívá v esterifikací chráněného baccatinu III nebo 10-desacetylbaccatinu III obecného vzorce III aktivovanou kyselinou obecného vzorce III. Estery obecného vzorce I jsou užitečné pro přípravu derivátů taxanu, majících protileukemické a protinádorové vlastnosti. V obecných vzorcích I, II a III Ar znamená aryl, R.sub.1.n. znamená atom vodíku, aroyl nebo skupinu R.sub.4.n.-O-CO-, kde R.sub.4.n. je případně substituovaná alkenylová, alkinylová nebo alkylová skupina, cykloalkylová skupina, cykloalkenylová skupina, bicykloalkylová skupina, fenylová skupina, heterocyklická skupina a R.sub.2.n. znamená atom vodíku a R.sub.3.n. znamená ochrannou skupinu hydroxy-funkce nebo také R.sub.1.n. má výše uvedený význam a R.sub.2.n. a R.sub.3.n. dohromady tvoří 5- nebo 6-členný nasycený herocykl, G.sub.1.n. znamená acetyl nebo ochrannou skupinu hydroxy-funkce, G.sub.2.n. znamená ochrannou skupinu hydroxy-funkce a X zŕ
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9211739A FR2696464B1 (fr) | 1992-10-05 | 1992-10-05 | Nouveau procédé d'estérification de la baccatine III et de la désacétyl-10 baccatine III. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CZ83995A3 CZ83995A3 (en) | 1995-09-13 |
| CZ284818B6 true CZ284818B6 (cs) | 1999-03-17 |
Family
ID=9434116
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CZ95839A CZ284818B6 (cs) | 1992-10-05 | 1993-10-04 | Nový způsob esterifikace baccatinu III a 10-desacetylbaccatinu |
Country Status (24)
| Country | Link |
|---|---|
| US (2) | US5717103A (cs) |
| EP (1) | EP0663905B1 (cs) |
| JP (1) | JP3064419B2 (cs) |
| KR (1) | KR100290663B1 (cs) |
| AT (1) | ATE147734T1 (cs) |
| AU (1) | AU689446B2 (cs) |
| CA (1) | CA2146372C (cs) |
| CZ (1) | CZ284818B6 (cs) |
| DE (1) | DE69307526T2 (cs) |
| DK (1) | DK0663905T3 (cs) |
| ES (1) | ES2096328T3 (cs) |
| FI (1) | FI115909B (cs) |
| FR (1) | FR2696464B1 (cs) |
| GR (1) | GR3022286T3 (cs) |
| HU (1) | HU225973B1 (cs) |
| MX (1) | MX9305764A (cs) |
| NO (1) | NO313141B1 (cs) |
| NZ (1) | NZ256443A (cs) |
| PL (1) | PL178090B1 (cs) |
| RU (1) | RU2123493C1 (cs) |
| SK (1) | SK281035B6 (cs) |
| TW (1) | TW372234B (cs) |
| WO (1) | WO1994007876A1 (cs) |
| ZA (1) | ZA937316B (cs) |
Families Citing this family (75)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6794523B2 (en) | 1991-09-23 | 2004-09-21 | Florida State University | Taxanes having t-butoxycarbonyl substituted side-chains and pharmaceutical compositions containing them |
| FR2697522B1 (fr) * | 1992-10-30 | 1994-11-25 | Rhone Poulenc Rorer Sa | Procédé de préparation de dérivés du taxane. |
| FR2698361B1 (fr) * | 1992-11-20 | 1995-01-13 | Rhone Poulenc Rorer Sa | Procédé de préparation d'un acide oxazolidine-1,3 carboxylique-5. |
| MX9307777A (es) | 1992-12-15 | 1994-07-29 | Upjohn Co | 7-HALO-Y 7ß, 8ß-METANO-TAXOLES, USO ANTINEOPLASTICO Y COMPOSICIONES FARMACEUTICAS QUE LOS CONTIENEN. |
| JPH09511212A (ja) * | 1993-06-11 | 1997-11-11 | ジ・アップジョン・カンパニー | Δ▲上６▼，▲上７▼−タキソール類の抗悪性腫瘍的使用およびそれらを含む医薬組成物 |
| PT2226085E (pt) | 1993-07-19 | 2014-03-04 | Angiotech Pharm Inc | Composições anti-angiogénicas e métodos de utilização |
| NZ276286A (en) * | 1993-11-12 | 2001-06-29 | Upjohn Co | Substituted pyrimidine thio- or oxy-alkyl derivatives and medicaments |
| IL127598A (en) * | 1994-01-28 | 2003-04-10 | Upjohn Co | Process for preparing isotaxol analogs |
| CA2178541C (en) | 1995-06-07 | 2009-11-24 | Neal E. Fearnot | Implantable medical device |
| CZ293480B6 (cs) * | 1996-05-08 | 2004-05-12 | Pharmaciaá@Áupjohnácompany | Oxazolidinové estery silylovaného baccatinu III |
| US6150537A (en) | 1997-12-12 | 2000-11-21 | Emory University | Methods for the esterification of alcohols and compounds useful therefor as potential anticancer agents |
| JP4502338B2 (ja) * | 1999-09-17 | 2010-07-14 | 株式会社横浜国際バイオ研究所 | タキソイド化合物の製造法 |
| EP2289549A3 (en) | 1999-10-01 | 2011-06-15 | Immunogen, Inc. | Immunoconjugates for treating cancer |
| CA2307393A1 (en) | 2000-05-01 | 2001-11-01 | The University Of British Columbia | Ginsenoside chemotherapy |
| AU2001288805A1 (en) | 2000-09-22 | 2002-04-02 | Bristol-Myers Squibb Company | Method for reducing toxicity of combined chemotherapies |
| US20030054036A1 (en) * | 2001-03-13 | 2003-03-20 | Richard Liggins | Micellar drug delivery vehicles and precursors thereto and uses thereof |
| US20030157170A1 (en) * | 2001-03-13 | 2003-08-21 | Richard Liggins | Micellar drug delivery vehicles and precursors thereto and uses thereof |
| DE60220519T2 (de) * | 2001-04-20 | 2007-09-27 | The University Of British Columbia, Vancouver | Mizellares arzneistoffverabreichungssystem für hydrophobe arzneistoffe |
| US7351542B2 (en) | 2002-05-20 | 2008-04-01 | The Regents Of The University Of California | Methods of modulating tubulin deacetylase activity |
| ITMI20021921A1 (it) * | 2002-09-10 | 2004-03-11 | Indena Spa | Funzionalizzazione della posizione 14 dei nuclei tassanici e sintesi di nuovi derivati antitumorali. |
| AU2003300076C1 (en) | 2002-12-30 | 2010-03-04 | Angiotech International Ag | Drug delivery from rapid gelling polymer composition |
| EP2390262A1 (en) | 2003-05-16 | 2011-11-30 | Intermune, Inc. | Synthetic chemokine receptor ligands and methods of use thereof |
| US7407973B2 (en) | 2003-10-24 | 2008-08-05 | Intermune, Inc. | Use of pirfenidone in therapeutic regimens |
| US7989490B2 (en) | 2004-06-02 | 2011-08-02 | Cordis Corporation | Injectable formulations of taxanes for cad treatment |
| US7846940B2 (en) | 2004-03-31 | 2010-12-07 | Cordis Corporation | Solution formulations of sirolimus and its analogs for CAD treatment |
| US8003122B2 (en) | 2004-03-31 | 2011-08-23 | Cordis Corporation | Device for local and/or regional delivery employing liquid formulations of therapeutic agents |
| US7597884B2 (en) | 2004-08-09 | 2009-10-06 | Alios Biopharma, Inc. | Hyperglycosylated polypeptide variants and methods of use |
| US8691780B2 (en) | 2005-02-17 | 2014-04-08 | The Board Of Trustees Of The Leland Stanford Junior University | Txr1 and enhanced taxane sensitivity based on the modulation of a pathway mediated thereby |
| RU2448697C2 (ru) | 2006-03-22 | 2012-04-27 | Медигене Аг | Лечение рака молочной железы, негативного по трем рецепторам |
| EP2380606B1 (en) | 2006-06-30 | 2018-03-21 | Cook Medical Technologies LLC | Methods of manufacturing and modifying taxane coatings for implantable medical devices |
| US8420110B2 (en) | 2008-03-31 | 2013-04-16 | Cordis Corporation | Drug coated expandable devices |
| US8409601B2 (en) | 2008-03-31 | 2013-04-02 | Cordis Corporation | Rapamycin coated expandable devices |
| US8273404B2 (en) | 2008-05-19 | 2012-09-25 | Cordis Corporation | Extraction of solvents from drug containing polymer reservoirs |
| US9198893B2 (en) | 2008-05-22 | 2015-12-01 | Galera Labs, Llc | Combination antitumor therapy |
| CA2724130C (en) | 2008-06-06 | 2016-04-26 | Harbor Biosciences, Inc. | Methods for preparing 17-alkynyl-7-hydroxy steroids and related compounds |
| US20110172293A1 (en) | 2008-07-08 | 2011-07-14 | Fish Jason E | Methods and Compositions for Modulating Angiogenesis |
| US8642063B2 (en) | 2008-08-22 | 2014-02-04 | Cook Medical Technologies Llc | Implantable medical device coatings with biodegradable elastomer and releasable taxane agent |
| PL388144A1 (pl) | 2009-05-29 | 2010-12-06 | Przedsiębiorstwo Produkcyjno-Wdrożeniowe Ifotam Spółka Z Ograniczoną Odpowiedzialnością | Solwaty (2R,3S)-3-tert-butoksykarbonylamino-2-hydroksy-3-fenylopropionianu 4-acetoksy-2α-benzoiloksy -5β,20-epoksy-1,7β,10β-trihydroksy-9-okso-taks-11-en-13α-ylu, sposób ich otrzymywania i zastosowanie |
| US20120302954A1 (en) | 2011-05-25 | 2012-11-29 | Zhao Jonathon Z | Expandable devices coated with a paclitaxel composition |
| US20120303115A1 (en) | 2011-05-25 | 2012-11-29 | Dadino Ronald C | Expandable devices coated with a rapamycin composition |
| US9956385B2 (en) | 2012-06-28 | 2018-05-01 | The Spectranetics Corporation | Post-processing of a medical device to control morphology and mechanical properties |
| CN104582717B (zh) | 2012-07-19 | 2018-03-13 | 雷德伍德生物科技股份有限公司 | 对cd22有特异性的抗体及其使用方法 |
| CN104884056A (zh) | 2012-11-12 | 2015-09-02 | 雷德伍德生物科技股份有限公司 | 用于制备缀合物的化合物和方法 |
| US20150368342A1 (en) | 2013-02-15 | 2015-12-24 | The Regents Of The University Of California | Chimeric antigen receptor and methods of use thereof |
| JP6410790B2 (ja) | 2013-03-14 | 2018-10-24 | ザ ボード オブ トラスティーズ オブ ザ レランド スタンフォード ジュニア ユニバーシティー | ミトコンドリアアルデヒドデヒドロゲナーゼ−２調節因子およびその使用方法 |
| WO2015081282A1 (en) | 2013-11-27 | 2015-06-04 | Redwood Bioscience, Inc. | Hydrazinyl-pyrrolo compounds and methods for producing a conjugate |
| JP6615769B2 (ja) | 2014-02-19 | 2019-12-04 | アルデア ファーマシューティカルズ インコーポレイテッド | ミトコンドリアアルデヒドデヒドロゲナーゼ２（ａｌｄｈ２）に結合する多環式アミド |
| JP6083815B2 (ja) * | 2014-03-07 | 2017-02-22 | 立川ブラインド工業株式会社 | タッセル |
| KR20180058759A (ko) | 2015-09-25 | 2018-06-01 | 제트와이 테라퓨틱스 인코포레이티드 | 폴리사카라이드-비타민 접합체를 포함하는 미립자를 기재로 하는 약물 제제 |
| EP3373977A4 (en) | 2015-11-12 | 2019-07-17 | The Board of Trustees of the Leland Stanford Junior University | CELL-PENETRATING, GUANIDINIUM-LICH OLIGOPHOSPHOTRIESTER FOR ACTIVE AND SPILL-RELIEF |
| TWI760319B (zh) | 2015-12-30 | 2022-04-11 | 杏國新藥股份有限公司 | 乳癌治療 |
| WO2017189432A1 (en) | 2016-04-26 | 2017-11-02 | R.P. Scherer Technologies, Llc | Antibody conjugates and methods of making and using the same |
| KR102473887B1 (ko) | 2016-06-01 | 2022-12-06 | 세르비에 아이피 유케이 리미티드 | 폴리알킬렌 옥시드-아스파라기나제의 제형, 및 그의 제조 및 사용 방법 |
| TWI852903B (zh) | 2017-01-05 | 2024-08-21 | 杏國新藥股份有限公司 | 胰臟癌治療 |
| CA3049674A1 (en) | 2017-01-18 | 2018-07-26 | F1 Oncology, Inc. | Chimeric antigen receptors against axl or ror2 and methods of use thereof |
| EP3388082A1 (en) | 2017-04-13 | 2018-10-17 | Galera Labs, LLC | Combination cancer immunotherapy with pentaaza macrocyclic ring complex |
| CN111065623B9 (zh) | 2017-05-24 | 2024-10-25 | 德克萨斯州大学系统董事会 | 用于抗体药物缀合物的接头 |
| EA202091832A1 (ru) | 2018-01-31 | 2021-01-11 | ГАЛЕРА ЛЭБЗ, ЭлЭлСи | Комбинированная терапия злокачественных новообразований макроциклическим кольцевым комплексом пентаазы и противоопухолевым агентом на основе платины |
| WO2019195586A1 (en) | 2018-04-06 | 2019-10-10 | The Regents Of The University Of California | Methods of treating egfrviii expressing glioblastomas |
| AU2019249221A1 (en) | 2018-04-06 | 2020-10-22 | The Regents Of The University Of California | Methods of treating glioblastomas |
| KR20210009315A (ko) | 2018-04-11 | 2021-01-26 | 오하이오 스테이트 이노베이션 파운데이션 | 안약 전달용 서방형 마이크로 입자를 이용한 방법 및 조성물 |
| CA3105879A1 (en) | 2018-07-18 | 2020-01-23 | Manzanita Pharmaceuticals, Inc. | Conjugates for delivering an anti-cancer agent to nerve cells, methods of use and methods of making thereof |
| WO2020148612A1 (en) | 2019-01-14 | 2020-07-23 | Ignite Immunotherapy, Inc. | Recombinant vaccinia virus and methods of use thereof |
| JP2022520220A (ja) | 2019-02-14 | 2022-03-29 | イグナイト イミュノセラピー インク | 組換えワクシニアウイルスおよびその使用方法 |
| WO2020206033A1 (en) | 2019-04-02 | 2020-10-08 | Kenjockety Biotechnology, Inc. | Efflux pump-cancer antigen multi-specific antibodies and compositions, reagents, kits and methods related thereto |
| CA3163805A1 (en) | 2019-12-12 | 2021-06-17 | Ignite Immunotherapy, Inc. | Variant oncolytic vaccinia virus and methods of use thereof |
| EP4097134A1 (en) | 2020-01-29 | 2022-12-07 | Kenjockety Biotechnology, Inc. | Anti-mdr1 antibodies and uses thereof |
| AU2021284240A1 (en) | 2020-06-04 | 2022-12-08 | William Robert ARATHOON | Anti-ABCG2 antibodies and uses thereof |
| CA3182969A1 (en) | 2020-06-04 | 2021-12-09 | Kenjockety Biotechnology, Inc. | Abcg2 efflux pump-cancer antigen multi-specific antibodies and compositions, reagents, kits and methods related thereto |
| MX2023000734A (es) | 2020-07-14 | 2023-02-13 | Pfizer | Virus vaccinia recombinante. |
| US20230272117A1 (en) | 2020-09-02 | 2023-08-31 | Kenjockety Biotechnology, Inc. | Anti abcc1 antibodies and uses thereof |
| US20240010747A1 (en) | 2020-11-13 | 2024-01-11 | Kenjockety Biotechnology, Inc. | Anti-mrp4 (encoded by abcc4 gene) antibodies and uses thereof |
| WO2022109335A1 (en) | 2020-11-20 | 2022-05-27 | R.P. Scherer Technologies, Llc | Glycoside dual-cleavage linkers for antibody-drug conjugates |
| US20250051471A1 (en) | 2021-12-13 | 2025-02-13 | William Robert Arathoon Living Trust Dated August 29, 2016 | Anti-Abcb1 Antibodies |
| WO2023159220A1 (en) | 2022-02-18 | 2023-08-24 | Kenjockety Biotechnology, Inc. | Anti-cd47 antibodies |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US34277A (en) * | 1862-01-28 | Improvement in lamps | ||
| US4942184A (en) * | 1988-03-07 | 1990-07-17 | The United States Of America As Represented By The Department Of Health And Human Services | Water soluble, antineoplastic derivatives of taxol |
| USRE34277E (en) * | 1988-04-06 | 1993-06-08 | Centre National De La Recherche Scientifique | Process for preparing taxol |
| FR2629818B1 (fr) * | 1988-04-06 | 1990-11-16 | Centre Nat Rech Scient | Procede de preparation du taxol |
| MX9102128A (es) * | 1990-11-23 | 1992-07-08 | Rhone Poulenc Rorer Sa | Derivados de taxano,procedimiento para su preparacion y composicion farmaceutica que los contiene |
| FR2696460B1 (fr) * | 1992-10-05 | 1994-11-25 | Rhone Poulenc Rorer Sa | Procédé de préparation de dérivés du taxane. |
| FR2696458B1 (fr) * | 1992-10-05 | 1994-11-10 | Rhone Poulenc Rorer Sa | Procédé de préparation de dérivés du taxane. |
-
1992
- 1992-10-05 FR FR9211739A patent/FR2696464B1/fr not_active Expired - Fee Related
-
1993
- 1993-09-21 MX MX9305764A patent/MX9305764A/es unknown
- 1993-10-01 ZA ZA937316A patent/ZA937316B/xx unknown
- 1993-10-02 TW TW082108116A patent/TW372234B/zh not_active IP Right Cessation
- 1993-10-04 KR KR1019950701300A patent/KR100290663B1/ko not_active Expired - Lifetime
- 1993-10-04 EP EP93921980A patent/EP0663905B1/fr not_active Expired - Lifetime
- 1993-10-04 CZ CZ95839A patent/CZ284818B6/cs not_active IP Right Cessation
- 1993-10-04 RU RU95110766A patent/RU2123493C1/ru active
- 1993-10-04 SK SK438-95A patent/SK281035B6/sk not_active IP Right Cessation
- 1993-10-04 HU HU9500970A patent/HU225973B1/hu unknown
- 1993-10-04 ES ES93921980T patent/ES2096328T3/es not_active Expired - Lifetime
- 1993-10-04 WO PCT/FR1993/000965 patent/WO1994007876A1/fr active IP Right Grant
- 1993-10-04 DE DE69307526T patent/DE69307526T2/de not_active Expired - Lifetime
- 1993-10-04 NZ NZ256443A patent/NZ256443A/en not_active IP Right Cessation
- 1993-10-04 AT AT93921980T patent/ATE147734T1/de active
- 1993-10-04 AU AU51148/93A patent/AU689446B2/en not_active Expired
- 1993-10-04 CA CA002146372A patent/CA2146372C/fr not_active Expired - Lifetime
- 1993-10-04 US US08/411,691 patent/US5717103A/en not_active Expired - Lifetime
- 1993-10-04 JP JP6508785A patent/JP3064419B2/ja not_active Expired - Lifetime
- 1993-10-04 PL PL93308239A patent/PL178090B1/pl unknown
- 1993-10-04 DK DK93921980.4T patent/DK0663905T3/da active
-
1995
- 1995-03-29 NO NO19951200A patent/NO313141B1/no not_active IP Right Cessation
- 1995-04-04 FI FI951593A patent/FI115909B/fi not_active IP Right Cessation
-
1997
- 1997-01-16 GR GR960402654T patent/GR3022286T3/el unknown
- 1997-10-31 US US08/962,452 patent/US5977375A/en not_active Expired - Lifetime
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CZ284818B6 (cs) | Nový způsob esterifikace baccatinu III a 10-desacetylbaccatinu | |
| FR2696458B1 (fr) | Procédé de préparation de dérivés du taxane. | |
| CA2077394A1 (en) | Substituted taxanes and pharmaceutical compositions containing them | |
| ATE148882T1 (de) | Verfahren zur herstellung von taxan-derivaten | |
| ZA938214B (en) | Furyl or thienyl carbonyl substituted taxanes and pharmaceutical compositions containing them | |
| TW427988B (en) | Process for the preparation of taxane derivatives | |
| GEP19981299B (en) | Method of Preparing Taxane Derivatives | |
| MX9306883A (es) | Nuevos derivados de taxano, procedimiento para su obtencion y composicionfarmaceutica que los contiene. | |
| RU94045799A (ru) | СПОСОБ ПОЛУЧЕНИЯ β-ФЕНИЛИЗОСЕРИНА И ЕГО АНАЛОГОВ, СПОСОБ ПОЛУЧЕНИЯ ПРОИЗВОДНЫХ ТАКСАНА И ПРОМЕЖУТОЧНЫЕ СОЕДИНЕНИЯ СИНТЕЗА | |
| FR2698360B1 (fr) | Procédé de préparation d'un acide oxazolidine-1,3 carboxylique-5. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| IF00 | In force as of 2000-06-30 in czech republic | ||
| MK4A | Patent expired |
Effective date: 20131004 |