HRP20040892A2 - Use of epothilones in the treatment of brain diseases associated with proliferative processes - Google Patents

Use of epothilones in the treatment of brain diseases associated with proliferative processes

Info

Publication number: HRP20040892A2
Authority: HR; Croatia
Prior art keywords: methyl; dihydroxy; dione; ethenyl; tetramethyl
Prior art date: 2002-03-01

Application number

Other languages

English (en)

Croatian (hr)

Inventor

Rosemarie Lichtner

Andrea Rotgeri

Ulrich Klar

Jens Hoffmann

Bernd Buchmann

Wolfgang Schwede

Werner Skuballa

Original Assignee

Schering Ag

Priority date (The priority date 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 date listed.)

2002-03-01

Filing date

2004-09-28

Publication date

2004-12-31

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27675676&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20040892(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2004-09-28 Application filed by Schering Ag filed Critical Schering Ag

2004-12-31 Publication of HRP20040892A2 publication Critical patent/HRP20040892A2/hr

Links

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238000011282 treatment Methods 0.000 title claims description 29
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230000008569 process Effects 0.000 title claims description 21
230000002062 proliferating effect Effects 0.000 title claims description 21
HESCAJZNRMSMJG-KKQRBIROSA-N epothilone A Chemical class C/C([C@@H]1C[C@@H]2O[C@@H]2CCC[C@@H]([C@@H]([C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1)O)C)=C\C1=CSC(C)=N1 HESCAJZNRMSMJG-KKQRBIROSA-N 0.000 title description 11
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239000001257 hydrogen Substances 0.000 claims description 46
150000001875 compounds Chemical class 0.000 claims description 38
150000002431 hydrogen Chemical class 0.000 claims description 30
125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 26
125000003118 aryl group Chemical group 0.000 claims description 23
150000003883 epothilone derivatives Chemical class 0.000 claims description 23
-1 heteroaromatic radical Chemical class 0.000 claims description 21
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UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
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125000002971 oxazolyl group Chemical group 0.000 description 1
125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
230000002688 persistence Effects 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
YJGVMLPVUAXIQN-XVVDYKMHSA-N podophyllotoxin Chemical compound COC1=C(OC)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@H](O)[C@@H]3[C@@H]2C(OC3)=O)=C1 YJGVMLPVUAXIQN-XVVDYKMHSA-N 0.000 description 1
229960001237 podophyllotoxin Drugs 0.000 description 1
YVCVYCSAAZQOJI-UHFFFAOYSA-N podophyllotoxin Natural products COC1=C(O)C(OC)=CC(C2C3=CC=4OCOC=4C=C3C(O)C3C2C(OC3)=O)=C1 YVCVYCSAAZQOJI-UHFFFAOYSA-N 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
CPTBDICYNRMXFX-UHFFFAOYSA-N procarbazine Chemical compound CNNCC1=CC=C(C(=O)NC(C)C)C=C1 CPTBDICYNRMXFX-UHFFFAOYSA-N 0.000 description 1
229960000624 procarbazine Drugs 0.000 description 1
108090000765 processed proteins & peptides Proteins 0.000 description 1
230000035755 proliferation Effects 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000009979 protective mechanism Effects 0.000 description 1
125000003373 pyrazinyl group Chemical group 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
125000002098 pyridazinyl group Chemical group 0.000 description 1
ILVXOBCQQYKLDS-UHFFFAOYSA-N pyridine N-oxide Chemical compound [O-][N+]1=CC=CC=C1 ILVXOBCQQYKLDS-UHFFFAOYSA-N 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
125000000714 pyrimidinyl group Chemical group 0.000 description 1
238000011002 quantification Methods 0.000 description 1
125000005493 quinolyl group Chemical group 0.000 description 1
125000006413 ring segment Chemical group 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000011255 standard chemotherapy Methods 0.000 description 1
238000011301 standard therapy Methods 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000000829 suppository Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000003826 tablet Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
ILMRJRBKQSSXGY-UHFFFAOYSA-N tert-butyl(dimethyl)silicon Chemical group C[Si](C)C(C)(C)C ILMRJRBKQSSXGY-UHFFFAOYSA-N 0.000 description 1
125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
125000000335 thiazolyl group Chemical group 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
ODLHGICHYURWBS-LKONHMLTSA-N trappsol cyclo Chemical compound CC(O)COC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](COCC(C)O)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)COCC(O)C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1COCC(C)O ODLHGICHYURWBS-LKONHMLTSA-N 0.000 description 1
125000000025 triisopropylsilyl group Chemical group C(C)(C)[Si](C(C)C)(C(C)C)* 0.000 description 1
125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 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
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
229960004528 vincristine Drugs 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents

Landscapes

Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Veterinary Medicine (AREA)
Medicinal Chemistry (AREA)
Public Health (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Epidemiology (AREA)
Organic Chemistry (AREA)
Neurology (AREA)
General Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Biomedical Technology (AREA)
Chemical Kinetics & Catalysis (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Neurosurgery (AREA)
Psychiatry (AREA)
Hospice & Palliative Care (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Plural Heterocyclic Compounds (AREA)

HRP20040892 2002-03-01 2004-09-28 Use of epothilones in the treatment of brain diseases associated with proliferative processes HRP20040892A2 (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US36106202P	2002-03-01	2002-03-01
EP02004745A EP1340498A1 (fr)	2002-03-01	2002-03-01	Utilisation d'épothilones dans le traitement de maladies du cerveau associées aux processus de prolifération
PCT/EP2003/002085 WO2003074053A1 (fr)	2002-03-01	2003-02-28	Utilisation d'epothilones pour le traitement de maladies du cerveau a caractere proliferatif

Publications (1)

Publication Number	Publication Date
HRP20040892A2 true HRP20040892A2 (en)	2004-12-31

Family

ID=27675676

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
HRP20040892 HRP20040892A2 (en)	2002-03-01	2004-09-28	Use of epothilones in the treatment of brain diseases associated with proliferative processes

Country Status (23)

Country	Link
US (1)	US20040019088A1 (fr)
EP (2)	EP1340498A1 (fr)
JP (1)	JP2005525360A (fr)
KR (1)	KR20040095244A (fr)
CN (1)	CN100473381C (fr)
AR (1)	AR038712A1 (fr)
AU (1)	AU2003215618B2 (fr)
BR (1)	BR0308154A (fr)
CA (1)	CA2477403A1 (fr)
CR (1)	CR7444A (fr)
EC (1)	ECSP045340A (fr)
HK (1)	HK1079998A1 (fr)
HR (1)	HRP20040892A2 (fr)
IL (1)	IL163752A0 (fr)
MX (1)	MXPA04008450A (fr)
NO (1)	NO20044175L (fr)
NZ (1)	NZ546617A (fr)
PL (1)	PL370768A1 (fr)
RU (1)	RU2351330C2 (fr)
UA (1)	UA83798C2 (fr)
WO (1)	WO2003074053A1 (fr)
YU (1)	YU76404A (fr)
ZA (1)	ZA200407905B (fr)

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EP0977563B1 (fr)	1996-12-03	2005-10-12	Sloan-Kettering Institute For Cancer Research	Synthese d'epothilones, intermediaires utilises dans leur synthese, analogues et utilisations de celles-ci
CA2299608A1 (fr) *	1997-08-09	1999-02-18	Schering Aktiengesellschaft	Nouveaux derives d'epothilone, leur procede de fabrication et leur utilisation pharmaceutique
BR0008206A (pt) *	1999-02-11	2002-02-19	Schering Ag	Derivados de epotilon, processos para a sua preparação e sua aplicação farmacêutica
US7125893B1 (en) *	1999-04-30	2006-10-24	Schering Ag	6-alkenyl-, 6-alkinyl- and 6-epoxy-epothilone derivatives, process for their production, and their use in pharmaceutical preparations
CN102532120A (zh)	2002-08-23	2012-07-04	索隆-基特林癌症研究协会	埃坡霉素(epothilone)，合成埃坡霉素的中间体，其类似物及其用途
US7649006B2 (en)	2002-08-23	2010-01-19	Sloan-Kettering Institute For Cancer Research	Synthesis of epothilones, intermediates thereto and analogues thereof
DE10331004A1 (de) *	2003-07-03	2005-02-24	Schering Ag	Verfahren für die Herstellung von C1-C15-Fragmenten von Epothilonen und deren Derivaten
EP1559447A1 (fr) *	2004-01-30	2005-08-03	Institut National De La Sante Et De La Recherche Medicale (Inserm)	Utilisation d'epothilone pour le traitement de defauts de connectivité neuronale comme par exemple la schizophrenie et l'autisme
US20060069136A1 (en) *	2004-09-24	2006-03-30	Ulrich Klar	Use of Epothilones in the treatment of bone metastasis
US20060121511A1 (en)	2004-11-30	2006-06-08	Hyerim Lee	Biomarkers and methods for determining sensitivity to microtubule-stabilizing agents
EP1674098A1 (fr) *	2004-12-23	2006-06-28	Schering Aktiengesellschaft	Formulations parenterales stables et tolérables des substances de haut réactivité ayant une solubilité basse ou inexistante dans l'eau
EP1700596A1 (fr) *	2005-03-09	2006-09-13	Max-Planck-Gesellschaft Zur Förderung Der Wissenschaften E.V.	Utilisation de composés stabilisant les microtubules pour le traitement des lesions axonales du SNC
DE102007016046A1 (de) *	2007-03-30	2008-10-23	Bayer Schering Pharma Aktiengesellschaft	Verfahren zur Herstellung von Epothilonderivaten durch selektive katalytische Epoxidierung
TWI472329B (zh)	2008-04-24	2015-02-11	必治妥美雅史谷比公司	埃坡徽素ｄ於治療包括阿茲海默症之ｔａｕ相關疾病的用途
EP2793947B1 (fr)	2011-12-23	2021-02-03	Innate Pharma	Conjugaison enzymatique de polypeptides
US10132799B2 (en)	2012-07-13	2018-11-20	Innate Pharma	Screening of conjugated antibodies
EP2916872B1 (fr)	2012-11-09	2019-02-27	Innate Pharma	Etiquettes de reconnaissance pour la conjugaison à médiation par la tgase
WO2014140300A1 (fr)	2013-03-15	2014-09-18	Innate Pharma	Conjugaison d'anticorps en phase solide médiée par la tgase
US10071169B2 (en)	2013-06-20	2018-09-11	Innate Pharma	Enzymatic conjugation of polypeptides
KR20160042871A (ko)	2013-06-21	2016-04-20	이나뜨 파르마, 에스.아.	폴리펩티드의 효소적 콘쥬게이션
WO2019092148A1 (fr)	2017-11-10	2019-05-16	Innate Pharma	Anticorps avec des résidus de glutamine fonctionnalisés

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JP3226545B2 (ja) *	1995-06-09	2001-11-05	ノバルティス・アクチエンゲゼルシャフト	ラパマイシン誘導体
US6515016B2 (en) *	1996-12-02	2003-02-04	Angiotech Pharmaceuticals, Inc.	Composition and methods of paclitaxel for treating psoriasis
US6495579B1 (en) *	1996-12-02	2002-12-17	Angiotech Pharmaceuticals, Inc.	Method for treating multiple sclerosis
BR9807418A (pt) *	1997-02-18	2002-01-22	Canji Inc	Terapia de gene supressor de tumor combinado e quimioterapia no tratamento de neoplasmas
GB9801231D0 (en) *	1997-06-05	1998-03-18	Merck & Co Inc	A method of treating cancer
US6605599B1 (en) *	1997-07-08	2003-08-12	Bristol-Myers Squibb Company	Epothilone derivatives
CA2299608A1 (fr) *	1997-08-09	1999-02-18	Schering Aktiengesellschaft	Nouveaux derives d'epothilone, leur procede de fabrication et leur utilisation pharmaceutique
JP4434484B2 (ja) *	1997-12-04	2010-03-17	ブリストル−マイヤーズスクイブカンパニー	オキシラニルエポチロン化合物のオレフィン性エポチロン化合物への還元法
FR2775187B1 (fr) *	1998-02-25	2003-02-21	Novartis Ag	Utilisation de l'epothilone b pour la fabrication d'une preparation pharmaceutique antiproliferative et d'une composition comprenant l'epothilone b comme agent antiproliferatif in vivo
US6302838B1 (en) *	1998-02-25	2001-10-16	Novartis Ag	Cancer treatment with epothilones
AU4775299A (en) *	1998-06-22	2000-01-10	Nicolaou, Kyriacos Costa	Desmethyl epothilones
ES2291194T3 (es) *	1999-02-18	2008-03-01	Bayer Schering Pharma Aktiengesellschaft	Derivados de 16-halogeno-epotilones, procedimiento acerca de su preparacion y su utilizacion farmaceutica.
AR023792A1 (es) *	1999-04-30	2002-09-04	Bayer Schering Pharma Ag	Derivados 6-alquenilo- y 6-alquinilo-epotilona, los procedimientos para prepararlos y su empleo en productos farmaceuticos
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DE10020517A1 (de) *	2000-04-19	2001-10-25	Schering Ag	Neue Epothilon-Derivate, Verfahren zu deren Herstellung und ihre pharmazeutische Verwendung
WO2001092255A2 (fr) *	2000-05-26	2001-12-06	Kosan Biosciences, Inc.	Derives d'epothilone, procedes de production et methodes d'utilisation
GB0013643D0 (en) *	2000-05-31	2000-07-26	Unilever Plc	Targeted moieties for use in bleach catalysts
CA2449077A1 (fr) *	2001-06-01	2002-12-12	Gregory D. Vite	Derives d'epothilone

2002
- 2002-03-01 EP EP02004745A patent/EP1340498A1/fr not_active Withdrawn
2003
- 2003-02-28 BR BR0308154-0A patent/BR0308154A/pt not_active Withdrawn
- 2003-02-28 RU RU2004129325/15A patent/RU2351330C2/ru active
- 2003-02-28 US US10/375,043 patent/US20040019088A1/en not_active Abandoned
- 2003-02-28 CN CNB038097613A patent/CN100473381C/zh not_active Expired - Fee Related
- 2003-02-28 IL IL16375203A patent/IL163752A0/xx unknown
- 2003-02-28 NZ NZ546617A patent/NZ546617A/en unknown
- 2003-02-28 EP EP03743360A patent/EP1480643A1/fr not_active Withdrawn
- 2003-02-28 CA CA002477403A patent/CA2477403A1/fr not_active Abandoned
- 2003-02-28 PL PL03370768A patent/PL370768A1/xx not_active Application Discontinuation
- 2003-02-28 AU AU2003215618A patent/AU2003215618B2/en not_active Expired - Fee Related
- 2003-02-28 KR KR10-2004-7013549A patent/KR20040095244A/ko not_active Application Discontinuation
- 2003-02-28 WO PCT/EP2003/002085 patent/WO2003074053A1/fr active Application Filing
- 2003-02-28 MX MXPA04008450A patent/MXPA04008450A/es not_active Application Discontinuation
- 2003-02-28 YU YU76404A patent/YU76404A/sh unknown
- 2003-02-28 JP JP2003572570A patent/JP2005525360A/ja active Pending
- 2003-02-28 UA UA20040907817A patent/UA83798C2/ru unknown
- 2003-03-03 AR ARP030100696A patent/AR038712A1/es unknown
2004
- 2004-09-01 CR CR7444A patent/CR7444A/es not_active Application Discontinuation
- 2004-09-28 HR HRP20040892 patent/HRP20040892A2/hr not_active Application Discontinuation
- 2004-09-30 ZA ZA200407905A patent/ZA200407905B/en unknown
- 2004-09-30 NO NO20044175A patent/NO20044175L/no not_active Application Discontinuation
- 2004-09-30 EC EC2004005340A patent/ECSP045340A/es unknown
2006
- 2006-01-04 HK HK06100157.3A patent/HK1079998A1/zh unknown

Also Published As

Publication number	Publication date
ECSP045340A (es)	2004-11-26
US20040019088A1 (en)	2004-01-29
AR038712A1 (es)	2005-01-26
NO20044175L (no)	2004-12-01
EP1340498A1 (fr)	2003-09-03
YU76404A (sh)	2006-08-17
BR0308154A (pt)	2005-01-04
IL163752A0 (en)	2005-12-18
EP1480643A1 (fr)	2004-12-01
RU2351330C2 (ru)	2009-04-10
UA83798C2 (ru)	2008-08-26
AU2003215618A1 (en)	2003-09-16
AU2003215618B2 (en)	2009-06-04
CA2477403A1 (fr)	2003-09-12
WO2003074053A1 (fr)	2003-09-12
PL370768A1 (en)	2005-05-30
ZA200407905B (en)	2006-04-26
CR7444A (es)	2005-10-05
NZ546617A (en)	2007-12-21
MXPA04008450A (es)	2005-07-13
CN100473381C (zh)	2009-04-01
HK1079998A1 (zh)	2006-04-21
CN1649587A (zh)	2005-08-03
RU2004129325A (ru)	2005-07-10
KR20040095244A (ko)	2004-11-12
JP2005525360A (ja)	2005-08-25

Publication	Publication Date	Title
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