PE20020997A1 - Compuestos de dihidropirimidina ciano sustituidos y su uso para tratar padecimientos - Google Patents
Compuestos de dihidropirimidina ciano sustituidos y su uso para tratar padecimientosInfo
- Publication number
- PE20020997A1 PE20020997A1 PE2002000257A PE2002000257A PE20020997A1 PE 20020997 A1 PE20020997 A1 PE 20020997A1 PE 2002000257 A PE2002000257 A PE 2002000257A PE 2002000257 A PE2002000257 A PE 2002000257A PE 20020997 A1 PE20020997 A1 PE 20020997A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- cyane
- pyrimidinecarboxyl
- dihydro
- oxo
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- WCFAPJDPAPDDAQ-UHFFFAOYSA-N 1,2-dihydropyrimidine Chemical compound C1NC=CC=N1 WCFAPJDPAPDDAQ-UHFFFAOYSA-N 0.000 title abstract 2
- -1 1-ETHYL Chemical class 0.000 abstract 4
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 abstract 2
- NKANXQFJJICGDU-QPLCGJKRSA-N Tamoxifen Chemical compound C=1C=CC=CC=1C(/CC)=C(C=1C=CC(OCCN(C)C)=CC=1)/C1=CC=CC=C1 NKANXQFJJICGDU-QPLCGJKRSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 229940124087 DNA topoisomerase II inhibitor Drugs 0.000 abstract 1
- ZDZOTLJHXYCWBA-VCVYQWHSSA-N N-debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)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 ZDZOTLJHXYCWBA-VCVYQWHSSA-N 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 229930012538 Paclitaxel Natural products 0.000 abstract 1
- 239000000317 Topoisomerase II Inhibitor Substances 0.000 abstract 1
- 239000002246 antineoplastic agent Substances 0.000 abstract 1
- 230000006907 apoptotic process Effects 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 abstract 1
- 229960004316 cisplatin Drugs 0.000 abstract 1
- KZZKOVLJUKWSKX-UHFFFAOYSA-N cyclobutanamine Chemical compound NC1CCC1 KZZKOVLJUKWSKX-UHFFFAOYSA-N 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229960003668 docetaxel Drugs 0.000 abstract 1
- 229960004679 doxorubicin Drugs 0.000 abstract 1
- VJJPUSNTGOMMGY-MRVIYFEKSA-N etoposide Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@H](C)OC[C@H]4O3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 VJJPUSNTGOMMGY-MRVIYFEKSA-N 0.000 abstract 1
- 229960005420 etoposide Drugs 0.000 abstract 1
- 230000011278 mitosis Effects 0.000 abstract 1
- 229960001592 paclitaxel Drugs 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
- 229960001603 tamoxifen Drugs 0.000 abstract 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 abstract 1
- UCFGDBYHRUNTLO-QHCPKHFHSA-N topotecan Chemical compound C1=C(O)C(CN(C)C)=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 UCFGDBYHRUNTLO-QHCPKHFHSA-N 0.000 abstract 1
- 229960000303 topotecan Drugs 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/20—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D239/22—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to ring carbon atoms
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- A—HUMAN NECESSITIES
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
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- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
- C07D211/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
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- 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
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
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- Heart & Thoracic Surgery (AREA)
- Immunology (AREA)
- Communicable Diseases (AREA)
- Orthopedic Medicine & Surgery (AREA)
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- Molecular Biology (AREA)
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- Hospice & Palliative Care (AREA)
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Abstract
SE REFIERE A DERIVADOS DE DIHIDROPIRIMIDINAS DE FORMULA I DONDE R1 ES H, ALQUILO, CICLOALQUILO; R2 Y R3 SON H, ALQUILO, ARILO, HETEROARILO, O JUNTOS FORMAN UN HETEROCICLO, CARBOCICLO, ENTRE OTROS; R4 ES ALQUILO, ARILALQUILO, CICLOALQUILALQUILO, CN, CONR5R6, ENTRE OTROS; R5 Y R6 SON H, ALQUILO, CICLOALQUILO, HIDROXIALQUILO, ALQUENILO, ALCOXI, TIOALCOXI, ALCOXIALQUILO, ENTRE OTROS; Z ES O, S, NR8; R8 ES H, CN, SULFONAMIDO, OR7, ALQUILO, CICLOALQUILO, ARILO, ENTRE OTROS; R7 ES H, ALQUILO ARILALQUILO, CICLOALQUILALQUILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS 1-ESTER ETILICO DEL ACIDO 6-(3-BIFENIL)-5-CIANO-3,6-DIHIDRO-4-METIL-2-OXO-1-(2H)-PIRIMIDINCARBOXILICO; 1-ESTER ETILO DEL ACIDO 5-CIANO-3,6-DIHIDRO-4-METIL-2-OXO-6-(3-(2-TIENIL)FENIL)-1-(2H)-PIRIMIDINCARBOXILICO. 1-CICLOBUTIL AMIDA DEL ACIDO 5-CINAO-3,6-DIHIDRO-4-METIL-2-OXO-6-(3-(3-PIRIDIL)FENIL)-1-(2H)-PIRIMIDINCARBOXILICO, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION QUE COMPRENDE ADEMAS UN AGENTE ANTICANCERIGENO COMO CISPLATIN, DOXORUBICIN, INHIBIDORES DE TOPOISOMERASAS II, ETOPOSIDE, TOPOTECAN, PACLITAXEL, DOCETAXEL, EPOTILONA, TAMOXIFEN, ENTRE OTROS. LOS COMPUESTOS INTERRUMPEN LA MITOSIS MODULANDO A LA PROTEINA MOTORA Eg5 Y/OP QUE INDUCE LA APOPTOSIS Y PUEDEN SER UTILES PARA EL TRATAMIENTO DE PADECIMIENTOS PROLIFERATIVOS COMO CANCER
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US27995601P | 2001-03-29 | 2001-03-29 | |
| US10/104,382 US6900214B2 (en) | 2001-03-29 | 2002-03-22 | Cyano-substituted dihydropyrimidine compounds and their use to treat diseases |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20020997A1 true PE20020997A1 (es) | 2002-11-08 |
Family
ID=26801480
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2002000257A PE20020997A1 (es) | 2001-03-29 | 2002-04-01 | Compuestos de dihidropirimidina ciano sustituidos y su uso para tratar padecimientos |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US6900214B2 (es) |
| EP (1) | EP1373223A4 (es) |
| JP (1) | JP2004529139A (es) |
| KR (1) | KR20030086328A (es) |
| CN (1) | CN1500082A (es) |
| AR (1) | AR035805A1 (es) |
| BG (1) | BG108195A (es) |
| BR (1) | BR0208353A (es) |
| CA (1) | CA2442484A1 (es) |
| CZ (1) | CZ20032643A3 (es) |
| EE (1) | EE200300473A (es) |
| HR (1) | HRP20030874A2 (es) |
| HU (1) | HUP0400341A3 (es) |
| IL (1) | IL157442A0 (es) |
| IS (1) | IS6966A (es) |
| MX (1) | MXPA03008635A (es) |
| NO (1) | NO20034301L (es) |
| NZ (1) | NZ527617A (es) |
| PE (1) | PE20020997A1 (es) |
| PL (1) | PL364005A1 (es) |
| RU (1) | RU2003131975A (es) |
| SK (1) | SK11072003A3 (es) |
| WO (1) | WO2002079169A1 (es) |
| YU (1) | YU75603A (es) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69734362T2 (de) | 1996-12-03 | 2006-07-20 | Sloan-Kettering Institute For Cancer Research | Synthese von epothilonen, zwischenprodukte dazu, analoga und verwendungen davon |
| US6809102B2 (en) | 2001-03-29 | 2004-10-26 | Bristol-Myers Squibb Company | Cyano-substituted dihydropyrimidine compounds and their use to treat diseases |
| PT1454903E (pt) * | 2001-12-11 | 2010-11-09 | Kyowa Hakko Kirin Co Ltd | Derivados de tiadiazolina para tratamento do cancro |
| ES2281692T3 (es) | 2002-08-23 | 2007-10-01 | Sloan-Kettering Institute For Cancer Research | Sintesis de epotilones, sus intermediarios, sus analogos y sus usos. |
| US7649006B2 (en) | 2002-08-23 | 2010-01-19 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| CA2522594C (en) | 2003-04-18 | 2012-01-24 | Kyowa Hakko Kogyo Co., Ltd. | Mitotic kinesin inhibitor |
| CN1802361A (zh) * | 2003-06-10 | 2006-07-12 | 协和发酵工业株式会社 | 噻二唑啉衍生物 |
| WO2005007124A2 (en) | 2003-07-23 | 2005-01-27 | Bristol-Myers Squibb Company | Substituted dihydropyrimidine inhibitors of calcium channel function |
| US7166603B2 (en) | 2003-07-23 | 2007-01-23 | Bristol-Myers Squibb Co. | Dihydropyrimidone inhibitors of calcium channel function |
| WO2005037799A1 (en) * | 2003-10-16 | 2005-04-28 | Cytokinetics, Inc. | Compounds, compositions, and methods |
| RU2447077C2 (ru) | 2004-08-18 | 2012-04-10 | Астразенека Аб | Энантиомеры выбранных конденсированных пиримидинов и их применение для лечения и предотвращения злокачественного новообразования |
| FR2883284A1 (fr) * | 2005-03-15 | 2006-09-22 | Commissariat Energie Atomique | Nouveaux derives dihydropyrimidines et leur utilisation comme agents anti-cancereux |
| CA2602559A1 (en) * | 2005-03-22 | 2006-09-28 | Kyowa Hakko Kogyo Co., Ltd. | Agent for treatment of hematopoietic tumor |
| CA2602397A1 (en) * | 2005-03-22 | 2006-09-28 | Kyowa Hakko Kogyo Co., Ltd. | Therapeutic agent for solid tumor |
| WO2006137490A1 (ja) * | 2005-06-24 | 2006-12-28 | Kyowa Hakko Kogyo Co., Ltd. | 再狭窄治療剤 |
| DE102006002065B4 (de) * | 2006-01-16 | 2007-11-29 | Infineon Technologies Austria Ag | Kompensationsbauelement mit reduziertem und einstellbarem Einschaltwiderstand |
| EP2455456A1 (en) | 2010-11-22 | 2012-05-23 | Institut Curie | Use of kinesin inhibitors in HIV infection treatment and a method for screening them |
| BR112014003989A2 (pt) * | 2011-08-26 | 2017-06-13 | Sanford-Burnham Medical Res Inst | composto, composições e métodos para inibir a replicação do hiv-1 em paciente, para tratar pacientes infectados com hiv/aids e para profilaxia de pré-exposição para tratar paciente e para prevenir a transmissão de pessoa infectada para pessoa não infectada |
| CN105237465B (zh) * | 2015-11-13 | 2017-07-21 | 吉林大学 | 一种具有神经保护作用的化合物及医用用途 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS422265Y1 (es) | 1965-10-21 | 1967-02-10 | ||
| US6211198B1 (en) | 1993-04-05 | 2001-04-03 | Synaptic Pharmaceutical Corporation | Dihydropyridines and new uses thereof |
| HUT77941A (hu) | 1994-11-16 | 1998-12-28 | Synaptic Pharmaceutical Corporation | Dihidropirimidinszármazékok és ezek alkalmazása |
| WO1997017969A1 (en) | 1995-11-16 | 1997-05-22 | Synaptic Pharmaceutical Corporation | Dihydropyrimidines and uses thereof |
| US6172066B1 (en) | 1996-05-16 | 2001-01-09 | Synaptic Pharmaceutical Corporation | Dihydropyrimidines and uses thereof |
| JP2000506904A (ja) | 1996-05-16 | 2000-06-06 | シナプティック・ファーマスーティカル・コーポレーション | ジヒドロピリミジン類およびその使用 |
| US6080760A (en) | 1997-06-18 | 2000-06-27 | Merck & Co., Inc. | Alpha 1A adrenergic receptor antagonists |
| EP1003511A1 (en) | 1997-06-18 | 2000-05-31 | Merck & Co., Inc. | ALPHA 1aADRENERGIC RECEPTOR ANTAGONISTS |
| AU1403099A (en) | 1997-11-14 | 1999-06-07 | Merck & Co., Inc. | Alpha-1a adrenergic receptor antagonists |
| US6346389B1 (en) | 1998-04-01 | 2002-02-12 | Yale University | Method for selectively modulating the interactions between survivin and tubulin |
| US6300084B1 (en) | 1998-10-08 | 2001-10-09 | The Regents Of The University Of California | Anti-mitotic agent screening process |
| GB9914258D0 (en) * | 1999-06-18 | 1999-08-18 | Celltech Therapeutics Ltd | Chemical compounds |
| AUPQ171999A0 (en) | 1999-07-20 | 1999-08-12 | University Of Sydney, The | Neurotropic virus transport |
| DE19935303A1 (de) | 1999-07-28 | 2001-02-08 | Aventis Pharma Gmbh | Oligonukleotide zur Inhibierung der Expression von humanem eg5 |
| US6617115B1 (en) | 1999-10-27 | 2003-09-09 | Cytokinetics, Inc. | Methods of screening for modulators of cell proliferation |
| ES2263501T3 (es) | 1999-10-27 | 2006-12-16 | Cytokinetics, Inc. | Procedimiento y composiciones que utilizan quinazolinonas. |
| US6284480B1 (en) | 2000-04-03 | 2001-09-04 | Cytokinetics, Inc. | Antifungal assay |
| US6809102B2 (en) | 2001-03-29 | 2004-10-26 | Bristol-Myers Squibb Company | Cyano-substituted dihydropyrimidine compounds and their use to treat diseases |
-
2002
- 2002-03-22 US US10/104,382 patent/US6900214B2/en not_active Expired - Lifetime
- 2002-03-26 EP EP02731175A patent/EP1373223A4/en not_active Withdrawn
- 2002-03-26 NZ NZ527617A patent/NZ527617A/en unknown
- 2002-03-26 HU HU0400341A patent/HUP0400341A3/hu unknown
- 2002-03-26 CN CNA028074564A patent/CN1500082A/zh active Pending
- 2002-03-26 PL PL02364005A patent/PL364005A1/xx not_active Application Discontinuation
- 2002-03-26 WO PCT/US2002/009494 patent/WO2002079169A1/en not_active Ceased
- 2002-03-26 RU RU2003131975/04A patent/RU2003131975A/ru not_active Application Discontinuation
- 2002-03-26 HR HR20030874A patent/HRP20030874A2/xx not_active Application Discontinuation
- 2002-03-26 CA CA002442484A patent/CA2442484A1/en not_active Abandoned
- 2002-03-26 BR BR0208353-1A patent/BR0208353A/pt not_active IP Right Cessation
- 2002-03-26 JP JP2002577796A patent/JP2004529139A/ja not_active Withdrawn
- 2002-03-26 MX MXPA03008635A patent/MXPA03008635A/es unknown
- 2002-03-26 YU YU75603A patent/YU75603A/sh unknown
- 2002-03-26 KR KR10-2003-7012607A patent/KR20030086328A/ko not_active Withdrawn
- 2002-03-26 SK SK1107-2003A patent/SK11072003A3/sk unknown
- 2002-03-26 EE EEP200300473A patent/EE200300473A/xx unknown
- 2002-03-26 CZ CZ20032643A patent/CZ20032643A3/cs unknown
- 2002-03-26 IL IL15744202A patent/IL157442A0/xx unknown
- 2002-04-01 PE PE2002000257A patent/PE20020997A1/es not_active Application Discontinuation
- 2002-04-02 AR ARP020101175A patent/AR035805A1/es unknown
-
2003
- 2003-09-24 BG BG108195A patent/BG108195A/bg unknown
- 2003-09-24 IS IS6966A patent/IS6966A/is unknown
- 2003-09-26 NO NO20034301A patent/NO20034301L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| NO20034301D0 (no) | 2003-09-26 |
| NO20034301L (no) | 2003-11-10 |
| AR035805A1 (es) | 2004-07-14 |
| IL157442A0 (en) | 2004-03-28 |
| JP2004529139A (ja) | 2004-09-24 |
| HUP0400341A2 (hu) | 2004-10-28 |
| EP1373223A1 (en) | 2004-01-02 |
| PL364005A1 (en) | 2004-11-29 |
| KR20030086328A (ko) | 2003-11-07 |
| BR0208353A (pt) | 2004-03-23 |
| YU75603A (sh) | 2006-05-25 |
| CN1500082A (zh) | 2004-05-26 |
| NZ527617A (en) | 2005-02-25 |
| CA2442484A1 (en) | 2002-10-10 |
| BG108195A (bg) | 2004-07-30 |
| IS6966A (is) | 2003-09-24 |
| EE200300473A (et) | 2004-02-16 |
| SK11072003A3 (sk) | 2004-06-08 |
| US6900214B2 (en) | 2005-05-31 |
| HRP20030874A2 (en) | 2004-04-30 |
| MXPA03008635A (es) | 2004-02-23 |
| US20020143026A1 (en) | 2002-10-03 |
| HUP0400341A3 (en) | 2004-11-29 |
| RU2003131975A (ru) | 2005-05-10 |
| EP1373223A4 (en) | 2004-09-29 |
| WO2002079169A8 (en) | 2004-04-29 |
| WO2002079169A1 (en) | 2002-10-10 |
| CZ20032643A3 (en) | 2004-06-16 |
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