HN2000000051A - Derivados heterociclicos utiles como agentes anticancerosos - Google Patents

Derivados heterociclicos utiles como agentes anticancerosos

Info

Publication number
HN2000000051A
HN2000000051A HN2000000051A HN2000000051A HN2000000051A HN 2000000051 A HN2000000051 A HN 2000000051A HN 2000000051 A HN2000000051 A HN 2000000051A HN 2000000051 A HN2000000051 A HN 2000000051A HN 2000000051 A HN2000000051 A HN 2000000051A
Authority
HN
Honduras
Prior art keywords
useful
target agents
derivatives
heterociclic
heterociclic derivatives
Prior art date
Application number
HN2000000051A
Other languages
English (en)
Original Assignee
Pfizer Prod Inc
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.)
Filing date
Publication date
Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of HN2000000051A publication Critical patent/HN2000000051A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
    • C07D275/03—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • 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
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • 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
    • C07D409/12—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 chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Abstract

LA PRESENTE INVENCION SE REFIERE A DERIVADOS NOVEDOSOS DE ISOTIAZOL QUE SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES HIPERPOLIFERATIVAS, TALES COMO CANCERES EN MAMIFEROS.
HN2000000051A 1999-05-19 2000-04-12 Derivados heterociclicos utiles como agentes anticancerosos HN2000000051A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US13493399P 1999-05-19 1999-05-19

Publications (1)

Publication Number Publication Date
HN2000000051A true HN2000000051A (es) 2001-02-02

Family

ID=22465672

Family Applications (1)

Application Number Title Priority Date Filing Date
HN2000000051A HN2000000051A (es) 1999-05-19 2000-04-12 Derivados heterociclicos utiles como agentes anticancerosos

Country Status (21)

Country Link
US (1) US6380214B1 (es)
EP (1) EP1187826B1 (es)
JP (2) JP3692041B2 (es)
AR (1) AR029634A1 (es)
AT (1) ATE349440T1 (es)
AU (1) AU4137400A (es)
BR (1) BR0010746A (es)
CA (1) CA2374247C (es)
CO (1) CO5170417A1 (es)
DE (1) DE60032601T2 (es)
DZ (1) DZ3042A1 (es)
ES (1) ES2276681T3 (es)
GT (1) GT200000069A (es)
HN (1) HN2000000051A (es)
MA (1) MA26733A1 (es)
MX (1) MXPA01011920A (es)
PA (1) PA8494101A1 (es)
PE (1) PE20010152A1 (es)
TN (1) TNSN00104A1 (es)
UY (1) UY26143A1 (es)
WO (1) WO2000071532A1 (es)

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US6924276B2 (en) 2001-09-10 2005-08-02 Warner-Lambert Company Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors
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CA2491802C (en) * 2002-07-09 2012-04-10 Fasgen, Inc. Novel compounds, pharmaceutical compositions containing same, and methods of use for same
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WO2004050681A2 (en) * 2002-11-15 2004-06-17 Exelixis, Inc. Kinase modulators
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SE0300092D0 (sv) * 2003-01-15 2003-01-15 Astrazeneca Ab Novel compounds
SE0300091D0 (sv) * 2003-01-15 2003-01-15 Astrazeneca Ab Novel compounds
TWI369353B (en) * 2003-03-07 2012-08-01 Santen Pharmaceutical Co Ltd Novel compound having 4-pyridylalkylthio group as substituent
PT1626714E (pt) 2003-05-20 2007-08-24 Bayer Pharmaceuticals Corp Diarilureias para doenças mediadas por pdgfr
SI1663978T1 (sl) 2003-07-23 2008-02-29 Bayer Pharmaceuticals Corp Fluoro substituirana omega-karboksiaril difenil secnina za zdravljenje ali preprecevanje bolezni instanj
WO2005085201A1 (ja) * 2004-02-17 2005-09-15 Santen Pharmaceutical Co., Ltd. 置換又は無置換アミノ基を導入した４－ピリジルアルキルチオ基を有する新規環式化合物
JP4626353B2 (ja) * 2004-02-17 2011-02-09 参天製薬株式会社 置換又は無置換アミノ基を導入した４−ピリジルアルキルチオ基を有する新規環式化合物
ES2368153T3 (es) * 2004-02-17 2011-11-14 Santen Pharmaceutical Co., Ltd. Nuevo compuesto cíclico que presenta un grupo 4-piridilalquiltio que presenta amino (no) sustituido introducido en el mismo.
AU2005223483B2 (en) 2004-03-18 2009-04-23 Zoetis Llc N-(1-arylpyrazol-4l)sulfonamides and their use as parasiticides
ATE517885T1 (de) 2004-04-30 2011-08-15 Bayer Healthcare Llc Substituierte pyrazolyl-harnstoff-derivate zur behandlung von krebs
PT1784183E (pt) 2004-08-26 2012-03-09 Pfizer Processos para a preparação de derivados de isotiazole
JP4585978B2 (ja) * 2005-03-03 2010-11-24 参天製薬株式会社 キノリルアルキルチオ基を有する新規環式化合物
JP5030947B2 (ja) 2005-05-13 2012-09-19 ヴァイロケム・ファーマ・インコーポレーテッド フラビウイルス感染の治療及び予防のための化合物及び方法
US7932390B2 (en) 2006-06-29 2011-04-26 Hoffman-La Roche Inc. Substituted thieno[3,2-C]pyridine carboxylic acid derivatives
SG176488A1 (en) 2006-11-15 2011-12-29 Virochem Pharma Inc Thiophene analogues for the treatment or prevention of flavivirus infections
CN101622229B (zh) * 2007-02-26 2013-02-27 参天制药株式会社 具有脲基和氨基羰基作为取代基的吡咯衍生物
WO2008153042A1 (ja) * 2007-06-11 2008-12-18 Kyowa Hakko Kirin Co., Ltd. 抗腫瘍剤
MX2010001636A (es) 2007-08-14 2010-03-15 Hoffmann La Roche Derivados de pirazolo[3,4-d]-pirimidina como agentes antiproliferativos.
WO2010151710A2 (en) * 2009-06-25 2010-12-29 Medolution Limited Substituted heterocyclic compounds as kinases inhibitors and method of use thereof
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Also Published As

Publication number Publication date
AU4137400A (en) 2000-12-12
PE20010152A1 (es) 2001-02-08
JP3692041B2 (ja) 2005-09-07
DE60032601D1 (de) 2007-02-08
DZ3042A1 (fr) 2004-03-27
JP2005008641A (ja) 2005-01-13
CA2374247A1 (en) 2000-11-30
WO2000071532A1 (en) 2000-11-30
ES2276681T3 (es) 2007-07-01
AR029634A1 (es) 2003-07-10
GT200000069A (es) 2001-11-08
EP1187826B1 (en) 2006-12-27
PA8494101A1 (es) 2003-09-05
EP1187826A1 (en) 2002-03-20
MA26733A1 (fr) 2004-12-20
BR0010746A (pt) 2002-02-13
TNSN00104A1 (fr) 2005-11-10
US6380214B1 (en) 2002-04-30
ATE349440T1 (de) 2007-01-15
CO5170417A1 (es) 2002-06-27
MXPA01011920A (es) 2002-05-06
UY26143A1 (es) 2000-12-29
JP2003500401A (ja) 2003-01-07
DE60032601T2 (de) 2007-11-15
CA2374247C (en) 2008-01-22

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