AU2001265008A1 - Caspase inhibitors and uses thereof - Google Patents

Caspase inhibitors and uses thereof

Info

Publication number
AU2001265008A1
AU2001265008A1 AU2001265008A AU6500801A AU2001265008A1 AU 2001265008 A1 AU2001265008 A1 AU 2001265008A1 AU 2001265008 A AU2001265008 A AU 2001265008A AU 6500801 A AU6500801 A AU 6500801A AU 2001265008 A1 AU2001265008 A1 AU 2001265008A1
Authority
AU
Australia
Prior art keywords
caspase inhibitors
caspase
inhibitors
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.)
Abandoned
Application number
AU2001265008A
Inventor
Julian Golec
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Vertex Pharmaceuticals Inc
Original Assignee
Vertex Pharmaceuticals 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 Vertex Pharmaceuticals Inc filed Critical Vertex Pharmaceuticals Inc
Publication of AU2001265008A1 publication Critical patent/AU2001265008A1/en
Abandoned legal-status Critical Current

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    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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 chain containing hetero atoms as chain links
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    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30Oxygen atoms
    • CCHEMISTRY; METALLURGY
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    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen 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
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic 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
    • C07D333/06Heterocyclic 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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/14Radicals substituted by singly bound hetero atoms other than halogen
    • C07D333/16Radicals substituted by singly bound hetero atoms other than halogen by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic 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
AU2001265008A 2000-05-23 2001-05-23 Caspase inhibitors and uses thereof Abandoned AU2001265008A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US20636200P 2000-05-23 2000-05-23
US60206362 2000-05-23
US21700600P 2000-07-10 2000-07-10
US60217006 2000-07-10
PCT/US2001/017075 WO2001090070A2 (en) 2000-05-23 2001-05-23 Caspase inhibitors and uses thereof

Publications (1)

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AU2001265008A1 true AU2001265008A1 (en) 2001-12-03

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AU2001265008A Abandoned AU2001265008A1 (en) 2000-05-23 2001-05-23 Caspase inhibitors and uses thereof

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US (1) US7053057B2 (en)
EP (1) EP1283827A2 (en)
JP (1) JP2003534325A (en)
KR (1) KR20020025959A (en)
AP (1) AP2002002407A0 (en)
AR (1) AR028619A1 (en)
AU (1) AU2001265008A1 (en)
CA (1) CA2380935A1 (en)
MX (1) MXPA02000823A (en)
NO (1) NO20020343L (en)
NZ (1) NZ516918A (en)
PE (1) PE20020058A1 (en)
PL (1) PL357713A1 (en)
SK (1) SK1192002A3 (en)
TR (1) TR200200767T1 (en)
WO (1) WO2001090070A2 (en)

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BR0013666A (en) 1999-08-27 2002-05-14 Cytovia Inc "alpha" -hydroxy acids substituted for caspase inhibitors and their use
PE20011350A1 (en) 2000-05-19 2002-01-15 Vertex Pharma PROPHARMAC OF AN INHIBITOR OF INTERLEUKIN-1ß CONVERTER ENZYME (ICE)
US6878743B2 (en) 2001-09-18 2005-04-12 Sunesis Pharmaceuticals, Inc. Small molecule inhibitors of caspases
EP1485107A1 (en) 2002-02-11 2004-12-15 Vertex Pharmaceuticals Incorporated Phospholipids as caspase inhibitor prodrugs
EP1499898A2 (en) * 2002-04-19 2005-01-26 Vertex Pharmaceuticals Incorporated Regulation of tnf-alpha
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US20060241034A1 (en) * 2003-05-22 2006-10-26 David Chauvier Means for preventing and treating cellular death and their biological applications
AU2003902704A0 (en) * 2003-05-29 2003-06-19 Crc For Waste Management And Pollution Control Limited Of Unsw Process for producing a nanoscale zero-valent metal
AR047981A1 (en) * 2004-02-27 2006-03-15 Vertex Pharma CASPASA INHIBITORS AND THEIR CORRESPONDING USES
KR101135765B1 (en) 2004-03-12 2012-04-23 버텍스 파마슈티칼스 인코포레이티드 Processes and intermediates for the preparation of aspartic acetal caspase inhibitors
JP4691549B2 (en) * 2004-04-07 2011-06-01 ノバルティス アーゲー Inhibitors of IAP
JP5053836B2 (en) * 2004-04-30 2012-10-24 テラプトシス エス アー Caspase-2 inhibitors and their biological applications
JP4848367B2 (en) * 2004-05-15 2011-12-28 バーテックス ファーマシューティカルズ インコーポレイテッド Treatment of seizures using ICE inhibitors
EP2295054A1 (en) 2004-05-27 2011-03-16 Vertex Pharmaceuticals Incorporated Ice inhibitors for the treatment of autoinflammatory diseases
WO2006030437A2 (en) * 2004-09-17 2006-03-23 Biomas Ltd. Novel tellurium compounds and their use as immunomodulators
CA2616337A1 (en) * 2005-07-28 2007-02-08 Vertex Pharmaceuticals Incorporated Caspase inhibitor prodrugs
PE20110224A1 (en) 2006-08-02 2011-04-05 Novartis Ag PROCEDURE FOR THE SYNTHESIS OF A PEPTIDOMIMETIC OF Smac INHIBITOR OF IAP, AND INTERMEDIARY COMPOUNDS FOR THE SYNTHESIS OF THE SAME
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