WO2002088091A3 - Inhibitors of human rhinovirus 2a cysteine protease - Google Patents

Inhibitors of human rhinovirus 2a cysteine protease Download PDF

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Publication number
WO2002088091A3
WO2002088091A3 PCT/US2002/013270 US0213270W WO02088091A3 WO 2002088091 A3 WO2002088091 A3 WO 2002088091A3 US 0213270 W US0213270 W US 0213270W WO 02088091 A3 WO02088091 A3 WO 02088091A3
Authority
WO
WIPO (PCT)
Prior art keywords
human rhinovirus
inhibitors
halo
amino
cysteine protease
Prior art date
Application number
PCT/US2002/013270
Other languages
French (fr)
Other versions
WO2002088091A2 (en
Inventor
Raymond A Kim
David Shivak
Dongxu Sun
Original Assignee
Iconix Pharm Inc
Raymond A Kim
David Shivak
Dongxu Sun
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 Iconix Pharm Inc, Raymond A Kim, David Shivak, Dongxu Sun filed Critical Iconix Pharm Inc
Publication of WO2002088091A2 publication Critical patent/WO2002088091A2/en
Publication of WO2002088091A3 publication Critical patent/WO2002088091A3/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic 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
    • C07D231/14Heterocyclic 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
    • C07D231/18One oxygen or sulfur atom
    • C07D231/20One oxygen atom attached in position 3 or 5
    • C07D231/22One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
    • C07D231/261-Phenyl-3-methyl-5- pyrazolones, unsubstituted or substituted on the phenyl ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic 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
    • C07D231/14Heterocyclic 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
    • C07D231/18One oxygen or sulfur atom
    • C07D231/20One oxygen atom attached in position 3 or 5
    • C07D231/22One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Compounds of formula I are effective inhibitors of human rhinovirus 2A protease: (I) where R1 is H, lower alkyl, lower alkenyl, lower alkynyl, lower acyl, or lower acyloxy, substituted with 0-3 substituents selected from the group consisting of OH, halo, amino, nitro; R2 is H, lower alkyl, OH, halo, or amino; R3, R4, R5, R6, and R7 are each independently H, halo, OH, amino, nitro, lower alkyl, aryl, aralkyl, lower alkoxy, or lower alkylamino; or a pharmaceutically acceptable salt thereof.
PCT/US2002/013270 2001-04-26 2002-04-26 Inhibitors of human rhinovirus 2a cysteine protease WO2002088091A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US28708301P 2001-04-26 2001-04-26
US60/287,083 2001-04-26

Publications (2)

Publication Number Publication Date
WO2002088091A2 WO2002088091A2 (en) 2002-11-07
WO2002088091A3 true WO2002088091A3 (en) 2002-12-19

Family

ID=23101374

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2002/013270 WO2002088091A2 (en) 2001-04-26 2002-04-26 Inhibitors of human rhinovirus 2a cysteine protease

Country Status (1)

Country Link
WO (1) WO2002088091A2 (en)

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
DATABASE CAPLUS [online] TANAKA E. ET AL.: "Comparison of trimethadione and antipyrine as indicators of oxidative drug metabolizing capacity in man", XP002958361, accession no. STN Database accession no. 1989:508460 *
DATABASE CAPLUS [online] USUI Y. ET AL.: "Fungicides. XII. Synthesis and antifungal activity of halogen-substituted phenylpyrazolone derivatives", XP002958362, accession no. STN Database accession no. 1967:411452 *
EUR. J. OF CLIN. PHARM., vol. 36, no. 6, 1989, pages 29 - 32 *
YAKAGAKU ZASSHI, vol. 87, no. 1, 1967, pages 38 - 42 *

Also Published As

Publication number Publication date
WO2002088091A2 (en) 2002-11-07

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