ZA911101B - Inhibition of modified ldl products - Google Patents

Inhibition of modified ldl products

Info

Publication number
ZA911101B
ZA911101B ZA911101A ZA911101A ZA911101B ZA 911101 B ZA911101 B ZA 911101B ZA 911101 A ZA911101 A ZA 911101A ZA 911101 A ZA911101 A ZA 911101A ZA 911101 B ZA911101 B ZA 911101B
Authority
ZA
South Africa
Prior art keywords
inhibition
modified ldl
products
ldl products
modified
Prior art date
Application number
ZA911101A
Other languages
English (en)
Inventor
Yasuyuki Kato
Kato Yasuyuki
Kunio Tamura
Tamura Kunio
Yasuhiro Ohba
Ohba Yasuhiro
Yoshiki Kawabe
Kawabe Yoshiki
Osamu Cynshi
Cynshi Osamu
Original Assignee
Chugai Pharmaceutical Co Ltd
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 Chugai Pharmaceutical Co Ltd filed Critical Chugai Pharmaceutical Co Ltd
Publication of ZA911101B publication Critical patent/ZA911101B/xx

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    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
    • C07D207/32Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D207/33Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • A61K31/10Sulfides; Sulfoxides; Sulfones
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    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00Systems containing two condensed rings
    • C07C2602/02Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04One of the condensed rings being a six-membered aromatic ring
    • C07C2602/10One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/56Ring systems containing bridged rings
    • C07C2603/58Ring systems containing bridged rings containing three rings
    • C07C2603/70Ring systems containing bridged rings containing three rings containing only six-membered rings
    • C07C2603/74Adamantanes

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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ZA911101A 1990-02-14 1991-02-14 Inhibition of modified ldl products ZA911101B (en)

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EP0761214A3 (en) * 1995-07-21 1999-06-09 Kao Corporation N,N-disubstituted anilines or alkylamines as singlet oxygen quenchers, topical compositions comprising them
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JP5278983B2 (ja) * 1999-11-17 2013-09-04 塩野義製薬株式会社 アミド化合物の新規用途
US7429593B2 (en) 2001-09-14 2008-09-30 Shionogi & Co., Ltd. Utilities of amide compounds
US20050228017A1 (en) * 2001-10-31 2005-10-13 Morphochem Aktiengesellschaft Fur Kombinatorische Chemie Novel anticancer compounds
AR043507A1 (es) * 2003-03-14 2005-08-03 Lundbeck & Co As H Derivados de anilina sustituidos y composiciones farmaceuticas
EP1606247A1 (en) * 2003-03-14 2005-12-21 H. Lundbeck A/S Substituted aniline derivatives
EP1663999A2 (en) * 2003-08-29 2006-06-07 Ranbaxy Laboratories, Ltd. Inhibitors of phosphodiesterase type-iv
JP2008518003A (ja) * 2004-10-29 2008-05-29 アストラゼネカ・アクチエボラーグ 医薬品としての不飽和キノリンもしくはナフタレン誘導体の使用
US8008312B2 (en) 2005-01-07 2011-08-30 Emory University CXCR4 antagonists for the treatment of HIV infection
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CN101137379B (zh) * 2005-01-07 2015-02-11 埃莫里大学 用于治疗医学病症的cxcr4拮抗剂
CA2599331A1 (en) 2005-02-28 2006-09-08 Meiji Dairies Corporation Hydroquinone long-chain derivatives and/or phenoxy long-chain derivatives, and pharmaceuticals preparation comprising the same
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EP0515684A1 (en) 1992-12-02
EP0515684A4 (en) 1993-04-21
WO1991011994A1 (en) 1991-08-22
AU7317391A (en) 1991-09-03
CA2076012A1 (en) 1991-08-15

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