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Title:
MEDICINE CONTAINING HYDROXAMIC ACID DERIVATIVE
Document Type and Number:
Japanese Patent JPH111430
Kind Code:
A
Abstract:

To obtain the subject medicine having matrix metalloproteinase- inhibiting activities and useful as metastatic infiltration- or growth-inhibiting agents, etc., for various cancer cells, by bringing the medicine to contain a specific hydoxamic acid derivative.

The objective medicine is obtained by bringing the medicine to contain a hydroxamic acid derivative expressed by formula I [R1 is an alkyl, a cycloalkyl-methyl or an arylmethyl; R2 and R3 are a (substituted) alkyl, H or a cyclic amino group formed together with R1, R2 and bound N; R4 is an alkyl; R5 is H, a (substituted) carbamoyl or an aliphatic acyl; R6 is H, a heteroaryl-substituted alkyl, etc.], {e.g. N-[3-(S)-hydroxy-4-(N- hydroxylamino)-2-(R)-nonylsuccinyl]-L-tert-leucin-N-methyl amide}. The compound of formula I is a new compound and can be produced by using a compound of formula II (R1a expresses that a hydroxyl group in R1 is protected) as a starting material.


Inventors:
SHIBATA TOMOYUKI
OKAWA NOBUYUKI
TAKEMOTO TOSHIYASU
TAMAKI KAZUHIKO
KURIHARA NOBUKAZU
SATO SUSUMU
TANZAWA KAZUHIKO
KOBAYASHI TOMOO
FUJIWARA KOSAKU
Application Number:
JP10248298A
Publication Date:
January 06, 1999
Filing Date:
April 14, 1998
Export Citation:
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Assignee:
SANKYO CO
International Classes:
C07D295/12; A61K31/16; A61K31/165; A61K31/18; A61K31/195; A61K31/215; A61K31/44; A61K31/535; A61K31/5375; A61K38/00; A61P1/02; A61P1/04; A61P9/10; A61P13/02; A61P15/00; A61P17/00; A61P19/10; A61P27/02; A61P29/00; A61P35/00; A61P43/00; C07C259/06; C07C311/45; C07C311/51; C07D207/08; C07D207/12; C07D211/22; C07K5/062; (IPC1-7): A61K31/16; A61K31/16; A61K31/165; A61K31/18; A61K31/195; A61K31/215; A61K31/44; A61K31/535; A61K38/00
Attorney, Agent or Firm:
大野 彰夫 (外2名)



 
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