The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Mar. 09, 1999

Filed:

Sep. 18, 1996
Applicant:
Inventors:

Akira Yoshida, Tokyo, JP;

Kozo Oda, Tokyo, JP;

Takashi Kasai, Tokyo, JP;

Kousei Shimada, Tokyo, JP;

Hiroshi Kogen, Tokyo, JP;

Ichiro Hayakawa, Tokyo, JP;

Sadao Ishihara, Tokyo, JP;

Teiichiro Koga, Tokyo, JP;

Eiichi Kitazawa, Tokyo, JP;

Taro Tokui, Tokyo, JP;

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K / ; A61K / ; C07D / ; C07C / ;
U.S. Cl.
CPC ...
514452 ; 514464 ; 514465 ; 514469 ; 514524 ; 514563 ; 514617 ; 514618 ; 514619 ; 549377 ; 549378 ; 549441 ; 549467 ; 549468 ; 554 35 ; 554 36 ; 554 37 ; 558412 ; 558411 ; 558415 ; 564154 ; 564155 ; 564158 ;
Abstract

Compounds of formula (I): ##STR1## wherein: R.sup.1 is alkyl; R.sup.2a, R.sup.2b, R.sup.2c and R.sup.2d are the same or different and each is hydrogen, optionally substituted alkyl, --(C.dbd.O)--B.sup.1 (wherein B.sup.1 is hydrogen or alkyl), nitro, --NR.sup.c R.sup.d (wherein R.sup.c is hydrogen or alkyl and Rd is alkyl), hydroxy, protected hydroxy group, alkoxy, cyano, alkylthio, alkylsulfinyl, alkylsulfonyl or halogen; R.sup.3 is alkyl; R.sup.4 is a group of the formula (II) ##STR2## wherein A.sup.1 is a single bond, alkylene or alkenylene; R.sup.5a and R.sup.5b are the same or different and each is hydrogen, alkyl or --A.sup.4 R.sup.5.sub.c wherein A is a single bond, alkylene or alkenylene and R.sup.5.sub.c is alkoxy; and n is 0, and pharmaceutically acceptable salts thereof. Such compounds have valuable inhibitory activity against acyl-CoA (cholesterol acyl transferase).


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