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Peng C Tang, 69New Brunswick, NJ

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New Brunswick, NJ   

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Peng Tang

Location:
United States

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Us Patents

Methods For Treating Cancer And Other Cell Proliferative Diseases

US Patent:
5783568, Jul 21, 1998
Filed:
Jun 10, 1994
Appl. No.:
8/258307
Inventors:
Joseph Schlessinger - New York NY
Irit Lax - Fair Lawn NJ
John E. Ladbury - New York NY
Peng Cho Tang - Moraga CA
Assignee:
Sugen, Inc. - Redwood City CA
New York University - New York NY
International Classification:
A61K 31715
C08B 3710
US Classification:
514 53
Abstract:
The present invention relates to a method of treating in a mammal certain cancers, other cell proliferative diseases, and/or angiogenesis by using a salt or complex of a sulfated saccharide. The invention also relates to the use of mutant heparin binding growth factors that bind to the growth factor receptor, but not to heparin. The invention also provides pharmaceutical compositions for such methods.

Antipsoriatic Agents

US Patent:
5075327, Dec 24, 1991
Filed:
Nov 14, 1988
Appl. No.:
7/270991
Inventors:
Peng C. Tang - Bloomfield NJ
Milan R. Uskokovic - Upper Montclair NJ
Assignee:
Hoffmann-La Roche Inc. - Nutley NJ
International Classification:
A61K 3135
C07D30930
US Classification:
514460
Abstract:
A compound and process of making thereof of formula ##STR1## wherein R. sub. 1 is hydrogen; and A is alkyl; cycloalkyl; alkenyl; alkyl substituted with trifluoromethyl; phenyl; halophenyl; phenyl-C. sub. 1-3 alkyl; phenyl-C. sub. 1-3 alkyl substituted on the phenyl with 1 to 3 substituents selected from the group consisting of halo, C. sub. 1-3 alkyl, and C. sub. 1-3 alkoxy; or A is ##STR2## wherein Z is lower alkyl; R. sub. 2 is hydrogen or ##STR3## R. sub. 3 is hydrogen or methyl, and n is 1 to 5; Y is phenyl, is phenyl substituted by 1 to 3 substituents selected from the group consisting of halo, lower alkyl, and lower alkoxy; Y' is hydrogen or methyl; and b and d are carbon-carbon bonds or c is a carbon-carbon bond; or the corresponding hydroxy acid of formula ##STR4## wherein A, and R. sub. 1, R. sub. 2, R. sub. 3, Y and Y' are as described above, or a pharmaceutically acceptable salt of said acid, an alkyl ester of said acid, an acetylamino-substituted-C. sub. 1-4 alkyl ester of said acid, a phenyl-dimethylamino ester of said acid or a. alpha.

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