The George Washington University Law School, J.D., 1988
Isbn (Books And Publications)
Oral Contraceptives and Steroid Chemistry in the People's Republic of China: A Trip Report of the American Steroid Chemistry and Biochemistry Delegation
Richard H. Peters - San Jose CA Jyanwei Liu - Sunnyvale CA John G. Johansson - Menlo Park CA Kenneth J. Ryan - Sunnyvale CA Masato Tanabe - Palo Alto CA
Assignee:
SRI International - Menlo Park CA
International Classification:
A61K 3156
US Classification:
514182, 514176, 540112, 552558, 552600
Abstract:
Syntheses of steroids such as 3-hydroxy-7-methyl-21-[2â-methoxy-4â-(diethylaminomethyl)-phenoxy]-19-norpregna-1,3,5(10)triene citrate (âSR 16234â) and analogs thereof are provided, wherein 21-hydroxy-19-norpregna-4-en-3-one serves as a starting material or intermediate. The latter compound may be readily prepared from estrone-3-methyl ether. Certain intermediates in these syntheses also have value as therapeutic agents, for example in the treatment of prostate disorders such as prostatic cancer.
Synthesis Of Anti-Estrogenic And Other Therapeutic Steroids From 21-Hydroxy-19-Norpregna-4-En-3-One
Richard H. Peters - San Jose CA, US Jyanwei Liu - Sunnyvale CA, US John G. Johansson - Menlo Park CA, US Kenneth J. Ryan - Sunnyvale CA, US Masato Tanabe - Palo Alto CA, US
Assignee:
SRI International - Menlo Park CA
International Classification:
C07J 41/00 C07J 43/00
US Classification:
514169, 514174, 514178, 552526, 552530, 552531
Abstract:
Syntheses of steroids such as 3-hydroxy-7α-methyl-21-[2′-methoxy-4′-(diethylaminomethyl)-phenoxy]-19-norpregna-1,3,5(10)triene citrate (“SR 16234”) and analogs thereof are provided, wherein 21-hydroxy-19-norpregna-4-en-3-one serves as a starting material or intermediate. The latter compound may be readily prepared from estrone-3-methyl ether. Certain intermediates in these syntheses also have value as therapeutic agents, for example in the treatment of prostate disorders such as prostatic cancer.
Benzotriazine Oxides As Drugs Targeting Mycobacterium Tuberculosis
Charles K. Hiebert - Mountain View CA Alan Laibelman - Menlo Park CA Kenneth J. Ryan - Sunnyvale CA
Assignee:
SRI International - Menlo Park CA
International Classification:
A61K 3805 A61K 3806 A61K 31535 C07D26524
US Classification:
514 18
Abstract:
Novel therapeutic agents useful as inhibitors of HLE are provided. The compounds have the structural formula (I) ##STR1## wherein R. sup. 1 through R. sup. 9, m, n and p are as defined herein. Methods of using the compounds of formula (I) to inhibit serine proteases and to treat physiological conditions and disease states associated with elevated HLE levels are also provided, as are pharmaceutical compositions containing the compounds.
Edward M. Acton - Menlo Park CA Kenneth J. Ryan - Sunnyvale CA
Assignee:
Stanford Research Institute - Menlo Park CA
International Classification:
C07H 1916
US Classification:
536 24
Abstract:
Septacidin analogs, useful as antitumor agents, having the structure ##STR1## where R is a branched or straight chain alkanoyl group of from 12 to 16 carbon atoms. A preferred compound is 6-[4,6-dideoxy-4-(isopalmitoylglycyl)-amino-. beta. -L-glucopyranosylamino]- 9H-purine.
Edward M. Acton - Menlo Park CA Kenneth J. Ryan - Sunnyvale CA Michael Tracy - Menlo Park CA
Assignee:
SRI International - Menlo Park CA
International Classification:
C07H 702 C07H 1524
US Classification:
536 11
Abstract:
Disclosed herein is a new procedure for preparing the C. 1-2,4-pentadienyl derivatives of 2-deoxyhexopyranoses, as well as a new procedure for allylation of daunosamine. These methods are particularly useful for the preparation of intermediates in the synthesis of adriamycin C-glycosidic analogs which are useful anti-tumor agents. These methods provide the first enabling disclosure of methods to prepare these desired adriamycin and anthrocyclinone C-glycosidic analogs.
Benzotriazine Oxides As Drugs Targeting Mycobacterium Tuberculosis