ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CYTOTOXICITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HEALTH CARE ORGANIZATION;
IN VIVO STUDY;
TUMOR CELL LINE;
UNITED STATES;
XENOGRAFT;
ANDROSTENES;
ANIMALS;
ANTINEOPLASTIC AGENTS;
BIOLOGICAL ASSAY;
CELL PROLIFERATION;
CRYSTALLOGRAPHY, X-RAY;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMANS;
MICE;
NATIONAL CANCER INSTITUTE (U.S.);
QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP;
TRANSPLANTATION, HETEROLOGOUS;
TUMOR CELLS, CULTURED;
UNITED STATES;
Hybrid anticancer compounds. Steroidal lactam esters of carboxylic derivatives of N,N-bis(2-chloroethyl)aniline (review)
Catsoulacos P., and Catsoulacos D. Hybrid anticancer compounds. Steroidal lactam esters of carboxylic derivatives of N,N-bis(2-chloroethyl)aniline (review). Anticancer Res 11 (1991) 1773-1777
Steroids and steroidases. 10. Studies on some potentially antitumor active androstane compounds containing C-17 nitrogen mustard functions
Jones J.B., Adam D.J., and Leman J.D. Steroids and steroidases. 10. Studies on some potentially antitumor active androstane compounds containing C-17 nitrogen mustard functions. J Med Chem 14 (1971) 827-833
Pancuronium bromide and other steroidal neuromuscular blocking agents containing acetylcholine fragments
Buckett W.R., Hewett C.L., and Savage D.S. Pancuronium bromide and other steroidal neuromuscular blocking agents containing acetylcholine fragments. J Med Chem 16 (1973) 1116
Synthesis of 16α-bromoacetoxy androgens and 17β-bromoacetylamino-4-androsten-3-one: potential affinity labels of human placental aromatase
Numazawa M., and Osawa Y. Synthesis of 16α-bromoacetoxy androgens and 17β-bromoacetylamino-4-androsten-3-one: potential affinity labels of human placental aromatase. Steroids 38 (1981) 149-159
Synthesis and cytotoxic studies of hydroximino derivatives of some 16E-arylidenosteroids
Chattopadhaya R., Jindal D.P., Minu M., and Gupta R. Synthesis and cytotoxic studies of hydroximino derivatives of some 16E-arylidenosteroids. Arzneim Forsch/Drug Res 54 (2004) 551-556
Synthesis and in vitro antineoplastic evaluation of certain 16-(4-substituted benzylidiene) derivatives of androst-5-ene
Dubey S., Piplani P., and Jindal D.P. Synthesis and in vitro antineoplastic evaluation of certain 16-(4-substituted benzylidiene) derivatives of androst-5-ene. Chem Biodivers 1 (2004) 1529-1536
Adams R., Blatt A.H., Bockelheidie V., Cairns T.L., Cope A.C., Cram D.J., and House H.O. (Eds), John Wiley, New York
Nielsen A.T., and Houlihan W.J. In: Adams R., Blatt A.H., Bockelheidie V., Cairns T.L., Cope A.C., Cram D.J., and House H.O. (Eds). Organic reactions. 16th ed. (1968), John Wiley, New York 1-438
Two androst-5-ene derivatives: 16-[4-(3-chloropropoxy)-3-methoxybenzylidene]-17-oxoandrost-5-en-3β-ol and 16-[3-methoxy-4-(2-pyrrolidin-1-yl ethoxy)benzylidene]-3β-pyrrolidinoandrost-5-en-17β-ol mono-hydrate
Thamotharan S., Parthasarathi V., Gupta R., Guleria S., Jindal D.P., and Linden A. Two androst-5-ene derivatives: 16-[4-(3-chloropropoxy)-3-methoxybenzylidene]-17-oxoandrost-5-en-3β-ol and 16-[3-methoxy-4-(2-pyrrolidin-1-yl ethoxy)benzylidene]-3β-pyrrolidinoandrost-5-en-17β-ol mono-hydrate. Acta Cryst 60 (2004) o75-84
The National Cancer Institute: cancer drug discovery and development program
Grever M.R., Schepartz S.A., and Chabner B.A. The National Cancer Institute: cancer drug discovery and development program. Semin Oncol 19 (1992) 622-638
Some practical considerations and applications of the National Cancer Institute in vitro anticancer drug discovery screen
Boyd M.R., and Paull K.D. Some practical considerations and applications of the National Cancer Institute in vitro anticancer drug discovery screen. Drug Dev Res 34 (1995) 91-109
In vivo cultivation of tumor cells in hollow fibers
Hellingshead M., Alley M.C., Camalier R.F., Abbott M.J., Mayo J.G., Malspeis L., et al. In vivo cultivation of tumor cells in hollow fibers. Life Sci 57 (1995) 131-141
