Steroidal alkylating agents I. Some 16-substituted androstanes and pregnanes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry
Reference16 articles.
1. STEROIDS. I. A CASE OF WALDEN INVERSION WITH NUCLEOPHILIC SUBSTITUTION AT POSITION 3 OF Δ5–STEROIDS
2. Notes. Synthesis of a Steroidal Nitrogen Mustard
3. A Steroidal Mustard of the Androstane Series1
4. N-MUSTARD DERIVATIVES OF ESTROGENS
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1. Synthesis and aromatase inhibitory activity of some new 16E-arylidenosteroids;Bioorganic Chemistry;2012-12
2. Synthesis and antileukemic activity of 16E-[4-(2-carboxy)ethoxybenzylidene]-androstene amides;Steroids;2012-04
3. Synthesis and Biological Evaluation of 16E-Arylidenosteroids as Cytotoxic and Anti-aromatase Agents;Chemical and Pharmaceutical Bulletin;2011
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5. Preclinical activity of 17β-[N-[N′-(2-chloroethyl)-N′-nitrosocarbamoyl]-l-alanyl]-5α-dihydrotestosterone (E91) against tumour colony forming units and haematopoietic progenitor cells;European Journal of Cancer;1999-06
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