BIOMAT Database Logo BIOMAT Database Logo

Chlorosulfonation of 17-beta-acetoxy-3-methoxyestra-1,3,5(10)-triene. 1970

A H Goldkamp

UI MeSH Term Description Entries
D004967 Estrogens Compounds that interact with ESTROGEN RECEPTORS in target tissues to bring about the effects similar to those of ESTRADIOL. Estrogens stimulate the female reproductive organs, and the development of secondary female SEX CHARACTERISTICS. Estrogenic chemicals include natural, synthetic, steroidal, or non-steroidal compounds. Estrogen,Estrogen Effect,Estrogen Effects,Estrogen Receptor Agonists,Estrogenic Agents,Estrogenic Compounds,Estrogenic Effect,Estrogenic Effects,Agents, Estrogenic,Agonists, Estrogen Receptor,Compounds, Estrogenic,Effects, Estrogen,Effects, Estrogenic,Receptor Agonists, Estrogen
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D000924 Anticholesteremic Agents Substances used to lower plasma CHOLESTEROL levels. Cholesterol Inhibitors,Hypocholesteremic Agents,Anticholesteremic Drugs,Anticholesteremics,Inhibitors, Cholesterol,Agents, Anticholesteremic,Agents, Hypocholesteremic,Drugs, Anticholesteremic
D000970 Antineoplastic Agents Substances that inhibit or prevent the proliferation of NEOPLASMS. Anticancer Agent,Antineoplastic,Antineoplastic Agent,Antineoplastic Drug,Antitumor Agent,Antitumor Drug,Cancer Chemotherapy Agent,Cancer Chemotherapy Drug,Anticancer Agents,Antineoplastic Drugs,Antineoplastics,Antitumor Agents,Antitumor Drugs,Cancer Chemotherapy Agents,Cancer Chemotherapy Drugs,Chemotherapeutic Anticancer Agents,Chemotherapeutic Anticancer Drug,Agent, Anticancer,Agent, Antineoplastic,Agent, Antitumor,Agent, Cancer Chemotherapy,Agents, Anticancer,Agents, Antineoplastic,Agents, Antitumor,Agents, Cancer Chemotherapy,Agents, Chemotherapeutic Anticancer,Chemotherapy Agent, Cancer,Chemotherapy Agents, Cancer,Chemotherapy Drug, Cancer,Chemotherapy Drugs, Cancer,Drug, Antineoplastic,Drug, Antitumor,Drug, Cancer Chemotherapy,Drug, Chemotherapeutic Anticancer,Drugs, Antineoplastic,Drugs, Antitumor,Drugs, Cancer Chemotherapy
D051381 Rats The common name for the genus Rattus. Rattus,Rats, Laboratory,Rats, Norway,Rattus norvegicus,Laboratory Rat,Laboratory Rats,Norway Rat,Norway Rats,Rat,Rat, Laboratory,Rat, Norway,norvegicus, Rattus

Related Publications

A H Goldkamp
High-performance liquid chromatographic methods for monitoring of isomers of 17-hydroxy-16-hydroxymethyl-3-methoxyestra-1,3,5(10)-triene.
August 1999, Journal of chromatography. A,
A H Goldkamp
Aromatic steroids. I. Oxidation products of 3-methoxyestra-1,3,5(10-trien-17-beta-yl acetate.
January 1968, Journal of the Chemical Society. Perkin transactions 1,
A H Goldkamp
D-Secoestrone derivatives. VI. 17 beta-Benzyl-17 alpha-hydroxy-3-methoxyestra-1,3,5(10)-trien-16-one.
March 2002, Acta crystallographica. Section C, Crystal structure communications,
A H Goldkamp
Synthesis of 6,7-benzo-3-methoxyestra-1,3,5(10),8,14-pentaen-17-one.
January 1986, Steroids,
A H Goldkamp
[Conversion of 15 beta.16 beta-epoxy-3-methoxyestra-1.3.5(10)-triene-17-one using hydroxylamine derivatives. 43. Steroids].
January 1976, Die Pharmazie,
A H Goldkamp
Synthesis of (+/-)-3-methoxyestra-1,3,5(10)-triene: stitching and riveting as a tool for steroid synthesis.
September 1977, The Journal of organic chemistry,
A H Goldkamp
Synthesis and properties of benzo [d,e]estra-1,3,5(10)-triene-3, 17 beta-diol 17-acetate.
January 1981, Experientia,
A H Goldkamp
Formation of estra-1,3,5(10)-triene-3,15 alpha, 16 alpha, 17 beta-tetrol (estetrol) and estra-1,3,5(10)-triene-3,15 alpha, 17 beta-triol from neutral precursors.
November 1968, The Journal of clinical endocrinology and metabolism,
A H Goldkamp
D-Secoestrone derivatives. V1. 3-Methoxy-17-oxo-17-phenyl-16,17-secoestra-1,3,5(10)-triene-16-nitrile and 17-hydroxy-3-methoxy-17-phenyl-16,17-secoestra-1,3,5(10)-triene-16-nitrile.
February 2002, Acta crystallographica. Section C, Crystal structure communications,
A H Goldkamp
Total synthesis of steroids. X. Synthesis of 3-methoxyestra-1,3,5(10),8,14-pentaen-17-one.
October 1975, The Journal of organic chemistry,
Copied contents to your clipboard!