BIOMAT Database Logo BIOMAT Database Logo

[Synthesis of racemic 3-methoxy-17 -hydroxy-1.3.5(10)-estratriene-17 -carbonic acid and 3-methoxy-17 -hydroxy-1.3.5(10)-estratriene-17 -carbonic acid]. 1971

K Prezewowsky, and R Wiechert, and W Hohlweg

UI MeSH Term Description Entries
D002621 Chemistry A basic science concerned with the composition, structure, and properties of matter; and the reactions that occur between substances and the associated energy exchange.
D004962 Estranes A group of compounds forming the nucleus of the estrogenic steroid family. 19-Norandrostanes,19 Norandrostanes
D015065 17-Hydroxycorticosteroids A group of hydroxycorticosteroids bearing a hydroxy group at the 17-position. Urinary excretion of these compounds is used as an index of adrenal function. They are used systemically in the free alcohol form, but with esterification of the hydroxy groups, topical effectiveness is increased. 17 Hydroxycorticosteroids
D055598 Chemical Phenomena The composition, structure, conformation, and properties of atoms and molecules, and their reaction and interaction processes. Chemical Concepts,Chemical Processes,Physical Chemistry Concepts,Physical Chemistry Processes,Physicochemical Concepts,Physicochemical Phenomena,Physicochemical Processes,Chemical Phenomenon,Chemical Process,Physical Chemistry Phenomena,Physical Chemistry Process,Physicochemical Phenomenon,Physicochemical Process,Chemical Concept,Chemistry Process, Physical,Chemistry Processes, Physical,Concept, Chemical,Concept, Physical Chemistry,Concept, Physicochemical,Concepts, Chemical,Concepts, Physical Chemistry,Concepts, Physicochemical,Phenomena, Chemical,Phenomena, Physical Chemistry,Phenomena, Physicochemical,Phenomenon, Chemical,Phenomenon, Physicochemical,Physical Chemistry Concept,Physicochemical Concept,Process, Chemical,Process, Physical Chemistry,Process, Physicochemical,Processes, Chemical,Processes, Physical Chemistry,Processes, Physicochemical

Related Publications

K Prezewowsky, and R Wiechert, and W Hohlweg
Synthesis and biological activity of the superestrogen (E)-17-oximino-3-O-sulfamoyl-1,3,5(10)-estratriene: x-ray crystal structure of (E)-17-oximino-3-hydroxy-1,3,5(10)-estratriene.
August 1999, Journal of medicinal chemistry,
K Prezewowsky, and R Wiechert, and W Hohlweg
[Estrogenic activity and pharmacological characteristics of 2-(3-hydroxy-1,3,5(10)-estratriene-17-one)-isobutyric acid].
January 1954, Il Farmaco; edizione scientifica,
K Prezewowsky, and R Wiechert, and W Hohlweg
Conversion of an equilenane to the estrane: synthesis of d1-3-methoxy-17 beta-carboxy-1,3,5(10)-estratriene(1).
December 1970, Steroids,
K Prezewowsky, and R Wiechert, and W Hohlweg
Racemic 17-beta-hydroxy-17-alpha-vinyloestr-5(10)-en-3-one.
October 1965, Journal of the Chemical Society. Perkin transactions 1,
K Prezewowsky, and R Wiechert, and W Hohlweg
An affinity labeling of estrogen receptor. II. Synthesis and biological activity of 3-hydroxy-17 beta-(p-nitrophenyldithio)-1,3,5(10)-estratriene.
October 1983, Chemical & pharmaceutical bulletin,
K Prezewowsky, and R Wiechert, and W Hohlweg
The percutaneous absorption and excretion of promestriene (3-propoxy-17 beta-methoxy-1,3,5(10)-estratriene) in rats and humans.
January 1983, Steroids,
K Prezewowsky, and R Wiechert, and W Hohlweg
[Metabolism of steroid conjugates. 3. In vivo metabolism (6,7-3H)3-hydroxy-1,3,5(10)-estratriene-17-one (35S)sulfate].
June 1969, Hoppe-Seyler's Zeitschrift fur physiologische Chemie,
K Prezewowsky, and R Wiechert, and W Hohlweg
Structure of 3-hydroxy-1-methyl-1,3,5(10)-estratriene-11,17-dione.
June 1990, Acta crystallographica. Section C, Crystal structure communications,
K Prezewowsky, and R Wiechert, and W Hohlweg
3-O-phosphate ester conjugates of 17-β-O-{1-[2-carboxy-(2-hydroxy-4-methoxy-3-carboxamido)anilido]ethyl}1,3,5(10)-estratriene as novel bone-targeting agents.
December 2010, Bioorganic & medicinal chemistry letters,
K Prezewowsky, and R Wiechert, and W Hohlweg
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,
Copied contents to your clipboard!