38393-52-1 Usage
Description
(13S,14S)-13-ethyl-3-methoxy-6,7,11,12,13,14,15,16-octahydro-cyclopenta[a]phenanthren-17-one is a synthetic steroid compound characterized by a cyclopenta[a]phenanthren-17-one skeleton. It features an ethyl group at the 13th position and a methoxy group at the 3rd position. This unique structure suggests potential biological activity and may be involved in various biological processes, making it a candidate for pharmacological and medicinal applications. Further research is required to determine its specific properties and potential uses.
Uses
Used in Pharmaceutical Industry:
(13S,14S)-13-ethyl-3-methoxy-6,7,11,12,13,14,15,16-octahydro-cyclopenta[a]phenanthren-17-one is used as a potential pharmaceutical agent for its possible involvement in biological processes. Its unique structure and synthetic nature suggest that it could be developed into a drug candidate for treating specific conditions or diseases, pending further research and evaluation.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (13S,14S)-13-ethyl-3-methoxy-6,7,11,12,13,14,15,16-octahydro-cyclopenta[a]phenanthren-17-one serves as a subject for study to explore its potential biological activity and interactions with biological targets. Understanding its properties and mechanisms of action can contribute to the development of new therapeutic agents and a deeper understanding of molecular interactions in biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 38393-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,9 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38393-52:
(7*3)+(6*8)+(5*3)+(4*9)+(3*3)+(2*5)+(1*2)=141
141 % 10 = 1
So 38393-52-1 is a valid CAS Registry Number.
38393-52-1Relevant articles and documents
Total synthesis with a chirogenic opening move demonstrated on steroids with estrane or 18a-homoestrane skeleton
Quinkert,Del Grosso,Doring,Doring,Schenkel,Bauch,Dambacher,Bats,Zimmermann,Durner
, p. 1345 - 1391 (2007/10/02)
A concept of first choice for the synthesis of the title compounds had been proposed by Dane in the late 1930s. It was soon turned down, because the opening move - a chirogenic Diels-Alder reaction - did not work. With Lewis acids as mediators, however, a successful start has been achieved now. With Ti complexes of chelating ligands (Seebach's TADDOLs (= α,α,α',α'-tetraaryl-1,3-dioxolane-4,5-dimethanols)), enantioselective formation of the desired adducts does occur. Efficient total syntheses of 2 and 3a have been accomplished.
Synthesis of 13-alkyl-gon-4-ones
-
, (2008/06/13)
The preparation of 13-methylgon-4-enes and novel 13-polycarbonalkylgon-4-enes by a new total synthesis is described. 13-Alkylgon-4-enes having progestational, anabolic and androgenic activities are prepared by forming a tetracylic gonane structure unsaturated in the 1,3,5(10),9(11) and 14-positions, selectively reducing in the B- and C-rings, and converting the aromatic A-ring compounds so-produced to gon-4-enes by Birch reduction and hydrolysis.
