190006-01-0 Usage
Derived from androstane
This compound is synthesized from androstane, a steroid hormone.
Synthetic compound
It is a synthetic compound and is not found naturally in the human body.
Norsteroid
It is a modified version of a steroid hormone, specifically a norsteroid.
Research purposes
It is designed for research purposes to study the effects of modifying androstane derivatives on biological processes and hormone signaling pathways.
Tert-butyl carbamoyl group
It has a tert-butyl carbamoyl group attached to the 17β carbon.
Keto group
It has a keto group at the 5 carbon.
Carboxylic acid moiety
It has a carboxylic acid group at the 3 carbon.
Potential applications
As a synthetic norsteroid, it may have potential applications in drug discovery and development for diseases or conditions related to steroid hormone imbalance or dysfunction.
Chemical structure
The specific structure and chemical properties of this compound make it useful for studying the effects of modifying androstane derivatives on biological processes and hormone signaling pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 190006-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,0,0 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 190006-01:
(8*1)+(7*9)+(6*0)+(5*0)+(4*0)+(3*6)+(2*0)+(1*1)=90
90 % 10 = 0
So 190006-01-0 is a valid CAS Registry Number.
190006-01-0Relevant articles and documents
Synthesis of N-substituted 3-oxo-17β -carboxamide-4-aza-5α-androstanes and the tautomerism of 3-oxo-4-aza-5-androstenes
Xia, Peng,Yang, Zheng-Yu,Xia, Yi,Zhang, Hao-Bing,Zhang, Ke-Hua,Sun, Xun,Chen, Ying,Zheng, Yun-Qing
, p. 703 - 716 (1998)
An N-aryl-3-oxo-4-aza-5α -androst-1-ene-17β carboxamide and three N-aryl or alkyl substituted 17α -hydroxy-3-oxo-4-aza-5α -androstane-17β -carboxamides were synthesized as antiandrogen candidates from 3-oxoandrost-4-ene-17β - carboxylic acid and androst-4-ene-3,17-dione respectively. The chemo- and stereoselective reduction of 3-oxo-4-aza-5-ene intermediates with formic acid and their tautomerism in a solution of chloroform and methanol were described.
