21058-62-8 Usage
Uses
Used in Medicinal Chemistry:
(8E)-5a,7a-dimethyl-3,4,5,5a,5b,6,7,7a,9,10,10a,10b,11,12-tetradecahydrocyclopenta[5,6]naphtho[1,2-d]azepine-2,8-dione 8-oxime is used as a compound in medicinal chemistry for its unique structural features that may contribute to the development of new pharmaceutical agents. Its specific functional groups could be leveraged to target various biological pathways or to enhance the compound's interaction with biological targets.
Used in Pharmacology Research:
In pharmacology, (8E)-5a,7a-dimethyl-3,4,5,5a,5b,6,7,7a,9,10,10a,10b,11,12-tetradecahydrocyclopenta[5,6]naphtho[1,2-d]azepine-2,8-dione 8-oxime is used as a research tool to study the effects of structural modifications on the activity and selectivity of drug candidates. Its complex structure allows researchers to investigate how different functional groups and stereochemistry influence the compound's pharmacological properties, potentially leading to the discovery of novel therapeutic agents.
Used in Drug Design and Optimization:
(8E)-5a,7a-dimethyl-3,4,5,5a,5b,6,7,7a,9,10,10a,10b,11,12-tetradecahydrocyclopenta[5,6]naphtho[1,2-d]azepine-2,8-dione 8-oxime is utilized in drug design and optimization processes to create new molecules with improved potency, selectivity, and pharmacokinetic profiles. Its unique features can be incorporated into drug candidates to address specific therapeutic needs or to overcome challenges associated with existing medications.
Check Digit Verification of cas no
The CAS Registry Mumber 21058-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,5 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21058-62:
(7*2)+(6*1)+(5*0)+(4*5)+(3*8)+(2*6)+(1*2)=78
78 % 10 = 8
So 21058-62-8 is a valid CAS Registry Number.
21058-62-8Relevant academic research and scientific papers
Beckmann rearrangement of 3-aza-A-homo-4α-androsten-4,17-dione oxime and 3-oxo-13α-amino-13,17-seco-4-androsten-17-oic 13,17-lactam oxime
Camoutsis,Catsoulacos
, p. 1093 - 1094 (2007/10/02)
Rearragements of 3-aza-A-homo-4α-androsten-4,17-dione oxime produced a mixture of the normal lactam product and the product of a 'second order' cleavage, an unsaturated nitrile. The lactam 3,17α-diaza-A,D-bishomoandrost-4α-ene-4,17-dione was also obtained from the rearrangement of the syn-3-oxo-13α-amino-13,17-seco-4-androsten-17-oic-13,17-lactam oxime. The resolution of syn- and anti-isomers of VIII was effected by column chromatography and their structure was determined by spectral data.
