CAS 128255-08-3
:Pregn-5-en-20-amine,3-methoxy-N,N-dimethyl-, (3b,20S)-
Description:
Pregn-5-en-20-amine, 3-methoxy-N,N-dimethyl-, (3b,20S)-, with the CAS number 128255-08-3, is a synthetic compound that belongs to the class of steroid derivatives. It is characterized by a steroid backbone, which typically includes a four-ring structure that is common to all steroids. The presence of the amine group at the 20-position and the methoxy group at the 3-position indicates specific functional modifications that can influence its biological activity and solubility. The N,N-dimethyl substitution suggests enhanced lipophilicity, potentially affecting its pharmacokinetics. This compound may exhibit various biological activities, including potential hormonal effects, due to its structural similarity to natural steroid hormones. Its stereochemistry, indicated by the (3b,20S) designation, suggests specific spatial arrangements of atoms that can be crucial for its interaction with biological targets. Overall, this compound's unique structural features may contribute to its potential applications in medicinal chemistry and pharmacology.
Formula:C24H41NO
Synonyms:- (-)-PachyaximineA
- Pachyaximine A
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Found 4 products.
Pachyaximine A
CAS:Pachyaximine A fights E. coli, S. aureus, and Corynebacteria; enhances tamoxifen's antiestrogenic effects in Ishikawa cells.Formula:C24H41NOPurity:98%Color and Shape:SolidMolecular weight:359.59Pachyaximine A
CAS:Controlled ProductPachyaximine A is a bioactive alkaloid, which is isolated from marine sponges. This natural compound is extracted from marine organisms, primarily sponges, which are known for their rich chemical diversity and potential pharmaceutical applications. Pachyaximine A exhibits its mode of action through the disruption of key cellular processes, particularly targeting DNA synthesis and cell cycle progression, making it a promising candidate for anticancer therapy.
Formula:C24H41NOPurity:Min. 95%Molecular weight:359.6 g/mol
