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(13α,14β,17S,20S,21R,23R,24S)-21,23:24,25-Diepoxy5α-lanost-7-ene-3α,21-diol 3-acetate is a complex steroidal compound characterized by its unique molecular structure that includes two epoxide groups, a lanostane backbone, and an acetate group. This natural product, derived from specific fungi and plants, features a three-dimensional arrangement of carbon atoms with distinct stereochemical configurations at various positions. Its distinctive structure and stereochemistry endow it with potential biological activities, making it a promising candidate for medicinal and pharmaceutical research, particularly as a drug lead or a tool for investigating biological processes.

22415-24-3

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22415-24-3 Usage

Uses

Used in Pharmaceutical Research:
(13α,14β,17S,20S,21R,23R,24S)-21,23:24,25-Diepoxy5α-lanost-7-ene-3α,21-diol 3-acetate serves as a valuable compound in pharmaceutical research due to its potential biological activities. Its unique structure allows it to be explored as a drug lead, where it may exhibit therapeutic effects against various diseases or conditions.
Used in Drug Development:
In the drug development industry, (13α,14β,17S,20S,21R,23R,24S)-21,23:24,25-Diepoxy5α-lanost-7-ene-3α,21-diol 3-acetate is utilized as a starting material or a template for the synthesis of new pharmaceutical agents. Its complex steroidal nature and stereochemistry make it a suitable candidate for the development of innovative drugs with novel mechanisms of action.
Used in Biological Process Studies:
(13α,14β,17S,20S,21R,23R,24S)-21,23:24,25-Diepoxy5α-lanost-7-ene-3α,21-diol 3-acetate also finds application in the study of biological processes. Its unique structure and stereochemistry enable researchers to use it as a tool for probing and understanding complex biological mechanisms, potentially leading to new insights and therapeutic targets.
Used in Natural Product Chemistry:
In the field of natural product chemistry, (13α,14β,17S,20S,21R,23R,24S)-21,23:24,25-Diepoxy5α-lanost-7-ene-3α,21-diol 3-acetate is employed as a subject of study for understanding the biosynthesis and metabolic pathways of natural compounds. Its isolation from fungi and plants provides insights into the chemical diversity and bioactivity of secondary metabolites in these organisms.

Check Digit Verification of cas no

The CAS Registry Mumber 22415-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,1 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22415-24:
(7*2)+(6*2)+(5*4)+(4*1)+(3*5)+(2*2)+(1*4)=73
73 % 10 = 3
So 22415-24-3 is a valid CAS Registry Number.

22415-24-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3α,13α,14β,17α,20S,21R,23R,24S)-21-Hydroxy-21,23:24,25-diepoxyla nost-7-en-3-yl acetate

1.2 Other means of identification

Product number -
Other names aphanamixin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22415-24-3 SDS

22415-24-3Upstream product

22415-24-3Downstream Products

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