56682-25-8 Usage
Description
(8R,12R,13R)-8,12-epoxy-13-hydroxylabd-14-ene is a naturally occurring chemical compound that belongs to the class of labdane diterpenoids. It is derived from the plant Salvia ballotiflora and has been found to exhibit various biological activities, including anticancer, antimicrobial, and anti-inflammatory properties. (8R,12R,13R)-8,12-epoxy-13-hydroxylabd-14-ene's epoxy and hydroxyl functional groups contribute to its reactivity and potential therapeutic benefits, making it a promising candidate for pharmaceutical development.
Uses
Used in Pharmaceutical Industry:
(8R,12R,13R)-8,12-epoxy-13-hydroxylabd-14-ene is used as a potential pharmaceutical agent for the treatment of various diseases and conditions. Its anticancer properties make it a candidate for the development of new cancer treatments, while its antimicrobial and anti-inflammatory activities suggest potential applications in the treatment of infections and inflammatory disorders.
Used in Anticancer Applications:
(8R,12R,13R)-8,12-epoxy-13-hydroxylabd-14-ene is used as an anticancer agent due to its ability to exhibit various biological activities that can potentially target and treat cancer cells. (8R,12R,13R)-8,12-epoxy-13-hydroxylabd-14-ene's reactivity and functional groups may contribute to its effectiveness in inhibiting tumor growth and progression.
Used in Antimicrobial Applications:
(8R,12R,13R)-8,12-epoxy-13-hydroxylabd-14-ene is used as an antimicrobial agent, leveraging its natural ability to combat and inhibit the growth of harmful microorganisms. This property can be harnessed for the development of new treatments for bacterial and fungal infections.
Used in Anti-inflammatory Applications:
(8R,12R,13R)-8,12-epoxy-13-hydroxylabd-14-ene is used as an anti-inflammatory agent, potentially providing relief from inflammation and associated pain in various conditions. Its anti-inflammatory properties may be beneficial in the treatment of chronic inflammatory diseases and acute inflammatory responses.
Check Digit Verification of cas no
The CAS Registry Mumber 56682-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,8 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56682-25:
(7*5)+(6*6)+(5*6)+(4*8)+(3*2)+(2*2)+(1*5)=148
148 % 10 = 8
So 56682-25-8 is a valid CAS Registry Number.
56682-25-8Relevant articles and documents
Tobacco Chemistry 81. Biotransformations of (Z)-Abienol using Plant Cell Cultures of Nicotiana silvestris
Enzell, Curt R.,Nasiri, Ahmad,Forsblom, Ingrid,Johansson, Eva,Lundberg, Charlotta,et al.
, p. 375 - 379 (2007/10/02)
The transformations of (Z)-abienol (1) effected by cell cultures and cell-free extracts of Nicotiana silvestris and by horseradish peroxidase have been examined.Although this compound retarded the growth of the cell cultures in low doses and exhibited a toxic effect in high doses, a fairly rapid conversion was observed when low to moderate doses of cells cultivated under light were used.Of the many transformation products encountered twelve were identified.The major ones of these were (12R,13S)- and (12R,13R)-8,12-epoxy-14-labden-13-ols (2,5), (11E)-14,15-bisnor-8-hydroxy-11-labden-13-one (11), 12-norambreinolide (10), 12,15-epoxy-12,14-labdadien-8-ol (12) and 8-drimanol (13), and the minor (12R,13R)-, (12S,13R)-, (12S,13S)- and (12R,13S)-8,13-epoxy-14-labden-12-ols (6-9) and (12S,13S)- and (12S,13R)-8,12-epoxy-14-labden-13-ols (3,4).Horseradish peroxidase also transformed (Z)-abienol into these products.
