10207-79-1 Usage
Description
(+)-Isoabeinol is a naturally occurring diterpene compound found in the bark and wood of several tree species, such as the Japanese and Chinese red pine. It has been studied for its potential medicinal properties, including anti-inflammatory, analgesic, antimicrobial, and anti-tumor effects, making it a promising candidate for pharmaceutical and biotechnological applications.
Used in Pharmaceutical Industry:
(+)-Isoabeinol is used as a potential medicinal compound for its anti-inflammatory and analgesic effects, which can help in the treatment of various inflammatory and pain-related conditions.
Used in Biotechnological Applications:
(+)-Isoabeinol is used as a potential antimicrobial agent, which can be employed in the development of new antibiotics to combat drug-resistant bacteria.
Used in Antitumor Applications:
(+)-Isoabeinol is used as a potential anti-tumor agent, which can be explored for its potential in cancer treatment and prevention.
However, it is important to note that further studies are needed to fully understand the pharmacological and biological activities of (+)-Isoabeinol to ensure its safety and efficacy in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 10207-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,0 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10207-79:
(7*1)+(6*0)+(5*2)+(4*0)+(3*7)+(2*7)+(1*9)=61
61 % 10 = 1
So 10207-79-1 is a valid CAS Registry Number.
10207-79-1Relevant articles and documents
Oxidative degradation of the sclareol side chain: hemisyntheses of ambergris derivatives using in the key steps palladium complexes or ruthenium tetroxide generated in situ
Zahra, Jean-Pierre,Chauvet, Frederic,Coste-Maniere, Ivan,Martres, Paul,Perfetti, Patricia,Waegell, Bernard
, p. 1001 - 1024 (2007/10/03)
We report the hemisyntheses of various ambergris-type derivatives: ambraoxide 4, Ambrox 8, 13-methylambraoxide 13, ambraketal 14, norambraketal 15, non-norambraketal 16 and dioxepane 53.Sclareol 12 is used as starting material because it is currently available from Salvia sclarea.The key steps involve an oxidative degradation of the sclareol 12 side chain, using either palladium complexes or ruthenium tetroxide generated in situ. - Keywords: sclareol; Ambrox; ambraoxide; 13-methylambraoxide; ambraketal; norambraketal; nor-norambraketal; farnesylic aldehyde; palladium complex; ruthenium tetroxide generated in situ; oxidative degradation
