77658-38-9 Usage
Description
Pterokaurene L3 is a diterpene compound derived from the resin of the Brazilian medicinal plant, copaiba (Copaifera multijuga). It exhibits anti-inflammatory, anti-microbial, analgesic, and wound healing properties, positioning it as a potential natural therapeutic agent for various medical applications.
Uses
Used in Pharmaceutical Industry:
Pterokaurene L3 is used as an anti-inflammatory agent for its ability to inhibit the production of nitric oxide, a key inflammatory mediator in macrophages. This property makes it suitable for treating inflammatory conditions.
Used in Antimicrobial Applications:
Pterokaurene L3 is used as an antimicrobial agent due to its capacity to inhibit the growth of various bacteria and fungi, making it a potential candidate for treating infections.
Used in Pain Management:
Pterokaurene L3 is used as an analgesic agent, providing pain relief through its natural painkilling properties, which can be beneficial in managing various types of pain.
Used in Wound Healing:
Pterokaurene L3 is used to promote wound healing, accelerating the recovery process and improving the overall health of the affected area. Its wound healing properties make it a valuable component in treatments for various skin conditions and injuries.
Check Digit Verification of cas no
The CAS Registry Mumber 77658-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,5 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77658-38:
(7*7)+(6*7)+(5*6)+(4*5)+(3*8)+(2*3)+(1*8)=179
179 % 10 = 9
So 77658-38-9 is a valid CAS Registry Number.
77658-38-9Relevant articles and documents
ENT-KAURENOID METHYL ESTERS FROM VIGUIEMA STENOLOBA, STRUCTURAL REVISION OF STENOLOBIN AND ITS BIOMIMETIC CONVERSION TO ZOAPATLIN
Delgado, Guillermo,Vivar, Alfonso Romo de
, p. 1237 - 1240 (2007/10/02)
The structure of stenolobin, a diterpene from Viguiema stenoloba, was revised to 5.The new diterpene, 15α-angeloyloxy stenolobin, was also isolated from the same plant source.The biomimetic transformation of stenolobin (5) to zoapatlin is described.
