1962-14-7 Usage
Description
3β,16α,21β-Trihydroxyolean-12-en-28-oic acid is a pentacyclic triterpenoid, specifically the olean-12-ene molecule, which is characterized by the presence of a carboxy group at position 28 and hydroxy groups at positions 3, 16, and 21. 3β,16α,21β-Trihydroxyolean-12-en-28-oic acid is known for its 3β,16α,21β stereoisomer configuration, which plays a crucial role in its biological activities and potential applications.
Uses
Used in Pharmaceutical Industry:
3β,16α,21β-Trihydroxyolean-12-en-28-oic acid is used as a pharmaceutical compound for its potential therapeutic properties. The expression is: 3β,16α,21β-Trihydroxyolean-12-en-28-oic acid is used as a therapeutic agent for its potential to modulate various biological pathways and exhibit beneficial effects on human health.
Used in Cosmetic Industry:
In the cosmetic industry, 3β,16α,21β-Trihydroxyolean-12-en-28-oic acid is used as an active ingredient for its potential skin-friendly properties. The expression is: 3β,16α,21β-Trihydroxyolean-12-en-28-oic acid is used as a cosmetic ingredient for its potential to improve skin health and provide anti-aging benefits.
Used in Nutraceutical Industry:
3β,16α,21β-Trihydroxyolean-12-en-28-oic acid is also utilized in the nutraceutical industry as a dietary supplement due to its potential health-promoting properties. The expression is: 3β,16α,21β-Trihydroxyolean-12-en-28-oic acid is used as a nutraceutical ingredient for its potential to contribute to overall health and well-being.
Please note that the specific applications and reasons for using 3β,16α,21β-Trihydroxyolean-12-en-28-oic acid may vary depending on the research and development in each industry. The provided uses are based on the general properties of triterpenoids and their common applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1962-14-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1962-14:
(6*1)+(5*9)+(4*6)+(3*2)+(2*1)+(1*4)=87
87 % 10 = 7
So 1962-14-7 is a valid CAS Registry Number.
InChI:InChI=1/C30H48O5/c1-25(2)14-18-17-8-9-20-27(5)12-11-21(31)26(3,4)19(27)10-13-28(20,6)29(17,7)15-23(33)30(18,24(34)35)16-22(25)32/h8,18-23,31-33H,9-16H2,1-7H3,(H,34,35)/t18-,19+,20-,21+,22+,23-,27+,28-,29-,30-/m1/s1
1962-14-7Relevant articles and documents
Elucidation of the pharmacophore of echinocystic acid, a new lead for blocking HCV entry
Wang, Han,Wang, Qi,Xiao, Su-Long,Yu, Fei,Ye, Min,Zheng, Yong-Xiang,Zhao, Chuan-Ke,Sun, Di-An,Zhang, Li-He,Zhou, De-Min
, p. 160 - 168 (2013)
To elucidate the pharmacophore of echinocystic acid (EA), an oleanane-type triterpene displaying substantial inhibitory activity on HCV entry, two microbial strains, Rhizopus chinensis CICC 3043 and Alternaria alternata AS 3.4578, were utilized to modify the chemical structure of EA. Eight new metabolites with regio- and stereo-selective introduction of hydroxyl and lactone groups at various inert carbon positions were obtained. The anti-HCV entry activity of the metabolites 2-13, along with their parental compound EA and other analogs 14-15, were evaluated. Most of the metabolites showed no improvement but detrimental effect on potency except compound 5 and 6, which showed similar and even a litter higher anti-HCV entry activity than that of EA. The results demonstrated that ring A, B, C and the left side of ring E of EA are highly conserved, while ring D and the right side of ring E of EA are flexible. Introduction of a hydroxyl group at C-16 enhanced the triterpene potency. Further analysis indicated that the hemolytic effect of EA disappeared upon such modifications.
