22338-67-6 Usage
Uses
Used in Pharmaceutical Industry:
Grandiflorenic acid is used as an anti-inflammatory agent for its ability to reduce inflammation and alleviate symptoms associated with inflammatory and immune-related disorders.
Used in Antioxidant Applications:
Grandiflorenic acid is used as an antioxidant to protect cells from oxidative stress and prevent damage caused by free radicals, thereby promoting overall health and well-being.
Used in Antimicrobial Applications:
Grandiflorenic acid is used as an antimicrobial agent to combat infections caused by various microorganisms, including bacteria, fungi, and viruses.
Used in Anticancer Applications:
Grandiflorenic acid is used as an anticancer agent for its potential to induce apoptosis and inhibit cell proliferation in certain cancer cell lines, offering a natural alternative for cancer treatment.
Used in Drug Delivery Systems:
Grandiflorenic acid can be incorporated into drug delivery systems to enhance its bioavailability, targeting, and therapeutic efficacy, particularly in the treatment of cancer and inflammatory disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 22338-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,3 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22338-67:
(7*2)+(6*2)+(5*3)+(4*3)+(3*8)+(2*6)+(1*7)=96
96 % 10 = 6
So 22338-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O2/c1-13-11-20-10-7-15-18(2,16(20)6-5-14(13)12-20)8-4-9-19(15,3)17(21)22/h6,14-15H,1,4-5,7-12H2,2-3H3,(H,21,22)/t14?,15-,18+,19+,20?/m0/s1
22338-67-6Relevant academic research and scientific papers
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.
