3064-05-9 Usage
Uses
Used in Antioxidant Applications:
(+)-Cycloolivil is used as an antioxidant agent for its ability to scavenge free radicals, which can help protect cells from oxidative damage and contribute to the prevention of various diseases associated with oxidative stress.
Used in Anti-inflammatory Applications:
(+)-Cycloolivil is used as an anti-inflammatory agent for its capacity to inhibit the production of inflammatory mediators. This property suggests its potential use in the treatment of various inflammatory conditions, where reducing inflammation can alleviate symptoms and prevent disease progression.
Used in Neuroprotective Applications:
(+)-Cycloolivil is used as a neuroprotective agent due to its demonstrated effects in protecting neurons and potentially preventing neurodegenerative diseases. Its neuroprotective properties make it a candidate for therapeutic interventions aimed at preserving cognitive function and reducing the impact of neurodegenerative disorders.
Used in Pharmaceutical Industry:
(+)-Cycloolivil is used as a therapeutic compound in the pharmaceutical industry for its multifaceted potential in antioxidant, anti-inflammatory, and neuroprotective medicine. Its diverse applications make it a valuable asset in the development of new treatments for a range of conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 3064-05-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3064-05:
(6*3)+(5*0)+(4*6)+(3*4)+(2*0)+(1*5)=59
59 % 10 = 9
So 3064-05-9 is a valid CAS Registry Number.
3064-05-9Relevant articles and documents
Total Synthesis and Stereochemical Confirmation of (-)-Olivil, (+)-Cycloolivil, (-)-Alashinols F and G, (+)-Cephafortin A, and Their Congeners: Filling in Biosynthetic Gaps
Hanessian, Stephen,Reddy Vakiti, Jithender
, p. 3345 - 3350 (2020/04/30)
For the first time, we describe the stereocontrolled total syntheses of olivil, cephafortin A, 4-des-O-methyl-4-O-rhamnosyl cephafortin A, and alashinol F from a common precursor using a combination of chemoenzymatic and biomimetic methods for the systematic introduction of functional groups on three vicinal stereogenic carbon atoms. We revised the previously assigned stereochemistry of (+)-cephafortin A, which was reported as the enantiomer. Natural and unnatural congeners provide insights into the biogenetic interrelations of members of this family.