85344-33-8 Usage
Uses
Used in Pharmaceutical Industry:
Ginkgolic acid is used as a pharmaceutical agent for its anti-tumor properties, targeting various types of cancer. Its anti-bacterial and anti-inflammatory properties also contribute to its potential use in developing new drugs for treating infections and inflammatory conditions.
Used in Neurodegenerative Disorder Treatment:
Ginkgolic acid is used as a potential treatment for neurodegenerative disorders such as Alzheimer's disease, due to its demonstrated neuroprotective effects and ability to improve cognitive function.
Used in Cosmetic Industry:
Due to its anti-inflammatory and anti-bacterial properties, ginkgolic acid can be used in the cosmetic industry for developing skincare products that promote skin health and treat various skin conditions.
Used in Nutraceutical Industry:
Ginkgolic acid's health-promoting properties make it a potential candidate for use in the development of nutraceutical products, which can be consumed to improve overall health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 85344-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,4 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85344-33:
(7*8)+(6*5)+(5*3)+(4*4)+(3*4)+(2*3)+(1*3)=138
138 % 10 = 8
So 85344-33-8 is a valid CAS Registry Number.
85344-33-8Relevant academic research and scientific papers
Preparation of 13-Hydroxygibberellin A12-7-Aldehyde
Down, Graham J.,Lee, Michael,MacMillan, Jake,Staples, Karen S.
, p. 1103 - 1108 (2007/10/02)
7β- and 7α-Hydroxykaurenolides have been efficiently 13-hydroxylated by cultures of Rhizopus arrhizus.The products have been chemically converted into the title compound.In an alternative preparation, gibberellin A12-7-aldehyde, gibberellin A12-7-aldehyde (prepared from 7β,18-dihydroxykaurenolide), and gibberellin A12-7-aldehyde (prepared, by hydrogen-tritium exchange, from gibberellin A12-7-aldehyde), have been 13-hydroxylated by cultures of Rhizopus arrhizus to give the unlabelled and the - and -labelled title compound. 13-Hydroxylation of gibberellin A12-7-alcohol by cultures of Rhizopus arrhizus, followed by oxidation, also gave 13-hydroxygibberellin A12-7-aldehyde.
