77667-09-5 Usage
Description
(5Z,8Z,11Z)-14,15-dihydroxyicosa-5,8,11-trienoic acid, also known as a dihydroxyeicosatrienoic acid (DHET), is a biologically active compound derived from the metabolism of arachidonic acid. It is characterized by the presence of three double bonds at positions 5, 8, and 11, and two hydroxyl groups at positions 14 and 15. This molecule plays a crucial role in various physiological processes and has potential applications in different industries due to its unique structural features and biological activities.
Uses
Used in Pharmaceutical Industry:
(5Z,8Z,11Z)-14,15-dihydroxyicosa-5,8,11-trienoic acid is used as a therapeutic agent for its anti-inflammatory and vasodilatory properties. It helps in modulating the production of eicosanoids, which are involved in various physiological processes, including inflammation and blood pressure regulation.
Used in Research Applications:
In the field of scientific research, (5Z,8Z,11Z)-14,15-dihydroxyicosa-5,8,11-trienoic acid is used as a biochemical marker for studying the metabolism of arachidonic acid and its role in various diseases. It can also be used as a research tool to investigate the mechanisms underlying the production and actions of eicosanoids.
Used in Drug Development:
(5Z,8Z,11Z)-14,15-dihydroxyicosa-5,8,11-trienoic acid serves as a potential lead compound for the development of new drugs targeting inflammatory and cardiovascular diseases. Its unique structural features and biological activities make it an attractive candidate for the design and synthesis of novel therapeutic agents.
Used in Nutritional Supplements:
Due to its potential health benefits, (5Z,8Z,11Z)-14,15-dihydroxyicosa-5,8,11-trienoic acid may be used as an ingredient in nutritional supplements, particularly those aimed at promoting cardiovascular health and reducing inflammation.
Used in Cosmetics Industry:
(5Z,8Z,11Z)-14,15-dihydroxyicosa-5,8,11-trienoic acid could be utilized in the development of cosmetic products, such as anti-aging creams and lotions, due to its potential anti-inflammatory and skin-protective properties.
Check Digit Verification of cas no
The CAS Registry Mumber 77667-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,6 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77667-09:
(7*7)+(6*7)+(5*6)+(4*6)+(3*7)+(2*0)+(1*9)=175
175 % 10 = 5
So 77667-09-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H32O4/c1-2-3-12-15-18(21)19(22)16-13-10-8-6-4-5-7-9-11-14-17-20(23)24/h4,6-10,13,16,18-19,21-22H,2-3,5,11-12,14-15,17H2,1H3,(H,23,24)/b6-4+,9-7+,10-8+,16-13+
77667-09-5Relevant articles and documents
ON THE SYNTHESIS AND STRUCTURE OF LIPOXIN B
Corey, E. J.,Mehrotra, Mukund M.,Su, Wei-guo
, p. 1919 - 1922 (1985)
A synthesis of lipoxin B, a recently discovered biologically active eicosanoid, and the assignment of stereoformula 2 is reported.
