92950-25-9 Usage
Uses
Used in Pharmaceutical Industry:
5,14,15-Trihydroxy-6,8,10,12-eicosatetraenoic acid is used as a pharmaceutical agent for its potential therapeutic properties. The presence of multiple hydroxy and double bond groups may allow it to interact with biological targets and modulate various signaling pathways, making it a candidate for the development of new drugs.
Used in Cosmetic Industry:
In the cosmetic industry, 5,14,15-trihydroxy-6,8,10,12-eicosatetraenoic acid is used as an active ingredient for its potential skin benefits. The hydroxy groups and double bonds may contribute to its ability to moisturize, nourish, and protect the skin, as well as potentially improve skin elasticity and reduce the appearance of fine lines and wrinkles.
Used in Food Industry:
5,14,15-Trihydroxy-6,8,10,12-eicosatetraenoic acid can be used in the food industry as a functional ingredient due to its unique chemical structure. It may have potential health benefits, such as anti-inflammatory or antioxidant properties, which could be harnessed to develop healthier food products.
Used in Research Applications:
5,14,15-trihydroxy-6,8,10,12-eicosatetraenoic acid is also used in research settings as a chemical probe to study the interactions between fatty acids and biological systems. Its unique structure allows researchers to investigate its effects on various cellular processes and signaling pathways, contributing to a better understanding of its potential applications and mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 92950-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,5 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92950-25:
(7*9)+(6*2)+(5*9)+(4*5)+(3*0)+(2*2)+(1*5)=149
149 % 10 = 9
So 92950-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H32O5/c1-2-3-8-14-18(22)19(23)15-10-7-5-4-6-9-12-17(21)13-11-16-20(24)25/h4-7,9-10,12,15,17-19,21-23H,2-3,8,11,13-14,16H2,1H3,(H,24,25)/b6-4-,7-5+,12-9+,15-10+/t17-,18+,19-/m1/s1
92950-25-9Relevant academic research and scientific papers
Stereocontrolled Total Synthesis of Lipoxins B
Nicolaou, K. C.,Webber, S. E.
, p. 453 - 461 (2007/10/02)
A stereocontrolled total synthesis of six lipoxin B isomers are described.The flexible and stereoselective strategy involves Sharpless asymmetric epoxidation and pinylborane asymmetric reduction to secure the three hydroxyl-bearing stereocenters and a Wittig-type as well as palladium(0)-copper(I) coupling reactions to construct the carbon skeleton of the target molecules.
