192461-95-3 Usage
Uses
Used in Pharmaceutical Industry:
(5Z,8Z,14Z)-11,12-dihydroxyicosa-5,8,14-trienoic acid is used as a pharmaceutical agent for its potential anti-inflammatory and analgesic properties. The compound may help in modulating the inflammatory response and alleviating pain, making it a promising candidate for the development of new drugs targeting inflammation-related conditions.
Used in Research Applications:
In the field of scientific research, (5Z,8Z,14Z)-11,12-dihydroxyicosa-5,8,14-trienoic acid is used as a research tool for studying the biological effects of arachidonic acid and its metabolites. It can be employed in various experimental setups to investigate the role of DHETs in cellular signaling, inflammation, and other related processes.
Used in Drug Delivery Systems:
Similar to gallotannin, (5Z,8Z,14Z)-11,12-dihydroxyicosa-5,8,14-trienoic acid can also be incorporated into drug delivery systems to enhance its bioavailability and therapeutic efficacy. By utilizing nanoparticles or other carriers, the compound can be more effectively delivered to target cells or tissues, improving its overall performance in treating specific conditions.
Used in Cosmetics Industry:
(5Z,8Z,14Z)-11,12-dihydroxyicosa-5,8,14-trienoic acid may find applications in the cosmetics industry due to its potential anti-inflammatory and skin-soothing properties. It could be used as an active ingredient in skincare products designed to reduce inflammation, redness, and irritation, providing a soothing and calming effect on the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 192461-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,4,6 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 192461-95:
(8*1)+(7*9)+(6*2)+(5*4)+(4*6)+(3*1)+(2*9)+(1*5)=153
153 % 10 = 3
So 192461-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H34O4/c1-2-3-4-5-9-12-15-18(21)19(22)16-13-10-7-6-8-11-14-17-20(23)24/h6,8-10,12-13,18-19,21-22H,2-5,7,11,14-17H2,1H3,(H,23,24)/b8-6-,12-9-,13-10-
192461-95-3Relevant academic research and scientific papers
Wang, Steven S.,Rokach, Joshua
, p. 6239 - 6242 (1994)
The first total and enantioselective synthesis of 11-R,12-R-dihydroxy-5,8,14-eicosatrienoic acid 7 is reported.We have used the carbohydrate 2-deoxy-D-glucose as a masked 1,6-dialdehyde precursor 20 to perform the synthesis.The availability of this material will allow, among other things, the testing of the hypothesis that it can be a biochemical precursor to 12-R-HETE in vivo.
vic-Diol chirons: Enantiospecific synthesis of 11,12- and 14,15-dihydroxyeicosatrienoic acids
Chauhan,Chauhan, Kamlesh,Aravind,Aravind, Sivasubramanian,Lee,Lee, Sang-Gyeong,Falck,Capdevila,Capdevila, Jorge H.
, p. 6791 - 6794 (2007/10/02)
A differentiated, six-carbon vicinal-diol chiron was prepared from D-glucurono-6,3-lactone and exploited in the asymmetric synthesis of the erythro/threo-isomers of the title eicosanoids.
