10164-73-5 Usage
Uses
Used in Pharmaceutical Research:
9BETA,11ALPHA,15S-TRIHYDROXY-PROST-13E-EN-1-OIC ACID is used as a target for pharmaceutical research for the development of anti-inflammatory and pain-relieving drugs due to its crucial role in inflammation and immune response.
Used in Inflammation and Immune Response Regulation:
9BETA,11ALPHA,15S-TRIHDROXY-PROST-13E-EN-1-OIC ACID is used as a signaling molecule in the regulation of inflammation and immune response, modulating processes such as fever, pain perception, and blood vessel dilation.
Used in Gastrointestinal System Regulation:
9BETA,11ALPHA,15S-TRIHYDROXY-PROST-13E-EN-1-OIC ACID is used as a regulatory molecule in the gastrointestinal system, influencing its functioning and maintaining homeostasis.
Used in Reproductive System Regulation:
9BETA,11ALPHA,15S-TRIHYDROXY-PROST-13E-EN-1-OIC ACID is used as a regulatory molecule in the reproductive system, affecting processes such as fertility and pregnancy.
Used in Respiratory System Regulation:
9BETA,11ALPHA,15S-TRIHYDROXY-PROST-13E-EN-1-OIC ACID is used as a regulatory molecule in the respiratory system, influencing its functioning and maintaining respiratory health.
Check Digit Verification of cas no
The CAS Registry Mumber 10164-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,6 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10164-73:
(7*1)+(6*0)+(5*1)+(4*6)+(3*4)+(2*7)+(1*3)=65
65 % 10 = 5
So 10164-73-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H36O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h12-13,15-19,21-23H,2-11,14H2,1H3,(H,24,25)/b13-12+/t15-,16+,17+,18+,19+/m0/s1
10164-73-5Relevant academic research and scientific papers
Regio- and Stereoselectivity of the Reaction between Cyanocuprates and Cyclopentene Epoxides. Application to the Total Synthesis of Prostaglandins
Marino, Joseph P.,Pradilla, Roberto F. de la,Laborde, Edgardo
, p. 4898 - 4913 (2007/10/02)
A systematic study of the reaction between cyclopentene epoxides and alkyl-, alkenyl-, and arylcyanocuprates is described.Alkylcyanocuprates react with complete regio- and stereoselectivity to provide trans-4-alkylcyclopent-2-enols in excellent yields.Vin
Stereocontrolled Synthesis of Prostaglandins from Cyclopentadiene Monoepoxide
Marino, Joseph P.,Pradilla, Roberto Fernandez de la,Laborde, Edgardo
, p. 5279 - 5280 (2007/10/02)
Two complementary syntheses of prostaglandins from the same key intermediate 3, available in four steps from cyclopentadiene monoepoxide, are described.In one approach, a saturated α-chain is introduced via a 1,4-addition of an appropriately functionalized cyanocuprate reagent onto silyl enol ether 3.The resulting prostanoid compound was converted into the bronchodilator 1-decarboxy-1-hydroxymethyl PGE1, PGE1, and PGF1α.The second approach involves the transformation of silyl enol ether 3 into the known prostanoid precursor 11 via selective addition of carbethoxycarbene and subsequent fluoride-induced ring opening of the resulting (silyloxy)cyclopropane carboxylate ester.
