152561-64-3 Usage
General Description
"(+)-1-Decarboxy-1-methyl-20-nor-19-carboxyprostaglandin F(sub 2-alpha)" is a synthetic form of the prostaglandin F2-alpha hormone. It is a derivative of prostaglandins, which are lipid compounds with hormone-like effects in the body. The specific chemical structure of (+)-1-Decarboxy-1-methyl-20-nor-19-carboxyprostaglandin F(sub 2-alpha) includes a carboxylic acid group and a methyl group, as well as a nor-19-carboxy group, which gives it its unique properties. (+)-1-Decarboxy-1-methyl-20-nor-19-carboxyprostaglandin F(sub 2-alpha) has been synthesized for research purposes and has been studied for its potential therapeutic applications, particularly in the treatment of glaucoma and other ocular disorders. It functions by binding to prostaglandin receptors and has been shown to lower intraocular pressure, making it a promising candidate for the treatment of glaucoma. Additionally, it has also been investigated for its potential use in inducing labor and aborting pregnancies.
Check Digit Verification of cas no
The CAS Registry Mumber 152561-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,5,6 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 152561-64:
(8*1)+(7*5)+(6*2)+(5*5)+(4*6)+(3*1)+(2*6)+(1*4)=123
123 % 10 = 3
So 152561-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H34O5/c1-2-3-4-5-6-10-16-17(19(23)14-18(16)22)13-12-15(21)9-7-8-11-20(24)25/h5-6,12-13,15-19,21-23H,2-4,7-11,14H2,1H3,(H,24,25)/b6-5-,13-12+/t15-,16+,17+,18-,19+/m0/s1
152561-64-3Relevant academic research and scientific papers
PROSTANOIDS. LIV. ALTERNATIVES TO NATURAL PROSTAGLANDINS
Tolstikov, G. A.,Akhmetvaleev, R. R.,Zhurba, V. M.,Miftakhov, M. S.
, p. 1491 - 1496 (2007/10/02)
In order to check the hypothetically possible 9-cyclooxygenase path for the metabolism of arachidonic acid the expected (+)-1-decarboxy-1-methyl-20-nor-19-carboxyprostaglandin F2α was synthesized from (-)-7α-hydroxy-6-β-hydroxymethyl-cis-2-oxabicyclooctan-3-one.
