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1A,1B-DIHOMO PROSTAGLANDIN F2ALPHA is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57944-39-5

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57944-39-5 Usage

Naturally occurring chemical compound

1A,1B-DIHOMO PROSTAGLANDIN F2ALPHA is a naturally occurring chemical compound that belongs to the family of prostaglandins.

Derived from dihomo-gamma-linolenic acid (DGLA)

It is derived from the fatty acid dihomo-gamma-linolenic acid (DGLA).

Involved in various biological processes

1A,1B-DIHOMO PROSTAGLANDIN F2ALPHA plays a role in various biological processes, including inflammation, blood clotting, and smooth muscle contraction.

Regulates blood pressure

In the body, 1A,1B-DIHOMO PROSTAGLANDIN F2ALPHA is involved in the regulation of blood pressure.

Involved in immune response

It is also involved in the immune response.

Regulates reproductive functions

1A,1B-DIHOMO PROSTAGLANDIN F2ALPHA is involved in the regulation of reproductive functions.

Check Digit Verification of cas no

The CAS Registry Mumber 57944-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,4 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57944-39:
(7*5)+(6*7)+(5*9)+(4*4)+(3*4)+(2*3)+(1*9)=165
165 % 10 = 5
So 57944-39-5 is a valid CAS Registry Number.
InChI:InChI=1/C22H38O5/c1-2-3-8-11-17(23)14-15-19-18(20(24)16-21(19)25)12-9-6-4-5-7-10-13-22(26)27/h6,9,14-15,17-21,23-25H,2-5,7-8,10-13,16H2,1H3,(H,26,27)/b9-6-,15-14+/t17-,18+,19+,20-,21+/m0/s1

57944-39-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1A,1B-DIHOMO PROSTAGLANDIN F2ALPHA

1.2 Other means of identification

Product number -
Other names 9ALPHA,11ALPHA,15S-TRIHYDROXY-1A,1B-DIHOMO-PROSTA-5Z,13E-DIEN-1-OIC ACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57944-39-5 SDS

57944-39-5Downstream Products

57944-39-5Relevant academic research and scientific papers

Stereoselective preparation of key intermediates for the synthesis of iso-, neuro- and phyto-prostane family members: Inaugural asymmetric synthesis of 17-E2c-dihomo- and 17-F2c-dihomo-isoprostanes

Gandini, Andrea,Amin, Ahmed A.,Amin, Hawraz Ibrahim M.,Corriero, Davide,Porta, Alessio,Zanoni, Giuseppe

, p. 2393 - 2396 (2018/04/12)

A practical methodology for the synthesis of key intermediates for isoprostane, neuroprostane and dihomo-isoprostane preparation has been described. The key strategy involved a three stage C-12 stereocenter inversion of the configuration of a Corey lacton

Total synthesis of isoprostanes derived from adrenic acid and EPA

Oger, Camille,Bultel-Ponce, Valerie,Guy, Alexandre,Durand, Thierry,Galano, Jean-Marie

experimental part, p. 2621 - 2634 (2012/06/30)

Enantiomerically enriched F2-dihomo-isoprostanes and F 3-isoprostanes have been synthesized. Such compounds are derived from the action of reactive oxygen species on the phospholipid-bound polyunsaturated fatty acids (PUFA), adrenic

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