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9alpha, 15S-dihydroxy-11-oxo-prost-13e-en-1-oic-3,3,4,4-d4 acid

9alpha, 15S-dihydroxy-11-oxo-prost-13e-en-1-oic-3,3,4,4-d4 acid Suppliers list
Company Name: ChemeGen  
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9alpha, 15S-dihydroxy-11-oxo-prost-13e-en-1-oic-3,3,4,4-d4 acid Basic information
Product Name:9alpha, 15S-dihydroxy-11-oxo-prost-13e-en-1-oic-3,3,4,4-d4 acid
Synonyms:PROSTAGLANDIN D1-D4;9alpha, 15S-dihydroxy-11-oxo-prost-13e-en-1-oic-3,3,4,4-d4 acid
CAS:
MF:C20H30D4O5
MW:358.51
EINECS:
Product Categories:
Mol File:Mol File
9alpha, 15S-dihydroxy-11-oxo-prost-13e-en-1-oic-3,3,4,4-d4 acid Structure
9alpha, 15S-dihydroxy-11-oxo-prost-13e-en-1-oic-3,3,4,4-d4 acid Chemical Properties
solubility DMF: >100 mg/ml
DMSO: >50 mg/ml
Ethanol: >75 mg/mlPBS (pH 7.2): >5 mg/ml
Safety Information
MSDS Information
9alpha, 15S-dihydroxy-11-oxo-prost-13e-en-1-oic-3,3,4,4-d4 acid Usage And Synthesis
DescriptionProstaglandin D1-d4 (PGD1-d4) contains four deuterium atoms at the 3, 3', 4, and 4' positions. It is intended for use as an internal standard for the quantification of PGD1 by GC- or LC-mass spectrometry. PGD1 is the theoretical D-series metabolite of dihomo-γ-linolenic acid (DGLA), but to date it has not been isolated as a natural product. It is an inhibitor of ADP-induced platelet aggregation in humans with an IC50 value of 320 ng/ml, about 1/10 as potent as PGD2.1WARNING This product is not for human or veterinary use.
References[1] G. L. BUNDY. ChemInform Abstract: Synthesis and Platelet Aggregation Inhibiting Activity of Prostaglandin D Analogues.[J]. ChemInform, 1984, 15 8. DOI: 10.1002/chin.198408306
9alpha, 15S-dihydroxy-11-oxo-prost-13e-en-1-oic-3,3,4,4-d4 acid Preparation Products And Raw materials
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