Prostaglandin J2-d4

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Company Name: Shanghai isotope chemical co.,ltd  
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Products Intro: Product Name:Prostaglandin J2-d4
CAS:2738376-80-0
Purity:Purity: >=98% Package:100ug Remarks:CA19345
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Products Intro: Product Name:Prostaglandin J2-d4
CAS:2738376-80-0
Purity:95% Package:25μg;50μg;100μg
Company Name: Cayman Chemical Company  
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Products Intro: Product Name:Prostaglandin J2-d4
CAS:2738376-80-0
Company Name: Cayman Chemical Company  
Tel: (800) 364-9897
Email: cayman@caymanchem.com
Products Intro: Product Name:Prostaglandin J2-d4
CAS:2738376-80-0
Prostaglandin J2-d4 Basic information
Product Name:Prostaglandin J2-d4
Synonyms:(Z)-3,3,4,4-tetradeuterio-7-[(1S,5R)-5-[(E,3S)-3-hydroxyoct-1-enyl]-4-oxocyclopent-2-en-1-yl]hept-5-enoic acid
CAS:2738376-80-0
MF:C20H26D4O4
MW:338.48
EINECS:
Product Categories:
Mol File:2738376-80-0.mol
Prostaglandin J2-d4 Structure
Prostaglandin J2-d4 Chemical Properties
Boiling point 521.748±50.00 °C(Press: 760.00 Torr)(predicted)
density 1.103±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
solubility DMF: 50 mg/ml; DMSO: 50 mg/ml; Ethanol: 50 mg/ml; PBS (pH 7.2): 1 mg/ml
Safety Information
MSDS Information
Prostaglandin J2-d4 Usage And Synthesis
DescriptionProstaglandin J2-d4 is intended for use as an internal standard for the quantification of prostaglandin J2 by GC- or LC-MS. Prostaglandin J2 (PGJ2) is formed from PGD2 by the elimination of the C-9 hydroxyl group, a process which is accelerated by the presence of albumin.1 PGJ2 inhibits platelet aggregation with an IC50 of about 5-10 nM.2,3 PGJ2 has antimitotic and antiproliferative effects on a variety of cultured normal cells and tumor cell lines.4 However, this activity has been attributed to further metabolites of PGJ2 and not the parent compound itself.
UsesProstaglandin J2-d4 is the deuterium labeled Prostaglandin J2[1].
References1. Fitzpatrick, F.A., and Wynalda, M.A. Albumin-catalyzed metabolism of prostaglandin D2. Identification of products formed in vitro J. Biol. Chem. 258(19),11713-11718(1983).
2. Bundy, G.L., Morton, D.R., Peterson, D.C., et al. Synthesis and platelet aggregation inhibiting activity of prostaglandin D analogues J. Med. Chem. 26(6),790-799(1983).
3. Mahmud, I., Smith, D.L., Whyte, M.A., et al. On the identification and biological properties of prostaglandin J2 Prostaglandins Leukot. Med. 16(2),131-146(1984).
4. Fukushima, M. Prostaglandin J2 - anti-tumor and anti-viral activities and the mechanisms involved Eicosanoids 3(4),189-199(1990).
Prostaglandin J2-d4 Preparation Products And Raw materials
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