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13,14-DIHYDRO-15-KETO PROSTAGLANDIN E2

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Company Name: Wuhan Topule Biopharmaceutical Co., Ltd
Tel: +8618327326525
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Products Intro: Product Name:13,14-DIHYDRO-15-KETO PROSTAGLANDIN E2
CAS:363-23-5
Purity:98% Package:100mg;1g;500g Remarks:Topule Company operates with integrity and has its own laboratory, which supports packaging and customization. Payment will be made after the product has passed third-party testing
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
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Products Intro: Product Name:13,14-dihydro-15-keto Prostaglandin E2
CAS:363-23-5
Purity:95% Package:1mg;5mg;10mg
Company Name: Shanghai Hongye Biotechnology Co. Ltd  
Tel: 400-9205774
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Products Intro: Product Name:13,14-dihydro-15-keto Prostaglandin E2
CAS:363-23-5
Purity:>98% Package:1mg;10mg;50mg;100mg;
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
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Products Intro: Product Name:13,14-dihydro-15-keto Prostaglandin E2
CAS:363-23-5
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
Company Name: Hubei Kele Fine Chemical Co., Ltd  
Tel: 027-59101668 19945030958
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Products Intro: CAS:363-23-5
Purity:98% HPLC Package:1g;100g;1kg
13,14-DIHYDRO-15-KETO PROSTAGLANDIN E2 Basic information
Product Name:13,14-DIHYDRO-15-KETO PROSTAGLANDIN E2
Synonyms:9,15-DIOXO-11ALPHA-HYDROXY-PROST-5Z-EN-1-OIC ACID;15-keto-13,14-dihydroprostaglandine2;13,14-dihydro-15-oxo-prostaglandin E2;CUJMXIQZWPZMNQ-XYYGWQPLSA-N;13,14-dihydro-15-keto Prostaglandin E2 MaxSpecStandard;13,14-DIHYDRO-15-KETO PROSTAGLANDIN E2;(E)-7-[(1R,2R,3R)-3-hydroxy-5-oxo-2-(3-oxooctyl)cyclopentyl]hept-5-enoic acid;13,14-Dihydro-15-keto-PGE2
CAS:363-23-5
MF:C20H32O5
MW:352.47
EINECS:
Product Categories:
Mol File:363-23-5.mol
13,14-DIHYDRO-15-KETO PROSTAGLANDIN E2 Structure
13,14-DIHYDRO-15-KETO PROSTAGLANDIN E2 Chemical Properties
Boiling point 538.1±45.0 °C(Predicted)
density 1.086±0.06 g/cm3(Predicted)
storage temp. −20°C
solubility DMF: >100 mg/ml
DMSO: >100 mg/ml
Ethanol: >100 mg/mlPBS (pH 7.2): >5 mg/ml
form Liquid
pka4.75±0.10(Predicted)
color Colorless to light yellow
Safety Information
Hazard Codes F,Xn,Xi
Risk Statements 11-20/21/22-36/37/38-67-66-36
Safety Statements 16-26-36
RIDADR UN 1231 3/PG 2
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
13,14-DIHYDRO-15-KETO PROSTAGLANDIN E2 Usage And Synthesis
Description13,14-dihydro-15-keto Prostaglandin E2 (13,14-dihydro-15-keto PGE2) is a metabolite of PGE2 and the primary PGE2 metabolite in plasma. It is formed from PGE2 via a 15-keto PGE2 intermediate by 15-oxo-PG Δ13 reductase. Unlike PGE2, 13,14-dihydro-15-keto PGE2 does not bind effectively to the PGE2 receptors EP2 and EP4 expressed in CHO cells (Kis = 12 and 57 μM, respectively) or induce adenylate cyclase activity in the same cells (EC50s = >18 and >38 μM, respectively). Levels of 13,14-dihydro-15-keto PGE2 are increased in the plasma of women in the third trimester of pregnancy and in women during and immediately after labor and delivery. Levels of 13,14-dihydro-15-keto PGE2 levels are decreased in tumor tissue compared to adjacent non-cancerous tissue isolated from patients with non-small cell lung cancer (NSCLC).
Uses13,14-Dihydro-15-ketoPGE2 is a primary metabolite of PGE2 in plasma.
DefinitionChEBI: The 13,14-dihydro derivative of 15-oxo-prostaglandin E2.
References[1] P. HUSSLEIN  H. S. Concentration of 13,14-dihydro-15-keto-prostaglandin E2 in the maternal peripheral plasma during labour of spontaneous onset[J]. Bjog-An International Journal of Obstetrics and Gynaecology, 1984, 91 3: 228-231. DOI: 10.1111/j.1471-0528.1984.tb04757.x
[2] DUNCAN HUGHES. NAD+-dependent 15-hydroxyprostaglandin dehydrogenase regulates levels of bioactive lipids in non-small cell lung cancer.[J]. Cancer prevention research (Philadelphia, Pa.), 2008, 1 4: 241-249. DOI: 10.1158/1940-6207.capr-08-0055
[3] JOVANA MARIC PHD , PHD  Gerd G M  Nerea Ferreirós PhD, PHD  Danielle F M, et al. Cytokine-induced endogenous production of prostaglandin D2 is essential for human group 2 innate lymphoid cell activation[J]. Journal of Allergy and Clinical Immunology, 2019, 143 6: Pages 2202-2214.e5. DOI: 10.1016/j.jaci.2018.10.069
[4] M. HAMBERG B S. On the Metabolism of Prostaglandins E1 and E2 in Man[J]. Journal of Biological Chemistry, 1971, 246 1: 6713-6721. DOI: 10.1016/s0021-9258(19)45905-x
[5] N. NISHIGAKI A I M Negishi. Two Gs-coupled prostaglandin E receptor subtypes, EP2 and EP4, differ in desensitization and sensitivity to the metabolic inactivation of the agonist.[J]. Molecular Pharmacology, 1996, 146 1: 1031-1037. DOI: 10.1254/fpj.108.supplement_65
[6] DAVID MERIWETHER. Apolipoprotein A-I mimetics mitigate intestinal inflammation in COX2-dependent inflammatory bowel disease model.[J]. Journal of Clinical Investigation, 2019, 129 9: 3670-3685. DOI: 10.1172/jci123700
13,14-DIHYDRO-15-KETO PROSTAGLANDIN E2 Preparation Products And Raw materials
Tag:13,14-DIHYDRO-15-KETO PROSTAGLANDIN E2(363-23-5) Related Product Information
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