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13,14-Dihydro-15-keto prostaglandin E2

CAS No.
363-23-5
Chemical Name:
13,14-Dihydro-15-keto prostaglandin E2
Synonyms
PGEM;13,14-Dihydro-15-keto-PGE2;CUJMXIQZWPZMNQ-XYYGWQPLSA-N;15-keto-13,14-dihydroprostaglandine2;13,14-dihydro-15-oxo-prostaglandin E2;13,14-Dihydro-15-keto prostaglandin E2;13,14-Dihydro-15-ketoprostaglandinE2 solution;9,15-DIOXO-11ALPHA-HYDROXY-PROST-5Z-EN-1-OIC ACID;(5Z)-11α-Hydroxy-9,15-dioxoprosta-5-ene-1-oic acid;(5Z,11α)-11-Hydroxy-9,15-dioxoprost-5-en-1-oic acid
CBNumber:
CB8349316
Molecular Formula:
C20H32O5
Molecular Weight:
352.47
MDL Number:
MFCD00135217
MOL File:
363-23-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:55:41

13,14-Dihydro-15-keto prostaglandin E2 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
pka 4.75±0.10(Predicted)
color Colorless to light yellow

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
Signal word  Warning
Hazard statements  H302-H312-H315-H319-H332-H335-H351
Precautionary statements  P261-P280-P305+P351+P338
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
NFPA 704
3
2 0

13,14-Dihydro-15-keto prostaglandin E2 price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 14650 13,14-dihydro-15-keto Prostaglandin E2 ≥95% 363-23-5 1mg $76 2026-04-30 Buy
Cayman Chemical 14650 13,14-dihydro-15-keto Prostaglandin E2 ≥95% 363-23-5 5mg $343 2026-04-30 Buy
Cayman Chemical 14650 13,14-dihydro-15-keto Prostaglandin E2 ≥95% 363-23-5 10mg $646 2026-04-30 Buy
aablocks AA00C09Y 13,14-dihydro-15-keto Prostaglandin E2 ≥95% 363-23-5 1mg $76 2026-05-28 Buy
aablocks AA00C09Y 13,14-dihydro-15-keto Prostaglandin E2 ≥95% 363-23-5 5mg $343 2026-05-28 Buy
Product number Packaging Price Buy
14650 1mg $76 Buy
14650 5mg $343 Buy
14650 10mg $646 Buy
AA00C09Y 1mg $76 Buy
AA00C09Y 5mg $343 Buy

13,14-Dihydro-15-keto prostaglandin E2 Chemical Properties, Uses, Production

Description

13,14-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).

Uses

13,14-Dihydro-15-ketoPGE2 is a primary metabolite of PGE2 in plasma.

Definition

ChEBI: 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

Raw materials

Preparation Products

13,14-Dihydro-15-keto prostaglandin E2 Suppliers

Global Suppliers ( 30)
Supplier Tel Email Country ProdList Advantage
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9799 58
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TargetMol Chemicals Inc. 15002134094 marketing@targetmol.cn China 29874 58
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Wuhan Topule Biopharmaceutical Co., Ltd +86-18327326525 masar@topule.com China 8433 58
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 (E)-7-[(1R,2R,3R)-3-hydroxy-5-oxo-2-(3-oxooctyl)cyclopentyl]hept-5-enoic acid 13,14-Dihydro-15-keto-PGE2 13,14-Dihydro-15-ketoprostaglandinE2 solution (5Z)-11α-Hydroxy-9,15-dioxoprosta-5-ene-1-oic acid (5Z,11α)-11-Hydroxy-9,15-dioxoprost-5-en-1-oic acid PGEM 13,14-dihydro-15-keto Prostaglandin E2 Lipid Maps MS Standard Prost-5-en-1-oic acid, 11-hydroxy-9,15-dioxo-, (5Z,11α)- 13,14-Dihydro-15-keto prostaglandin E2 363-23-5