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59894-07-4

59894-07-4 Structure

59894-07-4 Structure
IdentificationBack Directory
[Name]

13,14-DIHYDRO-15-KETO PROSTAGLANDIN D2
[CAS]

59894-07-4
[Synonyms]

DK-PGD2
13,14-Dihydro-15-keto-PGD2
13,14-Dihydro-15-ketoprostadlandin D2
13,14-DIHYDRO-15-KETO PROSTAGLANDIN D2
9ALPHA-HYDROXY-11,15-DIOXO-PROST-5Z-EN-1-OIC ACID
13,14-dihydro-15-keto Prostaglandin D2
(5Z,9α)-9-Hydroxy-11,15-dioxoprost-5-en-1-oic acid
13,14-dihydro-15-keto Prostaglandin D2 MaxSpecStandard
13,14-dihydro-15-keto Prostaglandin D2 Lipid Maps MS Standard
[Molecular Formula]

C20H32O5
[MDL Number]

MFCD00885499
[MOL File]

59894-07-4.mol
[Molecular Weight]

352.47
Chemical PropertiesBack Directory
[Boiling point ]

542.1±40.0 °C(Predicted)
[density ]

1.086±0.06 g/cm3(Predicted)
[solubility ]

DMF: 50 mg/ml
DMSO: 30 mg/ml
Ethanol: 50 mg/mlPBS pH 7.2: 2.5 mg/ml
[pka]

4.76±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H319-H336
[Precautionary statements ]

P210-P240-P241-P242-P243-P261-P264-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P312-P337+P313-P370+P378-P403+P233-P403+P235-P405-P501
Hazard InformationBack Directory
[Description]

13,14-dihydro-15-keto Prostaglandin D2 (13,14-dihydro-15-keto PGD2) is a metabolite of PGD2 which is formed through the 15-hydroxy PGDH pathway. 13,14-dihydro-15-keto PGD2 was recently identified as a selective agonist for the CRTH2/DP2 receptor. It also inhibits ion flux in a canine colonic mucosa preparation. In humans, 13,14-dihydro-15-keto PGD2 is further metabolized to give 11β-hydroxy compounds which have also undergone β-oxidation of one or both side chains. Virtually no 13,14-dihydro-15-keto PGD2 survives intact in the urine.
[Uses]

13,14-Dihydro-15-keto-PGD2 is a metabolite of Prostaglandin D2 (CAT# P838575) and a selective CRTh2/DP2 receptor agonist. CRTh2/DP2 receptors play crucial roles in atopic dermatitis, asthma, and other inflammatory diseases.
[Definition]

ChEBI: 13,14-dihydro-15-ketoprostaglandin D2 is a prostaglandins D. It has a role as a metabolite. It is functionally related to a prostaglandin D2.
[References]

[1] P K RANGACHARI  P A B. Biological activity of metabolites of PGD2 on canine proximal colon.[J]. American Journal of Physiology, 1993, 264 5 Pt 1: G886-94. DOI: 10.1152/ajpgi.1993.264.5.g886
[2] H. HIRAI. Prostaglandin D2 Selectively Induces Chemotaxis in T Helper Type 2 Cells, Eosinophils, and Basophils via Seven-Transmembrane Receptor Crth2[J]. The Tokushima journal of experimental medicine, 2001, 1 1: 255-262. DOI: 10.1084/jem.193.2.255
[3] T E LISTON  L J R. Metabolic fate of radiolabeled prostaglandin D2 in a normal human male volunteer.[J]. The Journal of Biological Chemistry, 1985, 260 24: 13172-13180.
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