PROSTAGLANDIN H1
PROSTAGLANDIN H1 Basic information
- Product Name:
- PROSTAGLANDIN H1
- Synonyms:
-
- PROSTAGLANDIN H1
- PROST-13-EN-1-OIC, 9,11-EPIDIOXY-15-HYDROXY-, (9ALPHA,11ALPHA,13E,15S)
- PGH1
- Prostaglandin?H1?(PGH1)
- PGH1, 9,11-epi-Dioxy-15-hydroxy-(9α,11α,13E,15S)-prost-13-en-1-oic acid
- (13E,15S)-9α,11α-Epidioxy-15-hydroxyprost-13-en-1-oic acid
- PGR1
- Prostaglandin R1
- CAS:
- 52589-22-7
- MF:
- C20H34O5
- MW:
- 354.48
- Mol File:
- 52589-22-7.mol
PROSTAGLANDIN H1 Chemical Properties
- Boiling point:
- 486.2±38.0 °C(Predicted)
- Density
- 1.113±0.06 g/cm3(Predicted)
- Flash point:
- -17 °C
- storage temp.
- −70°C
- solubility
- Ethanol: >100 mg/ml; PBS pH 7.2: >2 mg/ml
- form
- acetone solution
- pka
- 4.78±0.10(Predicted)
Safety Information
- Hazard Codes
- F,Xi
- Risk Statements
- 11-36-66-67
- Safety Statements
- 9-16-26
- RIDADR
- UN 1090 3/PG 2
- WGK Germany
- 1
MSDS
- Language:English Provider:SigmaAldrich
PROSTAGLANDIN H1 Usage And Synthesis
Description
Prostaglandin H1 (PGH1) is the unstable precursor to all 1-series PGs and thromboxanes.1,2,3 It is produced from dihomo-γ-linolenic acid (DGLA; Item No. 90230) by COX-1 and COX-2. 4,2 PGH1 is an agonist of the PGD2 receptor CRTH2.5 It increases intracellular calcium levels in HEK293 cells expressing CRTH2 when used at a concentration of 3 µM and induces CRTH2 internalization at 1 µM, an effect that can be blocked by the CRTH2 antagonist TM30089 (CAY10471; Item No. 10006735). PGH1 is also a suicide inhibitor of platelet thromboxane synthase (Ki = 28 µM).6WARNING This product is not for human or veterinary use.
Definition
ChEBI: Prostaglandin H1 is a member of the class of prostaglandins H that is prostaglandin H2 lacking the double bond at position 5. It has a role as a human xenobiotic metabolite. It is a prostaglandins H, an oxylipin, a bridged compound, an olefinic compound, an organic peroxide and a secondary alcohol. It is a conjugate acid of a prostaglandin H1(1-).
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