13,14-DIHYDRO-15-KETO PROSTAGLANDIN D2
- Product Name
- 13,14-DIHYDRO-15-KETO PROSTAGLANDIN D2
- CAS No.
- 59894-07-4
- Chemical Name
- 13,14-DIHYDRO-15-KETO PROSTAGLANDIN D2
- Synonyms
- DK-PGD2;13,14-Dihydro-15-keto-PGD2;13,14-dihydro-15-keto Prostaglandin D;13,14-Dihydro-15-ketoprostadlandin D2;13,14-DIHYDRO-15-KETO PROSTAGLANDIN D2;13,14-dihydro-15-keto Prostaglandin D2;9ALPHA-HYDROXY-11,15-DIOXO-PROST-5Z-EN-1-OIC ACID;(5Z,9α)-9-Hydroxy-11,15-dioxoprost-5-en-1-oic acid;13,14-dihydro-15-keto Prostaglandin D2 MaxSpecStandard;Prost-5-en-1-oic acid, 9-hydroxy-11,15-dioxo-, (5Z,9α)-
- CBNumber
- CB5674543
- Molecular Formula
- C20H32O5
- Formula Weight
- 352.47
- MOL File
- 59894-07-4.mol
13,14-DIHYDRO-15-KETO PROSTAGLANDIN D2 Property
- 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)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H225Highly Flammable liquid and vapour
H319Causes serious eye irritation
H336May cause drowsiness or dizziness
- Precautionary statements
-
P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P240Ground/bond container and receiving equipment.
P241Use explosion-proof electrical/ventilating/lighting/…/equipment.
P242Use only non-sparking tools.
P243Take precautionary measures against static discharge.
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P312Call a POISON CENTER or doctor/physician if you feel unwell.
P337+P313IF eye irritation persists: Get medical advice/attention.
P370+P378In case of fire: Use … for extinction.
P403+P233Store in a well-ventilated place. Keep container tightly closed.
P403+P235Store in a well-ventilated place. Keep cool.
P405Store locked up.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- 12610
- Product name
- 13,14-dihydro-15-keto Prostaglandin D2
- Purity
- ≥95%
- Packaging
- 1mg
- Price
- $130
- Updated
- 2024/03/01
- Product number
- 12610
- Product name
- 13,14-dihydro-15-keto Prostaglandin D2
- Purity
- ≥95%
- Packaging
- 5mg
- Price
- $576
- Updated
- 2024/03/01
- Product number
- 12610
- Product name
- 13,14-dihydro-15-keto Prostaglandin D2
- Purity
- ≥95%
- Packaging
- 10mg
- Price
- $1019
- Updated
- 2024/03/01
- Product number
- 10007208
- Product name
- 13,14-dihydro-15-keto Prostaglandin D2 MaxSpec? Standard
- Purity
- >95%
- Packaging
- 100μg
- Price
- $185
- Updated
- 2023/06/20
- Product number
- D447790
- Product name
- 13,14-Dihydro-15-keto-PGD2
- Packaging
- 1mg
- Price
- $440
- Updated
- 2021/12/16
13,14-DIHYDRO-15-KETO PROSTAGLANDIN D2 Chemical Properties,Usage,Production
Description
13,14-
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.
[4] JASON D. MORROW. Quantification of the major urinary metabolite of prostaglandin D2 by a stable isotope dilution mass spectrometric assay[J]. Analytical biochemistry, 1991, 193 1: Pages 142-148. DOI: 10.1016/0003-2697(91)90054-w
[5] 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
[6] VICTORIA GÓMEZ-ABELLÁN . Professional phagocytic granulocyte-derived PGD2 regulates the resolution of inflammation in fish[J]. Developmental and comparative immunology, 2015, 52 2: Pages 182-191. DOI: 10.1016/j.dci.2015.04.017
[7] RALF SCHRÖDER. PGH1, the precursor for the anti-inflammatory prostaglandins of the 1-series, is a potent activator of the pro-inflammatory receptor CRTH2/DP2.[J]. PLoS ONE, 2012: e33329. DOI: 10.1371/journal.pone.0033329
13,14-DIHYDRO-15-KETO PROSTAGLANDIN D2 Preparation Products And Raw materials
Raw materials
Preparation Products
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