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PROSTAGLANDIN D2

CAS No.
41598-07-6
Chemical Name:
PROSTAGLANDIN D2
Synonyms
PGDS;PGD2;Prostaglandin D?;PROSTAGLANDIN D2;PROSTAGLANDINS D2;PGD2 (Prostaglandin D2);RP23-47P18.11-006, 21kDa;Prostaglandin D2;11-dehydroprostaglandinf2-alpha;Prostaglandin D2 MaxSpecStandard
CBNumber:
CB2433095
Molecular Formula:
C20H32O5
Molecular Weight:
352.47
MDL Number:
MFCD00077857
MOL File:
41598-07-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-21 11:20:27
Product description Number Pack Size Price
Prostaglandin D2 ≥95%, synthetic P5172 1mg $221
Anti-Ptgds antibody produced in goat affinity isolated antibody, buffered aqueous solution SAB2502046 100μG $628
Prostaglandin D? 538909 1mg $210
Prostaglandin D2 ≥98% 12010 1mg $49
Prostaglandin D2 ≥98% 12010 5mg $216

PROSTAGLANDIN D2 Properties

Melting point 68°C
alpha +7.5°(D/21℃)(c=1,THF)
Boiling point 406.07°C (rough estimate)
Density 1.0601 (rough estimate)
refractive index 1.6120 (estimate)
storage temp. -20°C
solubility Chloroform (Slightly), Ethanol (Slightly), Methanol (Slightly), THF (Slightly)
pka 4.76±0.10(Predicted)
form White solid
color White to Light Orange
biological source synthetic
BRN 2170623
Stability Light Sensitive
InChIKey BHMBVRSPMRCCGG-OUTUXVNYSA-N
SMILES [H][C@]1(C\C=C/CCCC(O)=O)[C@@H](O)CC(=O)[C@]1([H])\C=C\[C@@H](O)CCCCC
FDA UNII RXY07S6CZ2
UNSPSC Code 12352211
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Danger
Hazard statements  H302-H360
Precautionary statements  P201-P301+P312+P330-P308+P313
PPE Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  T
Risk Statements  60-22
Safety Statements  53-22-26-36
WGK Germany  3
RTECS  UK7930000
10
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 4 Oral
Repr. 1B
NFPA 704
0
2 0

PROSTAGLANDIN D2 price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P5172 Prostaglandin D2 ≥95%, synthetic 41598-07-6 1mg $221 2026-03-19 Buy
Sigma-Aldrich SAB2502046 Anti-Ptgds antibody produced in goat affinity isolated antibody, buffered aqueous solution 41598-07-6 100μG $628 2026-03-19 Buy
Sigma-Aldrich 538909 Prostaglandin D? 41598-07-6 1mg $210 2026-03-19 Buy
Cayman Chemical 12010 Prostaglandin D2 ≥98% 41598-07-6 1mg $49 2024-03-01 Buy
Cayman Chemical 12010 Prostaglandin D2 ≥98% 41598-07-6 5mg $216 2024-03-01 Buy
Product number Packaging Price Buy
P5172 1mg $221 Buy
SAB2502046 100μG $628 Buy
538909 1mg $210 Buy
12010 1mg $49 Buy
12010 5mg $216 Buy

PROSTAGLANDIN D2 Chemical Properties,Uses,Production

Description

Prostaglandin D2 (PGD2) is the major eicosanoid product of mast cells and is released in large quantities during allergic and asthmatic anaphylaxis. Mastocytosis patients produce excessive amounts of PGD2, which causes vasodilation, flushing, hypotension, and syncopal episodes. PGD2 is also produced in the brain via an alternative pathway involving a soluble, secreted PGD-synthase also known as β-trace. In the brain, PGD2 produces normal physiological sleep and lowering of body temperature. Further pharmacological actions include inhibition of platelet aggregation and relaxation of vascular smooth muscle. PGD2 inhibits human ovarian tumor cell proliferation with an IC50 of 6.8 μM.

Uses

Prostaglandin D2 is a fatty acid compound present in the human body. Elevated levels of localized Prostaglandin D2 has been linked to hair loss and growth inhibition. It has also been seen to contribute to the activity of allergic asthma.

Definition

ChEBI: A member of the class of prostaglandins D that is prosta-5,13-dien-1-oic acid substituted by hydroxy groups at positions 9 and 15 and an oxo group at position 11 (the 5Z,9alpha,13E,15S- s ereoisomer).

Biochem/physiol Actions

Primary prostaglandin in brain; induces inflammation; stimulates adenylyl cyclase.

in vivo

Prostaglandin D2 (PGD2; infused into the lateral ventricle; 5-50 pmol/min; for 6 hours between 20:00 and 2:00) induces sleep-wake profiles in A2AR KO mice[2].

Animal Model:Male WT and A2AR KO mice of the inbred C57BL/6 strain (weighing 23-27 g, 11-13 weeks old)[1]
Dosage:5, 10, 20, or 50 pmol/min
Administration:Infused into the lateral ventricle; for 6 hours between 20:00 and 2:00
Result:Induced sleep-wake profiles.

IC 50

DP; Human Endogenous Metabolite

References

[1] L.JACKSON ROBERTS II  Brian J S. Metabolic fate of endogenously synthesized prostaglandin D2 in a human female with mastocytosis[J]. Prostaglandins, 1985, 30 3: Pages 383-400. DOI: 10.1016/0090-6980(85)90114-5
[2] HAYAISHI O. Sleep-wake regulation by prostaglandins D2 and E2.[J]. The Journal of Biological Chemistry, 1988, 263 29: 14593-14596.
[3] H ONOE. Prostaglandin D2, a cerebral sleep-inducing substance in monkeys.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1988, 85 11: 4082-4086. DOI: 10.1073/pnas.85.11.4082
[4] Y KIKUCHI. Preclinical studies of antitumor prostaglandins by using human ovarian cancer cells.[J]. Cancer and Metastasis Reviews, 1994, 13 3-4: 309-315. DOI: 10.1007/bf00666101
[5] BRENDAN J. WHITTLE . Binding and activity of the prostacyclin receptor (IP) agonists, treprostinil and iloprost, at human prostanoid receptors: Treprostinil is a potent DP1 and EP2 agonist[J]. Biochemical pharmacology, 2012, 84 1: Pages 68-75. DOI: 10.1016/j.bcp.2012.03.012
[6] OYEBOLA O OYESOLA. The Prostaglandin D2 Receptor CRTH2 Promotes IL-33-Induced ILC2 Accumulation in the Lung.[J]. Journal of immunology, 2020, 204 4: 1001-1011. DOI: 10.4049/jimmunol.1900745
[7] AKIKO SUGANAMI. Human DP and EP2 prostanoid receptors take on distinct forms depending on the diverse binding of different ligands[J]. The FEBS journal, 2016, 283 21: 3931-3940. DOI: 10.1111/febs.13899
[8] D F WOODWARD. Pharmacological characterization of a novel antiglaucoma agent, Bimatoprost (AGN 192024).[J]. Journal of Pharmacology and Experimental Therapeutics, 2003, 305 2: 772-785. DOI: 10.1124/jpet.102.047837
[9] P. WAFFO-TéGUO. Potential Cancer-Chemopreventive Activities of Wine Stilbenoids and Flavans Extracted From Grape (Vitis vinifera) Cell Cultures[J]. Nutrition and Cancer-An International Journal, 2001, 40 1: 173-179. DOI: 10.1207/s15327914nc402_14

61305-35-9
41598-07-6
Synthesis of PROSTAGLANDIN D2 from (4R)-(+)-T-BUTYLDIMETHYLSILOXY-2-CYCLOPENTEN-1-ONE

PROSTAGLANDIN D2 Suppliers

Global( 92)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32467 58
Career Henan Chemica Co
+86-0371-86658258 +8613203830695 laboratory@coreychem.com China 30227 58
TargetMol Chemicals Inc.
+1-781-999-5354; support@targetmol.com United States 39040 58
Aladdin Scientific
tp@aladdinsci.com United States 57505 58
J & K SCIENTIFIC LTD. 18210857532; 18210857532 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15838 69
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32321 50
Syntechem Co.,Ltd info@syntechem.com China 12984 57
ShangHai Caerulum Pharma Discovery Co., Ltd. 18149758185 18149758185 sales-cpd@caerulumpharma.com China 3505 58
Shanghai Macklin Biochemical Co.,Ltd. 15221275939 shenlinxing@macklin.cn China 15781 55

View Lastest Price from PROSTAGLANDIN D2 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Prostaglandin D2 pictures 2026-04-21 Prostaglandin D2
41598-07-6
US $323.00 / μg 100.00% 10g TargetMol Chemicals Inc.
9,15-dihydroxy-11-oxo-,(5z,9-alpha,13e,15s)-prosta-13-dien-1-oicacid prostaglandin D2 cell culture tested prostaglandind2synthetichygroscopic (5z,9α,13e,15s)-9,15-dihydroxy-11-oxoprosta-5,13-dien-1-oic-acid 7-[(1R,2R,5S)-5-hydroxy-2-[(3S)-3-hydroxyoct-1-enyl]-3-oxocyclopentyl]hept-5-enoic acid PGD2, (5Z,9α,13E,15S)-9,15-Dihydroxy-11-oxoprosta-5,13-dien-1-oic-acid (5Z,13E,15S)-9α,15-Dihydroxy-11-oxoprosta-5,13-dien-1-oic acid Prostaglandin D2,(5Z,9α,13E,15S)-9,15-Dihydroxy-11-oxoprosta-5,13-dien-1-oic-acid, PGD2 Prostaglandin D2 Lipid Maps MS Standard (Z)-7-((1R,2R,5S)-5-hydroxy-2-((S,E)-3-hydroxyoct-1-en-1-yl)-3-oxocyclopentyl)hept-5-enoic acid Anti-Ptgds antibody produced in goat PGDS prostaglandin D2 synthase (brain) RP23-47P18.11-006, 21kDa PGD2 (Prostaglandin D2) Prostaglandin D? PROSTAGLANDIN D2 PROSTAGLANDINS D2 PGD2 9ALPHA,15S-DIHYDROXY-11-OXO-PROSTA-5Z,13E-DIEN-1-OIC ACID [5Z,9ALPHA,13E,15S]9,15-DIHYDROXY-11-OXOPROSTA-5,13-DIEN-1-OIC ACID 11-dehydroprostaglandinf2-alpha Prostaglandin D2 MaxSpecStandard Prostaglandin D - CAS 41598-07-6 - Calbiochem Prosta-5,13-dien-1-oic acid, 9,15-dihydroxy-11-oxo-, (5Z,9α,13E,15S)- Prostaglandin D2, HDP1 and CRTH2 receptor agonist Prostaglandin D2 41598-07-6 Fatty Acids Prostaglandins Lipids BioChemical Biochemicals and Reagents