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
| 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 |
| 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) | ![]() ![]() GHS07,GHS08 |
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|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||||||||
| F | 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 |
|
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 |
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-
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
PROSTAGLANDIN D2 Preparation Products And Raw materials
Raw materials
1of2
Preparation Products
PROSTAGLANDIN D2 Suppliers
| Supplier | Tel | 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 | |
|---|---|---|---|---|---|---|---|---|
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2026-04-21 | Prostaglandin D2
41598-07-6
|
US $323.00 / μg | 100.00% | 10g | TargetMol Chemicals Inc. |
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- Prostaglandin D2
41598-07-6
- US $323.00 / μg
- 100.00%
- TargetMol Chemicals Inc.








