
CAS Number41598-07-6
SynonymsPGD2; (5Z,9α,13E,15S)-9,15-Dihydroxy-11-oxoprosta-5,13-dien-1-oic acid; Prostaglandin D2; (5Z,9α,13E,15S)-9,15-dihydroxy-11-oxo-prosta-5,13-dien-1-oic acid; MFCD00077857
Molecular FormulaC20H32O5
Molecular Weight352.47
Purity≥98 (HPLC)%
Density1.1±0.1 g/cm3
Boiling Point549.6±50.0 °C at 760 mmHg
Appearancesolid
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 41598-07-6 |
| Catalog No. | 2A-9012179 |
| Chinese Name | 前列腺素 D2 |
| Synonyms | PGD2; (5Z,9α,13E,15S)-9,15-Dihydroxy-11-oxoprosta-5,13-dien-1-oic acid; Prostaglandin D2; (5Z,9α,13E,15S)-9,15-dihydroxy-11-oxo-prosta-5,13-dien-1-oic acid; MFCD00077857 |
| Molecular Formula | C20H32O5 |
| Molecular Weight | 352.47 |
| Purity | ≥98 (HPLC) |
| Density | 1.1±0.1 g/cm3 |
| Boiling Point | 549.6±50.0 °C at 760 mmHg |
| Appearance | solid |
| Storage Condition | Sealed with argon and stored dry below 0 ºC |
| Application | Prostaglandin D2 (PGD2) is one of the major prostaglandins actively produced in the brains of various mammals. Prostaglandin D2 is one of the most potent endogenous sleep promoters. Prostaglandin D2 p |
| MDL Number | MFCD00077857 |
| SMILES | O[C@@H]1[C@@H]([C@H](C(=O)C1)\C=C\[C@@H](O)CCCCC)C\C=C/CCCC(=O)O |
| InChI | 1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,15-18,21-22H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16+,17+,18-/m0/s1 |
| InChI Key | BHMBVRSPMRCCGG-OUTUXVNYSA-N |
| NACRES Code | NA.77 |
| eCl@ss | 42020658 |
| UNSPSC | 12352211 |
| Hazard Symbols | Transport |
| MSDS | msds/12179_1_41598_07_6.pdf |
| Bioactivity | Prostaglandin D2 (PGD2) is one of the major PGs actively produced in the brain of various mammals[1]. Prostaglandin D2 is one of the most potent endogenous sleep promoting substances[2]. PGD2 plays a protective role by suppressing inflammation[3]. Related Catalog Research Areas >> Inflammation/Immunology Target Human Endogenous Metabolite 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. References [1]. Suzuki F, et al. Transport of prostaglandin D2 into brain. Brain Res. 1986 Oct 22;385(2):321-8. [2]. Zhang BJ, et al. Adenosine A2A receptor deficiency attenuates the somnogenic effect of prostaglandin D2 in mice. Acta Pharmacol Sin. 2017 Apr;38(4):469-476. [3]. Kida T, et al. Prostaglandin D2 Attenuates Bleomycin-Induced Lung Inflammation and Pulmonary Fibrosis. PLoS One. 2016 Dec 19;11(12):e0167729. Chemical & Physical Properties Density 1.1±0.1 g/cm3 Boiling Point 549.6±50.0 °C at 760 mmHg Molecular Formula C20H32O5 Molecular Weight 352.465 Flash Point 300.3±26.6 °C Exact Mass 352.224976 PSA 94.83000 LogP 2.02 Vapour Pressure 0.0±3.4 mmHg at 25°C Index of Refraction 1.561 InChIKey BHMBVRSPMRCCGG-OUTUXVNYSA-N SMILES CCCCCC(O)C=CC1C(=O)CC(O)C1CC=CCCCC(=O)O Storage condition 20°C |
| Use of | Prostaglandin D2 (PGD2) is one of the major PGs actively produced in the brain of various mammals[1]. Prostaglandin D2 is one of the most potent endogenous sleep promoting substances[2]. PGD2 plays a protective role by suppressing inflammation[3]. Properties Articles143 Name prostaglandin D2 Synonym More Synonyms Prostaglandin D2 Biological Activity Description Prostaglandin D2 (PGD2) is one of the major PGs actively produced in the brain of various mammals[1]. Prostaglandin D2 is one of the most potent endogenous sleep promoting substances[2]. PGD2 plays a protective role by suppressing inflammation[3]. Related Catalog Research Areas >> Inflammation/Immunology Human Endogenous Metabolite References [1]. Suzuki F, et al. Transport of prostaglandin D2 into brain. Brain Res. 1986 Oct 22;385(2):321-8. [2]. Zhang BJ, et al. Adenosine A2A receptor deficiency attenuates the somnogenic effect of prostaglandin D2 in mice. Acta Pharmacol Sin. 2017 Apr;38(4):469-476. [3]. Kida T, et al. Prostaglandin D2 Attenuates Bleomycin-Induced Lung Inflammation and Pulmonary Fibrosis. PLoS One. 2016 Dec 19;11(12):e0167729. Chemical & Physical Properties Molecular Formula C20H32O5 Exact Mass 352.224976 PSA 94.83000 Index of Refraction 1.561 InChIKey BHMBVRSPMRCCGG-OUTUXVNYSA-N |
| Transport Info | Shipping Name: UN |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available |
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