Prostaglandin B2 structure
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Common Name | Prostaglandin B2 | ||
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CAS Number | 13367-85-6 | Molecular Weight | 334.45 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 537.0±50.0 °C at 760 mmHg | |
Molecular Formula | C20H30O4 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 292.6±26.6 °C | |
Symbol |
GHS02, GHS07 |
Signal Word | Danger |
Use of Prostaglandin B2Prostaglandin B2 is a prostaglandin. Prostaglandin B2 is the main substance in cord blood mesenchymal stem cells, to inhibit DC-T Cell proliferation. Prostaglandin B2 also induces cutaneous vasoconstriction of the canine hind paw[1][2]. |
Name | prostaglandin B2 |
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Synonym | More Synonyms |
Description | Prostaglandin B2 is a prostaglandin. Prostaglandin B2 is the main substance in cord blood mesenchymal stem cells, to inhibit DC-T Cell proliferation. Prostaglandin B2 also induces cutaneous vasoconstriction of the canine hind paw[1][2]. |
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Related Catalog | |
Target |
Human Endogenous Metabolite |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 537.0±50.0 °C at 760 mmHg |
Molecular Formula | C20H30O4 |
Molecular Weight | 334.45 |
Flash Point | 292.6±26.6 °C |
Exact Mass | 334.214417 |
PSA | 74.60000 |
LogP | 3.24 |
Appearance of Characters | solution |
Vapour Pressure | 0.0±3.2 mmHg at 25°C |
Index of Refraction | 1.564 |
Storage condition | −20°C |
Water Solubility | ethanol: ~100 mg/mL |
Symbol |
GHS02, GHS07 |
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Signal Word | Danger |
Hazard Statements | H225-H319-H336 |
Supplemental HS | Repeated exposure may cause skin dryness or cracking. |
Precautionary Statements | P210-P280-P304 + P340 + P312-P305 + P351 + P338-P337 + P313-P403 + P235 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xn,Xi,F |
Risk Phrases | 20/21/22-67-66-36-11 |
Safety Phrases | 36/37-26 |
RIDADR | UN 1231 3/PG 2 |
WGK Germany | 3 |
Precursor 3 | |
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DownStream 0 |
Identification of prostamides, fatty acyl ethanolamines, and their biosynthetic precursors in rabbit cornea.
J. Lipid Res. 56 , 1419-33, (2015) Arachidonoyl ethanolamine (anandamide) and pros-taglandin ethanolamines (prostamides) are biologically active derivatives of arachidonic acid. Although available through different precursor phospholip... |
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Differences in the Neuroprotective Effect of Orally Administered Virgin Olive Oil (Olea europaea) Polyphenols Tyrosol and Hydroxytyrosol in Rats.
J. Agric. Food Chem. 63 , 5957-63, (2015) The neuroprotective effect of virgin olive oil (VOO) polyphenols has been related to their antioxidant effect. The main objective was to analyze how tyrosol and hydroxytyrosol contribute to the antiox... |
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Cord blood mesenchymal stem cells suppress DC-T Cell proliferation via prostaglandin B2.
Stem Cells Dev. 23(14) , 1582-93, (2014) Immune suppression is a very stable property of multipotent stromal cells also known as mesenchymal stem cells (MSCs). All cell lines tested showed robust immune suppression not affected by a long cul... |
(5Z,13E,15R)-15-Hydroxy-9-oxoprosta-5,8(12),13-trien-1-oic acid |
MFCD00065730 |
EINECS 234-237-8 |
Prostaglandin B2 |
(5Z,13E,15S)-15-Hydroxy-9-oxoprosta-5,8(12),13-trien-1-oic acid PGB2 |
Prosta-5,8(12),13-trien-1-oic acid, 15-hydroxy-9-oxo-, (5Z,13E,15R)- |