LBF20207PG28

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Fatty acid (脂肪酸)

Glycerolipid (グリセロ脂質)

Sphingolipid (スフィンゴ脂質)

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Upper classes: LB LBF

IDs and Links
LipidBank	XPR1711
LipidMaps	LMFA03010148
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20207PG28

5-trans Prostaglandin E2
Structural Information
Systematic Name	9-oxo-11α,15S-dihydroxy-prosta-5E,13E-dien-1-oic acid
Common Name	5-trans Prostaglandin E2 9-oxo-11α,15S-dihydroxy-prosta-5E,13E-dien-1-oic acid
Symbol
Formula	C20H32O5
Exact Mass	352.224974134
Average Mass	352.46508
SMILES	C(CC[C@@H](O)C=C[C@H]([C@H]1CC=CCCCC(O)=O)[C@@H](CC1=O)O)CC
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility
Source	5-trans PGE2 is naturally produced by some gorgonian corals and is also a common impurity in commercial lots of PGE1.
Chemical Synthesis
Metabolism
Biological Activity	5-trans PGE2 has 18 times potency in activating adenylate cyclase compared to PGE2. Hensby_CN et al. 5-trans PGE2 accelerates fibrinolysis by enhancing plasminogen activation mediated dby tissue-type plasminogen activator. Shimokawa_M et al. And it also inhibits platelet
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF20207PG28 See above. Hensby_CN et al. 1979 n.a. LBF20207PG28 See above. Shimokawa_M et al. 1992