LBF16000PG02

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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	XPR1521
LipidMaps	LMFA03010139
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF16000PG02

8- [ 2 (R) - (2-Carboxyethyl) -3 (S) ,5 (R) -dihydroxycyclopentan-1 (R) -yl ] -6-oxooctanoic acid
Structural Information
Systematic Name	8- [ 2R- (2-Carboxyethyl) - (3S,5R) -dihydroxycyclopentan- 1R-yl ] -6-oxooctanoic acid
Common Name	8- [ 2 (R) - (2-Carboxyethyl) -3 (S) ,5 (R) -dihydroxycyclopentan-1 (R) -yl ] -6-oxooctanoic acid
Symbol	PGFα-MUM
Formula	C16H26O7
Exact Mass	330.167853186
Average Mass	330.37343999999996
SMILES	OC(=O)CCCCC(=O)CC[C@@H]([C@H](O)1)[C@@H](CCC(O)=O)[C@@H](O)C1
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility
Source	When prostaglandin F2 alpha was administered intravenously to female subjects, 5 alpha ,7 alpha -dihydroxy-11-keto-tetranor-prosta-1,16-dioic acid was found as a major urinary metabolite (PGF alpha -MUM) Granstrom_E et al..
Chemical Synthesis
Metabolism
Biological Activity
Genetic Information
Note
Spectral Information
Mass Spectra	DIMETHYL ESTER DI-TMS ETHER ; m/e 502(M+), 487, 412, 397, 325, 322, 291, 254, 241, 228, 217, 191, 179, 143 GranstromEet al.
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF16000PG02 See above. Granstrom_E et al. 1969 n.a. LBF16000PG02 See above. Granstrom_E et al. 1971