LBF20207PG22

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Fatty acid (脂肪酸)

Glycerolipid (グリセロ脂質)

Sphingolipid (スフィンゴ脂質)

Journals (雑誌一覧)

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Upper classes: LB LBF

IDs and Links
LipidBank	XPR1301
LipidMaps	LMFA03010004
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20207PG22

PROSTAGLANDIN D2
Structural Information
Systematic Name	7- [ 5 (S) -Hydroxy-2 (R) - (3 (S) -hydroxy-1 (E) -octenyl) -3-oxocyclopentan-1 (R) -yl ] -5 (Z) -heptenoic acid
Common Name	PROSTAGLANDIN D2 7- [ 5 (S) -Hydroxy-2 (R) - (3 (S) -hydroxy-1 (E) -octenyl) -3-oxocyclopentan-1 (R) -yl ] -5 (Z) -heptenoic 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(C[C@@H]1O)=O)CC
Physicochemical Information
Melting Point	68°C Hayashi_M et al.
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility	ETHYL ACETATE,THF,CHLOROFORM OgawaYet al.
Source	In most animal tissues prostanoids are synthesized enzymatically de novo upon physiological and pathological stimulations, and this is also the case of prostaglandin D2. Prostaglandin D2 is produced in barin, lung, spleen, mast cells and other tissues Urade_Y et al.;>.
Chemical Synthesis	Hayashi_M et al.;>
Metabolism	Prostaglandin D2 is produced by isomerization of 9,11-endoperoxide of prostaglandin H2. There are two isozymes of prostaglandin D synthase (hematopoietic type and lipocalin type) distinguished by glutathione reequirement and effect of inhibitor Urade_Y et al.;>. Prostaglandin D2 is either reduced to 9a,11b-prostaglandin F or oxidized to 15-keto-prostaglandin D2 by a specific dehydrogenase Giles_H et al.;>. Non-enzymatic transformation of prostaglandin D2 produces anti-neoplastic D12-prostaglandin J2 Negishi_M et al.;>.
Biological Activity
Genetic Information
Note
Spectral Information
Mass Spectra	m/e 334, 316, 246, 245, 191, 190, 161, 55 OgawaYet al.
UV Spectra
IR Spectra	KBr : 3400-2500, 1740, 1700, 975cm-1 HayashiMet al.
NMR Spectra	1H-NMR(270MHz, CDCl3) : d 5.63(dd,J=7 & 16Hz,1H,14-CH), 5.43(dd,J=16 & 8.5Hz,1H,13-CH), 4.47(m, 1H, 9-CH), 4.09(bq, J=7Hz, 1H, 15-CH), 2.87(dd, J=12 & 8.5Hz, 1H, 12-CH), 2.45(m, 2H, 10-CH2), 1.95(bm, 1H, 8-CH) Jenny_EF et al.
Other Spectra
Chromatograms

Reported Metabolites, References

Biospecies ID Compound Name Reference Comment n.a. LBF20207PG22 See above. Fukushima_M 1992 n.a. LBF20207PG22 See above. Giles_H et al. 1988 n.a. LBF20207PG22 See above. Hayaishi_O 1988 n.a. LBF20207PG22 See above. Hayashi_M et al. 1973 n.a. LBF20207PG22 See above. Jenny_EF et al. 1974 n.a. LBF20207PG22 See above. Negishi_M et al. 1995 n.a. LBF20207PG22 See above. Negishi_M et al. 1995 n.a. LBF20207PG22 See above. Ogawa_Y et al. 1986 n.a. LBF20207PG22 See above. Urade_Y et al. 1995