LBF20207PG51

LipidBank Top (トップ)

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)

How to edit (ページの書き方)

Upper classes: LB LBF

IDs and Links
LipidBank	XPR1801
LipidMaps	LMFA03010087
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20207PG51

PROSTAGLANDIN I2
Structural Information
Systematic Name	5 (Z) - [ 7 (R) -Hydroxy-6 (R) - (3 (S) -hydroxyocten-1 (E) -yl) -1 (S) ,5 (R) -2-oxabicyclo [ 3.3.0 ] oct-3-ylidenpentanoic acid
Common Name	PROSTAGLANDIN I2 5 (Z) - [ 7 (R) -Hydroxy-6 (R) - (3 (S) -hydroxyocten-1 (E) -yl) -1 (S) ,5 (R) -2-oxabicyclo [ 3.3.0 ] oct-3-ylidenpentanoic acid
Symbol
Formula	C20H32O5
Exact Mass	352.224974134
Average Mass	352.46508
SMILES	C(CC[C@@H](O)C=C[C@H]([C@H]12)[C@H](O)C[C@H](OC(C2)=CCCCC(O)=O)1)CC
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility
Source	In most animal tissues prostanoids are synthesized enzymatically de novo upon physiological and pathological stimulations, and this is also the case of prostaglandin I2. Prostaglandin I2 is produced in blood vessels, lung and other tissues Moncada_S et al..
Chemical Synthesis	Johnson_RA et al.
Metabolism	Prostaaglandin I2 is produced by isomerization of 9,11-endoperoxide of prostaglandin H2 by the catalysis of prostaglandin I synthaase Tanabe_T et al.. Prostaglandin I2 is unstable and decomposes readily to 6-keto-prostaglandin F2a. Its 2,3-dinor derivative is a major urinary metabolite Needleman_P et al..
Biological Activity
Genetic Information
Note
Spectral Information
Mass Spectra	11,15-BIS(TRIMETHYLSILYL) ETHER METHYL ESTER ; 495(M+-CH3), 479, 439, 423, 349, 327, 323, 315, 313, 199, 173 Johnson_RA et al.
UV Spectra
IR Spectra	METHYL ESTER ; LIQUID MELT n 3370, 1740, 1695cm-1 Johnson_RA et al.
NMR Spectra	1-H-NMR(D2O, GLYCINE BUFFER, pH10.4) : d 5.60(m, 2H, 13,14-CH), 4.66(m, 1H, 9-CH), 4.39(t, 1H, 5-CH), 4.15(q, 1H, 15-CH), 3.97(q, 1H, 11-CH), 2.20(t, 2H, 2-CH2) KotovychGet al.
Other Spectra
Chromatograms

Reported Metabolites, References

Biospecies ID Compound Name Reference Comment n.a. LBF20207PG51 See above. Johnson_RA et al. 1978 n.a. LBF20207PG51 See above. Kotovych_G et al. 1980 n.a. LBF20207PG51 See above. Moncada_S et al. 1978 n.a. LBF20207PG51 See above. Needleman_P et al. 1986 n.a. LBF20207PG51 See above. Negishi_M et al. 1995 n.a. LBF20207PG51 See above. Negishi_M et al. 1995 n.a. LBF20207PG51 See above. Pace-Asciak_CR et al. 1983 n.a. LBF20207PG51 See above. Tanabe_T et al. 1995 n.a. LBF20207PG51 See above. Yokoyama_C et al. 1996