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COMMON NAME | : | |
SYMBOL | : | |
FORMULA | : | C23H40O4 MOL.WT (average) : 380.561 |
BIOLOGICAL ACTIVITY |
PHYSICAL AND CHEMICAL PROPERTIES |
MELTING POINT | : | 120-122 (Ref. 0446) |
BOILING POINT | : | |
REFRACTIVE INDEX | : | |
OPTICAL ROTATION | : | |
DENSITY | : | |
SOLUBILITY | : |
SPECTRAL DATA |
UV SPECTRA | : | |
IR SPECTRA | : | 3400cm-1 (KBr disc) (Ref. 0446) |
NMR SPECTRA | : | 0.78(s,3H,18-CH3), 0.93(s,3H,19-CH3), 1.34(d, J=6Hz, 3H,21-CH3), 3.4-4.3(m,5H, CH-OH's)(Ref. 0446) |
MASS SPECTRA | : | |
OTHER SPECTRA | : | |
CHROMATOGRAM DATA |
SOURCE |
CHEMICAL SYNTHESIS |
METABOLISM |
GENETIC INFORMATION |
NOTE |
REFERENCES |
AUTHOR | : | Kihira,K.,Morioka,Y., and Hoshita,T. |
TITLE | : | Synthesis of (22R and 22S)-3a,7a,22-trihydroxy-5b-cholan-24-oic acids and structure of haemulcholic acid, a unique bile acid isolated from fish bile. PubMed ID:7320628 |
JOURNAL | : | J.Lipid Res. |
VOL | : | 22 PAGE : 1181 -1187 (1981) |