|
| COMMON NAME | : | |
| SYMBOL | : | |
| FORMULA | : | C23H38O2 MOL.WT (average) : 346.547 |
| BIOLOGICAL ACTIVITY |
| PHYSICAL AND CHEMICAL PROPERTIES |
| MELTING POINT | : | 129.5-130(Ref. 0446) |
| BOILING POINT | : | |
| REFRACTIVE INDEX | : | |
| OPTICAL ROTATION | : | |
| DENSITY | : | |
| SOLUBILITY | : | |
| SPECTRAL DATA |
| UV SPECTRA | : | |
| IR SPECTRA | : | 3400,991,908 cm-1 (KBr disc) (Ref. 0446) |
| NMR SPECTRA | : | 0.72(s,3H,18-CH3), 0.97(s,3H,19-CH3), 1.06(d, J=6Hz, 3H,21-CH3), 3.40-4.4 0 (m,2H, 3b-H, 7b-H), 4.90(m, 2H,23-H), 5.73(m,1H,22-H)(Ref. 0446) |
| MASS SPECTRA | : | m/z 400,385,345,310,295,255 (as TMS derivative)(Ref. 0446) |
| 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) |
| AUTHOR | : | Carlson, G. L., Belobaba, D. T., Hofmann, A. F., and Wedmid, Y. |
| TITLE | : | 24-Nor-5beta-chol-22-enes derived from the major bile acids by oxidative decarboxylation PubMed ID:611641 |
| JOURNAL | : | Steroids. |
| VOL | : | 30 PAGE : 787-793 (1977) |