![]() |
COMMON NAME | : | chlorovulone IV (Ref. 8025/8026) |
SYMBOL | : | |
FORMULA | : | C21H29O4Cl MOL.WT (average) : 380.905 |
BIOLOGICAL ACTIVITY |
PHYSICAL AND CHEMICAL PROPERTIES |
MELTING POINT | : | |
BOILING POINT | : | |
REFRACTIVE INDEX | : | |
OPTICAL ROTATION | : | 12-O-acetylchlorovulone IV[a]D -12![]() |
DENSITY | : | |
SOLUBILITY | : | Chlorovulones are soluble in MeOH, EtOH, CHCl3, or hexane. |
SPECTRAL DATA |
UV SPECTRA | : | |
IR SPECTRA | : | |
NMR SPECTRA | : | 12-O-acetylchlorovulone IV1H-NMR(400MHz,CDCl3)dppm0.88(3H,t,J=7.2Hz),1.79(2H,quint.,J=7.4Hz),1.81(2H,quint.,J=7.5Hz),1.97(2H,brq,J=7.4Hz),2.04(3H,s),2.35(2H,t,J=7.4Hz),2.70(1H,brdd,J=7.1,14.3Hz),2.94(1H,brdd,J=7.4,14.3Hz),3.67(3H,s),5.21(1H,brq,J=10.8Hz),5.54(1H,brtd,J=7.4,10.8Hz),6.02(1H,brtd,J=8.8,10.8Hz),6.98(1H,d,J=12.0Hz),7.44(1H,s),7.55(1H,brt,J=12.0Hz).(Ref. 8025) |
MASS SPECTRA | : | |
OTHER SPECTRA | : | |
CHROMATOGRAM DATA |
SOURCE |
CHEMICAL SYNTHESIS |
METABOLISM |
GENETIC INFORMATION |
NOTE |
REFERENCES |
AUTHOR | : | Iguchi,K., Kaneta,S., Mori,K., Yamada,Y., Honda,A., and Mori,Y. |
TITLE | : | Chlorovulones, New Halogenated Marine Prostanoids with Antitumor Activity from the Stolonifer Clavularia viridis Quoy and Gaimard. |
JOURNAL | : | Tetrahedron Lett. |
VOL | : | 26 PAGE : 5787 -5790 (1985) |
AUTHOR | : | Nagaoka,H., Iguchi,K., Miyakoshi,T., Yamada,N., and Yamada,Y. |
TITLE | : | Determination of Absolute Configuration of Chlorovulones by CD Measurement and by Enantioselective Synthesis of (-)-Chlorovulone II. |
JOURNAL | : | Tetrahedron Lett. |
VOL | : | 27 PAGE : 223 -226 (1986) |