Bioactive compounds and methods of uses thereof
In one aspect, the present invention provides compounds having formula I or IV as shown below: as further defined herein. In additional aspects, the present invention provides compositions and kits comprising the compounds of the invention and methods for their use, for example, for the prevention or treatment of a cancer.
1. A compound having the formula (I):
or a pharmaceutically acceptable salt, or solvate, thereof, wherein:
R 1 , R 2 , R 3 and R 4 are each independently hydrogen, (C 1 -C 6 )alkyl, or (C 1 -C 12 )acyl;
R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , and R 13 are each independently hydrogen or (C 1 -C 6 )alkyl; and
R 14 and R 15 are each independently hydrogen or (C 1 -C 6 ) alkyl.
2. The isolated compound of claim 1 , wherein R 1 , R 2 , R 3 R 4 are each independently selected from the group consisting of hydrogen, methyl, ethyl, acetyl, and propionyl.
3. The isolated compound of claim 2 , wherein R 14 and R 15 are methyl.
4. The isolated compound of claim 1 , wherein R 5 -R 13 are each independently selected from the group consisting of hydrogen, methyl, and ethyl.
5. The isolated compound of claim 1 , wherein at least four of R 5 -R 13 are hydrogen.
6. The isolated compound of claim 1 , having the formula (II):
or a pharmaceutically acceptable salt, or solvate thereof.
7. The isolated compound of claim 6 , wherein the compound has the formula:
8. A composition comprising a compound of claim 1 , wherein said composition is prepared by a method comprising adsorbing an extract of Rabdosia rubescens to a synthetic resin comprising polyamide moieties or styrene-divinylbenzene moieties, and eluting the synthetic resin with methanol or ethanol to obtain the composition.
9. The compound of claim 1 in the form of a solvate, wherein the solvent is methanol, and the solvate has a specific rotation, [α]D, equal to -28.6 (cO.06 14).