For research use only. Not for therapeutic Use.
Taccalonolides C is an anti-cancer agent[1].
| Catalog Number | I044885 |
| CAS Number | 117803-96-0 |
| Synonyms | [(1R,2S,3S,4R,6S,8S,10S,11R,12R,13S,14S,15R,16R,17S,18R,21S,22S,25R)-4,11,15-triacetyloxy-22-hydroxy-12,16,18,21,22-pentamethyl-5,20,23-trioxo-9,24-dioxaheptacyclo[15.7.1.02,16.03,13.06,12.08,10.021,25]pentacosan-14-yl] acetate |
| Molecular Formula | C36H46O14 |
| Purity | ≥95% |
| InChI | InChI=1S/C36H46O14/c1-12-10-19(41)35(8)24-21(12)34(7)22(28(24)50-32(43)36(35,9)44)20-23(29(46-14(3)38)31(34)48-16(5)40)33(6)17(25(42)27(20)45-13(2)37)11-18-26(49-18)30(33)47-15(4)39/h12,17-18,20-24,26-31,44H,10-11H2,1-9H3/t12-,17-,18+,20+,21+,22-,23-,24+,26+,27-,28-,29+,30+,31+,33+,34-,35+,36-/m1/s1 |
| InChIKey | RXQVUONAHNHYNF-XSUQWDDVSA-N |
| SMILES | CC1CC(=O)C2(C3C1C4(C(C3OC(=O)C2(C)O)C5C(C(C4OC(=O)C)OC(=O)C)C6(C(CC7C(C6OC(=O)C)O7)C(=O)C5OC(=O)C)C)C)C |
| Reference | [1]. Jing Li, et al. Hydrolysis reactions of the taccalonolides reveal structure-activity relationships. J Nat Prod. 2013 Jul 26;76(7):1369-75. |
