CAS 67667-71-4

Fórmula: C21H26O8

InChI: InChI=1S/C21H26O8/c1-11(2)18(23)27-15-8-12(3)21(25)7-6-20(5,29-21)9-16-17(15)14(19(24)28-16)10-26-13(4)22/h9,12,15,25H,1,6-8,10H2,2-5H3/b16-9+/t12-,15+,20-,21+/m1/s1

Chave InChI: YKIDGUZXBGGNBZ-GUNZAYKBSA-N

SMILES: C[C@@H]1C[C@@H](C\2=C(C(=O)O/C2=C/[C@]3(CC[C@@]1(O3)O)C)COC(=O)C)OC(=O)C(=C)C

8α-(2-Methylacryloyloxy)hirsutinolide 13-O-acetate

CAS: 67667-71-4

8alpha-(2-Methylacryloyloxy)hirsutinolide 13-O-acetate shows inhibitory activity toward CYP2A6 and MAO-A and MAO-B enzymes.

Fórmula: C₂₁H₂₆O₈

Pureza: 98%

Cor e Forma: Solid

Peso molecular: 406.43

Ref: TM-TN3294

8α-(2-Methylacryloyloxy)hirsutinolide 13-O-acetate

CAS: 67667-71-4

Fórmula: C₂₁H₂₆O₈

Pureza: 95%~99%

Peso molecular: 406.431

Ref: BP-SBP03704

[(1R,2E,8S,10R,11S)-6-(Acetyloxymethyl)-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-meth ylprop-2-enoate

CAS: 67667-71-4

[(1R,2E,8S,10R,11S)-6-(Acetyloxymethyl)-11-hydroxy-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-methylprop-2-enoate is a semisynthetic analog of a natural compound, which is derived from a compound found in certain plants. Its mode of action involves the inhibition of microtubule stabilization during cell division, primarily targeting rapidly dividing cancer cells. This disruption of mitotic spindle formation results in apoptosis, effectively reducing tumor growth.

Fórmula: C₂₁H₂₆O₈

Pureza: Min. 95%

Peso molecular: 406.4 g/mol

Ref: 3D-SCA66771