14581-83-0 , 2-甲?；交?2,3,4,6-O-四乙酰基-beta-D-吡喃葡萄糖苷, CAS:14581-83-0

14581-83-0 , 2-甲酰基苯基-2,3,4,6-O-四乙酰基-beta-D-吡喃葡萄糖苷, CAS:14581-83-0

14581-83-0 , 2-甲?；交?2,3,4,6-O-四乙?；?beta-D-吡喃葡萄糖苷,
2-Formylphenyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside,
CAS:14581-83-0
C21H24O11 / 452.41
MFCD08704116

2-Formylphenyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside

2-甲?；交?2,3,4,6-O-四乙?；?beta-D-吡喃葡萄糖苷,

2-Formylphenyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside is a natural product of the gentisyl family. It is synthesized from benzyl alcohol and acetic anhydride. This compound has been shown to have anticancer properties in animal studies. The acetyl groups are thought to be responsible for the cytotoxicity of this compound. Salireposide is one such analog that has been shown to inhibit protein synthesis and induce apoptosis in cancer cells.

CAS Number	14581-83-0
Product Name	2-Formylphenyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside
IUPAC Name	[(2R,3R,4S,5R,6S)-3,4,5-triacetyloxy-6-(2-formylphenoxy)oxan-2-yl]methyl acetate
Molecular Formula	C21H24O11
Molecular Weight	452.41 g/mol
InChI	InChI=1S/C21H24O11/c1-11(23)27-10-17-18(28-12(2)24)19(29-13(3)25)20(30-14(4)26)21(32-17)31-16-8-6-5-7-15(16)9-22/h5-9,17-21H,10H2,1-4H3/t17-,18-,19+,20-,21-/m1/s1
InChI Key	PCBZIIGBXBDLBK-YMQHIKHWSA-N
SMILES	CC(=O)OCC1C(C(C(C(O1)OC2=CC=CC=C2C=O)OC(=O)C)OC(=O)C)OC(=O)C
Canonical SMILES	CC(=O)OCC1C(C(C(C(O1)OC2=CC=CC=C2C=O)OC(=O)C)OC(=O)C)OC(=O)C
Isomeric SMILES	CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)OC2=CC=CC=C2C=O)OC(=O)C)OC(=O)C)OC(=O)C