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Details

Stereochemistry ABSOLUTE
Molecular Formula C30H38O16
Molecular Weight 654.6131
Optical Activity UNSPECIFIED
Defined Stereocenters 16 / 16
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of Saccatoside

SMILES

C[C@@H]1O[C@@H](O[C@@H]2[C@@H]3O[C@]3(CO)[C@@H]4[C@H]2C=CO[C@H]4O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)[C@H](OC(=O)\C=C\C6=CC=C(O)C=C6)[C@H](O)[C@H]1O

InChI

InChIKey=XIPQZLUSSJDAIC-UYESFEPRSA-N
InChI=1S/C30H38O16/c1-12-19(35)22(38)25(43-17(34)7-4-13-2-5-14(33)6-3-13)29(41-12)44-24-15-8-9-40-27(18(15)30(11-32)26(24)46-30)45-28-23(39)21(37)20(36)16(10-31)42-28/h2-9,12,15-16,18-29,31-33,35-39H,10-11H2,1H3/b7-4+/t12-,15+,16+,18+,19-,20+,21-,22+,23+,24-,25+,26-,27-,28-,29-,30+/m0/s1

HIDE SMILES / InChI

Approval Year

Name Type Language
?-D-Glucopyranoside, (1aS,1bS,2S,5aR,6S,6aS)-6-[[6-deoxy-2-O-[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propenyl]-?-L-mannopyranosyl]oxy]-1a,1b,2,5a,6,6a-hexahydro-1a-(hydroxymethyl)oxireno[4,5]cyclopenta[1,2-c]pyran-2-yl
Preferred Name English
Saccatoside
Common Name English
?-D-Glucopyranoside, 6-[[6-deoxy-2-O-[3-(4-hydroxyphenyl)-1-oxo-2-propenyl]-?-L-mannopyranosyl]oxy]-1a,1b,2,5a,6,6a-hexahydro-1a-(hydroxymethyl)oxireno[4,5]cyclopenta[1,2-c]pyran-2-yl, [1aS-(1a?,1b?,2?,5a?,6?,6a?)]-
Systematic Name English
(2S,3R,4R,5R,6S)-4,5-dihydroxy-2-{[(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl]oxy}-6-methyloxan-3-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate
Systematic Name English
6-O-?-L-(2-O-trans-p-Coumaroyl)rhamnopyranosylcatalpol
Common Name English
?-D-Glucopyranoside, (1aS,1bS,2S,5aR,6S,6aS)-6-[[6-deoxy-2-O-[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]-?-L-mannopyranosyl]oxy]-1a,1b,2,5a,6,6a-hexahydro-1a-(hydroxymethyl)oxireno[4,5]cyclopenta[1,2-c]pyran-2-yl
Systematic Name English
Code System Code Type Description
PUBCHEM
15736668
Created by admin on Mon Mar 31 22:41:48 GMT 2025 , Edited by admin on Mon Mar 31 22:41:48 GMT 2025
PRIMARY
EPA CompTox
DTXSID401345786
Created by admin on Mon Mar 31 22:41:48 GMT 2025 , Edited by admin on Mon Mar 31 22:41:48 GMT 2025
PRIMARY
CAS
85819-35-8
Created by admin on Mon Mar 31 22:41:48 GMT 2025 , Edited by admin on Mon Mar 31 22:41:48 GMT 2025
PRIMARY
FDA UNII
RJ46GBS6PY
Created by admin on Mon Mar 31 22:41:48 GMT 2025 , Edited by admin on Mon Mar 31 22:41:48 GMT 2025
PRIMARY