Matairesinoside

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C26H32O11
Molecular Weight	520.5257
Optical Activity	( - )
Defined Stereocenters	7 / 7
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

COC1=CC(C[C@H]2COC(=O)[C@@H]2CC3=CC=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C(OC)=C3)=CC=C1O

InChI

InChIKey=AAGCATAPYOEULE-LHHMAMHXSA-N

InChI=1S/C26H32O11/c1-33-19-9-13(3-5-17(19)28)7-15-12-35-25(32)16(15)8-14-4-6-18(20(10-14)34-2)36-26-24(31)23(30)22(29)21(11-27)37-26/h3-6,9-10,15-16,21-24,26-31H,7-8,11-12H2,1-2H3/t15-,16+,21+,22+,23-,24+,26+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C26H32O11
Molecular Weight	520.5257
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	7 / 7
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:31:01 GMT 2025` Edited by `admin` on `Mon Mar 31 22:31:01 GMT 2025`
Record UNII	XRE59W9FDD
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

Matairesinoside

Common Name

English

(-)-Matairesinol 4-O-glucoside

Preferred Name

English

2(3H)-Furanone, 3-[[4-(?-D-glucopyranosyloxy)-3-methoxyphenyl]methyl]dihydro-4-[(4-hydroxy-3-methoxyphenyl)methyl]-, (3R-trans)-

Systematic Name

English

2(3H)-Furanone, 3-[[4-(?-D-glucopyranosyloxy)-3-methoxyphenyl]methyl]dihydro-4-[(4-hydroxy-3-methoxyphenyl)methyl]-, (3R,4R)-

Systematic Name

English

(3R,4R)-4-(4-hydroxy-3-methoxybenzyl)-3-(3-methoxy-4-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)benzyl)dihydrofuran-2(3H)-one

Systematic Name

English

(3R,4R)-3-[[4-(?-D-Glucopyranosyloxy)-3-methoxyphenyl]methyl]dihydro-4-[(4-hydroxy-3-methoxyphenyl)methyl]-2(3H)-furanone

Systematic Name

English

Code System Code Type Description

PUBCHEM

486612

Created by admin on Mon Mar 31 22:31:01 GMT 2025 , Edited by admin on Mon Mar 31 22:31:01 GMT 2025

PRIMARY

CAS

23202-85-9

Created by admin on Mon Mar 31 22:31:01 GMT 2025 , Edited by admin on Mon Mar 31 22:31:01 GMT 2025

PRIMARY

EPA CompTox

DTXSID80177784

Created by admin on Mon Mar 31 22:31:01 GMT 2025 , Edited by admin on Mon Mar 31 22:31:01 GMT 2025

PRIMARY

FDA UNII

XRE59W9FDD

Created by admin on Mon Mar 31 22:31:01 GMT 2025 , Edited by admin on Mon Mar 31 22:31:01 GMT 2025

PRIMARY