LUTEOLIN 3'-GLUCOSIDE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C21H20O11
Molecular Weight	448.3769
Optical Activity	UNSPECIFIED
Defined Stereocenters	5 / 5
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC[C@H]1O[C@@H](OC2=C(O)C=CC(=C2)C3=CC(=O)C4=C(O3)C=C(O)C=C4O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

InChIKey=VNTMXJLNIJFLIF-QNDFHXLGSA-N

InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)31-14-3-8(1-2-10(14)24)13-6-12(26)17-11(25)4-9(23)5-15(17)30-13/h1-6,16,18-25,27-29H,7H2/t16-,18-,19+,20-,21-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C21H20O11
Molecular Weight	448.3769
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	5 / 5
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
Development of an HPLC-PAD-MS assay for the identification and quantification of major phenolic edelweiss (Leontopodium alpium Cass.) constituents.	2006-10-06	17019930

Substance Class	Chemical Created by `admin` on `Mon Mar 31 23:30:01 GMT 2025` Edited by `admin` on `Mon Mar 31 23:30:01 GMT 2025`
Record UNII	NE54EDY436
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LUTEOLIN 3'-GLUCOSIDE

Common Name

English

DRACOCEPHALOSIDE

Preferred Name

English

LUTEOLIN 3'-.BETA.-D-GLUCOPYRANOSIDE

Common Name

English

LUTEOLIN 3'-O-.BETA.-D-GLUCOPYRANOSIDE

Common Name

English

4H-1-BENZOPYRAN-4-ONE, 2-(3-(.BETA.-D-GLUCOPYRANOSYLOXY)-4-HYDROXYPHENYL)-5,7-DIHYDROXY-

Systematic Name

English

LUTEOLIN-3'-O-.BETA.-GLUCOSIDE

Common Name

English

LUTEOLIN-3'-O-GLUCURONIDE (CONSTITUENT OF ROSEMARY) [DSC]

Common Name

English

LUTEOLIN 3'-O-.BETA.-D-GLUCOSIDE

Common Name

English

LUTEOLIN 3'-O-GLUCOSIDE

Common Name

English

Code System Code Type Description

PUBCHEM

12309350

Created by admin on Mon Mar 31 23:30:01 GMT 2025 , Edited by admin on Mon Mar 31 23:30:01 GMT 2025

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CAS

5154-41-6

Created by admin on Mon Mar 31 23:30:01 GMT 2025 , Edited by admin on Mon Mar 31 23:30:01 GMT 2025

PRIMARY

FDA UNII

NE54EDY436

Created by admin on Mon Mar 31 23:30:01 GMT 2025 , Edited by admin on Mon Mar 31 23:30:01 GMT 2025

PRIMARY

EPA CompTox

DTXSID80385286

Created by admin on Mon Mar 31 23:30:01 GMT 2025 , Edited by admin on Mon Mar 31 23:30:01 GMT 2025

PRIMARY

Related Record Type Details


					8LGU7VM393

ROSEMARY OIL

PARENT -> CONSTITUENT ALWAYS PRESENT