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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H20O11
Molecular Weight 448.3777
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LUTEOLIN 3'-GLUCOSIDE

SMILES

c1cc(c(cc1-c2cc(=O)c3c(cc(cc3o2)O)O)O[C@@]4([H])[C@@]([H])([C@]([H])([C@@]([H])([C@@]([H])(CO)O4)O)O)O)O

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 448.3777
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Development of an HPLC-PAD-MS assay for the identification and quantification of major phenolic edelweiss (Leontopodium alpium Cass.) constituents.
2006 Sep-Oct
Substance Class Chemical
Created
by admin
on Sat Jun 26 01:30:10 UTC 2021
Edited
by admin
on Sat Jun 26 01:30:10 UTC 2021
Record UNII
NE54EDY436
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LUTEOLIN 3'-GLUCOSIDE
Common 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
DRACOCEPHALOSIDE
Common Name English
Code System Code Type Description
PUBCHEM
12309350
Created by admin on Sat Jun 26 01:30:10 UTC 2021 , Edited by admin on Sat Jun 26 01:30:10 UTC 2021
PRIMARY
CAS
5154-41-6
Created by admin on Sat Jun 26 01:30:10 UTC 2021 , Edited by admin on Sat Jun 26 01:30:10 UTC 2021
PRIMARY
FDA UNII
NE54EDY436
Created by admin on Sat Jun 26 01:30:10 UTC 2021 , Edited by admin on Sat Jun 26 01:30:10 UTC 2021
PRIMARY
EPA CompTox
5154-41-6
Created by admin on Sat Jun 26 01:30:10 UTC 2021 , Edited by admin on Sat Jun 26 01:30:10 UTC 2021
PRIMARY
Related Record Type Details
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