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Details

Stereochemistry ACHIRAL
Molecular Formula C15H11O5.Cl
Molecular Weight 306.698
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LUTEOLINIDOL CHLORIDE

SMILES

[Cl-].OC1=CC(O)=C2C=CC(=[O+]C2=C1)C3=CC=C(O)C(O)=C3

InChI

InChIKey=MMAGHFOHXGFQRZ-UHFFFAOYSA-N
InChI=1S/C15H10O5.ClH/c16-9-6-12(18)10-2-4-14(20-15(10)7-9)8-1-3-11(17)13(19)5-8;/h1-7H,(H3-,16,17,18,19);1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C15H10O5
Molecular Weight 270.2369
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The creation and physiological relevance of divergent hydroxylation patterns in the flavonoid pathway.
2010-02-04
Identification of flavone phytoalexins and a pathogen-inducible flavone synthase II gene (SbFNSII) in sorghum.
2010-02
(13)C CPMAS NMR and DFT calculations of anthocyanidins.
2008-02-09
Quantitative analysis of anticancer 3-deoxyanthocyanidins in infected sorghum seedlings.
2007-01-24
Synergistic effect of deoxyanthocyanins from symbiotic fern Azolla spp. on hrmA gene induction in the cyanobacterium Nostoc punctiforme.
2002-09
A novel acetylated 3-deoxyanthocyanidin laminaribioside from the fern Blechnum novae-zelandiae.
2001-05-24
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:33:54 GMT 2025
Edited
by admin
on Mon Mar 31 19:33:54 GMT 2025
Record UNII
M011G96EDA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LUTEOLINIDOL CHLORIDE
Common Name English
1-BENZOPYRYLIUM, 2-(3,4-DIHYDROXYPHENYL)-5,7-DIHYDROXY-, CHLORIDE (1:1)
Preferred Name English
LUTEOLINIDIN
Common Name English
Code System Code Type Description
CAS
1154-78-5
Created by admin on Mon Mar 31 19:33:54 GMT 2025 , Edited by admin on Mon Mar 31 19:33:54 GMT 2025
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FDA UNII
M011G96EDA
Created by admin on Mon Mar 31 19:33:54 GMT 2025 , Edited by admin on Mon Mar 31 19:33:54 GMT 2025
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PUBCHEM
6451196
Created by admin on Mon Mar 31 19:33:54 GMT 2025 , Edited by admin on Mon Mar 31 19:33:54 GMT 2025
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WIKIPEDIA
LUTEOLINIDIN
Created by admin on Mon Mar 31 19:33:54 GMT 2025 , Edited by admin on Mon Mar 31 19:33:54 GMT 2025
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CHEBI
6584
Created by admin on Mon Mar 31 19:33:54 GMT 2025 , Edited by admin on Mon Mar 31 19:33:54 GMT 2025
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EPA CompTox
DTXSID20921728
Created by admin on Mon Mar 31 19:33:54 GMT 2025 , Edited by admin on Mon Mar 31 19:33:54 GMT 2025
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