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
SMILES
[Cl-].OC1=CC2=[O+]C(=CC=C2C(O)=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
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
Title | Date | PubMed |
---|---|---|
A novel acetylated 3-deoxyanthocyanidin laminaribioside from the fern Blechnum novae-zelandiae. | 2001 Mar-Apr |
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Synergistic effect of deoxyanthocyanins from symbiotic fern Azolla spp. on hrmA gene induction in the cyanobacterium Nostoc punctiforme. | 2002 Sep |
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Quantitative analysis of anticancer 3-deoxyanthocyanidins in infected sorghum seedlings. | 2007 Jan 24 |
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(13)C CPMAS NMR and DFT calculations of anthocyanidins. | 2008 Jul-Sep |
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Identification of flavone phytoalexins and a pathogen-inducible flavone synthase II gene (SbFNSII) in sorghum. | 2010 Feb |
|
The creation and physiological relevance of divergent hydroxylation patterns in the flavonoid pathway. | 2010 Feb 4 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:09:37 GMT 2023
by
admin
on
Fri Dec 15 19:09:37 GMT 2023
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Record UNII |
M011G96EDA
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Record Status |
Validated (UNII)
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Record Version |
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-
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1154-78-5
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M011G96EDA
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6451196
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LUTEOLINIDIN
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6584
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DTXSID20921728
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