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=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
| 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 |
|---|---|---|
| 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
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:33:54 GMT 2025
by
admin
on
Mon Mar 31 19:33:54 GMT 2025
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| Record UNII |
M011G96EDA
|
| Record Status |
Validated (UNII)
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| Record Version |
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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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