6-Methoxy-7-hydroxydihydroflavonol

Details

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Internal ID 4ced1651-55c9-4c3b-96f6-6ab3ece429ca
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 6-O-methylated flavonoids
IUPAC Name 3,7-dihydroxy-6-methoxy-2-phenyl-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H14O5/c1-20-13-7-10-12(8-11(13)17)21-16(15(19)14(10)18)9-5-3-2-4-6-9/h2-8,15-17,19H,1H3
InChI Key GUMFPOIJOXLCLA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H14O5
Molecular Weight 286.28 g/mol
Exact Mass 286.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.08
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Methoxy-7-hydroxydihydroflavonol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9779 97.79%
Caco-2 - 0.6370 63.70%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8113 81.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8847 88.47%
OATP1B3 inhibitior + 0.9877 98.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7851 78.51%
P-glycoprotein inhibitior - 0.5993 59.93%
P-glycoprotein substrate - 0.9418 94.18%
CYP3A4 substrate + 0.5150 51.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7112 71.12%
CYP3A4 inhibition - 0.6447 64.47%
CYP2C9 inhibition + 0.8876 88.76%
CYP2C19 inhibition + 0.9315 93.15%
CYP2D6 inhibition - 0.8064 80.64%
CYP1A2 inhibition + 0.9264 92.64%
CYP2C8 inhibition + 0.5056 50.56%
CYP inhibitory promiscuity + 0.7815 78.15%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5580 55.80%
Eye corrosion - 0.9749 97.49%
Eye irritation + 0.8322 83.22%
Skin irritation - 0.5737 57.37%
Skin corrosion - 0.9616 96.16%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7677 76.77%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.9457 94.57%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6440 64.40%
Acute Oral Toxicity (c) III 0.7641 76.41%
Estrogen receptor binding - 0.5419 54.19%
Androgen receptor binding - 0.6110 61.10%
Thyroid receptor binding - 0.5083 50.83%
Glucocorticoid receptor binding - 0.4800 48.00%
Aromatase binding - 0.5381 53.81%
PPAR gamma - 0.4858 48.58%
Honey bee toxicity - 0.8934 89.34%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8637 86.37%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.69% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.49% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.13% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.00% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.37% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.84% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 91.65% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.94% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.44% 89.00%
CHEMBL2535 P11166 Glucose transporter 85.63% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.71% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.63% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Dalbergia ecastaphyllum

Cross-Links

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PubChem 129650648
LOTUS LTS0029142
wikiData Q105020269