Wightin

Details

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Internal ID 5aa9f0a9-50c1-4f74-a0b4-5291a7953e01
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 8-O-methylated flavonoids
IUPAC Name 5-hydroxy-2-(3-hydroxy-2-methoxyphenyl)-7,8-dimethoxychromen-4-one
SMILES (Canonical) COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=C(C(=CC=C3)O)OC)OC
SMILES (Isomeric) COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=C(C(=CC=C3)O)OC)OC
InChI InChI=1S/C18H16O7/c1-22-14-8-12(21)15-11(20)7-13(25-18(15)17(14)24-3)9-5-4-6-10(19)16(9)23-2/h4-8,19,21H,1-3H3
InChI Key ZYWSNHKXAZICNY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H16O7
Molecular Weight 344.30 g/mol
Exact Mass 344.08960285 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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SCHEMBL23728055
LMPK12111307
4825-18-7

2D Structure

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2D Structure of Wightin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9711 97.11%
Caco-2 + 0.8501 85.01%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7936 79.36%
OATP2B1 inhibitior - 0.7127 71.27%
OATP1B1 inhibitior + 0.9169 91.69%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6030 60.30%
P-glycoprotein inhibitior + 0.7442 74.42%
P-glycoprotein substrate - 0.6776 67.76%
CYP3A4 substrate + 0.5655 56.55%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.7237 72.37%
CYP2C9 inhibition - 0.6863 68.63%
CYP2C19 inhibition + 0.6566 65.66%
CYP2D6 inhibition - 0.8329 83.29%
CYP1A2 inhibition + 0.8642 86.42%
CYP2C8 inhibition + 0.5749 57.49%
CYP inhibitory promiscuity + 0.7231 72.31%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5851 58.51%
Eye corrosion - 0.9825 98.25%
Eye irritation + 0.8291 82.91%
Skin irritation - 0.7275 72.75%
Skin corrosion - 0.9759 97.59%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5075 50.75%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.9511 95.11%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.4611 46.11%
Acute Oral Toxicity (c) III 0.4741 47.41%
Estrogen receptor binding + 0.9097 90.97%
Androgen receptor binding + 0.7568 75.68%
Thyroid receptor binding + 0.6858 68.58%
Glucocorticoid receptor binding + 0.7887 78.87%
Aromatase binding + 0.6881 68.81%
PPAR gamma + 0.8046 80.46%
Honey bee toxicity - 0.8519 85.19%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.8969 89.69%

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 95.68% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.33% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.91% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.20% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.50% 86.33%
CHEMBL2535 P11166 Glucose transporter 92.40% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.90% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.91% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.54% 99.17%
CHEMBL3194 P02766 Transthyretin 87.38% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 86.56% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.77% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.81% 93.99%
CHEMBL1255126 O15151 Protein Mdm4 84.30% 90.20%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.67% 96.95%
CHEMBL1951 P21397 Monoamine oxidase A 83.54% 91.49%
CHEMBL1907 P15144 Aminopeptidase N 82.78% 93.31%

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.
Phytolacca americana

Cross-Links

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PubChem 12444943
NPASS NPC172333
LOTUS LTS0019486
wikiData Q105386494