8-(3-Hydroxy-3-methylbut-1-enyl)-7-methoxy-2-phenylchromen-4-one

Details

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Internal ID 5fb6950d-1e66-4a37-80c3-e1b7c0cbaf54
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 8-(3-hydroxy-3-methylbut-1-enyl)-7-methoxy-2-phenylchromen-4-one
SMILES (Canonical) CC(C)(C=CC1=C(C=CC2=C1OC(=CC2=O)C3=CC=CC=C3)OC)O
SMILES (Isomeric) CC(C)(C=CC1=C(C=CC2=C1OC(=CC2=O)C3=CC=CC=C3)OC)O
InChI InChI=1S/C21H20O4/c1-21(2,23)12-11-16-18(24-3)10-9-15-17(22)13-19(25-20(15)16)14-7-5-4-6-8-14/h4-13,23H,1-3H3
InChI Key GWHQUBFEZSVTKH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O4
Molecular Weight 336.40 g/mol
Exact Mass 336.13615911 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 3.50
Atomic LogP (AlogP) 4.25
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-(3-Hydroxy-3-methylbut-1-enyl)-7-methoxy-2-phenylchromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.6941 69.41%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8141 81.41%
OATP2B1 inhibitior - 0.7207 72.07%
OATP1B1 inhibitior + 0.9156 91.56%
OATP1B3 inhibitior + 0.9839 98.39%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9286 92.86%
P-glycoprotein inhibitior + 0.7935 79.35%
P-glycoprotein substrate - 0.7515 75.15%
CYP3A4 substrate + 0.5815 58.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8074 80.74%
CYP3A4 inhibition + 0.7167 71.67%
CYP2C9 inhibition + 0.5558 55.58%
CYP2C19 inhibition + 0.8890 88.90%
CYP2D6 inhibition - 0.8614 86.14%
CYP1A2 inhibition + 0.6386 63.86%
CYP2C8 inhibition + 0.7471 74.71%
CYP inhibitory promiscuity + 0.7333 73.33%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.4462 44.62%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.7873 78.73%
Skin corrosion - 0.9744 97.44%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6792 67.92%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.5292 52.92%
skin sensitisation - 0.9160 91.60%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6587 65.87%
Acute Oral Toxicity (c) III 0.4710 47.10%
Estrogen receptor binding + 0.9605 96.05%
Androgen receptor binding + 0.9555 95.55%
Thyroid receptor binding + 0.7465 74.65%
Glucocorticoid receptor binding + 0.8978 89.78%
Aromatase binding + 0.8425 84.25%
PPAR gamma + 0.8998 89.98%
Honey bee toxicity - 0.8287 82.87%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9775 97.75%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.30% 95.56%
CHEMBL2581 P07339 Cathepsin D 97.16% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.46% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.02% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.27% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.37% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 86.86% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.15% 92.08%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.60% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.60% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 85.16% 90.20%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.06% 95.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.61% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.33% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.25% 85.14%

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.
Tephrosia hookeriana
Tephrosia purpurea

Cross-Links

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PubChem 179523
LOTUS LTS0024979
wikiData Q105022387