7-(3-Methylbut-2-enoxy)-2-phenylchromen-4-one

Details

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Internal ID ed6a74a5-fdf2-4f03-aaf3-35ecf8d459ce
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones
IUPAC Name 7-(3-methylbut-2-enoxy)-2-phenylchromen-4-one
SMILES (Canonical) CC(=CCOC1=CC2=C(C=C1)C(=O)C=C(O2)C3=CC=CC=C3)C
SMILES (Isomeric) CC(=CCOC1=CC2=C(C=C1)C(=O)C=C(O2)C3=CC=CC=C3)C
InChI InChI=1S/C20H18O3/c1-14(2)10-11-22-16-8-9-17-18(21)13-19(23-20(17)12-16)15-6-4-3-5-7-15/h3-10,12-13H,11H2,1-2H3
InChI Key HOXANYZGDSXVJG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O3
Molecular Weight 306.40 g/mol
Exact Mass 306.125594432 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.81
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(3-Methylbut-2-enoxy)-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 + 1.0000 100.00%
Caco-2 + 0.6215 62.15%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8140 81.40%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9513 95.13%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9603 96.03%
P-glycoprotein inhibitior + 0.9168 91.68%
P-glycoprotein substrate - 0.8978 89.78%
CYP3A4 substrate + 0.5311 53.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7963 79.63%
CYP3A4 inhibition - 0.6446 64.46%
CYP2C9 inhibition + 0.7782 77.82%
CYP2C19 inhibition + 0.9288 92.88%
CYP2D6 inhibition - 0.7790 77.90%
CYP1A2 inhibition + 0.9529 95.29%
CYP2C8 inhibition + 0.5625 56.25%
CYP inhibitory promiscuity + 0.9563 95.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.6558 65.58%
Eye corrosion - 0.9664 96.64%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.7600 76.00%
Skin corrosion - 0.9719 97.19%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8264 82.64%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.5792 57.92%
skin sensitisation - 0.7034 70.34%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.5595 55.95%
Acute Oral Toxicity (c) III 0.7708 77.08%
Estrogen receptor binding + 0.9564 95.64%
Androgen receptor binding + 0.9468 94.68%
Thyroid receptor binding + 0.5935 59.35%
Glucocorticoid receptor binding + 0.8963 89.63%
Aromatase binding + 0.9141 91.41%
PPAR gamma + 0.8723 87.23%
Honey bee toxicity - 0.8357 83.57%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9898 98.98%

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 98.94% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.50% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.79% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.15% 95.56%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 94.05% 83.57%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.94% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.91% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.06% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 88.76% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.07% 95.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.47% 85.14%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.69% 94.62%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.42% 92.08%
CHEMBL1951 P21397 Monoamine oxidase A 84.68% 91.49%
CHEMBL1907 P15144 Aminopeptidase N 83.70% 93.31%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.52% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.55% 99.23%

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.
Millettia erythrocalyx

Cross-Links

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PubChem 15541792
LOTUS LTS0097816
wikiData Q104939273