(Z)-6-(2-Methoxyvinyl)-7-methyl-2H-1-benzopyran-2-one

Details

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Internal ID e3f0ef84-819c-4c00-987d-ba090448dcc8
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 6-[(Z)-2-methoxyethenyl]-7-methylchromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H12O3/c1-9-7-12-11(3-4-13(14)16-12)8-10(9)5-6-15-2/h3-8H,1-2H3/b6-5-
InChI Key GENWIQAWAHKDHA-WAYWQWQTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O3
Molecular Weight 216.23 g/mol
Exact Mass 216.078644241 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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6-[(Z)-2-methoxyethenyl]-7-methylchromen-2-one
CHEBI:174093
DTXSID301201933
195259-91-7
6-[(Z)-2-methoxyethenyl]-7-methyl-2H-chromen-2-one
6-[(1Z)-2-Methoxyethenyl]-7-methyl-2H-1-benzopyran-2-one

2D Structure

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2D Structure of (Z)-6-(2-Methoxyvinyl)-7-methyl-2H-1-benzopyran-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.8716 87.16%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7302 73.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8846 88.46%
OATP1B3 inhibitior + 0.9920 99.20%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.5861 58.61%
P-glycoprotein inhibitior - 0.8674 86.74%
P-glycoprotein substrate - 0.9059 90.59%
CYP3A4 substrate - 0.5695 56.95%
CYP2C9 substrate - 0.6562 65.62%
CYP2D6 substrate - 0.8534 85.34%
CYP3A4 inhibition - 0.6758 67.58%
CYP2C9 inhibition + 0.7258 72.58%
CYP2C19 inhibition + 0.7177 71.77%
CYP2D6 inhibition - 0.8699 86.99%
CYP1A2 inhibition + 0.9432 94.32%
CYP2C8 inhibition - 0.8071 80.71%
CYP inhibitory promiscuity + 0.7968 79.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9523 95.23%
Carcinogenicity (trinary) Non-required 0.4687 46.87%
Eye corrosion - 0.9363 93.63%
Eye irritation + 0.8494 84.94%
Skin irritation - 0.6202 62.02%
Skin corrosion - 0.9871 98.71%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3895 38.95%
Micronuclear + 0.7659 76.59%
Hepatotoxicity - 0.6768 67.68%
skin sensitisation - 0.8640 86.40%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6962 69.62%
Acute Oral Toxicity (c) II 0.6029 60.29%
Estrogen receptor binding + 0.8632 86.32%
Androgen receptor binding + 0.6225 62.25%
Thyroid receptor binding - 0.6041 60.41%
Glucocorticoid receptor binding + 0.7553 75.53%
Aromatase binding + 0.8544 85.44%
PPAR gamma - 0.5150 51.50%
Honey bee toxicity - 0.9066 90.66%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9796 97.96%

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
CHEMBL3492 P49721 Proteasome Macropain subunit 91.82% 90.24%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.50% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.31% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.12% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.98% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.17% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.03% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.64% 94.00%
CHEMBL3959 P16083 Quinone reductase 2 84.25% 89.49%
CHEMBL4208 P20618 Proteasome component C5 81.23% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.59% 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.
Dalbergia odorifera
Ficus carica

Cross-Links

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PubChem 5319497
NPASS NPC285067