4-Methoxy-6-phenylpyran-2-one

Details

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Internal ID c3ee72bc-8821-4375-9eb4-799b54b85335
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 4-methoxy-6-phenylpyran-2-one
SMILES (Canonical) COC1=CC(=O)OC(=C1)C2=CC=CC=C2
SMILES (Isomeric) COC1=CC(=O)OC(=C1)C2=CC=CC=C2
InChI InChI=1S/C12H10O3/c1-14-10-7-11(15-12(13)8-10)9-5-3-2-4-6-9/h2-8H,1H3
InChI Key JRKYMPFHUAZGIS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H10O3
Molecular Weight 202.21 g/mol
Exact Mass 202.062994177 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.32
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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4225-45-0
DTXSID10290450
RefChem:99606
DTXCID40241596
4-methoxy-6-phenyl-2H-pyran-2-one
NSC68684
4-Methoxy-6-phenyl-pyran-2-one
NSC-68684

2D Structure

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2D Structure of 4-Methoxy-6-phenylpyran-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 + 0.9942 99.42%
Caco-2 + 0.8612 86.12%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8788 87.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9561 95.61%
OATP1B3 inhibitior + 0.9864 98.64%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4844 48.44%
P-glycoprotein inhibitior - 0.7885 78.85%
P-glycoprotein substrate - 0.9831 98.31%
CYP3A4 substrate - 0.6404 64.04%
CYP2C9 substrate - 0.8363 83.63%
CYP2D6 substrate - 0.8441 84.41%
CYP3A4 inhibition - 0.8531 85.31%
CYP2C9 inhibition + 0.6645 66.45%
CYP2C19 inhibition + 0.9137 91.37%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition + 0.9057 90.57%
CYP2C8 inhibition - 0.7561 75.61%
CYP inhibitory promiscuity + 0.7390 73.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8313 83.13%
Carcinogenicity (trinary) Non-required 0.4414 44.14%
Eye corrosion - 0.7605 76.05%
Eye irritation + 0.9401 94.01%
Skin irritation - 0.5276 52.76%
Skin corrosion - 0.9746 97.46%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6189 61.89%
Micronuclear + 0.6300 63.00%
Hepatotoxicity - 0.5540 55.40%
skin sensitisation - 0.9550 95.50%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5629 56.29%
Acute Oral Toxicity (c) III 0.7738 77.38%
Estrogen receptor binding + 0.7274 72.74%
Androgen receptor binding + 0.8689 86.89%
Thyroid receptor binding - 0.6989 69.89%
Glucocorticoid receptor binding + 0.6681 66.81%
Aromatase binding + 0.8400 84.00%
PPAR gamma - 0.4939 49.39%
Honey bee toxicity - 0.9008 90.08%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.8518 85.18%

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 95.53% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.80% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.44% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.53% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.92% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.58% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.99% 95.50%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.07% 99.15%
CHEMBL1907 P15144 Aminopeptidase N 86.01% 93.31%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.73% 92.08%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.42% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.82% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.81% 97.14%

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.
Aniba firmula
Aniba rosaeodora

Cross-Links

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PubChem 249888
LOTUS LTS0204795
wikiData Q82028113