5-Methyl-4-(methylsulfanyl)-2H-1-benzopyran-2-one

Details

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Internal ID ebfa198a-6bb1-4e9f-b0e5-cba6aed098fb
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 5-methyl-4-methylsulfanylchromen-2-one
SMILES (Canonical) CC1=C2C(=CC=C1)OC(=O)C=C2SC
SMILES (Isomeric) CC1=C2C(=CC=C1)OC(=O)C=C2SC
InChI InChI=1S/C11H10O2S/c1-7-4-3-5-8-11(7)9(14-2)6-10(12)13-8/h3-6H,1-2H3
InChI Key ZYPOGPAECURRGL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O2S
Molecular Weight 206.26 g/mol
Exact Mass 206.04015073 g/mol
Topological Polar Surface Area (TPSA) 51.60 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.82
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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5-Methyl-4-(methylsulfanyl)-2H-1-benzopyran-2-one
DTXSID30564226

2D Structure

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2D Structure of 5-Methyl-4-(methylsulfanyl)-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 + 0.9941 99.41%
Caco-2 + 0.7717 77.17%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.4724 47.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9489 94.89%
OATP1B3 inhibitior + 0.9639 96.39%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8135 81.35%
P-glycoprotein inhibitior - 0.9266 92.66%
P-glycoprotein substrate - 0.8980 89.80%
CYP3A4 substrate - 0.5917 59.17%
CYP2C9 substrate - 0.6396 63.96%
CYP2D6 substrate - 0.8551 85.51%
CYP3A4 inhibition + 0.6059 60.59%
CYP2C9 inhibition + 0.6183 61.83%
CYP2C19 inhibition - 0.5353 53.53%
CYP2D6 inhibition - 0.8707 87.07%
CYP1A2 inhibition + 0.9283 92.83%
CYP2C8 inhibition - 0.8855 88.55%
CYP inhibitory promiscuity - 0.5719 57.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8923 89.23%
Carcinogenicity (trinary) Non-required 0.5006 50.06%
Eye corrosion - 0.9299 92.99%
Eye irritation + 0.9589 95.89%
Skin irritation - 0.6523 65.23%
Skin corrosion - 0.9630 96.30%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5683 56.83%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.7621 76.21%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6617 66.17%
Acute Oral Toxicity (c) III 0.6519 65.19%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding + 0.5341 53.41%
Thyroid receptor binding - 0.7494 74.94%
Glucocorticoid receptor binding + 0.6812 68.12%
Aromatase binding + 0.6671 66.71%
PPAR gamma + 0.5333 53.33%
Honey bee toxicity - 0.8921 89.21%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.8873 88.73%

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 95.68% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.85% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 93.77% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.72% 91.11%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 91.31% 93.65%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.15% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.28% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.24% 99.23%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.17% 81.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.81% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.08% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 80.51% 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.
Clutia abyssinica
Onoseris albicans
Onoseris lopezii

Cross-Links

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PubChem 14804142
LOTUS LTS0004996
wikiData Q82448848