4,5-Dimethyl-3-sulfanylchromen-2-one

Details

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Internal ID 20c2ad41-ff83-4b50-ade2-62218b495ca4
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 4,5-dimethyl-3-sulfanylchromen-2-one
SMILES (Canonical) CC1=C2C(=C(C(=O)OC2=CC=C1)S)C
SMILES (Isomeric) CC1=C2C(=C(C(=O)OC2=CC=C1)S)C
InChI InChI=1S/C11H10O2S/c1-6-4-3-5-8-9(6)7(2)10(14)11(12)13-8/h3-5,14H,1-2H3
InChI Key NTMGVAJAVVIPNL-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) 27.30 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.70
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,5-Dimethyl-3-sulfanylchromen-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 + 0.9956 99.56%
Caco-2 + 0.7893 78.93%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5662 56.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9373 93.73%
OATP1B3 inhibitior + 0.9726 97.26%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8703 87.03%
P-glycoprotein inhibitior - 0.9505 95.05%
P-glycoprotein substrate - 0.9380 93.80%
CYP3A4 substrate - 0.6203 62.03%
CYP2C9 substrate - 0.6498 64.98%
CYP2D6 substrate - 0.8786 87.86%
CYP3A4 inhibition + 0.5234 52.34%
CYP2C9 inhibition + 0.6634 66.34%
CYP2C19 inhibition + 0.5053 50.53%
CYP2D6 inhibition - 0.8990 89.90%
CYP1A2 inhibition + 0.8976 89.76%
CYP2C8 inhibition - 0.9151 91.51%
CYP inhibitory promiscuity + 0.5403 54.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.5362 53.62%
Eye corrosion - 0.9689 96.89%
Eye irritation + 0.8263 82.63%
Skin irritation - 0.6291 62.91%
Skin corrosion - 0.9649 96.49%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6244 62.44%
Micronuclear + 0.6659 66.59%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.6603 66.03%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.4665 46.65%
Acute Oral Toxicity (c) III 0.6140 61.40%
Estrogen receptor binding - 0.6579 65.79%
Androgen receptor binding - 0.5799 57.99%
Thyroid receptor binding - 0.7397 73.97%
Glucocorticoid receptor binding + 0.6495 64.95%
Aromatase binding - 0.6445 64.45%
PPAR gamma - 0.4900 49.00%
Honey bee toxicity - 0.9451 94.51%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9764 97.64%

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 93.84% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 93.58% 94.73%
CHEMBL2581 P07339 Cathepsin D 92.99% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 90.60% 93.65%
CHEMBL2039 P27338 Monoamine oxidase B 89.72% 92.51%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.61% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.05% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.96% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.20% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.83% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 82.60% 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.
Onoseris lopezii

Cross-Links

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PubChem 163192443
LOTUS LTS0273151
wikiData Q105185514