8-Hydroxy-3,5-dimethyl-4-methylsulfanylchromen-2-one

Details

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Internal ID 406c4cbc-057f-44b7-924f-dde4ff1e8c8d
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins
IUPAC Name 8-hydroxy-3,5-dimethyl-4-methylsulfanylchromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12O3S/c1-6-4-5-8(13)10-9(6)11(16-3)7(2)12(14)15-10/h4-5,13H,1-3H3
InChI Key BSEFNMUDJWBKLO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O3S
Molecular Weight 236.29 g/mol
Exact Mass 236.05071541 g/mol
Topological Polar Surface Area (TPSA) 71.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.84
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Hydroxy-3,5-dimethyl-4-methylsulfanylchromen-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 + 0.9839 98.39%
Caco-2 + 0.5465 54.65%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6557 65.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9458 94.58%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8921 89.21%
P-glycoprotein inhibitior - 0.8998 89.98%
P-glycoprotein substrate - 0.9433 94.33%
CYP3A4 substrate - 0.5798 57.98%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8505 85.05%
CYP3A4 inhibition - 0.7920 79.20%
CYP2C9 inhibition - 0.8357 83.57%
CYP2C19 inhibition - 0.8196 81.96%
CYP2D6 inhibition - 0.9087 90.87%
CYP1A2 inhibition + 0.7535 75.35%
CYP2C8 inhibition - 0.8174 81.74%
CYP inhibitory promiscuity - 0.6685 66.85%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9710 97.10%
Carcinogenicity (trinary) Non-required 0.5813 58.13%
Eye corrosion - 0.9766 97.66%
Eye irritation + 0.7985 79.85%
Skin irritation - 0.6421 64.21%
Skin corrosion - 0.9612 96.12%
Ames mutagenesis + 0.5636 56.36%
Human Ether-a-go-go-Related Gene inhibition - 0.7322 73.22%
Micronuclear + 0.7959 79.59%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.8628 86.28%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.6250 62.50%
Acute Oral Toxicity (c) III 0.5473 54.73%
Estrogen receptor binding + 0.7553 75.53%
Androgen receptor binding + 0.5570 55.70%
Thyroid receptor binding - 0.6315 63.15%
Glucocorticoid receptor binding + 0.6797 67.97%
Aromatase binding + 0.6614 66.14%
PPAR gamma + 0.6812 68.12%
Honey bee toxicity - 0.9147 91.47%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9627 96.27%

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 95.97% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.43% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 94.42% 83.82%
CHEMBL2581 P07339 Cathepsin D 92.29% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 90.05% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.76% 94.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.55% 93.65%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.47% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.10% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.93% 99.15%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 81.13% 90.93%

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

Cross-Links

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PubChem 14804143
LOTUS LTS0064464
wikiData Q104945200