6-(4-Methylsulfanylpenta-1,2,3-trienyl)pyran-2-one

Details

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Internal ID 4751b48d-f296-4e94-8591-1f8192170ff3
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 6-(4-methylsulfanylpenta-1,2,3-trienyl)pyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10O2S/c1-9(14-2)5-3-6-10-7-4-8-11(12)13-10/h4,6-8H,1-2H3
InChI Key UHKQQAVHSXDUBK-UHFFFAOYSA-N
Popularity 2 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 1.30
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(4-Methylsulfanylpenta-1,2,3-trienyl)pyran-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 + 0.9936 99.36%
Caco-2 + 0.7990 79.90%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6786 67.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9347 93.47%
OATP1B3 inhibitior + 0.9701 97.01%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8621 86.21%
P-glycoprotein inhibitior - 0.9447 94.47%
P-glycoprotein substrate - 0.9258 92.58%
CYP3A4 substrate - 0.5507 55.07%
CYP2C9 substrate - 0.6330 63.30%
CYP2D6 substrate - 0.8928 89.28%
CYP3A4 inhibition - 0.7978 79.78%
CYP2C9 inhibition - 0.7696 76.96%
CYP2C19 inhibition + 0.5114 51.14%
CYP2D6 inhibition - 0.9124 91.24%
CYP1A2 inhibition + 0.6824 68.24%
CYP2C8 inhibition - 0.9076 90.76%
CYP inhibitory promiscuity - 0.5544 55.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7958 79.58%
Carcinogenicity (trinary) Non-required 0.5781 57.81%
Eye corrosion - 0.6611 66.11%
Eye irritation + 0.6397 63.97%
Skin irritation + 0.6323 63.23%
Skin corrosion - 0.9175 91.75%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7545 75.45%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.6682 66.82%
skin sensitisation + 0.5920 59.20%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.7592 75.92%
Acute Oral Toxicity (c) III 0.5943 59.43%
Estrogen receptor binding - 0.6337 63.37%
Androgen receptor binding - 0.7418 74.18%
Thyroid receptor binding - 0.6059 60.59%
Glucocorticoid receptor binding - 0.6299 62.99%
Aromatase binding + 0.7003 70.03%
PPAR gamma - 0.7184 71.84%
Honey bee toxicity - 0.8488 84.88%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8101 81.01%

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 94.25% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.24% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.84% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 90.91% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.20% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.49% 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.
Cota austriaca

Cross-Links

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PubChem 101415107
LOTUS LTS0225462
wikiData Q105272943