(1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,8-tetrahydro-1H-naphthalen-2-yl) 3-methylsulfanylprop-2-enoate

Details

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Internal ID dbdd84cb-9db2-4ff7-8888-8693fab9ef6c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name (1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,8-tetrahydro-1H-naphthalen-2-yl) 3-methylsulfanylprop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H26O3S/c1-12(2)15-11-19(4)13(3)17(22-18(21)8-9-23-5)7-6-14(19)10-16(15)20/h8-10,13,17H,6-7,11H2,1-5H3
InChI Key YGBHBIXCSYCCOR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H26O3S
Molecular Weight 334.50 g/mol
Exact Mass 334.16026586 g/mol
Topological Polar Surface Area (TPSA) 68.70 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.45
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,8-tetrahydro-1H-naphthalen-2-yl) 3-methylsulfanylprop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.6783 67.83%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8499 84.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9084 90.84%
OATP1B3 inhibitior + 0.9612 96.12%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.6420 64.20%
P-glycoprotein inhibitior - 0.5533 55.33%
P-glycoprotein substrate - 0.7254 72.54%
CYP3A4 substrate + 0.6595 65.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9059 90.59%
CYP3A4 inhibition - 0.8100 81.00%
CYP2C9 inhibition - 0.7844 78.44%
CYP2C19 inhibition - 0.5852 58.52%
CYP2D6 inhibition - 0.9490 94.90%
CYP1A2 inhibition - 0.8974 89.74%
CYP2C8 inhibition - 0.6630 66.30%
CYP inhibitory promiscuity - 0.8626 86.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8863 88.63%
Carcinogenicity (trinary) Non-required 0.5582 55.82%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9515 95.15%
Skin irritation - 0.6323 63.23%
Skin corrosion - 0.9752 97.52%
Ames mutagenesis - 0.7054 70.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6617 66.17%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.6106 61.06%
skin sensitisation - 0.5621 56.21%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.4944 49.44%
Acute Oral Toxicity (c) III 0.7902 79.02%
Estrogen receptor binding + 0.6688 66.88%
Androgen receptor binding + 0.5198 51.98%
Thyroid receptor binding + 0.5546 55.46%
Glucocorticoid receptor binding - 0.4929 49.29%
Aromatase binding - 0.7308 73.08%
PPAR gamma + 0.5901 59.01%
Honey bee toxicity - 0.7954 79.54%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.93% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.59% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 92.09% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.72% 95.56%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 91.03% 92.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.01% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.84% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.69% 94.45%
CHEMBL2581 P07339 Cathepsin D 86.41% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.01% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.88% 86.33%

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.
Petasites hybridus

Cross-Links

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PubChem 156603037
LOTUS LTS0129753
wikiData Q105347951