3-Methoxy-4a-methyl-7-propan-2-yl-5,6-dihydronaphthalen-2-one

Details

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Internal ID 0bc288a3-b85e-4fcb-8913-66ef7f5228a3
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name 3-methoxy-4a-methyl-7-propan-2-yl-5,6-dihydronaphthalen-2-one
SMILES (Canonical) CC(C)C1=CC2=CC(=O)C(=CC2(CC1)C)OC
SMILES (Isomeric) CC(C)C1=CC2=CC(=O)C(=CC2(CC1)C)OC
InChI InChI=1S/C15H20O2/c1-10(2)11-5-6-15(3)9-14(17-4)13(16)8-12(15)7-11/h7-10H,5-6H2,1-4H3
InChI Key CSLOJDYGJYLHDO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O2
Molecular Weight 232.32 g/mol
Exact Mass 232.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.41
H-Bond Acceptor 2
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 3-Methoxy-4a-methyl-7-propan-2-yl-5,6-dihydronaphthalen-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 + 1.0000 100.00%
Caco-2 + 0.8295 82.95%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.6709 67.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9280 92.80%
OATP1B3 inhibitior + 0.9640 96.40%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6213 62.13%
P-glycoprotein inhibitior - 0.9394 93.94%
P-glycoprotein substrate - 0.9131 91.31%
CYP3A4 substrate + 0.5149 51.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8751 87.51%
CYP3A4 inhibition - 0.7725 77.25%
CYP2C9 inhibition - 0.7303 73.03%
CYP2C19 inhibition + 0.5286 52.86%
CYP2D6 inhibition - 0.8589 85.89%
CYP1A2 inhibition - 0.6613 66.13%
CYP2C8 inhibition - 0.9160 91.60%
CYP inhibitory promiscuity - 0.6266 62.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8963 89.63%
Carcinogenicity (trinary) Non-required 0.4721 47.21%
Eye corrosion - 0.9857 98.57%
Eye irritation + 0.5914 59.14%
Skin irritation - 0.5828 58.28%
Skin corrosion - 0.9707 97.07%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.5219 52.19%
skin sensitisation + 0.6150 61.50%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5684 56.84%
Acute Oral Toxicity (c) III 0.7801 78.01%
Estrogen receptor binding - 0.7145 71.45%
Androgen receptor binding - 0.4868 48.68%
Thyroid receptor binding - 0.5070 50.70%
Glucocorticoid receptor binding - 0.5142 51.42%
Aromatase binding + 0.6199 61.99%
PPAR gamma - 0.6994 69.94%
Honey bee toxicity - 0.7447 74.47%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9603 96.03%

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 96.08% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.73% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.23% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.87% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.80% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.47% 93.99%
CHEMBL4208 P20618 Proteasome component C5 87.02% 90.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.24% 97.25%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.00% 93.40%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.36% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.88% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.77% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.40% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.61% 91.07%

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.
Parthenium argentatum

Cross-Links

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PubChem 85157806
LOTUS LTS0072926
wikiData Q104969429