1-tert-Butyl-7-methoxynaphthalene

Details

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Internal ID 4dda750e-ea88-4c3b-adc4-e43971ca4ba0
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 1-tert-butyl-7-methoxynaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H18O/c1-15(2,3)14-7-5-6-11-8-9-12(16-4)10-13(11)14/h5-10H,1-4H3
InChI Key KGIHXPXSMAHFPD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O
Molecular Weight 214.30 g/mol
Exact Mass 214.135765193 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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60683-42-3
DTXSID00345928
RefChem:235435
DTXCID70297001
Naphthalene, 1-(1,1-dimethylethyl)-7-methoxy-
SCHEMBL22967806
KGIHXPXSMAHFPD-UHFFFAOYSA-N
1-tert-Butyl-7-methoxynaphthalene #

2D Structure

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2D Structure of 1-tert-Butyl-7-methoxynaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.9287 92.87%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6239 62.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9681 96.81%
OATP1B3 inhibitior + 0.9713 97.13%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.5519 55.19%
P-glycoprotein inhibitior - 0.9341 93.41%
P-glycoprotein substrate - 0.8788 87.88%
CYP3A4 substrate - 0.5703 57.03%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate + 0.4119 41.19%
CYP3A4 inhibition - 0.7806 78.06%
CYP2C9 inhibition - 0.7066 70.66%
CYP2C19 inhibition - 0.5932 59.32%
CYP2D6 inhibition - 0.8901 89.01%
CYP1A2 inhibition + 0.7804 78.04%
CYP2C8 inhibition - 0.6067 60.67%
CYP inhibitory promiscuity - 0.5757 57.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7662 76.62%
Carcinogenicity (trinary) Non-required 0.4860 48.60%
Eye corrosion - 0.9263 92.63%
Eye irritation + 0.9619 96.19%
Skin irritation - 0.8302 83.02%
Skin corrosion - 0.9838 98.38%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3965 39.65%
Micronuclear - 0.7367 73.67%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.5811 58.11%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.6846 68.46%
Acute Oral Toxicity (c) III 0.8153 81.53%
Estrogen receptor binding + 0.8548 85.48%
Androgen receptor binding + 0.6641 66.41%
Thyroid receptor binding - 0.5507 55.07%
Glucocorticoid receptor binding - 0.7415 74.15%
Aromatase binding - 0.5564 55.64%
PPAR gamma - 0.5776 57.76%
Honey bee toxicity - 0.9495 94.95%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.8600 86.00%
Fish aquatic toxicity + 0.9453 94.53%

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
CHEMBL1907 P15144 Aminopeptidase N 95.91% 93.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.42% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.66% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.60% 95.56%
CHEMBL3959 P16083 Quinone reductase 2 92.49% 89.49%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 89.85% 94.67%
CHEMBL2535 P11166 Glucose transporter 89.51% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.65% 94.00%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 85.49% 100.00%
CHEMBL2581 P07339 Cathepsin D 84.54% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.44% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.32% 92.62%
CHEMBL2039 P27338 Monoamine oxidase B 81.25% 92.51%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.88% 100.00%

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.
Cornus officinalis

Cross-Links

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PubChem 608110
NPASS NPC155679