1,4-Dimethylnaphthalene

Details

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Internal ID 1c62134b-2f61-4f55-ba6d-524e31998cfc
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 1,4-dimethylnaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12/c1-9-7-8-10(2)12-6-4-3-5-11(9)12/h3-8H,1-2H3
InChI Key APQSQLNWAIULLK-UHFFFAOYSA-N
Popularity 196 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12
Molecular Weight 156.22 g/mol
Exact Mass 156.093900383 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.46
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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571-58-4
Naphthalene, 1,4-dimethyl-
DTXSID8035423
BQH3S1I0SO
NSC-61779
DTXCID6015423
CHEBI:48609
RefChem:73311
209-335-9
1,4-Dimethylnapthalene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,4-Dimethylnaphthalene

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 + 0.9323 93.23%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.8360 83.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9683 96.83%
OATP1B3 inhibitior + 0.9673 96.73%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7136 71.36%
P-glycoprotein inhibitior - 0.9700 97.00%
P-glycoprotein substrate - 0.9857 98.57%
CYP3A4 substrate - 0.7147 71.47%
CYP2C9 substrate - 0.8375 83.75%
CYP2D6 substrate - 0.6845 68.45%
CYP3A4 inhibition - 0.8310 83.10%
CYP2C9 inhibition - 0.9412 94.12%
CYP2C19 inhibition - 0.8671 86.71%
CYP2D6 inhibition - 0.8842 88.42%
CYP1A2 inhibition + 0.5723 57.23%
CYP2C8 inhibition - 0.9232 92.32%
CYP inhibitory promiscuity - 0.5588 55.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Warning 0.4226 42.26%
Eye corrosion + 0.4873 48.73%
Eye irritation + 0.9969 99.69%
Skin irritation + 0.7638 76.38%
Skin corrosion - 0.9479 94.79%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5084 50.84%
Micronuclear - 0.6753 67.53%
Hepatotoxicity + 0.8698 86.98%
skin sensitisation + 0.9127 91.27%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6468 64.68%
Acute Oral Toxicity (c) II 0.5992 59.92%
Estrogen receptor binding - 0.7358 73.58%
Androgen receptor binding - 0.8274 82.74%
Thyroid receptor binding - 0.6906 69.06%
Glucocorticoid receptor binding - 0.7659 76.59%
Aromatase binding - 0.6927 69.27%
PPAR gamma - 0.7532 75.32%
Honey bee toxicity - 0.9740 97.40%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.8700 87.00%
Fish aquatic toxicity + 0.9793 97.93%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3356 P05177 Cytochrome P450 1A2 3600 nM
IC50
PMID: 15916432

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.86% 95.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 89.09% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 86.09% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.64% 91.11%
CHEMBL2581 P07339 Cathepsin D 83.60% 98.95%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.15% 96.25%

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.
Meconopsis punicea

Cross-Links

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PubChem 11304
NPASS NPC1008
ChEMBL CHEMBL362076