1,8-Dimethylnaphthalene

Details

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Internal ID a318f4ba-b25c-456a-b8b6-c32e8315c535
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 1,8-dimethylnaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12/c1-9-5-3-7-11-8-4-6-10(2)12(9)11/h3-8H,1-2H3
InChI Key XAABPYINPXYOLM-UHFFFAOYSA-N
Popularity 75 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 4.30
Atomic LogP (AlogP) 3.46
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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Naphthalene, 1,8-dimethyl-
UNII-22P9FW1L76
1,8-DMN
22P9FW1L76
EINECS 209-314-4
DTXSID6060347
CHEBI:48610
RefChem:73759
DTXCID8042137
209-314-4
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,8-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 + 0.9458 94.58%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.8360 83.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9724 97.24%
OATP1B3 inhibitior + 0.9673 96.73%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7545 75.45%
P-glycoprotein inhibitior - 0.9800 98.00%
P-glycoprotein substrate - 0.9820 98.20%
CYP3A4 substrate - 0.7697 76.97%
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 - 0.9110 91.10%
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 + 0.9967 99.67%
Skin irritation + 0.7638 76.38%
Skin corrosion - 0.9479 94.79%
Ames mutagenesis + 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5977 59.77%
Micronuclear - 0.6753 67.53%
Hepatotoxicity + 0.8625 86.25%
skin sensitisation + 0.9127 91.27%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.6272 62.72%
Acute Oral Toxicity (c) II 0.5992 59.92%
Estrogen receptor binding - 0.7676 76.76%
Androgen receptor binding - 0.9268 92.68%
Thyroid receptor binding - 0.6650 66.50%
Glucocorticoid receptor binding - 0.7801 78.01%
Aromatase binding - 0.7640 76.40%
PPAR gamma - 0.7766 77.66%
Honey bee toxicity - 0.9809 98.09%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.8600 86.00%
Fish aquatic toxicity + 0.9793 97.93%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3401 O75469 Pregnane X receptor 87.81% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.15% 95.56%
CHEMBL2581 P07339 Cathepsin D 84.22% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 82.85% 93.31%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.88% 93.65%
CHEMBL3959 P16083 Quinone reductase 2 81.81% 89.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.25% 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.
Cannabis sativa
Cornus officinalis

Cross-Links

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PubChem 11287
NPASS NPC163030