1,6,7-Trimethylnaphthalene

Details

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Internal ID bf3b97a5-4ae0-44ca-a911-0c880cdcaea2
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 1,6,7-trimethylnaphthalene
SMILES (Canonical) CC1=C2C=C(C(=CC2=CC=C1)C)C
SMILES (Isomeric) CC1=C2C=C(C(=CC2=CC=C1)C)C
InChI InChI=1S/C13H14/c1-9-5-4-6-12-7-10(2)11(3)8-13(9)12/h4-8H,1-3H3
InChI Key JBXULKRNHAQMAS-UHFFFAOYSA-N
Popularity 80 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14
Molecular Weight 170.25 g/mol
Exact Mass 170.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.77
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2245-38-7
2,3,5-Trimethylnaphthalene
Naphthalene, 1,6,7-trimethyl-
Naphthalene, 2,3,5-trimethyl-
UNII-4WC055TBJ9
4WC055TBJ9
EINECS 218-833-5
NSC 89511
NSC-89511
AI3-28792
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,6,7-Trimethylnaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.9400 94.00%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.6632 66.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9673 96.73%
OATP1B3 inhibitior + 0.9627 96.27%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5818 58.18%
P-glycoprotein inhibitior - 0.9722 97.22%
P-glycoprotein substrate - 0.9559 95.59%
CYP3A4 substrate - 0.6965 69.65%
CYP2C9 substrate - 0.8375 83.75%
CYP2D6 substrate - 0.6845 68.45%
CYP3A4 inhibition - 0.8356 83.56%
CYP2C9 inhibition - 0.8229 82.29%
CYP2C19 inhibition - 0.6497 64.97%
CYP2D6 inhibition - 0.8793 87.93%
CYP1A2 inhibition + 0.6363 63.63%
CYP2C8 inhibition - 0.8194 81.94%
CYP inhibitory promiscuity + 0.6652 66.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Warning 0.4014 40.14%
Eye corrosion - 0.8805 88.05%
Eye irritation + 0.9857 98.57%
Skin irritation + 0.7957 79.57%
Skin corrosion - 0.9805 98.05%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4693 46.93%
Micronuclear - 0.7917 79.17%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.8766 87.66%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.6589 65.89%
Acute Oral Toxicity (c) II 0.5875 58.75%
Estrogen receptor binding - 0.6267 62.67%
Androgen receptor binding - 0.5888 58.88%
Thyroid receptor binding - 0.7126 71.26%
Glucocorticoid receptor binding - 0.6717 67.17%
Aromatase binding + 0.5441 54.41%
PPAR gamma - 0.8336 83.36%
Honey bee toxicity - 0.9862 98.62%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.8600 86.00%
Fish aquatic toxicity + 0.9926 99.26%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.53% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 88.09% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 87.26% 94.73%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 86.34% 96.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.92% 86.33%
CHEMBL2581 P07339 Cathepsin D 85.81% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 84.46% 89.63%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.48% 93.65%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 82.52% 94.67%
CHEMBL1936 P10721 Stem cell growth factor receptor 81.38% 84.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.31% 91.11%

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.
Atractylodes lancea
Atractylodes macrocephala

Cross-Links

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PubChem 16732
NPASS NPC42886