1,4,5,8-Tetramethylnaphthalene

Details

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Internal ID 74c523cb-a6fc-46ad-b002-bcc62cd08814
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 1,4,5,8-tetramethylnaphthalene
SMILES (Canonical) CC1=C2C(=CC=C(C2=C(C=C1)C)C)C
SMILES (Isomeric) CC1=C2C(=CC=C(C2=C(C=C1)C)C)C
InChI InChI=1S/C14H16/c1-9-5-6-11(3)14-12(4)8-7-10(2)13(9)14/h5-8H,1-4H3
InChI Key DWUSGRRPJCRNCI-UHFFFAOYSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16
Molecular Weight 184.28 g/mol
Exact Mass 184.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.07
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2717-39-7
DWUSGRRPJCRNCI-UHFFFAOYSA-
DTXSID60873252
DWUSGRRPJCRNCI-UHFFFAOYSA-N
1,4,5,8-tetramethyl-naphthalene
Naphthalene, 1,4,5,8-tetramethyl-
AKOS006279129
InChI=1/C14H16/c1-9-5-6-11(3)14-12(4)8-7-10(2)13(9)14/h5-8H,1-4H3

2D Structure

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2D Structure of 1,4,5,8-Tetramethylnaphthalene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.8155 81.55%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Lysosomes 0.8185 81.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9763 97.63%
OATP1B3 inhibitior + 0.9639 96.39%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7501 75.01%
P-glycoprotein inhibitior - 0.9427 94.27%
P-glycoprotein substrate - 0.9816 98.16%
CYP3A4 substrate - 0.8326 83.26%
CYP2C9 substrate - 0.8375 83.75%
CYP2D6 substrate - 0.6845 68.45%
CYP3A4 inhibition - 0.8163 81.63%
CYP2C9 inhibition - 0.9514 95.14%
CYP2C19 inhibition - 0.8890 88.90%
CYP2D6 inhibition - 0.8920 89.20%
CYP1A2 inhibition + 0.5077 50.77%
CYP2C8 inhibition - 0.9767 97.67%
CYP inhibitory promiscuity - 0.5404 54.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Warning 0.4633 46.33%
Eye corrosion - 0.6451 64.51%
Eye irritation + 0.9808 98.08%
Skin irritation + 0.7132 71.32%
Skin corrosion - 0.9372 93.72%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3952 39.52%
Micronuclear - 0.7061 70.61%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation + 0.8792 87.92%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.5270 52.70%
Acute Oral Toxicity (c) II 0.4758 47.58%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.6527 65.27%
Thyroid receptor binding - 0.5410 54.10%
Glucocorticoid receptor binding - 0.5415 54.15%
Aromatase binding - 0.6020 60.20%
PPAR gamma - 0.7715 77.15%
Honey bee toxicity - 0.9867 98.67%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.8500 85.00%
Fish aquatic toxicity + 0.9801 98.01%

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
CHEMBL2581 P07339 Cathepsin D 85.02% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.12% 93.65%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.38% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 82.21% 94.73%

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 137689
NPASS NPC40521