1,5-Dimethylnaphthalene

Details

Top
Internal ID 235c1144-11fa-4bbc-b43a-e111aec6bb1e
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 1,5-dimethylnaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12/c1-9-5-3-8-12-10(2)6-4-7-11(9)12/h3-8H,1-2H3
InChI Key SDDBCEWUYXVGCQ-UHFFFAOYSA-N
Popularity 116 references in papers

Physical and Chemical Properties

Top
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

Top
571-61-9
Naphthalene, 1,5-dimethyl-
1,5-DMN
UNII-60CM3233U9
CHEBI:48608
EINECS 209-338-5
NSC 59388
NSC-59388
60CM3233U9
DTXSID0060351
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 1,5-Dimethylnaphthalene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
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 + 0.8571 85.71%
Subcellular localzation Lysosomes 0.8360 83.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9709 97.09%
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 - 0.9766 97.66%
CYP3A4 substrate - 0.7076 70.76%
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 - 0.9426 94.26%
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 + 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5084 50.84%
Micronuclear - 0.6753 67.53%
Hepatotoxicity + 0.8823 88.23%
skin sensitisation + 0.9127 91.27%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6784 67.84%
Acute Oral Toxicity (c) II 0.5992 59.92%
Estrogen receptor binding - 0.7358 73.58%
Androgen receptor binding - 0.9250 92.50%
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 - 0.9834 98.34%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 0.9793 97.93%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3356 P05177 Cytochrome P450 1A2 42000 nM
IC50
PMID: 15916432
CHEMBL5282 P11509 Cytochrome P450 2A6 31000 nM
30974.19 nM
IC50
IC50
PMID: 15658857
PMID: 19110342

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.68% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.16% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.96% 93.65%
CHEMBL2581 P07339 Cathepsin D 85.21% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 84.61% 93.31%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 81.24% 96.42%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.14% 96.25%

Plants that contains it

Top
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.
Ephedra sinica
Trichosanthes kirilowii

Cross-Links

Top
PubChem 11306
NPASS NPC213570
ChEMBL CHEMBL435106