8-(2,5-Dimethylanilino)naphtho-1,2-quinone

Details

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Internal ID 687eae28-a8b6-447a-915d-651531d98054
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 8-(2,5-dimethylanilino)naphthalene-1,2-dione
SMILES (Canonical) CC1=CC(=C(C=C1)C)NC2=CC=CC3=C2C(=O)C(=O)C=C3
SMILES (Isomeric) CC1=CC(=C(C=C1)C)NC2=CC=CC3=C2C(=O)C(=O)C=C3
InChI InChI=1S/C18H15NO2/c1-11-6-7-12(2)15(10-11)19-14-5-3-4-13-8-9-16(20)18(21)17(13)14/h3-10,19H,1-2H3
InChI Key AYUZCCIJHYEPCB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H15NO2
Molecular Weight 277.30 g/mol
Exact Mass 277.110278721 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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SCHEMBL16296934
AYUZCCIJHYEPCB-UHFFFAOYSA-N

2D Structure

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2D Structure of 8-(2,5-Dimethylanilino)naphtho-1,2-quinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.9259 92.59%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.8714 87.14%
Subcellular localzation Mitochondria 0.6547 65.47%
OATP2B1 inhibitior - 0.8607 86.07%
OATP1B1 inhibitior + 0.9601 96.01%
OATP1B3 inhibitior + 0.9625 96.25%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7845 78.45%
P-glycoprotein inhibitior - 0.6229 62.29%
P-glycoprotein substrate - 0.8570 85.70%
CYP3A4 substrate - 0.5401 54.01%
CYP2C9 substrate - 0.7778 77.78%
CYP2D6 substrate - 0.8322 83.22%
CYP3A4 inhibition + 0.5618 56.18%
CYP2C9 inhibition - 0.5890 58.90%
CYP2C19 inhibition + 0.5657 56.57%
CYP2D6 inhibition - 0.7354 73.54%
CYP1A2 inhibition + 0.7966 79.66%
CYP2C8 inhibition - 0.8066 80.66%
CYP inhibitory promiscuity + 0.7184 71.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8643 86.43%
Carcinogenicity (trinary) Warning 0.3943 39.43%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.6063 60.63%
Skin irritation - 0.7194 71.94%
Skin corrosion - 0.9741 97.41%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5157 51.57%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7006 70.06%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.8656 86.56%
Acute Oral Toxicity (c) III 0.8307 83.07%
Estrogen receptor binding + 0.9620 96.20%
Androgen receptor binding + 0.8647 86.47%
Thyroid receptor binding + 0.6493 64.93%
Glucocorticoid receptor binding + 0.8248 82.48%
Aromatase binding + 0.7076 70.76%
PPAR gamma + 0.6742 67.42%
Honey bee toxicity - 0.9499 94.99%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9708 97.08%

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 97.97% 95.56%
CHEMBL2581 P07339 Cathepsin D 96.75% 98.95%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 93.35% 93.03%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 90.79% 96.67%
CHEMBL3401 O75469 Pregnane X receptor 90.79% 94.73%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 88.56% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.14% 81.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.91% 96.00%
CHEMBL2535 P11166 Glucose transporter 87.26% 98.75%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 86.19% 83.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.80% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 85.55% 91.49%
CHEMBL230 P35354 Cyclooxygenase-2 85.10% 89.63%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 85.02% 90.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.75% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.49% 99.23%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 83.26% 81.29%
CHEMBL3568 P29475 Nitric-oxide synthase, brain 81.34% 95.46%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.88% 94.80%
CHEMBL4581 P52732 Kinesin-like protein 1 80.01% 93.18%

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.
Humulus lupulus

Cross-Links

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PubChem 624013
NPASS NPC48959