5-Methoxy-7-methyl-naphthalene-1,4-dione

Details

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Internal ID 973be9d3-fda6-4061-8637-682f898f9fb8
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 5-methoxy-7-methylnaphthalene-1,4-dione
SMILES (Canonical) CC1=CC2=C(C(=O)C=CC2=O)C(=C1)OC
SMILES (Isomeric) CC1=CC2=C(C(=O)C=CC2=O)C(=C1)OC
InChI InChI=1S/C12H10O3/c1-7-5-8-9(13)3-4-10(14)12(8)11(6-7)15-2/h3-6H,1-2H3
InChI Key CRXUROREGJAECD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H10O3
Molecular Weight 202.21 g/mol
Exact Mass 202.062994177 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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CHEMBL239879

2D Structure

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2D Structure of 5-Methoxy-7-methyl-naphthalene-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5680 56.80%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.8355 83.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9349 93.49%
OATP1B3 inhibitior + 0.9899 98.99%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8814 88.14%
P-glycoprotein inhibitior - 0.9330 93.30%
P-glycoprotein substrate - 0.9553 95.53%
CYP3A4 substrate - 0.5362 53.62%
CYP2C9 substrate - 0.7983 79.83%
CYP2D6 substrate - 0.8150 81.50%
CYP3A4 inhibition - 0.6151 61.51%
CYP2C9 inhibition + 0.5583 55.83%
CYP2C19 inhibition + 0.5286 52.86%
CYP2D6 inhibition - 0.8716 87.16%
CYP1A2 inhibition + 0.9827 98.27%
CYP2C8 inhibition - 0.8951 89.51%
CYP inhibitory promiscuity + 0.7359 73.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7873 78.73%
Carcinogenicity (trinary) Non-required 0.5262 52.62%
Eye corrosion - 0.8762 87.62%
Eye irritation + 0.9782 97.82%
Skin irritation - 0.5927 59.27%
Skin corrosion - 0.9628 96.28%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6662 66.62%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.7449 74.49%
skin sensitisation - 0.6899 68.99%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.7482 74.82%
Acute Oral Toxicity (c) II 0.6740 67.40%
Estrogen receptor binding + 0.5689 56.89%
Androgen receptor binding + 0.5868 58.68%
Thyroid receptor binding - 0.7600 76.00%
Glucocorticoid receptor binding - 0.7717 77.17%
Aromatase binding - 0.6441 64.41%
PPAR gamma - 0.8020 80.20%
Honey bee toxicity - 0.9160 91.60%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9754 97.54%

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 94.09% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.09% 98.95%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.50% 96.67%
CHEMBL4208 P20618 Proteasome component C5 86.60% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.80% 86.33%
CHEMBL2535 P11166 Glucose transporter 83.32% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.17% 94.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.73% 96.21%
CHEMBL1907 P15144 Aminopeptidase N 82.57% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.36% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.28% 96.00%

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.
Diospyros chloroxylon

Cross-Links

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PubChem 11830482
LOTUS LTS0176508
wikiData Q104969000