8-Hydroxy-2-methoxynaphthalene-1,4-dione

Details

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Internal ID 009f8d5d-ccaa-44c8-8fce-8784f25fcfd0
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 8-hydroxy-2-methoxynaphthalene-1,4-dione
SMILES (Canonical) COC1=CC(=O)C2=C(C1=O)C(=CC=C2)O
SMILES (Isomeric) COC1=CC(=O)C2=C(C1=O)C(=CC=C2)O
InChI InChI=1S/C11H8O4/c1-15-9-5-8(13)6-3-2-4-7(12)10(6)11(9)14/h2-5,12H,1H3
InChI Key HOFSOQDUZIZMBA-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C11H8O4
Molecular Weight 204.18 g/mol
Exact Mass 204.04225873 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.30
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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15254-76-9
1,4-Naphthalenedione, 8-hydroxy-2-methoxy-
8-Hydroxy-2-methoxy-1,4-naphthalenedione
1,4-Naphthoquinone, 8-hydroxy-2-methoxy-
3-Methoxyjuglone
SCHEMBL5174769
CHEMBL2204407
DTXSID90346065
HOFSOQDUZIZMBA-UHFFFAOYSA-N
8-Hydroxy-2-methoxynaphthoquinone #

2D Structure

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2D Structure of 8-Hydroxy-2-methoxynaphthalene-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 + 0.9969 99.69%
Caco-2 + 0.5745 57.45%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.7995 79.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9538 95.38%
OATP1B3 inhibitior + 0.9876 98.76%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8667 86.67%
P-glycoprotein inhibitior - 0.9367 93.67%
P-glycoprotein substrate - 0.9427 94.27%
CYP3A4 substrate - 0.5697 56.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8492 84.92%
CYP3A4 inhibition - 0.6885 68.85%
CYP2C9 inhibition + 0.5791 57.91%
CYP2C19 inhibition - 0.5653 56.53%
CYP2D6 inhibition - 0.8596 85.96%
CYP1A2 inhibition + 0.9402 94.02%
CYP2C8 inhibition - 0.7156 71.56%
CYP inhibitory promiscuity + 0.6069 60.69%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8656 86.56%
Carcinogenicity (trinary) Non-required 0.4547 45.47%
Eye corrosion - 0.9591 95.91%
Eye irritation + 0.9564 95.64%
Skin irritation + 0.5811 58.11%
Skin corrosion - 0.9511 95.11%
Ames mutagenesis + 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8748 87.48%
Micronuclear + 0.7759 77.59%
Hepatotoxicity + 0.7084 70.84%
skin sensitisation - 0.7041 70.41%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.8299 82.99%
Acute Oral Toxicity (c) II 0.4741 47.41%
Estrogen receptor binding + 0.6104 61.04%
Androgen receptor binding + 0.6552 65.52%
Thyroid receptor binding - 0.6858 68.58%
Glucocorticoid receptor binding - 0.7934 79.34%
Aromatase binding - 0.6292 62.92%
PPAR gamma - 0.5887 58.87%
Honey bee toxicity - 0.9406 94.06%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9792 97.92%

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 97.16% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 95.75% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.68% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.15% 91.11%
CHEMBL2535 P11166 Glucose transporter 90.35% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.74% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.01% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 88.06% 96.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.48% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.90% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.33% 93.99%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.88% 82.69%
CHEMBL1907 P15144 Aminopeptidase N 81.83% 93.31%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.41% 93.03%
CHEMBL3401 O75469 Pregnane X receptor 80.81% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.70% 99.15%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.24% 90.24%

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 morrisiana
Engelhardia roxburghiana

Cross-Links

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PubChem 609303
LOTUS LTS0058025
wikiData Q82118931