8-Methoxynaphthalene-1,7-diol

Details

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Internal ID b4664ad0-0e6a-456c-9b95-08655594165a
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 8-methoxynaphthalene-1,7-diol
SMILES (Canonical) COC1=C(C=CC2=C1C(=CC=C2)O)O
SMILES (Isomeric) COC1=C(C=CC2=C1C(=CC=C2)O)O
InChI InChI=1S/C11H10O3/c1-14-11-9(13)6-5-7-3-2-4-8(12)10(7)11/h2-6,12-13H,1H3
InChI Key MXKCIJHLIAYIAO-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O3
Molecular Weight 190.19 g/mol
Exact Mass 190.062994177 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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RefChem:107249
CHEBI:220939

2D Structure

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2D Structure of 8-Methoxynaphthalene-1,7-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 - 0.5212 52.12%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7817 78.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9580 95.80%
OATP1B3 inhibitior + 0.9822 98.22%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8334 83.34%
P-glycoprotein inhibitior - 0.9394 93.94%
P-glycoprotein substrate - 0.9805 98.05%
CYP3A4 substrate - 0.6533 65.33%
CYP2C9 substrate - 0.7933 79.33%
CYP2D6 substrate + 0.4916 49.16%
CYP3A4 inhibition - 0.9201 92.01%
CYP2C9 inhibition + 0.6264 62.64%
CYP2C19 inhibition + 0.7666 76.66%
CYP2D6 inhibition - 0.8680 86.80%
CYP1A2 inhibition + 0.9582 95.82%
CYP2C8 inhibition - 0.7424 74.24%
CYP inhibitory promiscuity + 0.6529 65.29%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Warning 0.5232 52.32%
Eye corrosion - 0.9615 96.15%
Eye irritation + 0.9900 99.00%
Skin irritation + 0.6659 66.59%
Skin corrosion - 0.8817 88.17%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7356 73.56%
Micronuclear + 0.6059 60.59%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.7263 72.63%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5159 51.59%
Acute Oral Toxicity (c) III 0.6472 64.72%
Estrogen receptor binding + 0.7947 79.47%
Androgen receptor binding - 0.5893 58.93%
Thyroid receptor binding + 0.6116 61.16%
Glucocorticoid receptor binding + 0.6134 61.34%
Aromatase binding - 0.6075 60.75%
PPAR gamma + 0.6105 61.05%
Honey bee toxicity - 0.9639 96.39%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9245 92.45%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.78% 91.11%
CHEMBL3959 P16083 Quinone reductase 2 92.01% 89.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.97% 95.56%
CHEMBL2535 P11166 Glucose transporter 88.92% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.17% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.56% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.08% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.86% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.02% 93.99%
CHEMBL1937 Q92769 Histone deacetylase 2 82.35% 94.75%
CHEMBL3401 O75469 Pregnane X receptor 80.31% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 86279732
LOTUS LTS0228762
wikiData Q77569655