4-(2-Hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-3-methylnaphthalene-1,7-diol

Details

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Internal ID cbfc3102-beec-4f4d-9899-9e51506b852b
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 4-(2-hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-3-methylnaphthalene-1,7-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H22O5/c1-12-5-6-14-16(9-12)22(19(27)11-20(14)28-3)21-13(2)10-18(26)23-15(21)7-8-17(25)24(23)29-4/h5-11,25-27H,1-4H3
InChI Key OPQFKTYILPXVOC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H22O5
Molecular Weight 390.40 g/mol
Exact Mass 390.14672380 g/mol
Topological Polar Surface Area (TPSA) 79.20 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.41
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(2-Hydroxy-4-methoxy-7-methylnaphthalen-1-yl)-8-methoxy-3-methylnaphthalene-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 + 0.9906 99.06%
Caco-2 + 0.6984 69.84%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8037 80.37%
OATP2B1 inhibitior - 0.5761 57.61%
OATP1B1 inhibitior + 0.9266 92.66%
OATP1B3 inhibitior + 0.8818 88.18%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7581 75.81%
P-glycoprotein inhibitior + 0.6117 61.17%
P-glycoprotein substrate - 0.8182 81.82%
CYP3A4 substrate + 0.5282 52.82%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate + 0.4558 45.58%
CYP3A4 inhibition - 0.7586 75.86%
CYP2C9 inhibition - 0.6456 64.56%
CYP2C19 inhibition + 0.5359 53.59%
CYP2D6 inhibition - 0.8730 87.30%
CYP1A2 inhibition + 0.8383 83.83%
CYP2C8 inhibition + 0.6833 68.33%
CYP inhibitory promiscuity + 0.6860 68.60%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.4770 47.70%
Eye corrosion - 0.9885 98.85%
Eye irritation + 0.7778 77.78%
Skin irritation - 0.7062 70.62%
Skin corrosion - 0.9579 95.79%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3755 37.55%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.9064 90.64%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6256 62.56%
Acute Oral Toxicity (c) III 0.5425 54.25%
Estrogen receptor binding + 0.8912 89.12%
Androgen receptor binding + 0.7151 71.51%
Thyroid receptor binding + 0.8059 80.59%
Glucocorticoid receptor binding + 0.8300 83.00%
Aromatase binding + 0.7515 75.15%
PPAR gamma + 0.8135 81.35%
Honey bee toxicity - 0.9003 90.03%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.9666 96.66%

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 98.83% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.82% 99.15%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 94.72% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.24% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.29% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.10% 94.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.19% 96.21%
CHEMBL2535 P11166 Glucose transporter 87.16% 98.75%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 86.22% 91.79%
CHEMBL4208 P20618 Proteasome component C5 85.37% 90.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 85.09% 80.78%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.69% 89.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 83.75% 98.11%
CHEMBL4581 P52732 Kinesin-like protein 1 83.69% 93.18%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.44% 93.99%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.31% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.02% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.61% 97.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.72% 96.09%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.38% 93.65%

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 10408060
LOTUS LTS0159145
wikiData Q105196502