4-Hydroxy-3,5-dimethoxy-2-naphthaldehyde

Details

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Internal ID 80769986-03c6-43e4-b879-b275fd3513a9
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 4-hydroxy-3,5-dimethoxynaphthalene-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H12O4/c1-16-10-5-3-4-8-6-9(7-14)13(17-2)12(15)11(8)10/h3-7,15H,1-2H3
InChI Key ZNGJSXDIYKTOFV-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O4
Molecular Weight 232.23 g/mol
Exact Mass 232.07355886 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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4-hydroxy-3,5-dimethoxynaphthalene-2-carbaldehyde

2D Structure

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2D Structure of 4-Hydroxy-3,5-dimethoxy-2-naphthaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.7903 79.03%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8114 81.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7282 72.82%
OATP1B3 inhibitior + 0.9809 98.09%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7394 73.94%
P-glycoprotein inhibitior - 0.9061 90.61%
P-glycoprotein substrate - 0.9238 92.38%
CYP3A4 substrate + 0.5074 50.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7008 70.08%
CYP3A4 inhibition - 0.5654 56.54%
CYP2C9 inhibition - 0.8456 84.56%
CYP2C19 inhibition + 0.5608 56.08%
CYP2D6 inhibition - 0.8745 87.45%
CYP1A2 inhibition + 0.9447 94.47%
CYP2C8 inhibition + 0.5065 50.65%
CYP inhibitory promiscuity - 0.5506 55.06%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8920 89.20%
Carcinogenicity (trinary) Non-required 0.5197 51.97%
Eye corrosion - 0.9609 96.09%
Eye irritation + 0.8394 83.94%
Skin irritation + 0.5315 53.15%
Skin corrosion - 0.9829 98.29%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5856 58.56%
Micronuclear + 0.7818 78.18%
Hepatotoxicity + 0.5284 52.84%
skin sensitisation - 0.8803 88.03%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6708 67.08%
Acute Oral Toxicity (c) II 0.4898 48.98%
Estrogen receptor binding + 0.8499 84.99%
Androgen receptor binding - 0.6429 64.29%
Thyroid receptor binding + 0.5195 51.95%
Glucocorticoid receptor binding + 0.5483 54.83%
Aromatase binding + 0.6683 66.83%
PPAR gamma - 0.5836 58.36%
Honey bee toxicity - 0.9244 92.44%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5655 56.55%
Fish aquatic toxicity + 0.9641 96.41%

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 96.53% 95.56%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 96.25% 98.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.04% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.92% 86.33%
CHEMBL2535 P11166 Glucose transporter 91.24% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.82% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.79% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.29% 96.00%
CHEMBL2581 P07339 Cathepsin D 86.74% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 86.43% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.33% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 82.65% 94.03%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.07% 94.45%

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 ebenum

Cross-Links

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PubChem 16086621
LOTUS LTS0000227
wikiData Q105380056