5-Hydroxy-4,6-dimethoxy-2-naphthalenecarboxylic acid

Details

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Internal ID f57df3b9-92a7-41cc-9f1a-eed4705f816d
Taxonomy Benzenoids > Naphthalenes > Naphthalenecarboxylic acids and derivatives > Naphthalenecarboxylic acids
IUPAC Name 5-hydroxy-4,6-dimethoxynaphthalene-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H12O5/c1-17-9-4-3-7-5-8(13(15)16)6-10(18-2)11(7)12(9)14/h3-6,14H,1-2H3,(H,15,16)
InChI Key SOWWUWXEZSXOBX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O5
Molecular Weight 248.23 g/mol
Exact Mass 248.06847348 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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2-Naphthalenecarboxylic acid, 5-hydroxy-4,6-dimethoxy-
2-Naphthalenecarboxylic acid,5-hydroxy-4,6-dimethoxy-

2D Structure

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2D Structure of 5-Hydroxy-4,6-dimethoxy-2-naphthalenecarboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9867 98.67%
Caco-2 + 0.6490 64.90%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8139 81.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9287 92.87%
OATP1B3 inhibitior + 0.9110 91.10%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6051 60.51%
P-glycoprotein inhibitior - 0.9285 92.85%
P-glycoprotein substrate - 0.9266 92.66%
CYP3A4 substrate - 0.6418 64.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8281 82.81%
CYP3A4 inhibition - 0.8570 85.70%
CYP2C9 inhibition - 0.7157 71.57%
CYP2C19 inhibition - 0.8002 80.02%
CYP2D6 inhibition - 0.8765 87.65%
CYP1A2 inhibition + 0.7170 71.70%
CYP2C8 inhibition + 0.5376 53.76%
CYP inhibitory promiscuity - 0.6590 65.90%
UGT catelyzed + 0.5362 53.62%
Carcinogenicity (binary) - 0.8720 87.20%
Carcinogenicity (trinary) Non-required 0.5547 55.47%
Eye corrosion - 0.9779 97.79%
Eye irritation + 0.9619 96.19%
Skin irritation - 0.5298 52.98%
Skin corrosion - 0.9726 97.26%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7714 77.14%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.5659 56.59%
skin sensitisation - 0.9127 91.27%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7059 70.59%
Acute Oral Toxicity (c) II 0.6451 64.51%
Estrogen receptor binding + 0.7627 76.27%
Androgen receptor binding - 0.5455 54.55%
Thyroid receptor binding + 0.5265 52.65%
Glucocorticoid receptor binding + 0.5891 58.91%
Aromatase binding - 0.6523 65.23%
PPAR gamma + 0.6220 62.20%
Honey bee toxicity - 0.9660 96.60%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.9813 98.13%

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
CHEMBL1255126 O15151 Protein Mdm4 95.00% 90.20%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 93.73% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.44% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.30% 99.17%
CHEMBL3194 P02766 Transthyretin 89.01% 90.71%
CHEMBL4208 P20618 Proteasome component C5 87.54% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.34% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.96% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.28% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.55% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.95% 94.00%

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 paniculata

Cross-Links

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PubChem 73013845
LOTUS LTS0194910
wikiData Q105257269