4-hydroxy-4-methoxy-3H-naphthalene-2-carboxylic acid

Details

Top
Internal ID 82eabb3f-2723-4b0d-b2ec-96da752d5fbc
Taxonomy Benzenoids > Naphthalenes > Naphthalenecarboxylic acids and derivatives > Naphthalenecarboxylic acids
IUPAC Name 4-hydroxy-4-methoxy-3H-naphthalene-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12O4/c1-16-12(15)7-9(11(13)14)6-8-4-2-3-5-10(8)12/h2-6,15H,7H2,1H3,(H,13,14)
InChI Key JBXVEZZUYXXFMC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H12O4
Molecular Weight 220.22 g/mol
Exact Mass 220.07355886 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.35
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4-hydroxy-4-methoxy-3H-naphthalene-2-carboxylic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 - 0.5297 52.97%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8042 80.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9264 92.64%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8638 86.38%
P-glycoprotein inhibitior - 0.9794 97.94%
P-glycoprotein substrate - 0.9256 92.56%
CYP3A4 substrate - 0.5316 53.16%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.8595 85.95%
CYP3A4 inhibition - 0.8370 83.70%
CYP2C9 inhibition - 0.7232 72.32%
CYP2C19 inhibition - 0.5645 56.45%
CYP2D6 inhibition - 0.7570 75.70%
CYP1A2 inhibition + 0.6362 63.62%
CYP2C8 inhibition - 0.7531 75.31%
CYP inhibitory promiscuity - 0.7834 78.34%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8286 82.86%
Carcinogenicity (trinary) Non-required 0.6011 60.11%
Eye corrosion - 0.9864 98.64%
Eye irritation + 0.8288 82.88%
Skin irritation - 0.6488 64.88%
Skin corrosion - 0.9617 96.17%
Ames mutagenesis - 0.7154 71.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8663 86.63%
Micronuclear - 0.5141 51.41%
Hepatotoxicity + 0.6302 63.02%
skin sensitisation - 0.6394 63.94%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6581 65.81%
Acute Oral Toxicity (c) III 0.5914 59.14%
Estrogen receptor binding - 0.7460 74.60%
Androgen receptor binding + 0.5700 57.00%
Thyroid receptor binding - 0.7745 77.45%
Glucocorticoid receptor binding - 0.6413 64.13%
Aromatase binding - 0.7146 71.46%
PPAR gamma - 0.5605 56.05%
Honey bee toxicity - 0.9436 94.36%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9639 96.39%

Targets

Top

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.96% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.77% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.92% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.38% 95.56%
CHEMBL4208 P20618 Proteasome component C5 88.70% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.09% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.21% 94.62%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.13% 90.24%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.06% 93.00%
CHEMBL5028 O14672 ADAM10 80.85% 97.50%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 163194012
LOTUS LTS0162605
wikiData Q105124636