2-Hydroxy-8-methoxyquinoline-4-carboxylic acid

Details

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Internal ID 50e154df-bf99-4f2e-9b63-4b7acb9c622f
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinoline carboxylic acids
IUPAC Name 8-methoxy-2-oxo-1H-quinoline-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H9NO4/c1-16-8-4-2-3-6-7(11(14)15)5-9(13)12-10(6)8/h2-5H,1H3,(H,12,13)(H,14,15)
InChI Key ZIMKBZCDBGZJGS-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H9NO4
Molecular Weight 219.19 g/mol
Exact Mass 219.05315777 g/mol
Topological Polar Surface Area (TPSA) 75.60 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.23
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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AKOS001752366
SR-01000118542
Quinoline-4-carboxylic acid, 2-hydroxy-8-methoxy-
SR-01000118542-1

2D Structure

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2D Structure of 2-Hydroxy-8-methoxyquinoline-4-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9647 96.47%
Caco-2 - 0.7808 78.08%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6504 65.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9676 96.76%
OATP1B3 inhibitior + 0.9619 96.19%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8541 85.41%
P-glycoprotein inhibitior - 0.9570 95.70%
P-glycoprotein substrate - 0.8980 89.80%
CYP3A4 substrate - 0.5645 56.45%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition - 0.9464 94.64%
CYP2C9 inhibition - 0.8760 87.60%
CYP2C19 inhibition - 0.9840 98.40%
CYP2D6 inhibition - 0.9649 96.49%
CYP1A2 inhibition - 0.5966 59.66%
CYP2C8 inhibition - 0.7839 78.39%
CYP inhibitory promiscuity - 0.9356 93.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9362 93.62%
Carcinogenicity (trinary) Non-required 0.6121 61.21%
Eye corrosion - 0.9949 99.49%
Eye irritation + 0.7273 72.73%
Skin irritation - 0.8539 85.39%
Skin corrosion - 0.9816 98.16%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7866 78.66%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.6698 66.98%
skin sensitisation - 0.9650 96.50%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.4853 48.53%
Acute Oral Toxicity (c) III 0.7323 73.23%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding + 0.7708 77.08%
Thyroid receptor binding - 0.6316 63.16%
Glucocorticoid receptor binding + 0.6232 62.32%
Aromatase binding + 0.6291 62.91%
PPAR gamma + 0.5901 59.01%
Honey bee toxicity - 0.9532 95.32%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity - 0.5960 59.60%

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 97.26% 95.56%
CHEMBL2535 P11166 Glucose transporter 96.88% 98.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.22% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.86% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.03% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.88% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.66% 91.11%
CHEMBL1255126 O15151 Protein Mdm4 89.48% 90.20%
CHEMBL4040 P28482 MAP kinase ERK2 89.03% 83.82%
CHEMBL213 P08588 Beta-1 adrenergic receptor 88.68% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.47% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.28% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.42% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.02% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.17% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.37% 91.71%
CHEMBL1907 P15144 Aminopeptidase N 81.31% 93.31%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.12% 81.11%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.76% 94.80%

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.
Cynoglossum gansuense

Cross-Links

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PubChem 713865
LOTUS LTS0099656
wikiData Q105377353