2-Quinoxalinecarboxylic acid

Details

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Internal ID 77b6fbf5-f5cf-48ce-80b1-de4b82f77d4d
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines
IUPAC Name quinoxaline-2-carboxylic acid
SMILES (Canonical) C1=CC=C2C(=C1)N=CC(=N2)C(=O)O
SMILES (Isomeric) C1=CC=C2C(=C1)N=CC(=N2)C(=O)O
InChI InChI=1S/C9H6N2O2/c12-9(13)8-5-10-6-3-1-2-4-7(6)11-8/h1-5H,(H,12,13)
InChI Key UPUZGXILYFKSGE-UHFFFAOYSA-N
Popularity 136 references in papers

Physical and Chemical Properties

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Molecular Formula C9H6N2O2
Molecular Weight 174.16 g/mol
Exact Mass 174.042927438 g/mol
Topological Polar Surface Area (TPSA) 63.10 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.33
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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879-65-2
Quinoxaline-2-carboxylic acid
2-Quinoxalinecarboxylicacid
2-Carboxyquinoxaline
MFCD00012334
M5OE8SN42M
CHEMBL151797
NSC-86873
UNII-M5OE8SN42M
2-QCA
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Quinoxalinecarboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.6102 61.02%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.6561 65.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9662 96.62%
OATP1B3 inhibitior + 0.9580 95.80%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8613 86.13%
P-glycoprotein inhibitior - 0.9851 98.51%
P-glycoprotein substrate - 0.9899 98.99%
CYP3A4 substrate - 0.7256 72.56%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8938 89.38%
CYP3A4 inhibition - 0.9359 93.59%
CYP2C9 inhibition - 0.9465 94.65%
CYP2C19 inhibition - 0.9047 90.47%
CYP2D6 inhibition - 0.9697 96.97%
CYP1A2 inhibition - 0.6113 61.13%
CYP2C8 inhibition - 0.5826 58.26%
CYP inhibitory promiscuity - 0.9701 97.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8957 89.57%
Carcinogenicity (trinary) Non-required 0.8096 80.96%
Eye corrosion - 0.9911 99.11%
Eye irritation + 0.9900 99.00%
Skin irritation + 0.6692 66.92%
Skin corrosion - 0.9607 96.07%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8210 82.10%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.8803 88.03%
skin sensitisation - 0.8815 88.15%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5621 56.21%
Acute Oral Toxicity (c) III 0.5747 57.47%
Estrogen receptor binding - 0.7729 77.29%
Androgen receptor binding - 0.7761 77.61%
Thyroid receptor binding - 0.6976 69.76%
Glucocorticoid receptor binding + 0.5642 56.42%
Aromatase binding + 0.5353 53.53%
PPAR gamma + 0.6712 67.12%
Honey bee toxicity - 0.9717 97.17%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.7172 71.72%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.84% 94.62%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 90.01% 81.11%
CHEMBL2039 P27338 Monoamine oxidase B 89.66% 92.51%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.61% 86.33%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 87.24% 87.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.07% 99.23%
CHEMBL1811 P34995 Prostanoid EP1 receptor 84.83% 95.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.64% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.60% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 81.47% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.76% 99.17%

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 96695
LOTUS LTS0156623
wikiData Q27283516