8-(3-Methylbut-2-enyl)quinoline-2-carboxylic acid

Details

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Internal ID 4f28288a-a64d-47e0-8de0-e8e894b2faba
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinoline carboxylic acids
IUPAC Name 8-(3-methylbut-2-enyl)quinoline-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H15NO2/c1-10(2)6-7-11-4-3-5-12-8-9-13(15(17)18)16-14(11)12/h3-6,8-9H,7H2,1-2H3,(H,17,18)
InChI Key ZIFDBDYESJDTSE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H15NO2
Molecular Weight 241.28 g/mol
Exact Mass 241.110278721 g/mol
Topological Polar Surface Area (TPSA) 50.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.44
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-(3-Methylbut-2-enyl)quinoline-2-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 + 1.0000 100.00%
Caco-2 + 0.8127 81.27%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4774 47.74%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.9583 95.83%
OATP1B3 inhibitior + 0.9395 93.95%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.6885 68.85%
P-glycoprotein inhibitior - 0.9290 92.90%
P-glycoprotein substrate - 0.9062 90.62%
CYP3A4 substrate - 0.6420 64.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8876 88.76%
CYP3A4 inhibition - 0.8715 87.15%
CYP2C9 inhibition - 0.8167 81.67%
CYP2C19 inhibition - 0.8000 80.00%
CYP2D6 inhibition - 0.8522 85.22%
CYP1A2 inhibition - 0.8487 84.87%
CYP2C8 inhibition - 0.8613 86.13%
CYP inhibitory promiscuity - 0.7067 70.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8339 83.39%
Carcinogenicity (trinary) Non-required 0.7873 78.73%
Eye corrosion - 0.9903 99.03%
Eye irritation + 0.8268 82.68%
Skin irritation - 0.5503 55.03%
Skin corrosion - 0.9172 91.72%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5378 53.78%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.6926 69.26%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6319 63.19%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6710 67.10%
Acute Oral Toxicity (c) III 0.7648 76.48%
Estrogen receptor binding + 0.7756 77.56%
Androgen receptor binding - 0.6044 60.44%
Thyroid receptor binding + 0.5570 55.70%
Glucocorticoid receptor binding + 0.8104 81.04%
Aromatase binding + 0.8302 83.02%
PPAR gamma + 0.7791 77.91%
Honey bee toxicity - 0.9576 95.76%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.8966 89.66%

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
CHEMBL3401 O75469 Pregnane X receptor 92.54% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.05% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 90.85% 90.17%
CHEMBL3959 P16083 Quinone reductase 2 90.83% 89.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.22% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.63% 99.23%
CHEMBL2581 P07339 Cathepsin D 87.26% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.72% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.93% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.37% 91.11%

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 46909978
LOTUS LTS0144450
wikiData Q104202426