3-Hydroxyquinoline

Details

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Internal ID 7f2e0628-25c6-4d19-bdf7-e2da812c27ea
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives
IUPAC Name quinolin-3-ol
SMILES (Canonical) C1=CC=C2C(=C1)C=C(C=N2)O
SMILES (Isomeric) C1=CC=C2C(=C1)C=C(C=N2)O
InChI InChI=1S/C9H7NO/c11-8-5-7-3-1-2-4-9(7)10-6-8/h1-6,11H
InChI Key IQQDNMHUOLMLNJ-UHFFFAOYSA-N
Popularity 80 references in papers

Physical and Chemical Properties

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Molecular Formula C9H7NO
Molecular Weight 145.16 g/mol
Exact Mass 145.052763847 g/mol
Topological Polar Surface Area (TPSA) 33.10 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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580-18-7
Quinolin-3-ol
3-QUINOLINOL
3-Quinolol
MFCD00169018
12PZ582CI0
CCRIS 4328
EINECS 209-456-7
BRN 0113185
UNII-12PZ582CI0
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Hydroxyquinoline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.9120 91.20%
Blood Brain Barrier + 0.7379 73.79%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5166 51.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9555 95.55%
OATP1B3 inhibitior + 0.9701 97.01%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8783 87.83%
P-glycoprotein inhibitior - 0.9863 98.63%
P-glycoprotein substrate - 0.9904 99.04%
CYP3A4 substrate - 0.6839 68.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7024 70.24%
CYP3A4 inhibition - 0.9401 94.01%
CYP2C9 inhibition - 0.9236 92.36%
CYP2C19 inhibition - 0.7385 73.85%
CYP2D6 inhibition - 0.8461 84.61%
CYP1A2 inhibition + 0.8585 85.85%
CYP2C8 inhibition + 0.8903 89.03%
CYP inhibitory promiscuity - 0.8180 81.80%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9023 90.23%
Carcinogenicity (trinary) Non-required 0.7354 73.54%
Eye corrosion - 0.9910 99.10%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.6082 60.82%
Skin corrosion - 0.9761 97.61%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5926 59.26%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.7679 76.79%
skin sensitisation - 0.6936 69.36%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.4865 48.65%
Acute Oral Toxicity (c) III 0.7863 78.63%
Estrogen receptor binding - 0.5111 51.11%
Androgen receptor binding - 0.8522 85.22%
Thyroid receptor binding - 0.6125 61.25%
Glucocorticoid receptor binding - 0.7098 70.98%
Aromatase binding - 0.6162 61.62%
PPAR gamma + 0.6056 60.56%
Honey bee toxicity - 0.9105 91.05%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.8329 83.29%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.20% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.51% 94.62%
CHEMBL1951 P21397 Monoamine oxidase A 89.69% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.36% 86.33%
CHEMBL2535 P11166 Glucose transporter 87.19% 98.75%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 86.67% 93.10%
CHEMBL3401 O75469 Pregnane X receptor 85.06% 94.73%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 84.48% 85.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.89% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.40% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.23% 94.00%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 80.74% 89.67%
CHEMBL2243 O00519 Anandamide amidohydrolase 80.02% 97.53%

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.
Ruta montana

Cross-Links

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PubChem 11376
LOTUS LTS0258390
wikiData Q27251431