Jineol

Details

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Internal ID e6fe05e5-9f74-4796-8cc1-4f8cc4cb0453
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > 8-hydroxyquinolines
IUPAC Name quinoline-3,8-diol
SMILES (Canonical) C1=CC2=CC(=CN=C2C(=C1)O)O
SMILES (Isomeric) C1=CC2=CC(=CN=C2C(=C1)O)O
InChI InChI=1S/C9H7NO2/c11-7-4-6-2-1-3-8(12)9(6)10-5-7/h1-5,11-12H
InChI Key IGDFDIZIHMFYGR-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C9H7NO2
Molecular Weight 161.16 g/mol
Exact Mass 161.047678466 g/mol
Topological Polar Surface Area (TPSA) 53.40 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.65
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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quinoline-3,8-diol
178762-28-2
3,8-Quinolinediol
3,8-Dihydroxyquinoline
TG4DD1DY9O
CHEBI:66125
NSC694081
NSC-694081
NSC 694081
UNII-TG4DD1DY9O
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Jineol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.8231 82.31%
Blood Brain Barrier + 0.5629 56.29%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5796 57.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9763 97.63%
OATP1B3 inhibitior + 0.9626 96.26%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9525 95.25%
P-glycoprotein inhibitior - 0.9846 98.46%
P-glycoprotein substrate - 0.9720 97.20%
CYP3A4 substrate - 0.6784 67.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7024 70.24%
CYP3A4 inhibition - 0.8953 89.53%
CYP2C9 inhibition - 0.7897 78.97%
CYP2C19 inhibition - 0.6817 68.17%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition + 0.7718 77.18%
CYP2C8 inhibition + 0.5846 58.46%
CYP inhibitory promiscuity - 0.7352 73.52%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8936 89.36%
Carcinogenicity (trinary) Non-required 0.6926 69.26%
Eye corrosion - 0.9949 99.49%
Eye irritation + 1.0000 100.00%
Skin irritation - 0.6321 63.21%
Skin corrosion - 0.9853 98.53%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7049 70.49%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.7552 75.52%
skin sensitisation - 0.7599 75.99%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5207 52.07%
Acute Oral Toxicity (c) III 0.6040 60.40%
Estrogen receptor binding - 0.5514 55.14%
Androgen receptor binding - 0.7768 77.68%
Thyroid receptor binding - 0.5388 53.88%
Glucocorticoid receptor binding - 0.6147 61.47%
Aromatase binding - 0.6775 67.75%
PPAR gamma + 0.7487 74.87%
Honey bee toxicity - 0.9497 94.97%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.8506 85.06%

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
CHEMBL1951 P21397 Monoamine oxidase A 92.75% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.65% 99.15%
CHEMBL2535 P11166 Glucose transporter 92.54% 98.75%
CHEMBL1937 Q92769 Histone deacetylase 2 92.28% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.25% 91.11%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 86.55% 93.10%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.33% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.32% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.91% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.28% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 82.22% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.53% 94.62%

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 177338
LOTUS LTS0019677
wikiData Q27134646