5,6,7,8-Tetrahydro-2,4-dimethylquinoline

Details

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Internal ID 765713c7-2164-4a0b-bb92-689e8be947cd
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Hydroquinolines
IUPAC Name 2,4-dimethyl-5,6,7,8-tetrahydroquinoline
SMILES (Canonical) CC1=CC(=NC2=C1CCCC2)C
SMILES (Isomeric) CC1=CC(=NC2=C1CCCC2)C
InChI InChI=1S/C11H15N/c1-8-7-9(2)12-11-6-4-3-5-10(8)11/h7H,3-6H2,1-2H3
InChI Key ZBIKAJHAGKBFKR-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H15N
Molecular Weight 161.24 g/mol
Exact Mass 161.120449483 g/mol
Topological Polar Surface Area (TPSA) 12.90 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.58
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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2,4-dimethyl-5,6,7,8-tetrahydroquinoline
60169-66-6
SCHEMBL527227
DTXSID801276347

2D Structure

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2D Structure of 5,6,7,8-Tetrahydro-2,4-dimethylquinoline

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 + 0.9223 92.23%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.6197 61.97%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.9712 97.12%
OATP1B3 inhibitior + 0.9593 95.93%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.8319 83.19%
P-glycoprotein inhibitior - 0.9797 97.97%
P-glycoprotein substrate - 0.9318 93.18%
CYP3A4 substrate - 0.7289 72.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7551 75.51%
CYP3A4 inhibition - 0.8216 82.16%
CYP2C9 inhibition - 0.8608 86.08%
CYP2C19 inhibition - 0.5187 51.87%
CYP2D6 inhibition - 0.7527 75.27%
CYP1A2 inhibition + 0.6744 67.44%
CYP2C8 inhibition - 0.8939 89.39%
CYP inhibitory promiscuity - 0.7340 73.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.7346 73.46%
Eye corrosion - 0.8547 85.47%
Eye irritation + 0.6837 68.37%
Skin irritation + 0.6322 63.22%
Skin corrosion - 0.7487 74.87%
Ames mutagenesis - 0.6554 65.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4490 44.90%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.7053 70.53%
skin sensitisation - 0.5718 57.18%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5608 56.08%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7706 77.06%
Acute Oral Toxicity (c) III 0.5518 55.18%
Estrogen receptor binding - 0.8966 89.66%
Androgen receptor binding - 0.6963 69.63%
Thyroid receptor binding - 0.6822 68.22%
Glucocorticoid receptor binding - 0.8343 83.43%
Aromatase binding - 0.8316 83.16%
PPAR gamma - 0.8524 85.24%
Honey bee toxicity - 0.9804 98.04%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7700 77.00%
Fish aquatic toxicity + 0.8248 82.48%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.06% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 86.64% 91.49%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.25% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 85.24% 94.73%
CHEMBL2581 P07339 Cathepsin D 84.11% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.38% 93.40%
CHEMBL2039 P27338 Monoamine oxidase B 82.27% 92.51%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.18% 94.00%

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.
Glycyrrhiza
Glycyrrhiza uralensis
Mitracarpus hirtus

Cross-Links

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PubChem 5321849
NPASS NPC124263