1-Methyl-2,3-dihydroquinolin-4-imine

Details

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Internal ID d0ff7d73-b035-4377-9bd7-39c9a508d510
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Hydroquinolines
IUPAC Name 1-methyl-2,3-dihydroquinolin-4-imine
SMILES (Canonical) CN1CCC(=N)C2=CC=CC=C21
SMILES (Isomeric) CN1CCC(=N)C2=CC=CC=C21
InChI InChI=1S/C10H12N2/c1-12-7-6-9(11)8-4-2-3-5-10(8)12/h2-5,11H,6-7H2,1H3
InChI Key GKGBJWPUGWCYNT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12N2
Molecular Weight 160.22 g/mol
Exact Mass 160.100048391 g/mol
Topological Polar Surface Area (TPSA) 27.10 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Methyl-2,3-dihydroquinolin-4-imine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9763 97.63%
Caco-2 + 0.9549 95.49%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.6539 65.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9635 96.35%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.7000 70.00%
BSEP inhibitior - 0.8441 84.41%
P-glycoprotein inhibitior - 0.9932 99.32%
P-glycoprotein substrate - 0.8471 84.71%
CYP3A4 substrate - 0.6572 65.72%
CYP2C9 substrate + 0.5905 59.05%
CYP2D6 substrate + 0.4308 43.08%
CYP3A4 inhibition + 0.6900 69.00%
CYP2C9 inhibition - 0.8690 86.90%
CYP2C19 inhibition - 0.8199 81.99%
CYP2D6 inhibition + 0.7345 73.45%
CYP1A2 inhibition + 0.8332 83.32%
CYP2C8 inhibition - 0.9788 97.88%
CYP inhibitory promiscuity - 0.7516 75.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7551 75.51%
Eye corrosion - 0.9773 97.73%
Eye irritation + 0.8725 87.25%
Skin irritation - 0.5142 51.42%
Skin corrosion - 0.7697 76.97%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6021 60.21%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8310 83.10%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6281 62.81%
Acute Oral Toxicity (c) III 0.5327 53.27%
Estrogen receptor binding - 0.8839 88.39%
Androgen receptor binding - 0.7486 74.86%
Thyroid receptor binding - 0.7852 78.52%
Glucocorticoid receptor binding - 0.8365 83.65%
Aromatase binding - 0.7385 73.85%
PPAR gamma - 0.7264 72.64%
Honey bee toxicity - 0.9851 98.51%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.6599 65.99%

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
CHEMBL2581 P07339 Cathepsin D 96.27% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.27% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.97% 95.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 91.59% 93.65%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.44% 86.33%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.14% 93.40%
CHEMBL4208 P20618 Proteasome component C5 86.84% 90.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 86.14% 96.25%
CHEMBL258 P06239 Tyrosine-protein kinase LCK 81.71% 94.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.27% 82.69%

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.
Echinops echinatus
Echinops niveus

Cross-Links

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PubChem 161462
LOTUS LTS0273029
wikiData Q5332581