2-Benzyl-1-methyl-2,3-dihydroquinazolin-4-one

Details

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Internal ID 236aff9a-8864-4667-a8d7-8719b5e08808
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinazolines
IUPAC Name 2-benzyl-1-methyl-2,3-dihydroquinazolin-4-one
SMILES (Canonical) CN1C(NC(=O)C2=CC=CC=C21)CC3=CC=CC=C3
SMILES (Isomeric) CN1C(NC(=O)C2=CC=CC=C21)CC3=CC=CC=C3
InChI InChI=1S/C16H16N2O/c1-18-14-10-6-5-9-13(14)16(19)17-15(18)11-12-7-3-2-4-8-12/h2-10,15H,11H2,1H3,(H,17,19)
InChI Key KRKWVLLKCHDMKS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16N2O
Molecular Weight 252.31 g/mol
Exact Mass 252.126263138 g/mol
Topological Polar Surface Area (TPSA) 32.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Benzyl-1-methyl-2,3-dihydroquinazolin-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9378 93.78%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4460 44.60%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.8956 89.56%
OATP1B3 inhibitior + 0.9483 94.83%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6069 60.69%
BSEP inhibitior + 0.6498 64.98%
P-glycoprotein inhibitior - 0.9302 93.02%
P-glycoprotein substrate - 0.5743 57.43%
CYP3A4 substrate - 0.5305 53.05%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.8380 83.80%
CYP3A4 inhibition - 0.5242 52.42%
CYP2C9 inhibition - 0.6661 66.61%
CYP2C19 inhibition - 0.5603 56.03%
CYP2D6 inhibition - 0.8446 84.46%
CYP1A2 inhibition - 0.5544 55.44%
CYP2C8 inhibition - 0.9271 92.71%
CYP inhibitory promiscuity - 0.5206 52.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6528 65.28%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9920 99.20%
Skin irritation - 0.7781 77.81%
Skin corrosion - 0.9547 95.47%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3786 37.86%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.9012 90.12%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.6038 60.38%
Acute Oral Toxicity (c) II 0.5660 56.60%
Estrogen receptor binding + 0.8032 80.32%
Androgen receptor binding - 0.5367 53.67%
Thyroid receptor binding - 0.6908 69.08%
Glucocorticoid receptor binding - 0.6779 67.79%
Aromatase binding + 0.8442 84.42%
PPAR gamma - 0.5980 59.80%
Honey bee toxicity - 0.9339 93.39%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity - 0.5939 59.39%

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 99.32% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.82% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.65% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.77% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.17% 86.33%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 83.53% 97.64%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.31% 82.69%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.16% 92.67%

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 15408355
LOTUS LTS0090272
wikiData Q105145101