2-methyl-1H-quinazolin-4-one

Details

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Internal ID abe11d89-4bef-460e-a714-f327845364b5
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinazolines
IUPAC Name 2-methyl-1H-quinazolin-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H8N2O/c1-6-10-8-5-3-2-4-7(8)9(12)11-6/h2-5H,1H3,(H,10,11,12)
InChI Key FIEYHAAMDAPVCH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C9H8N2O
Molecular Weight 160.17 g/mol
Exact Mass 160.063662883 g/mol
Topological Polar Surface Area (TPSA) 41.50 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.23
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 2-methyl-1H-quinazolin-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 + 1.0000 100.00%
Caco-2 - 0.5554 55.54%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6622 66.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9388 93.88%
OATP1B3 inhibitior + 0.9603 96.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8091 80.91%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9723 97.23%
CYP3A4 substrate - 0.5533 55.33%
CYP2C9 substrate - 0.5892 58.92%
CYP2D6 substrate - 0.8995 89.95%
CYP3A4 inhibition - 0.9797 97.97%
CYP2C9 inhibition - 0.9443 94.43%
CYP2C19 inhibition - 0.9562 95.62%
CYP2D6 inhibition - 0.9624 96.24%
CYP1A2 inhibition + 0.9287 92.87%
CYP2C8 inhibition - 0.8978 89.78%
CYP inhibitory promiscuity - 0.8850 88.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9223 92.23%
Carcinogenicity (trinary) Non-required 0.6122 61.22%
Eye corrosion - 0.9899 98.99%
Eye irritation + 0.9118 91.18%
Skin irritation - 0.8856 88.56%
Skin corrosion - 0.9809 98.09%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7403 74.03%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.7501 75.01%
skin sensitisation - 0.7871 78.71%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.5718 57.18%
Acute Oral Toxicity (c) III 0.6953 69.53%
Estrogen receptor binding - 0.8978 89.78%
Androgen receptor binding - 0.7856 78.56%
Thyroid receptor binding - 0.6058 60.58%
Glucocorticoid receptor binding - 0.8839 88.39%
Aromatase binding - 0.5690 56.90%
PPAR gamma - 0.7718 77.18%
Honey bee toxicity - 0.9770 97.70%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity - 0.7998 79.98%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.87% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.60% 99.23%
CHEMBL2581 P07339 Cathepsin D 90.87% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 87.86% 94.75%
CHEMBL3524 P56524 Histone deacetylase 4 86.50% 92.97%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.25% 93.65%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.95% 94.00%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 83.89% 85.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.81% 96.67%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.59% 93.99%
CHEMBL255 P29275 Adenosine A2b receptor 83.36% 98.59%
CHEMBL3401 O75469 Pregnane X receptor 83.23% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.91% 94.62%
CHEMBL3310 Q96DB2 Histone deacetylase 11 82.76% 88.56%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 81.70% 96.39%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.68% 85.49%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.95% 90.08%

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 15674
LOTUS LTS0048008
wikiData Q27463113