2(1H)-Quinazolinone

Details

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Internal ID 397746ba-5304-4eea-b351-75ece67828ab
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinazolines
IUPAC Name 1H-quinazolin-2-one
SMILES (Canonical) C1=CC=C2C(=C1)C=NC(=O)N2
SMILES (Isomeric) C1=CC=C2C(=C1)C=NC(=O)N2
InChI InChI=1S/C8H6N2O/c11-8-9-5-6-3-1-2-4-7(6)10-8/h1-5H,(H,9,10,11)
InChI Key AVRPFRMDMNDIDH-UHFFFAOYSA-N
Popularity 955 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6N2O
Molecular Weight 146.15 g/mol
Exact Mass 146.048012819 g/mol
Topological Polar Surface Area (TPSA) 41.50 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.92
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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7471-58-1
Quinazolin-2(1H)-one
2(1H)-Quinazolinone
2-Quinazolinone
1H-quinazolin-2-one
2(3H)-Quinazolinone
2-Quinazolinol
hydroxyquinazoline
2-hydroxyquinazoline
NSC-401245
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2(1H)-Quinazolinone

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 + 0.6938 69.38%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7121 71.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9713 97.13%
OATP1B3 inhibitior + 0.9580 95.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8570 85.70%
P-glycoprotein inhibitior - 0.9914 99.14%
P-glycoprotein substrate - 0.9877 98.77%
CYP3A4 substrate - 0.6625 66.25%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8354 83.54%
CYP3A4 inhibition - 0.9649 96.49%
CYP2C9 inhibition - 0.9111 91.11%
CYP2C19 inhibition - 0.9646 96.46%
CYP2D6 inhibition - 0.9446 94.46%
CYP1A2 inhibition + 0.8488 84.88%
CYP2C8 inhibition - 0.8951 89.51%
CYP inhibitory promiscuity - 0.8626 86.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9123 91.23%
Carcinogenicity (trinary) Non-required 0.6578 65.78%
Eye corrosion - 0.9841 98.41%
Eye irritation + 0.9859 98.59%
Skin irritation - 0.8003 80.03%
Skin corrosion - 0.9785 97.85%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7915 79.15%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.7052 70.52%
skin sensitisation - 0.8472 84.72%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.6159 61.59%
Acute Oral Toxicity (c) III 0.7573 75.73%
Estrogen receptor binding - 0.8846 88.46%
Androgen receptor binding - 0.8712 87.12%
Thyroid receptor binding - 0.6499 64.99%
Glucocorticoid receptor binding - 0.8686 86.86%
Aromatase binding - 0.5701 57.01%
PPAR gamma - 0.6970 69.70%
Honey bee toxicity - 0.9415 94.15%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.6709 67.09%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.48% 94.62%
CHEMBL1937 Q92769 Histone deacetylase 2 91.26% 94.75%
CHEMBL3310 Q96DB2 Histone deacetylase 11 87.84% 88.56%
CHEMBL2535 P11166 Glucose transporter 87.48% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.45% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.20% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.44% 99.23%
CHEMBL3524 P56524 Histone deacetylase 4 84.95% 92.97%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 84.19% 85.49%
CHEMBL1781 P11387 DNA topoisomerase I 82.37% 97.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.77% 96.67%
CHEMBL2424504 P29375 Lysine-specific demethylase 5A 80.47% 99.23%

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.
Isatis tinctoria

Cross-Links

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PubChem 344381
NPASS NPC218255