2-(quinoline-3-carbonyl)-1H-quinazolin-4-one

Details

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Internal ID 4755b3ea-72a5-4d80-80e2-234ab07c68c3
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinazolines
IUPAC Name 2-(quinoline-3-carbonyl)-1H-quinazolin-4-one
SMILES (Canonical) C1=CC=C2C(=C1)C=C(C=N2)C(=O)C3=NC(=O)C4=CC=CC=C4N3
SMILES (Isomeric) C1=CC=C2C(=C1)C=C(C=N2)C(=O)C3=NC(=O)C4=CC=CC=C4N3
InChI InChI=1S/C18H11N3O2/c22-16(12-9-11-5-1-3-7-14(11)19-10-12)17-20-15-8-4-2-6-13(15)18(23)21-17/h1-10H,(H,20,21,23)
InChI Key HSEIGGKZBVNIDH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H11N3O2
Molecular Weight 301.30 g/mol
Exact Mass 301.085126602 g/mol
Topological Polar Surface Area (TPSA) 71.40 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.70
H-Bond Acceptor 4
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-(quinoline-3-carbonyl)-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 + 0.5157 51.57%
Blood Brain Barrier + 0.9379 93.79%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6939 69.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9096 90.96%
OATP1B3 inhibitior + 0.9584 95.84%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5783 57.83%
P-glycoprotein inhibitior - 0.6940 69.40%
P-glycoprotein substrate - 0.9094 90.94%
CYP3A4 substrate + 0.5313 53.13%
CYP2C9 substrate - 0.7882 78.82%
CYP2D6 substrate - 0.8884 88.84%
CYP3A4 inhibition - 0.9778 97.78%
CYP2C9 inhibition - 0.5194 51.94%
CYP2C19 inhibition + 0.5857 58.57%
CYP2D6 inhibition - 0.9224 92.24%
CYP1A2 inhibition + 0.9181 91.81%
CYP2C8 inhibition + 0.7431 74.31%
CYP inhibitory promiscuity - 0.8672 86.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9023 90.23%
Carcinogenicity (trinary) Non-required 0.6666 66.66%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.7114 71.14%
Skin irritation - 0.9032 90.32%
Skin corrosion - 0.9821 98.21%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5654 56.54%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.6803 68.03%
skin sensitisation - 0.9069 90.69%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6863 68.63%
Acute Oral Toxicity (c) III 0.6909 69.09%
Estrogen receptor binding + 0.9499 94.99%
Androgen receptor binding + 0.6147 61.47%
Thyroid receptor binding + 0.5838 58.38%
Glucocorticoid receptor binding + 0.7658 76.58%
Aromatase binding + 0.8916 89.16%
PPAR gamma + 0.7327 73.27%
Honey bee toxicity - 0.9395 93.95%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity - 0.8928 89.28%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.37% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 93.62% 94.75%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 93.27% 85.49%
CHEMBL3524 P56524 Histone deacetylase 4 92.72% 92.97%
CHEMBL2535 P11166 Glucose transporter 91.79% 98.75%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 91.68% 89.44%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.56% 99.23%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.48% 94.62%
CHEMBL5393 Q9UNQ0 ATP-binding cassette sub-family G member 2 90.41% 97.50%
CHEMBL4302 P08183 P-glycoprotein 1 90.37% 92.98%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.22% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.47% 95.56%
CHEMBL1829 O15379 Histone deacetylase 3 89.21% 95.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.87% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.07% 93.99%
CHEMBL1781 P11387 DNA topoisomerase I 87.94% 97.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.44% 89.00%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 85.76% 89.67%
CHEMBL3310 Q96DB2 Histone deacetylase 11 83.77% 88.56%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 83.48% 81.14%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 82.44% 96.47%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.11% 86.33%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 81.90% 92.67%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 81.72% 87.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.19% 99.17%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.97% 81.11%
CHEMBL213 P08588 Beta-1 adrenergic receptor 80.78% 95.56%
CHEMBL325 Q13547 Histone deacetylase 1 80.27% 95.92%

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.
Peganum nigellastrum

Cross-Links

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PubChem 11771062
LOTUS LTS0266266
wikiData Q105033000