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N-benzhydryl-3-(4-oxo-3,4-dihydroquinazolin-2-yl)propanamide ID: ALA3092546
PubChem CID: 135724863
Max Phase: Preclinical
Molecular Formula: C24H21N3O2
Molecular Weight: 383.45
Molecule Type: Small molecule
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: O=C(CCc1nc2ccccc2c(=O)[nH]1)NC(c1ccccc1)c1ccccc1
Standard InChI: InChI=1S/C24H21N3O2/c28-22(16-15-21-25-20-14-8-7-13-19(20)24(29)26-21)27-23(17-9-3-1-4-10-17)18-11-5-2-6-12-18/h1-14,23H,15-16H2,(H,27,28)(H,25,26,29)
Standard InChI Key: HUBGQSZPQXLUOF-UHFFFAOYSA-N
Molfile:
RDKit 2D
29 32 0 0 0 0 0 0 0 0999 V2000
1.4183 -18.8944 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4172 -19.7140 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1252 -20.1229 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1235 -18.4856 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8321 -18.8908 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8355 -19.7160 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.5478 -20.1234 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
4.2614 -19.7102 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
4.2580 -18.8850 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
3.5411 -18.4730 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
3.5366 -17.6558 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
4.9702 -20.1168 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6768 -19.7063 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
6.3856 -20.1130 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.0922 -19.7025 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
6.3879 -20.9302 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
7.8010 -20.1091 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.5076 -19.6986 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.2123 -20.1077 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.9184 -19.6979 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.9166 -18.8798 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
9.2028 -18.4733 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.4997 -18.8855 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8043 -20.9256 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.0961 -21.3355 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.0980 -22.1519 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
7.8073 -22.5594 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.5163 -22.1445 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
8.5109 -21.3294 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
1 2 2 0
2 3 1 0
3 6 2 0
5 4 2 0
4 1 1 0
5 6 1 0
5 10 1 0
6 7 1 0
7 8 2 0
8 9 1 0
9 10 1 0
10 11 2 0
8 12 1 0
12 13 1 0
13 14 1 0
14 15 1 0
14 16 2 0
15 17 1 0
17 18 1 0
18 19 2 0
19 20 1 0
20 21 2 0
21 22 1 0
22 23 2 0
23 18 1 0
24 25 2 0
25 26 1 0
26 27 2 0
27 28 1 0
28 29 2 0
29 24 1 0
17 24 1 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 383.45Molecular Weight (Monoisotopic): 383.1634AlogP: 3.76#Rotatable Bonds: 6Polar Surface Area: 74.85Molecular Species: NEUTRALHBA: 3HBD: 2#RO5 Violations: ┄HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): ┄CX Acidic pKa: 9.92CX Basic pKa: 5.40CX LogP: 3.52CX LogD: 3.54Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.53Np Likeness Score: -1.17
References 1. Lindgren AE, Karlberg T, Ekblad T, Spjut S, Thorsell AG, Andersson CD, Nhan TT, Hellsten V, Weigelt J, Linusson A, Schüler H, Elofsson M.. (2013) Chemical probes to study ADP-ribosylation: synthesis and biochemical evaluation of inhibitors of the human ADP-ribosyltransferase ARTD3/PARP3., 56 (23): [PMID:24188023 ] [10.1021/jm401394u ]