ID: ALA4229013

Max Phase: Preclinical

Molecular Formula: C26H23N3O4

Molecular Weight: 441.49

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1nc2cc(-c3ccccc3)cc(-c3cccc(C(=O)O)c3)c2c(=O)n1CC1CCCO1

Standard InChI:  InChI=1S/C26H23N3O4/c27-26-28-22-14-19(16-6-2-1-3-7-16)13-21(17-8-4-9-18(12-17)25(31)32)23(22)24(30)29(26)15-20-10-5-11-33-20/h1-4,6-9,12-14,20H,5,10-11,15H2,(H2,27,28)(H,31,32)

Standard InChI Key:  YZGHWKNHLHTVCA-UHFFFAOYSA-N

Associated Targets(Human)

Cathepsin D 3201 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmepsin 1 207 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plasmepsin 4 112 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plasmepsin 2 774 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 441.49Molecular Weight (Monoisotopic): 441.1689AlogP: 4.19#Rotatable Bonds: 5
Polar Surface Area: 107.44Molecular Species: ACIDHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.01CX Basic pKa: 2.53CX LogP: 3.92CX LogD: 0.93
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.48Np Likeness Score: -0.44

References

1. Rasina D, Stakanovs G, Borysov OV, Pantelejevs T, Bobrovs R, Kanepe-Lapsa I, Tars K, Jaudzems K, Jirgensons A..  (2018)  2-Aminoquinazolin-4(3H)-one based plasmepsin inhibitors with improved hydrophilicity and selectivity.,  26  (9): [PMID:29636223] [10.1016/j.bmc.2018.04.012]

Source