ID: ALA431789

Max Phase: Preclinical

Molecular Formula: C31H29N3O4

Molecular Weight: 507.59

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(CN(C)Cc2ccc(NC(=O)c3cccc4c(O)c5ccccc5nc34)cc2)cc1OC

Standard InChI:  InChI=1S/C31H29N3O4/c1-34(19-21-13-16-27(37-2)28(17-21)38-3)18-20-11-14-22(15-12-20)32-31(36)25-9-6-8-24-29(25)33-26-10-5-4-7-23(26)30(24)35/h4-17H,18-19H2,1-3H3,(H,32,36)(H,33,35)

Standard InChI Key:  CDIOUAPPWVXPJV-UHFFFAOYSA-N

Associated Targets(non-human)

CHRC5 cell line 91 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: 507.59Molecular Weight (Monoisotopic): 507.2158AlogP: 6.00#Rotatable Bonds: 8
Polar Surface Area: 83.92Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 8.33CX Basic pKa: 7.92CX LogP: 5.12CX LogD: 4.81
Aromatic Rings: 5Heavy Atoms: 38QED Weighted: 0.25Np Likeness Score: -0.93

References

1. Dodic N, Dumaitre B, Daugan A, Pianetti P..  (1995)  Synthesis and activity against multidrug resistance in Chinese hamster ovary cells of new acridone-4-carboxamides.,  38  (13): [PMID:7608906] [10.1021/jm00013a017]

Source