ID: ALA3706592

Max Phase: Preclinical

Molecular Formula: C34H32N2O6

Molecular Weight: 564.64

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(CCN(C)CCOc2ccc(NC(=O)c3cccc4c3C(=O)c3ccccc3C4=O)cc2)cc1OC

Standard InChI:  InChI=1S/C34H32N2O6/c1-36(18-17-22-11-16-29(40-2)30(21-22)41-3)19-20-42-24-14-12-23(13-15-24)35-34(39)28-10-6-9-27-31(28)33(38)26-8-5-4-7-25(26)32(27)37/h4-16,21H,17-20H2,1-3H3,(H,35,39)

Standard InChI Key:  OYNLGCAQMCPMDH-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: 564.64Molecular Weight (Monoisotopic): 564.2260AlogP: 5.28#Rotatable Bonds: 11
Polar Surface Area: 94.17Molecular Species: BASEHBA: 7HBD: 1
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 8.91CX LogP: 5.57CX LogD: 4.05
Aromatic Rings: 4Heavy Atoms: 42QED Weighted: 0.23Np Likeness Score: -0.63

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