ID: ALA78571

Max Phase: Preclinical

Molecular Formula: C32H30FN3O4

Molecular Weight: 539.61

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(CN(C)CCc2ccc(NC(=O)c3cccc4c(O)c5cccc(F)c5nc34)cc2)cc1OC

Standard InChI:  InChI=1S/C32H30FN3O4/c1-36(19-21-12-15-27(39-2)28(18-21)40-3)17-16-20-10-13-22(14-11-20)34-32(38)25-8-4-6-23-29(25)35-30-24(31(23)37)7-5-9-26(30)33/h4-15,18H,16-17,19H2,1-3H3,(H,34,38)(H,35,37)

Standard InChI Key:  RRHUXEZDYUVVEE-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: 539.61Molecular Weight (Monoisotopic): 539.2220AlogP: 6.18#Rotatable Bonds: 9
Polar Surface Area: 83.92Molecular Species: BASEHBA: 6HBD: 2
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 8.00CX Basic pKa: 9.07CX LogP: 5.12CX LogD: 4.68
Aromatic Rings: 5Heavy Atoms: 40QED Weighted: 0.22Np Likeness Score: -1.03

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