ID: ALA3706600

Max Phase: Preclinical

Molecular Formula: C34H33N3O5

Molecular Weight: 563.65

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc2c(cc1OC)CN(CCCOc1ccc(NC(=O)c3cccc4c(=O)c5ccccc5[nH]c34)cc1)CC2

Standard InChI:  InChI=1S/C34H33N3O5/c1-40-30-19-22-15-17-37(21-23(22)20-31(30)41-2)16-6-18-42-25-13-11-24(12-14-25)35-34(39)28-9-5-8-27-32(28)36-29-10-4-3-7-26(29)33(27)38/h3-5,7-14,19-20H,6,15-18,21H2,1-2H3,(H,35,39)(H,36,38)

Standard InChI Key:  ZOTIYZJFSIBQJB-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: 563.65Molecular Weight (Monoisotopic): 563.2420AlogP: 5.78#Rotatable Bonds: 9
Polar Surface Area: 92.89Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 8.21CX LogP: 6.66CX LogD: 5.79
Aromatic Rings: 5Heavy Atoms: 42QED Weighted: 0.17Np Likeness Score: -0.78

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