ID: ALA4276676

Max Phase: Preclinical

Molecular Formula: C24H15N5O3

Molecular Weight: 421.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N#CC1=CC2(c3ccccc3Nc3ccccc32)N(/N=C/c2ccccc2[N+](=O)[O-])C1=O

Standard InChI:  InChI=1S/C24H15N5O3/c25-14-17-13-24(18-8-2-4-10-20(18)27-21-11-5-3-9-19(21)24)28(23(17)30)26-15-16-7-1-6-12-22(16)29(31)32/h1-13,15,27H/b26-15+

Standard InChI Key:  SZOGZODSNALIDA-CVKSISIWSA-N

Associated Targets(Human)

DNA topoisomerase II alpha 6317 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Serum albumin 1163 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Calf thymus DNA 4845 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: 421.42Molecular Weight (Monoisotopic): 421.1175AlogP: 4.22#Rotatable Bonds: 3
Polar Surface Area: 111.63Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.23CX LogD: 4.23
Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.39Np Likeness Score: -0.64

References

1. Gouveia RG, Ribeiro AG, Segundo MÂSP, de Oliveira JF, de Lima MDCA, de Lima Souza TRC, de Almeida SMV, de Moura RO..  (2018)  Synthesis, DNA and protein interactions and human topoisomerase inhibition of novel Spiroacridine derivatives.,  26  (22): [PMID:30420325] [10.1016/j.bmc.2018.10.038]

Source