ID: ALA4080584

Max Phase: Preclinical

Molecular Formula: C25H27N5O6

Molecular Weight: 493.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cnc2c(c1)C(=O)c1c-2n(CCCNCCN2CCOCC2)c(=O)c2cc([N+](=O)[O-])ccc12

Standard InChI:  InChI=1S/C25H27N5O6/c1-35-17-14-20-22(27-15-17)23-21(24(20)31)18-4-3-16(30(33)34)13-19(18)25(32)29(23)7-2-5-26-6-8-28-9-11-36-12-10-28/h3-4,13-15,26H,2,5-12H2,1H3

Standard InChI Key:  VPADSKSPZOJDAY-UHFFFAOYSA-N

Associated Targets(Human)

SN12C 47755 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

DNA topoisomerase I 7553 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Tyrosyl-DNA phosphodiesterase 1 345557 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Tyrosyl-DNA phosphodiesterase 2 864 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

OVCAR-3 48710 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

UACC-62 47335 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

SF-539 44845 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HOP-62 47048 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MCF7 126967 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: 493.52Molecular Weight (Monoisotopic): 493.1961AlogP: 1.84#Rotatable Bonds: 9
Polar Surface Area: 128.83Molecular Species: BASEHBA: 10HBD: 1
#RO5 Violations: 0HBA (Lipinski): 11HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 9.81CX LogP: 0.56CX LogD: -1.79
Aromatic Rings: 3Heavy Atoms: 36QED Weighted: 0.21Np Likeness Score: -0.87

References

1. Wang P, Elsayed MSA, Plescia CB, Ravji A, Redon CE, Kiselev E, Marchand C, Zeleznik O, Agama K, Pommier Y, Cushman M..  (2017)  Synthesis and Biological Evaluation of the First Triple Inhibitors of Human Topoisomerase 1, Tyrosyl-DNA Phosphodiesterase 1 (Tdp1), and Tyrosyl-DNA Phosphodiesterase 2 (Tdp2).,  60  (8): [PMID:28418653] [10.1021/acs.jmedchem.6b01565]

Source