ID: ALA4861486

Max Phase: Preclinical

Molecular Formula: C23H24N8

Molecular Weight: 412.50

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  N#Cc1c(N2CCNCC2)c2ccc(N3CCNCC3)cc2n2c1nc1ncccc12

Standard InChI:  InChI=1S/C23H24N8/c24-15-18-21(30-12-8-26-9-13-30)17-4-3-16(29-10-6-25-7-11-29)14-20(17)31-19-2-1-5-27-22(19)28-23(18)31/h1-5,14,25-26H,6-13H2

Standard InChI Key:  UAUOUUMIFKJDMO-UHFFFAOYSA-N

Associated Targets(Human)

HCT-116 91556 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

NCI-H460 60772 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MCF7 126967 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HEK293 82097 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

quadruplex DNA 2700 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Calf thymus DNA 4845 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 412.50Molecular Weight (Monoisotopic): 412.2124AlogP: 1.73#Rotatable Bonds: 2
Polar Surface Area: 84.52Molecular Species: BASEHBA: 8HBD: 2
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.11CX LogP: 1.29CX LogD: -1.55
Aromatic Rings: 4Heavy Atoms: 31QED Weighted: 0.52Np Likeness Score: -1.02

References

1. Lončar B, Perin N, Mioč M, Boček I, Grgić L, Kralj M, Tomić S, Stojković MR, Hranjec M..  (2021)  Novel amino substituted tetracyclic imidazo[4,5-b]pyridine derivatives: Design, synthesis, antiproliferative activity and DNA/RNA binding study.,  217  [PMID:33751978] [10.1016/j.ejmech.2021.113342]

Source