ID: ALA4871724

Max Phase: Preclinical

Molecular Formula: C25H35BrN2O2

Molecular Weight: 395.57

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCn1c2c([n+](CCCCC)c1C)C(=O)c1ccccc1C2=O.[Br-]

Standard InChI:  InChI=1S/C25H35N2O2.BrH/c1-4-6-8-9-10-14-18-27-19(3)26(17-13-7-5-2)22-23(27)25(29)21-16-12-11-15-20(21)24(22)28;/h11-12,15-16H,4-10,13-14,17-18H2,1-3H3;1H/q+1;/p-1

Standard InChI Key:  VRESXBJACKRYCE-UHFFFAOYSA-M

Associated Targets(non-human)

Mycobacterium tuberculosis variant bovis BCG 1626 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: 395.57Molecular Weight (Monoisotopic): 395.2693AlogP: 5.41#Rotatable Bonds: 11
Polar Surface Area: 42.95Molecular Species: HBA: 3HBD: 0
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 1.83CX LogD: 1.83
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.32Np Likeness Score: -0.03

References

1. Fridianto KT, Li M, Hards K, Negatu DA, Cook GM, Dick T, Lam Y, Go ML..  (2021)  Functionalized Dioxonaphthoimidazoliums: A Redox Cycling Chemotype with Potent Bactericidal Activities against Mycobacterium tuberculosis.,  64  (21.0): [PMID:34706190] [10.1021/acs.jmedchem.1c01383]

Source