ID: ALA4863965

Max Phase: Preclinical

Molecular Formula: C24H33BrN2O2

Molecular Weight: 381.54

Molecule Type: Unknown

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C24H33N2O2.BrH/c1-5-7-8-9-10-13-16-25-18(4)26(17(3)6-2)22-21(25)23(27)19-14-11-12-15-20(19)24(22)28;/h11-12,14-15,17H,5-10,13,16H2,1-4H3;1H/q+1;/p-1

Standard InChI Key:  ONBCWCBRWXYYDN-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: 381.54Molecular Weight (Monoisotopic): 381.2537AlogP: 5.19#Rotatable Bonds: 9
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: 1.35CX LogD: 1.35
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.38Np 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