ID: ALA4583170

Max Phase: Preclinical

Molecular Formula: C14H14BrN3O2S

Molecular Weight: 368.26

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)c1sc(N/N=C/c2ccccc2Br)nc1C

Standard InChI:  InChI=1S/C14H14BrN3O2S/c1-3-20-13(19)12-9(2)17-14(21-12)18-16-8-10-6-4-5-7-11(10)15/h4-8H,3H2,1-2H3,(H,17,18)/b16-8+

Standard InChI Key:  ZBFMKTIIERSZST-LZYBPNLTSA-N

Associated Targets(non-human)

Leucine--tRNA ligase 91 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: 368.26Molecular Weight (Monoisotopic): 366.9990AlogP: 3.84#Rotatable Bonds: 5
Polar Surface Area: 63.58Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.31CX Basic pKa: 4.25CX LogP: 4.54CX LogD: 4.53
Aromatic Rings: 2Heavy Atoms: 21QED Weighted: 0.49Np Likeness Score: -2.20

References

1. Kovalenko OP, Volynets GP, Rybak MY, Starosyla SA, Gudzera OI, Lukashov SS, Bdzhola VG, Yarmoluk SM, Boshoff HI, Tukalo MA..  (2019)  Dual-target inhibitors of mycobacterial aminoacyl-tRNA synthetases among N-benzylidene-N'-thiazol-2-yl-hydrazines.,  10  (12): [PMID:32206244] [10.1039/C9MD00347A]

Source