ID: ALA4555781

Max Phase: Preclinical

Molecular Formula: C15H15N3O4S

Molecular Weight: 333.37

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)c1sc(N/N=C/c2ccc(C(=O)O)cc2)nc1C

Standard InChI:  InChI=1S/C15H15N3O4S/c1-3-22-14(21)12-9(2)17-15(23-12)18-16-8-10-4-6-11(7-5-10)13(19)20/h4-8H,3H2,1-2H3,(H,17,18)(H,19,20)/b16-8+

Standard InChI Key:  QJIJOKACRAGPDP-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: 333.37Molecular Weight (Monoisotopic): 333.0783AlogP: 2.77#Rotatable Bonds: 6
Polar Surface Area: 100.88Molecular Species: ACIDHBA: 7HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.82CX Basic pKa: 4.65CX LogP: 2.46CX LogD: 0.24
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.48Np Likeness Score: -1.80

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