Compound ID | 3633

Update compound information

N-(5-Benzyl-thiazol-2-yl)-2-[4-(4-methoxy-phenyl)-1H-tetrazol-5-ylsulfanyl]-acetamide

Synonym(s): GTPL13929; Compound 4b

Class: Small molecule antibacterial agent

Agent Type: Synthetic; Small molecule; Direct acting;
Spectrum of activity: Antimycobacterial
Mechanism of action: Protein synthesis inhibitor. Aminoacyl-tRNA synthetase inhibitor (boron-heterocyclic leucyl-tRNA synthetase [LeuRS] inhibitor)
Target Pathogen: Active against Mycobacterium tuberculosis
Description: Synthetic boron-heterocyclic compound identified by virtual screening of LeuRS inhibitors
Year first mentioned: 2025
Development status: Experimental
Chemical structure(s):
Click here for structure editor
Molecular weight: 439.54
Iso. SMILES: COC1=CC=C(C=C1)[N+]2=C(N=NN2)SCC(=O)NC3=NC=C(S3)CC4=CC=CC=C4
InChI Key: QDYCZFKMORSJMN-UHFFFAOYSA-O
Can. SMILES: COC1=CC=C(C=C1)[N+]2=C(N=NN2)SCC(=O)NC3=NC=C(CC4=CC=CC=C4)S3
InChI: InChI=1S/C20H18N6O2S2/c1-28-16-9-7-15(8-10-16)26-20(23-24-25-26)29-13-18(27)22-19-21-12-17(30-19)11-14-5-3-2-4-6-14/h2-10,12H,11,13H2,1H3,(H,21,22,27)/p+1
External links:
Structure link: https://pubchem.ncbi.nlm.nih.gov/compound/175670510
Guide to Pharmacology: compound 4b [PMID: 40259683]
Citation: https://doi.org/10.1080/17568919.2025.2485673

AntibioticDB is supported by GARDP.

If you have feedback, experience problems, or are interested in a collaboration, please contact us. | Terms and conditions

The content of this site is intended for educational and scientific research purposes only and not as a source of medical advice or consultation.