25 250 125 250 125 125 5b 1000 1000 1000 1000 1000 1000 5c 500 250 500 500 1000 250 5d 1000 >1000 >1000 >1000 BIBW2992 datasheet 500 >1000 5g 1000 >1000 >1000 >1000 500 >1000 5h 1000 1000 1000 >1000 >1000 1000 5i >1000 1000 >1000 >1000 >1000

>1000 6h 250 nd 500 15.63 nd 125 Cefuroxime 0.49 1.95 0.24 0.49 62.5 0.49 Bold values indicate the lowest MIC nd Not determined, Sa25923 S. aureus ATCC 25923, Sa6538 S. aureus ATCC 6538, Se12228 S. epidermidis ATCC 12228, Bs6633 B. subtilis ATCC 6633, Bc10876 B. cereus ATCC 10876, Ml10240 M. luteus ATCC 10240 The somewhat lower activity against reference strains of Gram-positive bacteria was shown by compound 5c (MIC values from 250 to 1,000 μg/mL). According to our results, MICs of cefuroxime, which has been extensively used to treat bacterial infections, were 0.24–1.95 μg/mL for Staphylococcus species and 0.49–62.5 μg/mL for the other Gram-positive bacteria. With our research, it has been established that the introduction of the benzoyl group in thiosemicarbazide and the benzyl group in 1,3,4-thiadiazole

derivative yielded active compounds endowed with a wide spectrum of antimicrobial activities. The compounds 4l and 6h with potential activity against the reference strains of Gram-positive bacteria may be regarded as precursor compounds for searching for new derivatives showing antimicrobial activity against pathogenic (e.g. S. aureus) or opportunistic

(e.g. S. epidermidis, AZD5363 M. luteus, B. subtilis, or B. cereus) bacteria. Experimental Selleckchem Bafilomycin A1 Chemistry Melting points were determined in Fisher–Johns blocks (Pittsburgh, US) and presented without any corrections. The IR spectra (ν, cm−1) were recorded in KBr tablets using a Specord IR-75 spectrophotometer (Germany). The NMR spectra were recorded on a Bruker Avance 300 apparatus (Bruker BioSpin GmbH, Rheinstetten/Karlsruhe, Germany) in dimethyl sulfoxide (DMSO)-d 6 with TMS as the internal standard, and chemical shifts are given in ppm (δ-scale). The MS spectra were recorded on a Thermo-Finnigan Trace DSQ GC MS apparatus (Waltham, Massachusetts, US). Chemicals were purchased Sitaxentan from Merck Co., or Lancaster and used without further purification. The purity of the obtained compounds was checked by TLC on aluminum oxide 60 F254 plates (Merck Co., Whitehouse Station, New Jersey, US), in a CHCl3/C2H5OH (10:1, v/v) solvent system with UV visualization (λ = 254 nm). Elemental analysis of the obtained compounds was performed for C, H, N, S. The maximum percentage differences between calculated and found values for each element were within the error and amounted to ±0.4 %. Crystal data for 2 C18H17N3O2S, colorless prism, 0.45 × 0.29 × 0.14 mm3, monoclinic, P21/n, a = 11.692(1) Å, b = 9.414(1) Å, c = 15.740(2) Å, β = 100.24(1)°, V = 1,704.