Synthesis of novel piperazine-based bis(thiazole)(1,3,4-thiadiazole) hybrids as anti-cancer agents through caspase-dependent apoptosis. [PDF]
Mohamed DM +5 more
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Design, Synthesis, Antibacterial, and Antifungal Evaluation of Phenylthiazole Derivatives Containing a 1,3,4-Thiadiazole Thione Moiety. [PDF]
Mao G +9 more
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Identification of Benzothiazoles Bearing 1,3,4-Thiadiazole as Antiproliferative Hybrids Targeting VEGFR-2 and BRAF Kinase: Design, Synthesis, BIO Evaluation and In Silico Study. [PDF]
Ewes WA +10 more
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Novel quinazolines bearing 1,3,4-thiadiazole-aryl urea derivative as anticancer agents: design, synthesis, molecular docking, DFT and bioactivity evaluations. [PDF]
Masoudinia S +4 more
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Heterocycles 52: The Drug-Likeness Analysis of Anti-Inflammatory Thiazolo[3,2-b][1,2,4]triazole and Imidazo[2,1-b][1,3,4]thiadiazole Derivatives. [PDF]
Apan A +6 more
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Novel [1,3,4]Thiadiazole[3,2-a]pyrimidin-5-ones as Promising Biofilm Dispersal Agents against Relevant Gram-Positive and Gram-Negative Pathogens. [PDF]
Carbone D +8 more
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Synthesis and antiproliferative potency of 1,3,4-thiadiazole and 1,3-thiazolidine-4-one based new binary heterocyclic molecules: <i>in vitro</i> cell-based anticancer studies. [PDF]
Maji A +9 more
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Three antiviral 1,3,4-thiadiazoles caused, when incubated together with 3H-uridine, a reduction of the incorporation rate into acid-insoluble material of FL cells.
Marion Tonew, Elke Klimke
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Abstract The microwave spectra of 1, 3, 4-thiadiazole (I) and [ 34 S] 1, 3, 4-thiadiazole (II) have been recorded in the 15,000–30,000 Mc/sec region. Twelve and ten transitions, respectively, were assigned. The rotational constants of (I) are, A = 8907.51 ± 0.10, B = 5569.27 ± 0.02, and C = 3424.80 ± 0.03 Mc/sec. For (II), A = 8908.15 ± 0.20,
Børge Bak +4 more
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Kristallin‐flüssige 1,3,4‐Thiadiazole. II [1]. 1,3,4‐Thiadiazole mit Cyclohexanstrukturfragmenten
Journal für Praktische Chemie, 1989Liquid Crystalline 1,3,4‐Thiadiazoles. II. 1,3,4‐Thiadiazoles with CyclohexanefragmentsPreparation and liquid crystalline properties of disubstituted 1,3,4‐thiadiazoles (1 and 2) are described. The mesomorphic behaviour of the title compounds is compared with their benzoate analogues. The dielectric anisotropy of these compounds is negative.
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