Results 151 to 160 of about 18,261 (204)

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]

open access: yesMolecules
Ewes WA   +10 more
europepmc   +1 more source

1,3,4-Thiadiazole Based Anticancer Agents

Anti-Cancer Agents in Medicinal Chemistry, 2016
In recent years, researchers like medicinal chemists in the field of medicinal chemistry have widely utilized the 1,3,4-thiadiazole nucleus to investigate its biological and pharmacological effects. This heterocyclic structure has demonstrated various bioactivities such as antifungal, antimicrobial, antiviral, antileishmanial, anti-inflammatory ...
Alireza Aliabadi
exaly   +3 more sources

Antiviral 1,3,4-Thiadiazoles

Chemotherapy, 2009
Nine 1,3,4-thiadiazoles showed an antiviral action against Mengo virus; four of them were also active against vaccinia virus and one against fowl plague virus. Investigations with Mengo virus revealed plaque reduction, inhibition of the cytopathic effect and depression of virus multiplication, with the maximum activity after substance addition from 0–2
Marion Tonew, Elke Klimke
openaire   +2 more sources

Solid-Phase Synthesis of 1,3,4-Thiadiazole Derivatives via Desulfurative Cyclization of Thiosemicarbazide Intermediate Resin

open access: yesACS Combinatorial Science, 2016
A 1,3,4-thiadiazole library was constructed by solid-phase organic synthesis. The key step of this solid-phase synthesis involves the preparation of polymer-bound 2-amido-5-amino-1,3,4-thiadiazole resin by the cyclization of thiosemicarbazide resin using
Young-Dae Gong, Seung-Ju Yang
exaly   +2 more sources

Microwave spectra of 1,3,4-thiadiazole and [34S]1,3,4-thiadiazole. Dipole moment of 1,3,4-thiadiazole

Journal of Molecular Spectroscopy, 1962
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
openaire   +1 more source

Synthesis and antifungal activity of thiadiazole-functionalized chitosan derivatives

open access: yesCarbohydrate Research, 2013
A groups of novel water soluble chitosan derivatives containing 1,3,4-thiadiazole group were synthesized including 1,3,4-thiadiazole (TPCTS), 2-methyl-1,3,4-thiadiazole (MTPCTS), and 2-phenyl-1,3,4-thiadiazole (PTPCTS).
Qing Li, Zhanyong Guo, Guodong Gu
exaly   +2 more sources

Synthesis of 1,3,4-thiadiazole oligomers

Journal of the Chemical Society, Perkin Transactions 1, 2002
AbstractFor Abstract see ChemInform Abstract in Full Text.
Van‐Duc Le   +2 more
openaire   +1 more source

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