Results 41 to 50 of about 5,263 (174)

Synthesis of Benzimidazole–Based Analogs as Anti Alzheimer’s Disease Compounds and Their Molecular Docking Studies

open access: yesMolecules, 2020
We synthesized 10 analogs of benzimidazole-based thiosemicarbazide 1 (a–j) and 13 benzimidazole-based Schiff bases 2 (a–m), and characterized by various spectroscopic techniques and evaluated in vitro for acetylcholinesterase (AchE) and ...
Bushra Adalat   +8 more
doaj   +1 more source

Pharmacophore Mapping Approach for Drug Target Identification: A Chemical Synthesis and in Silico Study on Novel Thiadiazole Compounds [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2017
Introduction: Compounds containing thiadiazole moiety are cognized to possess with variety of clinical and therapeutic activity. Finding a suitable drug target for newly synthesized compounds remain a major bottle neck in current high throughout ...
Rohan J. Meshram   +4 more
doaj   +1 more source

1,1,4-Derivatives of Thiosemicarbazide—New Non-Staining Antiozonants

open access: yes, 1973
In the nature of non-staining antiozonants, a new class of compounds, 1,1,4-derivatives of thiosemicarbazide, are proposed. The mechanism of reaction of thiosemicarbazide derivatives with ozone is analogous to the mechanism of this reaction with thiourea
L. K. Zolotarevskaya   +3 more
core   +1 more source

Synthesis and Characterization of Novel Corrosion Inhibitor Derived from Oleic Acid: 2-Amino 5-Oleyl-1,3,4-Thiadiazol (AOT)

open access: yesInternational Journal of Electrochemical Science, 2012
Novel corrosion inhibitor as a green chemical product namely derivative, 2-amino 5-oleyl-1,3,4-thiadiazol (AOT) was synthesized by cyclization of oleic acid. The new corrosion inhibitor was characterized by FT-IR and NMR spectroscopical methods.
Sutiana Junaedi   +4 more
doaj   +1 more source

Design, Synthesis, Antibacterial Evaluations and In Silico Studies of Novel Thiosemicarbazides and 1,3,4-Thiadiazoles

open access: yesMolecules, 2022
The emergence of drug-resistant bacterial strains continues to be one of the major challenges of medicine. For this reason, the importance of searching for novel structures of antibacterial drugs chemically different from the currently known antibiotics ...
Sara Janowska   +3 more
doaj   +1 more source

N‐Amidinyl‐Benzodiazaborines as Novel Boron‐Based Scaffolds: Synthesis and Application in Retromer Stabilization

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 11, 3 June 2026.
In this work, we successfully synthesized a library of novel N‐amidinyl‐benzodiazaborines, showing how these heteroaryl guanyl hydrazones are able to stabilize the retromer, a protein complex involved in the disposal of misfolded and aggregated proteins, whose malfunction is observed in multiple neurodegenerative diseases.
Alessandro Dimasi   +10 more
wiley   +1 more source

Monoamine Oxidase and Cholinesterase Inhibition Profiles of Semicarbazone and Thiosemicarbazone Derivatives

open access: yesChemistry &Biodiversity, Volume 23, Issue 6, June 2026.
Thiosemicarbazones generally show higher MAO‐B inhibitory potential than their corresponding semicarbazones, and particularly T6 is the most potent, which contains R = H and X = S in its Tail Unit, with an IC50 value of 6.45 µM with SI of 3.6. ABSTRACT Twenty semicarbazone and thiosemicarbazone derivatives (T1–T20) were synthesized and evaluated for ...
Sandeep Bindra   +11 more
wiley   +1 more source

Effects of Thiosemicarbazide on Audiogenic Seizures

open access: yes, 1966
35 male albino rats were tested for audiogenic seizures and then divided into 5 time-delay groups. These time delays preceded bell-can stimulations following the administration of thiosemicarbazide. It was found that 1-hr. and 5-hr.
Emery E. Benson, Herman C. Salzberg
core   +1 more source

A novel intermediate in the interaction of thiosemicarbazide with sheep liver serine hydroxymethyltransferase [PDF]

open access: yes, 1992
An unusual intermediate bound to the enzyme was detected in the interaction of thiosemicarbazide with sheep liver serine hydroxymethyltransferase. This intermediate had absorbance maxima at 464 and 440 nm.
Rao, NA, Acharya, JK
core   +2 more sources

Synthesis, characterization, antimicrobial, and pharmacological evaluation of some 2, 5-disubstituted sulfonyl amino 1,3,4-oxadiazole and 2-amino-disubstituted 1,3,4-thiadiazole derivatives

open access: yesJournal of Advanced Pharmaceutical Technology & Research, 2014
The presence of heterocyclic structures in diverse types of compounds, this is strongly indicative of the profound effect like structure exerts on physiologic activity, and recognition of this is abundantly reflected in efforts to find useful synthetic ...
Dilipkumar Pal   +3 more
doaj   +1 more source

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