The therapeutic journey of benzimidazoles: A review
Y Bansal, O Silakari - Bioorganic & medicinal chemistry, 2012 - Elsevier
Presence of benzimidazole nucleus in numerous categories of therapeutic agents such as
antimicrobials, antivirals, antiparasites, anticancer, anti-inflammatory, antioxidants, proton …
antimicrobials, antivirals, antiparasites, anticancer, anti-inflammatory, antioxidants, proton …
Opportunities and challenges in developing stearoyl-coenzyme A desaturase-1 inhibitors as novel therapeutics for human disease: miniperspective
Z Zhang, NA Dales, MD Winther - Journal of medicinal chemistry, 2014 - ACS Publications
This review provides an overview of stearoyl-coenzyme A desaturase-1 (SCD1) as a novel
therapeutic target for metabolic disorders and other indications. Target validation is …
therapeutic target for metabolic disorders and other indications. Target validation is …
Selective Synthesis of Benzimidazoles from o-Phenylenediamine and Aldehydes Promoted by Supported Gold Nanoparticles
MA Tzani, C Gabriel, IN Lykakis - Nanomaterials, 2020 - mdpi.com
We investigated the catalytic efficacy of supported gold nanoparticles (AuNPs) towards the
selective reaction between o-phenylenediamine and aldehydes that yields 2-substituted …
selective reaction between o-phenylenediamine and aldehydes that yields 2-substituted …
Non-clinical pharmacology of YTX-7739: a clinical stage stearoyl-CoA desaturase inhibitor being developed for Parkinson's disease
DF Tardiff, M Lucas, I Wrona, B Chang, CY Chung… - Molecular …, 2022 - Springer
Stearoyl-CoA desaturase (SCD) is a potential therapeutic target for Parkinson's and related
neurodegenerative diseases. SCD inhibition ameliorates neuronal toxicity caused by …
neurodegenerative diseases. SCD inhibition ameliorates neuronal toxicity caused by …
Benzimidazole derivatives endowed with potent antileishmanial activity
Two sets of benzimidazole derivatives were synthesised and tested in vitro for activity
against promastigotes of Leishmania tropica and L. infantum. Most of the tested compounds …
against promastigotes of Leishmania tropica and L. infantum. Most of the tested compounds …
[HTML][HTML] Accelerated bottom-up drug design platform enables the discovery of novel stearoyl-CoA desaturase 1 inhibitors for cancer therapy
CA von Roemeling, TR Caulfield, L Marlow, I Bok… - Oncotarget, 2018 - ncbi.nlm.nih.gov
Here we present an innovative computational-based drug discovery strategy, coupled with
machine-based learning and functional assessment, for the rational design of novel small …
machine-based learning and functional assessment, for the rational design of novel small …
Discovery of potent and liver-targeted stearoyl-CoA desaturase (SCD) inhibitors in a bispyrrolidine series
N Lachance, Y Gareau, S Guiral, Z Huang… - Bioorganic & medicinal …, 2012 - Elsevier
Inhibition of stearoyl-CoA desaturase (SCD) activity represents a potential novel mechanism
for the treatment of metabolic disorders including obesity and type II diabetes. To circumvent …
for the treatment of metabolic disorders including obesity and type II diabetes. To circumvent …
[PDF][PDF] Applying nanotechnology in the synthesis of benzimidazole derivatives: a pharmacological approach
A El-Sayed, S Abu-Bakr, S Swelam… - Biointerface …, 2022 - biointerfaceresearch.com
Benzimidazoles are classified as a category of heterocyclic compounds. They possess an
essential structural feature of 6-membered benzene fused to 5-membered imidazole moiety …
essential structural feature of 6-membered benzene fused to 5-membered imidazole moiety …
An overview of patented small molecule stearoyl coenzyme-A desaturase inhibitors (2009–2013)
DA Powell - Expert opinion on therapeutic patents, 2014 - Taylor & Francis
Introduction: Stearoyl coenzyme-A desaturase (SCD) is a critical lipogenic enzyme that
converts a range of unsaturated lipids to their corresponding monounsaturated fatty acids …
converts a range of unsaturated lipids to their corresponding monounsaturated fatty acids …
Discovery of novel SCD1 inhibitors: 5-alkyl-4, 5-dihydro-3H-spiro [1, 5-benzoxazepine-2, 4′-piperidine] analogs
Y Uto, Y Ueno, Y Kiyotsuka, Y Miyazawa… - European journal of …, 2011 - Elsevier
Expansion of the 6-membered ring and subsequent fine-tuning of the newly obtained 7-
membered spiropiperidine structure resulted in the discovery of a series of novel and potent …
membered spiropiperidine structure resulted in the discovery of a series of novel and potent …