نتایج جستجو برای: 4 thiazolidinone

تعداد نتایج: 1303703  

Journal: :Asian Journal of Chemistry 2014

Journal: :Journal of pharmaceutical research international 2021

Background: Cancer is the world's second leading cause of death, accounting for an estimate more than 10 million deaths annually. The most common type cancers in women are breast, endometrial, cervical, ovarian, colorectal, lung, and skin cancers.Among these, breast cancer all ages. Human epidermal growth factor receptor 2 widely seen which test positive protein HER2. This present one-fifth eve...

2015
Daniel Spinks Victoria Smith Stephen Thompson David A Robinson Torsten Luksch Alasdair Smith Leah S Torrie Stuart McElroy Laste Stojanovski Suzanne Norval Iain T Collie Irene Hallyburton Bhavya Rao Stephen Brand Ruth Brenk Julie A Frearson Kevin D Read Paul G Wyatt Ian H Gilbert

The enzyme N-myristoyltransferase (NMT) from Trypanosoma brucei has been validated both chemically and biologically as a potential drug target for human African trypanosomiasis. We previously reported the development of some very potent compounds based around a pyrazole sulfonamide series, derived from a high-throughput screen. Herein we describe work around thiazolidinone and benzomorpholine s...

Journal: :The Journal of pharmacology and experimental therapeutics 2008
N D Sonawane Olga Zegarra-Moran Wan Namkung Luis J V Galietta A S Verkman

Inhibitors of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel have potential applications in the therapy of secretory diarrheas and polycystic kidney disease. In a recent study, several highly polar alpha-aminoazaheterocyclic-methylglyoxal adducts were reported to reversibly inhibit CFTR chloride channel activity with IC50 values in the low picomolar range (J Pha...

Journal: :Chemistry & biology 2006
Erin E Carlson John F May Laura L Kiessling

Many pathogenic prokaryotes and eukaryotes possess the machinery required to assemble galactofuranose (Galf)-containing glycoconjugates; these glycoconjugates can be critical for virulence or viability. Accordingly, compounds that block Galf incorporation may serve as therapeutic leads or as probes of the function of Galf-containing glycoconjugates. The enzyme UDP-galactopyranose mutase (UGM) i...

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