نتایج جستجو برای: thiazolidinone

تعداد نتایج: 272  

2012
Habibullah Khalilullah Shamshir Khan Mohamed Jawed Ahsan Bahar Ahmed

In continuance of our search for newer antihepatotoxic agents some novel thiazolidinone derivatives containing 1,4-benzodioxane ring system were synthesized starting from 2,3-dihydro-1,4-benzodioxane-2-carbohydrazide. The synthesized compounds were evaluated for antihepatotoxic activity against CCl4-induced hepatotoxicity in rats. Among them some compounds have shown significant antihepatotoxic...

Journal: :Beilstein Journal of Organic Chemistry 2008
Deepa Pandey Wahajul Haq Seturam B Katti

In search of new erythromycin derivatives 3-O-[gamma-(4-oxo-2-aryl-thiazolidin-3-yl)butyryl]erythromycin A derivatives have been synthesized. The 3-hydroxy group was derivatised to a primary amine and subsequently the thiazolidinone nucleus was generated at the amino functionality through DCC mediated one-pot three-component reaction in good yields.

Journal: :iranian journal of pharmaceutical research 0
nb patel vn patel

synthesis of 2-[2-(2,6-dichlorophenyl)amino]phenylmethyl-3-[4-(2-substitutedphenyl-4-oxo-thiazolidinyl)aryl]-6-bromo quinazolin-4(3h)ones via-j have been achieved from the starting material 2-[(2,6-dichlorophenyl)amino] phenylacetic acid i to benzoxazine iii, further reaction with p-phenylindiamine and substituted aromatic aldehyde gave 2-[2-(2,6-dichlorophenyl)amino]phenyl methyl-3-(4-aminoary...

Journal: :Scientia Pharmaceutica 2022

It was determined that the studied 5-[(Z)-(4-nitrobenzylidene)]-2-(thiazol-2-ylimino)-4-thiazolidinone (Les-6222) affects cyclooxygenase pathway of arachidonic acid cascade, markers damage to neurons on models PTZ kindling. In model chronic epileptogenesis in mice (pentylenetetrazole kindling), a 4-thiazolidinone derivative showed high anticonvulsant activity, which is weaker than effect sodium...

Journal: :iranian journal of allergy, asthma and immunology 0
hossein ghafoori department of biology, university of guilan, rasht, iran mehrnaz rezaei department of biology, university of guilan, university campus 2, rasht, iran asadollah mohammadi department of chemistry, university of guilan, rasht, iran

the inhibition of the inducible nitric oxide synthase (inos), cyclooxygenase 2 (cox-2) and nuclear factor-κb (nf-κb) production are research targets of attract in the field of anti-inflammatory drug development. therefore, this study was designed to investigate the anti-inflammatory effects of novel thiazolidinone derivatives using a cellular model of lipopolysaccharide (lps)-stimulated murine ...

Journal: :Asian Journal of Chemistry 2014

Journal: :Journal of advanced scientific research 2022

A N-methyl-2-pyrrolidonium hydrogensulfate [NMP][HSO4] bronsted acidic ionic liquid-promoted cyclocondensation-cyclization pathway has been established using one pot reaction of anilines, aldehydes and mercaptoacetic acid to give 4-thiazolidinone derivatives in good promising yields microwave irradiation. Applications for this protocol are easy workup, high yields, short times, variability func...

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...

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