نتایج جستجو برای: antimalarial activity

تعداد نتایج: 1138771  

Journal: :Antimicrobial agents and chemotherapy 2000
P Newton Y Suputtamongkol P Teja-Isavadharm S Pukrittayakamee V Navaratnam I Bates N White

The pharmacokinetic properties of oral and intravenous artesunate (2 mg/kg of body weight) were studied in 19 adult patients with acute uncomplicated Plasmodium falciparum malaria by using a randomized crossover design. A sensitive bioassay was used to measure the antimalarial activity in plasma which results from artesunate and its principal metabolite, dihydroartemisinin. The oral study was r...

2007
Sanjay Kumar Mithu Guha Vinay Choubey Pallab Maity Uday Bandyopadhyay

Digestion of hemoglobin in the food vacuole of the malaria parasite produces very high quantities of redox active toxic free heme. Hemozoin (β-hematin) formation is a unique process adopted by Plasmodium sp. to detoxify free heme. Hemozoin formation is a validated target for most of the well-known existing antimalarial drugs and considered to be a suitable target to develop new antimalarials. H...

Journal: :Journal of medicinal chemistry 2008
Sandra Gemma Giuseppe Campiani Stefania Butini Gagan Kukreja Salvatore Sanna Coccone Bhupendra P Joshi Marco Persico Vito Nacci Isabella Fiorini Ettore Novellino Ernesto Fattorusso Orazio Taglialatela-Scafati Luisa Savini Donatella Taramelli Nicoletta Basilico Silvia Parapini Giulia Morace Vanessa Yardley Simon Croft Massimiliano Coletta Stefano Marini Caterina Fattorusso

We describe herein the design, synthesis, biological evaluation, and structure-activity relationship (SAR) studies of an innovative class of antimalarial agents based on a polyaromatic pharmacophore structurally related to clotrimazole and easy to synthesize by low-cost synthetic procedures. SAR studies delineated a number of structural features able to modulate the in vitro and in vivo antimal...

Journal: :Revista da Sociedade Brasileira de Medicina Tropical 2014
Daniele Ribatski-Silva Carmen Lucia Bassi Thamires Oliveira Gasquez Martin Eduardo Alves-Junior Luciano Teixeira Gomes Cor Jésus Fernandes Fontes

INTRODUCTION We evaluated the in vitro antimalarial activity of tigecycline as an alternative drug for the treatment of severe malaria. METHODS A chloroquine-sensitive Plasmodium falciparum reference strain, a chloroquine-resistant reference strain, and three clinical isolates were tested for in vitro susceptibility to tigecycline. A histidine-rich protein in vitro assay was used to evaluate ...

Journal: :Antimicrobial agents and chemotherapy 1995
J L Vennerstrom M T Makler C K Angerhofer J A Williams

In 1891 Guttmann and Ehrlich (P. Guttmann and P. Ehrlich, Berlin Klin. Wochenschr. 28:953-956, 1891) were the first to report the antimalarial properties of a synthetic, rather than a natural, material when they described the clinical cure of two patients after oral administration of a thiazine dye, methylene blue. Since that time, sporadic reports of the antimalarial properties of several xant...

2016
Lukman Adewale Alli Abdulfatai Ayoade Adesokan Adeola Oluwakanyinsola Salawu

BACKGROUND The problem of resistance of malarial parasites to available antimalarial drugs makes the development of new drugs imperative, with natural plant products providing an alternative source for discovering new drugs. AIM To evaluate the antimalarial activity of eluted fractions of Acacia nilotica root extract and determine the phytochemicals responsible for its antimalarial activity. ...

Journal: :Biological & pharmaceutical bulletin 2012
Sunanta Tangnitipong Thitiporn Thaptimthong Sirada Srihirun Supeenun Unchern Dusadee Kittikool Rachanee Udomsangpetch Nathawut Sibmooh

Artemisinin exerts the antimalarial activity through activation by heme. The hemolysis in malaria results in the elevated levels of plasma heme which may affect the activity of artemisinin. We hypothesized that the extracellular heme would potentiate the antimalarial activity of artemisinin. Hemin (ferric heme) at the pathologic concentrations enhanced the activity of artemisinin against Plasmo...

Journal: :Bioorganic & medicinal chemistry 2014
Timothy J Hubin Prince N-A Amoyaw Kimberly D Roewe Natalie C Simpson Randall D Maples TaRynn N Carder Freeman Amy N Cain Justin G Le Stephen J Archibald Shabana I Khan Babu L Tekwani M O Faruk Khan

Using transition metals such as manganese(II), iron(II), cobalt(II), nickel(II), copper(II), and zinc(II), several new metal complexes of cross-bridged tetraazamacrocyclic chelators namely, cyclen- and cyclam-analogs with benzyl groups, were synthesized and screened for in vitro antimalarial activity against chloroquine-resistant (W2) and chloroquine-sensitive (D6) strains of Plasmodium falcipa...

Journal: :Bioorganic & medicinal chemistry letters 2013
Katherine T Andrews Gillian M Fisher Subathdrage D M Sumanadasa Tina Skinner-Adams Janina Moeker Marie Lopez Sally-Ann Poulsen

Despite the urgent need for effective antimalarial drugs with novel modes of action no new chemical class of antimalarial drug has been approved for use since 1996. To address this, we have used a rational approach to investigate compounds comprising the primary benzene sulfonamide fragment as a potential new antimalarial chemotype. We report the in vitro activity against Plasmodium falciparum ...

Journal: :The Journal of infectious diseases 2005
Paul Monaghan Maria Fardis W Peter Revill Angus Bell

The polyketide macrolactone FK506 inhibits the growth of Plasmodium falciparum in culture and the enzymatic (peptidyl-prolyl cis-trans isomerase [PPIase]) and chaperone activities of a recently identified P. falciparum FK506-binding protein (PfFKBP35). However, the potent immunosuppressive properties of FK506 exclude it from consideration as an antimalarial drug. We describe the antimalarial ac...

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