نتایج جستجو برای: adrafinil analogues

تعداد نتایج: 28279  

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2005
hassan hadadzadeh ali reza rezvani

[ru(terpy)(bpy)(l)]pf6 complexes, where terpy is 2,2΄:6′,2″– terpyridine, bpy is 2,2΄ - bipyridine and l is monoanions of  4 - bromophenylcyanamide (4 - brpcyd), 4-methoxyphenylcyanamide (4 - meopcyd), 2, 4 - dibromophenylcyanamide (2,4 - br2pcyd), 2,4-dimethylphenylcyanamide (2,4 - me2pcyd), 2 - methylphenylcyanamide  (2 - mepcyd), phenylcyanamide  (pcyd) and naphtylcyanamide  (ncyd)  have bee...

Journal: :iranian journal of pharmaceutical sciences 0
bhatia manish sudesh drug development sciences research group department of pharmaceutical chemistry, bharatividyapeeth college of pharmacy, kolhapur maharastara india choudhari prafulla balkrishna drug development sciences research group department of pharmaceutical chemistry, bharatividyapeeth college of pharmacy, kolhapur maharastara india ingale kundan bhanudas drug development sciences research group department of pharmaceutical chemistry, bharatividyapeeth college of pharmacy, kolhapur maharastara india

this paper describes 3d-qsar analysis and biological evaluation of 1,5-benzodiazepine analogues. benzodiazepine nucleus with its simple structure gives a good opportunity for further modification regarding an increase of its antimicrobial activity. we synthesized a series of benzodiazepine analogues from condensation of various chalcones and halo substituted o-phenelynene diamines. all compound...

Journal: :Bioorganic & Medicinal Chemistry Letters 2016

Journal: :Chemical reviews 2000
S Singh

H. Piperidine Analogues of Phenyltropanes 967 III. Cocaine Analogues 969 A. Stereoisomers of Cocaine 970 B. Phenyl Ring Substituted Cocaines 970 C. 2â-Substituted Cocaines 973 1. 2â-Substituted Cocaines 973 2. 2â-Substituted 4′-Iodococaines 977 D. N-Modified Cocaines 978 E. 3â-Carbamoyl Analogues of Cocaine 981 F. 3â-Alkylphenyltropanes 982 G. 6/7-Substituted Cocaine and Pseudococaine 982 H. 6-...

Journal: :Current topics in medicinal chemistry 2014
Pedro Merino Mattia Ghirardello Tomas Tejero Ignacio Delso Rosa Matute

This review will describe the recent advances in the synthesis of C-nucleosides with inhibitory activity of inosine monophosphate dehydrogenase (IMPDH), a key enzyme in the biosynthesis of guanine nucleotides. The review will cover synthetic approaches of structural analogues showing modifications in the furanose ring as well as in the heterocyclic base. Heterocyclic sugar nucleoside analogues ...

CW Wright

Natural product-derived drugs exemplified by quinine, isolated from South American Cinchona species and artemisinin discovered in China are of immense importance for the treatment of malaria. Although malaria parasites resistant to artemisinin have not yet been found in malaria patients, the need for new antimalarial agents remains. The burden of malaria is heaviest in Africa where over a milli...

2009
Cheuk-Chun Szeto Philip Kam-Tao Li

Chronic kidney disease (CKD) is a common and costly medical condition, and currently available therapeutic options remain unsatisfactory. Vitamin D analogues are widely used for the bone and mineral disorder associated with CKD. However, accumulating evidence suggests that vitamin D analogues may have actions other than their effects on bone and mineral metabolism. In this article, we review th...

2014
Michail Syrpas Ewout Ruysbergh Christian V Stevens Norbert De Kimpe Sven Mangelinckx

Novel N-α-haloacylated homoserine lactones, in which a halogen atom was introduced at the α-position of the carbonyl function of the N-acyl chain, have been studied as quorum sensing (QS) modulators and compared with a library of natural N-acylated homoserine lactones (AHLs). The series of novel analogues consists of α-chloro, α-bromo and α-iodo AHL analogues. Furthermore, the biological QS act...

Journal: :The Journal of biological chemistry 1983
A K Samanta A Bhaduri

UDP-glucose 4-epimerase from Saccharomyces fragilis has 1 mol of NAD firmly bound per mol of the dimeric apoenzyme. This prevents a direct study of the coenzyme binding site of the protein. Dissociation of the dimer with p-chloromercuribenzoate and its reconstitution with exogenous NAD or one of its analogues and 2-mercaptoethanol provides an indirect method of study of the site. Depending on t...

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