Results 31 to 40 of about 2,042 (119)
Human synenkephalin [1–53] (hSYN), an analogue peptide of shrew saliva neurotoxins, was synthesized and its structural characteristics studied. Synthetic hSYN potently activated the T‐type voltage‐gated Ca channel hCav3.2 but did not paralyze mealworms. These findings offer new insight into neurological disorder treatment and evolutionary mechanisms of
Ryo Fukuoka +5 more
wiley +1 more source
Solid phase extraction of biogenic amines using immobilized new hydrazone ligands. [PDF]
Dalam kajian ini, sebatian hidrazin dan hidrazid melalui tindak balas kondensasi dengan keton dan terbitan berbeza aldehid menghasilkan hidrazon sepadan yang dijangkakan. Kesemua ligan yang dipisahkan memperolehi hasil yang memuaskan (82-94 %).
Alfergani, Abdassalam Abdelhafiz
core
Assessment of enzyme inhibition : a review with examples from the development of monoamine oxidase and cholinesterase inhibitory drugs [PDF]
Both authors are grateful for the collaborations on multi-target drugs facilitated by COST Action CM1103 (2011-2015).The actions of many drugs involve enzyme inhibition.
Ramsay, Rona R., Tipton, Keith F.
core +1 more source
Quinazolinone‐based compounds emerge as potent antimycobacterial agents, showing low minimum inhibitory concentrations against drug‐resistant Mycobacterium tuberculosis. Molecular modeling uncovers a novel allosteric site in PonA1 targeted by these derivatives.
Marek Kerda +15 more
wiley +1 more source
Advances in Metal‐Free Transamidation: A Sustainable Approach to Amide Bond Formation
This review highlights the recent developments of transamidation reactions under metal‐free reaction conditions. Various amines including weak nucleophilic amines such as aromatic amines have been used to achieve the transamidation reactions under mild and relatively green reaction conditions. Abstract The amide functionalities are a crucial functional
Niharan Sivaraj +2 more
wiley +1 more source
Synthesis and antimicrobial evaluation of some ethoxyphthalimide derivatives of 3-(substitutedphenyl)-4-methyl-3a, 6-dihydropyrazolo[3,4-c]pyrazol-2(3H)-yl(pyridin-3-yl)methanone [PDF]
5-Methyl-2,4-dihydro-3H-pyrazol-3-one (1) reacted with substituted benzaldehydes (2a-d) in the presence of anhydrous sodium acetate to gave corresponding 4-arylidene-5-methyl-2,4-dihyro-3H-pyrazol-3-ones (3a-d).
Dangi, Raja +3 more
core
This study synthesizes novel pyrimidine–pyrazole hybrids and evaluates their antimicrobial activity against bacterial pathogens by targeting penicillin‐binding protein 3 (PBP3). Several compounds show significant activity against E. faecium. Docking studies reveal strong binding with HMG‐CoA synthase, while in silico pharmacokinetic predictions ...
Suresh Choppadandi +4 more
wiley +1 more source
Design, synthesis and anticonvulsant activity of some new 5,7-dibromoisatin semicarbazone derivatives [PDF]
A series of 5,7-dibromoisatin semicarbazones have been synthesized in good yield, involving aryl urea and aryl semicarbazide formation. The structures of the synthesized compounds were confirmed on the basis of their spectral data. All the compounds were
Kumar, Dheeraj +6 more
core
Studies on synthesis of pyrazole from dibromo and hydrazine compounds. [PDF]
Depression has become the fourth leading case for mortality and morbidity in the world. It is a leading cause of disability worldwide and is a major contributor to the overall global burden of disease. Current treatments of depression are inadequate, and
Trivedi, Riya
core +1 more source
This review summarizes the synthetic methodologies of the nitro‐substituted Donor‐Acceptor cyclopropanes (NCPs). Particularly from nitroalkenes including the Michael Initiated Ring Closure and the Oxidative Ring Closure of Michael Adducts, from Diazo Compounds bearing Nitro Group, from Nitromethane and its Derivatives; and after Oxidation of ...
Andriani G. Chaidali +2 more
wiley +1 more source

