نتایج جستجو برای: dihydropyridine

تعداد نتایج: 2508  

Journal: :Chemical science 2017
Darrin M Flanigan Tomislav Rovis

NHC-catalyzed nucleophilic dearomatization of alkyl pyridiniums has been achieved to generate 1,4-dihydropyridines with high enantioselectivity. This is a rare example of catalytic, asymmetric addition of a nucleophile to the activated pyridinium that prefers C-4 functionalization leading to the 1,4-dihydropyridine with high selectivity.

2010
Heloise Brice Jonathan Clayden Stuart D Hamilton

The silyl enol ether derivatives of ketones or esters tethered by a hydrocarbon or ether linkage to the 3-position of a pyridine ring undergo dearomatising nucleophilic attack on the ring once it is activated (as an acylpyridinium species) by the addition of methyl chloroformate. The bicyclic dihydropyridine products are in some cases unstable, but may be isolated after hydrogenation as fused b...

Journal: :iranian journal of pharmaceutical research 0
afshin zarghi shahid beheshti univ. med. sci. iman sabakhi department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences vigen topuzyan the scientific thechnological centre of organic and pharmaceutical chemistry nasraal. mnjoyan institute of fine organic chemistry, yerevan, armenia. zahra hajimahdi department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences bahram daraei department of toxicology, faculty of medical sciences, tarbiat modares university hadi arefi department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran.

as a continuous research for discovery of new cox-2 inhibitors, chemical synthesis, in vitro biological activity and molecular docking study of anew group of 1,4-dihydropyridine (dhp) derivatives were presented. novel synthesized compounds possessing a cox-2 so2me pharmacophore at the para position of c-4 phenyl ring, different hydrophobic groups (r1) at c-2 position and alkoxycarbonyl groups (...

Journal: :Acta Crystallographica Section E Structure Reports Online 2009

Journal: :Oxidative Medicine and Cellular Longevity 2017

Journal: :Circulation research 1987
A C Maan M M Hosey

The interaction of 1,4-dihydropyridine derivatives with their receptors on voltage-dependent calcium channels in cardiac membranes was studied to determine if there are basic differences in the binding properties of ligands that cause inhibition or activation of calcium channels. The binding characteristics of 6 pure stereoisomers, (-) and (+)202-791, (-) and (+)Bay k 8644, (-) and (+)PN 200-11...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2006
Valérie De Crescenzo Kevin E Fogarty Ronghua Zhuge Richard A Tuft Lawrence M Lifshitz Jeffrey Carmichael Karl D Bellvé Stephen P Baker S Zissimopoulos F Anthony Lai José R Lemos John V Walsh

Ca2+ stores were studied in a preparation of freshly dissociated terminals from hypothalamic magnocellular neurons. Depolarization from a holding level of -80 mV in the absence of extracellular Ca2+ elicited Ca2+ release from intraterminal stores, a ryanodine-sensitive process designated as voltage-induced Ca2+ release (VICaR). The release took one of two forms: an increase in the frequency but...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1985
M C Nowycky A P Fox R W Tsien

A large-conductance calcium channel in chicken dorsal root ganglion neurons was studied with patch-clamp recordings of unitary currents. In addition to the conventional pattern of Ca-channel gating previously described in neurons ("mode 1"), we observed a different form of gating behavior ("mode 2"). Unlike the brief (approximately equal to 1 ms) openings in mode 1, mode 2 openings tend to be l...

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