نتایج جستجو برای: 2 dimethylamino substituted dihydropyridines

تعداد نتایج: 2552240  

Journal: :Chemical & pharmaceutical bulletin 2002
Takeshi Koike Naoki Takeuchi

The reactions of sec-aminodienyl esters 3 with acetylacetone (4) afforded N-alkyl 3-acetyl-4-methoxycarbonylmethyl-2-methyl-1,4-dihydropyridines 5 and enamines 6, providing a new azaelectrocyclization reaction.

Journal: :Molecular pharmacology 2000
A Adams J M Guss C A Collyer W A Denny A S Prakash L P Wakelin

For a series of antitumor-active 5-substituted 9-aminoacridine-4-carboxamide topoisomerase II poisons, we have used X-ray crystallography and stopped-flow spectrophotometry to explore relationships between DNA binding kinetics, biological activity, and the structures of their DNA complexes. The structure of 5-F-9-amino-[N-(2-dimethylamino)ethyl]-acridine-4-carboxamide bound to d(CGTACG)(2) has ...

2001
William M. Davis Allen D. Hunter

The reaction of [Et3NHI[@-CO)Cu-RS)Fe2(C0)6] with bis(1-alkyny1)mercw-y compounds gave different products depending on the nature of the organomercurial. Bis(phenylethyny1)mercury and bis( 1-hexyny1)mercury gave p-q1:q2-acetylide complexes, @-q1:q2-CsCR1)@-RS)Fe2(CO)6, while bis(3-methoxy-1-propyny1)mercury and bis(3-(dimethylamino)-l-propynyl)mercury formed doubly bridging vinylcarbyne product...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1999
V Morisset F Nagy

Approximately 28% of dorsal horn neurons (DHNs) in lamina V of the rat spinal cord generate voltage-dependent plateau potentials underlying accelerating discharges and prolonged afterdischarges in response to steady current pulses or stimulation of nociceptive primary afferent fibers. Using intracellular recordings in a transverse slice preparation of the cervical spinal cord, we have analyzed ...

Journal: :Neuron 2007
David Sulzer Yvonne Schmitz

Pacemaking activity in adult substantia nigra (SN) dopamine neurons relies on L-type Ca2+ channels, but a surprising study in Nature by Chan et al. demonstrates that blockade of these channels by dihydropyridines re-establishes the pacemaking driven by sodium and HCN channels found in juvenile SN. This shift protects SN neurons in chemical models of Parkinson's disease (PD), suggesting that ele...

2003
Smeet Deshmukh Lev Bromberg

Facile, one-step synthesis of self-assembling, cationic block copolymers of poly(2-N-(dimethylaminoethyl) methacrylate) (pDMAEMA) and PEO-PPO-PEO (Pluronic®) is developed. The copolymers are obtained via free-radical polymerization of DMAEMA initiated by Pluronic-radicals generated by cerium (IV). The copolymers possess surface activity, are polycationic at pH<7.1, and self-assemble into micell...

Journal: :Dalton transactions 2012
Kenneth Hanson Luke Roskop Niral Patel Laurent Griffe Peter I Djurovich Mark S Gordon Mark E Thompson

A series of twelve platinum(II) complexes of the form (N^N^N)PtX have been synthesized and characterized where N^N^N is 1,3-bis(2-pyridylimino)isoindolate ligands (BPI) or BPI ligands whose aryl moieties are substituted with tert-butyl, nitro, alkoxy, iodo or chloro groups, and X is a chloride, fluoride, cyano, acetate, phenyl or 4-(dimethylamino)phenyl ligand. All complexes display at least on...

2006
Andreas Schmidt Thorsten Mordhorst

2,4-Dichloro-, 4,6-dichloro-, 2,4,6-trichloroand tetrachloropyrimidine undergo nucleophilic displacements by 4-(dimethylamino)pyridine to give (pyrimidine-2,4-diyl)-1,1’-bis[4-(dimethylamino)pyridinium] dichloride, (pyrimidine-4,6-diyl)-1,1’-bis[4-(dimethylamino)-pyridinium] dichloride, (pyrimidine-2,4,6-triyl)-1,1’,1”-tris[4-(dimethylamino)pyridinium] trichloride, and (5chloropyrimidine-2,4,6-...

Journal: :Chemical communications 2012
Lixin Li Wenchao Chen Wenguo Yang Yuanhang Pan Hongjun Liu Choon-Hong Tan Zhiyong Jiang

A bicyclic guanidine-catalyzed Michael addition of 3-benzyl substituted oxindoles to N-maleimides has been developed to produce oxindole derivatives with a quaternary carbon chiral center at the 3-position in excellent yields and enantio- and diastereoselectivities. This is the first incorporation of N-benzylic α-branched succinimides into 3,3-disubstituted oxindoles.

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