نتایج جستجو برای: benzyl pyridin 2 yl methylcarbamodithioate

تعداد نتایج: 2534431  

Journal: :Acta Crystallographica Section E Structure Reports Online 2014

Journal: :Acta Crystallographica Section E Crystallographic Communications 2015

Journal: :Dalton transactions 2008
Zhengliang Lu José Sánchez Costa Olivier Roubeau Ilpo Mutikainen Urho Turpeinen Simon J Teat Patrick Gamez Jan Reedijk

A new bifunctional, triazine-based ligand has been designed with the aim to generate a copper(II) complex holding a TEMPO (2,2,6,6-tetramethylpiperidinyloxy) moiety. The coordination compound obtained from the ligand 4-(2-(3-(pyridin-2-yl)-1H-pyrazol-1-yl)ethoxy)-6-(4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl)-N,N-diphenyl-1,3,5-triazin-2-amine (pypzt-1) and copper(II) bromide (i.e. complex 8)...

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2008
Tapan K Nayak Helen J Hathaway Chinnasamy Ramesh Jeffrey B Arterburn Donghai Dai Larry A Sklar Jeffrey P Norenberg Eric R Prossnitz

UNLABELLED Breast and endometrial cancers are the most common invasive malignancies in women, with more than 217,000 new diagnoses per year in the United States. These cancers are often classified into 2 subtypes based on the expression of the classical estrogen receptor. In this study, we describe a new structural class of neutral tridentate 99mTc(I)-estradiol-pyridin-2-yl hydrazine derivative...

2014
Lukas K. Filak Danuta S. Kalinowski Theresa J. Bauer Des R. Richardson Vladimir B. Arion

In this study, the indoloquinoline backbone and piperazine were combined to prepare indoloquinoline-piperazine hybrids and their ruthenium- and osmium-arene complexes in an effort to generate novel antitumor agents with improved aqueous solubility. In addition, the position of the metal-binding unit was varied, and the effect of these structural alterations on the aqueous solubility and antipro...

Journal: :Acta Crystallographica Section E Structure Reports Online 2012

Journal: :The Journal of pharmacology and experimental therapeutics 2009
Daniel S Lorrain Gretchen Bain Lucia D Correa Charles Chapman Alex R Broadhead Angelina M Santini Pat Prodanovich Janice V Darlington John H Hutchinson Christopher King Catherine Lee Christopher Baccei Yiwei Li Jeannie M Arruda Jilly F Evans

Leukotrienes (LTs) are proinflammatory lipid mediators synthesized by the conversion of arachidonic acid (AA) to LTA(4) by the enzyme 5-lipoxygenase (5-LO) in the presence of 5-LO-activating protein (FLAP). 3-[3-tert-Butylsulfanyl-1-[4-(6-methoxy-pyridin-3-yl)-benzyl]-5-(pyridin-2-ylmethoxy)-1H-indol-2-yl]-2,2-dimethyl-propionic acid (AM103) is a novel selective FLAP inhibitor in development fo...

Journal: :Acta Crystallographica Section E Structure Reports Online 2011

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