نتایج جستجو برای: ligand urea

تعداد نتایج: 144786  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه علوم کشاورزی و منابع طبیعی گرگان - دانشکده علوم کشاورزی 1392

تاثیر لیپاز و پروتئاز استارتری در تسریع رسیدن و توسعه عطر و طعم پنیر فتای فراپالایش بررسی شد. آنزیم های حاصل از تجزیه سلولی لاکتوباسیلوس پلانتاروم به وسیله التراسوند در 2 غلظت 5/2 میلی لیتر در لیتر و 5 میلی لیتر در لیتر و لیپاز ریزوموکورمهی در 2 غلظت12/0 گرم در لیتر و 24/0 گرم در لیتر به رتنتیت افزوده شدند. خصوصیات فیزیکوشیمیایی نمونه ها در روزهای 15، 30، 45 و 60 آنالیز شـد. بررسـی فرایند پروتئ...

2014
Min Li Weng Ieong Tou Hong Zhou Fei Li Huiwen Ren Calvin Yu-Chian Chen Baoxue Yang

Urea transporter B (UT-B) is a membrane channel protein that specifically transports urea. UT-B null mouse exhibited urea selective urine concentrating ability deficiency, which suggests the potential clinical applications of the UT-B inhibitors as novel diuretics. Primary high-throughput virtual screening (HTVS) of 50000 small-molecular drug-like compounds identified 2319 hit compounds. These ...

2011
R. Alan Howie Geraldo M. de Lima Edward R. T. Tiekink James L. Wardell Solange M. S. V. Wardell

The Sn atom in the title compound, [Sn(C(3)H(6)NO)Cl(3)(CH(4)N(2)O)], is octa-hedrally coordinated within a CCl(3)NO donor set provided by a chelating amido-ethyl ligand (C and O), a urea-O atom and three facially arranged Cl atoms. Systematic variations in the Sn-Cl bond distances are correlated with the relative trans influence exerted by the C and carbonyl-O atoms. The three-dimensional crys...

2018
Michael R. Michaelides Arthur Kluge Michael Patane John H. Van Drie Ce Wang T. Matthew Hansen Roberto M. Risi Robert Mantei Carmen Hertel Kannan Karukurichi Alexandre Nesterov David McElligott Peter de Vries J. William Langston Philip A. Cole Ronen Marmorstein Hong Liu Loren Lasko Kenneth D. Bromberg Albert Lai Edward A. Kesicki

p300 and its paralog CBP can acetylate histones and other proteins and have been implicated in a number of diseases characterized by aberrant gene activation, such as cancer. A novel, highly selective, orally bioavailable histone acetyltransferase (HAT) domain inhibitor has been identified through virtual ligand screening and subsequent optimization of a unique hydantoin screening hit. Conforma...

2017
Arunpatcha Nimthong-Roldán Paramee Sripa Yupa Wattanakanjana

In the title compound, [AgCl(C7H7N3O2S)(C18H15P)2], the AgI ion is in a distorted tetra-hedral coordination environment formed by P atoms from two tri-phenyl-phosphane ligands, one terminal S atom from the 1-(4-nitro-phen-yl)thio-urea ligand and a chloride ion. In the crystal, bifurcated (N-H)2⋯Cl hydrogen bonds [with graph-set motif R21(6)] connect complex mol-ecules, forming zigzag chains alo...

2017
Arunpatcha Nimthong-Roldán Nichakan Promsuwhan Walailak Puetpaiboon Yupa Wattanakanjana

The mononuclear mixed-ligand title complex, [CuCl(C7H7N3O2S)(C18H15P)2], displays a distorted tetra-hedral coordination sphere around the CuI atom, with two P atoms from two tri-phenyl-phosphane mol-ecules, one terminal S atom from a 1-(4-nitro-phen-yl)thio-urea mol-ecule and a chloride ion as ligands. An intra-molecular N-H⋯Cl hydrogen bond stabilizes the mol-ecular conformation [graph-set mot...

2009
Latipah La-o Chaveng Pakawatchai Saowanit Saithong Brian W. Skelton

The title compound, [CuCl(C(3)H(8)N(2)S)(C(18)H(15)P)(2)]·0.5CH(3)CN, was prepared by the reaction of copper(I) chloride with 1,3-dimethyl-thio-urea (dmtu) and triphenyl-phosphine (PPh(3)) in acetonitrile. The Cu(I) atom has a distorted tetra-hedral environment formed by two P atoms from triphenyl-phosphine, one S atom from the dmtu ligand and one Cl atom. In addition, the mol-ecules exhibit in...

Journal: :Molecular pharmacology 2011
Petra de Kruijf Herman D Lim Luc Roumen Véronique A Renjaän Jiuqiao Zhao Maria L Webb Douglas S Auld Jac C H M Wijkmans Guido J R Zaman Martine J Smit Chris de Graaf Rob Leurs

We have shown previously that different chemical classes of small-molecule antagonists of the human chemokine CXCR2 receptor interact with distinct binding sites of the receptor. Although an intracellular binding site for diarylurea CXCR2 antagonists, such as N-(2-bromophenyl)-N'-(7-cyano-1H-benzotriazol-4-yl)urea (SB265610), and thiazolopyrimidine compounds was recently mapped by mutagenesis s...

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