Search results for "DamID"

showing 10 items of 73 documents

CCDC 1541820: Experimental Crystal Structure Determination

2017

Related Article: Svetlana A. Katkova, Mikhail A. Kinzhalov, Peter M. Tolstoy, Alexander S. Novikov, Vadim P. Boyarskiy, Anastasiia Yu. Ananyan, Pavel V. Gushchin, Matti Haukka, Andrey A. Zolotarev, Alexander Yu. Ivanov, Semen S. Zlotsky, Vadim Yu. Kukushkin|2017|Organometallics|36|4145|doi:10.1021/acs.organomet.7b00569

Space GroupCrystallographyCrystal SystemCrystal Structure{[(26-dimethylphenyl)amino][(NN'-diphenylcarbamimidoyl)imino]methyl}-{[(26-dimethylphenyl)imino](N'N''-diphenylcarbamimidamido)methyl}-platinum(ii)Cell ParametersExperimental 3D Coordinates
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CCDC 881315: Experimental Crystal Structure Determination

2013

Related Article: A.N.Chernyshev, N.A.Bokach, P.V.Gushchin, M.Haukka, V.Yu.Kukushkin|2012|Dalton Trans.|41|12857|doi:10.1039/c2dt30986f

Space GroupCrystallographyCrystal SystemTetrachloro-bis(N-(3-nitrophenyl)propanimidamide)-platinum(iv)Crystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1009524: Experimental Crystal Structure Determination

2015

Related Article: Pavel V. Gushchin, Maxim L. Kuznetsov, Matti Haukka, and Vadim Yu. Kukushkin|2014|J.Phys.Chem.A|118|9529|doi:10.1021/jp506256a

Space GroupCrystallographyCrystal Systembis(N-phenyl-N-(N'-phenylcarbamimidoyl-kappaN')piperidine-1-carboximidamide)-platinum(ii) dibromide methanol solvateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 966548: Experimental Crystal Structure Determination

2013

Related Article: Dmitrii S. Bolotin, Nadezhda A. Bokach, Andreii S. Kritchenkov, Matti Haukka, Vadim Yu. Kukushkin|2013|Inorg.Chem.|52|6378|doi:10.1021/ic4000878

Space GroupCrystallographyDichloro-(N-((4-methylphenyl)(piperidin-1-ylimino)methyl)piperidine-1-carboximidamide)-platinum nitromethane solvate monohydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 881319: Experimental Crystal Structure Determination

2013

Related Article: A.N.Chernyshev, N.A.Bokach, P.V.Gushchin, M.Haukka, V.Yu.Kukushkin|2012|Dalton Trans.|41|12857|doi:10.1039/c2dt30986f

Space GroupCrystallographyTetrachloro-(methyl propanimidoate)-(N-(3-nitrophenyl)propanimidamide)-platinum(iv)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1937786: Experimental Crystal Structure Determination

2019

Related Article: Florian Chotard, Rosita Lapenta, Anaëlle Bolley, Audrey Trommenschlager, Cédric Balan, Jérôme Bayardon, Raluca Malacea-Kabbara, Quentin Bonnin, Ewen Bodio, Hélène Cattey, Philippe Richard, Stefano Milione, Alfonso Grassi, Samuel Dagorne, Pierre Le Gendre|2019|Organometallics|38|4147|doi:10.1021/acs.organomet.9b00501

Space GroupCrystallographybis(mu-isopropoxo)-bis(N'-[(2-oxyphenyl)methyl]-NN-dimethylbenzenecarboximidamide)-di-zincCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 881317: Experimental Crystal Structure Determination

2013

Related Article: A.N.Chernyshev, N.A.Bokach, P.V.Gushchin, M.Haukka, V.Yu.Kukushkin|2012|Dalton Trans.|41|12857|doi:10.1039/c2dt30986f

Space GroupCrystallographytrichloro-(2-((1-(imino)propyl)amino)-4-nitrophenyl)-(N-(3-nitrophenyl)propanimidamide)-platinum(iv) monohydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2081829: Experimental Crystal Structure Determination

2021

Related Article: Alexandros A. Kitos, Diogo A. Gálico, Niki Mavragani, Raúl Castañeda, Jani O. Moilanen, Jaclyn L. Brusso, Muralee Murugesu|2021|Chem.Commun.|57|7818|doi:10.1039/D1CC02407H

Space GroupCrystallographytris(acetylacetonato)-(pyrimidine-2-carboximidamide)-dysprosiumCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Impact du système endocannabinoïdien sur la physiologie de l'obésité : effets de l'antagonisme des récepteurs CB1 sur le métabolisme glucido-lipidiqu…

2010

The endocannabinoïd system (ECS) is involved in many biological functions such as regulation of energy metabolism. Recently, several studies have shown an association between obesity and ECS overactivity. In addition, specific CB1R antagonists such as Rimonabant (SR141716) improved metabolic parameters in obese patients essentially through inactivation of central CB1R. However, peripheral CB1R inactivation could also contribute to the improvement of these parameters and it is this notion that we have studied. To this purpose, we tested the effects of SR141716 on obese mice in order to establish relationships between the ECS activity and lipid metabolism by looking more specifically to its r…

[SDV.SA]Life Sciences [q-bio]/Agricultural sciences[SDV.SA] Life Sciences [q-bio]/Agricultural sciences[SDV.MHEP] Life Sciences [q-bio]/Human health and pathologyStéatoseTissu adipeuxAnandamideMétabolisme glucido-lipidiqueEndocannabinoïde[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathologyCb1rNo english keywordsCb2rSystème endocannabinoïdienAdiponectineSr141716Foie[ SDV.SA ] Life Sciences [q-bio]/Agricultural sciences[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology
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Cyclic Sulfoximine and Sulfonimidamide Derivatives by Copper‐Catalyzed Cross‐Coupling Reactions with Elemental Sulfur

2023

Copper-catalyzed cross-coupling reactions of α-bromoaryl NH-sulfoximines with elemental sulfur lead to benzo[d][1,3,2]dithiazole-1-oxides, which represent a new class of three-dimensional heterocycles. The reactions proceed under mild conditions showing good functional group and heterocycle tolerance. By imination/oxidation, the initial cross-coupling products can be converted to unprecedented cyclic sulfonimidamides derivatives. Furthermore, a seven-membered heterocycle was obtained by a ruthenium-catalyzed ring-expansion with ethyl propiolate. peerReviewed

kemiallinen synteesicopper catalysissulfonimidamideskatalyytitcross-coupling reactionssulfoximineskatalyysirikkiyhdisteetkupariGeneral Chemistryheterosykliset yhdisteetrikkielemental sulfurAdvanced Synthesis & Catalysis
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