Search results for "Thiol"

showing 5 items of 485 documents

CCDC 863726: Experimental Crystal Structure Determination

2013

Related Article: G.A.Horley, G.Kociok-Kohn, K.C.Molloy, J.R.Castro, S.Morreale|2012|Z.Anorg.Allg.Chem.|638|1699|doi:10.1002/zaac.201200024

tris(2-(Dimethylamino)ethanethiolato)-antimonySpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 921190: Experimental Crystal Structure Determination

2013

Related Article: Pilar Amo-Ochoa, Simone S. Alexandre, Samira Hribesh, Miguel A. Galindo, Oscar Castillo, Carlos J. Gómez-García, Andrew R. Pike, José M. Soler, Andrew Houlton, Ross W. Harrington, William Clegg, Félix Zamora|2013|Inorg.Chem.|52|5290|doi:10.1021/ic400237h

tris(2-amino-9-pentofuranosyl-9H-purine-6-thiolato)-cobalt(iii) sesquihydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1814033: Experimental Crystal Structure Determination

2018

Related Article: Guocheng Deng, Sami Malola, Juanzhu Yan, Yingzi Han, Peng Yuan, Chaowei Zhao, Xiting Yuan, Shuichao Lin, Zichao Tang, Boon K. Teo, Hannu Häkkinen, Nanfeng Zheng|2018|Angew.Chem.,Int.Ed.|57|3421|doi:10.1002/anie.201800327

tris(mu-(2S4S)-(-)-24-bis(diphenylphosphino)pentane)-hexakis(mu-pyridine-2-thiolato)-di-copper-trideca-goldSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1814032: Experimental Crystal Structure Determination

2018

Related Article: Guocheng Deng, Sami Malola, Juanzhu Yan, Yingzi Han, Peng Yuan, Chaowei Zhao, Xiting Yuan, Shuichao Lin, Zichao Tang, Boon K. Teo, Hannu Häkkinen, Nanfeng Zheng|2018|Angew.Chem.,Int.Ed.|57|3421|doi:10.1002/anie.201800327

tris(mu-13-bis(diphenylphosphino)propane)-hexakis(mu-pyridine-2-thiolato)-di-copper-trideca-goldSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Dipeptidyl Enoates As Potent Rhodesain Inhibitors That Display a Dual Mode of Action

2015

Dipeptidyl enoates were prepared through a high-yielding two-step synthetic route. They have a dipeptidic structure with a 4-oxoenoate moiety as a warhead with multiple reactive sites. Dipeptidyl enoates were screened against rhodesain and human cathepsins B and L, and were found to be potent and selective inhibitors of rhodesain. Among them (S,E)-ethyl 5-((S)-2-{[(benzyloxy)carbonyl]amino}-3-phenylpropanamido)-7-methyl-4-oxooct-2-enoate (6) was the most potent, with an IC50 value of 16.4 nm and kinact/Ki=1.6×106 m−1 s−1 against rhodesain. These dipeptidyl enoates display a reversible mode of inhibition at very low concentrations and an irreversible mode at higher concentrations. Inhibition…

trypanosomiasisStereochemistrysleeping sicknessCathepsin LDrug Evaluation PreclinicalChemistry Techniques SyntheticInhibition kineticsCysteine Proteinase InhibitorsBiochemistryCathepsin BInhibitory Concentration 50Structure-Activity RelationshipinhibitorsDrug DiscoveryHumansMoietyMolecular Targeted TherapyGeneral Pharmacology Toxicology and PharmaceuticsIC50Volume concentrationrhodesainPharmacologyChemistryOrganic ChemistryDual modeDipeptidesTrypanocidal AgentsCombinatorial chemistryMolecular Docking SimulationCysteine EndopeptidasesKineticsdipeptidyl enoatesTrypanosomiasis AfricanDocking (molecular)Molecular MedicineCysteine thiolateChemMedChem
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