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Nombre químico: N-Biotinyl-N’-cysteinyl ethylenediamine*TFA // Sinónimos: Biotin-NH-CH2-CH2-NH-Cys*TFA, N-(2-((R)-2-amino-3-mercaptopropanamido)ethyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide
from 200,00 €
Multicomponent Oxidative Nitrile Thiazolidination Reaction for Selective Modification of N-terminal Dimethylation Posttranslational Modification; B. Emenike, J. Donovan, M. Raj; J. Am. Chem. Soc. 2023; 145(30): 16417-16428. https://doi.org/10.1021/jacs.3c02369
Semisynthesis of Functional Glycosylphosphatidylinositol-Anchored Proteins; R. F. Roller, A. Malik, M. A. Carillo, M. Garg, A. Rella, M.-K. Raulf, B. Lepenies, P. H. Seeberger, D. V. Silva; Angew. Chem. Int. Ed. 2020; 59(29): 12035-12040. https://doi.org/10.1002/anie.202002479
Synthesis and application of cNGR-containing imaging agents for detection of angiogenesis; I. Dijkgraaf, P. van de Vijver, A. Dirksen, T. M. Hackeng; Bioorg. Med. Chem. 2013; 21(12): 3555-3564. https://doi.org/10.1016/j.bmc.2013.04.002
A supramolecular approach to multivalent target-specific MRI contrast agents for angiogenesis; A. Dirksen, S. Langereis, B. F. M. de Waal, M. H. O. van Genderen, T. M. Hackeng, E. W. Meijer; Chem. Commun. 2005. 2811-2813. https://doi.org/10.1039/B502347E
A ribozyme with Michaelase activity: Synthesis of the substrate precursors; A. Eisenführ, P. S. Arora, G. Sengle, L. R. Takaoka, J. S. Nowick, M. Famulok; Bioorg. Med. Chem. 2003; 11(2): 235-249. https://doi.org/10.1016/S0968-0896(02)00311-5
Novel RNA catalysts for the Michael reaction; G. Sengle, A. Eisenführ, P. S. Arora, J. S. Nowick; Chem. Biol. 2001; 8(5): 459-473. https://doi.org/10.1016/S1074-5521(01)00026-6
Intein-Mediated Synthesis of Proteins Containing Carbohydrates and Other Molecular Probes; T. J. Tolbert, C.-H. Wong; J. Am. Chem. Soc. 2000; 122(23): 5421–5428. https://doi.org/10.1021/ja0000192
