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Chemical name: Biotinyl-N-propargylamide // Synonyms: 5‐[(3aS,4S,6aR)‐2‐oxohexahydro‐1H‐thieno[3,4‐d]imidazol‐4‐yl]‐N‐(prop‐2‐yn‐1‐yl)pentanamide, Biotin alkyne, Biotin propargylamide, N-Propargylbiotinamide
|Molecular weight:||281,37 g/mol|
Used as a biotinylation reagent that can be attached using Click-chemistry.
An Entry of the Chemoselective Sulfo-Click Reaction into the Sphere of Nucleic Acids; G. Clave, E. Dursun, J. J. Vasseur and M. Smietana; Org Lett 2020; 22: 1914-1918. https://doi.org/10.1021/acs.orglett.0c00265
Dynamic and Functional Profiling of Xylan-Degrading Enzymes in Aspergillus Secretomes Using Activity-Based Probes; S. P. Schroder, C. de Boer, N. G. S. McGregor, R. J. Rowland, O. Moroz, E. Blagova, J. Reijngoud, M. Arentshorst, D. Osborn, M. D. Morant, E. Abbate, M. A. Stringer, K. Krogh, L. Raich, C. Rovira, J. G. Berrin, G. P. van Wezel, A. F. J. Ram, B. I. Florea, G. A. van der Marel, J. D. C. Codee, K. S. Wilson, L. Wu, G. J. Davies and H. S. Overkleeft; ACS Cent Sci 2019; 5: 1067-1078. https://doi.org/10.1021/acscentsci.9b00221
Site-Specific Modification of Proteins through N-Terminal Azide Labeling and a Chelation-Assisted CuAAC Reaction; N. Inoue, A. Onoda and T. Hayashi; Bioconjug Chem 2019; 30: 2427-2434. https://doi.org/10.1021/acs.bioconjchem.9b00515
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