H-L-Phe(4-MeTz)-OH*TFA

Nombre químico: (S)-2-amino-3-(4-(6-methyl-1,2,4,5-tetrazin-3-yl)phenyl)propanoic acid trifluoroacetic acid salt // Sinónimos: H-Phe(4-MeTz)-OH*TFA, Methyltetrazin phenylalanine trifluoroacetate

  • Nº Artículo:HAA9470
  • Nº CAS:1698038-85-5 net
  • Fórmula:C12H13N5O2*CF3COOH
  • Storage temperature:-20°C
  • Masa molecular:259,27*114,02 g/mol

from 200,00 €

Grouped product items
Cantidad Unidad de venta Precio Unidad de almacenamiento de stock (SKU) Disponibilidad
25 mg
200,00 €
HAA9470.0025
peticón
100 mg
600,00 €
HAA9470.0100
peticón
references

Ideal Bioorthogonal Reactions Using A Site-Specifically Encoded Tetrazine Amino Acid; R. J. Blizzard, D. R. Backus, W. Brown, C. G. Bazewicz, Y. Li, R. A. Mehl; J. Am. Chem. Soc. 2015; 137(32): 10044-10047. https://doi.org/10.1021/jacs.5b03275


Bicyclo[6.1.0]nonyne and tetrazine amino acids for Diels–Alder reactions; X. Li, T. Liu, S. Dong; RSC Adv. 2017; 7: 44470-44473. https://doi.org/10.1039/C7RA08136G


Computationally guided discovery of a reactive, hydrophilic trans-5-oxocene dienophile for bioorthogonal labeling; W. D. Lambert, S. L. Scinto, O. Dmitrenko, S. J. Boyd, R. Magboo, R. A. Mehl, J. W. Chin, J. M. Fox, S. Wallace; Org. Biomol. Chem. 2017; 15: 6640-6644. https://doi.org/10.1039/C7OB01707C


Cellular interactions with hydrogel microfibers synthesized via interfacial tetrazine ligation; S. Liu, A. C. Moore, A. B. Zerdoum, H. Zhang, S. L. Scinto, H. Zhang, L. Gong, D. L. Burris, A. K. Rajasekaran, J. M. Fox, X. Jia; Biomaterials 2018; 180: 24-35. https://doi.org/10.1016/j.biomaterials.2018.06.042


Engineering Heterodimeric Kinesins through Genetic Incorporation of Noncanonical Amino Acids; A. R. Popchock, S. Jana, R. A. Mehl, W. Qiu; ACS Chem. Biol. 2018; 13(8): 2229-2236. https://doi.org/10.1021/acschembio.8b00399


Immobilization of Proteins with Controlled Load and Orientation; R. M. Bednar, T. W. Golbek, K. M. Kean, W. J. Brown, S. Jana, J. E. Baio, P. A. Karplus, R. A. Mehl; ACS Appl. Mater. Interfaces 2019; 11(40): 36391-36398. https://doi.org/10.1021/acsami.9b12746


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