N3-PEG(3)-NH-Suc

Chemical name: 1-azido-13-oxo-3,6,9-trioxa-12-azahexadecan-16-oic acid // Synonyms: N3-PEG3-NH-Suc, N3-PEG3-NH-Suc-OH, N3-PEG(3)-NHSuc, 11-azido-3,6,9-trioxaundecan-1-N-Succinoyl, SucNH-PEG3-CH2CH2N3, Succinoyl-N-Amido-PEG3-azide,1-azido-3,6,9-trioxaundecan-11-N-Succinoyl

  • Product code:RL-4320
  • CAS No.:1202400-17-6
  • Formula:C12H22N4O6
  • Storage temperature:-20°C
  • Molecular weight:318,33 g/mol
  • Purity :min.98,0%

from €108.00

Grouped product items
Qty Packing unit Price SKU Availability
500 mg
€108.00
RL-4320.0500
Please inquire
1 g
€168.00
RL-4320.1000
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5 g
€600.00
RL-4320.5000
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25 g
€2,400.00
RL-4320.9025
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description

Carboxylic-acid and azide containing PEG-linker that can be used in Click-chemistry.

references

Induction of apoptosis in MDA-MB-231 breast cancer cells by a PARP1-targeting PROTAC small molecule; Q. Zhao, T. Lan, S. Su, Y. Rao; Chem. Commun. 2019, 55: 369-372. https://doi.org/10.1039/C8CC07813K

Design, Synthesis, and Biological Evaluations of Tumor-Targeting Dual-Warhead Conjugates for a Taxoid–Camptothecin Combination Chemotherapy; J. G. Vineberg, E. S. Zuniga, A. Kamath, Y. J. Chen, J. D. Seitz, I. Ojima; J. Med. Chem. 2014, 57(13): 5777–5791. https://doi.org/10.1021/jm500631u

Polymer Multilayer Films Obtained by Electrochemically Catalyzed Click Chemistry; G. Rydzek, J. S. Thomann, N. B. Ameur, L. Jierry, P. Mesini, A. Ponche, C. Contal, A. E. El Haitami, J. C. Voegel, B. Senger, P. Schaaf, B. Frisch, F. Boulmedais; Langmuir 2010, 26(4): 2816–2824. https://doi.org/10.1021/la902874k

Carbon dot-based fluorescent antibody nanoprobes as brain tumour glioblastoma diagnostics; M. Ghirardello, R. Shyam, X. Liu, T. Garcia-Millan, I. Sittel, J. Ramos-Soriano, K. M. Kurian, M. C. Galan; Nanoscale Adv. 2022, 4: 1770-1778. https://doi.org/10.1039/D2NA00060A

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