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Code Name Synonym
BO-149 Boc-Pro(4-N3).DCHA (2R, 4S) (2R,4S)-4-azido-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid // Boc-(2R,4S )-4-azidoproline // Boc-4-azidoproline
CAS 132622-77-6 net /upload/more_svg/small/small_BO-149.svg
Formula C22H39N5O4
MW 437.6
Purity >98%
Storage +2 ... +8 °C
Note Boc-Pro(4-N3) is incorporated into peptides and proteins that can be further selectively modified using Staudinger ligation or Click-chemistry. The Azido-group can be reduced to amino-group. J. Org. Chem. (1991), 56(9), 3009-16. DOI:10.1021/jo00009a016; Bioorg. Med. Chem. Lett. (2003), 13(23), 4241-4244. DOI:10.1016/j.bmcl.2003.07.030.
Code Name Synonym
BO-138 Boc-Pro(4-N3) (2S,4R).DCHA (2S,4R)-4-azido-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid // Boc-(2S,4R )-4-azidoproline // Boc-4-azidoproline // Boc-Azp
CAS 132622-68-5 net /upload/more_svg/small/small_BO-138.svg
Formula C22H39N5O4
MW 437.6
Purity >98%
Storage +2 ... +8 °C
Note Boc-Pro(4-N3) is incorporated into peptides and proteins that can be further selectively modified using Staudinger ligation or Click-chemistry. The Azido-group can be reduced to amino-group. J. Am. Chem. Soc. (2012), 134(41), 17117-17124. DOI:10.1021/ja3066418; J. Med. Chem. (2012), 55(22), 9856-9867. DOI:10.1021/jm301060g.
Code Name Synonym
FM-227 Fmoc-Pro(4-N3) (2R,4R) Fmoc-(2R, 4R)-4-azidoproline // (2R,4R)-Fmoc-gamma-azidoproline // Fmoc-Azp (2R,4R)
CAS 1378847-51-8 /upload/more_svg/small/small_fm-227.svg
Formula C20H18N4O4
MW 378.4
Purity >98%
Storage +2 ... +8 °C
Note Fmoc-Pro(4-N3) is incorporated into peptides and proteins that can be further selectively modified using Staudinger ligation or Click-chemistry. The Azido-group can be reduced to amino-group under neutral conditions.
Code Name Synonym
FM-177 Fmoc-Pro(4-N3) (2S,4S) Fmoc-(2S, 4S)-4-azidoproline // (2S,4S)-Fmoc-gamma-azidoproline // Fmoc-Azp (2S,4S) // Fmoc-4-azidoproline
CAS 263847-08-1 /upload/more_svg/small/small_FM-177.svg
Formula C20H18N4O4
MW 378.4
Purity >98%
Storage +2 ... +8 °C
Note Fmoc-Pro(4-N3) is incorporated into peptides and proteins that can be further selectively modified using Staudinger ligation or Click-chemistry. The Azido-group can be reduced to amino-group under neutral conditions. Angew. Chem. Int. Ed. (2010), 49(36), 6324-6327, S6324/1-S6324/23. DOI:10.1002/anie.201001851;
J. Am. Chem. Soc. (2013), 135(14), 5250-5253. DOI:10.1021/ja312143h; J. Med. Chem. (2018), 61(11), 5020-5033. DOI:10.1021/acs.jmedchem.8b00477.
Code Name Synonym
FM-182 Fmoc-Pro(4-N3) (2S,4R) Fmoc-(2S,4R)-4-azidoproline // (2S,4R)-Fmoc-gamma-azidoproline // Fmoc-Azp (2S,4R) // Fmoc-4-azidoproline
CAS 702679-55-8 /upload/more_svg/small/small_FM-182.svg
Formula C20H18N4O4
MW 378.4
Purity >98%
Storage +2 ... +8 °C
Note Fmoc-Pro(4-N3) is incorporated into peptides and proteins that can be further selectively modified using Staudinger ligation or Click-chemistry. The Azido-group can be reduced to amino-group under neutral conditions. Angew. Chem. Int. Ed. (2010), 49(36), 6324-6327. DOI:10.1002/anie.201001851; Nature Chem. (2017), 9(11), 1068-1072. DOI:10.1038/nchem.2823.
Code Name Synonym
FM-223 Fmoc-Pro(4-N3) (2R,4S) Fmoc-(2R,4S)-4-azidoproline // (2R,4S)-Fmoc-gamma-azidoproline // Fmoc-Azp (2R,4S) // Fmoc-4-azidoproline
CAS 2137142-63-1 /upload/more_svg/small/small_FM-223.svg
Formula C20H18N4O4
MW 378.4
Purity >98%
Storage +2 ... +8 °C
Note Fmoc-Pro(4-N3) is incorporated into peptides and proteins that can be further selectively modified using Staudinger ligation or Click-chemistry. The Azido-group can be reduced to amino-group under neutral conditions.
Code Name Synonym
ET-163 N3-C10H20-COOSu 2,5‐dioxopyrrolidin‐1‐yl 11‐azidoundecanoate // 11-azido undecanoic acid NHS ester // 11-azido undecanoic acid N-hydroxysuccinimide ester
CAS 850080-13-6 /upload/small/small_et-163.svg
Formula C15H24N4O4
MW 324.4
Purity >98% (HPLC)
Storage +2 ... +8 °C
Note Used as a hydrophobic bioconjugation linker that can be further modified at the azido-position using Staudinger ligation or Click-chemistry. Bundle, D. R. et al Organic & Biomolecular Chem. (2006), 4(1), 142-154. DOI:10.1039/B513595H; Liu, J.-N. et al Biomacromolecules (2009), 10(4), 877-883. DOI:10.1021/bm8014076; Zundel, M. A. et al PCT Int. Appl. (2005), WO 2005035553.
Code Name Synonym
AA-123 H-Dap(N3).HCl L-beta-azidoalanine.HCl // L-Aza.HCl // L-Dpr(N3).HCl // 2-(S)-amino-3-azidopropionic acid // hydrochloride // L-Ala(N3).HCl // 2-(S)-amino-3-azidopropanoic acid
CAS 105661-40-3 net /upload/more_svg/small/small_AA-123.svg
Formula C3H7ClN4O2
MW 166.6
Purity >98%
Storage +2 ... +8 °C
Note H-Dap(N3) is incorporated into proteins that can be further selectively modified using Staudinger ligation or Click-chemistry. Proc. Natl. Acad. Sci. USA, DOI:10.1073/pnas.012583299; J. Am. Chem. Soc. (2004), 126(34), 10598-10602. DOI:10.1021/ja047629c; PCT Int. Appl. (2018), WO 2018219619 A1; U.S. (2018), US 9975951 B2.
Code Name Synonym
AA-124 H-D-Dap(N3).HCl D-beta-azidoalanine.HCl // D-beta-azidoalanine.HCl // D-Aza.HCl // D-Dpr(N3).HCl // 2-(R)-amino-3-azidopropionic acid.HCl // 2-(R)-amino-3-azidopropanoic acid // D-Ala(N3).HCl
CAS 1379690-01-3
105928-88-9 net
/upload/more_svg/small/small_AA-124.svg
Formula C3H7ClN4O2
MW 166.6
Purity >98%
Storage +2 ... +8 °C
Note H-D-Dap(N3) is incorporated into peptides and proteins that can be further selectively modified using Staudinger ligation or Click-chemistry. Angew. Chem. Int. Ed. (2012), 51(50), 12519-12523. DOI:10.1002/anie.201206749; Bioconjugate Chem. (2016), 27(5), 1222-1226. DOI:10.1021/acs.bioconjchem.6b00063.
Code Name Synonym
DD-162 Boc-Dap(N3) CHA salt N-alpha-Boc-N-beta-azido-L-2,3-diaminopropionic acid cyclohexylamine salt // Boc-L-beta-azidoalanine CHA salt // Boc-L-beta-azidoalanine CHA salt // Boc-Dap(N3).CHA // Boc-Dpr(N3).CHA // Boc-Dapa(N3).CHA
CAS 122225-54-1 net /upload/more_svg/small/small_DD-162.svg
Formula C14H27N5O4
MW 329.4
Purity >99%
Storage +2 ... +8 °C
Note Boc-Dap(N3) is incorporated into peptides and proteins that can be further selectively modified using Staudinger ligation or Click-chemistry. J. Am. Chem. Soc. (2006), 128(47), 15096-15097. DOI:10.1021/ja066779f; J. Am. Chem. Soc. (2010), 132(41), 14327-14329. DOI:10.1021/ja104393t; European J. Med. Chem. (2018), 145, 661-672. DOI:10.1016/j.ejmech.2018.01.022.

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