| Code | Name | Synonym |
| ET-127 | Azido diglycine.DCHA | N-(2-azidoacetyl)-glycine DCHA salt // azido diglycine DCHA salt // azido glycylglycine DCHA salt // N3-diglycine.DCHA // 2-(2-azidoacetamido)acetic acid dicyclohexylamine salt |
| CAS | 855750-87-7 (net) |  |
| Formula | C16H29N5O3 | |
| MW | 339.4 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Note | N3-Gly-Gly is used as a linker that can be further modified at the azido-position using Staudinger ligation or Click-chemistry. ACS Macro Letters (2014), 3(3), 291-294. DOI:10.1021/mz5000575. | |
| Code | Name | Synonym |
| ET-128 | Azido triglycine | N-(2-azidoacetyl)-glycylglycine // azido triglycine // azido glycylglycylglycine // N3-triglycine // 2-[2-(2-azidoacetamido)acetamido]acetic acid |
| CAS | 1993176-75-2 |  |
| Formula | C6H9N5O4 | |
| MW | 215.2 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Note | N3-Gly-Gly-Gly is used as a linker that can be further modified at the azido-position using Staudinger ligation or Click-chemistry. | |
| Code | Name | Synonym |
| ET-130 | Azido pentaglycine | azidoacetyl tetraglycine // N3-Gly-Gly-Gly-Gly-Gly-OH // N3-(Gly)5-OH // N3-GGGGG-OH // 2-(2-{2-[2-(2-azidoacetamido)acetamido]acetamido}acetamido)acetic acid |
| CAS |  |
|
| Formula | C10H15N7O6 | |
| MW | 329.3 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Code | Name | Synonym |
| AA-143 | H-Pro(4-N3).HCl (2R,4S) | (4S)-4-Azido-D-proline // (2R,4S)-4-azidopyrrolidine-2-carboxylic acid hydrochloride |
| CAS | 2137086-50-9 |  |
| Formula | C5H9ClN4O2 | |
| MW | 192.6 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Note | H-Pro(4-N3) is incorporated into peptides and proteins that can be further selectively modified using Staudinger ligation or Click-chemistry. | |
| 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 |  |
| 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 |
| PE-012 | Fmoc-D-Lys(Palm-Glu-OtBu) | Fmoc-D-Lys(Pal-Glu-OtBu)-OH // Fmoc-D-Lys(palmitoyl-Glu-OtBu)-OH |
| CAS |  |
|
| Formula | C46H69N3O8 | |
| MW | 792.1 | |
| Purity | >98% | |
| Storage | +2 ... +8 °C | |
| Note | Used in solid-phase peptide synthesis to introduce Liraglutide side-chain. | |
| Code | Name | Synonym |
| AA-151 | H-D-Phe(4-N3).HCl | 4-Azido-D-phenylalanine hydrochloride // 3-(p-Azidophenyl)-D-alanine Hydrochloride // D-4-Azidophenylalanine Hydrochloride // p-Azido-D-phenylalanine Hydrochloride // D-p-Azidophenylalanine Hydrochloride // H-4-Azido-D-Phe.HCl // D-Phe(pN3).HCl // para-azido-D-Phe.HCl |
| CAS | 1241681-80-0 net |  |
| Formula | C9H11ClN4O2 | |
| MW | 242.7 | |
| Purity | >98% | |
| Storage | -15 ... -25°C | |
| Note | H-D-Phe(4-N3).HCl is used in protein and peptide synthesis as unnatural amino acid. The azido-funcionality can be further utilized to cross-link various functionalities to proteins utilizing click-chemistry. Chang, Tse-Wen; Chu, Hsing-Mao; Chen, Jou-Han; Lin, Chun-Yu; Lin, Chien-Jen PCT Int. Appl. (2016), WO 2016112870 A1; U.S. (2018), US 9994638 B2; U.S. (2018), US 9988454 B2. | |
| Code | Name | Synonym |
| SU-002 | H-Ala-AMC.TFA | L-Alanine 7-amido-4-methylcoumarin trifluoroacetate salt |
| CAS | 96594-10-4, 77471-41-1 net |  |
| Formula | C15H15F3N2O5 | |
| MW | 360.3 | |
| Purity | >99% | |
| Storage | +2 ... +8 °C | |
| Code | Name | Synonym |
| SU-006 | H-Ala-pNA.HCl | H-L-Ala-pNA.HCl // L-2-amino-4'-nitropropionanilide hydrochloride // L-alanine-4-nitroanilide hydrochloride // L-alanine-p-nitroanilide hydrochloride // L-alanyl-p-nitroanilide, hydrochloride // alanine-pNA.HCl // alanine-p-nitroanilide hydrochloride // Ala-pNA.HCl |
| CAS | 31796-55-1 , 1668-13-9 net |  |
| Formula | C9H12ClN3O3 | |
| MW | 254.7 | |
| Purity | >99% | |
| Storage | +2 ... +8 °C | |
| Code | Name | Synonym |
| SU-054 | H-Ala-Ala-Phe-pNA | Ala-Ala-Phe p-nitroanilide |
| CAS | 61043-41-2 |  |
| Formula | C21H25N5O5 | |
| MW | 427.5 | |
| Purity | >99% | |
| Storage | +2 ... +8 °C | |
| Note | Used as enzyme substrate and in the synthesis of various enzyme substrates. Journal of Biological Chemistry (1985), 260(23), 12600-6; Journal of Biological Chemistry (2004), 279(49), 51275-51281. DOI:10.1074/jbc.M409455200; Biomacromolecules (2015), 16(1), 411-421. DOI:10.1021/bm501671r. |
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