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(2S,4R)-1-((S)-23-azido-2-(tert-butyl)-4-oxo-6,9,12,15,18,21-hexaoxa-3-azatricosanoyl)-4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide
ACAZNH420
2086298-71-5
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Azides (126)
Azide click chemistry is a chemical reaction that creates a stable triazole bond by combining azides and alkynes under gentle conditions. It is extensively utilized in biomolecule labeling, drug delivery, and bioimaging because of its mild conditions, rapid reaction rate, and excellent biocompatibility.
(3R,4R,5R,6R)-3-acetamido-6-(azidomethyl)tetrahydro-2H-pyran-2,4,5-triyl triacetate
ACKSIO524
487027-19-0
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73-azido-2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47,50,53,56,59,62,65,68,71-tetracosaoxatriheptacontane
ACNGTA841
2563873-82-3
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23-azido-3,6,9,12,15,18,21-heptaoxatricosyl 4-methylbenzenesulfonate
ACVMIT624
857892-34-3
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N,N'-(disulfanediylbis(ethane-2,1-diyl))bis(4-azido-2-hydroxybenzamide)
ACRANV084
199804-21-2
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(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(2-azidoethoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
ACJARX297
140428-81-5
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2-((1E,3E)-5-((E)-1-(6-((3-azidopropyl)amino)-6-oxohexyl)-3,3-dimethyl-5-sulfoindolin-2-ylidene)penta-1,3-dien-1-yl)-1,3,3-trimethyl-3H-indol-1-ium-5-sulfonate
ACGVSQ950
1481447-40-8
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Total: 7