1994331-17-7
![N6-[(2-Azidoethoxy)carbonyl]-L-lysine hydrochloride Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-111434a.gif "N6-[(2-Azidoethoxy)carbonyl]-L-lysine hydrochloride Chemical Structure")
Chemical Structure
N6-[(2-Azidoethoxy)carbonyl]-L-lysine hydrochloride
Synonym(s): UAA crosslinker 1 hydrochloride
- CAS No.: 1994331-17-7
- Formula:C9H18ClN5O4
- Molecular Weight:295.72
IUPAC Name: N6-((2-azidoethoxy)carbonyl)-L-lysine hydrochloride
InChIKey: USQKPJVGUFZIJQ-FJXQXJEOSA-N
SMILES: N[C@@H](CCCCNC(OCCN=[N+]=[N-])=O)C(O)=O.[H]Cl
Biological Activity: N6-[(2-Azidoethoxy)carbonyl]-L-lysine hydrochloride (UAA crosslinker 1 hydrochloride) is a click chemistry-reactive amino acid derivative. N6-[(2-Azidoethoxy)carbonyl]-L-lysine hydrochloride mediates the generation of antibody-drug conjugates (ADCs). N6-[(2-Azidoethoxy)carbonyl]-L-lysine hydrochloride is used for site-specific incorporation into recombinant proteins, or for synthesizing chemical probes and tools for biological research[1].
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N6-[(2-Azidoethoxy)carbonyl]-L-lysine hydrochloride | 98.0% | N6-[(2-Azidoethoxy)carbonyl]-L-lysine hydrochloride (UAA crosslinker 1 hydrochloride) is a click chemistry-reactive amino acid derivative. N6-[(2-Azidoethoxy)carbonyl]-L-lysine hydrochloride mediates the generation of antibody-drug conjugates (ADCs). N6-[(2-Azidoethoxy)carbonyl]-L-lysine hydrochloride is used for site-specific incorporation into recombinant proteins, or for synthesizing chemical probes and tools for biological research. | ||||||||||||||||||||
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