1. Click Chemistry
  2. BCN PROTAC Synthesis
  3. (Rac)-BCN-L-Lysine

(Rac)-BCN-L-Lysine is a Click Amino Acid that can be used as a linker in the synthesis of PROTAC molecules. (Rac)-BCN-L-Lysine contains a BCN group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

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(Rac)-BCN-L-Lysine Chemical Structure

(Rac)-BCN-L-Lysine Chemical Structure

CAS No. : 1580501-90-1

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Description

(Rac)-BCN-L-Lysine is a Click Amino Acid that can be used as a linker in the synthesis of PROTAC molecules. (Rac)-BCN-L-Lysine contains a BCN group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

In Vitro

Click chemistry is used to describe the selective, modular, wide range and high-yield chemical reactions that allow rapid synthesis of new compounds through heteroatom linking (C-X-C). Bertozzi developed click chemistry in a new dimension —Bioorthogonal chemistry. It is defined as a rapid and selective reaction that does not interfere with biological processes under physiological conditions. Common reaction structures of click chemistry, such as Azide, Alkyne, DBCO, BCN, TCO and Tetrazine.

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

322.40

Formula

C17H26N2O4

CAS No.
SMILES

OC([C@@H](N)CCCCNC(OCC1[C@@]2([H])[C@]1([H])CCC#CCC2)=O)=O

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Please store the product under the recommended conditions in the Certificate of Analysis.

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(Rac)-BCN-L-Lysine Related Classifications

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Product Name:
(Rac)-BCN-L-Lysine
Cat. No.:
HY-157054A
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