Azido-Proline

Proline derivatives with azido function at position 4 enable Click conjugation just at the edge of a beta-turn. Both optical configurations, 4S and 4R, are available, in order to direct the conjugate specifically in the direction of desire.


 

Boc-L-Pro(4-N3)-OH*CHA (2S,4S)
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cis-N-alpha-(t-Butyloxycarbonyl)-4-azido-L-proline
Code Quantity Price (EUR)
BAA1905.0001
BAA1905.0005
BAA1905.0025

 1 g
5 g
25 g		 200
700
2800
Boc-L-Pro(4-N3)-OH*CHA (2S,4S)
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trans-N-alpha-(t-Butyloxycarbonyl)-4-azido-L-proline dicyclohexylamine
Code Quantity Price (EUR)
BAA1930.0001
BAA1930.0005
BAA1930.0025		 1 g
5 g
25 g		 225
800
3200
Fmoc-L-Pro(4-N3)-OH (2S,4S)
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cis-N-alpha-(9-Flourenylmethyloxycarbonyl)-4-azido-L-proline
Code Quantity Price (EUR)
FAA2050.0001
FAA2050.0005 

 1 g
5 g		 250
900
Fmoc-L-Pro(4-N3)-OH (2S,4R)
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trans-N-alpha-(9-Fluorenylmethyloxycarbonyl)-4-azido-L-proline
Code Quantity Price (EUR)
FAA3000.0001
FAA3000.0005 

 1 g
5 g		 300
1200

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