282729-06-0
282729-06-0
Chemical Structure
DL-Proline-2-d1
- CAS No.: 282729-06-0
- Formula:C5H8DNO2
- Molecular Weight:116.14
IUPAC Name: N-(4-benzoylbenzyl)-4-sulfamoylbenzamide
InChIKey: ONIBWKKTOPOVIA-QYKNYGDISA-N
SMILES: OC(C1([2H])CCCN1)=O
Biological Activity: DL-Proline-2-d is the deuterium labeled DL-Proline-2.
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DL-Proline-2-d1 | 98.0% | DL-Proline-2-d is the deuterium labeled DL-Proline-2. | ||||||||||||||||||||
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DL-Proline-d3 | 99.67% | DL-Proline-d3 is the deuterium labeled DL-Proline. | ||||||||||||||||||||
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DL-Proline-d7 | 98.0% | DL-Proline-d7 is the deuterium labeled DL-Proline (HY-W012908). H-DL-Pro-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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DL-Proline | 98.0% | DL-Proline is a racemic mixture of D-Proline and L-Prolin. DL-Proline is a cyclic imino acid with a five-membered ring structure. DL-Proline is a key structural unit in peptide synthesis. DL-Proline can stabilize the β-turn conformation and affect the secondary structure of the peptide. DL-Proline has biological activities such as regulating peptide conformation and enhancing the stability of cyclic peptides. DL-Proline can be used to study diseases related to peptide structure and function, such as cancer and bacterial infection. | ||||||||||||||||||||
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