68-95-1
68-95-1
Chemical Structure
N-Acetyl-L-proline
- CAS No.: 68-95-1
- Formula:C7H11NO3
- Molecular Weight:157.17
IUPAC Name: acetyl-L-proline
InChIKey: GNMSLDIYJOSUSW-LURJTMIESA-N
SMILES: OC([C@H]1N(CCC1)C(C)=O)=O
Biological Activity: N-Acetyl-L-proline is an N-acetylated amino acid derivative of L-proline (HY-Y0252), as well as a stereospecific substrate of N-acyl-L-proline-acylase. N-Acetyl-L-proline can be used for the synthesis of the non-steroidal anti-inflammatory drug Aceprol[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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N-Acetyl-L-proline | 99.92% | N-Acetyl-L-proline is an N-acetylated amino acid derivative of L-proline (HY-Y0252), as well as a stereospecific substrate of N-acyl-L-proline-acylase. N-Acetyl-L-proline can be used for the synthesis of the non-steroidal anti-inflammatory drug Aceprol. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 1.00
HY-W017258N-Acetyl-D-proline -
Similarity Score 0.85
HY-137772Captopril EP Impurity E -
Similarity Score 0.85
HY-W016887RGlycyl-L-proline (Standard) -
Similarity Score 0.83
HY-21754Hygric acid -
Similarity Score 0.83
HY-17490Oxaceprol -
Similarity Score 0.82
HY-137768RCaptopril EP Impurity B (Standard) -
Similarity Score 0.82
HY-136511Epicaptopril -
Similarity Score 0.82
HY-B0368BD-Captopril -
Similarity Score 0.82
HY-B0368Cepi-D-Captopril -
Explore the MedChemAI to find more analogs
References
- [1]. Romanovskaya II, et al. Preparation and use of N-acetyl-α-amino acids. Drug synthesis methods and manufacturing technology. Pharm Chem J. 2009;43:615-618.
- [2]. Groeger U, et al. Isolation of an L-Stereospecific N-Acyl-L-proline-Acylase and its Use as Catalyst in Organic Synthesis. Angewandte Chemie International Edition in English. 1990;29(4):417-419.
