704-15-4
Chemical Structure
Glycyl-L-proline
Synonym(s): H-Gly-Pro-OH; Gly-Pro
- CAS No.: 704-15-4
- Formula:C7H12N2O3
- Molecular Weight:172.18
IUPAC Name: glycyl-L-proline
InChIKey: KZNQNBZMBZJQJO-YFKPBYRVSA-N
SMILES: NCC(N1CCC[C@H]1C(O)=O)=O
Biological Activity: Glycyl-L-proline (H-Gly-Pro-OH) is a dipeptide. Glycyl-L-proline can induce MCF-7 cells apoptosis. Glycyl-L-proline can enhance the inhibitory effect of the PRODH/POX knockout on collagen and DNA biosynthesis. Glycyl-L-proline can inhibit Gly-Sar and L-proline transport. Glycyl-L-proline can be used for the researches of cancer and metabolic disease, such as breast cancer[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Glycyl-L-proline | 99.51% | Glycyl-L-proline (H-Gly-Pro-OH) is a dipeptide. Glycyl-L-proline can induce MCF-7 cells apoptosis. Glycyl-L-proline can enhance the inhibitory effect of the PRODH/POX knockout on collagen and DNA biosynthesis. Glycyl-L-proline can inhibit Gly-Sar and L-proline transport. Glycyl-L-proline can be used for the researches of cancer and metabolic disease, such as breast cancer. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Glycyl-L-proline (Standard) | 98.54% | H-Gly-Pro-OH (Standard) is the analytical standard of H-Gly-Pro-OH. This product is intended for research and analytical applications. H-Gly-Pro-OH is an end product of collagen metabolism that is further cleaved by prolidase. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Glycyl-L-proline-15N,d2 trifluoroacetate | 98.86% | Glycyl-L-proline-15N,d2 (trifluoroacetate) is a 15N-labeled and deuterium labeled Glycyl-L-proline. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
-
Similarity Score 0.85
HY-W004114N-Acetyl-L-proline -
Similarity Score 0.85
HY-W017258N-Acetyl-D-proline -
Similarity Score 0.84
HY-W061571H-Gly-Hyp-OH -
Similarity Score 0.84
HY-P4569H-Ser-Pro-OH -
Similarity Score 0.82
HY-137772Captopril EP Impurity E -
Similarity Score 0.81
HY-137768RCaptopril EP Impurity B (Standard) -
Similarity Score 0.81
HY-136511Epicaptopril -
Similarity Score 0.81
HY-B0368BD-Captopril -
Similarity Score 0.81
HY-B0368Cepi-D-Captopril -
Explore the MedChemAI to find more analogs
References
- [1]. Zareba I, et al. Proline oxidase silencing induces proline-dependent pro-survival pathways in MCF-7 cells. Oncotarget. 2018;9(17):13748-13757. Published 2018 Feb 9. [Content Brief]
- [2]. von Linde T, et al. Rapid and Sensitive Quantification of Intracellular Glycyl-Sarcosine for Semi-High-Throughput Screening for Inhibitors of PEPT-1. Pharmaceutics. 2021;13(7):1019. Published 2021 Jul 3. [Content Brief]
- [3]. Boyd CA, et al. L-proline transport by brush border membrane vesicles prepared from human placenta. J Physiol. 1981;315:9-19. [Content Brief]