CAS 13485-59-1
:L-Alanyl-L-proline
Description:
L-Alanyl-L-proline, with the CAS number 13485-59-1, is a dipeptide composed of the amino acids alanine and proline. This compound is characterized by its unique structure, which includes an amide bond linking the two amino acids. L-Alanyl-L-proline is known for its role in protein synthesis and its potential biological activities, including antioxidant properties and involvement in cellular signaling pathways. It is typically found in various biological systems and can be synthesized through peptide coupling methods. The compound is soluble in water, which facilitates its use in biochemical applications. Additionally, L-Alanyl-L-proline may exhibit specific conformational properties due to the presence of proline, which can influence the overall stability and functionality of peptides and proteins. Its applications extend to nutrition, pharmaceuticals, and research, particularly in studies related to peptide behavior and interactions. Overall, L-Alanyl-L-proline is a significant compound in biochemistry, contributing to our understanding of peptide dynamics and biological functions.
Formula:C8H14N2O3
InChI:InChI=1S/C8H14N2O3/c1-5(9)7(11)10-4-2-3-6(10)8(12)13/h5-6H,2-4,9H2,1H3,(H,12,13)/t5-,6-/m0/s1
InChI key:InChIKey=WPWUFUBLGADILS-WDSKDSINSA-N
SMILES:C([C@H](C)N)(=O)N1[C@H](C(O)=O)CCC1
Synonyms:- 1-L-Alanyl-L-proline
- 101: PN: US20070066537 PAGE: 17 claimed protein
- 12: PN: WO2014170713 SEQID: 112 claimed protein
- 150: PN: EP2161028 PAGE: 10 claimed protein
- 20: PN: WO2020097235 SEQID: 249 claimed protein
- 443: PN: WO2005081628 SEQID: 445 claimed protein
- <span class="text-smallcaps">L</smallcap>-Alanyl-<smallcap>L</span>-proline
- <span class="text-smallcaps">L</smallcap>-Proline, 1-<smallcap>L</span>-alanyl-
- <span class="text-smallcaps">L</smallcap>-Proline, <smallcap>L</span>-alanyl-
- <span class="text-smallcaps">L</smallcap>-α-Alanyl-<smallcap>L</span>-proline
- Alanylproline
- N-Alanylproline
- Nsc 97932
- Proline, 1-<span class="text-smallcaps">L</smallcap>-alanyl-, <smallcap>L</span>-
- Proline, 1-<span class="text-smallcaps">L</span>-alanyl-
- Proline, 1-L-alanyl-
- Proline, 1-L-alanyl-, L-
- L-Alanyl-L-proline
- L-Proline, 1-L-alanyl-
- See more synonyms
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Found 11 products.
L-Alanyl-L-proline
CAS:Formula:C8H14N2O3Purity:>96.0%(T)Color and Shape:White to Almost white powder to crystalMolecular weight:186.21(S)-1-((S)-2-Aminopropanoyl)pyrrolidine-2-carboxylic acid
CAS:Formula:C8H14N2O3Purity:97%Color and Shape:SolidMolecular weight:186.2084(2S)-1-[(2S)-2-Aminopropanoyl]pyrrolidine-2-carboxylic Acid (L-Alanyl-L-proline)
CAS:Color and Shape:NeatL-Alanyl-L-proline
CAS:Controlled Product<p>Applications L-Alanyl-L-proline is a dipeptide that contains a sterically constrained proline, a well-known turn inducer in proteins.<br>References Moriuchi, T., et al.: J. Organomet. Chem., 589, 50 (1999)<br></p>Formula:C8H14N2O3Color and Shape:NeatMolecular weight:186.21H-Ala-Pro-OH
CAS:<p>H-Ala-Pro-OH is a molecule that has the ability to bind to the active site of enzymes. It inhibits the activity of esterases and proteases by binding to their active sites and blocking access to substrates. This drug also inhibits the uptake of drugs in cells by competitively inhibiting membrane transport proteins, such as P-glycoprotein. H-Ala-Pro-OH binds to gamma-aminobutyric acid receptors and shows a kinetic effect on this neurotransmitter’s activity. The conformational properties of H-Ala-Pro-OH are not fully understood, but it is thought that its low energy allows it to bind to intracellular proteins more easily than other molecules.</p>Formula:C8H14N2O3Purity:Min. 95%Color and Shape:White Off-White PowderMolecular weight:186.21 g/molH-Ala-Pro-OH
CAS:<p>Substrate for skin fibroblast prolidase.</p>Formula:C8H14N2O3Purity:> 99%Color and Shape:White PowderMolecular weight:186.21










