CAS 13485-59-1
:L-Alanyl-L-proline
- 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-
- Voir plus de synonymes
L-Alanyl-L-proline
CAS :Formule :C8H14N2O3Degré de pureté :>96.0%(T)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :186.21(S)-1-((S)-2-Aminopropanoyl)pyrrolidine-2-carboxylic acid
CAS :Formule :C8H14N2O3Degré de pureté :97%Couleur et forme :SolidMasse moléculaire :186.2084(2S)-1-[(2S)-2-Aminopropanoyl]pyrrolidine-2-carboxylic Acid (L-Alanyl-L-proline)
CAS :Couleur et forme :NeatL-Alanyl-L-proline
CAS :Produit contrôléApplications L-Alanyl-L-proline is a dipeptide that contains a sterically constrained proline, a well-known turn inducer in proteins.
References Moriuchi, T., et al.: J. Organomet. Chem., 589, 50 (1999)Formule :C8H14N2O3Couleur et forme :NeatMasse moléculaire :186.21H-Ala-Pro-OH
CAS :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.
Formule :C8H14N2O3Degré de pureté :Min. 95%Couleur et forme :White Off-White PowderMasse moléculaire :186.21 g/molH-Ala-Pro-OH
CAS :Substrate for skin fibroblast prolidase.
Formule :C8H14N2O3Degré de pureté :> 99%Couleur et forme :White PowderMasse moléculaire :186.21










