TargetMol

Alanylphenylalanine

Product Code:
 
TAR-T20504
Product Group:
 
Inhibitors and Activators
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20℃
1 / 1
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Further Information

Bioactivity:
Alanylphenylalanine may be used in physicochemical studies or to evaluate dipeptide separation technologies. It can also be used for studying cell uptake mechanisms.
CAS:
3061-90-3
Formula:
C12H16N2O3
Molecular Weight:
236.271
Purity:
0.98
SMILES:
C[C@H](N)C(=O)N[C@@H](Cc1ccccc1)C(O)=O

References

1. Shi G, Dang Y, Pan T, Liu X, Liu H, Li S, Zhang L, Zhao H, Li S, Han J, Tai R, Zhu Y, Li J, Ji Q, Mole RA, Yu D, Fang H. Unexpectedly Enhanced Solubility of Aromatic Amino Acids and Peptides in an Aqueous Solution of Divalent Transition-Metal Cations. Phys Rev Lett. 2016 Dec 2;117(23):238102. Epub 2016 Dec 2. PubMed PMID: 27982649. 2. Facchin G, Veiga N, Kramer MG, Batista AA, V?rnagy K, Farkas E, Moreno V, Torre MH. Experimental and theoretical studies of copper complexes with isomeric dipeptides as novel candidates against breast cancer. J Inorg Biochem. 2016 Sep;162:52-61. doi: 10.1016/j.jinorgbio.2016.06.005. Epub 2016 Jun 4. PubMed PMID: 27369466. 3. Li J, Waldron KC. Estimation of the pH-independent binding constants of alanylphenylalanine and leucylphenylalanine stereoisomers with beta-cyclodextrin in the presence of urea. Electrophoresis. 1999 Jan;20(1):171-9. PubMed PMID: 10065974. 4. Verteeg DH, Witter A. Isolation and identification of alpha-aspartyl-serine, alanylphenylalanine and isoleucylleucine from calf brain stem. J Neurochem. 1970 Jan;17(1):41-52. PubMed PMID: 5494038.