4313-73-9
4313-73-9
Chemical Structure
Z-Phe-Leu-OH
Synonym(s): NSC 334018
- CAS. Nr.: 4313-73-9
- Formula:C23H28N2O5
- Molecular Weight:412.48
IUPAC Name: ((benzyloxy)carbonyl)-L-phenylalanyl-L-leucine
InChIKey: IBOXOGVHBFUSFH-PMACEKPBSA-N
SMILES: O=C(N[C@@H](CC(C)C)C(O)=O)[C@H](CC1=CC=CC=C1)NC(OCC2=CC=CC=C2)=O
Biological Activity: Z-Phe-Leu-OH (NSC 334018) is a dipeptide acid. Z-Phe-Leu-OH undergoes hydrolysis by carboxypeptidase Y to release L-leucine. Z-Phe-Leu-OH acts as a substrate to assay carboxypeptidase Y peptidase activity[1][2][3].
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Z-Phe-Leu-OH | 98.0% | Z-Phe-Leu-OH (NSC 334018) is a dipeptide acid. Z-Phe-Leu-OH undergoes hydrolysis by carboxypeptidase Y to release L-leucine. Z-Phe-Leu-OH acts as a substrate to assay carboxypeptidase Y peptidase activity. | ||||||||||||||||||||
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References
- [1]. Shimizu H, et al. Role of carbohydrate moiety in carboxypeptidase Y: structural study of mutant enzyme lacking carbohydrate moiety. Biosci Biotechnol Biochem. 1999;63(6):1045-1050. [Content Brief]
- [2]. Makino M, et al. Amino acid substitution reveals the role of V-shape helix on construction of yeast carboxypeptidase Y. J. Biol. Macromol. 2014 Feb 4;14(1):27-41.
- [3]. Könnecke A, et al. Model studies on the utility of nucleophiles bound to insoluble supports for enzymatic peptide synthesis. Monatsh Chem. 1981 Sep 28;113:331–337.
