730-08-5
Chemical Structure
H-Tyr-Ala-OH
Synonym(s): Tyr-Ala
- CAS No.: 730-08-5
- Formula:C12H16N2O4
- Molecular Weight:252.27
IUPAC Name: L-tyrosyl-L-alanine
InChIKey: NLKUJNGEGZDXGO-XVKPBYJWSA-N
SMILES: C[C@@H](C(O)=O)NC([C@H](CC1=CC=C(O)C=C1)N)=O
Biological Activity: H-Tyr-Ala-OH (Tyr-Ala) is a dipeptide containing tyrosine and alanine[1].
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H-Tyr-Ala-OH | 99.81% | H-Tyr-Ala-OH (Tyr-Ala) is a dipeptide containing tyrosine and alanine. | ||||||||||||||||||||
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Tyrosylleucine | 99.82% | Tyrosylleucine (Tyr-Leu, YL), an orally active dipeptide, exhibits a potent antidepressant-like activity. | ||||||||||||||||||||
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Lactoyl-L-tyrosine | Lactoyl-L-tyrosine is an endogenous N-lactoyl-amino acid formed from L-lactic acid and L-tyrosine. Lactoyl-L-tyrosine can be used to study flavor development during cheese ripening or as a natural flavor enhancer in the food industry. | |||||||||||||||||||||
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Leucyltyrosine | Leucyltyrosine is an ACE inhibitor (IC50s: 44 μM (HHL as substrate) and 534 μM (HPA as substrate)). | |||||||||||||||||||||
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H-Ser-Tyr-OH | 98.87% | H-Ser-Tyr-OH is a dipeptide. H-Ser-Tyr-OH can form a copper(II) complex. | ||||||||||||||||||||
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H-Tyr-Ile-OH | H-Tyr-Ile-OH is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development. | |||||||||||||||||||||
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Tyrosylvaline | Tyrosylvaline is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development. | |||||||||||||||||||||
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H-Val-Tyr-OH (Standard) | ≥98% | H-Val-Tyr-OH is an endogenous metabolite. | ||||||||||||||||||||
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Phenylalanylalanine | 99.47% | Phenylalanylalanine (Phe-ala) is an enkephalinase inhibitor and belongs to the class of dipeptides. Phenylalanylalanine inhibits dipeptidyl carboxypeptidase-mediated enkephalin degradation by cleaving the Gly3-Phe4 bond, and when co-administered with Leu-enkephalin, it produces analgesic effects with a synergistic enhancement, which can be reversed by Naloxone (HY-17417A). Phenylalanylalanine can be used in pain-related research. | ||||||||||||||||||||
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L-Alanyl-L-tyrosin | 99.94% | L-Alanyl-L-tyrosin is a tyrosine derivative. | ||||||||||||||||||||
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H-Tyr-Gly-OH | H-Tyr-Gly-OH is an amino acid building block commonly used in biochemical and peptide synthesis. | |||||||||||||||||||||
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References
- [1]. Koleva BB, et al. Spectroscopic and structural elucidation of L-tyrosine-containing dipeptides valyl-tyrosine and tyrosyl-alanine: solid-state IR-LD spectroscopy, quantum chemical calculations and vibrational analysis. Spectrochim Acta A Mol Biomol Spectrosc. 2007;68(5):1187-1196. [Content Brief]