587-33-7
587-33-7
Chemical Structure
L-m-Tyrosine
- CAS No.: 587-33-7
- Formula:C9H11NO3
- Molecular Weight:181.19
IUPAC Name: (S)-2-amino-3-(3-hydroxyphenyl)propanoic acid
InChIKey: JZKXXXDKRQWDET-QMMMGPOBSA-N
SMILES: N[C@H](C(O)=O)CC1=CC(O)=CC=C1
Biological Activity: L-m-Tyrosine is an unnatural amino acid. L-m-Tyrosine reduces dopamine, norepinephrine and serotonin in rats. L-m-Tyrosine has potential in the research of Parkinsons disease, Alzheimers disease, and arthritis[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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L-m-Tyrosine | 99.94% | L-m-Tyrosine is an unnatural amino acid. L-m-Tyrosine reduces dopamine, norepinephrine and serotonin in rats. L-m-Tyrosine has potential in the research of Parkinsons disease, Alzheimers disease, and arthritis. | ||||||||||||||||||||
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L-Tyrosine | 98.73% | L-Tyrosine is a non-essential amino acid which can inhibit citrate synthase activity in the posterior cortex. | ||||||||||||||||||||
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L-Tyrosine-15N | 99.31% | L-Tyrosine-15N is the 15N-labeled L-Tyrosine. L-Tyrosine is a non-essential amino acid which can inhibit citrate synthase activity in the posterior cortex. | ||||||||||||||||||||
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L-Tyrosine-13C,15N | L-Tyrosine-13C,15N is the 13C and 15N labeled L-Tyrosine. L-Tyrosine is a non-essential amino acid which can inhibit citrate synthase activity in the posterior cortex. | |||||||||||||||||||||
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L-Tyrosine-13C6 | 99.20% | L-Tyrosine-13C6 is the 13C-labeled L-Tyrosine. L-Tyrosine is a non-essential amino acid which can inhibit citrate synthase activity in the posterior cortex. | ||||||||||||||||||||
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L-Tyrosine-13C9 | 99.81% | L-Tyrosine-13C9 is the 13C-labeled L-Tyrosine. L-Tyrosine is a non-essential amino acid which can inhibit citrate synthase activity in the posterior cortex. | ||||||||||||||||||||
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L-Tyrosine-13C | 99.42% | L-Tyrosine-13C is the 13C-labeled L-Tyrosine. L-Tyrosine is a non-essential amino acid which can inhibit citrate synthase activity in the posterior cortex. | ||||||||||||||||||||
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DL-m-Tyrosine (Standard) | ≥98% | DL-m-Tyrosine (Standard) is the analytical standard of DL-m-Tyrosine (HY-W001940). This product is intended for research and analytical applications. DL-m-Tyrosine is a non-protein amino acid. DL-m-Tyrosine inhibits microbial growth and spore formation. DL-m-Tyrosine also inhibits root growth in various plants, such as lettuce and Arabidopsis. DL-m-Tyrosine, when used in combination with Carbidopa (HY-B0311), has a potent antihypertensive effect. DL-m-Tyrosine can be used in research on biopesticide design. | ||||||||||||||||||||
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DL-Tyrosine | 98.0% | DL-Tyrosine is an aromatic nonessential amino acid synthesized from the essential amino acid phenylalanine. DL-Tyrosine is a precursor for several important neurotransmitters (epinephrine, norepinephrine, dopamine). | ||||||||||||||||||||
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L-Tyrosine-13C9,15N | 98.0% | L-Tyrosine-13C9,15N is the 13C- and 15N-labeled L-Tyrosine. L-Tyrosine is an aromatic nonessential amino acid synthesized from the essential amino acid phenylalanine. L-Tyrosine is a precursor for several important neurotransmitters (epinephrine, norepinephrine, dopamine). | ||||||||||||||||||||
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D-Tyrosine (Standard) | ≥98% | D-Tyrosine (Standard) is the analytical standard of D-Tyrosine (HY-Y0444). This product is intended for research and analytical applications. D-Tyrosine is the D-isomer of tyrosine. D-Tyrosine negatively regulates melanin synthesis by inhibiting tyrosinase activity. D-Tyrosine inhibits biofilm formation and trigger the self-dispersal of biofilms without suppressing bacterial growth. | ||||||||||||||||||||
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References
- [1]. M H Fukami ,et al. Phenylalanine as Substrate for Tyrosine Hydroxylase in Bovine Adrenal Chromaffin Cells. Biochem J. 1990 Jun 1;268(2):525-8. [Content Brief]
- [2]. Ishimitsu S, et al. Studies on the formation of 3,4-dihydroxyphenylalanine, m-tyrosine and o-tyrosine from L-phenylalanine by rat liver and adrenal. Chem Pharm Bull (Tokyo). 1988 Jan;36(1):279-85. [Content Brief]
- [3]. Smyth RG, et al. Studies on the depletion of brain amines by m-tyrosine. Eur J Pharmacol. 1977 Apr 7;42(3):267-73. [Content Brief]
