L-m-Tyrosine
Based on 1 Customer Validation
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.
For research use only. We do not sell to patients.
- Purity: 99.94%
- CAS No.: 587-33-7
- Formula: C9H11NO3
- Molecular Weight:181.19
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biological Activity
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Chemical Information
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Solvent & Solubility
- Purity & Documentation
- References
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Help & FAQs
Biological Activity
L-m-tyrosine is converted to dopamine by partially purified rat liver phenylalanine hydroxylase and bovine adrenal medullary tyrosine hydroxylase[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 587-33-7
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Appearance Solid
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Molecular Weight 181.19
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Formula C9H11NO3
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Color Off-white to light yellow
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SMILES
N[C@H](C(O)=O)CC1=CC(O)=CC=C1
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Solvent & Solubility
DMSO : < 1 mg/mL (insoluble or slightly soluble)
Purity & Documentation
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Data Sheet (269 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
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]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
L-m-Tyrosine Related Classifications
HY-W016443 Related Classifications
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