4-O-Methyldopa-d3

Product Name 4-O-Methyldopa-d3
Alternate Names Methyldopa Stable Isotopes, Stable Isotopes of Methyldopa
CAT No. CS-P-02899
CAS No. 35296-56-1(Unlabeled)
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Methyldopa
Smileys N[C@H](C(O)=O)CC1=CC(O)=C(OC([2H])([2H])[2H])C=C1
Canonical Smiles COC1=C(C=C(C=C1)CC(C(=O)O)N)O
InchIKey QRXPIKKZQGWJMW-ZETCQYMHSA-N
Inchl InChI=1S/C10H13NO4/c1-15-9-3-2-6(5-8(9)12)4-7(11)10(13)14/h2-3,5,7,12H,4,11H2,1H3,(H,13,14)/t7-/m0/s1
IUPAC (2S)-2-amino-3-(3-hydroxy-4-methoxyphenyl)propanoic acid
Controlled No
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4-O-Methyldopa-d3 is a stable isotope-labeled analogue of the neurotransmitter dopamine. It is a pharmaceutical intermediate that is commonly used in the production of drugs used to treat hypertension and Parkinson's disease. This compound is available in its pure form and is used by chemists and researchers for a range of applications. One of the primary uses for 4-O-Methyldopa-d3 is as a reference standard in mass spectrometry analysis. It is often used as a stable isotope internal standard for the quantification of dopamine and its metabolites in biological samples. The compound is also used in research studies to investigate the metabolism of dopamine and to understand the underlying mechanisms involved in the development of neurological disorders. Chemically, 4-O-Methyldopa-d3 is a labeled analogue of L-DOPA, an amino acid that is converted into dopamine in the brain. It is an inhibitor of the enzyme DOPA decarboxylase, which is responsible for the conversion of L-DOPA into dopamine. This results in an increase in the levels of L-DOPA in the brain, which can be used to treat Parkinson's disease and other conditions. In conclusion, 4-O-Methyldopa-d3 is a valuable tool for researchers and chemists studying the metabolism of dopamine and related compounds. It is a stable isotope-labeled analogue with a range of applications in mass spectrometry analysis and drug development. Its chemical properties make it an effective inhibitor of DOPA decarboxylase, and it has potential for use in the treatment of neurological disorders.

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