7,8-Dihydro-L-biopterin-d3

Product Name 7,8-Dihydro-L-biopterin-d3
CAT No. CS-T-90539
CAS No. 1217782-44-9
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
Smileys O=C1NC(N)=NC2=C1N=C([C@@H](O)[C@@H](O)C([2H])([2H])[2H])CN2
Canonical Smiles CC(C(C1=NC2=C(NC1)N=C(NC2=O)N)O)O
InchIKey FEMXZDUTFRTWPE-OERXLRDQSA-N
Inchl InChI=1S/C9H13N5O3/c1-3(15)6(16)4-2-11-7-5(12-4)8(17)14-9(10)13-7/h3,6,15-16H,2H2,1H3,(H4,10,11,13,14,17)/t3-,6-/m0/s1/i1D3
IUPAC 2-amino-6-[(1R,2S)-3,3,3-trideuterio-1,2-dihydroxypropyl]-7,8-dihydro-3H-pteridin-4-one
Controlled No
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7,8-Dihydro-L-biopterin-d3 is a stable isotope-labeled compound that is commonly used in biochemical and medical research. This compound is a derivative of 7,8-Dihydro-L-biopterin, which is an important cofactor in many enzymatic reactions in the body, particularly those involving the production of neurotransmitters and nitric oxide. The primary use of 7,8-Dihydro-L-biopterin-d3 is in studies of the enzymatic pathways that involve the cofactor. Researchers use this compound to investigate the role of the cofactor in various biological processes, including the biosynthesis of neurotransmitters like dopamine, serotonin, and norepinephrine. Additionally, 7,8-Dihydro-L-biopterin-d3 is used in the study of nitric oxide production, which is also dependent on the cofactor. Chemically, 7,8-Dihydro-L-biopterin-d3 is a stable isotope-labeled compound, which means that it has been modified to contain a specific number of heavy isotopes of hydrogen (deuterium). This modification does not significantly alter the chemical properties of the compound, but it allows researchers to track the movement and metabolism of the compound within biological systems using mass spectrometry. Overall, 7,8-Dihydro-L-biopterin-d3 is an important tool in the study of enzymatic pathways and the role of cofactors in biological processes. Its stable isotope labeling makes it a valuable tool in mass spectrometry-based studies of these pathways.

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