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Product Name: | D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid | CAS No: | 103733-65-9 |
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M.W: | 177.2 | Appearance: | White Powder |
Assay: | 99+ | Storage: | Room Temperature |
Highlight: | D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid,CAS 103733-65-9 D-Tic-OH |
Product Description
D-Tic-OH CAS 103733-65-9 D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
Name: D-Tic-OH
CAS NO: 103733-65-9
M.W: 177.2
Appearance: White Powder
Purity: 99+
Synonyms: D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
Application
Synthesis and Structure:
D-THIQ-3-CA has a carboxylic acid group at the 3-position on the isoquinoline ring. This carboxyl group makes it reactive and potentially useful for chemical modifications, allowing for the development of derivatives with different bioactivities.
The D-enantiomer of the compound is often used in research because it can have different biological properties compared to the L-enantiomer, especially in terms of stereoselectivity in enzyme interactions or receptor binding.
Neurochemical Research:
Tetrahydroisoquinolines are of particular interest in neurochemistry, especially because they are precursors to neurotransmitters like dopamine. The isoquinoline scaffold is structurally related to the dopamine and noradrenaline pathways, and THIQ derivatives can interact with these systems.
D-THIQ-3-CA might be used in studies on dopamine receptor modulation, since isoquinoline derivatives are sometimes involved in influencing dopaminergic signaling. Additionally, some THIQ compounds have been studied for their roles in Parkinson’s disease and other neurodegenerative conditions.
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