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Catalog Number:
05010
CAS Number:
152286-30-1
Acide 3 R -1,2,3,4-tétrahydroisoquinoléine-7-hydroxy-3-carboxylique
Purity:
≥ 98 % (HPLC)
Synonym(s):
D-Tic(OH)-OH, 7-hydroxy-D-Tic-OH, HD-Tic(OH)-OH
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$67.60 /100 mg
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Product Information

(3R)-1,2,3,4-Tetrahydroisoquinoline-7-hydroxy-3-carboxylic acid is a versatile compound that has garnered attention in various fields, particularly in medicinal chemistry and pharmacology. This compound is recognized for its potential applications in the development of novel therapeutic agents, particularly in the treatment of neurological disorders. Its unique structure allows it to interact with biological systems effectively, making it a valuable candidate for research focused on neuroprotective and anti-inflammatory properties.

Researchers have explored its efficacy in modulating neurotransmitter systems, which could lead to advancements in treating conditions such as depression and anxiety. Additionally, its carboxylic acid functionality enhances its solubility and bioavailability, making it suitable for formulation in pharmaceutical applications. The compound's ability to cross the blood-brain barrier further underscores its potential in central nervous system therapies. With ongoing studies, (3R)-1,2,3,4-Tetrahydroisoquinoline-7-hydroxy-3-carboxylic acid stands out as a promising candidate for innovative drug development.

Synonyms
D-Tic(OH)-OH, 7-hydroxy-D-Tic-OH, HD-Tic(OH)-OH
CAS Number
152286-30-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 10 H 11 NON 3
Molecular Weight
193.2
MDL Number
MFCD00171281
PubChem ID
4429537
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +160 ± 2 (C = 1 dans AcOH)
Conditions
Conserver à 0-8°C
General Information
Synonyms
D-Tic(OH)-OH, 7-hydroxy-D-Tic-OH, HD-Tic(OH)-OH
CAS Number
152286-30-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 10 H 11 NON 3
Molecular Weight
193.2
MDL Number
MFCD00171281
PubChem ID
4429537
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +160 ± 2 (C = 1 dans AcOH)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(3R)-1,2,3,4-Tetrahydroisoquinoline-7-hydroxy-3-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Neuroscience Research: Its properties make it a useful tool for studying neurotransmitter systems, helping researchers understand mechanisms behind mood regulation and cognitive function.
  • Antioxidant Applications: The compound exhibits antioxidant properties, making it beneficial in formulations aimed at reducing oxidative stress in biological systems, which is crucial for developing health supplements.
  • Biochemical Assays: It is employed in biochemical assays to evaluate enzyme activity, particularly in studies related to metabolic pathways, providing insights into cellular processes.
  • Natural Product Synthesis: This chemical is involved in the synthesis of natural products, allowing researchers to explore new compounds with potential therapeutic benefits, thus expanding the pharmaceutical repertoire.

Citations