Cas no 1177303-46-6 (Isoquinolin-1-ylmethanamine hydrochloride)

Isoquinolin-1-ylmethanamine hydrochloride is a heterocyclic organic compound featuring an isoquinoline core substituted with an aminomethyl group, isolated as its hydrochloride salt. This derivative is of interest in pharmaceutical and agrochemical research due to its potential as a versatile intermediate in the synthesis of bioactive molecules. The hydrochloride form enhances stability and solubility, facilitating handling and storage. Its structural framework allows for further functionalization, making it valuable in medicinal chemistry for developing ligands or inhibitors targeting specific biological pathways. The compound is typically characterized by high purity and consistent performance, ensuring reliability in synthetic applications. Proper handling requires adherence to standard safety protocols for amine hydrochlorides.
Isoquinolin-1-ylmethanamine hydrochloride structure
1177303-46-6 structure
Product Name:Isoquinolin-1-ylmethanamine hydrochloride
CAS No:1177303-46-6
MF:C10H11ClN2
MW:194.660741090775
CID:1088563
PubChem ID:43810665
Update Time:2025-06-14

Isoquinolin-1-ylmethanamine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • Isoquinolin-1-ylmethanamine hydrochloride
    • 1-isoquinolin-1-ylmethanamine hydrochloride
    • 1-isoquinolinylmethanamine hydrochloride
    • A825196
    • AC1Q3D67
    • AG-B-82691
    • AK136083
    • CTK7E6920
    • EN300-37106
    • MolPort-005-312-474
    • DTXSID90656398
    • E74125
    • isoquinolin-1-ylmethanaminehydrochloride
    • isoquinolin-1-ylmethanamine HCl
    • isoquinolin-1-ylmethanamine;hydrochloride
    • CXB30346
    • AKOS022176139
    • WS-01319
    • (isoquinolin-1-yl)methanamine hydrochloride
    • 1-(Isoquinolin-1-yl)methanamine--hydrogen chloride (1/1)
    • DB-129974
    • CS-0270348
    • 1-(ISOQUINOLIN-1-YL)METHANAMINE HYDROCHLORIDE
    • 1177303-46-6
    • Inchi: 1S/C10H10N2.ClH/c11-7-10-9-4-2-1-3-8(9)5-6-12-10;/h1-6H,7,11H2;1H
    • InChI Key: WKDWEZVBPUQBNW-UHFFFAOYSA-N
    • SMILES: Cl.N1C=CC2C=CC=CC=2C=1CN

Computed Properties

  • Exact Mass: 194.0610761g/mol
  • Monoisotopic Mass: 194.0610761g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 147
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 38.9?2

Isoquinolin-1-ylmethanamine hydrochloride Pricemore >>

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Additional information on Isoquinolin-1-ylmethanamine hydrochloride

Recent Advances in Isoquinolin-1-ylmethanamine Hydrochloride (CAS: 1177303-46-6) Research: A Comprehensive Review

Isoquinolin-1-ylmethanamine hydrochloride (CAS: 1177303-46-6) is a chemical compound of significant interest in the field of medicinal chemistry and drug discovery. This compound, characterized by its isoquinoline scaffold, has garnered attention due to its potential pharmacological applications, particularly in the development of novel therapeutic agents. Recent studies have explored its synthesis, biological activity, and potential as a lead compound in various disease models. This research brief aims to provide an up-to-date overview of the latest findings related to Isoquinolin-1-ylmethanamine hydrochloride, highlighting its chemical properties, mechanisms of action, and therapeutic potential.

The synthesis of Isoquinolin-1-ylmethanamine hydrochloride has been optimized in recent years to improve yield and purity, making it more accessible for research and development. Advanced synthetic routes, including multi-step organic reactions and catalytic processes, have been reported in peer-reviewed journals. These methods not only enhance the efficiency of production but also allow for the introduction of structural modifications that can fine-tune the compound's biological activity. Researchers have particularly focused on the role of the hydrochloride salt form in improving solubility and bioavailability, which are critical factors for drug development.

In terms of biological activity, Isoquinolin-1-ylmethanamine hydrochloride has demonstrated promising results in preclinical studies. Its mechanism of action appears to involve interactions with various molecular targets, including enzymes and receptors implicated in inflammatory and neurodegenerative diseases. For instance, recent in vitro studies have shown that this compound exhibits inhibitory effects on key enzymes involved in oxidative stress pathways, suggesting potential applications in conditions such as Alzheimer's disease and Parkinson's disease. Additionally, its modulatory effects on neurotransmitter systems have sparked interest in its use as a potential anxiolytic or antidepressant agent.

One of the most significant advancements in the research of Isoquinolin-1-ylmethanamine hydrochloride is its evaluation in cancer models. Preliminary data indicate that this compound may interfere with cell proliferation and induce apoptosis in certain cancer cell lines. These findings are particularly relevant given the ongoing search for novel chemotherapeutic agents with improved selectivity and reduced side effects. Researchers are currently investigating the compound's structure-activity relationship to identify derivatives with enhanced potency and specificity against various cancer types.

Despite these promising developments, challenges remain in the clinical translation of Isoquinolin-1-ylmethanamine hydrochloride. Pharmacokinetic studies are needed to fully understand its absorption, distribution, metabolism, and excretion profiles. Furthermore, comprehensive toxicological assessments must be conducted to ensure its safety profile meets regulatory standards for human use. Collaborative efforts between academic institutions and pharmaceutical companies are crucial to advancing this compound through the drug development pipeline.

In conclusion, Isoquinolin-1-ylmethanamine hydrochloride (CAS: 1177303-46-6) represents a versatile chemical entity with substantial potential in medicinal chemistry. Recent research has shed light on its synthetic accessibility, diverse biological activities, and therapeutic applications across multiple disease areas. As investigations continue to unravel its full pharmacological potential, this compound may emerge as a valuable tool for drug discovery and a promising candidate for further development. The coming years are likely to witness significant progress in understanding and harnessing the therapeutic benefits of this intriguing molecule.

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