H-89
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- Molecular formula
- C20H24BrN3O3S
- CAS Number
- 130964-39-5
- IUPAC Name
- N-[2-[3-(4-bromophenyl)allylamino]ethyl]isoquinoline-5-sulfonamide
- Molecular Weight
- 458.40g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4500g/cm3
- Appearance
- and efficacy.
- Synonyms
- N-[2-[3-(4-bromophenyl)prop-2-enylamino]ethyl]isoquinoline-5-sulfonamide
Identification
Interesting facts
Interesting Facts about N-[2-[3-(4-bromophenyl)allylamino]ethyl]isoquinoline-5-sulfonamide
N-[2-[3-(4-bromophenyl)allylamino]ethyl]isoquinoline-5-sulfonamide is an intriguing compound within the field of organic chemistry, particularly in medicinal chemistry. Here are some fascinating insights about this compound:
- Pharmaceutical Relevance: This compound belongs to a class of sulfonamides, which are known for their diverse therapeutic applications. They have been utilized as antibiotics and are being explored for their potential in cancer treatment.
- Structural Complexity: The compound features a multi-functional structure that includes both isoquinoline and sulfonamide moieties. This complexity can enhance its biological activity and specificity.
- Bridging Two Worlds: The presence of a bromophenyl group indicates potential for various substitution reactions, allowing chemists to modify the compound for improved efficacy.
- Mechanism of Action: Sulfonamides generally work by inhibiting bacterial synthesis of folic acid, which is crucial for their growth. Understanding this mechanism is essential for developing new drugs with minimized resistance.
- Research Applications: Ongoing studies often explore the potential of isoquinoline derivatives in treating conditions like neurodegenerative diseases, demonstrating the compound's importance beyond antibiotics.
In summary, N-[2-[3-(4-bromophenyl)allylamino]ethyl]isoquinoline-5-sulfonamide exemplifies the intersection of structure and function in medicinal chemistry. Its unique composition and potential therapeutic applications make it a subject of continuous interest and research in scientific communities.