Interesting facts
Exploring N-[4-Guanidino-1-(2-naphthylcarbamoyl)butyl]benzamide
N-[4-Guanidino-1-(2-naphthylcarbamoyl)butyl]benzamide is a fascinating compound, particularly noteworthy in the realm of medicinal chemistry. Here are some engaging facts about this compound:
- Biological Significance: This compound exhibits potential therapeutic properties, especially in the field of cancer research. Studies suggest that it may play a role in cellular apoptosis, making it a subject of interest for developing cancer treatments.
- Structural Complexity: The compound is characterized by a complex structure that includes a benzamide core and guanidino group. This multifaceted design can interact with various biological targets, enhancing its medicinal potential.
- Mechanism of Action: Compounds like N-[4-Guanidino-1-(2-naphthylcarbamoyl)butyl]benzamide often work as enzyme inhibitors, impacting pathways that are crucial for cell proliferation and survival.
- Research Interest: Given its multifactorial nature, researchers are actively investigating how modifications to its structure can augment its efficacy and selectivity against particular cancer types.
- Synergistic Potential: There is ongoing research into how this compound can be used in combination with other therapeutic agents to create synergistic effects, potentially leading to more effective treatment regimens.
- Pharmacophore Elements: The combination of naphthyl and carbonyl moieties contributes to its pharmacophoric characteristics, which are crucial for biological activity and interaction with target receptors.
As scientists continue to unravel the complexities of N-[4-Guanidino-1-(2-naphthylcarbamoyl)butyl]benzamide, it exemplifies how intricate organic compounds can have profound implications in the biotechnology and pharmaceutical industries. Its potential as a therapeutic agent showcases the importance of structural diversity and innovation in drug design.
Synonyms
305-09-9
N-{5-carbamimidamido-1-[(naphthalen-2-yl)amino]-1-oxopentan-2-yl}benzamide
BENZOYLARGININE-2-NAPHTHYLAMIDE
N-[5-(diaminomethylideneamino)-1-(naphthalen-2-ylamino)-1-oxopentan-2-yl]benzamide
CBDivE_003067
Nalpha-Benzoyl-DL-arginine beta-naphthylamide hydrochloride
MLS002177847
SCHEMBL676271
2 Naphthylamide, Benzoylarginine
CHEMBL1553126
CHEBI:91069
Benzoylarginine beta-naphthylamide
DTXSID00952813
HMS2236D05
HMS3372B13
n-benzoyl-dl-arginine-2-naphthylamide
NCGC00246973-01
SMR000857298
NS00041997
Q27163044
N-(5-Guanidino-1-(naphthalen-2-ylamino)-1-oxopentan-2-yl)benzamide
Benzamide, N-(4-((aminoiminomethyl)amino)-1-((2-naphthalenylamino)carbonyl)butyl)-, (+-)-
N-{5-Carbamimidamido-1-hydroxy-1-[(naphthalen-2-yl)imino]pentan-2-yl}benzenecarboximidic acid
Solubility of N-[4-guanidino-1-(2-naphthylcarbamoyl)butyl]benzamide
N-[4-guanidino-1-(2-naphthylcarbamoyl)butyl]benzamide is a compound that presents intriguing characteristics when it comes to solubility. Its solubility can be influenced by various factors including:
It's important to note that while the compound has potential solubility in water due to these factors, its exact solubility remains subject to empirical measurement, and may vary based on the specific conditions. As a general observation, many compounds with similar structures tend to exhibit moderate to good solubility in commonly used organic solvents like DMSO or methanol, making them viable for various applications in biochemical settings.
In conclusion, solubility is an essential property that influences the utility and application of N-[4-guanidino-1-(2-naphthylcarbamoyl)butyl]benzamide. Understanding the solubility behavior of this compound allows scientists to better harness its potential in specific environments or formulations.