Interesting facts
Interesting Facts about N4-(3-bromophenyl)quinazoline-4,6,7-triamine
N4-(3-bromophenyl)quinazoline-4,6,7-triamine is a fascinating compound that belongs to the quinazoline family, known for their diverse biological activities. This particular compound has garnered attention due to its potential applications in the fields of medicinal chemistry and pharmaceuticals. Here are some intriguing aspects:
- Anticancer Activity: Compounds like this one, containing quinazoline structures, have been studied for their ability to inhibit cancer cell growth, making them candidates for cancer treatment development.
- Inhibition of Kinases: Quinazoline derivatives are often employed as kinase inhibitors, particularly in targeting pathways associated with various cancers.
- Pharmacophoric Features: The presence of the bromophenyl group enhances the lipophilicity of the molecule, which can improve its cell membrane permeability and biological activity.
- Versatility in Synthesis: N4-(3-bromophenyl)quinazoline-4,6,7-triamine can be synthesized through various organic reactions, leading to a rich array of derivatives that can be explored for different biological properties.
- Potential for Customization: The ability to modify the substituents on the quinazoline ring allows chemists to tailor the compound's characteristics, such as solubility and reactivity, to better suit specific applications.
This compound serves as a prime example of how a seemingly simple modification in molecular structure can lead to significant changes in chemical behavior and efficacy in medicinal applications. As research continues, the potential of compounds like N4-(3-bromophenyl)quinazoline-4,6,7-triamine will likely unveil new therapeutic targets and deepen our understanding of disease mechanisms.
Synonyms
bpdq
169205-87-2
N4-(3-bromophenyl)quinazoline-4,6,7-triamine
N4-(3-bromophenyl)-4,6,7-Quinazolinetriamine
4-N-(3-bromophenyl)quinazoline-4,6,7-triamine
72M7S95J3U
N-(3-Bromophenyl)quinazoline-4,6,7-triamine
UNII-72M7S95J3U
CHEMBL328216
4,6,7-Quinazolinetriamine, N4-(3-bromophenyl)-
4-[(3-Bromophenyl)amino]-6,7-diaminoquinazoline
K00041
BDBM3303
SCHEMBL7221302
4-Anilinoquinazoline deriv. 54
ADXSZLCTQCWMTE-UHFFFAOYSA-N
DTXSID101257447
HSCI1_000040
AKOS025149794
PD187049
4-(3-bromoanilino)-6,7-diaminoquinazoline
DB-343769
4[ (3-Bromophenyl)aminol-6,7-diaminoquinazoline
BRD-K65185756-001-01-0
Solubility of N4-(3-bromophenyl)quinazoline-4,6,7-triamine (C14H11BrN6)
The solubility of N4-(3-bromophenyl)quinazoline-4,6,7-triamine can be somewhat complex due to its molecular structure and the presence of functional groups. It is essential to consider the following factors that greatly influence its solubility:
For N4-(3-bromophenyl)quinazoline-4,6,7-triamine, its solubility is likely to be limited in water due to the bulk of its brominated structure, which may hinder interactions with water molecules. However, it could exhibit better solubility in organic solvents such as dimethyl sulfoxide (DMSO) or dimethylformamide (DMF), where similar compounds typically dissolve more readily.
In summary, when considering the solubility of N4-(3-bromophenyl)quinazoline-4,6,7-triamine, one should focus on the polar or non-polar characteristics of the solvent, the structural properties of the compound, and environmental conditions. As always, empirical testing should confirm expected solubility behaviors.