Interesting facts
Interesting Facts about N'-(2-chloroethyl)-N-(6-chloro-2-methoxy-acridin-9-yl)-N'-ethyl-propane-1,3-diamine
N'-(2-chloroethyl)-N-(6-chloro-2-methoxy-acridin-9-yl)-N'-ethyl-propane-1,3-diamine is a fascinating compound with several intriguing aspects that merit discussion. Here are some highlights about this compound:
- Pharmaceutical Significance: This compound has been researched for its potential roles in medicinal chemistry, particularly in the development of anticancer agents. Its unique structure holds promise for targeted therapy against certain types of cancer cells.
- Mechanism of Action: The acridine structure is known for its ability to intercalate with DNA, thereby inhibiting the replication process. This mechanism is vital for its anticancer properties, making it a subject of interest in drug development.
- Chlorinated Moiety: The presence of chlorine atoms in its structure enhances its biological activity. Chlorinated compounds often exhibit increased potency and stability, which can lead to improved efficacy in therapeutic applications.
- Synthetic Pathways: The synthesis of this compound involves intricate synthetic routes that can include both aromatic substitution and alkylation reactions. Such synthetic methodologies are key for producing a range of similarly structured compounds for research.
- Potential for Novel Therapeutics: As researchers continue to explore the compound's characteristics, there is potential for discovering novel therapeutic strategies. Its unique combination of functional groups could lead to derivatives with enhanced properties.
- Research Studies: Investigations into this compound have revealed promising results in preclinical models, highlighting its utility in the quest for new cancer therapies. Ongoing studies aim to elucidate its full pharmacological profile.
In conclusion, N'-(2-chloroethyl)-N-(6-chloro-2-methoxy-acridin-9-yl)-N'-ethyl-propane-1,3-diamine is more than just a chemical compound; it represents a beacon of hope in the field of medicinal chemistry. As researchers expand their understanding of its properties and mechanisms, this compound may lead to significant advancements in cancer treatment and therapy development.
Synonyms
Acridine mustard free base
ICR-170 free base
UNII-568MU7Q5YZ
568MU7Q5YZ
13015-79-7
CHEBI:37594
1,3-Propanediamine, N-(2-chloroethyl)-N'-(6-chloro-2-methoxy-9-acridinyl)-N-ethyl-
N-(2-chloroethyl)-N'-(6-chloro-2-methoxyacridin-9-yl)-N-ethylpropane-1,3-diamine
CHEMBL3416994
SCHEMBL20305454
DTXSID50156369
N'-(2-chloroethyl)-N-(6-chloro-2-methoxyacridin-9-yl)-N'-ethylpropane-1,3-diamine
Q27117199
6-chloro-9-[3-([2-chloroethyl]ethylamino)propylamino]-2-methoxy -acridine
Solubility of N'-(2-chloroethyl)-N-(6-chloro-2-methoxy-acridin-9-yl)-N'-ethyl-propane-1,3-diamine
The solubility of N'-(2-chloroethyl)-N-(6-chloro-2-methoxy-acridin-9-yl)-N'-ethyl-propane-1,3-diamine can be influenced by several factors due to its complex structure. While specific solubility data may not be extensively available, we can draw some general conclusions based on its functional groups and chemical properties.
Factors Affecting Solubility:
Generally, compounds that contain both polar and non-polar characteristics can dissolve well in mixed solvents, such as water-chloroform or ethanol-water mixtures.
Key Considerations:
In summary, the solubility of this compound may demonstrate:
Understanding the solubility behavior of N'-(2-chloroethyl)-N-(6-chloro-2-methoxy-acridin-9-yl)-N'-ethyl-propane-1,3-diamine is essential for its practical applications, including pharmacological activity, formulation, and stability studies.