2-Chloro-N-(piperidin-4-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine hydrochloride
Names and Identifiers of 1000207-51-1
CAS Number |
1000207-51-1 |
|---|---|
IUPAC Name |
2-chloro-N-piperidin-4-yl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine;hydrochloride |
InChI |
InChI=1S/C12H17ClN4.ClH/c13-12-16-10-3-1-2-9(10)11(17-12)15-8-4-6-14-7-5-8;/h8,14H,1-7H2,(H,15,16,17);1H |
InChIKey |
LPZSDDKVDLYBAA-UHFFFAOYSA-N |
Canonical SMILES |
C1CC2=C(C1)N=C(N=C2NC3CCNCC3)Cl.Cl |
Physical and chemical properties of 1000207-51-1
Exact Mass |
288.090851 |
|---|---|
Molecular Formula |
C12H18Cl2N4 |
Molecular Weight |
289.204 |
Applications of 1000207-51-1
The primary applications of 2-Chloro-N-(piperidin-4-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine hydrochloride are in pharmaceutical research and development. Its unique structure allows it to serve as a lead compound for designing new drugs targeting various diseases, particularly in oncology and neurology.
Interaction Studies of 1000207-51-1
Interaction studies have shown that this compound can bind effectively to specific biological targets such as enzymes and receptors involved in disease pathways. These interactions are crucial for understanding its mechanism of action and potential therapeutic benefits. In vitro assays have demonstrated its efficacy against certain cancer cell lines, suggesting a promising role in cancer therapy.
Biological Activity of 1000207-51-1
Research indicates that 2-Chloro-N-(piperidin-4-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine hydrochloride exhibits significant biological activities. It has been investigated for its potential as an inhibitor of specific enzymes and receptors, making it a candidate for therapeutic applications in treating various diseases. For instance, it has shown promise in inhibiting certain cancer cell lines, demonstrating its potential as an anticancer agent.