6-Acetyl-8-cyclopentyl-5-methyl-2-(5-(piperazin-1-yl)pyridin-2-ylamino)pyrido[2,3-d]pyrimidin-7(8H)-one hydrochloride

98%

  • Product Code: 110624
  CAS:    827022-32-2
Molecular Weight: 483.99 g./mol Molecular Formula: C₂₄H₂₉N₇O₂HCl
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: -20°C
Product Description: This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a potent and selective inhibitor of cyclin-dependent kinases (CDKs), which are crucial regulators of cell cycle progression. By targeting specific CDKs, it has potential applications in cancer therapy, particularly in halting the proliferation of cancer cells. Its mechanism involves inducing cell cycle arrest and promoting apoptosis in malignant cells, making it a candidate for treating various cancers, including breast, lung, and leukemia. Additionally, its structural features allow for further optimization and modification to enhance efficacy and reduce off-target effects, contributing to its role in preclinical research and the development of novel anticancer agents.
Product Specification:
Test Specification
Appearance White To Beige Powder
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.005 10-20 days ฿590.00
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-
0.010 10-20 days ฿990.00
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0.050 10-20 days ฿2,840.00
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-
0.100 10-20 days ฿4,820.00
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-
0.250 10-20 days ฿7,362.00
+
-
1.000 10-20 days ฿12,510.00
+
-
5.000 10-20 days ฿39,420.00
+
-
6-Acetyl-8-cyclopentyl-5-methyl-2-(5-(piperazin-1-yl)pyridin-2-ylamino)pyrido[2,3-d]pyrimidin-7(8H)-one hydrochloride
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a potent and selective inhibitor of cyclin-dependent kinases (CDKs), which are crucial regulators of cell cycle progression. By targeting specific CDKs, it has potential applications in cancer therapy, particularly in halting the proliferation of cancer cells. Its mechanism involves inducing cell cycle arrest and promoting apoptosis in malignant cells, making it a candidate for treating various cancers, including breast, lung, and leukemia. Additionally, its structural features allow for further optimization and modification to enhance efficacy and reduce off-target effects, contributing to its role in preclinical research and the development of novel anticancer agents.
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