PHA-680632
10mM in DMSO
- Product Code: 223885
CAS:
398493-79-3
Molecular Weight: | 501.62 g./mol | Molecular Formula: | C₂₈H₃₅N₇O₂ |
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EC Number: | MDL Number: | MFCD16038900 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C |
Product Description:
PHA-680632 is a potent Aurora kinase inhibitor primarily used in cancer research. It interferes with the activity of Aurora A and Aurora B kinases, which play critical roles in cell division and mitotic regulation. By inhibiting these enzymes, PHA-680632 disrupts proper spindle formation, chromosome segregation, and cytokinesis, leading to cell cycle arrest and apoptosis in rapidly dividing tumor cells.
This compound is widely applied in preclinical studies to investigate the role of Aurora kinases in tumorigenesis and as a potential therapeutic agent in oncology. It has shown antiproliferative effects in various cancer cell lines, including leukemia, breast, and colon cancers. Researchers also use PHA-680632 to study mechanisms of drug resistance and to evaluate combination therapies with other anticancer agents. Its selectivity and potency make it a valuable tool in the development of targeted cancer treatments.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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1ml | 10-20 days | ฿5,300.00 |
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PHA-680632
PHA-680632 is a potent Aurora kinase inhibitor primarily used in cancer research. It interferes with the activity of Aurora A and Aurora B kinases, which play critical roles in cell division and mitotic regulation. By inhibiting these enzymes, PHA-680632 disrupts proper spindle formation, chromosome segregation, and cytokinesis, leading to cell cycle arrest and apoptosis in rapidly dividing tumor cells.
This compound is widely applied in preclinical studies to investigate the role of Aurora kinases in tumorigenesis and as a potential therapeutic agent in oncology. It has shown antiproliferative effects in various cancer cell lines, including leukemia, breast, and colon cancers. Researchers also use PHA-680632 to study mechanisms of drug resistance and to evaluate combination therapies with other anticancer agents. Its selectivity and potency make it a valuable tool in the development of targeted cancer treatments.
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