RO5126766 (CH5126766)
99%
- Product Code: 230319
CAS:
946128-88-7
| Molecular Weight: | 471.46 g./mol | Molecular Formula: | C₂₁H₁₈FN₅O₅S |
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| Density: | Storage Condition: | -20℃ |
Product Description:
RO5126766 is a potent and selective dual inhibitor of MEK and RAF kinases, which are key components of the MAPK signaling pathway. This pathway is frequently dysregulated in various cancers, particularly those with mutations in BRAF or RAS genes. By inhibiting both MEK and RAF, RO5126766 effectively suppresses aberrant signaling in this pathway, leading to reduced tumor cell proliferation and induction of apoptosis.
It has been investigated primarily in preclinical and early clinical studies for the treatment of solid tumors, including melanoma, non-small cell lung cancer, and colorectal cancer. Its dual inhibition mechanism offers a potential advantage in overcoming resistance seen with single-pathway inhibitors, especially in tumors that develop escape mechanisms upon MEK or RAF inhibition alone.
RO5126766 shows promise in targeting tumors with acquired resistance to first-generation BRAF inhibitors, making it a candidate for use in combination therapies or as a second-line treatment. Research continues to explore optimal dosing, safety profiles, and patient selection based on genetic markers to maximize therapeutic benefit.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5mg | 10-20 days | ฿15,000.00 |
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RO5126766 (CH5126766)
RO5126766 is a potent and selective dual inhibitor of MEK and RAF kinases, which are key components of the MAPK signaling pathway. This pathway is frequently dysregulated in various cancers, particularly those with mutations in BRAF or RAS genes. By inhibiting both MEK and RAF, RO5126766 effectively suppresses aberrant signaling in this pathway, leading to reduced tumor cell proliferation and induction of apoptosis.
It has been investigated primarily in preclinical and early clinical studies for the treatment of solid tumors, including melanoma, non-small cell lung cancer, and colorectal cancer. Its dual inhibition mechanism offers a potential advantage in overcoming resistance seen with single-pathway inhibitors, especially in tumors that develop escape mechanisms upon MEK or RAF inhibition alone.
RO5126766 shows promise in targeting tumors with acquired resistance to first-generation BRAF inhibitors, making it a candidate for use in combination therapies or as a second-line treatment. Research continues to explore optimal dosing, safety profiles, and patient selection based on genetic markers to maximize therapeutic benefit.
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