E7820
10mM in DMSO
- Product Code: 181265
CAS:
289483-69-8
Molecular Weight: | 336.37 g./mol | Molecular Formula: | C₁₇H₁₂N₄O₂S |
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Density: | Storage Condition: | -20°C |
Product Description:
E7820 is an investigational anti-cancer agent primarily studied for its potential in treating solid tumors. It functions as a sulfonamide-based small molecule with anti-angiogenic properties, meaning it helps inhibit the formation of new blood vessels that tumors need to grow and spread. This compound has shown activity in preclinical models against various cancer types, including multiple myeloma and leukemia, by inducing G1 cell cycle arrest and promoting apoptosis in tumor cells.
One of the key mechanisms involves downregulation of integrin β4 signaling, which plays a role in tumor cell survival and metastasis. Due to its oral bioavailability and favorable pharmacokinetic profile in early studies, E7820 has been evaluated in phase I and II clinical trials to assess efficacy and safety in patients with advanced malignancies. While still under investigation, it represents a promising candidate in targeted cancer therapy, particularly for tumors dependent on angiogenesis and specific integrin pathways.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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1ml | 10-20 days | ฿7,970.00 |
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E7820
E7820 is an investigational anti-cancer agent primarily studied for its potential in treating solid tumors. It functions as a sulfonamide-based small molecule with anti-angiogenic properties, meaning it helps inhibit the formation of new blood vessels that tumors need to grow and spread. This compound has shown activity in preclinical models against various cancer types, including multiple myeloma and leukemia, by inducing G1 cell cycle arrest and promoting apoptosis in tumor cells.
One of the key mechanisms involves downregulation of integrin β4 signaling, which plays a role in tumor cell survival and metastasis. Due to its oral bioavailability and favorable pharmacokinetic profile in early studies, E7820 has been evaluated in phase I and II clinical trials to assess efficacy and safety in patients with advanced malignancies. While still under investigation, it represents a promising candidate in targeted cancer therapy, particularly for tumors dependent on angiogenesis and specific integrin pathways.
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