Bioymifi,DR5 Activator

10mM in DMSO

  • Product Code: 142763
  CAS:    1420071-30-2
Molecular Weight: 494.32 g./mol Molecular Formula: C₂₂H₁₂BrN₃O₄S
EC Number: MDL Number:
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Density: Storage Condition: -20°C
Product Description: Bioymifi, DR5 Activator is primarily used in cancer research due to its ability to selectively activate the DR5 (Death Receptor 5) pathway. This activation triggers apoptosis, or programmed cell death, in tumor cells, making it a valuable tool in the development of targeted cancer therapies. It shows particular promise in studies involving resistant cancer cell lines, where conventional treatments fail to induce apoptosis effectively. The compound enhances the sensitivity of cancer cells to TRAIL (TNF-Related Apoptosis-Inducing Ligand), supporting combination therapies that improve treatment efficacy. It is widely applied in preclinical studies to investigate apoptosis signaling mechanisms and to screen potential anticancer agents. Its role in promoting cancer cell death with minimal effect on normal cells highlights its potential as a selective and efficient therapeutic agent in oncology research.
Sizes / Availability / Pricing:
Size Availability Price Quantity
1ml 10-20 days ฿6,230.00
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Bioymifi,DR5 Activator
Bioymifi, DR5 Activator is primarily used in cancer research due to its ability to selectively activate the DR5 (Death Receptor 5) pathway. This activation triggers apoptosis, or programmed cell death, in tumor cells, making it a valuable tool in the development of targeted cancer therapies. It shows particular promise in studies involving resistant cancer cell lines, where conventional treatments fail to induce apoptosis effectively. The compound enhances the sensitivity of cancer cells to TRAIL (TNF-Related Apoptosis-Inducing Ligand), supporting combination therapies that improve treatment efficacy. It is widely applied in preclinical studies to investigate apoptosis signaling mechanisms and to screen potential anticancer agents. Its role in promoting cancer cell death with minimal effect on normal cells highlights its potential as a selective and efficient therapeutic agent in oncology research.
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