MRK-003

≥95%

  • Product Code: 210092
  CAS:    623165-93-5
Molecular Weight: 551.59 g./mol Molecular Formula: C₂₅H₃₁F₆N₃O₂S
EC Number: MDL Number: MFCD23136012
Melting Point: Boiling Point: 591.3±60.0 °C(Predicted)
Density: 1.41 Storage Condition: Room temperature
Product Description: MRK-003 is a gamma-secretase inhibitor that has been primarily investigated for its potential in cancer research, particularly in targeting Notch signaling pathways. The Notch pathway plays a critical role in cell differentiation, proliferation, and survival, and its dysregulation is associated with several cancers, including T-cell acute lymphoblastic leukemia (T-ALL), breast cancer, and glioblastoma. MRK-003 has demonstrated the ability to suppress the activation of Notch receptors by inhibiting gamma-secretase, the enzyme responsible for the final proteolytic cleavage that releases the active intracellular domain of Notch. In preclinical studies, MRK-003 has shown antitumor activity in xenograft models by inducing cell cycle arrest and apoptosis in tumor cells. It has also been explored in combination with other chemotherapeutic agents and radiation, where it enhances sensitivity and improves treatment outcomes. Its application extends to research on cancer stem cells, where inhibition of Notch signaling may reduce self-renewal and tumor initiation capacity. Due to its role in modulating key oncogenic pathways, MRK-003 serves as a valuable tool compound in oncology research, aiding in the validation of gamma-secretase and Notch as therapeutic targets. However, its use remains largely confined to laboratory and preclinical settings due to challenges related to toxicity and selectivity.
Sizes / Availability / Pricing:
Size Availability Price Quantity
1mg 10-20 days ฿14,240.00
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5mg 10-20 days ฿42,640.00
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MRK-003
MRK-003 is a gamma-secretase inhibitor that has been primarily investigated for its potential in cancer research, particularly in targeting Notch signaling pathways. The Notch pathway plays a critical role in cell differentiation, proliferation, and survival, and its dysregulation is associated with several cancers, including T-cell acute lymphoblastic leukemia (T-ALL), breast cancer, and glioblastoma. MRK-003 has demonstrated the ability to suppress the activation of Notch receptors by inhibiting gamma-secretase, the enzyme responsible for the final proteolytic cleavage that releases the active intracellular domain of Notch. In preclinical studies, MRK-003 has shown antitumor activity in xenograft models by inducing cell cycle arrest and apoptosis in tumor cells. It has also been explored in combination with other chemotherapeutic agents and radiation, where it enhances sensitivity and improves treatment outcomes. Its application extends to research on cancer stem cells, where inhibition of Notch signaling may reduce self-renewal and tumor initiation capacity. Due to its role in modulating key oncogenic pathways, MRK-003 serves as a valuable tool compound in oncology research, aiding in the validation of gamma-secretase and Notch as therapeutic targets. However, its use remains largely confined to laboratory and preclinical settings due to challenges related to toxicity and selectivity.
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