TAK-733

10mM in DMSO

Reagent Code: #239088
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CAS Number 1035555-63-5

science Other reagents with same CAS 1035555-63-5

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scatter_plot Molecular Information
Weight 504.23 g/mol
Formula C₁₇H₁₅F₂IN₄O₄
badge Registry Numbers
MDL Number MFCD24386349
inventory_2 Storage & Handling
Storage -20°C

description Product Description

TAK-733 is a potent and selective inhibitor of MEK1/2 (mitogen-activated protein kinase kinase), which plays a key role in the RAS/RAF/MEK/ERK signaling pathway. This pathway is frequently dysregulated in various cancers, especially those with mutations in BRAF or RAS genes. TAK-733 has been investigated primarily for its antitumor activity in preclinical cancer models. It has shown efficacy in inhibiting the proliferation of cancer cells by blocking MEK-dependent signaling, leading to cell cycle arrest and apoptosis. Studies have demonstrated its activity against melanoma, non-small cell lung cancer, and colorectal cancer cell lines, particularly those harboring BRAF mutations. Due to its high selectivity and pharmacokinetic profile, TAK-733 has been used as a research tool to understand MEK inhibition mechanisms and pathway dynamics. Although it did not advance into late-stage clinical trials, it contributed valuable insights into the development of other MEK inhibitors for oncology therapeutics.

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inventory 1ml
10-20 days ฿14,680.00

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TAK-733
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TAK-733 is a potent and selective inhibitor of MEK1/2 (mitogen-activated protein kinase kinase), which plays a key role in the RAS/RAF/MEK/ERK signaling pathway. This pathway is frequently dysregulated in various cancers, especially those with mutations in BRAF or RAS genes. TAK-733 has been investigated primarily for its antitumor activity in preclinical cancer models. It has shown efficacy in inhibiting the proliferation of cancer cells by blocking MEK-dependent signaling, leading to cell cycle arrest and apoptosis. Studies have demonstrated its activity against melanoma, non-small cell lung cancer, and colorectal cancer cell lines, particularly those harboring BRAF mutations. Due to its high selectivity and pharmacokinetic profile, TAK-733 has been used as a research tool to understand MEK inhibition mechanisms and pathway dynamics. Although it did not advance into late-stage clinical trials, it contributed valuable insights into the development of other MEK inhibitors for oncology therapeutics.
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