TAK-733 5mg 5mg | Purity Not Available
Adooq Bioscience
TAK-733 is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity.
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TAK-733 10mM * 1mL in DMSO 10mM * 1mL in DMSO | Purity Not Available
Adooq Bioscience
TAK-733 is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity.
More Information Supplier PageTAK-733 100mg 100mg | Purity Not Available
Adooq Bioscience
TAK-733 is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity.
More Information Supplier PageTubastatin A HCl 10mg 10mg | Purity Not Available
Adooq Bioscience
Tubastatin A HCl is a potent HDAC inhibitor that demonstrates over more selectivity than all other HDAC isoforms (IC50s >16 uM), excluding HDAC8 (IC50 = 0.9 M).
More Information Supplier PageTubastatin A HCl 100mg 100mg | Purity Not Available
Adooq Bioscience
Tubastatin A HCl is a potent HDAC inhibitor that demonstrates over more selectivity than all other HDAC isoforms (IC50s >16 uM), excluding HDAC8 (IC50 = 0.9 M).
More Information Supplier PageTAK-700 100mg 100mg | Purity Not Available
Adooq Bioscience
TAK-700 (Orteronel) is an oral, non-steroidal androgen synthesis inhibitor that selectively inhibits the 17,20 lyase enzyme.
More Information Supplier PageTAK-700 10mg 10mg | Purity Not Available
Adooq Bioscience
TAK-700 (Orteronel) is an oral, non-steroidal androgen synthesis inhibitor that selectively inhibits the 17,20 lyase enzyme.
More Information Supplier PageMG-132 50mg 50mg | Purity Not Available
Adooq Bioscience
MG-132 is a potent cell-permeable inhibitor of proteasome (IC50 = 100 nM) and calpain (IC50 = 1.2 ??M).
More Information Supplier PageMG-132 25mg 25mg | Purity Not Available
Adooq Bioscience
MG-132 is a potent cell-permeable inhibitor of proteasome (IC50 = 100 nM) and calpain (IC50 = 1.2 ??M).
More Information Supplier PageMG-132 10mM * 1mL in DMSO 10mM * 1mL in DMSO | Purity Not Available
Adooq Bioscience
MG-132 is a potent cell-permeable inhibitor of proteasome (IC50 = 100 nM) and calpain (IC50 = 1.2 ??M).
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