CTEP 10mM * 1mL in DMSO 10mM * 1mL in DMSO | Purity Not Available
Adooq Bioscience
CTEP is a highly potent, selective and orally bioavailable allosteric antagonist of mGlu5 receptor with an IC50 of 2.2 nM.
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CTEP 10mg 10mg | Purity Not Available
Adooq Bioscience
CTEP is a highly potent, selective and orally bioavailable allosteric antagonist of mGlu5 receptor with an IC50 of 2.2 nM.
More Information Supplier PageTCS PIM-1 4a 50mg 50mg | Purity Not Available
Adooq Bioscience
TCS PIM-1 4a is a selective and ATP-competitive Pim kinase inhibitor (IC50 values = 24 and 100 nM for Pim-1 and Pim-2, respectively).
More Information Supplier PageTCS PIM-1 4a 25mg 25mg | Purity Not Available
Adooq Bioscience
TCS PIM-1 4a is a selective and ATP-competitive Pim kinase inhibitor (IC50 values = 24 and 100 nM for Pim-1 and Pim-2, respectively).
More Information Supplier PageBafilomycin A1 5mg 5mg | Purity Not Available
Adooq Bioscience
Bafilomycin A1 prevents maturation of autophagic vacuoles by inhibiting fusion between autophagosomes and lysosomes in rat hepatoma cell line, H-4-II-E cells.
More Information Supplier PageBafilomycin A1 25mg 25mg | Purity Not Available
Adooq Bioscience
Bafilomycin A1 prevents maturation of autophagic vacuoles by inhibiting fusion between autophagosomes and lysosomes in rat hepatoma cell line, H-4-II-E cells.
More Information Supplier PageBafilomycin A1 2mg 2mg | Purity Not Available
Adooq Bioscience
Bafilomycin A1 prevents maturation of autophagic vacuoles by inhibiting fusion between autophagosomes and lysosomes in rat hepatoma cell line, H-4-II-E cells.
More Information Supplier PageBafilomycin A1 10mg 10mg | Purity Not Available
Adooq Bioscience
Bafilomycin A1 prevents maturation of autophagic vacuoles by inhibiting fusion between autophagosomes and lysosomes in rat hepatoma cell line, H-4-II-E cells.
More Information Supplier PageLY 2183240 50mg 50mg | Purity Not Available
Adooq Bioscience
LY 2183240 acts both as a potent inhibitor of the reuptake of the endocannabinoid anandamide, and as an inhibitor of fatty acid amide hydrolase (FAAH), the primary enzyme responsible for degrading anandamide.
More Information Supplier PageLY 2183240 25mg 25mg | Purity Not Available
Adooq Bioscience
LY 2183240 acts both as a potent inhibitor of the reuptake of the endocannabinoid anandamide, and as an inhibitor of fatty acid amide hydrolase (FAAH), the primary enzyme responsible for degrading anandamide.
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