BML-275 5mg 5mg | Purity Not Available
Adooq Bioscience
BML-275 is a cell-permeable pyrazolopyrimidine compound shown to be an AMP-activated protein kinase (AMPK) and fatty acid synthase inhibitor.
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BML-275 10mg 10mg | Purity Not Available
Adooq Bioscience
BML-275 is a cell-permeable pyrazolopyrimidine compound shown to be an AMP-activated protein kinase (AMPK) and fatty acid synthase inhibitor.
More Information Supplier PageTCS JNK 5a 50mg 50mg | Purity Not Available
Adooq Bioscience
TCS JNK 5a is a highly selective inhibitor of JNK2 and JNK3 (pIC50 values are 6.7, 6.5,
More Information Supplier PageNF 279 50mg 50mg | Purity Not Available
Adooq Bioscience
NF279 is a suramin analog that acts as a highly selective, competitive, and reversible ATP-antagonist of P2X receptor (IC50/KB ~ 1 ??M in smooth muscle).
More Information Supplier PageNecrostatin-1 10mg 10mg | Purity Not Available
Adooq Bioscience
Necrostatin-1 is an ATP-competitive, allosteric inhibitor of receptor-interacting protein kinase 1 (RIPK1) (EC50 = 182 nM).
More Information Supplier PageMethoctramine hydrate 50mg 50mg | Purity Not Available
Adooq Bioscience
Methoctramine hydrate is a selective M2 muscarinic receptor antagonist at nM concentrations
More Information Supplier PageMethoctramine hydrate 25mg 25mg | Purity Not Available
Adooq Bioscience
Methoctramine hydrate is a selective M2 muscarinic receptor antagonist at nM concentrations
More Information Supplier PageMethoctramine hydrate 10mg 10mg | Purity Not Available
Adooq Bioscience
Methoctramine hydrate is a selective M2 muscarinic receptor antagonist at nM concentrations
More Information Supplier PageGW 4869 50mg 50mg | Purity Not Available
Adooq Bioscience
W4869 is a cell permeable, selective inhibitor of N-SMase (neutral sphingomyelinase).
More Information Supplier PageGW 4869 5mg 5mg | Purity Not Available
Adooq Bioscience
W4869 is a cell permeable, selective inhibitor of N-SMase (neutral sphingomyelinase).
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