AM1241 25mg | Purity Not Available
Selleck Chemicals
AM-1241 is a selective cannabinoid CB2 receptor agonist with Ki of 3.4 nM, exhibits 82-fold selectivity over CB1 receptor.
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AM1241 2mg | Purity Not Available
Selleck Chemicals
AM-1241 is a selective cannabinoid CB2 receptor agonist with Ki of 3.4 nM, exhibits 82-fold selectivity over CB1 receptor.
More Information Supplier PageAM1241 10mM/1mL | Purity Not Available
Selleck Chemicals
AM-1241 is a selective cannabinoid CB2 receptor agonist with Ki of 3.4 nM, exhibits 82-fold selectivity over CB1 receptor.
More Information Supplier PageSB408124 5mg | Purity Not Available
Selleck Chemicals
SB408124 is a non-peptide antagonist for OX1 receptor with Ki of 57 nM and 27 nM in both whole cell and membrane, respectively, exhibits 50-fold selectivity over OX2 receptor.
More Information Supplier PageOrg 27569 50mg | Purity Not Available
Selleck Chemicals
Org 27569 is an allosteric modulator of cannabinoid CB1 receptor, induces a CB1 receptor state that is characterized by enhanced agonist affinity and decreased inverse agonist affinity.
More Information Supplier PageOrg 27569 10mg | Purity Not Available
Selleck Chemicals
Org 27569 is an allosteric modulator of cannabinoid CB1 receptor, induces a CB1 receptor state that is characterized by enhanced agonist affinity and decreased inverse agonist affinity.
More Information Supplier PageR406 (free base) 50mg | Purity Not Available
Selleck Chemicals
R406 (free base) is a potent Syk inhibitor with IC50 of 41 nM in a cell-free assay, strongly inhibits Syk but not Lyn, 5-fold less potent to Flt3. R406 (free base) triggers apoptosis. Phase 1.
More Information Supplier PageR406 (free base) 10mg | Purity Not Available
Selleck Chemicals
R406 (free base) is a potent Syk inhibitor with IC50 of 41 nM in a cell-free assay, strongly inhibits Syk but not Lyn, 5-fold less potent to Flt3. R406 (free base) triggers apoptosis. Phase 1.
More Information Supplier PageAZD7762 10mM/1mL | Purity Not Available
Selleck Chemicals
AZD7762 is a potent and selective inhibitor of Chk1 with IC50 of 5 nM in a cell-free assay. It is equally potent against Chk2 and less potent against CAM, Yes, Fyn, Lyn, Hck and Lck. Phase 1.
More Information Supplier PageAZD7762 2mg | Purity Not Available
Selleck Chemicals
AZD7762 is a potent and selective inhibitor of Chk1 with IC50 of 5 nM in a cell-free assay. It is equally potent against Chk2 and less potent against CAM, Yes, Fyn, Lyn, Hck and Lck. Phase 1.
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