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A646895-1mgA-836339 is a cannabinoid CB2 receptor-selective agonist: exhibits high potencies at CB(2) and selectivity over CB(1) receptors.IC50 value: 1.6 nM(EC50) Target: CB2 agonist in vitro: In radioligand binding assays, A-836339 displays high affinities
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A646895-50mgA-836339 is a cannabinoid CB2 receptor-selective agonist: exhibits high potencies at CB(2) and selectivity over CB(1) receptors.IC50 value: 1.6 nM(EC50) Target: CB2 agonist in vitro: In radioligand binding assays, A-836339 displays high affinities
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A646895-5mgA-836339 is a cannabinoid CB2 receptor-selective agonist: exhibits high potencies at CB(2) and selectivity over CB(1) receptors.IC50 value: 1.6 nM(EC50) Target: CB2 agonist in vitro: In radioligand binding assays, A-836339 displays high affinities
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A654783-1mlA-836339 is a cannabinoid CB2 receptor-selective agonist: exhibits high potencies at CB(2) and selectivity over CB(1) receptors.IC50 value: 1.6 nM(EC50) Target: CB2 agonist in vitro: In radioligand binding assays, A-836339 displays high affinities
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A650965-10mgA-908292 is a potent and selective acetyl-CoA carboxylase 2 (ACC2) inhibitor, with an IC 50 of 38 nM. A-908292 can be used for the research of fatty acid metabolismForm:SolidIC50&: Target:IC50: 38 nM (ACC2).
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A650965-25mgA-908292 is a potent and selective acetyl-CoA carboxylase 2 (ACC2) inhibitor, with an IC 50 of 38 nM. A-908292 can be used for the research of fatty acid metabolismForm:SolidIC50&: Target:IC50: 38 nM (ACC2).
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A650965-5mgA-908292 is a potent and selective acetyl-CoA carboxylase 2 (ACC2) inhibitor, with an IC 50 of 38 nM. A-908292 can be used for the research of fatty acid metabolismForm:SolidIC50&: Target:IC50: 38 nM (ACC2).
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A651043-100mgA2AR-agonist-1 is a potent A2AR and ENT1 agonist with Ki of 4.39 and 3.47 for A2AR and ENT1.IC50 value: 4.39 and 3.47 (Ki) Target: A2AR and ENT1A2AR-agonist-1 is a novel dual-action compound, targeting the Adenosine A2A Receptor and Adenosine
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A651043-10mgA2AR-agonist-1 is a potent A2AR and ENT1 agonist with Ki of 4.39 and 3.47 for A2AR and ENT1.IC50 value: 4.39 and 3.47 (Ki) Target: A2AR and ENT1A2AR-agonist-1 is a novel dual-action compound, targeting the Adenosine A2A Receptor and Adenosine
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A651043-1mgA2AR-agonist-1 is a potent A2AR and ENT1 agonist with Ki of 4.39 and 3.47 for A2AR and ENT1.IC50 value: 4.39 and 3.47 (Ki) Target: A2AR and ENT1A2AR-agonist-1 is a novel dual-action compound, targeting the Adenosine A2A Receptor and Adenosine
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A651043-50mgA2AR-agonist-1 is a potent A2AR and ENT1 agonist with Ki of 4.39 and 3.47 for A2AR and ENT1.IC50 value: 4.39 and 3.47 (Ki) Target: A2AR and ENT1A2AR-agonist-1 is a novel dual-action compound, targeting the Adenosine A2A Receptor and Adenosine
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A651043-5mgA2AR-agonist-1 is a potent A2AR and ENT1 agonist with Ki of 4.39 and 3.47 for A2AR and ENT1.IC50 value: 4.39 and 3.47 (Ki) Target: A2AR and ENT1A2AR-agonist-1 is a novel dual-action compound, targeting the Adenosine A2A Receptor and Adenosine