Molecular Biology Reagents

Reactant for synthesis of: DPP-4 inhibitors JAK2 inhibitors Serotonin and noradrenaline reuptake inhibitors Human tryptase inhibitors Anti-thrombotic nicecotamides Reactive for oxidative C-arylation of free (NH)-heterocycles via direct (sp3) C-H

Reactant for synthesis of: DPP-4 inhibitors JAK2 inhibitors Serotonin and noradrenaline reuptake inhibitors Human tryptase inhibitors Anti-thrombotic nicecotamides Reactive for oxidative C-arylation of free (NH)-heterocycles via direct (sp3) C-H

Reactant for synthesis of: DPP-4 inhibitors JAK2 inhibitors Serotonin and noradrenaline reuptake inhibitors Human tryptase inhibitors Anti-thrombotic nicecotamides Reactive for oxidative C-arylation of free (NH)-heterocycles via direct (sp3) C-H

Reactant for synthesis of: DPP-4 inhibitors JAK2 inhibitors Serotonin and noradrenaline reuptake inhibitors Human tryptase inhibitors Anti-thrombotic nicecotamides Reactive for oxidative C-arylation of free (NH)-heterocycles via direct (sp3) C-H

FTY720 (S)-Phosphate is an agonist of S1P receptor 1 (S1PR1) , used in the research of acute inflammatory diseases such as acute lung injury.In VitroFTY720 (S)-Phosphate is an agonist of S1PR1. FTY720 (S)-Phosphate (Tys, 1 μM) maintains S1PR1

FTY720 (S)-Phosphate is an agonist of S1P receptor 1 (S1PR1) , used in the research of acute inflammatory diseases such as acute lung injury.In VitroFTY720 (S)-Phosphate is an agonist of S1PR1. FTY720 (S)-Phosphate (Tys, 1 μM) maintains S1PR1

A potent, specific, ATP-competitive, and cell permeable inhibitor of ROCK (Ki = 1.6 nM) more potent inhibitor of ROCK than either Y-27632 (Ki = 140 nM) or HA-1077 (Ki = 330 nM) poorly inhibits PKA, PKC, and MLCK.

(S)-JQ-35 (TEN-010) is an inhibitor of the Bromodomain and Extra-Terminal (BET) family bromodomain-containing proteins with potential antineoplastic activity.Form:Solid.

(S)-JQ-35 (TEN-010) is an inhibitor of the Bromodomain and Extra-Terminal (BET) family bromodomain-containing proteins with potential antineoplastic activity.Form:Solid.

(S)-JQ-35 (TEN-010) is an inhibitor of the Bromodomain and Extra-Terminal (BET) family bromodomain-containing proteins with potential antineoplastic activity.Form:Solid.

(S)-JQ-35 (TEN-010) is an inhibitor of the Bromodomain and Extra-Terminal (BET) family bromodomain-containing proteins with potential antineoplastic activity.Form:Solid.

(S)-Mephenytoin is a hydantoin small molecule, originally discovered and implemented for its anticonvulsant effects. Individuals present a variable ability to perform hydroxylation of (S)-Mephenytoin at the 4'-position associated with polymorphism