Imiloxan hydrochloride

Adrenochrome Monoaminoguanidine Mesilate is a adrenochrome derivative that is used as a hemostatic agent.

ANTI-ALPHA FODRIN ANTIBODY CLONE 9H5V8 RABBIT MONOCLONAL

AZD9056 hydrochloride is a selective orally active inhibitor of P2X7 which plays a significant role in inflammation and pain-causing diseases.In VitroThe antagonist AZD9056 blocks P2X7 receptors with an IC 50 of 11.2 nM in HEK-hP2X7 cell line,

Block 5 ml x 24

CCR1 is a GPCR that binds to a variety of CC ligands, including MIP-1a, RANTES, MCP-3, HCC-1, HCC-2, HCC-4, and MPIF-1 (Olson and Ley, 2002). Lymphocytes, macrophages, dendritic cells, and GM-CSF-activated neutrophils express CCR1 (Kaufmann et al.

Desethyl Amiodarone Hydrochloride is a metabolite of Amiodarone and a non-selective ion channel blocker.

Biochem/physiol Actions (+)-Isomer is a selective &#945-adrenoceptor antagonist (&#8722)-isomer is an imidazoline ligand that induces insulin secretion, mediated by the blockade of ATP-sensitive potassium channels in pancreatic &#946 cells I 1

Biochem/physiol Actions (+)-Isomer is a selective &#945-adrenoceptor antagonist (&#8722)-isomer is an imidazoline ligand that induces insulin secretion, mediated by the blockade of ATP-sensitive potassium channels in pancreatic &#946 cells I 1

Enpatoran (M5049) hydrochloride is a potent, orally active and dual TLR7/8 inhibitor with IC 50 s of 11.1 nM and 24.1 nM in HEK293 cells, respectively. Enpatoran hydrochloride is inactive against TLR3 , TLR4 and TLR9 . Enpatoran hydrochloride can

Enpatoran (M5049) hydrochloride is a potent, orally active and dual TLR7/8 inhibitor with IC 50 s of 11.1 nM and 24.1 nM in HEK293 cells, respectively. Enpatoran hydrochloride is inactive against TLR3 , TLR4 and TLR9 . Enpatoran hydrochloride can

Enpatoran (M5049) hydrochloride is a potent, orally active and dual TLR7/8 inhibitor with IC 50 s of 11.1 nM and 24.1 nM in HEK293 cells, respectively. Enpatoran hydrochloride is inactive against TLR3 , TLR4 and TLR9 . Enpatoran hydrochloride can

A potent, selective antagonist of the &beta2-adrenergic receptor (Ki = 0.7 nM for the &beta2 receptor, compared with 49.