Dutasteride/tamsulosin

Evacuation Traps, 2-1/4, 144/bx";MPN=UBC-85502"

Evacuation Traps, 2-3/4, 144/bx";MPN=UBC-85512"

Evacuation Traps, 1-1/4, 144/bx";MPN=UBC-85500"

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

Biochem/physiol Actions Dynarrestin is a potent and selective reversible inhibitor of cytoplasmic dyneins 1 and 2 that inhibits dynein 1-dependent microtubule binding and motility without affecting ATP hydrolysis. It inhibits endosome movement and

A cell-permeable, reversible inhibitor of dynamin 1, dynamin 2, and mitochondrial dynamin, Drp1 GTPase activity (IC₅₀ = 15 &muM) inhibits clathrin-dependent vesicle formation and endocytosis can also augment the release of

A cell-permeable, reversible inhibitor of dynamin 1, dynamin 2, and mitochondrial dynamin, Drp1 GTPase activity (IC₅₀ = 15 &muM) inhibits clathrin-dependent vesicle formation and endocytosis can also augment the release of

A cell-permeable, reversible inhibitor of dynamin 1, dynamin 2, and mitochondrial dynamin, Drp1 GTPase activity (IC₅₀ = 15 &muM) inhibits clathrin-dependent vesicle formation and endocytosis can also augment the release of

A cell-permeable, reversible inhibitor of dynamin 1, dynamin 2, and mitochondrial dynamin, Drp1 GTPase activity (IC₅₀ = 15 &muM) inhibits clathrin-dependent vesicle formation and endocytosis can also augment the release of

An inhibitor of the ERAD pathway, blocking the degradation of misfolded proteins at a dose of 8 &microM associates with the p97-associated deubiquitinating complex in cells, preventing deubiquitination of substrates by ataxin-3 interferes with

An inhibitor of the ERAD pathway, blocking the degradation of misfolded proteins at a dose of 8 &microM associates with the p97-associated deubiquitinating complex in cells, preventing deubiquitination of substrates by ataxin-3 interferes with

An inhibitor of the ERAD pathway, blocking the degradation of misfolded proteins at a dose of 8 &microM associates with the p97-associated deubiquitinating complex in cells, preventing deubiquitination of substrates by ataxin-3 interferes with