BAY 41-8543 ME1 Smiles: [2H]C([2H])([2H])C(O)([C@@H](C)/C=C/[C@@H](C)[C@H]1CC[C@H]2/C(/CCC[C@@]21C)=C/C=C1C[C@@H](O)C[C@H](O)C1)C([2H])([2H])[2H]

Smiles: [2H]C([2H])([2H])C(O)([C@@H](C)/C=C/[C@@H](C)[C@H]1CC[C@H]2/C(/CCC[C@@]21C)=C/C=C1C[C@@H](O)C[C@H](O)C1)C([2H])([2H])[2H]

InChi: InChI=1S/C23H31N5O8

10 μM) dose-dependently reduces expression of toll-like receptor-4 evoked by palmitic acid (100 μM)

demonstrates biological activities against Aldose reductase (AR) and the formation of advanced glycation endproducts (AGEs)

CAS Number: 59-50-7

BAY 41-8543 ME1 Smiles: [2H]C([2H])([2H])C(O)([C@@H](C)/C=C/[C@@H](C)[C@H]1CC[C@H]2/C(/CCC[C@@]21C)=C/C=C1C[C@@H](O)C[C@H](O)C1)C([2H])([2H])[2H]BAY 41 8543 is an orally active, nitric oxide (NO) independent stimulator of soluble guanylyl cyclase (sGC). BAY 41 8543 has vasodilator activity in the pulmonary and systemic vascular beds in the rat. BAY 41 8543 has antiplatelet effects and has the potential for cardiovascular diseases research. Product information CAS Number: 256498 66 5 Molecular Weight: 420. 44 Formula: C21H21FN8O Chemical Name: 2 {1 [(2 fluorophenyl)methyl] 1H pyrazolo[3,4