Bay-K-8644 (R) 26 SE Smiles: CC(C)(C)[C@@H]1C[C@H]2OC(=O)[C@@]34O[C@@H]5OC(=O)[C@H](O)[C@]51[C@]32[C@H](O)[C@@H]1OC(=O)[C@@H](C)[C@]41O

Smiles: CC(C)(C)[C@@H]1C[C@H]2OC(=O)[C@@]34O[C@@H]5OC(=O)[C@H](O)[C@]51[C@]32[C@H](O)[C@@H]1OC(=O)[C@@H](C)[C@]41O

Hep 3B cells) treatment increases CYP7A1 mRNA expression and the expression of the proliferative marker EGR1 is inhibited

C57/Bl6 mice) treatment could promote a strong increase of γ-H2AX and apoptosis throughout the lymphoma

8 nmol/l for efonidipine

Chemical Name: 2-(2-(2-aminopyrimidin-5-yl)-4-morpholinothieno[3

Bay-K-8644 (R) 26 SE Smiles: CC(C)(C)[C@@H]1C[C@H]2OC(=O)[C@@]34O[C@@H]5OC(=O)[C@H](O)[C@]51[C@]32[C@H](O)[C@@H]1OC(=O)[C@@H](C)[C@]41O(R) (+) BAY K 8644 is an L type channel blocker that has negative inotropic and vasodilatory effects. Intracerebroventricular administration of this enantiomer has no effect on motor function in mice, whereas (S) () BAY K 8644 impairs rotarod and motor activity, an effect that is blocked by (R) (+) BAY K 8644. Product information CAS Number: 98791 67 4 Molecular Weight: 356. 30 Formula: C16H15F3N2O4 Synonym: (R) (+) Bay K 8644 R 4407 NI 105 (+) BAY K