Zaltidine is a H2-receptor antagonist, which has the antisecretory action.

Zaltidine is a H2-receptor antagonist, which has the antisecretory action.

Zaltidine is a H2-receptor antagonist, which has the antisecretory action.

Zaltidine is a H2-receptor antagonist, which has the antisecretory action.

Zaltidine is a H2-receptor antagonist, which has the antisecretory action.

Zamifenacin fumarate is a selective M3 muscarinic receptor antagonist with pKi value of 8.52.

Zamifenacin fumarate is a selective M3 muscarinic receptor antagonist with pKi value of 8.52.

Zanthobungeanine, a natural product isolated and purified from the roots of Zanthoxylum nitidum with anti-inflammatory activity, shows the inhibitory action on the development of A549 cell only in high concentration and has no antipersonnel effect on A549 cell, moderate NO production inhibitory activity with an IC50 value of 37.26 mg /L, and obviously inhibitoryactivity to […]

Zanthobungeanine, a natural product isolated and purified from the roots of Zanthoxylum nitidum with anti-inflammatory activity, shows the inhibitory action on the development of A549 cell only in high concentration and has no antipersonnel effect on A549 cell, moderate NO production inhibitory activity with an IC50 value of 37.26 mg /L, and obviously inhibitoryactivity to […]

Zaprinast is selective inhibitor of cGMP-specific phosphodiesterases V and VI (PDE5/6) and an agonist at the G protein-coupled receptor 35 (GPR35).

Zaprinast is selective inhibitor of cGMP-specific phosphodiesterases V and VI (PDE5/6) and an agonist at the G protein-coupled receptor 35 (GPR35).

Zatebradine is a potent HCN channels antagonist, which decreased the heartbeat in a reversible manner, with 92% inhibition of the hHCN1-mediated current at 10 uM.

Zatebradine is a potent HCN channels antagonist, which decreased the heartbeat in a reversible manner, with 92% inhibition of the hHCN1-mediated current at 10 uM.

Zatebradine is a potent HCN channels antagonist, which decreased the heartbeat in a reversible manner, with 92% inhibition of the hHCN1-mediated current at 10 uM.

Zatebradine is a potent HCN channels antagonist, which decreased the heartbeat in a reversible manner, with 92% inhibition of the hHCN1-mediated current at 10 uM.

Zatebradine HCl is a potent HCN channels antagonist, which decreased the heartbeat in a reversible manner with 92% inhibition of the hHCN1-mediated current at 10 μM.

Zatebradine HCl is a potent HCN channels antagonist, which decreased the heartbeat in a reversible manner with 92% inhibition of the hHCN1-mediated current at 10 μM.

Zatebradine HCl is a potent HCN channels antagonist, which decreased the heartbeat in a reversible manner with 92% inhibition of the hHCN1-mediated current at 10 μM.

Zatebradine HCl is a potent HCN channels antagonist, which decreased the heartbeat in a reversible manner with 92% inhibition of the hHCN1-mediated current at 10 μM.

ZD 7155 hydrochloride is selective competitive antagonist of the angiotensin II type 1 (AT1) receptor.

A phytoestrogenic mycotoxin and ER activator

A phytoestrogenic mycotoxin and ER activator

A phytoestrogenic mycotoxin and ER activator

A phytoestrogenic mycotoxin and ER activator

Zibotentan is an orally administered, potent and specific ETA-receptor (endothelin A receptor) antagonist (IC50 = 21 nM).

Zibotentan is an orally administered, potent and specific ETA-receptor (endothelin A receptor) antagonist (IC50 = 21 nM).

Zibotentan is an orally administered, potent and specific ETA-receptor (endothelin A receptor) antagonist (IC50 = 21 nM).

Zibotentan is an orally administered, potent and specific ETA-receptor (endothelin A receptor) antagonist (IC50 = 21 nM).

Zibotentan is an orally administered, potent and specific ETA-receptor (endothelin A receptor) antagonist (IC50 = 21 nM).