Budiodarone（ATI-2042）is a chemical analog of an antiarrhythmic drug and amiodarone. Budedalone is promising as an antiarrhythmic agent for the prevention of atrial fibrillation.

Bifemelane 是一种益智化合物， 通过刺激细胞内 Ca2+储存的释放产生第一个峰值，通过储存操作的 Ca2+通道的电容进入产生第二个峰值。Bifemelane 可作为星形胶质细胞基础研究的药理学工具。

Azumolene sodium anhydrous is a muscle relaxant that inhibits the release of calcium from skeletal muscle sarcoplasmic reticulum. Azumolene inhibits a component of store-operated calcium entry coupled to the skeletal muscle ryanodine receptor. Azumolene, an equipotent dantrolene analog, inhibits a component of SOCE coupled to activation of RyR1 by caffeine and ryanodine, whereas the SOCE component induced by thapsigargin is not affected.

Selective CaV3.1 channel blocker (IC50 values are 0.2 and 31.8 μM for hCaV3.1 and hCaV3.2 respectively). Also reversibly inhibits NaV1.8 and blocks KV2.1 channels.

O-Des[2-aminoethyl]-O-carboxymethyl dehydroamlodipine is a major metabolite of the calcium channel inhibitor amlodipine .1 1.Taguchi, R., Naito, T., Sato, H., et al.Validated LC-MS/MS method for the simultaneous determination of amlodipine and its major metabolites in human plasma of hypertensive patientsTher. Drug Monit.39(6)625-631(2017)

(R)-Lercanidipine hydrochloride is the R-enantiomer of Lercanidipine. (R)-lercanidipine hydrochloride is a blocker of calcium channel.

Nelutroctiv 是心肌肌钙蛋白的有效激活剂。

L-Phenylalanine-13C9是13C 标记的L-Phenylalanine (T3377)。L-Phenylalanine ( (S)-2-Amino-3-phenylpropionic acid)是从大肠杆菌中分离出的必需氨基酸，作为电压依赖性 α2δ 亚基 Ca2+ 通道拮抗剂，其Ki为980 nM。此外，L-Phenylalanine是NMDARs (KB573 μM)和非NMDARs上甘氨酸和谷氨酸结合位点的竞争性拮抗剂，广泛应用于食品香料和药品的生产过程。

Fargesone B inhibits the vascular smooth muscle contraction by suppressing the voltage- and receptor-activated calcium influxes in a nonselective manner.