Ascorbic acid-13C6是Ascorbic acid (T22039)的 13C 的标记化合物。Ascorbic acid的CAS号为50-81-7。L-Ascorbic acid是一种电子供体，是一种内源性抗氧化剂。它选择性抑制 Cav3.2 通道，IC50为 6.5 μM。它还是一种胶原沉积促进剂和弹性生成抑制剂，可对抗细菌感染、解毒反应和胶原蛋白的形成。

D-myo-Inositol-1,3,4,5-tetraphosphate (Ins(1,3,4,5)-P4) is formed by the phosphorylation of Ins(1,4,5)P3 by inositol 1,4,5-triphosphate 3-kinase. Ins(1,3,4,5)-P4 increases intracellular calcium levels by two distinct mechanisms: opening calcium channels on both the endoplasmic reticulum to release calcium from internal stores and on the plasma membrane to allow the influx of calcium from outside the cell.

piCRAC-1 is a powerful inhibitor of the photoinducible Ca2+ release-activated Ca2+ (CRAC) channel. It effectively alleviates thrombocytopenia and hemorrhage [1].

JTV-519 free base (K201 free base), recognized for its antiarrhythmic and cardioprotective properties, functions as a Ca2+-dependent blocker of sarcoplasmic reticulum Ca2+-stimulated ATPase (SERCA) and serves as a partial agonist of ryanodine receptors in striated muscle.

Cinnamyl caffeate has cardiovascular protective effects, it can increase H9c2 cellular antioxidant potential, decrease intracellular calcium ion ([Ca2+]i) level, and prevent cell apoptosis; it possesses potent antiproliferative activity with the EC(50) value of 0.114 microM, toward colon 26-L5 carcinoma. Cinnamyl caffeate possesses potent NO inhibitory activity with the IC(50) value of 9.53 microM.

G-Glu-Ser is a calcium receptor activator and Flavor-enriching agent.

SM-6586 是一种有效的钙离子通道拮抗剂，对 Na+/H+ 和 Na+/Ca2+ 交换通道有抑制作用，可用于研究脑血管疾病和高血压等疾病。

2',3'-Cyclic NADP disodium (2',3'-cNADP+; β-Nicotinamide adenine dinucleotide-2',3'-cyclic phosphate) 是 2',3'-环状核苷酸 3'-磷酸二酯酶 (CNP) 的一种底物，CNP 在髓鞘中丰富存在。此化合物被用于偶联酶测定以量化 CNP 活性。使用 2',3'-Cyclic NADP disodium (5 μM) 可以增加钙超载引发的钙释放并防止大鼠脑线粒体发生钙诱导的肿胀。

1-Octanol-D17是1-Octanol (T10024)的氘代物。1-Octanol (Octanol）是一种饱和脂肪醇，作为T型钙通道 (T-channels）抑制剂，对天然T电流的IC50值为4 μM。1-Octanol是一种具有柴油特性的极具吸引力的生物燃料。