Calcium Channels
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Dantrolene
Catalog No. A13928 -
Berbamine
Catalog No. A14794 -
(S)-Amlodipine
Catalog No. A14935 -
NNC 55-0396
Catalog No. A15188 Calcium channel blockerNNC 55-0396是Mibefradil衍生物,是一种高度选择性的T型钙通道阻滞剂;分别在INS-1细胞中抑制Cav3.1 T型通道和HVA电流的IC50值为6.8和> 100μM。 了解更多 -
NP118809
Catalog No. A15192 -
Bay K 8644
Catalog No. A15875 -
Mibefradil dihydrochloride
Catalog No. A12482 Calcium channel blockerMibefradil dihydrochloride是钙通道阻滞剂,对T型Ca2+通道具有中等选择性,对T型和L型通道的IC50值分别为2.7 uM和18.6 uM。 了解更多 -
Dantrolene sodium Hemiheptahydrate
Catalog No. A16146 Dantrolene sodium是一种骨骼肌松弛剂,其通过干扰肌肉纤维中的激发-收缩偶联起作用。 了解更多 -
Cinepazide maleate
Catalog No. A16454 Cinepazide maleate是Cinepazide的马来酸盐形式,其为血管扩张剂。 了解更多 -
Cinnarizine
Catalog No. A16455 -
Aranidipine
Catalog No. A18291 Calcium channel antagonistAranidipine (MPC1304) is a Ca2+ channel antagonist with potent and long-lasting antihypertensive effects. 了解更多 -
Ca2+ channel agonist 1
Catalog No. A12186 Ca2+ channel agonist/CDK2 inhibitorCa2+ channel agonist 1 is an agonist of N-type Ca2+ channel and an inhibitor of Cdk2, with EC50s of 14.23 μM and 3.34 μM, respectively, and is used as a potential treatment for motor nerve terminal dysfunction. 了解更多 -
Barnidipine
Catalog No. A21940 L-type calcium antagonistBarnidipine (Mepirodipine) is an L-type calcium antagonist (CaA) with high affinity for [3H] initrendipine binding sites (Ki=0.21 nmol/l), has selective action against CaA receptors. 了解更多 -
Dantrolene sodium
Catalog No. A17644 Calcium channel proteins inhibitorDantrolene sodium is a inhibitor of calcium channel proteins, inhibiting the release of Ca2+ from the sarcoplasm. Dantrolene sodium is a skeletal muscle relaxant which acts by blocking muscle contraction beyond the neuromuscular junction. 了解更多 -
Tetrandrine (Fanchinine)
Catalog No. A10921 Calcium Channel 抑制剂Tetrandrine (Fanchinine)是一种钙通道阻滞剂。粉防己碱具有抗炎和抗纤维化作用,使粉防己碱及其相关化合物潜在地用于治疗肺矽肺,肝硬化和类风湿性关节炎。 了解更多 -
Astragaloside A
Catalog No. A11405 Ca2+ signaling modulatorAstragaloside A是缺氧条件下人脐静脉内皮细胞HIF-1α和通过PI3K/Akt途径血管生成的一种新型调节因子。 了解更多 -
CK-1827452 (Omecamtiv mecarbil)
Catalog No. A11206 Myosin activatorCK-1827452 (Omecamtiv mecarbil)是选择性的心脏特异性肌球蛋白激活剂。 了解更多 -
Manidipine 2HCl
Catalog No. A10554 Manidipine dihydrochloride是Manidipine的HCl盐形式,Manidipine是Ca2+电流的钙通道阻滞剂,IC50为2.6 nM。 了解更多 -
Amlodipine
Catalog No. A10068 L-type calcium channel blockerAmlodipine是一种L型钙通道阻滞剂,具有降压作用。它抑制去极化大鼠主动脉中Ca2 +诱导的收缩(IC50 = 1.9 nM),并在心血管疾病中显示出血管保护作用。 了解更多 -
Amlodipine besylate (Norvasc)
Catalog No. A10069 L-type calcium channel blockerAmlodipine besylate是一种L型钙通道阻滞剂,具有降压作用。它抑制去极化大鼠主动脉中Ca2 +诱导的收缩(IC50 = 1.9 nM)。 了解更多 -
Cilnidipine
Catalog No. A10215 Calcium channel blockerCilnidipine是提供血管平滑肌中L型电压门控钙通道和交感神经末梢N型钙通道的双重阻滞剂。 了解更多 -
Isradipine
Catalog No. A10487 -
Azelnidipine
Catalog No. A11219 calcium channel blockerAzelnidipine是一种钙阻断剂,可减轻肝纤维化并可能增加抗氧化防御能力。可以减轻肝纤维化并可能增加抗氧化防御能力。 了解更多 -
BAPTA tetrapotassium
Catalog No. A13989 Selective calcium chelatorBAPTA tetrapotassium是一种选择性钙螯合剂,对Ca2+的亲和力大于Mg2+。 了解更多 -
Nimodipine
Catalog No. A10645 -
Nifedipine
Catalog No. A10643 -
Pinaverium Bromide
Catalog No. A12684 Pinaverium Bromide是一种痉挛剂,抗胆碱能作用的发生率低。吡那溴铵也是解痉药。 了解更多 -
Manidipine (Manyper)
Catalog No. A10553 Manidipine (Manyper)是二氢吡啶化合物和钙通道蛋白抑制剂和拮抗剂。 了解更多 -
Diltiazem HCl
Catalog No. A10311 Diltiazem HCl是一种非二氢吡啶(非DHP)药物,称为钙通道阻滞剂,用于治疗高血压,心绞痛和某些类型的心律不齐。 了解更多 -
Diethylstilbestrol
Catalog No. A10309 Diethylstilbestrol是一种合成的非甾体雌激素,于1938年首次合成。它也被分类为内分泌干扰物。 了解更多 -
Clevidipine
Catalog No. A11746 Calcium channel blockerClevidipine是一种二氢吡啶类钙通道阻滞剂,用于在口服治疗不可行或不理想时降低血压。 了解更多 -
Nilvadipine (ARC029)
Catalog No. A11731 -
Benidipine hydrochloride
Catalog No. A11730 Benidipine hydrochloride是一种长效的T型钙通道阻滞剂,对高血压糖尿病患者的血压和肾功能有影响。 了解更多 -
ABT-639 hydrochloride
Catalog No. A12571 T-type Ca2+ channel blockerABT-639 hydrochloride is a novel, peripherally acting, selective T-type Ca2+ channel blocker. 了解更多 -
(S)-(-)-Bay-K-8644
Catalog No. A21164 L-type Ca2+ channel agonist(S)-(-)-Bay-K-8644 is an agonist of L-type Ca2+ channel. (S)-(-)-Bay-K-8644 activates Ba2+ currents (IBa) (EC50=32 nM). 了解更多 -
TTA-Q6(isomer)
Catalog No. A21724 T-type Ca2+ channel antagonistTTA-Q6(isomer) is an isomer of TTA-Q6. TTA-Q6 is a selective T-type Ca2+ channel antagonist. 了解更多 -
JTV-519 free base
Catalog No. A21846 Ca2+-dependent blockerTV-519 free base (K201 free base) is a Ca2+-dependent blocker of sarcoplasmic reticulum Ca2+-stimulated ATPase (SERCA) and a partial agonist of ryanodine receptors in striated muscle. Antiarrhythmic and cardioprotective properties. 了解更多