Calcium Channel

A calcium channel is an ion channel which shows selective permeability to calcium ions. It is sometimes synonymous with voltage-gated calcium channel, although there are also ligand-gated calcium channels.

Cat. No.	Product Name	CAS No.	Purity
TN3260	8(14),15-Isopimaradien-3-ol 化合物 TN3260	4728-30-7	98%
TN3260	ent-8(14),15-pimaradien-3beta-ol (8(14),15-Isopimaradien-3-ol) can induce vascular relaxation. It displays high antibacterial activities (MIC values lower than 1...
TN1913	Marmin 化合物Marmin	14957-38-1	98%
TN1913	Marmin have anti-ulcer effects, which are ascribed primarily to the maintenance of the mucosal barrier integrity and inhibition of gastric motor activity and sec...
T10713	CCR4 antagonist 2 化合物 T10713	2206788-99-8	98%
T10713	CCR4 antagonist 2 (Compound 31) is a novel potent, orally bioavailable small molecule antagonists of CC chemokine receptor 4 (CCR4) that inhibits Treg traffickin...
TN1367	Alismol 化合物Alismol	87827-55-2	98%
TN1367	Alismol has antihypertensive action, it decreases cardiac output, heart rate and left ventricular pressure, but it increases coronary flow, it has been used for ...
TQ0153	Mibefradil 米贝地尔	116644-53-2	98%
TQ0153	Mibefradil is a calcium channel blocker with moderate selectivity for T-type Ca2+ channels (IC50s: 2.7 μM and 18.6 μM for T-type and L-type currents).
T35935	D-myo-Inositol-1,4,5-triphosphate trisodium D-肌醇-1,4,5-三磷酸钠盐	141611-10-1	98%
T35935	D-myo-Inositol-1,4,5-triphosphate trisodium (Inositol 1,4,5-trisphosphate trisodium) 是由磷脂酶 C 介导的磷脂酰肌醇-4,5-二磷酸酯水解在细胞中产生的第二信使。D-myo-Inositol-1,4,5-triphosphate (so...
T11080	Dopropidil 多普吡地	79700-61-1	98%
T11080	Dopropidil is a new anti-angina pectoris calcium regulator, which has intracellular calcium antagonist activity and anti-ischemic effects in various predicted an...
T12625	(R)-Lercanidipine-d3 hydrochloride 化合物 T12625	1217724-52-1	98%
T12625	(R)-lercanidipine D3 hydrochloride is a deuterium labeled (R)-Lercanidipine hydrochloride. (R)-Lercanidipine D3 (hydrochloride) is a calcium channel blocker.
TN5109	Taxezopidine L 化合物 TN5109	219749-76-5	98%
TN5109	Taxezopidines K and taxezopidine L can markedly inhibit Ca2+-induced depolymerization of microtubules.
TN2641	15-Methoxypinusolidic acid 化合物 TN2641	769928-72-5	98%
TN2641	15-Methoxypinusolidic acid has anti-inflammatory effects, it inhibits LPS-induced iNOS expression and NO production, independent on MAPK and NF-kappaB. 15-Methox...
T12205L	Trans-Ned 19 化合物 T12205L	1354235-96-3	98%
T12205L	trans-Ned 19 is a NAADP antagonist and TPC blocker and inhibits the calcium signal in human umbilical vein endothelial cells and the rat aorta relaxation in resp...
T15366	Gabapentin enacarbil 加巴喷丁酯	478296-72-9	98%
T15366	Gabapentin enacarbil (XP-13512) 是抗惊厥和镇痛药物加巴喷丁的前药。Gabapentin enacarbil 提供持续剂量比例的 Gabapentin 暴露和可预测的生物利用度。
T13879	(S)-Verapamil hydrochloride 化合物 T13879	36622-28-3	98%
T13879	(S)-Verapamil hydrochloride is an inhibitor of leukotriene C4 (LTC4) and calcein transport by MRP1,and leads to the death of potentially resistant tumor cells.
TN4051	Fargesone B 化合物 TN4051	116424-70-5	98%
TN4051	Fargesone B inhibits the vascular smooth muscle contraction by suppressing the voltage- and receptor-activated calcium influxes in a nonselective manner.
TN3568	Calceolarioside A 化合物 TN3568	84744-28-5	98%
TN3568	Calceolarioside A shows potent activity against visceral leishmaniasis. It can induce a dose-related aggregant effect on rabbit platelets, which may be partly re...
T12244	Norverapamil 化合物 T12244	67018-85-3	98%
T12244	Norverapamil is a blocker of L-type calcium channel and an inhibitor of P-glycoprotein (P-gp) function .
T2782L	Catharanthine Tartrate(2468-21-5(free base)) 化合物Catharanthine Tartrate	T2782L	99.98%
T2782L	Catharanthine Tartrate(2468-21-5(free base)) 是从马达加斯加长春花中分离得到的天然产物，Catharanthine Tartrate 抑制电压操作的L 型Ca2+通道，具有抗癌和降血压活性。
T13219	TTA-Q6 化合物 TTA-Q6	910484-28-5	99.97%
T13219	TTA-Q6 是一种选择性 T 型 Ca2+ 通道拮抗剂，具有潜在的抗肿瘤和免疫调节活性，可抑制肿瘤细胞摄取细胞外钙离子，诱导细胞内钙缺乏和内质网（ER）应激，用于治疗神经系统疾病。
T6777	Bay K 8644 化合物Bay K 8644	71145-03-4	99.97%
T6777	Bay K 8644 (SQ 28,873)是一种二氢吡啶化合物，是一种选择性的 L 型 Ca2+ 通道激活剂，IC50 为 17.3 nM。它通过增加通道的开放时间来增加通过肌膜 Ca2+通道的 Ca2+流入。
T30188L	Atagabalin HCl Atagabalin盐酸盐	223445-67-8	99.96%
T30188L	Atagabalin HCl 是一种新型电压依赖性钙通道（VDCC）α2δ亚基（1 和 2）配体，会影响慢波睡眠,可用于治疗失眠。