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￥ 0.00 Membrane Transporters/Ion Channels
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Brefeldin A
Catalog No. A11156 Protein translocation 抑制剂Brefeldin A阻断ADP-核糖基化因子与高尔基体的结合并抑制GDP-GTP交换。 了解更多 -
Sodium orthovanadate
Catalog No. A10854 protein tyrosine phosphatases inhibitorSodium orthovanadate是化合物Na3VO4。 它是蛋白质酪氨酸磷酸酶，碱性磷酸酶和许多ATPase的抑制剂，很可能充当磷酸盐类似物。 了解更多 -
Ouabain
Catalog No. A12755 -
Oligomycin A
Catalog No. A10669 ATPase 抑制剂Oligomycin A是线粒体ATPase抑制剂。寡霉素A抑制与细胞膜结合的ATP5（线粒体ATP酶，F1F0）。 了解更多 -
Omeprazole
Catalog No. A10672 -
(-)-Blebbistcitin
Catalog No. A13647 -
BTB06584
Catalog No. A14308 -
Oligomycin
Catalog No. A14000 -
Cyclopiazonic Acid
Catalog No. A14002 SERCA 抑制剂Cyclopiazonic acid是SERCA（内质网Ca2+ -ATPase）的抑制剂，可诱导细胞内储存的Ca2+释放，而不会增加IP3水平。 了解更多 -
Thapsigargin
Catalog No. A14007 SERCA ATPase 抑制剂Thapsigargin是在Thapsia garganica的根中发现的一种细胞可渗透的倍半萜烯内酯。它是肿瘤的启动子，可通过抑制肌浆/内质网Ca2+ -ATPase（SERCA，IC50 = 30 nM）诱导细胞内储存的Ca2+释放，而不会水解肌醇磷脂。 了解更多 -
Glucagon (19-29), human
Catalog No. A14875 -
CFTR-Inhibitor-II
Catalog No. A13723 CFTR 抑制剂CFTR inhibitor II,也称为GlyH-101，是一种甘氨酸酰肼，可选择性和可逆地阻断CFTR通道（Ki = 4.3 uM）。 了解更多 -
Oridonin (Isodonol)
Catalog No. A10675 CFTR 抑制剂Oridonin (Isodonol)是一种从鼠李木中分离出来的Entkaurane二萜类化合物，是一种重要的传统中草药。 了解更多 -
CFTRinh-172
Catalog No. A12897 CFTR 抑制剂CFTRinh-172是电压无关的选择性CFTR抑制剂。在2分钟内可逆地抑制CFTR短路电流的 Ki 值为300 nM。 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 -
Nimodipine
Catalog No. A10645 -
Dantrolene
Catalog No. A13928 -
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 -
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 -
Nav1.7-IN-3
Catalog No. A13626 voltage-gated sodium channel Nav1.7 inhibitorNav1.7-IN-3 is a selective, orally bioavailable voltage-gated sodium channel Nav1.7 inhibitor with an IC50 of 8 nM. Pain relief. Limited CNS penetration. 了解更多 -
Raxatrigine hydrochloride
Catalog No. A21645 Nav1.7 sodium channel inhibitorRaxatrigine hydrochloride (GSK-1014802 hydrochloride) is a novel small molecule state-dependent sodium channel blocker; Nav1.7 sodium channel inhibitor. 了解更多 -
Orphenadrine citrate
Catalog No. A11712 -
Procainamide HCl
Catalog No. A14240 -
Oxcarbazepine
Catalog No. A13943 -
ICA-121431
Catalog No. A13773 NaV1.3 and NaV1.1 channels 抑制剂ICA-121431是人NaV1.3和NaV1.1通道的有效和选择性抑制剂（IC50值分别为13和23 nM）。 了解更多 -
Sodium Channel inhibitor 1
Catalog No. A15243 -
Levobupivacaine
Catalog No. A15979 -
Procaine
Catalog No. A16131 -
PF-05089771
Catalog No. A16365 -
Ambroxol HCl
Catalog No. A16398 Sodium Channel 抑制剂Ambroxol HCl是神经元Na+通道的有效抑制剂，可抑制TTX耐受的Na+电流，IC50为35.2 uM，对于补品和相阻滞的IC50为22.5 μM，抑制TTX敏感的Na+电流，IC50为100 μM。第三阶段。 了解更多 -
Glimepiride
Catalog No. A10430 Kir6.2/SUR 抑制剂Glimepiride是一种强效Kir6.2/SUR抑制剂，SUR1、SUR2A和SURB的IC50分别为3.0 nM、5.4 nM和7.3 nM，用于治疗2型糖尿病化合物。 了解更多 -
Repaglinide
Catalog No. A10783 Potassium Channel 抑制剂Repaglinide是一种有效的短效胰岛素促分泌剂，可通过关闭胰岛β细胞质膜中的ATP敏感性钾（KATP）通道发挥作用。 了解更多 -
K+ Channel inhibitor
Catalog No. A16182 -
MK-7145
Catalog No. A21030 -
CaCCinh-A01
Catalog No. A15469 CaCCs 抑制剂CaCCinh-A01抑制人支气管和肠道细胞中的CaCC电流。还抑制TMEM16A通道（表达TMEM16A的FRT细胞中IC50 = 2.1 uM）。 了解更多 -
T16Ainh-A01
Catalog No. A15470
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- DNMT (1)
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