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Sodium Channel

Sodium Channel

Sodium channels are integral membrane proteins that form ion channels, conducting sodium ions (Na+) through a cell's plasma membrane.
TargetMol
1 2 3 4 5 6 7 8 9 10 11 12 13
Cat. No. Product Name CAS No. Purity Chemical Structure
T80495 MHuwentoxin-IV
化合物 mHuwentoxin-IV
98%
TargetMol Chemical Structure mHuwentoxin-IV
mHuwentoxin-IV是一种经天然修饰的Huwentoxin-IV。该化合物针对背根神经节中河豚毒素敏感(TTX-S)电压门控钠通道(sodium channels)表现出抑制作用,IC50值为54.16 nM。mHuwentoxin-IV对这些钠通道的抑制作用并不会因强去极化电压而逆转。
T80499 Jingzhaotoxin XI
化合物 Jingzhaotoxin XI
98%
TargetMol Chemical Structure Jingzhaotoxin XI
Jingzhaotoxin XI (JZTX-XI) 为抑制钠电导的化合物,其IC50值为124 nM。该化合物能够减缓CHO-K1细胞中Nav1.5通道的快速失活,EC50值为1.18±0.2 μM。
T80518 Mambalgin-3
化合物 Mambalgin-3
98%
TargetMol Chemical Structure Mambalgin-3
Mambalgin-3为针对酸敏感离子通道1 (ASIC1) 的抑制肽,适用于镇痛研究领域。
T80519 M3-Huwentoxin IV
化合物 m3-Huwentoxin IV
98%
TargetMol Chemical Structure m3-Huwentoxin IV
m3-Huwentoxin IV (m3-HwTx-IV) 是针对多种 hNaV 子型的有效 NaV 抑制剂,其 IC50 值针对 hNaV1.7、hNaV1.6、hNaV1.3、hNaV1.1、hNaV1.2 和 hNaV1.4 分别为 3.3、6.8、7.2、8.4、11.9 和 369 nM。该化合物还能剂量依赖性...
T80533 Pterinotoxin-2
化合物 Pterinotoxin-2
98%
TargetMol Chemical Structure Pterinotoxin-2
Pterinotoxin-2为一种肽类毒素,其作用机制为抑制(sodium channel)。
T80534 Pterinotoxin-1
化合物 Pterinotoxin-1
98%
TargetMol Chemical Structure Pterinotoxin-1
Pterinotoxin-1是一种肽类毒素,具有抑制(sodium channel)的活性。
T81134 Sodium Channel inhibitor 4
化合物 Sodium Channel inhibitor 4
587843-16-1 98%
TargetMol Chemical Structure Sodium Channel inhibitor 4
Sodium Channel Inhibitor4 是一种抑制钠通道的化合物。
T82936 ATX-II TFA
化合物 ATX-II TFA
98%
TargetMol Chemical Structure ATX-II TFA
ATX-II TFA为源自海葵(Anemonia sulcata)毒素的特定Na+通道调节剂,能使细胞培养物对Na+、Halothane、Caffeine和Ryanodine敏感,并可诱发肺静脉心律失常和心房颤动。
T22829 GX-674
化合物GX-674
1432913-36-4 98%
TargetMol Chemical Structure GX-674
GX-674 是一种具有高效和选择性的电压门控钠通道 1.7 (Nav1.7) 拮抗剂,在 -40 mV 时测得 IC50 值为 0.1 nM,可用于研究炎症和神经性疼痛。
TP1852 Myomodulin
肌调蛋白
110570-93-9 98%
TargetMol Chemical Structure Myomodulin
Myomodulin 是一种存在于软体动物、昆虫和腹足类动物中的神经肽。它存在于两个已确定的海兔神经元中,它们包含肌调节蛋白 A、ARC 运动神经元 B16 和腹部神经元 L10。
TN4697 Odoroside H
化合物 TN4697
18810-25-8 98%
TargetMol Chemical Structure Odoroside H
Odoroside H has anticancer activities, the cytotoxic effects are induced by the inhibition of the plasma membrane bound Na(+)/K(+)-ATPase.
TN5141 Thevetin B
黄夹甙 B
27127-79-3 98%
TargetMol Chemical Structure Thevetin B
Thevetin B 是一种强心苷,是Na+-, K+-依赖性腺苷三磷酸酶 (Na+,K+-ATPase) 的抑制剂,来自 Thevetia peruviana。
TCA2511 11Beta-hydroxyprogesterone
11β-羟孕酮
600-57-7 98%
TargetMol Chemical Structure 11Beta-hydroxyprogesterone
The progesterone derivatives 11 alpha- and 11 beta-hydroxyprogesterone are potent inhibitors of 11 beta-hydroxysteroid dehydrogenase (isoforms 1 and 2) in vitro ...
TN4276 Isocudraniaxanthone B
化合物 TN4276
199851-52-0 98%
TargetMol Chemical Structure Isocudraniaxanthone B
Isocudraniaxanthone B may have antimalarial activity.
T12951 Sodium Channel inhibitor 2
化合物 T12951
653573-60-5 98%
TargetMol Chemical Structure Sodium Channel inhibitor 2
Sodium Channel inhibitor 2 is a blocker of sodium channel.
TN5234 Vindorosine
化合物 TN5234
5231-60-7 98%
TargetMol Chemical Structure Vindorosine
Vindorosine has blood vessel relaxation effect, possible underlying mechanisms involving the inhibition of Ca(2+) entry via L-type Ca(2+) channels in vascular sm...
TN2306 Wilfordine
雷公藤定碱
37239-51-3 98%
TargetMol Chemical Structure Wilfordine
Wilfordine is an insecticidally active alkaloid, Na+-K+-ATPase may be an acting target of wilfordine against some larvae of insect.
TN5060 Stauntosaponin A
化合物 TN5060
1417887-91-2 98%
TargetMol Chemical Structure Stauntosaponin A
Stauntosaponin A and stauntosaponin B show moderate inhibitory activities against Na+/K+-ATPase with IC50 values of 21 and 29 uM, respectively.
TN4183 Hardwickiic acid
左旋哈氏豆属酸
1782-65-6 98%
TargetMol Chemical Structure Hardwickiic acid
Hardwickiic acid ((-)-Hardwikiic acid) 是一种从Pulicaria gnaphalodes 中提取的天然化合物,是一种抗伤害性感受作用化合物。Hardwickiic acid 能阻断河豚毒素敏感的电压依赖性钠通道 (sodium channels)。Hardwickiic acid ...
T13830 Propoxycaine hydrochloride
盐酸丙氧卡因
550-83-4 98%
TargetMol Chemical Structure Propoxycaine hydrochloride
Propoxycaine hydrochloride is an inhibit of voltage-gated sodium channels.
mHuwentoxin-IV
T80495
mHuwentoxin-IV是一种经天然修饰的Huwentoxin-IV。该化合物针对背根神经节中河豚毒素敏感(TTX-S)电压门控钠通道(sodium channels)表现出抑制作用,IC50值为54.16 nM。mHuwentoxin-IV对这些钠通道的抑制作用并不会因强去极化电压而逆转。
Jingzhaotoxin XI
T80499
Jingzhaotoxin XI (JZTX-XI) 为抑制钠电导的化合物,其IC50值为124 nM。该化合物能够减缓CHO-K1细胞中Nav1.5通道的快速失活,EC50值为1.18±0.2 μM。
Mambalgin-3
T80518
Mambalgin-3为针对酸敏感离子通道1 (ASIC1) 的抑制肽,适用于镇痛研究领域。
m3-Huwentoxin IV
T80519
m3-Huwentoxin IV (m3-HwTx-IV) 是针对多种 hNaV 子型的有效 NaV 抑制剂,其 IC50 值针对 hNaV1.7、hNaV1.6、hNaV1.3、hNaV1.1、hNaV1.2 和 hNaV1.4 分别为 3.3、6.8、7.2、8.4、11.9 和 369 nM。该化合物还能剂量依赖性...
Pterinotoxin-2
T80533
Pterinotoxin-2为一种肽类毒素,其作用机制为抑制(sodium channel)。
Pterinotoxin-1
T80534
Pterinotoxin-1是一种肽类毒素,具有抑制(sodium channel)的活性。
Sodium Channel inhibitor 4
T81134
Sodium Channel Inhibitor4 是一种抑制钠通道的化合物。
ATX-II TFA
T82936
ATX-II TFA为源自海葵(Anemonia sulcata)毒素的特定Na+通道调节剂,能使细胞培养物对Na+、Halothane、Caffeine和Ryanodine敏感,并可诱发肺静脉心律失常和心房颤动。
GX-674
T22829
GX-674 是一种具有高效和选择性的电压门控钠通道 1.7 (Nav1.7) 拮抗剂,在 -40 mV 时测得 IC50 值为 0.1 nM,可用于研究炎症和神经性疼痛。
Myomodulin
TP1852
Myomodulin 是一种存在于软体动物、昆虫和腹足类动物中的神经肽。它存在于两个已确定的海兔神经元中,它们包含肌调节蛋白 A、ARC 运动神经元 B16 和腹部神经元 L10。
Odoroside H
TN4697
Odoroside H has anticancer activities, the cytotoxic effects are induced by the inhibition of the plasma membrane bound Na(+)/K(+)-ATPase.
Thevetin B
TN5141
Thevetin B 是一种强心苷,是Na+-, K+-依赖性腺苷三磷酸酶 (Na+,K+-ATPase) 的抑制剂,来自 Thevetia peruviana。
11Beta-hydroxyprogesterone
TCA2511
The progesterone derivatives 11 alpha- and 11 beta-hydroxyprogesterone are potent inhibitors of 11 beta-hydroxysteroid dehydrogenase (isoforms 1 and 2) in vitro ...
Isocudraniaxanthone B
TN4276
Isocudraniaxanthone B may have antimalarial activity.
Sodium Channel inhibitor 2
T12951
Sodium Channel inhibitor 2 is a blocker of sodium channel.
Vindorosine
TN5234
Vindorosine has blood vessel relaxation effect, possible underlying mechanisms involving the inhibition of Ca(2+) entry via L-type Ca(2+) channels in vascular sm...
Wilfordine
TN2306
Wilfordine is an insecticidally active alkaloid, Na+-K+-ATPase may be an acting target of wilfordine against some larvae of insect.
Stauntosaponin A
TN5060
Stauntosaponin A and stauntosaponin B show moderate inhibitory activities against Na+/K+-ATPase with IC50 values of 21 and 29 uM, respectively.
Hardwickiic acid
TN4183
Hardwickiic acid ((-)-Hardwikiic acid) 是一种从Pulicaria gnaphalodes 中提取的天然化合物,是一种抗伤害性感受作用化合物。Hardwickiic acid 能阻断河豚毒素敏感的电压依赖性钠通道 (sodium channels)。Hardwickiic acid ...
Propoxycaine hydrochloride
T13830
Propoxycaine hydrochloride is an inhibit of voltage-gated sodium channels.
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