Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T80495 | MHuwentoxin-IV
化合物 mHuwentoxin-IV
|
98% |
|
|
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% |
|
|
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% |
|
|
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% |
|
|
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% |
|
|
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% |
|
|
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% |
|
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% |
|
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
Isocudraniaxanthone B may have antimalarial activity. | ||||
T12951 | Sodium Channel inhibitor 2
化合物 T12951
|
653573-60-5 | 98% |
|
Sodium Channel inhibitor 2 is a blocker of sodium channel. | ||||
TN5234 | Vindorosine
化合物 TN5234
|
5231-60-7 | 98% |
|
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% |
|
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% |
|
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% |
|
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% |
|
Propoxycaine hydrochloride is an inhibit of voltage-gated sodium channels. |