23
3
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T22408 |
Proflavine
吡啶-3,6-二胺,3,6-Diaminoacridine |
Antibacterial | Microbiology/Virology |
Proflavine (3,6-Diaminoacridine) 是吖啶染料,可用作抗菌剂。它是 DNA 嵌入剂,能够阻滞Kir3.2孔。它用作与 Kir3.2 相关的神经系统疾病的研究。 | |||
T0438 |
Proflavine Hemisulfate
3,6-Diaminoacridine hemisulfate,Proflavin hemisulfate,硫酸原黄素 |
Others; Potassium Channel; DNA; Thrombin; Antibacterial; Autophagy | Autophagy; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Others; Proteases/Proteasome |
Proflavine Hemisulfate (3,6-Diaminoacridine hemisulfate) 是一种 DNA 嵌入剂,也是一种吖啶染料。它是抗菌剂,也可作为 Kir3.2孔阻滞剂,可研究与 Kir3.2 相关的神经系统疾病。 | |||
T22745 |
DPO-1
|
Potassium Channel | Membrane transporter/Ion channel |
DPO-1 可以高效抑制电压门控钾离子通道Kv1.5,也可以阻断超快速延迟整流钾电流。它能够预防房性心律失常。 | |||
T5585 |
AM-92016 hydrochloride
|
Potassium Channel | Membrane transporter/Ion channel |
AM-92016 hydrochloride 是一种整流钾电流的特异性阻断剂。它能够延迟整流钾通道,使膜复极化,限制神经冲动的持续时间。 | |||
T27205 |
DPI 201-106
DPI-201-106 |
Sodium Channel | Membrane transporter/Ion channel |
DPI 201-106对电压门控钠通道的有心脏选择性调节活性,从而产生正性肌力作用。DPI 201-106 具有协同肌膜和细胞内作用机制。 | |||
T7505 |
Azimilide Dihydrochloride
NE-10064 Dihydrochloride,盐酸阿齐利特 |
Potassium Channel | Membrane transporter/Ion channel |
Azimilide Dihydrochloride (NE-10064 Dihydrochloride) 是 I(Ks) 和 I(Kr) 抑制剂,具有抗心律失常活性。 | |||
T3574 |
Sematilide hydrochloride
司美利特,CK-1752A,CK-1752,Sematilide HCl |
Potassium Channel | Membrane transporter/Ion channel |
Sematilide hydrochloride (CK-1752) 是一种选择性的 IKr 通道阻滞剂。Sematilide 以浓度依赖性抑制延迟整流钾通道 (K+current),IC50为 25 μM。Sematilide 是一种 III 类抗心律不齐剂。 | |||
T15555 |
IK1 inhibitor PA-6
|
Potassium Channel | Membrane transporter/Ion channel |
IK1 inhibitor PA-6 是一种喷他脒类似物,是选择性的 IK1(KIR2.x 离子通道携带向内整流电流) 抑制剂,对人和老鼠中 KIR2.x 电流的 IC50值为 12-15 nM。它可上调 KIR2.1 的蛋白表达,诱导细胞内 KIR2.1 的蛋白的积累。它在房颤和心律失常的研究中具有潜力。 | |||
T6476 |
Dofetilide
UK 68789,UK-68798,Tikosyn,多非利特 |
Potassium Channel | Membrane transporter/Ion channel |
Dofetilide (UK 68789) 是一种具有口服活性、有效的且特异性的IKr 阻滞剂,作为 III 类抗心律失常药物。Dofetilide 可用于心血管疾病研究。 | |||
T31011 |
Coralyne chloride
|
Topoisomerase | DNA Damage/DNA Repair |
Coralyne chloride 是一种具有强抗癌活性的原小檗碱。它可用于制备 Coralyne 衍生物,是一种基于荧光 DNA 的分子整流剂,通过位点特异性插入构建成 DNA 双链体。它可作为一种拓扑异构酶 I 毒性分子,诱导拓扑异构酶 I 介导 DNA 裂解。 | |||
T24948 |
VU625
VU007625,VU 625,VU 007625,VU-625,VU-007625 |
Others | Others |
VU625 is an effective inhibitor of Aedes aegypti inward rectifier potassium channels. | |||
T22662 |
Chromanol 293B
|
Others | Others |
slow delayed rectifier K+ current (IKs) blocker | |||
T70194 |
AM92016
|
Others | Others |
AM92016 is a specific blocker of the time dependent delayed rectifier potassium current. AM92016 does not show any β-adrenoceptor blocking activity. | |||
T14189 |
Almokalant
H 234/09 |
Potassium Channel | Membrane transporter/Ion channel |
Almokalant is a class III antiarrhythmic drug, acts as a potassium channel blocker. And it inhibits a specific component (Ikr) of the time-dependent delayed rectifier K+ current. | |||
T80510 |
Tertiapin-RQ
|
Potassium Channel | Membrane transporter/Ion channel |
Tertiapin-RQ为抗抑郁特性的内向整流K+通道阻滞剂肽。 | |||
T61685 |
Ibutilide
|
Others | Others |
Ibutilide (U70226E free base) is a potent antiarrhythmic compound that extends the action potential duration. It effectively blocks the rapidly activating delayed rectifier potassium current (I Kr ) in AT-1 cells [1]. | |||
T5336L |
Zacopride
Racemic zacopride |
Others | Others |
Zacopride is a selective agonist of inward rectifier potassium current (I K1) channel, inhibiting ventricular arrhythmias without affecting atrial arrhythmias. | |||
T15460 |
Halofantrine hydrochloride
WR-171669,SKF-102886 |
Others | Others |
Halofantrine hydrochloride is a blocker of delayed rectifier potassium current. Halofantrine hydrochloride also via the inhibition of the human-ether-a-go-go-related gene (HERG) channel and a potent antimalarial agent. | |||
T17240 |
VU041
|
Others | Others |
VU041 is an inhibitor of Anopheles gambiae and Aedes aegypti inward rectifier potassium 1 channels (IC50: 2.5 μM and 1.7 μM, respectively). VU041 inhibits appreciably is mammalian Kir2.1 (IC50: 12.7 μM) and has less inhibitory effect on mammalian Kir1.1, Kir4.1, Kir6.2/SUR1, and Kir7.1. | |||
TP2114 |
Tertiapin-Q
|
||
A high affinity blocker for inward-rectifier K+ channels, this compound is a stable derivative of the bee venom toxin tertiapin. Binds to ROMK1 (Kir1.1) and GIRK1/4 (Kir3.1/3.4) channels with high affinity (Ki values are 1.3 and 13.3 nM respectively) and | |||
T36740 |
Guanosine 5’-diphosphate (sodium salt hydrate)
|
Others | Others |
Guanosine 5’-diphosphate (GDP) is a purine nucleotide and biosynthetic precursor of guanosine 5’-triphosphate .1It has been used to study the conformations of GTPases.2GDP (100 μM) activates sulfonylurea receptor 2B (SUR2B) linked to the inward-rectifier potassium channel 6.1 (Kir6.1) in HEK293T cells in a patch-clamp assay.3 1.Berg, J.M., Tymoczko, J.L., and Stryer, L.Biochemistry(2002) 2.Vetter, I.R., and Wittinghofer, A.The guanine nucleotide-binding switch in three dimensionsScience294(5545)... | |||
T80426 |
Jingzhaotoxin-IX
|
Sodium Channel | Membrane transporter/Ion channel |
Jingzhaotoxin-IX是由35个氨基酸残基组成的C端酰胺化神经毒素。该化合物既抑制电压门控钠通道(包括河豚毒素抗性和河豚毒素敏感亚型)又抑制Kv2.1通道,但对延迟整流钾通道Kv1.1、1.2和1.3无效。 | |||
T83749 |
Tertiapin LQ TFA
TPNLQ |
||
Tertiapin LQ是源自蜜蜂毒素肽tertiapin的肽衍生物,同时也是向内整流钾(Kir)通道的抑制剂。它能够抑制由G蛋白激活的向内整流钾通道1(GIRK1)和GIRK4(即Kir3.1和Kir3.4)组成的异源多聚钾通道,以及向内整流钾通道1(Kir1.1)。在活体内,tertiapin LQ抑制在雪貂中对条件刺激的Purkinje细胞暂停响应。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8040 |
Cholesterol myristate
胆甾烯基豆蔻酸酯,Cholesteryl myristate,胆固醇肉豆蔻酸,Cholesteryl tetradecanoate |
Others; Potassium Channel; GABA Receptor; Endogenous Metabolite; AChR | Membrane transporter/Ion channel; Metabolism; Neuroscience; Others |
Cholesterol myristate (Cholesteryl myristate) 是粗吻海龙中的一种类固醇,可与多种离子通道结合,例如nAChR、GABAA 受体和内向整流钾离子通道。 | |||
T4A2458 |
Resibufogenin
酯蟾毒配基,Bufogenin,Recibufogenin,酯蟾毒配基,蟾力苏 |
Others | Others |
Resibufogenin (Bufogenin) 是华蟾素的成分之一,表现出抑制氧化应激及肿瘤再生的活性。 | |||
TN3636 |
Chlorahololide C
|
Potassium Channel | Membrane transporter/Ion channel |
Chlorahololide C is a potent and selective potassium channel blocker, it exerts potent and selective inhibition on the delayed rectifier (I(K)) K(+) current with the IC(50) value of 3.6 +/- 10.1 mu M. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01889 |
KCNK3 Protein, Human, Recombinant (His & Myc)
Potassium channel subfamily K member 3,TWIK-related acid-sen... |
Human | E. coli |
pH-dependent, voltage-insensitive, background potassium channel protein. Rectification direction results from potassium ion concentration on either side of the membrane. Acts as an outward rectifier when external potassium concentration is low. When external potassium concentration is high, current is inward. KCNK3 Protein, Human, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 50.5 kDa and the accession number is O... | |||
TMPH-03399 |
VAMP2 Protein, Rat, Recombinant (His)
Vesicle-associated membrane protein 2,Vamp2,Synaptobrevin-2 |
Rat | E. coli |
Involved in the targeting and/or fusion of transport vesicles to their target membrane. Major SNARE protein of synaptic vesicles which mediates fusion of synaptic vesicles to release neurotransmitters. Essential for fast vesicular exocytosis and activity-dependent neurotransmitter release as well as fast endocytosis that mediates rapid reuse of synaptic vesicles. Modulates the gating characteristics of the delayed rectifier voltage-dependent potassium channel KCNB1. VAMP2 Protein, Rat, Recombina... |