Cat. No. | Product Name | Target | Signaling Pathways |
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T3470 |
Cis-ACBD
cis-1-aminocyclobutane-1,3-dicarboxylic acid,氨基二羧酸 |
Amino Acids and Derivatives | Metabolism |
Cis-ACBD (cis-1-aminocyclobutane-1,3-dicarboxylic acid) 是一种有效的选择性 N-甲基-D-天冬氨酸受体激动剂。 | |||
T21469 |
Cyclopenthiazide
Cyclomethiazide,Su-8341,SU 8341,环戊噻嗪 |
Others | Others |
Cyclopenthiazide (Cyclomethiazide) 是一种噻嗪类利尿剂,用于治疗高血压和心力衰竭。减少钙离子和尿酸的排泄,增加钠和钾离子的排泄。 | |||
T0796 |
Prilocaine hydrochloride
Prilocaine HCl,Propitocaine hydrochloride,Xylonest,盐酸丙胺卡因 |
ATPase; Sodium Channel | Membrane transporter/Ion channel |
Prilocaine hydrochloride (Prilocaine HCl) 是一种氨基酰胺类局部麻醉剂,作用于神经元膜上的钠通道并限制癫痫发作的扩散。它是Na/K-ATPase 抑制剂,具有神经毒性作用。 | |||
T0018 |
Procainamide hydrochloride
Procapan,Procainamide HCl,Pronestyl,Procanbid,盐酸普鲁卡因胺 |
DNA Methyltransferase; Sodium Channel; AChR; Autophagy | Autophagy; Chromatin/Epigenetic; Membrane transporter/Ion channel; Neuroscience |
Procainamide hydrochloride (Procapan) 是一种用于研究心律失常的抗心律失常制剂。 | |||
T0030 |
Bupivacaine hydrochloride
Vivacaine,Bupivacaine HCl,盐酸布比卡因 |
Sodium Channel | Membrane transporter/Ion channel |
Bupivacaine hydrochloride (Vivacaine) 是NMDA 受体抑制剂,可用于慢性疼痛的研究。它可阻断钠、L-钙和钾通道,还阻断SCN5A 通道,IC50为 69.5 μM。 | |||
T1756 |
Ilaprazole sodium
IY-81149 sodium,艾普拉唑钠 |
Proton pump; TOPK | MAPK; Membrane transporter/Ion channel |
Ilaprazole sodium (IY-81149 sodium) 是一种具有口服活性质子泵抑制剂,以剂量依赖性方式不可逆地抑制 H+/K+-ATPase,在兔壁细胞制剂中的 IC50为 6 μM。它也是一种有效的 T 细胞起源蛋白激酶(TOPK)抑制剂,用于胃溃疡的研究。 | |||
T2189 |
Sodium orthovanadate
Sodium vanadate,钒酸钠,Trisodium vanadate,Sodium pervanadate |
ATPase; Phosphatase | Membrane transporter/Ion channel; Metabolism |
Sodium orthovanadate 是一种蛋白酪氨酸磷酸酶,碱性磷酸酶和一些ATP 酶的抑制剂,有可能充当磷酸盐类似物。它具有胰岛素样作用、对心室肌的正性肌力作用和其他代谢作用。 | |||
T0866 |
Propafenone
Rythmol,普罗帕酮,Propafenonum |
Potassium Channel; MRP; Sodium Channel | Immunology/Inflammation; Membrane transporter/Ion channel |
Propafenone (Propafenonum) 是钠通道阻滞剂,它对 β 受体具有高亲和力 (IC50=32 nM)。它能够阻断瞬时外向钾电流 (Ito) (IC50: 4.9 nM) 和持续延迟整流器K+电流 (Isus) (IC50: 8.6 nM) ,具有抗心律失常的作用。它能够诱导线粒体功能障碍及诱导细胞凋亡,从而抑制食管癌增殖。 | |||
T0378L |
Oxybuprocaine
Butoxyprocaine,BNX,Benoxinate,Novescine,Novesin |
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Oxybuprocaine is an ester-type local anesthetic that is used especially in ophthalmology and otolaryngology. Oxybuprocaine binds to sodium channels and reversibly stabilizes the neuronal membrane which decreases its permeability to sodium ions. | |||
T35842 |
5-chloro Hydrochlorothiazide
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5-chloro Hydrochlorothiazide is a derivative of hydrochlorothiazide, which is a diuretic and antihypertensive agent that increases renal excretion of sodium, potassium, chloride, and bicarbonate ions by inhibiting tubular reabsorptive mechanisms. | |||
T81067 |
Sulfo-Cy3(Me)COOH sodium
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Sulfo-Cy3(Me)COOH sodium 为含磺酸根离子的 Cy3(Cyanine3)染料衍生物,而 Trisulfo-Cy3-acid disodium 含 sulfonate (磺酸根离子),水溶性更佳。 | |||
T22014 |
8-CPT-2Me-cAMP, sodium salt
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8-CPT-2Me-cAMP sodium is a sodium salt compound that selectively activates exchange proteins activated by cAMP (Epac). These Epac proteins are cAMP-sensitive guanine nucleotide exchange factors (GEFs) responsible for activating small GTPases Rap1 and Rap2. 8-CPT-2Me-cAMP sodium specifically activates Epac1 with an EC50 value of 2.2 μM, while showing no activation of PKA with an EC50 value greater than 10 μM [1]. Additionally, 8-CPT-2Me-cAMP sodium stimulates the Epac-mediated release of calcium ... | |||
T83943 |
ING-2 AM
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ING-2 AM是一种能透过细胞膜的荧光钠离子(Na+)指示剂,与钠结合(Kd=20 mM)。激发和发射峰值(λ)分别为525 nm和545 nm。该化合物对K+离子具有20倍的选择性。在体外和原位实验中用于检测实时的钠流入。 | |||
T83944 |
IPG-4 AM
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IPG-4 AM 是一种可渗透膜的荧光钾离子 (K+) 指示剂,具有与钾结合的特性 (Kd= 7 mM)。其激发和发射峰值 (λ) 分别为 525 和 545 nm。它对 K+ 比 Na+ 离子具有 100:1 的选择性。可用于实时检测细胞内 K+ 的变化,也用于监测体内外 K+ 的变化。 | |||
T35731 |
Deethylindanomycin
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Deethylindanomycin is a polyether antibiotic that has been found in S. setonii. It is active against a variety of Gram-positive bacteria, including various strains of S. aureus and Streptococcus, as well as one strain of S. pneumoniae (MICs = 4, 4, and 2 μg/ml, respectively). It is also active against coccidia in vitro, inhibiting E. tenella development, but is inactive against E. tenella infection in chicks when administered at a dose of 200 μg/g in the diet. Deethylindanomycin acts as an ionop... | |||
T62272 |
TRPC6-IN-3
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TRPC6-IN-3 (compound 17) 是一种口服具有活力的瞬时受体电位 C6 离子通道 (TRPC6) 抑制剂。TRPC6-IN-3 能够调节细胞内钙浓度,也能够调节包括钙离子和钠离子在内的阳离子通量来调节膜电位。TRPC6-IN-3 可以用于研究呼吸系统。 | |||
T37052 |
Tetranactin
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Tetranactin is a macrotetrolide and a monovalent cation ionophore that has been found in S. aureus and has antibacterial, insecticidal, and mitogenic activities. It exhibits an equilibrium permeability ratio 1,000-fold greater for lithium than sodium or cesium ions accross bilayer membranes at low voltages. Tetranactin inhibits the growth of Gram-positive bacteria and C. miyabeanus and R. solani fungi when used at concentrations less than 0.9 μg/ml. Tetranactin (0.5-1.5 μg per insect) dose-depen... |