69
4
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0440 |
Oxcarbazepine
GP 47680,奥卡西平 |
Apoptosis; Sodium Channel | Apoptosis; Membrane transporter/Ion channel |
Oxcarbazepine (GP 47680) 是一种钠通道阻滞剂,有效抑制胶质母细胞瘤细胞生长并诱导胶质母细胞瘤细胞凋亡或 G2/M 停滞,具有抗癌和抗惊厥作用。 | |||
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。 | |||
T7806 |
Licarbazepine
10,11-hydroxy-10,11 Dihydrocarbamezer,10,11-二氢-10-羟基卡马西平 |
Others | Others |
Licarbazepine (10,11-hydroxy-10,11 Dihydrocarbamezer) 是一种有效的电压门控钠通道阻滞剂,具有抗惊厥和稳定情绪的功效。 | |||
T79835 |
Aneratrigine hydrochloride
|
Sodium Channel | Membrane transporter/Ion channel |
Aneratrigine hydrochloride 是一种钠通道蛋白9型亚基阻断剂,可用于预防或治疗钠通道阻断剂相关疾病。 | |||
T31614 |
Elpetrigine
GW-273293,JZP 4,JZP4,GW273293,JZP-4,GW 273293 |
||
Elpetrigine( GW 273293, JZP-4) is effective calcium and sodium channel blocker and is currently being evaluated in patients as an anticonvulsant and mood stabilizer. | |||
T22675 |
Co 102862
V 102862 |
Others; Sodium Channel | Membrane transporter/Ion channel; Others |
Co 102862 是一种电压门控钠通道阻滞剂。 Co 102862 可用于抗惊厥的研究。 | |||
T31716 |
Etidocaine Hydrochloride
W-19053,Duranest,W19053,W 19053 |
Sodium Channel | Membrane transporter/Ion channel |
Etidocaine Hydrochloride (W19053) 是一种长效麻醉剂和电压门控钠通道阻滞剂。 | |||
T7182 |
Metaflumizone
BAS-320I,氰氟虫腙 |
Sodium Channel; Parasite | Membrane transporter/Ion channel; Microbiology/Virology |
Metaflumizone (BAS-320I) 是一种缩氨基脲杀虫剂,是钠离子通道阻滞剂。 | |||
T7811 |
Pilsicainide HCl
SUN 1165,盐酸吡西卡呢 |
Sodium Channel | Membrane transporter/Ion channel |
Pilsicainide HCl (SUN 1165) 是一种纯钠通道阻滞剂。 | |||
T12608 |
QX-314 chloride
|
Sodium Channel | Membrane transporter/Ion channel |
QX-314 chloride 是钠离子通道电荷阻滞剂,具有膜不渗透性。 | |||
T13177L |
Tocainide
|
Sodium Channel | Membrane transporter/Ion channel |
Tocainide 是口服有活性的 sodium channel 阻滞剂,阻断产生疼痛的病灶中(神经膜上)的钠通道。它是利多卡因 (lignocaine) 的伯胺类似物,可用于研究心律不齐。 | |||
T2523 |
Rufinamide
CGP 33101,E 2080,卢非酰胺,RUF 331 |
Sodium Channel | Membrane transporter/Ion channel |
Rufinamide (E 2080) 是一种新型镇痫化合物,可用于研究 Lennox-Gastaut 综合症。 | |||
T23213 |
QX-222 chloride
QX 222,Lidocaine N-Methyl Hydrochloride |
Sodium Channel | Membrane transporter/Ion channel |
QX-222 chloride (Lidocaine N-Methyl Hydrochloride) 是 Lignocaine 的一种三甲基类似物,是有效的 Na+通道阻滞剂。 | |||
T68143 |
Solpecainol
|
Sodium Channel | Membrane transporter/Ion channel |
solpecainol 是一种钠离子通道阻滞剂,可用于研究神经系统和心血管疾病。 | |||
T1041 |
Risedronate Sodium
NE 58095 Sodium,Risedronic Acid Sodium,利塞膦酸钠,利赛膦酸钠 |
HBV; Transferase | Metabolism; Microbiology/Virology |
Risedronate Sodium (NE 58095 Sodium) 是一种双磷酸盐,对破骨细胞介导的骨吸收具有抑制作用。 | |||
T12424 |
PF-06305591
PF-6305591 |
Others | Others |
PF-06305591是一种有效的、选择性的电压门钠通道NaV1.8的阻断剂(IC50=15 nM)。 | |||
T7066 |
Fosphenytoin disodium
Fosphenytoin sodium,ACC-9653,磷苯妥英钠 |
Sodium Channel | Membrane transporter/Ion channel |
Fosphenytoin disodium (ACC-9653) 是 phenytoin 的前体药物,具有抗惊厥等活性。它是电压门控钠通道阻滞剂。 | |||
T5850 |
Benzamil
Benzamil (hydrochloride) |
Na+/Ca2+ Exchanger; Sodium Channel | Membrane transporter/Ion channel |
Benzamil 是 Amiloride 类似物,是 Na+/Ca2+交换体抑制剂,抑制 TRPP3 介导的 Ca2+激活电流,IC50为 1.1 μM。它也是一种非选择性上皮钠通道 (ENaC) 阻滞剂,能增强肌源性血管收缩。 | |||
T27830L |
Lifarizine FA
Lifarizine FA(119514-66-8 Free base) |
Sodium Channel | Membrane transporter/Ion channel |
Lifarizine FA 是一种钠通道阻滞剂,可用于治疗神经系统疾病和心血管疾病,研究脑卒中。 | |||
T15260 |
Evenamide
NW-3509 |
Sodium Channel | Membrane transporter/Ion channel |
Evenamide (NW-3509) 是一种口服有效的电压门控钠通道 (sodium channel, VGSC) 阻滞剂,Ki 为 0.4 µM,在精神分裂症中有研究价值。Evenamide 在精神病,躁狂症,抑郁和攻击性的各种啮齿动物模型中具有显著功效。 | |||
T39630 |
Zandatrigine
NBI-921352,XEN901 |
Sodium Channel | Membrane transporter/Ion channel |
Zandatrigine (NBI-921352) 是钠通道蛋白 8 型亚基 α 的阻断剂,可用于癫痫治疗的神经系统病理学研究。 | |||
T29457L |
5-Hydroxydecanoate sodium
|
Potassium Channel | Membrane transporter/Ion channel |
5-Hydroxydecanoate sodium 是一种选择性 ATP 敏感的 K+ (KATP) 通道阻滞剂,IC50 约为 30 μM。 它是线粒体外膜酰基辅酶A 合成酶的底物,具有抗氧化性。 | |||
T13177 | Taquidil | ||
Tocainide hydrochloride 是一种sodium channel 阻滞剂,它阻断神经膜中产生疼痛的病灶中的钠通道。Tocainide hydrochloride 是利多卡因 (lignocaine) 的一种伯胺类似物,可有效抑制各种情况下的室性心律失常。 | |||
T9234 |
Tocainide hydrochloride
2-amino-n-(2,6-dimethylphenyl)propanamide hydrochloride |
Sodium Channel | Membrane transporter/Ion channel |
Tocainide hydrochloride (2-amino-n-(2,6-dimethylphenyl)propanamide hydrochloride) 是利多卡因的伯胺类似物,是钠通道阻滞剂,在产生疼痛的病灶中(神经膜上) 阻断钠通道。Tocainide hydrochloride 具有用于心律不齐研究的价值。 | |||
T5391 |
Bepridil hydrochloride
CERM 1978,盐酸苄普地尔 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Bepridil hydrochloride (CERM 1978) 是一种钙通道阻滞剂,还抑制 Na+/Ca2+ 交换(NCX)、钠通道和心脏肌膜 KATP 通道,具有抗心绞痛的作用。 | |||
T0024 |
Primidone
Primaclone,Mysoline,去氧苯比妥,扑米酮,NCI-C56360 |
GABA Receptor; Sodium Channel; GluR; AChR | Membrane transporter/Ion channel; Neuroscience |
Primidone (NCI-C56360) 是一种强效抗惊厥试剂。它是神经元性电压门控钠通道阻滞剂,在癫痫、原发性震颤和精神疾病的研究中具有价值。 | |||
T0119 |
Nitrendipine
BAY-E-5009,Bayotensin,尼群地平 |
Calcium Channel; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Nitrendipine (BAY-E-5009) 是 Nifedipine 的类似物,是一种钙通道阻滞剂,具有显着的血管扩张作用。它是一种有效的抗高血压药且不会降低肾小球滤过率,并且具有轻微的利钠作用。 | |||
T1046 |
Mexiletine hydrochloride
KOE-1173 (hydrochloride),Mexiletine HCl,KO1173,盐酸美西律 |
AhR; Sodium Channel | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism |
Mexiletine hydrochloride (KOE-1173 hydrochloride) 是一种电压门控钠通道阻滞剂,是 IB 类抗心律失常药。 Mexiletine hydrochloride 通过抑制心肌细胞内钠电流,从而降低心脏动作电位(0相)上升速率,并且降低浦肯野纤维的自律性而发挥抗心律失常作用。 | |||
T7502 |
PF 05089771 tosylate
|
Sodium Channel | Membrane transporter/Ion channel |
PF 05089771 tosylate 是口服有效的、选择性的Nav1.7丙烯酰胺抑制剂。PF 05089771 tosylate 具有用于疼痛和糖尿病神经性疾病的研究。 | |||
T28778 |
Silperisone HCl
RGH5002,SILA336,RGH-5002,Silperisone hydrochloride,SILA-336 |
||
Silperisone HCl (RGH-5002) 阻断细胞中的钠和钙通道,使肌肉细胞的兴奋度和收缩度降低,降低外周张力,充当肌肉松弛剂和外周血管扩张剂。 Silperisone HCl 可用于治疗脊髓损伤引起的复发性疼痛性肌阵挛、脑血管病引起的异常高肌张力、肌张力症状、锥体紧张综合征、多发性硬化症肌痉挛和脊髓炎。Silperisone 是钠通道蛋白2型α通道阻滞剂。Silperisone 是一种类似于tolperisone 的有机硅化合物,具有中枢作用的肌肉松弛剂特性。 | |||
T24283 |
L 30
L30,L-30 |
||
L 30 is a blocker of the sodium channel. | |||
T14992 |
Raxatrigine hydrochloride
GSK-1014802 hydrochloride,CNV1014802 (hydrochloride) |
Others | Others |
Raxatrigine hydrochloride is a state-dependent sodium channel blocker and a Nav1.7 sodium channel inhibitor. | |||
T22887 | KC 12291 hydrochloride | Others | Others |
voltage-gated sodium channel blocker | |||
T26036 |
Rad 243
Rad243,Rad-243 |
||
Rad 243 is a sodium channel blocker with antiarrhythmic activity. | |||
T12951 |
Sodium Channel inhibitor 2
|
Sodium Channel | Membrane transporter/Ion channel |
Sodium Channel inhibitor 2 is a blocker of sodium channel. | |||
T31627 |
Englitazone sodium
CP-72,467-2,D03996,CP-72467-2,Englitazone sodium (USAN) |
||
Englitazone sodium is an antidiabetic agent and a novel NSCA and KATP channel blocker. | |||
T22266 |
Benzamil hydrochloride
Benzylamiloride hydrochloride,3,5-二氨基-N-[(E)-氨基(苄基氨基)亚甲基]-6-氯-2-吡嗪甲酰胺盐酸盐(1:1) |
Others | Others |
Benzamil hydrochloride is a specific and potent sodium channel (ENaC) blocker. | |||
T27297 |
Evenamide HCl
NW 3509,NW-3509,NW3509 |
||
Evenamide, a nav sodium channel blocker, is used potentially for the treatment of schizophrenia. | |||
T70199 | Enecadin HCl | ||
Enecadin HCl is a voltage-dependent sodium and calcium channel blocker. | |||
T69610 | Taplucainium chloride | ||
Taplucainium chloride is a sodium channel blocker with applications as a pain reliever. | |||
T68748 |
Saxitoxinol
|
||
Saxitoxinol is an analog of saxitoxin, a known voltage-gated sodium channel blocker. | |||
T25506 |
Homotyrosine, (+)-
alpha-Homotyrosine, (+)-,L-Homotyrosine |
||
Homotyrosine, (+)- is an amino acid used as a very stable, selective, and renally safe sodium channel blocker. | |||
T27734 |
KM-003 (sulfite)
KM 003,P-552,KM003,P552,P 552,KM-003 |
||
KM-003, a sodium channel blocker, is used potentially for the treatment of cystic fibrosis. | |||
T69027 | Procaine merethoxylline | ||
Procaine merethoxylline is a noted sodium channel blocker with a variety of inhibitory effects. | |||
T61241 | Bliretrigine | ||
Bliretrigine 是一种钠通道 (sodium channel) 阻滞剂。Bliretrigine 有缓解疼痛的作用。 | |||
TP1680 |
ProTx II
|
||
Selective NaV1.7 channel blocker. Shifts activation gating positively and decreases current magnitude. Displays 100-fold selectivity over other sodium channel subtypes. | |||
T69052 | P552-02 free base | ||
P552-02, also known as KM-003, PS 552-02, or 552-02, is a sodium channel blocker potentially for the treatment of cystic fibrosis. | |||
T28160 |
Nerispirdine HCl
HP-184,HP 184,Nerispirdine hydrochloride,HP184 |
||
Nerispirdine is a acetylcholine release enhancer, sodium channel blocker and K(V) 2.1 channel blocker. Nerispirdine inhibits voltage-dependent Na(+) channel currents recorded from human SH-SY5Y cells with an IC(50) of 11.9 micromol/L when measured from a | |||
T12023 |
Mexiletine-d6 hydrochloride
KOE-1173 D6 hydrochloride,Mexiletine D6 hydrochloride |
Others | Others |
Mexiletine D6 hydrochloride is a non-selective voltage-gated sodium channel blocker,is a Class IB antianhythmic. | |||
TP2070 |
BDS I
|
||
Potent and reversible Kv3.4 potassium channel blocker (IC50 = 47 nM); also attenuates inactivation of sodium currents by acting on Nav1.7 and Nav1.3 channels. Enhances TTX-sensitive sodium currents in rat small dorsal root ganglion neurons. Neuroprotective. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0792 |
(-)-Sparteine sulfate pentahydrate
(-)-Sparteine Sulfate,Lupinidine sulfate pentahydrate,(-)-Sparteine sulfate salt,sulfate pentahydrate,五水合硫酸司巴丁 |
Sodium Channel | Membrane transporter/Ion channel |
(-)-Sparteine sulfate pentahydrate ((-)-Sparteine Sulfate) 是一种生物碱,是钠通道抑制剂,属于1a 类抗心律失常药。 | |||
T7853 |
(+)-Sparteine
鹰爪豆碱,(+)-鹰爪豆碱,Pachycarpine |
AChR | Neuroscience |
(+)-Sparteine (Pachycarpine) 是从苏格兰扫帚中提取的一种生物碱,是钠通道阻滞剂和 1a 类抗心律失常剂。它在神经细胞中竞争性地抑制烟碱型乙酰胆碱受体活性,是神经节阻滞剂。 | |||
TMA2106 | (-)-Sparteine | P450 | Metabolism |
Sparteine is a class 1a antiarrhythmic agent, a sodium channel blocker. The deficient debrisoquine hydroxylation of Sparteine is due to the absence of P-450IID1 protein in the livers of poor metabolizers. | |||
T3029 |
Sparteine sulfate
硫酸司巴丁,Depasan,Tocosimplex,Actospar |
Others; Sodium Channel | Membrane transporter/Ion channel; Others |
Sparteine sulfate (Tocosimplex) 是一种 1a 类抗心律失常药和钠通道阻滞剂。它可以螯合二价钙和镁。 |