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Search Results for " sodium channel "

Targets Recommended: Sodium Channel Sodium Channel

210

抑制剂 & 化合物

27

天然产物

1

化合物库

10

重组蛋白

6

同位素标记化合物

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Cat. No.	Product Name
L7400	钠通道分子库		118 compounds
	118 种钠通道相关化合物的独特集合，可用于高通量筛选和高内涵筛选；

化合物库

钠通道分子库

Cat.No: L7400

Compounds: 118

Cat. No.	Product Name	Target	Signaling Pathways
T12951	Sodium Channel inhibitor 2	Sodium Channel	Membrane transporter/Ion channel
	Sodium Channel inhibitor 2 is a blocker of sodium channel.
T12948	Sodium Channel inhibitor 1	Others	Others
	Sodium Channel inhibitor1 is a novel and selective voltage-gated sodium channel for pain treatment. (IC50 Value of 0.16 uM and 0.41 uM for Na v1.7, V hold-90mV and Na v1.7, V hold-90mV)
T1320	Disopyramide Triombrin,Hypaque sodium,amidotrizoate sodium,达舒平	Potassium Channel; Sodium Channel; AChR	Membrane transporter/Ion channel; Neuroscience
	Disopyramide (Triombrin) 是用于研究房性和室性心律失常的 IA 类抗心律失常试剂。它阻断心肌快速内向钠电流，延长心肌动作电位持续时间。它抑制 HERG 编码的钾通道。它也表现出复杂的蛋白质结合，并具有强大的负性肌力作用。
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。
T4054	Dantrolene sodium hemiheptahydrate Dantrolene sodium hydrate,Dantrolene sodium salt,Dantrium,丹曲林钠五水合物,Sodium dantrolene	Calcium Channel; Autophagy	Autophagy; Membrane transporter/Ion channel; Metabolism
	Dantrolene sodium hemiheptahydrate (Sodium dantrolene) 是一种钙通道蛋白抑制剂, 抑制钙离子从肌浆释放, 它是一种乙内酰脲衍生物和直接作用的骨骼肌松弛剂。
T3956	Sodium ionophore III ETH2120	Sodium Channel	Membrane transporter/Ion channel
	Sodium ionophore III (ETH2120) 是一种Na+载体，适用于测定血液、血浆、血清中的钠活性。
T2024	A-803467 A 803467,A803467	Sodium Channel	Membrane transporter/Ion channel
	A-803467 是有效的、选择性的河豚毒素不敏感型Nav1.8 钠通道阻断剂。它在炎症性疼痛和神经性疼痛模型中有缓解疼痛作用。它通过与 ATP-binding cassette subfamily G member 2 (ABCG2) 转运蛋白的相互作用，增强了传统抗癌物的化疗敏感性。
T0008	Phenytoin sodium 5,5-Diphenylhydantoin sodium salt,Diphantoine,苯妥英钠,Dilantin sodium,Diphenylhydantoin Sodium	Virus Protease; Sodium Channel	Membrane transporter/Ion channel; Microbiology/Virology
	Phenytoin sodium (Diphantoine) 是一种有效的电压门控钠离子通道阻滞剂，可减少小鼠乳腺肿瘤的生长和转移，具有抗癫痫活性。
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。
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。
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。
T12421	PF-04885614	Sodium Channel	Membrane transporter/Ion channel
	PF-04885614是一种有效的NaV1.8抑制剂。PF-04885614有用于神经系统疾病和神经发育疾病研究的潜力。
T8711	PF-05186462 PF-05150122	Sodium Channel	Membrane transporter/Ion channel
	PF-05186462 (PF-05150122)是选择性的人Nav1.7电压依赖性钠通道抑制剂，IC50为 21 nM，与其他钠通道 (Nav 1.1、1.2、1.3、1.4、1.5、1.6 和 1.8) 相比，它对 Nav1.7显示出显著的选择性。PF-05186462在急性或慢性疼痛中具有研究价值。
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。
T0077	Dantrolene sodium Lapatinib ditosylate monohydrate,丹曲林钠,Dantrolene sodium salt	Others; Calcium Channel	Membrane transporter/Ion channel; Metabolism; Others
	Dantrolene sodium (Lapatinib ditosylate monohydrate) salt 是一种骨骼肌松弛药，是一种钙通道蛋白抑制剂，可抑制钙离子从肌浆释放。
T8581	Flecainide hydrochloride	Others	Others
	Flecainide hydrochloride 是一种用于预防和治疗异常快速心率的药物。这包括室性和室上性心动过速。
T23070	Nisoxetine hydrochloride	Sodium Channel; Monoamine Transporter; Norepinephrine	Membrane transporter/Ion channel; Neuroscience
	Nisoxetine hydrochloride 是一种去甲肾上腺素转运蛋白 (NET) 抑制剂，Kd 值为 0.76 nM。它是抗抑郁药和局部麻药，可以阻断电压门控性钠通道。
T19723	AMTB hydrochloride AMTB	TRP/TRPV Channel	Membrane transporter/Ion channel
	AMTB hydrochloride (AMTB HCl) 是TRPM8通道的选择性阻滞剂。它抑制 icilin 诱导的 TRPM8 通道激活，pIC50为 6.23。它在膀胱过度活动和膀胱疼痛综合征中有研究的价值。它是电压门控钠通道的非选择性抑制剂 (NaV)。
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。
T12786	RY785	Potassium Channel	Membrane transporter/Ion channel
	RY785 是电压门控钾 (KV2)通道的选择性抑制剂， KV2.2 的 IC50为 0.05 μM。它在缓解疼痛方面具有研究价值。
T15174	DSP-2230	Sodium Channel	Membrane transporter/Ion channel
	DSP-2230 是有效的Nav1.7/Nav1.8通道选择性阻断剂。
TQ0014	GNE-131	Sodium Channel	Membrane transporter/Ion channel
	GNE-131 是有效的人类钠离子通道 NaV1.7(hNaV1.7)选择性抑制剂，IC50为 3 nM。
T0916	Butamben Butyl 4-aminobenzoate,4-氨基苯甲酸丁酯	Potassium Channel; Calcium Channel; Sodium Channel	Membrane transporter/Ion channel; Metabolism
	Butamben (Butyl 4-aminobenzoate) 是一种长效局部麻醉剂，用于治疗慢性疼痛。
T0386L	Ropivacaine LEA-103 HCl,罗哌卡因	Potassium Channel; Sodium Channel	Membrane transporter/Ion channel
	Ropivacaine (LEA-103 HCl) 是有效的钠通道阻断剂，通过可逆地抑制钠离子内流从而引起神经纤维脉冲传导阻滞。Ropivacaine 也是一种 K2P(双孔钾通道)TREK-1的抑制剂，在 COS-7 细胞膜上的 IC50值为 402.7 μM。Ropivacaine 可以用于神经性疼痛的缓解的相关研究。
T5324	BI 01383298	Sodium Channel	Membrane transporter/Ion channel
	BI 01383298 是肝脏中高度表达的柠檬酸钠协同转运蛋白抑制剂。
TQ0011	PF-06869206	Sodium Channel	Membrane transporter/Ion channel
	PF-06869206 是口服有效的磷酸钠协同转运蛋白NaPi2a(SLC34A1) 选择性抑制剂，IC50为 380 nM。
T4490	PF-01247324	Sodium Channel	Membrane transporter/Ion channel
	PF01247324是一种选择性的、口服有效的Nav1.8通道阻断物，对人类重组Nav1.8 的IC50为196 nM。
T0275	Meticrane 美替克仑,Fontiliz,Arresten,蒲硫杂茶磺胺	Chloride channel; Sodium Channel	Membrane transporter/Ion channel
	Meticrane (Arresten) 是一种磺胺类衍生物，具有类似噻嗪类利尿剂的活性，可于研究原发性高血压。
T16514	PF 04531083	Others; Sodium Channel	Membrane transporter/Ion channel; Others
	PF 04531083 是 NaV1.8 通道的特异性阻断剂。 PF 04531083 可用于神经性和炎症性疼痛的相关研究。
T37688	Cyfluthrin	Reactive Oxygen Species; Sodium Channel	Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; NF-κB
	Cyfluthrin 属于 II 型拟除虫菊酯，对多种昆虫都有杀灭效果。Cyfluthrin 是Nav1.8钠通道调节剂。它可应用于农业、兽医、杀虫剂、拟除虫菊酯和贮存产品等领域。
T0924	Benzocaine 苯唑卡因,苯佐卡因	Others; MRP; Sodium Channel	Immunology/Inflammation; Membrane transporter/Ion channel; Others
	Benzocaine 作用电压门控 Na+通道的共同受体，+30 mV 下的 IC50为0.8 mM。
T19644	Benzonatate	Sodium Channel	Membrane transporter/Ion channel
	Benzonatate 是外周口服镇咳药，对咳嗽延伸受体 (cough stretch receptors) 的活性具有抑制作用。它是丁卡因样代谢物，能够阻断呼吸延伸受体的钠通道并产生局部麻醉作用。
T81134	Sodium Channel inhibitor 4	Sodium Channel	Membrane transporter/Ion channel
	Sodium Channel Inhibitor4 是一种抑制钠通道的化合物。
T0386	Ropivacaine hydrochloride 盐酸罗哌卡因,Ropivacaine monohydrochloride	Potassium Channel; Sodium Channel	Membrane transporter/Ion channel
	Ropivacaine hydrochloride (Ropivacaine monohydrochloride) 是钠通道阻断剂，通过可逆地抑制钠离子内流从而引起神经纤维脉冲传导阻滞。Ropivacaine hydrochloride 也是 K2P(双孔钾通道)TREK-1的抑制剂。在动物实验模型中，Ropivacaine hydrochloride 可用于神经性疼痛的缓解。
T9685	DS-1971a	Sodium Channel	Membrane transporter/Ion channel
	DS-1971a 是选择性、口服有效的 NaV1.7抑制剂，对 hNaV1.7 和 mNaV1.7 的 IC50分别为 22.8 和 59.4 nM。DS-1971a 在缓解疼痛方面有研究价值。
T0364	Dibucaine 地布卡因,Cinchocaine	CaMK; Sodium Channel; AChR	Membrane transporter/Ion channel; Neuroscience
	Dibucaine (Cinchocaine) 是钠通道抑制剂和有效的SChE 抑制剂。
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。
T9683	VX-150	Sodium Channel	Membrane transporter/Ion channel
	VX-150 是一种口服有效的，高选择性的 NaV1.8抑制剂。VX-150 在各种疼痛适应症中有研究的价值。
T1787	Levobupivacaine	Sodium Channel	Membrane transporter/Ion channel
	Levobupivacaine 是一种氨基酰胺类局麻药，属于n-alkylsubstituted pipecoloxylidide 家族。它是bupivacaine 的 S-对映异构体。
T12181	NaV1.7 inhibitor-1	Sodium Channel	Membrane transporter/Ion channel
	NaV1.7 inhibitor-1 是有效的、选择性的电压门控钠通道 (Nav) 1.7 抑制剂，对于hNaV1.7的IC50为 0.6 nM，其选择性是 hNaV1.5 的 80 倍。
T7547	Ralfinamide mesylate FCE-26742A (mesylate)	Sodium Channel	Membrane transporter/Ion channel
	Ralfinamide mesylate (FCE-26742A (mesylate)) 是一种口服有效，来源于 α-aminoamide 的钠离子通道阻滞剂, 在缓解疼痛方面有研究价值。
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。
T1260	Cromolyn sodium Disodium Cromoglycate,FPL 670 (Cromolyn) Disodium,FPL-670,色甘酸钠,Sodium cromoglycate	Others; Potassium Channel; GSK-3; Calcium Channel	Membrane transporter/Ion channel; Metabolism; Others; PI3K/Akt/mTOR signaling; Stem Cells
	Cromolyn sodium (FPL-670) 是一种GSK-3β抑制剂，IC50为 2.0 µM，有抗过敏作用。
T2049	GS967 GS458967	Sodium Channel	Membrane transporter/Ion channel
	GS967 是一种有效的、选择性的心脏晚期钠电流（late I Na）抑制剂，心室肌细胞和心脏中的IC50分别为0.13和0.21 μM。
T23280	Ruthenium Red 钌红,Ammoniated ruthenium oxychloride	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Ruthenium Red (Ammoniated ruthenium oxychloride) 是一种 L 型钙电流 (ICa) 阻断剂，是一种聚阳离子染料，广泛用于电子显微镜 (EM) 下细胞、组织和营养细菌的观察。它能与磷脂和脂肪酸反应强烈，并与酸性粘多糖结合。
T6633	Ranolazine 雷诺嗪,CVT 303,Ranexa,RS 43285-003	Calcium Channel; Sodium Channel	Membrane transporter/Ion channel; Metabolism
	Ranolazine (RS 43285-003) 具有抗心绞痛和抗缺血的功效，通过抑制内向钠电流的后期作用 (对INa 和IKr 的IC50值分别为 6 μM 和 12 μM) 发挥作用，而不会影响心率或血压。Ranolazine 还是脂肪酸氧化 (FAO) 的部分抑制剂。
T18975	DIDS sodium salt 4,4'-二异硫氰酸基-2,2'-二苯乙烯磺酸二钠[蛋白质改性试剂],MDL101114ZA	VDAC; ABC	Membrane transporter/Ion channel
	DIDS sodium salt (MDL101114ZA) 是有效的ABCA1和VDAC1双抑制剂。
T4539	Nicainoprol 尼卡普醇,RU-42924	Sodium Channel	Membrane transporter/Ion channel
	Nicainoprol (RU-42924) 是一种快速钠通道阻断剂，是有效的抗心律失常剂。
T15207	Eleclazine hydrochloride GS 6615 hydrochloride	Sodium Channel	Membrane transporter/Ion channel
	Eleclazine hydrochloride (GS 6615 hydrochloride) 是新型 Na+电流抑制剂，IC50是0.7 uM。

化合物

Sodium Channel inhibitor 2

Cat.No: T12951

Target: Sodium Channel

Sodium Channel inhibitor 1

Cat.No: T12948

Target: Others

Cat.No: T1320

Synonym: Triombrin,Hypaque sodium,amidotrizoate sodium,达舒平

Target: Potassium Channel, Sodium Channel, AChR

QX-314 chloride

Cat.No: T12608

Target: Sodium Channel

Cat.No: T13177L

Target: Sodium Channel

Dantrolene sodium hemiheptahydrate

Cat.No: T4054

Synonym: Dantrolene sodium hydrate,Dantrolene sodium salt,Dantrium,丹曲林钠五水合物,Sodium dantrolene

Target: Calcium Channel, Autophagy

Sodium ionophore III

Cat.No: T3956

Synonym: ETH2120

Target: Sodium Channel

Cat.No: T2024

Synonym: A 803467,A803467

Target: Sodium Channel

Phenytoin sodium

Cat.No: T0008

Synonym: 5,5-Diphenylhydantoin sodium salt,Diphantoine,苯妥英钠,Dilantin sodium,Diphenylhydantoin Sodium

Target: Virus Protease, Sodium Channel

Cat.No: T15260

Synonym: NW-3509

Target: Sodium Channel

Cat.No: T5850

Synonym: Benzamil (hydrochloride)

Target: Na+/Ca2+ Exchanger, Sodium Channel

Cat.No: T0440

Synonym: GP 47680,奥卡西平

Target: Apoptosis, Sodium Channel

Cat.No: T12421

Target: Sodium Channel

Cat.No: T8711

Synonym: PF-05150122

Target: Sodium Channel

Cat.No: T0866

Synonym: Rythmol,普罗帕酮,Propafenonum

Target: Potassium Channel, MRP, Sodium Channel

Dantrolene sodium

Cat.No: T0077

Synonym: Lapatinib ditosylate monohydrate,丹曲林钠,Dantrolene sodium salt

Target: Others, Calcium Channel

Flecainide hydrochloride

Cat.No: T8581

Target: Others

Nisoxetine hydrochloride

Cat.No: T23070

Target: Sodium Channel, Monoamine Transporter, Norepinephrine

AMTB hydrochloride

Cat.No: T19723

Synonym: AMTB

Target: TRP/TRPV Channel

Bupivacaine hydrochloride

Cat.No: T0030

Synonym: Vivacaine,Bupivacaine HCl,盐酸布比卡因

Target: Sodium Channel

Cat.No: T12786

Target: Potassium Channel

Cat.No: T15174

Target: Sodium Channel

Cat.No: TQ0014

Target: Sodium Channel

Cat.No: T0916

Synonym: Butyl 4-aminobenzoate,4-氨基苯甲酸丁酯

Target: Potassium Channel, Calcium Channel, Sodium Channel

Cat.No: T0386L

Synonym: LEA-103 HCl,罗哌卡因

Target: Potassium Channel, Sodium Channel

Cat.No: T5324

Target: Sodium Channel

Cat.No: TQ0011

Target: Sodium Channel

Cat.No: T4490

Target: Sodium Channel

Cat.No: T0275

Synonym: 美替克仑,Fontiliz,Arresten,蒲硫杂茶磺胺

Target: Chloride channel, Sodium Channel

Cat.No: T16514

Target: Others, Sodium Channel

Cat.No: T37688

Target: Reactive Oxygen Species, Sodium Channel

Cat.No: T0924

Synonym: 苯唑卡因,苯佐卡因

Target: Others, MRP, Sodium Channel

Cat.No: T19644

Target: Sodium Channel

Sodium Channel inhibitor 4

Cat.No: T81134

Target: Sodium Channel

Ropivacaine hydrochloride

Cat.No: T0386

Synonym: 盐酸罗哌卡因,Ropivacaine monohydrochloride

Target: Potassium Channel, Sodium Channel

Cat.No: T9685

Target: Sodium Channel

Cat.No: T0364

Synonym: 地布卡因,Cinchocaine

Target: CaMK, Sodium Channel, AChR

Cat.No: T7182

Synonym: BAS-320I,氰氟虫腙

Target: Sodium Channel, Parasite

Cat.No: T9683

Target: Sodium Channel

Levobupivacaine

Cat.No: T1787

Target: Sodium Channel

NaV1.7 inhibitor-1

Cat.No: T12181

Target: Sodium Channel

Ralfinamide mesylate

Cat.No: T7547

Synonym: FCE-26742A (mesylate)

Target: Sodium Channel

Cat.No: T7806

Synonym: 10,11-hydroxy-10,11 Dihydrocarbamezer,10,11-二氢-10-羟基卡马西平

Target: Others

Cromolyn sodium

Cat.No: T1260

Synonym: Disodium Cromoglycate,FPL 670 (Cromolyn) Disodium,FPL-670,色甘酸钠,Sodium cromoglycate

Target: Others, Potassium Channel, GSK-3, Calcium Channel

Cat.No: T2049

Synonym: GS458967

Target: Sodium Channel

Cat.No: T23280

Synonym: 钌红,Ammoniated ruthenium oxychloride

Target: Calcium Channel

Cat.No: T6633

Synonym: 雷诺嗪,CVT 303,Ranexa,RS 43285-003

Target: Calcium Channel, Sodium Channel

DIDS sodium salt

Cat.No: T18975

Synonym: 4,4'-二异硫氰酸基-2,2'-二苯乙烯磺酸二钠[蛋白质改性试剂],MDL101114ZA

Target: VDAC, ABC

Cat.No: T4539

Synonym: 尼卡普醇,RU-42924

Target: Sodium Channel

Eleclazine hydrochloride

Cat.No: T15207

Synonym: GS 6615 hydrochloride

Target: Sodium Channel

Cat. No.	Product Name	Target	Signaling Pathways
T4727	Taurolithocholic acid sodium salt 牛磺石胆酸钠,Sodium taurolithocholate	Others; Calcium Channel	Membrane transporter/Ion channel; Metabolism; Others
	Taurolithocholic acid sodium salt (Sodium taurolithocholate) 是抑胆剂和 Ca2+激动剂，可抑制放射性配体与毒蕈碱 M1 结合。
T2173	Veratridine	Sodium Channel	Membrane transporter/Ion channel
	Veratridine 是一种生物碱，来自百合科植物。Veratridine 是一种钠通道激动剂，对 Nav1.7 的峰值电流具有抑制作用，IC50为 18.39 µM。
T4S1876	3-Deoxyaconitine	Sodium Channel	Membrane transporter/Ion channel
	3-Deoxyaconitine 是一种二萜类生物碱，对钠离子通道有激活作用。
T6674	L-Ascorbic acid sodium salt (+)-Sodium L-ascorbate,Vitamin C sodium salt,Sodium ascorbate,L-Ascorbic acid sodium,抗坏血酸钠,Sodium L-ascorbate,维生素C钠	Apoptosis; Others; Calcium Channel; Reactive Oxygen Species; Endogenous Metabolite	Apoptosis; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; NF-κB; Others
	L-Ascorbic acid sodium salt (Vitamin C sodium salt) 是一种电子供体，是一种内源性抗氧化剂。它还是一种胶原沉积促进剂和弹性生成抑制剂。它选择性抑制 Cav3.2 通道(Cav3.2 channels)，IC50为 6.5 μM。
T2946	Tanshinone IIA sulfonate sodium 丹参酮IIA磺酸盐,丹参酮IIA-磺酸钠,Tanshinone IIA sulfonate,Sodium Tanshinone IIA sulfonate,Tanshinone IIA sodium sulfonate,sodium	CaMK; P450; Calcium Channel	Membrane transporter/Ion channel; Metabolism; Neuroscience
	Tanshinone IIA sulfonate sodium (Tanshinone IIA sodium sulfonate) 是从丹参中提取的丹参酮IIA 的水溶性衍生物，是SOCE 抑制剂，用于心血管疾病的研究。
T8125	Quinidine sulfate dihydrate 硫酸奎尼宁,硫酸奎尼丁二水合物,Chinidin Sodium,β-quinine Sodium,Pitayine Sodium,Quinidine sulfate	P450	Metabolism
	Quinidine sulfate dihydrate (Pitayine Sodium) 是抗心律失常剂，能够阻断 K+通道(IC50:19.9 μM)。它是细胞色素 P450db 的选择性抑制剂，可用于研究疟疾。
T3092	Nigericin sodium salt 尼日利亚菌素,尼日利亚菌素钠盐	Potassium Channel; NOD-like Receptor (NLR); Antibacterial; Antibiotic; NOD	Immunology/Inflammation; Membrane transporter/Ion channel; Microbiology/Virology; NF-κB
	Nigericin sodium salt 属于抗生素，是一种 NLRP3 激活剂，也是一种阳离子离子载体。Nigericin sodium 可以触发 NALP3 炎性体的激活，可抑制高尔基体功能并抑制革兰氏阳性菌的生长。
T8299	Dimethyl lithospermate B 丹酚酸B二甲酯,dmLSB	Sodium Channel	Membrane transporter/Ion channel
	Dimethyl lithospermate B (dmLSB) 是 Na+通道的选择性激动剂，减缓钠电流 (INa) 失活，导致动作电位 (AP) 早期内向电流增加。
T3021	Bulleyaconitine A 草乌甲素,Bulleyaconi cine A	Sodium Channel	Membrane transporter/Ion channel
	Bulleyaconitine A (Bulleyaconi cine A) 是一种分离自乌头属植物的抗炎活性化合物，也可用于缓解疼痛的研究。
T4590	(+)-Kavain 醉椒素,Kavain,L-KAWAIN,(R)-KAWAIN	Calcium Channel; GABA Receptor; Sodium Channel; Monoamine Transporter	Membrane transporter/Ion channel; Metabolism; Neuroscience
	(+)-Kavain ((R)-KAWAIN) 是从卡瓦胡椒中提取的一种主要的卡瓦内酯，可通过电压依赖性的 Na+和 Ca2+通道相互作用，减弱血管平滑肌的收缩，具有抗惊厥作用。它可与α4β2δ GABAA 受体结合，加强 GABA 的功效，用于炎症疾病研究。
T4550	Ajmaline Cardiorythmine,Raugalline,阿义吗啉,阿义马林,Tachmalin,(+)-Ajmaline	Sodium Channel	Membrane transporter/Ion channel
	Ajmaline (Cardiorythmine) 是一种钠通道阻断剂，属于1A 类抗心律失常剂。Ajmaline 阻断 HERG 电流，在 HEK 细胞的 IC50为 1 μM，爪蟾卵母细胞的IC50为 42.3 μM。Ajmaline 在室性心动过速方面具有研究价值。
T7056	Dronedarone 决奈达隆,SR 33589	P450; Potassium Channel; Calcium Channel; Sodium Channel; Adrenergic Receptor; AChR; Autophagy	Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience
	Dronedarone (SR 33589) 是一种胺碘酮类似物，对治疗心房颤动可能有效。它是CYP3A4的底物和中度抑制剂。它是多种离子电流的有效阻滞剂，通过非竞争性结合到肾上腺素能受体显示出抗肾上腺素能的效果。
T6856	Halofuginone 卤夫酮,常山酮,Tempostatin,empostatin,RU-19110	Calcium Channel; DNA/RNA Synthesis; Sodium Channel; Parasite; TGF-beta/Smad	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Stem Cells
	Halofuginone (RU-19110) 是Febrifugine 的衍生物，是一种竞争性脯氨酰-tRNA 合成酶抑制剂。它也是肺血管扩张剂，可激活Kv 通道并阻断电压门控、受体操作和存储操作的钙离子通道。它具有抗炎、抗癌、抗疟疾和抗纤维化作用。
T0167	Vinpocetine 长春西丁,RGH-4405,长春西汀,Ethyl apovincaminate	IκB/IKK; NF-κB; Sodium Channel; PDE	Membrane transporter/Ion channel; Metabolism; NF-κB
	Vinpocetine (RGH-4405) 是一种长春花生物碱衍生物，是阻断 Na+通道的阻断剂。Vinpocetine 抑制IKK 的IC50为 17.17 μM。Vinpocetine 也是PDE 抑制剂，并通过直接靶向IKK 抑制NF-κB 依赖性炎症反应，已被广泛用于研究脑血管疾病。
T3524	Halofuginone hydrobromide 卤夫酮溴氢酸盐,Tempostatin,RU-19110 (hydrobromide),Stenorol,常山酮溴酸盐	Others; Calcium Channel; DNA/RNA Synthesis; Sodium Channel; Parasite; TGF-beta/Smad	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Others; Stem Cells
	Halofuginone hydrobromid 是Febrifugine 的衍生物，是竞争性脯氨酰-tRNA 合成酶抑制剂。它是 I 型胶原合成的特异性抑制剂，并通过抑制TGF-β活性可减轻骨关节炎。它具有抗疟疾、抗炎、抗癌、抗纤维化作用。
TN6713	6-Benzoylheteratisine Heteratisan-14-one, 6-(benzoyloxy)-20-ethyl-8-hydroxy-1-methoxy-4-meth,苯甲酰新异乌头碱	Sodium Channel	Membrane transporter/Ion channel
	6-Benzoylheteratisine (Heteratisan-14-one, 6-(benzoyloxy)-20-ethyl-8-hydroxy-1-methoxy-4-meth) 是乌头碱的拮抗剂，乌头碱是天然 Na+通道激活剂。
T3402	20(S)-Ginsenoside Rg3 20(S)-人参皂苷 Rg3,人参皂苷 Rg3,20(S)-Ginsenoside-Rg3,Rg3,20S-Ginsenoside Rg3,Ginsenoside Rg3,S-Ginsenoside Rg3	EGFR; Beta Amyloid; Potassium Channel; NF-κB; COX; Sodium Channel; Endogenous Metabolite	Angiogenesis; Immunology/Inflammation; JAK/STAT signaling; Membrane transporter/Ion channel; Metabolism; Neuroscience; NF-κB; Tyrosine Kinase/Adaptors
	20(S)-Ginsenoside Rg3 (Rg3) 是红参的主要成分，通过抑制肿瘤细胞的粘附和侵袭来抑制肿瘤细胞肺转移。它抑制Na+和hKv1.4通道，IC50分别为 32.2±4.5 和 32.6±2.2 μM。它还抑制Aβ，NF-κB 活性和COX-2表达，抑制人脐静脉内皮细胞的增殖并具有抗血管生成活性。
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。
TN1254	3'-Methoxydaidzein 3'-甲氧基大豆苷元	Sodium Channel	Membrane transporter/Ion channel
	3'-Methoxydaidzein 是一种异黄酮和 Sodium Channel 双重抑制剂。3'-Methoxydaidzein 对NaV1.7、NaV1.8 和 NaV1.3有抑制作用，IC50 分别为 181 nM、397 nM 和 505 nM。 3'-Methoxydaidzein 对胶原诱导的血小板聚集具有特异性，IC50值分别为12.3和61.5µM。。3'-Methoxydaidzein 通过抑制电压门控钠通道发挥镇痛作用。 3'-Methoxydaidzein 具有抗氧化活性和抗血小板聚集活性。
T3604	Sodium dichloroacetate Sodium Dichloroacetate,DCA,bichloroacetic acid,二氯乙酸钠,Sodium dichloroacetate (DCA),二氯醋酸酯	Apoptosis; Dehydrogenase; Reactive Oxygen Species; PDK	Apoptosis; Immunology/Inflammation; Metabolism; NF-κB; PI3K/Akt/mTOR signaling
	Sodium dichloroacetate (DCA) 是一种肿瘤细胞线粒体中的代谢调节剂，一种丙酮酸脱氢酶激酶 (PDK) 抑制剂。Sodium dichloroacetate 具有抗肿瘤活性，可以降低肿瘤微环境中的乳酸，增加活性氧的产生并促进肿瘤细胞凋亡。
T4S0537	Neoline Bullatine B,雪上一枝蒿乙素	Others; Sodium Channel	Membrane transporter/Ion channel; Others
	Neoline 是一种乌头根 (PA) 的活性成分，可改善奥沙利铂引起的小鼠周围神经病变。Neoline 通对Nav1.7 电压门控钠通道电流 (VGSC)有抑制作用。它可用作标记化合物，从而测定用于研究神经性疼痛的 PA 产品的质量。
T5065	GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD Monosodium-GMP,cGMP sodium salt,鸟苷-3',5'-环磷酸一钠盐,Cyclic GMP	PKA	Tyrosine Kinase/Adaptors
	GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD (cGMP sodium salt) 也称为 cGMP，是一种细胞调节剂，被描述为第二信使。它的水平随着各种激素的增加而增加，包括乙酰胆碱、胰岛素和催产素。 cGMP 激活蛋白激酶 G(PKG) 并调节离子通道电导，信号传导影响多种过程，包括平滑肌松弛和增殖、光转导和能量稳态。
T0266	Quinidine hydrochloride monohydrate 奎宁树,奎尼丁盐酸盐一水合物,奎尼丁盐酸盐,Quinidine hydrochloride	Potassium Channel; Sodium Channel; Parasite	Membrane transporter/Ion channel; Microbiology/Virology
	Quinidine hydrochloride monohydrate 是一种抗心律失常剂，也是 K+通道 (K+channel) 的有效阻断剂，其IC50值为 19.9 μM。它是一种有效且选择性的细胞色素 P450db (cytochrome P450db) 抑制剂，也可用作疟疾的研究。
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。
T36068	Brevetoxin B	Others	Others
	Brevetoxin B is a polyketide neurotoxin produced by Karenia species and other dinoflagellates. It binds to site 5 on the alpha subunit of voltage-gated sodium channels (IC50 = 15 nM) on neurons at the neuromuscular junction, causing the channel to open irreversibly at potentials more negative than normal, discharging action potentials repetitively. Brevetoxin B is ichthyotoxic at nanomolar concentrations and is responsible for an illness described as neurotoxic shellfish poisoning.

天然产物

Taurolithocholic acid sodium salt

Cat.No: T4727

Synonym: 牛磺石胆酸钠,Sodium taurolithocholate

Target: Others, Calcium Channel

Cat.No: T2173

Target: Sodium Channel

3-Deoxyaconitine

Cat.No: T4S1876

Target: Sodium Channel

L-Ascorbic acid sodium salt

Cat.No: T6674

Synonym: (+)-Sodium L-ascorbate,Vitamin C sodium salt,Sodium ascorbate,L-Ascorbic acid sodium,抗坏血酸钠,Sodium L-ascorbate,维生素C钠

Target: Apoptosis, Others, Calcium Channel, Reactive Oxygen Species, Endogenous Metabolite

Tanshinone IIA sulfonate sodium

Cat.No: T2946

Synonym: 丹参酮IIA磺酸盐,丹参酮IIA-磺酸钠,Tanshinone IIA sulfonate,Sodium Tanshinone IIA sulfonate,Tanshinone IIA sodium sulfonate,sodium

Target: CaMK, P450, Calcium Channel

Quinidine sulfate dihydrate

Cat.No: T8125

Synonym: 硫酸奎尼宁,硫酸奎尼丁二水合物,Chinidin Sodium,β-quinine Sodium,Pitayine Sodium,Quinidine sulfate

Target: P450

Nigericin sodium salt

Cat.No: T3092

Synonym: 尼日利亚菌素,尼日利亚菌素钠盐

Target: Potassium Channel, NOD-like Receptor (NLR), Antibacterial, Antibiotic, NOD

Dimethyl lithospermate B

Cat.No: T8299

Synonym: 丹酚酸B二甲酯,dmLSB

Target: Sodium Channel

Bulleyaconitine A

Cat.No: T3021

Synonym: 草乌甲素,Bulleyaconi cine A

Target: Sodium Channel

Cat.No: T4590

Synonym: 醉椒素,Kavain,L-KAWAIN,(R)-KAWAIN

Target: Calcium Channel, GABA Receptor, Sodium Channel, Monoamine Transporter

Cat.No: T4550

Synonym: Cardiorythmine,Raugalline,阿义吗啉,阿义马林,Tachmalin,(+)-Ajmaline

Target: Sodium Channel

Cat.No: T7056

Synonym: 决奈达隆,SR 33589

Target: P450, Potassium Channel, Calcium Channel, Sodium Channel, Adrenergic Receptor, AChR, Autophagy

Cat.No: T6856

Synonym: 卤夫酮,常山酮,Tempostatin,empostatin,RU-19110

Target: Calcium Channel, DNA/RNA Synthesis, Sodium Channel, Parasite, TGF-beta/Smad

Cat.No: T0167

Synonym: 长春西丁,RGH-4405,长春西汀,Ethyl apovincaminate

Target: IκB/IKK, NF-κB, Sodium Channel, PDE

Halofuginone hydrobromide

Cat.No: T3524

Synonym: 卤夫酮溴氢酸盐,Tempostatin,RU-19110 (hydrobromide),Stenorol,常山酮溴酸盐

Target: Others, Calcium Channel, DNA/RNA Synthesis, Sodium Channel, Parasite, TGF-beta/Smad

6-Benzoylheteratisine

Cat.No: TN6713

Synonym: Heteratisan-14-one, 6-(benzoyloxy)-20-ethyl-8-hydroxy-1-methoxy-4-meth,苯甲酰新异乌头碱

Target: Sodium Channel

20(S)-Ginsenoside Rg3

Cat.No: T3402

Synonym: 20(S)-人参皂苷 Rg3,人参皂苷 Rg3,20(S)-Ginsenoside-Rg3,Rg3,20S-Ginsenoside Rg3,Ginsenoside Rg3,S-Ginsenoside Rg3

Target: EGFR, Beta Amyloid, Potassium Channel, NF-κB, COX, Sodium Channel, Endogenous Metabolite

(-)-Sparteine sulfate pentahydrate

Cat.No: T0792

Synonym: (-)-Sparteine Sulfate,Lupinidine sulfate pentahydrate,(-)-Sparteine sulfate salt,sulfate pentahydrate,五水合硫酸司巴丁

Target: Sodium Channel

Cat.No: T7853

Synonym: 鹰爪豆碱,(+)-鹰爪豆碱,Pachycarpine

Target: AChR

3'-Methoxydaidzein

Cat.No: TN1254

Synonym: 3'-甲氧基大豆苷元

Target: Sodium Channel

Sodium dichloroacetate

Cat.No: T3604

Synonym: Sodium Dichloroacetate,DCA,bichloroacetic acid,二氯乙酸钠,Sodium dichloroacetate (DCA),二氯醋酸酯

Target: Apoptosis, Dehydrogenase, Reactive Oxygen Species, PDK

Cat.No: T4S0537

Synonym: Bullatine B,雪上一枝蒿乙素

Target: Others, Sodium Channel

GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD

Cat.No: T5065

Synonym: Monosodium-GMP,cGMP sodium salt,鸟苷-3',5'-环磷酸一钠盐,Cyclic GMP

Target: PKA

Quinidine hydrochloride monohydrate

Cat.No: T0266

Synonym: 奎宁树,奎尼丁盐酸盐一水合物,奎尼丁盐酸盐,Quinidine hydrochloride

Target: Potassium Channel, Sodium Channel, Parasite

Cat.No: TMA2106

Target: P450

Sparteine sulfate

Cat.No: T3029

Synonym: 硫酸司巴丁,Depasan,Tocosimplex,Actospar

Target: Others, Sodium Channel

Cat.No: T36068

Target: Others

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPH-02118	SCN1A Protein, Human, Recombinant (His) Sodium channel protein brain I subunit alp...	Human	E. coli
	Mediates the voltage-dependent sodium ion permeability of excitable membranes. Assuming opened or closed conformations in response to the voltage difference across the membrane, the protein forms a sodium-selective channel through which Na(+) ions may pass in accordance with their electrochemical gradient. Plays a key role in brain, probably by regulating the moment when neurotransmitters are released in neurons. Involved in sensory perception of mechanical pain: activation in somatosensory neur...
TMPY-03183	SCN2B Protein, Human, Recombinant (hFc) sodium channel, voltage gated, type II bet...	Human	HEK293 Cells
	SCN2B Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 42.2 kDa and the accession number is O60939.
TMPY-03697	SCN2B Protein, Human, Recombinant (His) ATFB14,sodium channel, voltage gated, type...	Human	HEK293 Cells
	SCN2B Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 34.7 kDa and the accession number is O60939.
TMPY-02976	SCN3B Protein, Human, Recombinant (His) ATFB16,HSA243396,BRGDA7,SCNB3,sodium channel	Human	HEK293 Cells
	SCN3B Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 17.2 kDa and the accession number is Q9NY72.
TMPY-02722	SCN3B Protein, Human, Recombinant (hFc) ATFB16,HSA243396,sodium channel, voltage g...	Human	HEK293 Cells
	SCN3B Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 42.5 kDa and the accession number is Q9NY72.
TMPH-03623	Tb2-II Protein, Tityus bahiensis, Recombinant (His & Myc) Toxin Tb2-II,P-Mice-Ins-beta* NaTx5.4	Tityus bahiensis	Baculovirus Insect Cells
	Beta toxins bind voltage-independently at site-4 of sodium channels (Nav) and shift the voltage of activation toward more negative potentials thereby affecting sodium channel activation and promoting spontaneous and repetitive firing. This toxin is active against both mammals and insects. Tb2-II Protein, Tityus bahiensis, Recombinant (His & Myc) is expressed in Baculovirus insect cells with N-10xHis and C-Myc tag. The predicted molecular weight is 10.8 kDa and the accession number is P60276.
TMPH-00362	Beta-mammal toxin Css4 Protein, Centruroides suffusus, Recombinant (His & SUMO) Css IV,CssIV,Beta-mammal toxin Css4	Centruroides suffusus	E. coli
	Beta toxins bind voltage-independently at site-4 of sodium channels (Nav) and shift the voltage of activation toward more negative potentials thereby affecting sodium channel activation and promoting spontaneous and repetitive firing. This toxin is active only on mammals. Beta-mammal toxin Css4 Protein, Centruroides suffusus, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 23.6 kDa and the accession number is P60266.
TMPH-03624	Tb2-II Protein, Tityus bahiensis, Recombinant (E. coli, His & Myc) Toxin Tb2-II,P-Mice-Ins-beta* NaTx5.4	Tityus bahiensis	E. coli
	Beta toxins bind voltage-independently at site-4 of sodium channels (Nav) and shift the voltage of activation toward more negative potentials thereby affecting sodium channel activation and promoting spontaneous and repetitive firing. This toxin is active against both mammals and insects. Tb2-II Protein, Tityus bahiensis, Recombinant (E. coli, His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 12.0 kDa and the accession number is P...
TMPH-02405	LqqIT1 Protein, Leiurus quinquestriatus quinquestriatus, Recombinant (His & Myc) Beta-insect excitatory toxin LqqIT1	Egyptian scorpion	E. coli
	Excitatory insect beta-toxins induce a spastic paralysis. They bind voltage-independently at site-4 of sodium channels (Nav) and shift the voltage of activation toward more negative potentials thereby affecting sodium channel activation and promoting spontaneous and repetitive firing. This toxin induces a fast excitatory contraction paralysis on fly larvae. It is active only on insects. LqqIT1 Protein, Leiurus quinquestriatus quinquestriatus, Recombinant (His & Myc) is expressed in E. coli expre...
TMPH-03628	Beta-toxin Tz1 Protein, Tityus zulianus, Recombinant (His & Myc) PT-beta NaTx14.1,Beta-toxin Tz1	Tityus zulianus	E. coli
	Beta toxins bind voltage-independently at site-4 of sodium channels (Nav) and shift the voltage of activation toward more negative potentials thereby affecting sodium channel activation and promoting spontaneous and repetitive firing. Strongly affects skeletal muscle channels Nav1.4/SCN4A, poorly affects the neuronal channels Nav1.6/SCN8A and Nav1.2/SCN2A. Induces spastic paralysis of rear limbs, increased salivation, apnea, tachycardia and increased perspiration. Beta-toxin Tz1 Protein, Tityus ...

重组蛋白

SCN1A Protein, Human, Recombinant (His)

Cat.No: TMPH-02118

Species: Human

Expression System: E. coli

SCN2B Protein, Human, Recombinant (hFc)

Cat.No: TMPY-03183

Species: Human

Expression System: HEK293 Cells

SCN2B Protein, Human, Recombinant (His)

Cat.No: TMPY-03697

Species: Human

Expression System: HEK293 Cells

SCN3B Protein, Human, Recombinant (His)

Cat.No: TMPY-02976

Species: Human

Expression System: HEK293 Cells

SCN3B Protein, Human, Recombinant (hFc)

Cat.No: TMPY-02722

Species: Human

Expression System: HEK293 Cells

Tb2-II Protein, Tityus bahiensis, Recombinant (His & Myc)

Cat.No: TMPH-03623

Species: Tityus bahiensis

Expression System: Baculovirus Insect Cells

Beta-mammal toxin Css4 Protein, Centruroides suffusus, Recombinant (His & SUMO)

Cat.No: TMPH-00362

Species: Centruroides suffusus

Expression System: E. coli

Tb2-II Protein, Tityus bahiensis, Recombinant (E. coli, His & Myc)

Cat.No: TMPH-03624

Species: Tityus bahiensis

Expression System: E. coli

LqqIT1 Protein, Leiurus quinquestriatus quinquestriatus, Recombinant (His & Myc)

Cat.No: TMPH-02405

Species: Egyptian scorpion

Expression System: E. coli

Beta-toxin Tz1 Protein, Tityus zulianus, Recombinant (His & Myc)

Cat.No: TMPH-03628

Species: Tityus zulianus

Expression System: E. coli

Cat. No.	Product Name	Target	Signaling Pathways
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.
TMID-0295	Fosphenytoin Sodium-d10
	Fosphenytoin Sodium-d10 是 Fosphenytoin Sodium 的氘代化合物。Fosphenytoin Sodium 的 CAS 号为 92134-98-0。Fosphenytoin sodium 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。
TMID-0247	LacosaMide-d3
	LacosaMide-d3 是 LacosaMide 的氘代化合物。LacosaMide 的 CAS 号为 175481-36-4。Lacosamide是一种功能化氨基酸。Lacosamide以一种新的方式调节钠通道：它选择性地增强钠通道缓慢失活，而对快速失活没有影响Lacosamine在不同的啮齿类动物癫痫发作模型中显示出抗癫痫作用，在反映神经性疼痛和慢性炎性疼痛的不同类型和症状的实验动物模型中显示了抗伤害潜力。
TMIJ-0240	Lacosamide-d3 (Acetyl-d3)
	Lacosamide-d3 (Acetyl-d3) 是 Lacosamide 的氘代化合物。Lacosamide 的 CAS 号为 175481-36-4。Lacosamide是一种功能化氨基酸。Lacosamide以一种新的方式调节钠通道：它选择性地增强钠通道缓慢失活，而对快速失活没有影响Lacosamine在不同的啮齿类动物癫痫发作模型中显示出抗癫痫作用，在反映神经性疼痛和慢性炎性疼痛的不同类型和症状的实验动物模型中显示了抗伤害潜力。
TMID-0299	Zonisamide-d4
	Zonisamide-d4 是 Zonisamide 的氘代化合物。Zonisamide 的 CAS 号为 68291-97-4。Zonisamide 是锌酶碳酸酐酶 (carbonic anhydrase) 的有效抑制剂，对人类线粒体同工酶 hCA II 和 hCA V 作用的Ki值分别为 35.2 nM 和 20.6 nM。Zonisamide 具有抗癫痫活性，在癫痫、癫痫发作和帕金森病的研究中具有价值。
T37847	Zonisamide-13C2,15N Zonisamide-13C2,15N
	Zonisamide-13C2,15N is intended for use as an internal standard for the quantification of zonisamide by GC- or LC-MS. Zonisamide is an antiepileptic agent.1 It selectively inhibits the repeated firing of sodium channels (IC50 = 2 μg/ml) in mouse embryo spinal cord neurons and inhibits spontaneous channel firing when used at concentrations greater than 10 μg/ml.2 In rat cerebral cortex neurons, zonisamide (1-1,000 μM) inhibits T-type calcium channels with a maximum reduction of 60% of the calcium...

同位素标记化合物

Mexiletine-d6 hydrochloride

Cat.No: T12023

Synonym: KOE-1173 D6 hydrochloride,Mexiletine D6 hydrochloride

Target: Others

Fosphenytoin Sodium-d10

Cat.No: TMID-0295

Cat.No: TMID-0247

Lacosamide-d3 (Acetyl-d3)

Cat.No: TMIJ-0240

Cat.No: TMID-0299

Zonisamide-13C2,15N

Cat.No: T37847

Synonym: Zonisamide-13C2,15N

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