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51

抑制剂 & 化合物

8

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Cat. No. Product Name Target Signaling Pathways
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。
T72323 Antiarrhythmic agent-1

Antiarrhythmic agent-1 (示例 I) 是一种抗心律失常试剂,也是IKr 钾离子通道抑制剂 (IC50<1 μM)。
T23652 AFD-21

AFD21,NS-2 Class 1 antiarrhythmic agent

AFD-21是一种 I 类抗心律失常药物。它在钠通道失活状态下与钠通道结合,对钠通道具有使用和电压依赖性抑制作用,其解结合率与具有中等动力学的I 类抗心律失常药物相当。
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。
T24021 E 0747

E-0747,E0747

E 0747 is an antiarrhythmic agent of class 1C type. E-0747 suppresses arrhythmia by inhibiting the Na channels of cardiac cells.
T11099 Droxicainide

Others Others
Droxicainide 是一种抗心律失常剂。
T0249 N-Acetylprocainamide

NAPA,Acecainide,乙酰普卡胺,N-乙酰普鲁卡因胺

Potassium Channel; Sodium Channel; Drug Metabolite Membrane transporter/Ion channel; Metabolism
N-Acetylprocainamide (NAPA) 是K+通道抑制剂,是第三代抗心律失常剂。
T12858 Bidisomide

SC40230

Others Others
Bidisomide (SC40230) (SC40230) 属于 I 类抗心律失常剂。
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。
T7219 Flecainide acetate

Flecainide (acetate),氟卡胺,R-818,醋酸洗必太

Sodium Channel Membrane transporter/Ion channel
Flecainide acetate (R-818) 是位于心脏的 Nav1.5钠离子通道的阻断剂,具有抗心律失常的作用。
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。
T7198 E-4031

(1S)-1,5-脱水-1-C-[4-氯-3-[[4-[2-(环丙氧基)乙氧基]苯基]甲基]苯基]-D-山梨醇

EGFR; Potassium Channel Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors
E-4031是甲磺酰苯胺III 类抗心律失常药,选择性地阻断hERG 钾通道。
T60322 Procainamide

Biocoryl,Novocainamide

DNA Methyltransferase Chromatin/Epigenetic
Procainamide (Novocainamide) 是 DNA 甲基转移酶 1 (DNMT1) 的特异性强效抑制剂。Procainamide 是一种 1A 类抗心律失常药物。Procainamide 具有研究癌症和心律失常的潜力。
T11353 Gallopamil

Methoxyverapamil,戈洛帕米

Calcium Channel Membrane transporter/Ion channel; Metabolism
Gallopamil (Methoxyverapamil) 是一种苯烷基胺钙拮抗剂,以浓度依赖性方式抑制酸分泌 (IC50 = 10.9 μM)。Gallopamil 显示出抗心律失常和血管扩张剂的功效。
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。
T6541 Ibutilide Fumarate

Corvert Fumarate,U70226E,富马酸伊布利特

Calcium Channel; Sodium Channel Membrane transporter/Ion channel; Metabolism
Ibutilide Fumarate (U70226E) 是一种 III 类抗心律失常药物,可作用于急性心梗阻塞。
T1144 Lidocaine hydrochloride

Lidocaine HCL,盐酸利多卡因,Lignocaine hydrochloride,Xyloneural,Lidothesin

Apoptosis; ERK; NF-κB; MEK; Sodium Channel Apoptosis; MAPK; Membrane transporter/Ion channel; NF-κB
Lidocaine hydrochloride (Lignocaine hydrochloride) 抑制涉及复杂电压和依赖性的钠通道。它通过调节 miR-145 表达和进一步抑制 MEK/ERK 和 NF-κB 信号通路来减少胃癌细胞的生长,迁移和侵袭。Lidocaine 是一种酰胺衍生物,是一种研究室性心律失常的药物和有效的肿瘤抑制剂。
T0802 Procaine hydrochloride

Novocaine HCl,Procaine HCl,盐酸普鲁卡因

Histone Demethylase; 5-HT Receptor; DNA/RNA Synthesis; Sodium Channel; NMDAR; AChR Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair; GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
Procaine hydrochloride (Novocaine HCl) 是DNA 脱甲基剂,是一种苯甲酸衍生物,具有局部麻醉和抗心律失常特性。
T25157 Bisaramil

Bisaramil is a new class I antiarrhythmic agent.
T35114 WAY-123398 free base

Way-123398,Way 123398,Way 123,398,Way123398,Way-123,398,Way123,398

Way 123398 is a class III antiarrhythmic agent.
T12538 Prifuroline

Others Others
Prifuroline is an agent of antiarrhythmic.
T26033 RAC 109

RAC-109,RAC109

RAC 109 is a chiral antiarrhythmic agent.
T32032 GYKI-23107 HCl

GYKI23107,GYKI23,107,GYKI 23107,GYKI-23107,GYKI 23,107,GYKI-23,107

GYKI-23107 is an antiarrhythmic agent with a local anesthetic activity.
T30607 Budiodarone

ATI2042,ATI-2042,ATI 2042

Budiodarone(ATI-2042)is a chemical analog of an antiarrhythmic drug and amiodarone. Budedalone is promising as an antiarrhythmic agent for the prevention of atrial fibrillation.
T26136 RS 2135

RS2135,RS-2135

RS 2135 is a novel class I antiarrhythmic agent to inhibit ischemia-induced ventricular arrhythmias.
T70524 Tedisamil sesquifumarate

Tedisamil sesquifumarate is an Antiarrhythmic Agent (K(sup +) Channel Blocker)
T20732 Lignocaine N-oxide

Lignocaine N-oxide is a metabolite of Lidocaine, which is an antiarrhythmic and anesthetic agent.
T38434 (-)-(S)-Cibenzoline

(-)-(S)-Cibenzoline,Escibenzoline

Cibenzoline, also known as Escibenzoline, is the S(+)-enantiomer of Cibenzoline and functions as an antiarrhythmic agent.
T21370 Amiodarone

Nexterone,胺碘酮,Amiodarona,Cordarone,Aratac,Amiodaronum

Amiodarone is categorized as a class III antiarrhythmic agent and prolongs phase 3 of the cardiac action potential. It also has numerous other effects, including actions that are similar to those of antiarrhythmic classes Ia, II, and IV. Amiodarone chemic
T25755 Lorajmine

Lorajmina

Lorajmine, a monochloroacetyl derivative of ajmaline, is a class Ia antiarrhythmic agent that is rapidly hydrolyzed to ajmaline by plasma and tissue esterases.
T32030 GYKI-16638 HCl

GYKI 16,638,GYKI16,638,GYKI-16638,GYKI-16,638,GYKI16638,GYKI 16638

GYKI-16638 is a novel antiarrhythmic agent that demonstrates combined class IB and class III antiarrhythmic properties in human ventricular muscles, similar to the electrophysiological findings after chronic amiodarone treatment. In addition, GYKI 16638 h
T21373 Aprindine hydrochloride

Fiboran,Amidonal,Aprinidine,Aprindin,Aprindine HCl,Aprindina,Fibocil

Aprindine HCl is a Class 1b antiarrhythmic agent used to manage ventricular and supraventricular arrhythmias. In one study, it delayed atrial fibrillation more than digoxin did. It has shown effectiveness when given orally.
T12087 Modecainide

BMY 40327,MJ 14030

Others Others
Modecainide is metabolite of Encainide, is an antiarrhythmic agent.
T71021 Fendiline

Fendiline is a coronary vasodilator that inhibits calcium function in muscle cells in excitation-contraction coupling; proposed as an antiarrhythmic and antianginal agent.
T28567 Ro 22-9194

Ro-22-9194

Ro 22-9194 is a class I antiarrhythmic agent. Ro 22-9194 (>=10 μM) caused a concentration-dependent decrease in the maximum upstroke velocity and shortening of action potential duration in guinea-pig ventricular cells.
T4550L Ajmaline hydrochloride

Ajmaline hydrochloride is an alkaloid found in the root of Rauwolfia serpentina, and other plant sources. It is a class of Ia antiarrhythmic agent that apparently works by changing the shape and threshold of cardiac action potentials.
T33426 MK-142 dimethanesulfonate

MK142,MK 142,MK-142

MK-142 dimethyl sulfonate is a biologic active agent with antiarrhythmic properties, and the content of MK-142 is relatively high in cardiac muscle compared to that in skeletal muscle, indicating that the substance tested has a high affinity with cardiac
T21391 Flecainide

Tambocor,Apocard,Flecainida,Flecainidum

Flecainide acetate is a class Ic antiarrhythmic agent, it is used to treat a variety of cardiac arrhythmias including paroxysmal atrial fibrillation, paroxysmal supraventricular tachycardia, and ventricular tachycardia. It works by regulating the flow of
T60482 Pilsicainide

Pilsicainide (SUN 1165 free acid)是一种有效的 Ic 类抗心律失常药。Pilsicainide 是一种有效的钠通道阻滞剂。
T62207 KVI-020

KVI-020 是一种选择性的、口服具有活力的心房钾通道 Kv1.5 阻滞剂 (IC50: 480 nM)。KVI-020 对 hERG 表现出抑制作用 (IC50: 15100 nM)。 KVI-020 是一种有效的抗心律失常剂 (antiarrhythmic),能够用于研究房颤 (AF)。
T36561 (3S)-hydroxy Quinidine

(3S)-hydroxy Quinidine is an active quinidine metabolite. Quinidine, an antiarrhythmic agent, undergoes rapid first-pass metabolism by the cytochrome P450 (CYP) isoforms CYP3A4, CYP2C9, CYP2E1, and CYP3A5, with CYP3A4 being the most active enzyme in the (3S)-hydroxy quinidine formation. (3S)-hydroxy Quinidine prolongs repolarization of canine Purkinje fibers in vitro and prevents ventricular fibrillation and ventricular tachycardia after coronary reperfusion in isolated rat hearts in a dose-depe...
T25934 Pentisomide

Pentisomidum

Pentisomide 是一种抗心律失常的化合物,对去极化(Ia 和 Ic 类作用)和复极有显著作用。它可剂量依赖性地抑制缺血再灌注心律失常。Pentisomide 已进入治疗心律失常的 II 期临床试验。
T71122 Carsatrin (free base)

Carsatrin is purinylpiperazine derivative. as cardiotonic and antiarrhythmic. Carsatrin acts as positive inotropic agent that increases twitch tension and prolongs the action potential (AP) duration of ventricular muscle without affecting the Na+, K+-ATPase, adenylyl cyclase, phosphodiesterase isozymes, or cardiac myofilaments. Carsatrin’s positive inotropic effect can be prevented by tetrodotoxin but not by the adrenergic antagonists timolol, yohimbine, or prazosin
T62942 Moricizine Hydrochloride

Moricizine Hydrochloride (EN 313) 是一种口服具有活力的 I 类抗心律失常剂。Moricizine Hydrochloride 能够减少 0 相去极化的速率;提高 2 相和 3 相复极率,降低动作电位持续时间,减少有效不应期。
T70975 Carsatrin succinate

Carsatrin succinate is the salt form of Carsatin, a purinylpiperazine derivative used as a cardiotonic and antiarrhythmic. Carsatrin acts as positive inotropic agent that increases twitch tension and prolongs the action potential (AP) duration of ventricular muscle without affecting the Na+, K+-ATPase, adenylyl cyclase, phosphodiesterase isozymes, or cardiac myofilaments. Carsatrin’s positive inotropic effect can be prevented by tetrodotoxin but not by the adrenergic antagonists timolol, yohimbi...
T63635 Quinate

Quinate 是抗心律失常剂,是有效的、选择性的、口服具有活力的细胞色素 P450db (cytochrome P450db) 抑制剂,是一种有效的 K+通道 (K+channel) 阻断剂 (IC50: 19.9 μM)。Quinate 也能够用于研究疟疾。
T69119 Disopyramide HCl

Disopyramide HCl is the salt form of Disopyramide, an antiarrhythmic medication used in the treatment of ventricular tachycardia. It is a sodium channel blocker and therefore classified as a Class 1a anti-arrhythmic agent. Disopyramide has a negative inotropic effect on the ventricular myocardium, significantly decreasing the contractility. Disopyramide also has an anticholinergic effect on the heart which accounts for many adverse side effects. Disopyramide is available in both oral and intrave...
T61517 Quinidine Monosulfate

Quinidine Monosulfate 是一种抗心律失常剂。Quinidine Monosulfate 是一种有效的、具有口服活性的、选择性的细胞色素 P450db (cytochrome P450db) 抑制剂,也是 K+通道 (K+channel) 的有效阻断剂,其 IC50值为 19.9 μM。Quinidine Monosulfate 也可用作疟疾的研究。
T60428 Cibenzoline

Cibenzoline 是一种抗心律失常药,通过直接影响成孔 Kir6.2 亚基而不是 SUR1 亚基来抑制 KATP 通道。 Cibenzoline 几乎不具有抗胆碱能活性。 Cibenzoline 显着降低与心肌收缩力下降密切相关的LVPG。 Cibenzoline 具有研究肥厚型梗阻性心肌病的潜力[1][2]。
T60893 Ep vinyl quinidine

Ep vinyl quinidine (3-Epiquinine) 是Quinidine 的一种乙烯基立体异构体。Quinidine 可用于研究疟疾,也是一种抗心律失常剂。Quinidine 是口服有效的、选择性细胞色素 P450db 抑制剂,以及钾通道的有效阻断剂,IC50值为 19.9 μM。

化合物

Dofetilide
Cat.No: T6476
Synonym: UK 68789,UK-68798,Tikosyn,多非利特
Target: Potassium Channel
Antiarrhythmic agent-1
Cat.No: T72323
Synonym:
Target:
AFD-21
Cat.No: T23652
Synonym: AFD21,NS-2 Class 1 antiarrhythmic agent
Target:
Propafenone
Cat.No: T0866
Synonym: Rythmol,普罗帕酮,Propafenonum
Target: Potassium Channel, MRP, Sodium Channel
E 0747
Cat.No: T24021
Synonym: E-0747,E0747
Target:
Droxicainide
Cat.No: T11099
Synonym:
Target: Others
N-Acetylprocainamide
Cat.No: T0249
Synonym: NAPA,Acecainide,乙酰普卡胺,N-乙酰普鲁卡因胺
Target: Potassium Channel, Sodium Channel, Drug Metabolite
Bidisomide
Cat.No: T12858
Synonym: SC40230
Target: Others
Nicainoprol
Cat.No: T4539
Synonym: 尼卡普醇,RU-42924
Target: Sodium Channel
Flecainide acetate
Cat.No: T7219
Synonym: Flecainide (acetate),氟卡胺,R-818,醋酸洗必太
Target: Sodium Channel
Azimilide Dihydrochloride
Cat.No: T7505
Synonym: NE-10064 Dihydrochloride,盐酸阿齐利特
Target: Potassium Channel
E-4031
Cat.No: T7198
Synonym: (1S)-1,5-脱水-1-C-[4-氯-3-[[4-[2-(环丙氧基)乙氧基]苯基]甲基]苯基]-D-山梨醇
Target: EGFR, Potassium Channel
Procainamide
Cat.No: T60322
Synonym: Biocoryl,Novocainamide
Target: DNA Methyltransferase
Gallopamil
Cat.No: T11353
Synonym: Methoxyverapamil,戈洛帕米
Target: Calcium Channel
Taquidil
Cat.No: T13177
Synonym:
Target:
Ibutilide Fumarate
Cat.No: T6541
Synonym: Corvert Fumarate,U70226E,富马酸伊布利特
Target: Calcium Channel, Sodium Channel
Lidocaine hydrochloride
Cat.No: T1144
Synonym: Lidocaine HCL,盐酸利多卡因,Lignocaine hydrochloride,Xyloneural,Lidothesin
Target: Apoptosis, ERK, NF-κB, MEK, Sodium Channel
Procaine hydrochloride
Cat.No: T0802
Synonym: Novocaine HCl,Procaine HCl,盐酸普鲁卡因
Target: Histone Demethylase, 5-HT Receptor, DNA/RNA Synthesis, Sodium Channel, NMDAR, AChR
Bisaramil
Cat.No: T25157
Synonym:
Target:
WAY-123398 free base
Cat.No: T35114
Synonym: Way-123398,Way 123398,Way 123,398,Way123398,Way-123,398,Way123,398
Target:
Prifuroline
Cat.No: T12538
Synonym:
Target: Others
RAC 109
Cat.No: T26033
Synonym: RAC-109,RAC109
Target:
GYKI-23107 HCl
Cat.No: T32032
Synonym: GYKI23107,GYKI23,107,GYKI 23107,GYKI-23107,GYKI 23,107,GYKI-23,107
Target:
Budiodarone
Cat.No: T30607
Synonym: ATI2042,ATI-2042,ATI 2042
Target:
RS 2135
Cat.No: T26136
Synonym: RS2135,RS-2135
Target:
Tedisamil sesquifumarate
Cat.No: T70524
Synonym:
Target:
Lignocaine N-oxide
Cat.No: T20732
Synonym:
Target:
(-)-(S)-Cibenzoline
Cat.No: T38434
Synonym: (-)-(S)-Cibenzoline,Escibenzoline
Target:
Amiodarone
Cat.No: T21370
Synonym: Nexterone,胺碘酮,Amiodarona,Cordarone,Aratac,Amiodaronum
Target:
Lorajmine
Cat.No: T25755
Synonym: Lorajmina
Target:
GYKI-16638 HCl
Cat.No: T32030
Synonym: GYKI 16,638,GYKI16,638,GYKI-16638,GYKI-16,638,GYKI16638,GYKI 16638
Target:
Aprindine hydrochloride
Cat.No: T21373
Synonym: Fiboran,Amidonal,Aprinidine,Aprindin,Aprindine HCl,Aprindina,Fibocil
Target:
Modecainide
Cat.No: T12087
Synonym: BMY 40327,MJ 14030
Target: Others
Fendiline
Cat.No: T71021
Synonym:
Target:
Ro 22-9194
Cat.No: T28567
Synonym: Ro-22-9194
Target:
Ajmaline hydrochloride
Cat.No: T4550L
Synonym:
Target:
MK-142 dimethanesulfonate
Cat.No: T33426
Synonym: MK142,MK 142,MK-142
Target:
Flecainide
Cat.No: T21391
Synonym: Tambocor,Apocard,Flecainida,Flecainidum
Target:
Pilsicainide
Cat.No: T60482
Synonym:
Target:
KVI-020
Cat.No: T62207
Synonym:
Target:
(3S)-hydroxy Quinidine
Cat.No: T36561
Synonym:
Target:
Pentisomide
Cat.No: T25934
Synonym: Pentisomidum
Target:
Carsatrin (free base)
Cat.No: T71122
Synonym:
Target:
Moricizine Hydrochloride
Cat.No: T62942
Synonym:
Target:
Carsatrin succinate
Cat.No: T70975
Synonym:
Target:
Quinate
Cat.No: T63635
Synonym:
Target:
Disopyramide HCl
Cat.No: T69119
Synonym:
Target:
Quinidine Monosulfate
Cat.No: T61517
Synonym:
Target:
Cibenzoline
Cat.No: T60428
Synonym:
Target:
Ep vinyl quinidine
Cat.No: T60893
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T1334 Hydroquinidine

奎宁树,氢化奎宁定,Hydroconchinine,Dihydroquinidine,Hydroconquinine,(+)-Hydroquinidine,Dihydroquinine

Potassium Channel; Sodium Channel Membrane transporter/Ion channel
Hydroquinidine ((+)-Hydroquinidine) 是 Quinidine(一种抗心律不齐药) 的衍生物。它能够延长 QT 间隔,表现出抗心律不齐活性。
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。
T7938 Quinidine

奎尼丁,奎宁树

Parasite Microbiology/Virology
Quinidine 是一种抗心律失常剂,也是 K+通道的有效阻断剂,其 IC50值为 19.9 μM。它是一种选择性细胞色素 P450db 的有效抑制剂,也可研究疟疾。
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。
TN1412 Astringin

trans-Astringin,白皮杉醇葡萄糖苷

IL Receptor; Others Immunology/Inflammation; Others
Astringinin is a potent antiarrhythmic agent with cardioprotective activity in ischemic and ischemic-reperfused rat heart, the beneficial effects of astringinin in the ischemic and ischemic-reperfused hearts may be correlated with its antioxidant activity and upregulation of NO production.
T21266 Quinine sulfate

Quinidine sulfate 是一种抗心律失常剂。Quinidine sulfate 是一种口服有效的、选择性的细胞色素 P450db (cytochrome P450db) 抑制剂。Quinidine sulfate 是 K+通道 (K+channel) 的有效阻断剂,IC50值为 19.9 μM。Quinidine sulfate 同时具有抗疟疾的研究潜力。

天然产物

Hydroquinidine
Cat.No: T1334
Synonym: 奎宁树,氢化奎宁定,Hydroconchinine,Dihydroquinidine,Hydroconquinine,(+)-Hydroquinidine,Dihydroquinine
Target: Potassium Channel, Sodium Channel
(-)-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
Quinidine
Cat.No: T7938
Synonym: 奎尼丁,奎宁树
Target: Parasite
(+)-Sparteine
Cat.No: T7853
Synonym: 鹰爪豆碱,(+)-鹰爪豆碱,Pachycarpine
Target: AChR
(-)-Sparteine
Cat.No: TMA2106
Synonym:
Target: P450
Sparteine sulfate
Cat.No: T3029
Synonym: 硫酸司巴丁,Depasan,Tocosimplex,Actospar
Target: Others, Sodium Channel
Astringin
Cat.No: TN1412
Synonym: trans-Astringin,白皮杉醇葡萄糖苷
Target: IL Receptor, Others
Quinine sulfate
Cat.No: T21266
Synonym:
Target:
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