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56

抑制剂 & 化合物

3

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T2535	Ivabradine hydrochloride 盐酸伊伐布雷定,S 16257-2,Ivabradine HCl	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Ivabradine hydrochloride (S 16257-2) 是一种可口服的，超极化激活的环核苷酸门控离子通道通道阻滞剂。
T23535L	Xanthine amine congener trihydrochloride Xanthine amine congener trihydrochloride (96865-92-8 Free base)	Adenosine Receptor	GPCR/G Protein; Neuroscience
	Xanthine amine congener trihydrochloride 是一种有效的腺苷拮抗剂，可逆转由腺苷激动剂 N6-环己基腺苷产生的尿流量、钠排泄和心率的减少。
T28748	Selodenoson RG14202,DTI0009,DTI-0009,RG-14202,DT-009,DT009	Adenosine Receptor	GPCR/G Protein; Neuroscience
	Selodenoson (RG-14202) 是一种选择性腺苷 A1 受体激动剂，可用于减慢心房颤动患者的心率，治疗心律失常。
T61316	HTS07545	NADPH	Metabolism
	HTS07545 是一种有效的硫化物:醌氧化还原酶抑制剂（IC50： 30 nM）。HTS07545 可降低硫化氢 (H2S) 的分解速率。HTS07545 可用于研究心力衰竭。
T10364	Arbutamine GP 21213	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Arbutamine (GP 21213) 是一种新型非选择性β-肾上腺素受体激动剂，具有α-1-拟交感神经活性。Arbutamine 促进心脏应激，增加心率、心脏收缩力。Arbutamine 可用于研究心脏应激和冠状动脉疾病。
T0805	Quinapril hydrochloride CI-906,PD-109452-2,盐酸喹那普利,Quinapril HCl	RAAS	Endocrinology/Hormones
	Quinapril hydrochloride (PD-109452-2) 是一种血管紧张素转化酶(ACE) 抑制剂的原药。
T3126	Bethanechol chloride (±)-Bethanechol,Urecholine,Myocholine,氯贝胆碱,Carbamyl-β-methylcholine chloride	AChR	Neuroscience
	Bethanechol chloride (Carbamyl-β-methylcholine chloride) 是一种拟副交感神经剂，是毒蕈碱型受体 (mAChR) 激动剂，通过直接刺激副交感神经系统的 mAChR 发挥作用。
T0207	Ranolazine dihydrochloride 盐酸雷诺嗪,雷诺嗪二盐酸盐,RS 43285,Ranolazine 2HCl	Calcium Channel; Sodium Channel; Autophagy	Autophagy; Membrane transporter/Ion channel; Metabolism
	Ranolazine dihydrochloride (Ranolazine 2HCl) 是一种抗心绞痛和抗缺血剂，可通过抑制内向钠电流的后期作用来发挥功效，而不会影响心率或血压。它对 INa 和 IKr 的 IC50值分别为 6 μM 和 12 μM。它还是脂肪酸氧化的部分抑制剂。
TP1937L1	RFRP-1 (human) acetate(311309-25-8 free base)	Neuropeptide Y Receptor	GPCR/G Protein; Neuroscience
	RFRP-1 (human) acetate(311309-25-8 free base) 是一种有效的内源性 NPFF 受体激动剂（NPFF2 和 NPFF1 的 EC50 值分别为 0.0011 和 29 nM）。它减弱离体大鼠和兔心肌细胞的收缩功能。降低心率、每搏输出量、射血分数和心输出量，并增加大鼠的血浆催乳素水平。 GnIH 同系物。
T1496	Amiodarone hydrochloride 盐酸胺碘酮,Amiodar,Amiodarone HCl,Nexterone	Potassium Channel; Adrenergic Receptor; Autophagy	Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Amiodarone hydrochloride (Amiodarone HCl) 是一种抗心绞痛和 III 类抗心律失常药物，通过抑制钾通道和电压门控钠通道来增加心室和心房肌肉作用的持续时间，可导致心率和血管阻力降低。它通过成纤维细胞中的 ERK1/2和 p38 MAPK 信号传导诱导细胞增殖和肌成纤维细胞分化，可研究室上性和室性心律失常。
T1613	Hydralazine hydrochloride Hydralazine HCl,Apresoline,盐酸肼屈嗪	MAO; HIF/HIF Prolyl-Hydroxylase	Chromatin/Epigenetic; Metabolism; Neuroscience
	Hydralazine hydrochloride (Apresoline) 是一种直接作用的血管舒张剂，可抗高血压。
T50008	2,2-Dimethyl-5-(2,5-xylyloxy)valeramide 5-(2,5-二甲基苯氧基)-2,2-二甲基戊酰胺,5-(2,5-dimethylphenoxy)-2,2-dimethylpentanamide	Others	Others
	2,2-Dimethyl-5-(2,5-xylyloxy)valeramide (5-(2,5-dimethylphenoxy)-2,2-dimethylpentanamide) 是一种苯氧基家族化合物。它已被证明对神经系统具有刺激作用，包括神经元放电率的增加、突触传递的增加和神经递质释放的增加；还被证明对心血管系统有刺激作用，包括提高心率和血压。
TP1369L	[Sar9,Met(O2)11]-Substance P acetate [Sar9,Met(O2)11]-Substance P acetate(110880-55-2 free base)	Neurokinin receptor	GPCR/G Protein; Neuroscience
	[Sar9,Met(O2)11]-Substance P acetate(110880-55-2 free base) 是一种速激肽 NK1 受体选择性激动剂。它是一种选择性速激肽 NK1 受体激动剂。它和 septide（每只大鼠 10-100 pmol，i.c.v.）在增加平均动脉血压 (MAP) 和心率 (HR)，但它们的时间进程不同。两种激动剂都以剂量依赖性方式增加洗脸和吸鼻，而它是一种产生美容效果的化合物。
T25237	Chloracyzine Chloroacizine,Chloroacizin,Chlorazicine,Chloroacyzin
	Chloracyzine can produce a decrease in myocardial oxygen consumption accompanied by a reduction in coronary blood flow preceded by transient coronary dilatation. It produced an insignificant increase in arterial pressure; heart rate increased slightly in
T71800	Metoprolol HCl
	Metoprolol is a selective β1 receptor blocker medication. It is used to treat high blood pressure, chest pain due to poor blood flow to the heart, and a number of conditions involving an abnormally fast heart rate. It is also used to prevent further heart problems after myocardial infarction and to prevent headaches in those with migraines.
T36008	Nebentan potassium
	Nebentan potassium (YM598) is a potent, selective and orally active non-peptide endothelin ETA receptor antagonist through the modification of Bosentan . Nebentan potassium inhibits [125I] endothelin-1 binding to cloned human endothelin ETA and ETB receptor, with Ki of 0.697 nM and 569 nM, respectively[1]. YM598 can ameliorate the progression of cor pulmonale and myocardial infarction in vivo[2]. Nebentan potassium inhibits the specific binding of [125I] endothelin-1 to endothelin ETA and ETB re...
T60393	Clobutinol
	Clobutinol 具有止咳作用。Clobutinol 影响心率和血压，可用于咳嗽的相关研究。
T39063	Azilsartan mepixetil
	Azilsartan mepixetil is a potent angiotensin II receptor antagonist with enhanced efficacy and prolonged duration of action. It exhibits more prominent and sustained effects in lowering blood pressure and heart rate, while maintaining a high level of safety. Furthermore, Azilsartan mepixetil demonstrates optimal protective efficacy for cardiovascular and renal functions. Hence, it holds promise for the research and treatment of hypertension, chronic heart failure, and diabetic nephropathy.
T11692	Ivabradine-d3 hydrochloride 盐酸伊伐布雷定 D3,Ivabradine D3 Hydrochloride	Others	Others
	Ivabradine hydrochloride is a new If inhibitor with IC50 of 2.9 μM, and used as a pure heart rate lowering agent. Ivabradine D3 Hydrochloride is the deuterium labeled Ivabradine hydrochloride.
T11694	Ivabradine-d6 hydrochloride 盐酸伊伐布雷定 D6,Ivabradine D6 hydrochloride	Others	Others
	Ivabradine hydrochloride is a new If inhibitor with IC50 of 2.9 μM, and used as a pure heart rate lowering agent. Ivabradine D6 hydrochloride is the deuterium labeled Ivabradine hydrochloride.
T78523	Clobutinol hydrochloride	Potassium Channel	Membrane transporter/Ion channel
	Clobutinol hydrochloride是一种具有止咳作用的化合物，能够影响心率和血压，通常用于咳嗽相关的研究。
T75947	RFRP-1(human) TFA
	RFRP-1(human) TFA, an endogenous NPFF receptor agonist, exhibits potent activity with EC50 values of 0.0011 nM for NPFF2 and 29 nM for NPFF1. It significantly diminishes the contractile function of isolated rat and rabbit cardiac myocytes. Moreover, it decreases heart rate, stroke volume, ejection fraction, and cardiac output, while elevating plasma prolactin levels in rats.
T80121	Ac-(d-Arg)-CEH-(d-Phe)-RWC-NH2	Melanocortin Receptor	GPCR/G Protein; Neuroscience
	Ac-DArg-c[Cys-Glu-His-DPhe-Arg-Trp-Cys]-NH2 是一种环状八肽，能够激活MC4R。该化合物能显著提高心率与血压。
TP1937	RFRP-1(human) RFRP-1 (human)
	Potent endogenous NPFF receptor agonist (EC50 values are 0.0011 and 29 nM for NPFF2 and NPFF1, respectively). Attenuates contractile function of isolated rat and rabbit cardiac myocytes. Reduces heart rate, stroke volume, ejection fraction and cardiac out
T69232	Atropine Oxide Hydrochloride
	Atropine Oxide is a derivative of Atropine. Atropine is a medication to treat certain types of nerve agent and pesticide poisonings as well as some types of slow heart rate and to decrease saliva production during surgery. Atropine is a competitive antagonist of the muscarinic acetylcholine receptor types M1, M2, M3, M4 and M5. It is classified as an anticholinergic drug (parasympatholytic).
T78657	Azilsartan mepixetil potassium QR-01019K
	Azilsartan mepixetil potassium (QR-01019K)，是一种高效安全的血管紧张素 II 受体拮抗剂，展现出卓越的持久降压效应以及显著且持续的降心率功能，有望用于治疗高血压、慢性心力衰竭和糖尿病肾病。
T32426	KT 1 KT-1,KT1
	KT 1 decreased aortic pressure, renal blood flow, left ventricular enddiastolic pressure and resistances of total peripheral, vertebral, coronary and renal vasculatures and increased aortic blood flow, vertebral blood flow, coronary blood flow, peak posit
T81118	Spexin-2 (53-70), human,mouse,rat NPQ 53-70
	Spexin-2 (53-70), human, mouse, rat (NPQ 53-70) 是一种在哺乳动物中保守的非酰胺化Spexin-2肽段，具备生物活性。作为新型肽激素proNPQ的一个片段，它在调节心血管与肾功能方面发挥关键作用。在大鼠体内，Spexin-2能有效降低心率并促进尿流量增加。
T23763	Atropine Oxide NSC 72861,NSC72861,NSC-72861
	Atropine Oxide is a derivative of Atropine. Atropine is a competitive antagonist of the muscarinic acetylcholine receptor types M1, M2, M3, M4, and M5. Atropine is a medication to treat certain types of nerve agents and pesticide poisonings as well as som
T69085	Mabuterol, (S)-
	Mabuterol is a selective β2 adrenoreceptor agonist. Mabuterol has been found to decrease the blood pressure in rats and increase heart rate and contractile force in guinea pigs. Mabuterol inhibited the positive inotropic effect of isoprenaline but has no effect on alpha-adrenergic, acetylcholine and histamine receptors.
T35839	3-Iodothyronamine (hydrochloride)
	3-Iodothyronamine is derived from the deiodination and decarboxylation of endogenous thyroxine. It activates the G protein-coupled receptor known as trace amine-associated receptor 1 at nanomolar concentrations whereupon it rapidly influences thyroid hormone actions including body temperature, heart rate, and cardiac output. It has also been reported to function in controlling lipid and glucose utilization, hormonal secretion, and neuronal function, and has been considered for use in chemically-...
TP1369	[Sar9,Met(O2)11]-Substance P TFA(110880-55-2,free) [Sar9,Met(O2)11]-Substance P TFA
	[Sar9,Met(O2)11]-Substance P TFA is a selective tachykinin NK1 receptor agonist.[Sar9,Met(O2)11]-Substance P and septide (10-100 pmol per rat, i.c.v.) are equipotent in increasing mean arterial blood pressure (MAP) and heart rate (HR), yet they have dissi
T82567	Di-4-ANEPPS
	Di-4-ANEPPS为膜电位电压敏感染料，时间分辨率达1 ms优于，并能够呈现每100 mV荧光变化高至10%。常用于描绘心脏电活动图，对兔离体心脏模型的自发心率和心室冲动传导显示出显著直接不可逆影响。
T69084	Mabuterol, (R)-
	Mabuterol is a selective β2 adrenoreceptor agonist. Mabuterol has been found to decrease the blood pressure in rats and increase heart rate and contractile force in guinea pigs. Mabuterol inhibited the positive inotropic effect of isoprenaline but has no effect on alpha-adrenergic, acetylcholine and histamine receptors.
T72213	Efonidipine hydrochloride NZ-105 hydrochloride
	Efonidipine(NZ-105)盐酸盐是T 型和L 型钙离子通道双重阻断剂。
T68242	D-Mabuterol hydrochloride
	Mabuterol is a selective β2 adrenoreceptor agonist. Mabuterol has been found to decrease the blood pressure in rats and increase heart rate and contractile force in guinea pigs. Mabuterol inhibited the positive inotropic effect of isoprenaline but has no effect on alpha-adrenergic, acetylcholine and histamine receptors.
T82933	Auriculin A
	Auriculin A是一种合成ANF，它对血液动力学具有显著效应。该化合物可阻断犬的肾血管收缩，并在兔子的后肢灌注压、心率及动脉血压的全身调节中发挥作用。
T60368	Benzoctamine
	Benzoctamine 是一种口服有效作用精神剂，具有镇静作用。Benzoctamine 增加儿茶酚胺的周转率。Benzoctamine 增强大鼠心脏中 [3H] 去甲肾上腺素的摄取。Benzoctamine 也可加速脑内注射 [3H] 去甲肾上腺素的消失。
T36204	Methylatropine (nitrate)
	Methylatropine is an antagonist of muscarinic acetylcholine receptors (IC50= <0.1 nM in a radioligand binding assay using isolated porcine brain membranes) and a derivative of atropine .1,2It reduces acetylcholine-induced decreases in blood pressure in rats when administered intravenously with an ED50value of 5.5 μg/kg.2Methylatropine reduces salivation, induces mydriasis, and increases heart rate in dogs.3 1.Schmeller, T., Sporer, F., Sauerwein, M., et al.Binding of tropane alkaloids to nicotin...
T35543	Methyl Diethyldithiocarbamate
	Methyl diethyldithiocarbamate is an active metabolite of the aldehyde dehydrogenase inhibitor disulfiram .1It is produced by methylation of the disulfiram metabolite diethyldithiocarbamate in mouse liver microsomes.2Methyl diethyldithiocarbamate inhibits liver low Kmaldehyde dehydrogenase (ALDH) in rats (ID50= 15.5 mg/kg).1It decreases mean arterial pressure (MAP) and increases heart rate during ethanol challenge in rats when administered at a dose of 20.6 mg/kg. 1.Hart, B.W., Yourick, J.J., and...
T35871	Bopindolol (malonate)
	Bopindolol is a non-selective β-adrenergic receptor antagonist. In vivo, bopindolol decreases heart rate and blood pressure and attenuates ischemia-induced myocardial acidosis in dogs. Formulations containing bopindolol have been used to treat essential and renovascular hypertension.
T63014	Ivabradine
	Ivabradine 是一种有效的、口服具有活力的 HCN (超极化激活的环核苷酸门控) 通道阻滞剂，能够抑制心脏起搏器电流 (If)。Ivabradine 以剂量依赖性的方式降低心率，且不改变血压。Ivabradine 具有抗惊厥、抗缺血和抗心绞痛作用。
T73610	Lipoprotein lipase
	Lipoprotein lipase 是来自于脂肪组织、心肌和骨骼肌、胰岛和巨噬细胞的多功能酶。Lipoprotein lipase 促进正常脂蛋白代谢、组织特异性底物的输送和利用。Lipoprotein lipase 催化脂质在血液循环的限速步骤。
T78540	α-CGRP (mouse, rat) TFA	CGRP Receptor	GPCR/G Protein; Neuroscience
	α-CGRP (mouse, rat) TFA 是神经系统中的一种活性神经肽，位于神经肌肉接合部，具有显著的血管舒张功能。适用于心血管疾病、炎症、偏头痛及代谢研究领域。
T69598	Isoproterenol-d7 HCl
	Isoproterenol-d7 is intended for use as an internal standard for the quantification of isoproterenol by GC- or LC-MS. Isoproterenol is an agonist of β1- and β2-adrenergic receptors (β1- and β2-ARs; Kis = 224 and 458 nM, respectively). It is selective for β1- and β2-ARs over β3-ARs (Ki = 1,570 nM). Isoproterenol inhibits contractions in isolated field-stimulated rat vas deferens (EC50 = 45.6 nM). In vivo, isoproterenol (0.33 mg/kg) decreases blood pressure and increases water intake in nephrectom...
T75732	α-CGRP, rat TFA
	α-CGRP, rat TFA 是一种神经肽 (降钙素基因相关肽)，主要表达于神经肌肉交界处，是一种有效的血管扩张剂量。α-CGRP, rat TFA 外周给药可使大鼠血压下降、心率升高，并使结肠平滑肌松弛。α-CGRP, rat TFA 可用于心血管、促炎、偏头痛和代谢相关的研究。
T76334	Cenderitide
	Cenderitide 是一种有效的颗粒鸟酰基环化酶受体 (pGC) 激动剂。Cenderitide 是一种由 C 型利钠肽 (CNP) 与石斛利钠肽 (DNP) 的 C 端融合而成的利钠肽 (NP) 。Cenderitide 可激活 pGC-A 和 pGC-B，激活第二信使 cGMP，抑制醛固酮 (aldosterone)，在不降低血压的情况下保持 GFR 。Cenderitide 可用于心力衰竭的研究。
T71402	Nicorandil-d4
	Nicorandil-d4 is intended for use as an internal standard for the quantification of nicorandil by GC- or LC-MS. Nicorandil is an activator of sulfonylurea receptor 2B (SUR2B) linked to ATP-sensitive potassium channel Kir6.2 (EC50 = ~10 µM) and a nitric oxide (NO) donor. It is selective for SUR2B/Kir6.2 over the SUR2A/Kir6.2 channel (EC50 = >500 µM). Nicorandil activates soluble guanylate cyclase in a cell-free assay and relaxes partially depolarized isolated bovine coronary artery strips (EC50 =...
T79358	PF-07247685	Endogenous Metabolite	Metabolism
	PF-07247685是一种BCKDC激酶(BDK)抑制剂，具有较强的活性(EC50=2.2 nM)。该化合物能有效稳定BDK与BCKDH E2核心亚基之间的相互作用，并阻断E1亚基的磷酸化过程。BCKDH的活性受到BDK介导的磷酸化调控，从而控制支链氨基酸(BCAA)降解的关键步骤。BCAA的代谢失调与心力衰竭(HF)、2型糖尿病(T2DM)、非酒精性脂肪肝病(NAFLD)及肥胖等多种疾病相关联，尤其在心脏代谢疾病中表现明显。PF-07247685在小鼠模型中对心脏代谢终点产生改善效果，并提升了葡萄糖耐量。
T40869	Moxonidine hydrochloride BDF5895hydrochloride,盐酸莫索尼定
	Moxonidine Hydrochloride is a selective agonist at the imidazoline receptor subtype 1, used as antihypertensive agent. Target: I1-R Moxonidine Hydrochloride is a centrally acting antihypertensive agent. Mixed Nischarin (I1 imidazoline receptor) and α2-AR (adrenergic) agonist; displays 40-fold higher affinity for I1 receptors versus α2-adrenoceptors. Moxonidine reduced stimulated NE overflow (log EC50: -6.15 +/- 0.14). AGN192403, a selective ligand at I1-R, had no influence on the dose-response...

化合物

Ivabradine hydrochloride

Cat.No: T2535

Synonym: 盐酸伊伐布雷定,S 16257-2,Ivabradine HCl

Target: Adrenergic Receptor

Xanthine amine congener trihydrochloride

Cat.No: T23535L

Synonym: Xanthine amine congener trihydrochloride (96865-92-8 Free base)

Target: Adenosine Receptor

Cat.No: T28748

Synonym: RG14202,DTI0009,DTI-0009,RG-14202,DT-009,DT009

Target: Adenosine Receptor

Cat.No: T61316

Target: NADPH

Cat.No: T10364

Synonym: GP 21213

Target: Adrenergic Receptor

Quinapril hydrochloride

Cat.No: T0805

Synonym: CI-906,PD-109452-2,盐酸喹那普利,Quinapril HCl

Target: RAAS

Bethanechol chloride

Cat.No: T3126

Synonym: (±)-Bethanechol,Urecholine,Myocholine,氯贝胆碱,Carbamyl-β-methylcholine chloride

Target: AChR

Ranolazine dihydrochloride

Cat.No: T0207

Synonym: 盐酸雷诺嗪,雷诺嗪二盐酸盐,RS 43285,Ranolazine 2HCl

Target: Calcium Channel, Sodium Channel, Autophagy

RFRP-1 (human) acetate(311309-25-8 free base)

Cat.No: TP1937L1

Target: Neuropeptide Y Receptor

Amiodarone hydrochloride

Cat.No: T1496

Synonym: 盐酸胺碘酮,Amiodar,Amiodarone HCl,Nexterone

Target: Potassium Channel, Adrenergic Receptor, Autophagy

Hydralazine hydrochloride

Cat.No: T1613

Synonym: Hydralazine HCl,Apresoline,盐酸肼屈嗪

Target: MAO, HIF/HIF Prolyl-Hydroxylase

2,2-Dimethyl-5-(2,5-xylyloxy)valeramide

Cat.No: T50008

Synonym: 5-(2,5-二甲基苯氧基)-2,2-二甲基戊酰胺,5-(2,5-dimethylphenoxy)-2,2-dimethylpentanamide

Target: Others

[Sar9,Met(O2)11]-Substance P acetate

Cat.No: TP1369L

Synonym: [Sar9,Met(O2)11]-Substance P acetate(110880-55-2 free base)

Target: Neurokinin receptor

Cat.No: T25237

Synonym: Chloroacizine,Chloroacizin,Chlorazicine,Chloroacyzin

Cat.No: T71800

Nebentan potassium

Cat.No: T36008

Cat.No: T60393

Azilsartan mepixetil

Cat.No: T39063

Ivabradine-d3 hydrochloride

Cat.No: T11692

Synonym: 盐酸伊伐布雷定 D3,Ivabradine D3 Hydrochloride

Target: Others

Ivabradine-d6 hydrochloride

Cat.No: T11694

Synonym: 盐酸伊伐布雷定 D6,Ivabradine D6 hydrochloride

Target: Others

Clobutinol hydrochloride

Cat.No: T78523

Target: Potassium Channel

RFRP-1(human) TFA

Cat.No: T75947

Ac-(d-Arg)-CEH-(d-Phe)-RWC-NH2

Cat.No: T80121

Target: Melanocortin Receptor

Cat.No: TP1937

Synonym: RFRP-1 (human)

Atropine Oxide Hydrochloride

Cat.No: T69232

Azilsartan mepixetil potassium

Cat.No: T78657

Synonym: QR-01019K

Cat.No: T32426

Synonym: KT-1,KT1

Spexin-2 (53-70), human,mouse,rat

Cat.No: T81118

Synonym: NPQ 53-70

Cat.No: T23763

Synonym: NSC 72861,NSC72861,NSC-72861

Mabuterol, (S)-

Cat.No: T69085

3-Iodothyronamine (hydrochloride)

Cat.No: T35839

[Sar9,Met(O2)11]-Substance P TFA(110880-55-2,free)

Cat.No: TP1369

Synonym: [Sar9,Met(O2)11]-Substance P TFA

Cat.No: T82567

Mabuterol, (R)-

Cat.No: T69084

Efonidipine hydrochloride

Cat.No: T72213

Synonym: NZ-105 hydrochloride

D-Mabuterol hydrochloride

Cat.No: T68242

Cat.No: T82933

Cat.No: T60368

Methylatropine (nitrate)

Cat.No: T36204

Methyl Diethyldithiocarbamate

Cat.No: T35543

Bopindolol (malonate)

Cat.No: T35871

Cat.No: T63014

Lipoprotein lipase

Cat.No: T73610

α-CGRP (mouse, rat) TFA

Cat.No: T78540

Target: CGRP Receptor

Isoproterenol-d7 HCl

Cat.No: T69598

α-CGRP, rat TFA

Cat.No: T75732

Cat.No: T76334

Cat.No: T71402

Cat.No: T79358

Target: Endogenous Metabolite

Moxonidine hydrochloride

Cat.No: T40869

Synonym: BDF5895hydrochloride,盐酸莫索尼定

Cat. No.	Product Name	Target	Signaling Pathways
T8183	Deslanoside 洋地黄,去乙酰西地兰,Desacetyllanatoside C,Deacetyllanatoside C	ATPase; Drug Metabolite	Membrane transporter/Ion channel; Metabolism
	Deslanoside (Desacetyllanatoside C) 是一种快速作用的强心苷，可抑制Na-K-ATPase 膜泵，导致细胞内钠和钙浓度增加。它用于研究充血性心力衰竭和因折返机制引起的室上性心律失常，并在研究慢性心房颤动时控制心室率。
T4S1518	Pseudoginsenoside RT1 拟人参皂苷 RT1,假人参皂苷RT1	Others	Others
	Pseudoginsenoside RT1 是分离自 Randia siamensis 中，具有鱼毒素作用。它可导致血压下降、心率加快和子宫自发收缩力增加。
TN1367	Alismol 泽泻醇	Potassium Channel; Calcium Channel; PI3K	Membrane transporter/Ion channel; Metabolism; PI3K/Akt/mTOR signaling
	Alismol has antihypertensive action, it decreases cardiac output, heart rate and left ventricular pressure, but it increases coronary flow, it has been used for the prevention of anginal attacks.

天然产物

Cat.No: T8183

Synonym: 洋地黄,去乙酰西地兰,Desacetyllanatoside C,Deacetyllanatoside C

Target: ATPase, Drug Metabolite

Pseudoginsenoside RT1

Cat.No: T4S1518

Synonym: 拟人参皂苷 RT1,假人参皂苷RT1

Target: Others

Cat.No: TN1367

Synonym: 泽泻醇

Target: Potassium Channel, Calcium Channel, PI3K

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