52
3
4
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0075 |
Nicorandil
SG-75,尼可地尔 |
Potassium Channel | Membrane transporter/Ion channel |
Nicorandil (SG-75) 是一种有效的钾通道激活剂,靶向血管核苷二磷酸依赖性 K+通道和心脏 ATP 敏感 K+通道 (KATP)。Nicorandil 是一种烟酰胺酯,具有血管舒张和心脏保护作用,并具有治疗心绞痛和缺血性心脏病的潜力。 | |||
T21454 |
Nicardipine
Cardene,Dagan,尼卡地平,Antagonil,Flusemide |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Nicardipine (Cardene) 是一种二氢吡啶类钙通道阻滞剂,可阻断心脏钙通道,IC50为 1 μM,可用于治疗心绞痛和高血压。 | |||
T6551 |
Isosorbide
Devicoran,Isobide,异山梨酯,异山梨醇,Hydronol,Dianhydro-D-glucitol,D-Isosorbide |
Others | Others |
Isosorbide (Devicoran) 是一种血管舒张剂,也是一种高渗利尿剂,口服具有活性。可用于研究心力衰竭和心绞痛(胸痛)。 | |||
T1215 |
Nicardipine hydrochloride
盐酸尼卡地平,RS-69216,Nicardipine HCl,YC-93 Hydrochloride |
Calcium Channel; Adrenergic Receptor; AChR; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Nicardipine hydrochloride (YC-93 Hydrochloride) 是一种钙通道阻滞剂,IC50为 1 μM。它可阻断某些细胞壁中的钙离子并抑制冠状动脉和外周动脉的收缩,从而降低对氧气的需求心肌和减少动脉收缩和痉挛。它在临床上用作脑和冠状血管扩张剂。 | |||
T20656 |
Verapamil
NSC 135784,维拉帕米,NSC-135784,CP-16533-1,(±)-Verapamil |
P450; Calcium Channel; P-gp | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Verapamil (CP-16533-1) 是一种非二氢吡啶类钙通道阻滞剂,一种 P-gp 抑制剂,也是一种 CYP3A4 抑制剂,具有口服活性。Verapamil 可以用于治疗高血压、心绞痛、心肌梗塞等。 | |||
T0342 |
Carvedilol phosphate hemihydrate
Carvedilol phosphate,BM 14190 (phosphate hemihydrate),卡维地洛磷酸盐 |
VEGFR; Others; Potassium Channel; LDL; Integrin; Gap Junction Protein; NADPH; Adrenergic Receptor; Autophagy | Angiogenesis; Autophagy; Cytoskeletal Signaling; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience; Others; Tyrosine Kinase/Adaptors |
Carvedilol phosphate hemihydrate (BM 14190 phosphate hemihydrate) 是一种外消旋混合物,是一种非选择性β/α-1受体阻断剂,具有抗高血压活性且缺乏内在拟交感神经活性。 | |||
T1010 |
Verapamil hydrochloride
Manidon,盐酸维拉帕米,(±)-Verapamil hydrochlorid,Verapamil HCl,Calcan hydrochloride |
P450; Calcium Channel; P-gp | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Verapamil hydrochloride (Verapamil HCl) 是一种钙通道阻滞剂,是一种可口服的 P 糖蛋白 (P-gp) 抑制剂,可抑制CYP3A4,用于高血压、心律不齐和心绞痛的研究。 | |||
T0487 |
Metoprolol tartrate
酒石酸美托洛尔,CGP 2175E |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Metoprolol tartrate 是一种心脏选择性β1肾上腺素阻断剂。 | |||
T1203 |
Nadolol
Anabet,Corgard,Solgol,苯甲丁氮酮,纳多洛尔,SQ11725 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Nadolol 是一种有机阴离子转运多肽 1A2 (OATP1A2) 的底物,是一种非选择性的、具有口服活性的 β-肾上腺素受体 (β-adrenergic receptors) 阻滞剂,可用于高血压,心绞痛和血管性头痛的研究。 | |||
T11148 |
Ecastolol
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Ecastolol 是一种 beta adrenergic receptor 拮抗剂,具有防心绞痛的作用。 | |||
T35161 |
Xemilofiban
SC-54684A,SC54684A,SC 54684A |
Others | Others |
Xemilofiban (SC 54684A) 可中断血小板聚集,可促进血栓形成,可用于研究不稳定型心绞痛。 | |||
T27808 |
Lefradafiban
BIBU 104,BIBU104,BIBU-104 |
Others | Others |
Lefradafiban(BIBU-104) 是一种口服血小板糖蛋白 IIb/IIIa 受体拮抗剂,可用于研究心绞痛和急性冠状动脉综合症。 | |||
T34648 |
Sinitrodil
ITF296,ITF-296,ITF 296 |
Guanylate cyclase | GPCR/G Protein |
Sinitrodil (ITF-296) 是一种鸟苷酸环化酶兴奋剂,可用于治疗心肌缺血和心绞痛。 | |||
T1479 |
Isosorbide dinitrate
硝酸异山梨酯,Isordil,Nitrosorbide,Sorbide nitrate,Sorbidnitrate |
Others; NO Synthase | Immunology/Inflammation; Others |
Isosorbide dinitrate (Isordil) 是 NO 供体,可预防心肌梗死 (MI) 引起的左室重构及心功能退化。 | |||
T13154 |
Tiapamil hydrochloride
Ro 11-1781 hydrochloride,ORE 5002 hydrochloride |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Tiapamil hydrochloride (Ro 11-1781 hydrochloride) 是一种钙通道阻滞剂,具有抗高血压活性,可用于研究心绞痛和心血管疾病。 | |||
T8143 |
Bevantolol hydrochloride
贝凡洛尔盐酸盐,NC-1400 hydrochloride,盐酸贝凡洛尔 |
Calcium Channel; Adrenergic Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Bevantolol hydrochloride (NC-1400 hydrochloride) 是一种 β1-肾上腺素受体拮抗剂,可治疗心绞痛和高血压,在大鼠大脑皮层中的pKi 值分别为 7.83、6.9。 | |||
T27286L |
Esprolol
ACC-9369 free base |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Esprolol (ACC-9369 free base) 是一种新的 β 肾上腺素能受体拮抗剂,可用于研究劳力性心绞痛。 | |||
T0112L |
Diltiazem
CRD 401 free base,CRD-401 free base,Dilticard,CRD401 free base,Dilzen |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Diltiazem (CRD 401 free base) 是一种可口服的 L 型钙通道 (L-type Ca2+ channel) 阻滞剂,具有抗高血压、抗心律失常和心脏保护作用, 可预防再灌注后心肌损伤、心绞痛和与心血管相关的疾病。 | |||
T8580 |
Bupranolol
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bupranolol 是竞争性的、口服活性的、非选择性的β-adrenoceptor 拮抗剂,无固有的拟交感神经活性。 | |||
T68060 |
Elgodipine
|
Others | Others |
Elgodipine 显著降低了运动诱导的心绞痛系统的发生率和严重程度,能够通过独立于转录因子c-fos 和c-jun 表达的机制抑制血管平滑肌增殖。 Elgodipine 诱导的抑制是电压依赖性的。Elgodipine 是治疗心绞痛的潜在化合物。 | |||
T30586L |
Brefonalol HCl
Brefonalol HCl(103880-26-8 Free base) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Brefonalol HCl 是一种 ADRA 拮抗剂,可用于治疗神经系统疾病和心血管疾病,可用于研究心绞痛、心律失常和高血压。 | |||
T68073 |
Flosatidil
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Flosatidil是一种小分子电压门控性钙通道复合体(VDCCs)阻滞剂,可用于治疗神经系统疾病和心血管疾病,可用于研究心绞痛。 | |||
T83980 |
Alinidine
|
HCN Channel | Membrane transporter/Ion channel |
Alinidine 是一种 HCN 通道阻断剂,具有抗心律失常作用,可用于研究心绞痛。 | |||
T0988 |
Trimetazidine dihydrochloride
盐酸曲美他嗪,Yoshimilon,Kyurinett,Vastarel F |
Autophagy; Fatty Acid Synthase | Autophagy; Metabolism |
Trimetazidine dihydrochloride (Vastarel F) 是细胞保护性抗缺血剂,也用作缺血性心脏病或心绞痛的血管扩张剂,具有抗氧化,抗炎,抗伤害和胃保护作用。它可通过抑制脂肪酸代谢提高心肌葡萄糖利用率。 | |||
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。 | |||
T0230 |
Prasugrel
LY640315,CS-747,普拉格雷,PCR 4099 |
P2Y Receptor | GPCR/G Protein; Neuroscience |
Prasugrel (CS-747) 是一种噻吩吡啶和前药,是一种可口服的 P2Y12受体拮抗剂,抑制 ADP 诱导的血小板聚集,用于预防急性冠状动脉综合征患者的血栓形成、不稳定型心绞痛和心肌梗塞,以及接受经皮冠状动脉介入治疗的患者。 | |||
T50077 |
m-Nisoldipine
3-methyl 5-(2-methylpropyl) 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate |
Others | Others |
m-Nisoldipine (3-methyl 5-(2-methylpropyl) 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate) 是一种二氢吡啶类钙通道阻滞剂,尼索地平的衍生物,阻断心脏和平滑肌细胞中的 L-型钙通道,用于治疗高血压和心绞痛。 | |||
T1282 |
Carteolol hydrochloride
Arteoptic,Abbott-43326,OPC-1085 hydrochloride,盐酸卡替洛尔,Carteolol HCl,Mikelan |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Carteolol hydrochloride (Abbott-43326) 是一种非选择性的β肾上腺素受体阻断剂。 | |||
T36665 |
Dehydro Nifedipine
BAY-b 4759 |
Others | Others |
Dehydro Nifedipine (BAY-b 4759) 是人血浆中硝苯地平的主要代谢物。Dehydro Nifedipine 抑制PC-12细胞葡萄糖摄取,IC50值为130 μM,硝苯地平是一种钙通道阻滞剂,用于治疗高血压和心绞痛。当硝苯地平被细胞色素P450 (CYP)异构体CYP3A4和CYP3A5代谢时形成脱氢硝苯地平。 | |||
T31206 |
Darexaban
YM 150,Darexaban, Tanexaban,YM150 |
Factor Xa | Metabolism |
Darexaban (Tanexaban, YM-150) 是选择性的、口服具有活力的 Xa 因子 (FXa) 抑制剂,IC50=54.6 nM。它对其他相关丝氨酸蛋白酶(如胰蛋白酶、凝血酶和激肽释放酶)具有高选择性。它具有抗凝和抗血栓形成作用。 | |||
T24873 |
TGX-115
TGX 115 |
PI3K | PI3K/Akt/mTOR signaling |
TGX-115是一种细胞渗透性和有效的PI 3-K 异构体p110β/p110δ抑制剂(对p110β IC50值为 0.13 μM, 对p110δ值为0.63 μM),是一种调节血小板粘附过程的酶,可抑制磷酸肌苷(PI)3-激酶,可用来治疗冠状动脉闭塞、中风、急性冠状动脉综合征、急性心肌梗塞、血管再狭窄、动脉硬化和不稳定心绞痛等心血管疾病 。 | |||
T28800 |
SL-870495
SL870495 |
Others | Others |
SL-870495, a calcium channel antagonist, is used potentially for the treatment of angina pectoris. | |||
T25575 |
KF 14124
KF14124,Dptpp-2-ismn,KF-14124 |
Others | Others |
KF 14124 exhibits potent anti-ischemic activity in a lysine-vasopressin-induced angina pectoris model (rats). | |||
T28191 |
NP-252
NP252 |
Others | Others |
NP-252 is a calcium channel antagonist potentially for the treatment of angina pectoris and congestive heart failure. | |||
T8663L |
Nifenalol
|
Others | Others |
Nifenalol is an adrenergic beta-blocker with good antiarrhythmic properties. It tends to lower blood pressure and provide protection against angina. | |||
T69494 |
Toliprolol
|
Others | Others |
Toliprolol is an adrenergic receptor antagonist with some stimulant action; it has been proposed for angina pectoris. | |||
T11080 |
Dopropidil
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Dopropidil is a new anti-angina pectoris calcium regulator, which has intracellular calcium antagonist activity and anti-ischemic effects in various predicted animal models. | |||
T28457 |
Proxodolol hydrochloride
|
Others | Others |
Proxodolol, a β-adrenergic receptor antagonist, is used potentially for the treatment of glaucoma, hypertension and angina. | |||
T68213 |
Palonidipine HCl
|
Others | Others |
Palonidipine HCl is a calcium channel antagonist potentially for the treatment of angina pectoris and hypertension. | |||
T21010 |
Diacetolol
Acetylacebutolol,(+-)-Diacetolol,M and B 16942 |
Others | Others |
Diacetolol is the major metabolite of acebutolol, a selective beta blockers used to treat hypertension, angina pectoris and arrhythmia. | |||
T24659 |
Prenylamine lactate
Agozol,Angormin |
Others | Others |
Prenylamine lactate is a drug formerly used in the treatment of angina pectoris. Prenylamine depletes myocardial catecholamine stores and has some calcium channel blocking activity. | |||
T24631 |
Pheniprazine hydrochloride
Pheniprazine HCl,NSC 17766,CCRIS 1417,NSC-17766,NSC17766 |
Others | Others |
Pheniprazine is an irreversible and nonselective monoamine oxidase inhibitor of the hydrazine chemical class. It was also used in the treatment of angina pectoris and schizophrenia. | |||
T24863 |
Tedisamil
Tedisamilum,Pulzium |
Others | Others |
Tedisamil is a blocker of K+ currents in cardiac tissues, exerts bradycardic effects. It is an antiarrhythmic drug with predominantly class III activity. It has shown clinical efficacy in angina pectoris. | |||
T32770 |
Linsidomine
CV 664 |
Others | Others |
Lincydomine is a smooth muscle relaxant, beneficial to the treatment of unstable angina pectoris, but also can open the respiratory tract of humans and guinea pigs. | |||
T12358 |
Palonidipine
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Palonidipine is an antagonist of calcium, is potential for the therapy of angina-pectoris and hypertension. | |||
T27197 |
Dopropidil hydrochloride
ORG-30701,CERM-4205,CERM4205,ORG30701 |
Others | Others |
Dopropidil, a calcium channel antagonist, is used potentially for the treatment of arrhymia and angina pectoris. | |||
T33673 |
Niludipine
Niludipina,BAY-a 7168,Bay a 7168,Niludipinum |
Others | Others |
Nirudipine is a double (2-propoxyethyl) analogist of nifedipine and a calcium channel blocker, which is also a safe anti-angina Ca2+ antagonist with a broad range of efficacy for all types of angina. At the same time, Niludipine is a highly effective drug | |||
T61138 |
Bevantolol
|
Others | Others |
Bevantolol, a selective β-1 adrenoceptor antagonist, is utilized for the investigation of angina pectoris and hypertension [1]. | |||
T71583 |
Amlodipine hydrochloride, (R)-
|
Others | Others |
Amlodipine hydrochloride, (R)-, is a medication used to lower blood pressure and prevent chest pain. It belongs to a group of medications known as dihydropyridine-type calcium channel blockers. By widening of blood vessels it lowers blood pressure. In angina, amlodipine increases blood flow to the heart muscle to relieve pain due to angina. | |||
T68367 |
Amlodipine orotate
|
Others | Others |
Amlodipine orotate is a medication used to lower blood pressure and prevent chest pain. It belongs to a group of medications known as dihydropyridine-type calcium channel blockers. By widening of blood vessels it lowers blood pressure. In angina, amlodipine increases blood flow to the heart muscle to relieve pain due to angina. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3S0128 |
Hydroprotopine
氢化原阿片碱,氢化物碱 |
Others | Others |
Hydroprotopine 是一种来自Hypecoum leptocarpumand 的生物碱,能够有效的治疗冠心病及心绞痛。 | |||
TN2303 |
Viscumneoside III
槲寄生新甙III,槲寄生新苷III |
Tyrosinase | Proteases/Proteasome |
Viscumneoside III 是一种二氢黄酮 O-糖苷,抑制酪氨酸酶 (tyrosinase),IC50 为 0.5 mM。Viscumneoside III 具有抗心绞痛作用。 | |||
TN4323 |
Isorauhimbine
|
Antibiotic | Microbiology/Virology |
Isorauhimbine 是一种从萝芙藤 (R. serpentina) 中提取得到生物碱,具有抗癌、抗炎和抗菌活性,可用于治疗高血压、心律失常和心绞痛等心血管疾病。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10229 |
Acebutolol D7
|
Others | Others |
Acebutolol D7 is a deuterium-labeled Acebutolol. Acebutolol is a selective antagonist of the β1 adrenergic receptor used in the treatment of angina pectoris, hypertension, and cardiac arrhythmias. | |||
TMIJ-0426 |
Celiprolol-d9 Hydrochloride
|
||
Celiprolol-d9 Hydrochloride 是 Celiprolol Hydrochloride 的氘代化合物。Celiprolol Hydrochloride 的 CAS 号为 57470-78-7。Celiprolol hydrochloride 是一种选择性肾上腺素受体调节剂,是一种选择性的和具有口服活性的β1肾上腺素受体拮抗剂,具有部分β2激动剂活性,具有降压和抗心绞痛的作用。 | |||
TMIJ-0094 |
Trimetazidine-d8 Dihydrochloride
|
||
Trimetazidine-d8 Dihydrochloride 是 Trimetazidine Dihydrochloride 的氘代化合物。Trimetazidine Dihydrochloride 的 CAS 号为 13171-25-0。Trimetazidine dihydrochloride 是细胞保护性抗缺血剂,也用作缺血性心脏病或心绞痛的血管扩张剂,具有抗氧化,抗炎,抗伤害和胃保护作用。它可通过抑制脂肪酸代谢提高心肌葡萄糖利用率。 | |||
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 =... |