pectoris

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。

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。

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。

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。

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。

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。

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。

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。

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。

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。

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。

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。

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。

Celiprolol hydrochloride (Selectrol) 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。

Diacetolol is the major metabolite of acebutolol, a selective beta blockers used to treat hypertension, angina pectoris and arrhythmia.

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.

Palonidipine HCl is a calcium channel antagonist potentially for the treatment of angina pectoris and hypertension.

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.

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。

Etafenone is a vasodilator for the therapy of anigna pectoris.

NP-252 is a calcium channel antagonist potentially for the treatment of angina pectoris and congestive heart failure.

KF 14124 exhibits potent anti-ischemic activity in a lysine-vasopressin-induced angina pectoris model (rats).

SL-870495, a calcium channel antagonist, is used potentially for the treatment of angina pectoris.

Dopropidil is a new anti-angina pectoris calcium regulator, which has intracellular calcium antagonist activity and anti-ischemic effects in various predicted animal models.

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 = 4.4 µM). It decreases mean blood pressure, coronary resistance, and heart rate, as well as increases coronary sinus outflow, in dogs when administered intravenously at a dose of 1 mg/kg. Nicorandil increases survival and decreases infarct size in a rabbit model of myocardial ischemia-reperfusion injury induced by left coronary artery occlusion. Formulations containing nicorandil have been used in the treatment of angina pectoris.

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.

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.

Toliprolol is an adrenergic receptor antagonist with some stimulant action; it has been proposed for angina pectoris.

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.

Bevantolol, a selective β-1 adrenoceptor antagonist, is utilized for the investigation of angina pectoris and hypertension [1].

Dopropidil, a calcium channel antagonist, is used potentially for the treatment of arrhymia and angina pectoris.

Palonidipine is an antagonist of calcium, is potential for the therapy of angina-pectoris and hypertension.

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。

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。