57
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2320 |
Indacaterol
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Indacaterol 是一种超长效β-肾上腺素受体激动剂。 | |||
T15108 |
DG-041
|
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
DG-041 是高亲和力,选择性的,有效的 EP3受体拮抗剂,在结合和 FLIPR 试验中,IC50分别为 4.6 nM 和 8.1 nM。DG-041通过抑制 PGE2促进血小板聚集。DG-041具有血脑屏障渗透性。 | |||
T15418 |
GS-6201
CVT-6883 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
GS-6201 (CVT-6883) 是选择性腺苷 A2B 受体拮抗剂。它对人腺苷 A2B 受体具有高亲和力和选择性 (Ki=22 nM)。它降低了小鼠急性心肌梗死后心脏中 caspase-1 的活性,并减弱了心脏重塑。它减弱了致敏小鼠 NECA,AMP 或变应原诱导的气道反应性。 | |||
T5329 |
Trandolapril
|
Angiotensin-converting Enzyme (ACE) | Metabolism |
Trandolapril 是 Trandolaprilat 的前体药物。Trandolapril 是一种口服血管紧张素转换酶抑制剂,在高血压和充血性心力衰竭及心肌梗死领域有研究价值。 | |||
T1239 |
Indacaterol maleate
马来酸茚达特罗,QAB149 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Indacaterol maleate (QAB149) 是一种超长效的 β-肾上腺素受体激动剂。 | |||
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。 | |||
T7714 |
Temocapil
|
Tyrosinase | Proteases/Proteasome |
Temocapil 是一种酪氨酸激酶抑制剂。 | |||
T3461 |
Losartan Carboxylic Acid
EXP-3174,E-3174 |
RAAS | Endocrinology/Hormones |
Losartan Carboxylic Acid (E-3174) 是 Losartan 的活性羧酸代谢产物,是血管紧张素Ⅱ受体 1 型(AT1)拮抗剂。它能够阻断血管紧张素 II 诱导的血管平滑肌细胞反应,可以提高血浆肾素活性,降低平均动脉压。 | |||
T3230 |
NLRP3-IN-2
5-Chloro-N-(p-sulfamoylphenethyl)-o-anisamide,4-[2-(5-氯-2-甲氧基苯甲酰氨基)乙基]苯磺酰胺,NLRP3 Inflammasome Inhibitor I |
NOD-like Receptor (NLR); NOD | Immunology/Inflammation; NF-κB |
NLRP3-IN-2 (5-Chloro-N-(p-sulfamoylphenethyl)-o-anisamide) 是一种能够合成格列本脲的中间物,对心肌细胞中NLRP3炎症小体的形成具有抑制作用,在小鼠心肌缺血/再灌注后限制梗死面积,且对代谢无影响。 | |||
T6698 |
Temocapril hydrochloride
CS-622 HCl,Acecol,Temocapril HCl,CS-622,盐酸替莫普利 |
RAAS | Endocrinology/Hormones |
Temocapril hydrochloride (CS-622 HCl) 是血管紧张素转化酶 (ACE) 抑制剂。Temocapril HCl 能够用于充血性心力衰竭、急性心肌梗死、高血压、胰岛素抵抗和肾脏疾病的研究。 | |||
T11239 |
Ethacizine hydrochloride
NIK-244,Ethacizin,NIK-244 hydrochloride |
Sodium Channel | Membrane transporter/Ion channel |
Ethacizine hydrochloride (NIK-244) 具有抗心律失常活性,其作用于心脏活动有关,可用于研究心律失常和心肌梗死。 | |||
T83977 |
BIIB 722 Mesylate
|
Sodium Channel | Membrane transporter/Ion channel |
BIIB 722 Mesylate 是一种选择性钠氢交换抑制剂,具有心脏保护作用,可用于研究心肌缺血和心肌梗死。 | |||
T67941 |
PDE5-IN-9
|
||
PDE5-IN-9对Phosphodiesterase PDE1c 具有抑制作用,可用来治疗高血压、心力衰竭、心肌梗塞、肾衰竭、哮喘、支气管炎和痴呆。 | |||
T68022L |
Sulotroban potassium
BM 13177 potassium,Sulotroban potassium(72131-33-0 Free base) |
PPAR | DNA Damage/DNA Repair; Metabolism |
Sulotroban potassium 是一种小分子血栓素A2受体(TXA2R)拮抗剂,可用于研究心肌梗塞和血栓形成。 | |||
T24115 |
GSK854
GSK-854,GSK 854 |
Apoptosis | Apoptosis |
GSK854 是一种具有高选择性和有效性的肌钙蛋白 I 相互作用激酶 (TNNI3K) 抑制剂,抑制小鼠心肌梗死损伤细胞焦亡和细胞凋亡,可限制缺血性心脏的氧化应激、损伤和不良重塑。 | |||
T12078 |
ML334
LH601A |
Nrf2 | Immunology/Inflammation |
ML334 (LH601A) 是一种可穿过细胞膜且具有有效性的 NRF2 激活剂,抑制 Keap1-NRF2 蛋白质相互作用,抑制心脏成纤维细胞活化和增殖来改善心肌梗死诱导的心脏纤维化。 | |||
TP2279L |
Obestatin (rat) acetate
|
GHSR | GPCR/G Protein |
Obestatin (rat) acetate 是 G 蛋白偶联受体 39 (GPR39) 的内源性配体。它具有抗炎、抗心肌梗塞和抗氧化特性。 它抑制食物摄入,抑制空肠收缩,并减少体重增加。 | |||
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。 | |||
T39115 |
ABR-238901
|
TLR | Immunology/Inflammation |
ABR-238901是一种可口服的、有作用的 S100A8/A9阻滞剂,对 S100A8/A9与其受体 RAGE(晚期糖基化终产物受体)和TLR4 (toll 样受体4)的相互作用具有抑制作用。ABR-238901具有作为治疗心肌梗死(MI)化合物的潜力。 | |||
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。 | |||
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... | |||
T22323 |
Enoxaparin sodium
|
Thrombin | Proteases/Proteasome |
Enoxaparin sodium 是一种低分子量肝素 (LMWH),已获得美国 FDA 批准,可用于医疗管理的 ST 段心肌梗死 (STEMI) 或 STEMI 及随后的经皮冠状动脉介入治疗 (PCI) 患者。它与抗凝血酶结合并增强其作用,并抑制凝血因子 XIa、IXa、Xa 和 IIa(凝血酶),从而防止血栓形成。 | |||
T36569 |
KR-32568
|
Sodium Channel | Membrane transporter/Ion channel |
KR-32568是一种钠/氢交换器1(NHE-1)抑制剂(IC50:230 nM)。KR-32568具有强大的心脏保护作用。当使用浓度为10μM 时,它能在离体的缺血大鼠心脏模型中恢复心脏收缩功能。KR-32568(0.3mg/kg)在缺血和再灌注损伤的大鼠模型中减少了心肌梗死的大小。 | |||
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 。 | |||
T14390L | (2R,3S)-Azelaprag | Apelin receptor | GPCR/G Protein |
(2R,3S)-N-(4-(2,6-dimethoxyphenyl)-5-(5-methylpyridin-3-yl)-4H-1,2,4-triazol-3-yl)-3-(5-methylpyrimidin-2-yl)butane-2-sulfonamide 是一种Apelin 受体激动剂,对Apelin 受体的EC50为0.012 µM。(2R,3S)-N-(4-(2,6-dimethoxyphenyl)-5-(5-methylpyridin-3-yl)-4H-1,2,4-triazol-3-yl)-3-(5-methylpyrimidin-2-yl)butane-2-sulfonamide 可用于治疗心力衰竭、动脉粥样硬化、肥胖、糖尿病、肌萎缩侧索硬化、冠心病、高血压、中风和心肌梗塞等疾病。 | |||
T34327 |
Ridogrel
R-70416,R 68070,R-68070,R70416,R 70416,R68070 |
||
Lidogrell is a dual-acting agent that can be used to prevent systemic thromboembolism and as an adjunct to thrombolytic therapy in acute myocardial infarction. | |||
T28130 |
Naltiazem
RO 236152,RO-236152,RO236152 |
||
Naltiazem, a calcium channel antagonist, is used potentially for the treatment of arrhythmias, hypertension and myocardial infarction. | |||
T27581 |
Icrocaptide
ITF 1697,ITF-1697,ITF1697 |
||
Icrocaptide is used potentially for the treatment of acute myocardial infarction. | |||
T24746 |
Zalunfiban
RUC4,RUC 4,RUC-4 |
||
RUC-4 is an aIIb 3 antagonist. It is also used for prehospital therapy of myocardial infarction. | |||
T69078 |
Tiapamil Free Base
|
||
Tiapamil Free Base is a phenylethylamine derivative that acts as a calcium antagonist showing hemodynamic effects in patients with acute myocardial infarction. | |||
T37697 |
D-GsMTx4
D-GsMTx4 |
||
TRPC1/6 and Piezo2 inhibitor. Exhibits same effect as L-enantiomer, GsMTx4 (Cat. No. 4912) on TRPC channels. Inhibits mechanosensitive currents by ~70%. Protects against myocardial infarction in mouse ischemia/reperfusion model. Resistant to proteolytic digestion. | |||
T22685 |
CP-471474
CP 471474 |
Others | Others |
Broad spectrum MMP inhibitor (IC<sub>50</sub> values are 0.7, 0.9, 13, 16 and 1170 nM for MMP-2, MMP-13, MMP-9, MMP-3 and MMP-1 respectively). Attenuates early left ventricular dilation after experimental myocardial infarction in mice. | |||
T61540 | F15845 | ||
F 15845 is a potent and persistent blocker of the sodium current. It possesses cardioprotective properties and exhibits both anti-ischemic activity and short- and long-term cardioprotection following myocardial infarction. Furthermore, F 15845 finds utility in the investigation of myocardial functional impairment [1]. | |||
T62878 | Zalunfiban dihydrochloride | ||
Zalunfiban (RUC-4) dihydrochloride 是一种选择性的、有效的血小板αIIbβ3拮抗剂,其 IC50 值为 45 nM。Zalunfiban dihydrochloride 能够用于研究心肌梗死。 | |||
T11740L |
Delcasertib acetate
KAI-9803,KID1-1,CS-9803,BMS-875944,Delcasertib acetate(949100-39-4 free base) |
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
Delcasertib acetate 是一种选择性 δ 蛋白激酶C (δPKC) 抑制剂,可用于研究急性心肌梗死和疼痛。 | |||
T73240 |
PDE5-IN-4
|
||
PDE5-IN-4为磷酸二酯酶5(PDE5)抑制剂,应用于急性心肌梗死及再灌注损伤、消化系统疾病、糖尿病相关损害及肝功能衰竭的研究。 | |||
T73661 |
Delcasertib hydrochloride
|
||
Delcasertib (KAI-9803) hydrochloride 是有效,选择性的 δ 蛋白激酶 C (δPKC) 抑制剂。Delcasertib (KAI-9803) hydrochloride 可改善急性心肌梗死动物模型的缺血再灌注损伤。 | |||
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. | |||
T77026 | Goflikicept | ||
Goflikicept (RPH 104) 是一种可选择性结合并灭活循环中的 IL-1ß 和 IL-1α 的杂合蛋白。此化合物在研究ST段抬高型心肌梗死(STEMI)方面具有潜力。 | |||
T62507 | Protease-Activated Receptor-1 antagonist 1 | ||
Protease-Activated Receptor-1 antagonist 1 (Compound 13) 是一种蛋白酶激活受体 1 (PAR-1) 拮抗剂,通过 FLIPR 技术得到的 IC50 为 3 nM。Protease-Activated Receptor-1 antagonist 1 能够用于研究血栓性心血管、心肌梗塞和外周动脉疾病。 | |||
T77166 | Rovelizumab | ||
Rovelizumab是一种针对CD11/CD18细胞粘附蛋白的人源化单克隆抗白细胞整合素抗体,主要用于多发性硬化症(MS)、失血性休克、心肌梗死(MI)和中风研究。 | |||
T38800 |
MMPI-1154
|
||
MMPI-1154 is a highly promising imidazole-carboxylic acid (ICA) MMP-2 inhibitor (IC 50 = 6.6 μM) with excellent cardio-cytoprotective properties. It is specifically designed for the study of acute myocardial infarction. Additionally, MMPI-1154 exhibits significant inhibitory effects on MMP-13, MMP-1, and MMP-9 activities with IC 50 values of 1.8 μM, 10 μM, and 13 μM, respectively. | |||
T77163 | Pexelizumab | ||
Pexelizumab (h5G1.1-SC)为一种针对C5补体成分的人源化单克隆抗体。该化合物可抑制凋亡(apoptosis)和白细胞浸润,常用于研究脑缺血再灌注损伤和心肌梗死。 | |||
T62992 |
Trandolapril hydrochloride
|
||
Trandolapril (RU44570) hydrochloride 是一种非巯基前体化合物,水解为活性双乙酰 (Trandolapril hydrochlorideat)。Trandolapril hydrochloride 是一种口服具有活力的血管紧张素转换酶 (ACE) 抑制剂。Trandolapril hydrochloride 能够高血压和充血性心力衰竭及心肌梗死的研究。 | |||
T80130 |
SDF-1α (human)
|
CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation |
SDF-1α (human) 是一种能够与CXCR4受体相结合的单核细胞趋化剂,它在心肌梗死模型中的干细胞归巢、维持、生存、增殖、心肌细胞修复、血管形成以及心室重构过程扮演关键角色。SDF-1α (human) 常用于心血管病研究。 | |||
T36007 |
Nebentan
|
||
Nebentan (YM598) is a potent, selective and orally active non-peptide endothelin ETA receptor antagonist through the modification of Bosentan . Nebentan 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 inhibits the specific binding of [125I] endothelin-1 to endothelin ETA and ETB receptors in a concentration dep... | |||
T36223 |
MitoA
|
||
MitoA is a ratiometric mass spectrometry probe that can be used for assessing changes in H2S within mitochondria in vivo. MitoA contains a triphenylphosphonium cation component that drives its accumulation in mitochondria where its aryl azide moiety selectively reacts with H2S to produce an amine product, MitoN. Quantifying the MitoN/MitoA ratio by LC-MS/MS reflects the mitochondrial matrix H2S concentration. In a mouse model of acute myocardial infarction with MitoA administered prior to ischem... | |||
T62909 | SGC agonist 2 | ||
SGC agonist 2 是一种有效的可溶性鸟苷酸环化酶 (SGC) 激动剂。其中可溶性鸟苷酸环化酶是 NO-sGC-cGMP 信号通路中的关键信号转导酶。SGC agonist 2 具有潜力进行心血管疾病 (心力衰竭、心绞痛、肺动脉高压、心肌梗塞) 和纤维化疾病 (肾纤维化、系统性硬化症) 的研究。 | |||
T83043 |
Anti-MI/R injury agent 1
|
||
Anti-MI/R injury agent 1 (compound 18) 是一种口服有效的人参三醇衍生物,专用于抗心肌缺血/再灌注 (MI/R) 损伤。该化合物能增强经氧-葡萄糖剥夺和再灌注 (OGD/R) 诱导心肌细胞损伤模型中的细胞活力,显着缩小大鼠心肌梗死面积,减少循环心肌肌钙蛋白 I (cTnI) 的释放,并减轻心脏组织损害。 | |||
T75901 |
Obestatin(rat) TFA
|
||
Obestatin(rat) TFA 是一个包含23个氨基酸的肽,由Ghrelin基因编码。该化合物能够抑制食欲和空肠收缩,并能减缓体重增加。同时,Obestatin(rat) TFA 作为G 蛋白偶联受体 39 (GPR39) 的内源性配体,发挥抗炎、抗心肌梗塞和抗氧化功能。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2893 |
Muscone
3-Methylcyclopentadecanone,Methylexaltone,麝香酮 |
MMP; TNF; NF-κB; NOD-like Receptor (NLR); P-gp; Interleukin | Apoptosis; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience; NF-κB; Proteases/Proteasome |
Muscone (3-Methylcyclopentadecanone) 是中药麝香的一种主要活性单体。它抑制NF-κB 和NLRP3炎性小体的活化,显著降低炎性细胞因子水平,并最终改善心脏功能和存活率。 | |||
T3S0289 |
Araloside X
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Aralosides possess protective effect against experimental myocardial ischemia and infarction, the mechanism of myocardial protection may be attributed to the amelioration of FFA metabolic deterioration and membrane peroxidation induced by oxygen free radi |