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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10511 |
Anti-hypertensive sulfonanilide 1
|
Others | Others |
Anti-hypertensive sulfonanilide 1 is an antihypertensive compound. | |||
T22236 |
Alprenolol hydrochloride
阿普洛尔盐酸盐,盐酸阿普洛尔 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Alprenolol hydrochloride 是一种非选择性β受体阻滞剂,也是5-HT1A 受体拮抗剂。 | |||
T6835 |
Fenoldopam mesylate
Fenoldopam methanesulfonate,SKF-82526 mesylate,Corlopam mesylate,mesylate,SKF 82526,非诺多泮甲磺酸盐 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Fenoldopam mesylate (Corlopam mesylate) 是一种多巴胺受体D1选择性激动剂。 | |||
T9097 |
Guanadrel
|
Others | Others |
Guanadrel 是一种抗高血压药。 | |||
T17111 |
Todralazine hydrochloride
Ecarazine hydrochloride,盐酸托屈嗪 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Todralazine hydrochloride (Ecarazine hydrochloride) 是一种 β2AR 阻滞剂,具有抗氧化和自由基清除活性。 Todralazine hydrochloride 可用于抗高血压的研究。 | |||
T37496L |
Alamandine TFA
|
RAAS | Endocrinology/Hormones |
Alamandine TFA 是肾素-血管紧张素系统 (RAS) 的成员,是一种血管活性肽,是 G 蛋白偶联受体 MrgD 的内源性配体。它通过抗高血压作用来保护肾脏和心脏。 | |||
T31598 |
Ecadotril
S.049,BAY-y 7432,BAY y 7432,BP 1.02,S049 |
||
Ecadotril is a neutral endopeptidase (NEP) inhibitor, which plays an anti hypertensive role. | |||
T17112 |
Todralazine
Ecarazine |
Others | Others |
Todralazine is an anti-hypertensive agent and acts as a β2AR blocker. It also has an antioxidant and free radical scavenging activity. | |||
T21416 |
Hydroflumethiazide
Diurometon,Glomerulin,Diuredemina,Flutizide,Hidroflumetiazid |
||
Hydroflumethiazide is a thiazide diuretic. It has also shown the activity of anti-hypertensive. | |||
T15680 |
L-159282
MK 996 |
Others | Others |
L-159282 is an orally active and nonpeptide angiotensin II receptor antagonist. It also has anti-hypertensive activity. | |||
T62288 | AD013 | ||
AD013 是一种双重的 cACE 和 NEP 抑制剂。AD013 是通过 C 域选择性 ACE 抑制剂赖诺普利-色氨酸合成。AD013 具有潜力提供强效抗高血压和心脏保护作用。 | |||
T62831 | AD012 | ||
AD012 是一种 cACE/NEP 的双重抑制剂。AD012 利用先前报道的 C 域选择性 ACE 抑制剂赖诺普利-色氨酸合成。AD012 具有潜力提供强效抗高血压和心脏保护作用。 | |||
T62618 | SPH3127 | ||
SPH3127 (DRI 18) 是一种强有效的、口服具有活力的、新型的 direct renin 抑制剂,其对 recombinant human-renin,human plasma renin activity 的 IC50 值分别为0.4 nM 和 0.45 nM。SPH3127具有抗高血压效果,能够用于研究高血压。 | |||
T63160 | AD011 | ||
AD011 是一种双重的 cACE/NEP 抑制剂。AD011 是通过先前报道的 C 域选择性 ACE 抑制剂赖诺普利-色氨酸合成的。AD011 显示出提供高效抗高血压和心脏保护作用的潜力。 | |||
T62543 |
JNc-440
|
||
JNc-440 是一种有效的抗高血压剂。JNc-440 能够提高内皮细胞瞬时受体电位香草酸亚型 4 (TRPV4) 和钙离子激活钾通道 3 (KCa2.3) 的相互作用。JNc-440 也可以提高小鼠血管扩张,具有降压活性。 | |||
T35600 |
NO-Losartan A
|
||
Angiotensin II is a hormone that plays an important role in regulating blood pressure. Elevated levels of angiotensin II are implicated in inducing and maintaining hypertension, and also in the development of atherosclerosis. Both of these effects are mediated by the angiotensin II type 1 (AT1) receptor. Losartan is a mammalian AT1 receptor antagonist with a Ki value of 5-20 nM. In humans, losartan effectively controls hypertension while protecting renal function. Nitric oxide (NO) causes vasodi... | |||
T35642 | Tritylolmesartan Medoxomil | ||
Tritylolmesartan medoxomil is an intermediate in the synthesis of olmesartan medoxomil , a prodrug form of the angiotensin II receptor 1 (AT1) antagonist olmesartan .1 1.Hanumantha Rao, B., Subramanyeswara Rao, I.V., Ravi Kanth, V., et al.A competent and commercially viable process for the synthesis of the anti-hypertensive drug olmesartan medoxomilSci. Pharm.83(3)465-478(2015) |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6S1369 |
Vitexin
牡荆素,Apigenin-8-C-glucoside |
Antioxidant | oxidation-reduction |
Vitexin 是一种存在于多种药用植物(如榕树、螺旋藻)中的 c-糖基化的黄酮。 它具有广泛的药理作用,包括抗氧化,抗癌,抗炎,抗痛觉过敏和神经保护作用。 | |||
T8044 |
Ajmalicine
阿吗里新,Lamuran,Delta-Yohimbine,Raubasine,Ajmalicin |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Ajmalicine (Raubasine) 是一种有效的抗肾上腺素 (adrenolytic) 剂,优先阻断 α1-肾上腺素受体 (α1-adrenoceptor)。Ajmalicine 是一种可逆性但非竞争性尼古丁受体 (nicotine receptor) 完全抑制剂,IC50 为 72.3 μM。Ajmalicine 还可用于降压、蛇毒,具有镇静活性。 | |||
T4S1102 |
Liensinine diperchlorate
莲心碱高氯酸盐,莲心碱二高氯酸盐,Liensinine-Perchlorate |
Mitophagy; Others; Autophagy | Autophagy; Others |
Liensinine Diperchlorate 是从芙蕖种子胚中提取的一种异喹啉生物碱。它通过阻断自噬小体-溶酶体融合来抑制晚期自噬,具有抗心律不齐、抗高血压、抗肺纤维化和血管平滑肌松弛等生物学活性。 | |||
TCS1704 |
Artemitin
艾黄素,Artemetin,Artemisetin,Erianthin |
Antioxidant | oxidation-reduction |
Artemitin (Erianthin) 是一种存在于翼齿六棱菊中的天然黄酮,具有抗氧化、抗炎、抗病毒活性。 | |||
TN1065 |
Hirsutine
|
Apoptosis | Apoptosis |
Hirsutine 是一种来自钩藤的吲哚生物碱,可诱导细胞凋亡,是一种登革热病毒抑制剂,且毒性低。它具有抗癌、心脏保护、抗高血压、抗心律失常和血管舒张活性。 | |||
T1035 |
Hesperidin
橙皮甙,Hesperetin 7-rutinoside,Cirantin,橙皮苷 |
Apoptosis; Reactive Oxygen Species; Endogenous Metabolite; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; Metabolism; NF-κB |
Hesperidin (Cirantin) 是一种广泛存在于柑橘类水果中黄烷酮糖苷,具有减少炎症介质并发挥重要的抗氧化作用,还有抗肿瘤和抗过敏活性。 | |||
TN2990 |
3alpha-dihydrocadambine
|
Others | Others |
3alpha-Dihydrocadambine exhibits dose-dependent hypotensive and anti-hypertensive effects in anesthetized normotensive rats and in conscious spontaneously hypertensive rats. | |||
T69254 |
Ajmalicine hydrochloride
Raubasine hydrochloride |
||
Ajmalicine (Raubasine) hydrochloride 是一种有效的抗肾上腺素 (adrenolytic) 剂,优先阻断 α1-肾上腺素受体 (α1-adrenoceptor)。Ajmalicine hydrochloride 是一种可逆性但非竞争性尼古丁受体 (nicotine receptor) 完全抑制剂,其 IC50为 72.3 μM。Ajmalicine hydrochloride 还可用于降压、蛇毒,具有镇静活性。 |