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22

抑制剂 & 化合物

2

天然产物

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Cat. No. Product Name Target Signaling Pathways
T8462 Enoximone

依诺昔酮,烯氟酮

PDE Metabolism
Enoximone 是一种选择性的,具有口服活性的磷酸二酯酶 III 抑制剂,也是正性肌力血管舒张剂。它通过抑制 cGMP 抑制的 PDE 来诱导血管舒张并增加细胞内 cAMP 水平。它还表现出 PDE4抑制作用,对心肌 PDE4A 的 IC50为 21.1 μM。它用于充血性心力衰竭的研究,并具有支气管扩张,抗哮喘和抗炎作用。
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)。
T0109 Molsidomine

Morsydomine,SIN-10,吗多明,Corvaton

NOD Immunology/Inflammation; NF-κB
Molsidomine (Corvaton) 是一种长效的、口服活性的血管扩张药,在肝脏中代谢可被为活性代谢物Linsidomine。 其中Linsidomine 是一种不稳定的化合物,能够产生NO,可用作血管舒张剂。
TNU0864 HUP30

Potassium Channel; Calcium Channel Membrane transporter/Ion channel; Metabolism
HUP30是一种强效的血管舒张剂。HUP30可以刺激可溶性鸟苷酸环化酶,激活 K+离子通道,阻断细胞外 Ca2+的内流。
T0112 Diltiazem hydrochloride

CRD-401,盐酸地尔硫卓,RG 83606 HCl,Diltiazem HCl

Calcium Channel Membrane transporter/Ion channel; Metabolism
Diltiazem hydrochloride (RG 83606 HCl) 是一种苯并硫氮卓类钙通道阻滞剂,由于其拮抗钙离子对膜功能的作用而具有血管舒张作用。
T0903 Cinnarizine

Stugeron,桂利嗪,Cinarizine,Dimitronal,Stutgin

Calcium Channel; Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience
Cinnarizine (Stugeron) 是一种哌嗪衍生物,具有组胺 H1 受体和钙通道阻断活性,具有扩张血管和止吐的特性,可促进脑血流,用于脑中风、创伤后脑症状和脑动脉硬化的研究。
T15130 Dilazep dihydrochloride

Others Others
Dilazep dihydrochloride 是一种腺苷摄取的抑制剂。它可抑制缺血性损伤,血小板聚集和核苷的膜转运。它能够增强腺苷的作用,进而具有脑和冠状血管舒张作用。
T2671 Regadenoson

CVT-3146,瑞加德松,Lexiscan

Adenosine Receptor GPCR/G Protein; Neuroscience
Regadenoson (CVT-3146) 是一种腺苷衍生物和选择性 A2A 腺苷受体激动剂,具有冠状动脉舒张活性,对大鼠和猪腺苷 A2A 受体的Ki 分别为 290 和 1120 nM。它是血管扩张剂,可增加啮齿动物血脑屏障的通透性。
T26081 Ridazolol

Ridazololum

Ridazolol is a vasodilating and cardioselective beta adrenergic blocker.
T30586 Brefonalol

Brefonalol is a vasodilating beta-adrenergic receptor blocker.
T26201 Sorbinicate

LG10017,Sorbinicatum,LG10,017,LG-10017,LG 10017

Sorbinicate is an antihypercholesterolaemic and vasodilating nicotinic acid ester.
T30487 BMS 180448

BMS-180448,BMS180448

BMS 180448 is a prototype mitochondrial ATP-sensitive K+ (Mitok (ATP)) channel opener with cardioprotective and vasodilating properties.
T70678 Rwj 29009

Rwj 29009 is a potassium channel activator with prominent coronary and peripheral vasodilating actions.
T61495 Medroxalol

Medroxalol (RMI81968) is an orally active adrenergic receptor antagonist that effectively blocks both α- and β-adrenergic receptors, effectively producing antihypertensive and vasodilating effects [1].
T68600 Enoximone sulfoxide

Enoximone sulfoxide is a selective phosphodiesterase III (PDE3) inhibitor with vasodilating and positive inotropic activity that does not cause changes in myocardial oxygen consumption. Enoximone prevents the degradation of cAMP by PDE, which prolongs signal transduction and its subsequent effects. It is used in patients with congestive heart failure.
T11609 ICI 153110

Others Others
ICI 153110 is an orally active phosphodiesterase inhibitor with both inotropic and vasodilating properties. It is designed for the treatment of congestive cardiac failure.
T10371 Arotinolol

5-HT Receptor GPCR/G Protein; Neuroscience
Arotinolol is a nonselective α/β-adrenergic receptor blocker and a vasodilating β-blocker. Arotinolol also shows potency for inhibiting the binding of the radioligand 125I-ICYP to 5HT1B-serotonergic receptor sites. It is an antihypertensive agent.
T29213 Zelandopam free base

YM-435,YM435,MYD-37,MYD37,Zelandopam

Zelandopam is a dopamine D1 agonist. Zelandopam is a potent stimulant of pancreatic exocrine secretion by acting on DA D1 receptors of the pancreas in dogs. Intravenous administration of Zelandopam produces renal vasodilating and diuretic/natriuretic effe
T69303 Isoxsuprine Free Base

Isoxsuprine Free Base is a beta-adrenergic agonist that causes direct relaxation of uterine and vascular smooth muscle. Its vasodilating actions are greater on the arteries supplying skeletal muscle than on those supplying skin. It is used in the treatment of peripheral vascular disease and in premature labor.
T36547 Quazinone

Quazinone is a selective inhibitor of phosphodiesterase 3 (PDE3) with positive inotropic and vasodilating properties.1,2 It induces relaxation of precontracted isolated human cavernous smooth muscle (IC50 = 4.2 μM).1 Quazinone (10-300 μg/kg) increases myocardial contractile force in anesthetized open-chest dogs in a dose-dependent manner, as well as decreases systolic and diastolic blood pressure.2 It also inhibits DNA synthesis induced by the PDGF isoform PDGF-BB in bovine coronary artery smoot...
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...
T78007 Vasonatrin Peptide (VNP) TFA

Vasonatrin Peptide (VNP) TFA 是一种由心钠素 (ANP) 和C型利钠肽 (CNP) 嵌合而成的肽类化合物。它整合了CNP的静脉扩张功能、ANP的利尿效果,并展现出与ANP或CNP无关的特有动脉扩张特性。Vasonatrin Peptide TFA 透过cGMP-PKG信号途径发挥其对内质网应激介导的糖尿病心脏缺血再灌注损害的保护作用。

化合物

Enoximone
Cat.No: T8462
Synonym: 依诺昔酮,烯氟酮
Target: PDE
Isosorbide
Cat.No: T6551
Synonym: Devicoran,Isobide,异山梨酯,异山梨醇,Hydronol,Dianhydro-D-glucitol,D-Isosorbide
Target: Others
Molsidomine
Cat.No: T0109
Synonym: Morsydomine,SIN-10,吗多明,Corvaton
Target: NOD
HUP30
Cat.No: TNU0864
Synonym:
Target: Potassium Channel, Calcium Channel
Diltiazem hydrochloride
Cat.No: T0112
Synonym: CRD-401,盐酸地尔硫卓,RG 83606 HCl,Diltiazem HCl
Target: Calcium Channel
Cinnarizine
Cat.No: T0903
Synonym: Stugeron,桂利嗪,Cinarizine,Dimitronal,Stutgin
Target: Calcium Channel, Histamine Receptor
Dilazep dihydrochloride
Cat.No: T15130
Synonym:
Target: Others
Regadenoson
Cat.No: T2671
Synonym: CVT-3146,瑞加德松,Lexiscan
Target: Adenosine Receptor
Ridazolol
Cat.No: T26081
Synonym: Ridazololum
Target:
Brefonalol
Cat.No: T30586
Synonym:
Target:
Sorbinicate
Cat.No: T26201
Synonym: LG10017,Sorbinicatum,LG10,017,LG-10017,LG 10017
Target:
BMS 180448
Cat.No: T30487
Synonym: BMS-180448,BMS180448
Target:
Rwj 29009
Cat.No: T70678
Synonym:
Target:
Medroxalol
Cat.No: T61495
Synonym:
Target:
Enoximone sulfoxide
Cat.No: T68600
Synonym:
Target:
ICI 153110
Cat.No: T11609
Synonym:
Target: Others
Arotinolol
Cat.No: T10371
Synonym:
Target: 5-HT Receptor
Zelandopam free base
Cat.No: T29213
Synonym: YM-435,YM435,MYD-37,MYD37,Zelandopam
Target:
Isoxsuprine Free Base
Cat.No: T69303
Synonym:
Target:
Quazinone
Cat.No: T36547
Synonym:
Target:
NO-Losartan A
Cat.No: T35600
Synonym:
Target:
Vasonatrin Peptide (VNP) TFA
Cat.No: T78007
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T21047 Apovincamine

cis-Apovincamine

Apovincamine is a vinca alkaloid and a chemical precursor of Vinpocetine, which is a derivative of Vincamine with vasodilating activity.
T0879L Niacin hydrochloride

Niacin hydrochloride is a water-soluble vitamin of the B complex occurring in various animal and plant tissues. It is needed by the body for the formation of coenzymes NAD and NADP. It possesses PELLAGRA-curative, vasodilating, and antilipemic properties.

天然产物

Apovincamine
Cat.No: T21047
Synonym: cis-Apovincamine
Target:
Niacin hydrochloride
Cat.No: T0879L
Synonym:
Target:
TargetMol Loading
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