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Search Results for " atp-sensitive potassium "
Targets Recommended: Potassium Channel

24

抑制剂 & 化合物

1

天然产物

2

同位素标记化合物

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Cat. No. Product Name Target Signaling Pathways
T15385 Glibornuride

Potassium Channel Membrane transporter/Ion channel
Glibornuride 是对 ATP 敏感的 K+通道 (KATP 通道) 阻滞剂,pKi 为 5.75。Glibornuride 显示抗糖尿病活性。
T9714 Atpenin A5

Potassium Channel Membrane transporter/Ion channel
Atpenin A5 是高度特异性的complex II 抑制剂,IC50为 ~10 nM。Dolastatin 10也是有效的mKATP 通道激动剂,具有心脏保活的作用。
T1603 Glipizide

CP 28720,K 4024,格列吡嗪

Potassium Channel; PPAR; ABC DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism
Glipizide (CP 28720) 是一种有效的、具有口服活性的磺酰脲类抗糖尿病试剂 (anti-diabetic agent),在 2 型糖尿病的研究中具有价值,但不适用于1 型糖尿病。Glipizide 是通过部分阻断郎格汉斯胰岛细胞中 ATP 敏感钾通道 (KATP)发挥活性 。
T1634 Glibenclamide

格列本脲,Glyburide

Potassium Channel; Mitochondrial Metabolism; CFTR; P-gp; Autophagy Autophagy; Membrane transporter/Ion channel; Metabolism; Neuroscience
Glibenclamide (Glyburide) 是一种具有口服活性的 ATP 敏感的 K+通道抑制剂,可研究糖尿病和肥胖。它抑制 P-糖蛋白,可直接结合并阻断 KATP 的 SUR1亚基并抑制囊性纤维化跨膜传导调节蛋白。它通过诱导膜离子通透性干扰线粒体生物能,可诱导自噬。
T1101 Minocycline hydrochloride

Minocycline HCl,盐酸米诺环素,美满霉素

HIF/HIF Prolyl-Hydroxylase; Antibacterial; Antibiotic Chromatin/Epigenetic; Metabolism; Microbiology/Virology
Minocycline hydrochloride (Minocycline HCl) 属于四环素类抗生素,具有出色的吸收和组织渗透性。Minocycline hydrochloride 是一种广谱的抗菌剂,可用于多种细菌感染以及痤疮的治疗。
T10566 BMS-191095

Potassium Channel Membrane transporter/Ion channel
BMS-191095是一种线粒体 ATP 敏感性的钾离子通道活化剂。
T23563 ZM 226600

Potassium Channel Membrane transporter/Ion channel
ZM 226600是一种 ATP 敏感的钾通道开启剂 ,EC50值是500 nM。ZM226600 对膀胱自发活动有抑制作用。
T16420 P-1075

Potassium Channel Membrane transporter/Ion channel
P-1075 是磺酰脲受体2相关的 ATP 敏感性的钾通道(SUR2-KIR6)的激活剂,EC50为 45 nM。它在兔子中通过打开线粒体 K (ATP) 通道产生活性氧,产生保护心脏的功效。
T26086L (Iso)-Rilmakalim

Others Others
1-((3R,4S)-3-hydroxy-2,2-dimethyl-6-(phenylsulfonyl)chroman-4-yl)pyrrolidin-2-one 是 Rilmakalim 的异构体,Rilmakalim 是一种钾通道打开剂 (PCO),可以激活心脏或其它组织中 ATP-敏感 K+ 通道
T12315 OR-1896

PDE Metabolism
OR-1896 是 Levosimendan 的活性代谢产物,是一种高特异性磷酸二酯酶 (PDE III) 抑制剂,是一种血管扩张剂,具有部分抗炎特性,通过激活 ATP 敏感 (KATP) 和其他钾通道在不同类型的血管中产生血管舒张。OR-1896 可用于研究心力衰竭与血管功能障碍。
T27624 Iptakalim Hydrochloride

Potassium Channel; AChR Membrane transporter/Ion channel; Neuroscience
Iptakalim hydrochloride 是一种亲脂性的对氨基化合物,是 ATP 敏感的钾通道的开放剂,也是含α4β2的烟碱乙酰胆碱受体拮抗剂。它也是一种 K(ir) 6.1/SUR2B 激活剂,可通过保护内皮功能减轻大鼠缺氧引起的肺动脉高压。
T71929 Clamikalant

Others Others
Clamikalant inhibits ATP-sensitive potassium channel.
T35107 Way 120491

Way120491,Way-120,491,Way-120491,Celikalim

Others Others
Way 120491 activates ATP-sensitive potassium channels.
T70801 ZM-181037

Others Others
ZM-181037 is an ATP-sensitive potassium channel-blocker and a eukalemic diuretic.
T11243 Ethyl tosylcarbamate

Others Others
Gliclazide is a whole-cell beta-cell ATP-sensitive potassium currents blocker with an IC50 of 184 nM. Ethyl tosylcarbamate is an intermediate in the synthesis of Gliclazide (G409877).
T68602 AZ-DF 265

Others Others
AZ-DF 265 is a hypoglycaemic drug which stimulates insulin release. AZ-DF-265 inhibits ATP-sensitive potassium channels and displaces [3H]-glibenclamide from the sulphonylurea receptor.
T68745 U 56324

Others Others
U-56324 is a hypoglycemic agent derived from nicotinic acid. It was found to inhibit the activity of ATP-sensitive potassium channels in excised patches from mouse pancreatic B-cells.
T75084 Foslevcromakalim

Others Others
Foslevcromakalim (QLS-101 ) 是一种ATP 敏感的钾通道开启剂。Foslevcromakalim 是用于降眼压作用的前体。
T63330 Clamikalant sodium

Others Others
Clamikalant sodium 是非选择性的、 ATP 敏感性的钾 (KATP) 通道阻滞剂,能够用于研究心律不齐。
T84960 Nicorandil N-oxide

Others Others
Nicorandil N-oxide, a metabolite of nicorandil, functions as an activator of the ATP-sensitive potassium channel Kir6.2 (SUR2B/Kir6.2) and is associated with the sulfonylurea receptor 2B (SUR2B), while also serving as a nitric oxide donor.
T11002 Desethylamiodarone hydrochloride

N-desethylamiodarone hydrochloride,LB 33020 hydrochloride

Others Others
Desethylamiodarone hydrochloride (N-desethylamiodarone hydrochloride) is formed by the CYP3A isozyme. Amiodarone is an antiarrhythmic drug that inhibits ATP-sensitive potassium channels with an IC50 of 19.1 μM. It is the main active metabolite of amiodaro
T25739 Linogliride

McN-3935,McN3935,McN 3935,Linogliridum,Linoglirida

Others Others
Linogliride 是一种基于胍的胰岛素分泌抑制剂,也是 pirogliride 的结构类似物,具有降血糖活性。它可以阻断胰腺β细胞膜上对 ATP 敏感的钾通道,从而刺激胰岛素分泌并改善葡萄糖耐受性。
T25739L Linogliride fumarate

McN 3935,McN-3935,McN3935

Others Others
Linogliride fumarate 是Linogliride 的富马酸盐。Linogliride 是一种基于胍的胰岛素分泌抑制剂,也是pirogliride 的结构类似物,具有降血糖活性。它可以阻断胰腺β细胞膜上对ATP 敏感的钾通道,从而刺激胰岛素分泌并改善葡萄糖耐受性。
T36740 Guanosine 5’-diphosphate (sodium salt hydrate)

Others Others
Guanosine 5’-diphosphate (GDP) is a purine nucleotide and biosynthetic precursor of guanosine 5’-triphosphate .1It has been used to study the conformations of GTPases.2GDP (100 μM) activates sulfonylurea receptor 2B (SUR2B) linked to the inward-rectifier potassium channel 6.1 (Kir6.1) in HEK293T cells in a patch-clamp assay.3 1.Berg, J.M., Tymoczko, J.L., and Stryer, L.Biochemistry(2002) 2.Vetter, I.R., and Wittinghofer, A.The guanine nucleotide-binding switch in three dimensionsScience294(5545)...

化合物

Glibornuride
Cat.No: T15385
Synonym:
Target: Potassium Channel
Atpenin A5
Cat.No: T9714
Synonym:
Target: Potassium Channel
Glipizide
Cat.No: T1603
Synonym: CP 28720,K 4024,格列吡嗪
Target: Potassium Channel, PPAR, ABC
Glibenclamide
Cat.No: T1634
Synonym: 格列本脲,Glyburide
Target: Potassium Channel, Mitochondrial Metabolism, CFTR, P-gp, Autophagy
Minocycline hydrochloride
Cat.No: T1101
Synonym: Minocycline HCl,盐酸米诺环素,美满霉素
Target: HIF/HIF Prolyl-Hydroxylase, Antibacterial, Antibiotic
BMS-191095
Cat.No: T10566
Synonym:
Target: Potassium Channel
ZM 226600
Cat.No: T23563
Synonym:
Target: Potassium Channel
P-1075
Cat.No: T16420
Synonym:
Target: Potassium Channel
(Iso)-Rilmakalim
Cat.No: T26086L
Synonym:
Target: Others
OR-1896
Cat.No: T12315
Synonym:
Target: PDE
Iptakalim Hydrochloride
Cat.No: T27624
Synonym:
Target: Potassium Channel, AChR
Clamikalant
Cat.No: T71929
Synonym:
Target: Others
Way 120491
Cat.No: T35107
Synonym: Way120491,Way-120,491,Way-120491,Celikalim
Target: Others
ZM-181037
Cat.No: T70801
Synonym:
Target: Others
Ethyl tosylcarbamate
Cat.No: T11243
Synonym:
Target: Others
AZ-DF 265
Cat.No: T68602
Synonym:
Target: Others
U 56324
Cat.No: T68745
Synonym:
Target: Others
Foslevcromakalim
Cat.No: T75084
Synonym:
Target: Others
Clamikalant sodium
Cat.No: T63330
Synonym:
Target: Others
Nicorandil N-oxide
Cat.No: T84960
Synonym:
Target: Others
Desethylamiodarone hydrochloride
Cat.No: T11002
Synonym: N-desethylamiodarone hydrochloride,LB 33020 hydrochloride
Target: Others
Linogliride
Cat.No: T25739
Synonym: McN-3935,McN3935,McN 3935,Linogliridum,Linoglirida
Target: Others
Linogliride fumarate
Cat.No: T25739L
Synonym: McN 3935,McN-3935,McN3935
Target: Others
Guanosine 5’-diphosphate (sodium salt hydrate)
Cat.No: T36740
Synonym:
Target: Others
Cat. No. Product Name Target Signaling Pathways
T3929 Kaurenoic acid

Kauren-19-Oic Acid,异贝壳杉烯酸,kaurenoate,kaur-16-en-18-oic acid

Others Others
Kaurenoic acid (kaurenoate) 是一种二萜,来源于 Sphagneticola trilobata 中,可以抑制细胞因子的产生和激活 NO–cyclic GMP–PKG–ATP- 敏感型钾通道信号通路,并抑制炎症疼痛。

天然产物

Kaurenoic acid
Cat.No: T3929
Synonym: Kauren-19-Oic Acid,异贝壳杉烯酸,kaurenoate,kaur-16-en-18-oic acid
Target: Others
Cat. No. Product Name Target Signaling Pathways
T71981 Gliclazide-d4

Gliclazide-d4 is intended for use as an internal standard for the quantification of gliclazide by GC- or LC-MS. Gliclazide is a sulfonylurea and an inhibitor of pancreatic β-cell ATP-sensitive potassium (KATP) channels. It is selective for pancreatic β-cell over cardiac and arterial smooth muscle cell KATP channels. Gliclazide (5 μM) increases insulin-induced glucose uptake and glucose transporter 4 (GLUT4) translocation to the plasma membrane in a differentiated 3T3L1 adipocyte model of insulin...
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 =...

同位素标记化合物

Gliclazide-d4
Cat.No: T71981
Synonym:
Target:
Nicorandil-d4
Cat.No: T71402
Synonym:
Target:
TargetMol Loading
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