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55

抑制剂 & 化合物

3

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Cat. No. Product Name Target Signaling Pathways
T6928 Pantoprazole

SKF96022,泮托拉唑,BY1023

Apoptosis; Proton pump; Autophagy Apoptosis; Autophagy; Membrane transporter/Ion channel
Pantoprazole (BY1023) 是一种质子泵抑制剂,用于短期治疗由胃食管反流病引起的食管糜烂和溃疡。它联合阿霉素可显著增加肿瘤生长延迟。它是一种取代的苯并咪唑,是H+/K+-ATPase 抑制剂,可改善 pH 值稳定性,具有抗分泌和抗溃疡的作用。
T0161 Pantoprazole Sodium Hydrate

SKF96022 sodium hydrate,泮托拉唑钠水合物,BY1023 (sodium hydrate),SKF96022 (sodium hydrate)

Apoptosis; Potassium Channel; Proton pump; Autophagy Apoptosis; Autophagy; Membrane transporter/Ion channel
Pantoprazole Sodium Hydrate (BY1023 (sodium hydrate)) 是一种具有口服活性的质子泵抑制剂。它是取代的苯并咪唑,是H+/K+-ATPase 抑制剂。它可改善 pH 值稳定性,具有抗分泌和抗溃疡的作用。它联合阿霉素可显著增加肿瘤生长延迟。
T6929 Pantoprazole sodium

Pantecta,泮托拉唑钠盐,SKF96022 sodium,SKF96022 (sodium),BY1023 (sodium),泮托拉唑钠,BY-1023 sodium,Pantoloc

Apoptosis; Others; Proton pump; HIF; Autophagy Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; Membrane transporter/Ion channel; Others
Pantoprazole sodium (Pantecta) 是一种具有口服活性的质子泵抑制剂,是一种取代的苯并咪唑,是H+/K+-ATPase 抑制剂,IC50为 6.8 μM。它可以改善 pH 值稳定性,具有抗分泌和抗溃疡的作用。它联合阿霉素可显著增加肿瘤生长延迟。
T17030 Tegoprazan

ATPase; Proton pump Membrane transporter/Ion channel
Tegoprazan 是一种口服有效的、高选择性胃 H+/K+-ATP 酶 (H+/K+-ATPase) 抑制剂,能够控制胃酸分泌和运动,在体外检测的对猪、犬、人的 H+/K+-ATP 酶的 IC50为0.29-0.52 μM。
T2404 Vonoprazan fumarate

富马酸沃诺拉赞,TAK-438

ATPase Membrane transporter/Ion channel
Vonoprazan fumarate (TAK-438) 是一种新型 P-CAB(钾竞争性酸阻滞剂),可可逆地抑制 H+/K+、ATP 酶。
T21254 Vonoprazan Fumarate

TAK-438,TAK 438,Vonoprazan Fumurate,TAK438,富马酸沃诺拉赞

Proton pump Membrane transporter/Ion channel
Vonoprazan Fumarate (TAK438) 是质子泵的有效抑制剂,是口服有效的高效钾竞争性酸阻断剂,具有抗分泌活性。在 pH 为 6.5 时,它抑制猪胃微粒体中的 H+,K+-ATPase 酶活性,IC50为 19 nM。它被开发用于研究酸相关疾病,如消化性溃疡和胃食管反流病。
T16865 SCH28080

ATPase; Proton pump Membrane transporter/Ion channel
SCH28080 是一种可逆且具有 K+ 竞争性的胃 H+/K+-ATP 酶 (H+/K+-ATPase) 抑制剂,IC50 值为 20 nM (家兔微粒体膜)。SCH28080 在体内是有效的酸分泌抑制剂,具有抗溃疡活性、抗分泌和细胞保护活性。
T28136 NC-1300-B

NC1300B,NC 1300 B

ATPase Membrane transporter/Ion channel
NC-1300-B 抑制 H(+)-K(+)-ATP 酶,可用于研究胃溃疡。
T10435 Linaprazan

利那拉生,AZD0865

Potassium Channel Membrane transporter/Ion channel
Linaprazan (AZD0865) 通过K+竞争抑制胃中的H+,K+ -ATPase. (IC 50: 1.0 ± 0.2 μM)。Linaprazan 对酸有很强的抑制作用。
T9553 8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxylic acid

Others Others
8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-car 是一种 H+/K+ ATPase 抑制剂,IC50=0.38μM。
T27812 Leminoprazole

ATPase Membrane transporter/Ion channel
Leminoprazole 是一种可口服的 H+,K(+)-ATPase 抑制剂,可保护胃黏膜细胞免受各种细胞损伤,可用于治疗胃溃疡。
T19826 Rabeprazole

LY307640

Potassium Channel; STAT JAK/STAT signaling; Membrane transporter/Ion channel; Stem Cells
Rabeprazole (LY307640) 是一种 H+/K+-ATPase 抑制剂,通过靶向 STAT3 介导的糖酵解来抑制胃上皮细胞中的细胞增殖,可用于研究胃溃疡。
T1651 Rabeprazole sodium

Dexrabeprazole Sodium,LY307640 sodium,Habeprazole Sodium,雷贝拉唑钠,Rebeprazole sodium,Aciphex Sodium

Apoptosis; Proton pump Apoptosis; Membrane transporter/Ion channel
Rabeprazole sodium (Habeprazole Sodium) 是一种质子泵抑制剂,不可逆地抑制胃 H+/K+-ATPase,可研究胃溃疡和胃食管反流。它诱导细胞凋亡,也抑制尿苷核苷核糖水解酶 ,IC50为 0.3 μM。
T20714 Levolansoprazole

左旋兰索拉唑,(S)-Lansoprazole,(-)-Lansoprazole

Proton pump Membrane transporter/Ion channel
Levolansoprazole ((S)-Lansoprazole) 是一种质子泵抑制剂,不可逆地抑制壁细胞中 H+/K+ 刺激的 ATPase 泵 (IC50: 5.2 µM)。它还抑制分离的犬壁细胞中的酸形成(IC50:82 µM)。 (R)-和 (S)-兰索拉唑均具有药理活性,具有相似的效力。
T1756 Ilaprazole sodium

IY-81149 sodium,艾普拉唑钠

Proton pump; TOPK MAPK; Membrane transporter/Ion channel
Ilaprazole sodium (IY-81149 sodium) 是一种具有口服活性质子泵抑制剂,以剂量依赖性方式不可逆地抑制 H+/K+-ATPase,在兔壁细胞制剂中的 IC50为 6 μM。它也是一种有效的 T 细胞起源蛋白激酶(TOPK)抑制剂,用于胃溃疡的研究。
T0674 Lansoprazole

兰索拉唑,A-65006,AG-1749

Proton pump; Phospholipase; Antibacterial Membrane transporter/Ion channel; Metabolism; Microbiology/Virology
Lansoprazole (A-65006) 是一种可抑制胃酸生成的质子泵抑制剂。它是中性鞘磷脂酶的外泌体抑制剂。
T8388 Vonoprazan

TAK-438 (free base),沃诺拉赞

Proton pump Membrane transporter/Ion channel
Vonoprazan (TAK-438 (free base)) 是一种质子泵抑制剂,是口服活性钾竞争性酸阻断剂,有抗分泌作用。在 pH 为 6.5 时,它抑制猪胃微粒体中的 H+,K+-ATPase 酶活性,IC50值为 19 nM。它可用于研究胃酸相关疾病。
T1756L Ilaprazole

IY81149,艾普拉唑,IY 81149,IY-81149

Proton pump; TOPK MAPK; Membrane transporter/Ion channel
Ilaprazole (IY-81149) 是一种具有口服活性质子泵抑制剂,以剂量依赖性方式不可逆地抑制H+/K+-ATPase,在兔壁细胞制剂中的IC50为 6 μM。它也是一种有效的T 细胞起源蛋白激酶(TOPK)抑制剂,用于胃溃疡的研究。
T10221 Abeprazan hydrochloride

DWP14012 hydrochloride,Fexuprazan hydrochloride

Proton pump Membrane transporter/Ion channel
Abeprazan hydrochloride (Fexuprazan hydrochloride) 是一种有效的、可逆的、具有口服活性的potassium-competitive acid 阻滞剂,通过竞争性的与钾离子结合抑制 H+,K+- ATPase,而无需酸激活。Abeprazan hydrochloride 是一种质子泵抑制剂(PPI),通过减少胃酸的产生而起作用,可用于治疗胃酸相关疾病,如胃食管反流病(GERD)和消化性溃疡。
T2686L Esomeprazole Sodium

埃索美拉唑钠,(S)-Omeprazole sodium

ATPase; Proton pump Membrane transporter/Ion channel
Esomeprazole Sodium ((S)-Omeprazole sodium) 是一种口服有效的活性质子泵抑制剂。Esomeprazole sodium 通过抑制胃壁细胞中的 H+, K+-ATPase 来降低酸分泌,在胃食管反流疾病中有研究价值。Esomeprazole 是一种外泌体抑制剂,通过抑制 V-H+-ATPases 来阻断外泌体的释放。
T2686 Esomeprazole Magnesium

(S)-Omeprazole magnesium,NEXIUM,埃索美拉唑镁,(-)-Omeprazole magnesium

ATPase; Proton pump Membrane transporter/Ion channel
Esomeprazole Magnesium (NEXIUM) 是一种口服有效的 H+, K+-ATPase 抑制剂,在上消化道疾病和胃食管反流疾病中具有研究价值。Esomeprazole magnesium 是一种外泌体抑制剂,通过抑制 V-H+-ATPases 来阻断外泌体的释放。
T2093 PF 03716556

PF-3716556

ATPase Membrane transporter/Ion channel
PF 03716556 (PF-3716556) 是一种有效且特异性的 P-CAB(钾竞争性酸阻滞剂),用于治疗胃食管反流病。
T0825 Ebselen

SPI-1005,PZ-51,依布硒,CCG-39161

Phosphatase; Virus Protease; Calcium Channel; COX; HIV Protease Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience; Proteases/Proteasome
Ebselen (CCG-39161) 是一种谷胱甘肽过氧化物酶模拟物,是电压依赖性钙通道阻断剂。它抑制Mpro 和COVID-19病毒,是HIV-1衣壳 CTD 二聚化的抑制剂,具有抗炎、抗癌和抗氧化活性。
T8386 Esomeprazole Magnesium trihydrate

埃索美拉唑镁三水合物,埃索美拉唑镁(三水),(S)-Omeprazole magnesium trihydrate

Proton pump Membrane transporter/Ion channel
Esomeprazole Magnesium trihydrate ((S)-Omeprazole magnesium trihydrate) 是一种口服有效的H+, K+-ATPase 抑制剂,在上消化道疾病和胃食管反流疾病的研究中具有价值。它是一种外泌体抑制剂,通过抑制 V-H+-ATPases 来阻断外泌体的释放。
T1734 Rabeprazole Sulfide

雷贝拉唑相关物质E,Rabeprazole Related Compound E

Proton pump; Antibacterial Membrane transporter/Ion channel; Microbiology/Virology
Rabeprazole Sulfide (Rabeprazole Related Compound E) 是 Rabeprazole 的活性代谢产物。Rabeprazole 是一种质子泵抑制剂类的抗溃疡药物,有效抑制幽门螺旋杆菌的活性,可通过与胃壁细胞中的(H+/K+)-ATPase 相互作用来抑制胃酸分泌,可研究各种消化系统疾病。
T12471 Picoprazole

Others Others
Picoprazole is a specific H+/K+-ATPase inhibitor (IC50 of 3.1±0.4 μM).
T12822 S3337

Others Others
S3337 is an inhibitor of H+, K+-ATPase
T16894 SKF96067

Others Others
SKF96067 is a reversible gastric H+/K+-ATPase inhibitor.
T12977 Soraprazan

BYK61359

Others Others
Soraprazan is a reversible, and fast-acting gastric H+/K+ ATPase inhibitor.
T23685 AHR-9294

AHR-9294 is a novel inhibitor of H, K-ATPase. It also antagonizes gastric HCl secretion in vivo.
T30250 AZD0865

AZD-0865,AZD 0865

AZD0865 is an effective drug that inhibits gastric H(+), K(+) -ATPase activity and acid formation in vitro, with rapid onset.
T69801 AU-461

AU-461 is a gastric H(+)/K(+) ATPase inhibitor which acts as an anti-ulcer agent.
T28563 Ro 18-5364

Ro-18-5364,Ro 185364

Ro 18-5364 is a potent inhibitor of the gastric (H+ + K+)-ATPase with an apparent Ki of 0.1 μM at pH 6.
T76374 SPAI-1

SPAI-1,特异性单价阳离子ATP酶抑制剂,源自猪十二指肠。能体外抑制Na+,K+-ATP酶和H+,K+-ATP酶,同时刺激Mg2+-ATP酶。
T26450 A 80915A

A80915A,A-80915A

A 80915A is A semi-naphthoquinone antibiotic from Streptomyces aculeolatus. It is a potent inhibitor of gastric (H(+)-K+)-ATPase. Inhibition by A80915A is dependent on the conformation of gastric (H(+)-K+)-ATPase, potassium slows the rate of inhibition by
T27092 CS-526

R-105266,R 105266,R105266

CS-526 is a proton pump inhibitor. The inhibitory mechanism of CS-526 on H+,K+-ATPase was a competitive antagonism to the K+ binding site of H+,K+-ATPase, and it was also a reversible inhibition. CS-526 has a potent antisecretory effect on gastric acid se
T28609 Rohitukine

NSC623611,NSC-623611,NSC 623611

Rohitukine is an anti-cancer agent. It modulates apoptosis pathways through gastrin antagonism and H(+) K (+)-ATPase inhibition. Rohitukine ia an antiadipogenic, antidyslipidemic, gastroprotective, antifertility, and antileishmanial compound.
T20660 Revaprazan

SB-641257,SB 641257,SB641257

Revaprazan is a novel, selective potassium-competitive acid blocker, to be specific, it reversibly inhibits gastric H(+)/K(+)-ATPase and shows effective acid suppression comparable to PPIs.
T72812 (R)-Tegoprazan

(R)-Tegoprazan (example 3) 是一种苯并咪唑衍生物,是一种有效的胃H+/K+-ATP 酶抑制剂,对犬肾 Na+/K+-ATPase 的IC50为 98 nM。(R)-Tegoprazan 具有胃肠道疾病研究的潜力。
T36530 Pantoprazole sulfone

Pantoprazole sulfone is a metabolite of the gastric H+/K+ ATPase pump inhibitor pantoprazole . Pantoprazole is metabolized by the cytochrome P450 (CYP) isoforms CYP2C19 and CYP3A4 to form pantoprazole sulfone.
T37247 Pantoprazole Sulfide

Pantoprazole sulfide is a metabolite of the gastric H+/K+ ATPase pump inhibitor pantoprazole . Pantoprazole is metabolized by the cytochrome P450 (CYP) isomers CYP2C19 and CYP3A4 to form pantoprazole sulfide.
T28156 Nepaprazole

TY-11345,TY11345,TY 11345

Nepaprazole is a proton pump inhibitor. TY-11345 potently inhibited H+/K(+)-ATPase activity in isolated rabbit gastric mucosal microsomes, and the inhibitory effect was enhanced under weak acid conditions, the IC50 being 5.8 microM and 9.9 microM at pH 6.
T10221L Abeprazan

DWP14012

Others Others
Abeprazan (DWP14012) is a potassium-competitive acid blocker and it is developed as a potential alternative to proton pump inhibitor for the treatment of acid-related diseases[1]. Abeprazan inhibits H+, K+- ATPase by reversible potassium-competitive ionic
T61467 Esomeprazole magnesium salt

Esomeprazole magnesium salt is a potent and orally active proton pump inhibitor that effectively reduces acid secretion in gastric parietal cells by inhibiting the H+, K+-ATPase. This compound has shown promise for the research and treatment of symptomatic gastroesophageal reflux disease [1][2][3].
T61445 Tenatoprazole sodium

Tenatoprazole sodium (TU-199 sodium) is a potent proton pump inhibitor that effectively suppresses the activity of hog gastric H+/K+-ATPase, a vital enzymatic pump involved in acid secretion. It achieves this inhibition at an impressive IC50 value of 6.2 μM.
T62316 P-CAB agent 1

P-CAB agent 1 (compound B19) 是一种高效的钾离子竞争性酸阻滞剂,能够作用于 H+/K+-ATPase (IC50: 60.50 nM)。P-CAB agent 1 在大鼠中具表现出接受的口服吸收度。P-CAB agent 1 能够用于酸相关疾病 (ARDs) 的研究。
T61740 Esomeprazole hemistrontium

Esomeprazole hemistrontium, also known as (S)-Omeprazole, is a potent and orally active proton pump inhibitor that effectively reduces acid secretion by inhibiting the H+, K+-ATPase in gastric parietal cells. This compound exhibits promising potential for research in symptomatic gastroesophageal reflux disease [1] [2] [3].
T61667 Esomeprazole potassium salt

Esomeprazole potassium salt ((S)-Omeprazole potassium salt) is an effective and orally active proton pump inhibitor that works by inhibiting the H+, K+-ATPase enzyme in the gastric parietal cells, leading to a reduction in acid secretion. It is a promising compound for investigating symptomatic gastroesophageal reflux disease [1] [2] [3].
T78218 Ilaprazole sodium hydrate

IY-81149 sodium hydrate

Proton pump Membrane transporter/Ion channel
Ilaprazole (IY-81149) sodium hydrate是一种具有口服活性的质子泵抑制剂,可以量依赖性地不可逆抑制H+/K+-ATPase,并在兔壁细胞制剂中展示出IC50为6μM的效力。该化合物主要用于胃溃疡的研究,并已证实是一种有效的T细胞起源蛋白激酶(TOPK)抑制剂。
T37659 5-hydroxy Omeprazole

5-hydroxy Omeprazole is a major metabolite of omeprazole , an inhibitor of the gastric H+/K+-ATPase pump.[1] 5-hydroxy Omeprazole is produced from omeprazole by the action of cytochrome P450 (CYP) isoform 2C19, a monooxygenase. [2][3] CYP2C19 polymorphisms significantly influence the metabolism of omeprazole, and individuals may be classified as homozygous extensive metabolizers, heterozygous extensive metabolizers, and poor metabolizers.[1]

化合物

Pantoprazole
Cat.No: T6928
Synonym: SKF96022,泮托拉唑,BY1023
Target: Apoptosis, Proton pump, Autophagy
Pantoprazole Sodium Hydrate
Cat.No: T0161
Synonym: SKF96022 sodium hydrate,泮托拉唑钠水合物,BY1023 (sodium hydrate),SKF96022 (sodium hydrate)
Target: Apoptosis, Potassium Channel, Proton pump, Autophagy
Pantoprazole sodium
Cat.No: T6929
Synonym: Pantecta,泮托拉唑钠盐,SKF96022 sodium,SKF96022 (sodium),BY1023 (sodium),泮托拉唑钠,BY-1023 sodium,Pantoloc
Target: Apoptosis, Others, Proton pump, HIF, Autophagy
Tegoprazan
Cat.No: T17030
Synonym:
Target: ATPase, Proton pump
Vonoprazan fumarate
Cat.No: T2404
Synonym: 富马酸沃诺拉赞,TAK-438
Target: ATPase
Vonoprazan Fumarate
Cat.No: T21254
Synonym: TAK-438,TAK 438,Vonoprazan Fumurate,TAK438,富马酸沃诺拉赞
Target: Proton pump
SCH28080
Cat.No: T16865
Synonym:
Target: ATPase, Proton pump
NC-1300-B
Cat.No: T28136
Synonym: NC1300B,NC 1300 B
Target: ATPase
Linaprazan
Cat.No: T10435
Synonym: 利那拉生,AZD0865
Target: Potassium Channel
8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxylic acid
Cat.No: T9553
Synonym:
Target: Others
Leminoprazole
Cat.No: T27812
Synonym:
Target: ATPase
Rabeprazole
Cat.No: T19826
Synonym: LY307640
Target: Potassium Channel, STAT
Rabeprazole sodium
Cat.No: T1651
Synonym: Dexrabeprazole Sodium,LY307640 sodium,Habeprazole Sodium,雷贝拉唑钠,Rebeprazole sodium,Aciphex Sodium
Target: Apoptosis, Proton pump
Levolansoprazole
Cat.No: T20714
Synonym: 左旋兰索拉唑,(S)-Lansoprazole,(-)-Lansoprazole
Target: Proton pump
Ilaprazole sodium
Cat.No: T1756
Synonym: IY-81149 sodium,艾普拉唑钠
Target: Proton pump, TOPK
Lansoprazole
Cat.No: T0674
Synonym: 兰索拉唑,A-65006,AG-1749
Target: Proton pump, Phospholipase, Antibacterial
Vonoprazan
Cat.No: T8388
Synonym: TAK-438 (free base),沃诺拉赞
Target: Proton pump
Ilaprazole
Cat.No: T1756L
Synonym: IY81149,艾普拉唑,IY 81149,IY-81149
Target: Proton pump, TOPK
Abeprazan hydrochloride
Cat.No: T10221
Synonym: DWP14012 hydrochloride,Fexuprazan hydrochloride
Target: Proton pump
Esomeprazole Sodium
Cat.No: T2686L
Synonym: 埃索美拉唑钠,(S)-Omeprazole sodium
Target: ATPase, Proton pump
Esomeprazole Magnesium
Cat.No: T2686
Synonym: (S)-Omeprazole magnesium,NEXIUM,埃索美拉唑镁,(-)-Omeprazole magnesium
Target: ATPase, Proton pump
PF 03716556
Cat.No: T2093
Synonym: PF-3716556
Target: ATPase
Ebselen
Cat.No: T0825
Synonym: SPI-1005,PZ-51,依布硒,CCG-39161
Target: Phosphatase, Virus Protease, Calcium Channel, COX, HIV Protease
Esomeprazole Magnesium trihydrate
Cat.No: T8386
Synonym: 埃索美拉唑镁三水合物,埃索美拉唑镁(三水),(S)-Omeprazole magnesium trihydrate
Target: Proton pump
Rabeprazole Sulfide
Cat.No: T1734
Synonym: 雷贝拉唑相关物质E,Rabeprazole Related Compound E
Target: Proton pump, Antibacterial
Picoprazole
Cat.No: T12471
Synonym:
Target: Others
S3337
Cat.No: T12822
Synonym:
Target: Others
SKF96067
Cat.No: T16894
Synonym:
Target: Others
Soraprazan
Cat.No: T12977
Synonym: BYK61359
Target: Others
AHR-9294
Cat.No: T23685
Synonym:
Target:
AZD0865
Cat.No: T30250
Synonym: AZD-0865,AZD 0865
Target:
AU-461
Cat.No: T69801
Synonym:
Target:
Ro 18-5364
Cat.No: T28563
Synonym: Ro-18-5364,Ro 185364
Target:
SPAI-1
Cat.No: T76374
Synonym:
Target:
A 80915A
Cat.No: T26450
Synonym: A80915A,A-80915A
Target:
CS-526
Cat.No: T27092
Synonym: R-105266,R 105266,R105266
Target:
Rohitukine
Cat.No: T28609
Synonym: NSC623611,NSC-623611,NSC 623611
Target:
Revaprazan
Cat.No: T20660
Synonym: SB-641257,SB 641257,SB641257
Target:
(R)-Tegoprazan
Cat.No: T72812
Synonym:
Target:
Pantoprazole sulfone
Cat.No: T36530
Synonym:
Target:
Pantoprazole Sulfide
Cat.No: T37247
Synonym:
Target:
Nepaprazole
Cat.No: T28156
Synonym: TY-11345,TY11345,TY 11345
Target:
Abeprazan
Cat.No: T10221L
Synonym: DWP14012
Target: Others
Esomeprazole magnesium salt
Cat.No: T61467
Synonym:
Target:
Tenatoprazole sodium
Cat.No: T61445
Synonym:
Target:
P-CAB agent 1
Cat.No: T62316
Synonym:
Target:
Esomeprazole hemistrontium
Cat.No: T61740
Synonym:
Target:
Esomeprazole potassium salt
Cat.No: T61667
Synonym:
Target:
Ilaprazole sodium hydrate
Cat.No: T78218
Synonym: IY-81149 sodium hydrate
Target: Proton pump
5-hydroxy Omeprazole
Cat.No: T37659
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
TQ0184 Chebulinic acid

ATPase; Proton pump; DNA/RNA Synthesis; Antibacterial; TGF-beta/Smad Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Stem Cells
Chebulinic acid 是从诃子果中提取的一种天然产物,结核分枝杆菌 DNA 促旋酶的有效抑制剂。它也能抑制 SMAD-3 phosphorylation 和 H+ K+-ATPase 的活性。
TN4697 Odoroside H

ATPase; Potassium Channel; Sodium Channel Membrane transporter/Ion channel
Odoroside H has anticancer activities, the cytotoxic effects are induced by the inhibition of the plasma membrane bound Na(+)/K(+)-ATPase.
T38069 Aquastatin A

Aquastatin A is a fungal metabolite originally isolated fromF. aquaeductuumthat has diverse biological activities.1It is active againstS. aureus(MIC = 32 μg/ml) and inhibits enoyl-acyl carrier protein reductase (Fabl; IC50= 3.2 μM) andS. aureusfatty acid synthesis (IC50= 3.5 μM).2Aquastatin A also inhibits the Na+/K+-ATPase and H+/K+-ATPase (IC50s = 7.1 and 6.2 μM, respectively), as well as protein tyrosine phosphatase 1B (PTP1B; IC50= 0.19 μM).1,3 1.Hamano, K., Kinoshita-Okami, M., Minagawa, K....

天然产物

Chebulinic acid
Cat.No: TQ0184
Synonym:
Target: ATPase, Proton pump, DNA/RNA Synthesis, Antibacterial, TGF-beta/Smad
Odoroside H
Cat.No: TN4697
Synonym:
Target: ATPase, Potassium Channel, Sodium Channel
Aquastatin A
Cat.No: T38069
Synonym:
Target:
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