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搜索结果：“angiotensin converting enzyme ace”

“angiotensin converting enzyme ace”的搜索结果

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LY2886721

Catalog No. A10543
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BACE1 抑制剂

LY2886721是一种有效的，选择性的，口服活性的β位淀粉样蛋白前体蛋白裂解酶 1 (BACE1) 抑制剂。LY2886721是一种新型强效药物，用于治疗阿尔茨海默病的研究。了解更多

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- Naomi Ito, .et al. miR-15b mediates oxaliplatin-induced chronic neuropathic pain through BACE1 down-regulation, Br J Pharmacol, 2017, Mar; 174(5): 386-395 PMID: 28012171
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BMS-708163 (Avagacestat)

Catalog No. A10157
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Gamma-secretase 抑制剂

BMS-708163 (Avagacestat)是口服生物有效的，选择性的γ-分泌酶抑制剂，作用于Aβ40和Aβ42时，IC50分别为0.3 nM和0.27 nM。了解更多

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BTZ043 (BTZ038, BTZ044) Racemate

Catalog No. A10165
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DprE1 抑制剂

BTZ043 (BTZ038,BTZ044) Racemate 抑制癸二烯基磷酸基-β-d-核糖2α-表异构酶，它是一种产生致病细菌结核分枝杆菌细胞壁的酶。了解更多

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Anacetrapib (MK-0859)

Catalog No. A11084
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CETP 抑制剂

Anacetrapib (MK-0859)是一种有效的，选择性，可逆的rhCETP和突变CETP(C13S)抑制剂，IC50分别为7.9 nM和11.8 nM，提高HDL-C，降低LDL-C，不提高醛固酮和血压。了解更多

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Clinofibrate

Catalog No. A11184
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HMG-CoA Reductase 抑制剂

Clinofibrate是一种脂质清除剂，似乎可以改变脂质代谢，减少类固醇诱导的骨细胞内脂质堆积。它还可以有效降低血浆纤维蛋白原水平。抑制hydroxymethylglutaryl coenzyme A reductase (HMGCR)（羟甲基戊二酰辅酶A还原酶），IC50为0.47 mM。了解更多

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Semagacestat (LY450139)

Catalog No. A10836
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Gamma-secretase 抑制剂

Semagacestat (LY450139)是一种针对Aβ42，Aβ40和Aβ38的γ-分泌酶阻滞剂，IC50分别为10.9 nM，12.1 nM和12.0 nM。 Semagacestat还抑制Notch信号传导，IC50为14.1 nM。了解更多

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- Yesuvadian R, .et al. Potent γ-secretase inhibitors/modulators interact with amyloid-β fibrils but do not inhibit fibrillation: a high-resolution NMR study., Biochem Biophys Res Commun., 2014, May 16;447(4):590-5 PMID: 24747079
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Tubacin

Catalog No. A10954
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HDAC6 抑制剂

Tubacin (tubulin acetylation inducer)是一种高效且选择性强，可逆，可透过细胞的HDAC6抑制剂，IC50为4 nM。了解更多

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Acetanilide

Catalog No. A10031
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Hydrogen peroxide 抑制剂

Acetanilide在过氧化氢中用作抑制剂，并用于稳定纤维素酯清漆。了解更多

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LY2811376

Catalog No. A11776
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BACE1 抑制剂

LY2811376是第一种可口服的非肽类BACE1抑制剂，可在动物体内产生显着的Aβ降低作用。了解更多

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Aniracetam

Catalog No. A10078
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AMPA Receptor 抑制剂

Aniracetam是一种安非他命，属于消旋体化学类别的促智药，据称比吡乙酰胺更有效。了解更多

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Enalaprilat dihydrate

Catalog No. A10351
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RAAS 抑制剂

Enalaprilat dihydrate是依那普利的活性代谢产物。它是第一种含二羧酸盐的ACE抑制剂，IC50为1.2 nM。了解更多

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CI994 (Tacedinaline)

Catalog No. A11964
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HDAC 抑制剂

CI994 (Tacedinaline)是一种组蛋白脱乙酰基酶（HDAC）抑制剂，可在活细胞中诱导组蛋白超乙酰化。了解更多

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Apocynin (Acetovanillone)

Catalog No. A11989
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NADPH-oxidase 抑制剂

Apocynin (Acetovanillone)是NADPH氧化酶抑制剂。了解更多

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- Liling Su, .et al. Disruption of mitochondrial redox homeostasis as a mechanism of antimony-induced reactive oxygen species and cytotoxicity, Ecotoxicol Environ Saf, 2022, Jun 1;237:113519 PMID: 35453021
- Shimizu S, .et al. Angiotensin II, a stress-related neuropeptide in the CNS, facilitates micturition reflex in rats, Br J Pharmacol, 2018, Sep;175(18):3727-3737 PMID: 29981238
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Evacetrapib (LY2484595)

Catalog No. A11397
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CETP 抑制剂

Evacetrapib (LY2484595)是一种强效选择性CETP抑制剂，IC50为5.5 nM，可在不增加醛固酮或血压的情况下升高HDL胆固醇。了解更多

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Bay 11-7821

Catalog No. A11957
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E2 ubiquitin conjugating enzyme 抑制剂

Bay 11-7821是TNF-α刺激的IκBα磷酸化的不可逆抑制剂。了解更多

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- Ali Nasrollahzadeh, .et al. Blockade of Nuclear Factor-??b (NF-??b) Pathway Using Bay 11-7082 Enhances Arsenic Trioxide-Induced Antiproliferative Activity in U87 Glioblastoma Cells, Rep Biochem Mol Biol, 2022, Jan;10(4):602-613 PMID: 35291620
- Ali Nasrollahzadeh, .et al. Arsenic trioxide and BIBR1532 synergistically inhibit breast cancer cell proliferation through attenuation of NF-κB signaling pathway, Life Sci, 2020, Jul 6;257:118060 PMID: 32645343
- Momeny M, .et al. Blockade of nuclear factor-κB (NF-κB) pathway inhibits growth and induces apoptosis in chemoresistant ovarian carcinoma cells, Int J Biochem Cell Biol, 2018, Jun;99:1-9 PMID: 29567488
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Benazepril HCl

Catalog No. A10123
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RAAS 抑制剂

Benazepril hydrochloride是一种非肽血管紧张素转化酶（ACE）抑制剂。降低自发性高血压大鼠的血压和心肌肥大。了解更多

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Cilazapril monohydrate

Catalog No. A11747
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ACE 抑制剂

Cilazapril monohydrate是哒嗪血管紧张素转换酶抑制剂（ACE抑制剂），用于治疗高血压和充血性心力衰竭。了解更多

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Temocapril

Catalog No. A11749
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ACE 抑制剂

Temocapril是一种ACE抑制剂。了解更多

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Enalapril maleate

Catalog No. A10350
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ACE 抑制剂

Enalapril maleate是一种血管紧张素转换酶（ACE）抑制剂，用于治疗高血压和某些类型的慢性心力衰竭。了解更多

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