“angiotensin converting enzyme ace”的搜索结果
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GLP-1 receptor 激动剂
Lixisenatide抑制胰高血糖素释放,显着降低餐后胰高血糖素。对糖尿病(T2DM)有促进作用。
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2A-AR adrenergic 激动剂
Guanabenz acetate是a2A-AR肾上腺素能激动剂和IGRS(咪唑啉I2结合位点)选择性配体。
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GnRH 激动剂
Leuprolide Acetate是GnRH类似物;醋酸亮丙瑞林在垂体GnRH受体上起激动剂的作用。
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GnRH 激动剂
Triptorelin Acetate是一种促性腺激素释放激素激动剂(GnRH激动剂),用作乙酸盐或pamoate盐。
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GnRH 激动剂
Goserelin Acetate是具有抗肿瘤活性的促黄体激素释放激素(LHRH)的合成十肽类似物。
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progesterone receptor 激动剂
Medroxyprogesterone acetate是一种孕激素,是人激素黄体酮的合成变异体,也是一种强效的黄体酮受体激动剂。
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- Xijian Wang, .et al. Anxiety determination by antibody-conjugated nanoparticles on an interdigitated electrode sensor, 3 Biotech, 2020, Sep;10(9):377 PMID: 32802719
- Xiucui Bao, .et al. Coordinated Dispersion and Aggregation of Gold Nanorod in Aptamer-Mediated Gestational Hypertension Analysis, J Anal Methods Chem, 2019, Article ID 5676159
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TLR7 激动剂
Gardiquimod TFA是一种化合物,可选择性作用于小鼠和人类形式的Toll样受体7(TLR7)。它起免疫反应调节剂的作用。CAS:1020412-43-4(游离碱)
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5-HT1F receptor 激动剂
LY 344864 racemate是5-HT1F受体激动剂。
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Muscarinic receptor agonist
Methacholine chloride is a synthetic choline ester that acts as a non-selective muscarinic receptor agonist in the parasympathetic nervous system.
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GnRH/LHRH receptor agonist
Leuprorelin is a Gonadotropin-releasing hormone (GnRH, luteinizing hormone-releasing hormone, LHRH) receptor agonist. Suppresses estradiol, LH and FSH serum levels and represses the growth of experimental rat endometriosis.
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GnRH agonist
Nafarelin is a gonadotropin-releasing hormone agonist (GnRH agonist) which acts as an analog of GnRH.
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non-peptide PAR2 agonist
GB110 is a Novel potent non-peptide PAR2 agonist. GB-110 selectively induces PAR2-mediated intracellular Ca2+ release in HT29 cells with an EC50 of 0.28 μM.
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GPR35/CXCR8 拮抗剂
Kynurenic acid, an endogenous tryptophan metabolite, is a broad-spectrum antagonist targeting NMDA, glutamate, α7 nicotinic acetylcholine receptor. Kynurenic acid is also an agonist of GPR35/CXCR8.
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Wnt/β-catenin agonist
SKL2001 is an agonist of the Wnt/β-catenin pathway, with anti-cancer activity. SKL2001 stabilizes intracellular β-catenin via disruption of the Axin/β-catenin interaction.
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GABA receptor agonist
Acamprosate calcium(Campral EC) is a GABA receptor agonist and modulator of glutamatergic systems; reduces alcohol consumption in animal models of alcohol addiction.
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GPR35/CXCR8 agonist
Kynurenic acid sodium, an endogenous tryptophan metabolite, is a broad-spectrum antagonist targeting NMDA, glutamate, α7 nicotinic acetylcholine receptor. Kynurenic acid sodium is also an agonist of GPR35/CXCR8.
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glucocorticoid receptor agonist
Dexamethasone acetate (Dexamethasone 21-acetate) is a glucocorticoid receptor agonist.
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antinematodal thiophene nicotinic receptor agonist
Pyrantel tartrate is an antinematodal thiophene nicotinic receptor agonist and can elicit spastic muscle paralysis in parasitic worms due to prolonged activation of the excitatory nicotinic acetylcholine (nACh) receptors on body wall muscle.
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gonadotropin-releasing hormone agonist
Buserelin Acetate is a gonadotropin-releasing hormone agonist (GnRH agonist).
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glucagon-like peptide-1 receptor agonist
Exendin-4 Acetate (Exenatide acetate), a 39 amino acid peptide, is a long-acting glucagon-like peptide-1 receptor agonist with an IC50 of 3.22 nM.
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GC-C receptor agonist
Plecanatide acetate is a guanylate cyclase-C (GC-C) receptor agonist, with an EC50 of 190 nM in T84 cells. Plecanatide acetate shows anti-inflammatory activity in models of murine colitis.
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α4β2 nAChR partial agonist
Varenicline Hydrochloride (CP 526555 hydrochloride) is a high affinity, selective α4β2 nicotine acetylcholine receptor (nAChR) partial agonist and full α7 nAChR agonist.
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progesterone receptor agonist
Nomegestrol acetate is a potent, highly selective progestogen, which is characterized as a full agonist at the progesterone receptor, with no or minimal binding to other steroid receptors, including the androgen and glucocorticoid receptors.
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mAChR agonist
Oxotremorine M iodide is a potent and non-selective muscarinic acetylcholine receptor (mAChR) agonist.
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synthetic GnRH agonist
Alarelin acetate is a synthetic GnRH agonist.
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apelin agonist
Apelin agonist 1 is an oral selective apelin agonist AM-2995, a agonist of the APJ (APLNR, angiotensin receptor like-1) receptor, may be used in the treatment of cardiovascular conditions.
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Angiotensin-II subtype 2 receptor(AT2 R) agonist
CGP-42112(CGP-42112A) is a potent Angiotensin-II subtype 2 receptor(AT2 R) agonist.
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angiotensin-(1-7) receptor agonist
AVE 0991 is a nonpeptide and orally active angiotensin-(1-7) receptor agonist with an IC50 of 21 nM.
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