this compound

Antiasthmatic Compound 1 is an antiasthmatic agent.

Antimicrobial Compound 1 是一种烷基吡啶鎓化合物，尾部为 12C，头部为 4-羧基。 Antimicrobial Compound 1 对枯草芽孢杆菌和大肠杆菌具有抗菌活性。

Antibacterial compound 1 is an antibacterial compound.

Asthma relating compound 1是一种潜在的抗哮喘化合物。

Antibacterial compound 2 是一种有效的抗菌剂，对许多人类兽医病原体有效，对多重耐药葡萄球菌、肠球菌和链球菌，以及厌氧菌有抑制作用。

Neuromuscular-targeting compound 1 可用于研究肌肉萎缩和神经肌肉相关疾病。

Cancer-Targeting Compound 1可用于激素相关癌症的研究，包括治疗或预防肌瘤、子宫平滑肌瘤、多囊卵巢综合征或激素依赖性癌等等。

Compound H 通过Klotho 基因CpG 岛的去甲基化诱导Klotho 的表达。

Compound 1T-0216 是AKT1-FAK 相互作用的阻滞剂，在不影响基础FAK 磷酸化的情况下，减少对人类SW620结肠癌细胞细胞外压力的FAK 磷酸化的刺激。

Compound 48/80是一种组胺释放剂，通过激活肥大细胞表面的G蛋白偶联受体，提高细胞内钙离子浓度并激活phospholipase D，诱导细胞脱颗粒和类过敏性休克等炎症。

Neuromuscular Disorder-Targeting Compound 1 is utilized in research for neuromuscular disorders, including chronic fatigue syndrome and fibromyalgia syndrome symptoms.

NPS ALX Compound 4a is a potent and selective antagonist of 5-HT6 receptor (IC50 of 7.2 nM)

NPS ALX Compound 4a dihydrochloride is a potent and selective antagonist of 5-HT6 receptor (IC50 of 7.2 nM)

Barbaloin-related compound B 是一种有用的有机化合物，可用于生命科学领域的相关研究，其产品编号为 T124814。

Barbaloin-related compound A 是一种有用的有机化合物，可用于生命科学领域的相关研究，其产品编号为 T124815。

(R)-Clopidogrel bisulfate (Clopidogrel Related Compound C) 是一种氯吡格雷异构体。Clopidogrel 是一种 P2Y12 受体拮抗剂，可降低血小板聚集，用于抑制冠状动脉疾病、周围血管疾病和脑血管疾病中的血凝块。

Neurodegenerative Disorder-Targeting Compound 1 是一种靶向 calpain 的抑制剂。

Arrhythmias-Targeting Compound 1 is a compound. It is used in the research of arrhythmias.

Compound 48/80 trihydrochloride (C48/80 trihydrochloride) 是 N-甲基对甲氧基苯乙胺和甲醛发生缩合反应后的混合物。Compound 48/80 trihydrochloride 是一种肥大细胞 (mast cell) 脱颗粒剂和组胺 (histamine) 释放剂。Compound 48/80 trihydrochloride 对人血小板磷脂酰肌醇特异性磷脂酶 C (phosphatidylinositol-specific phospholipase C) 活性有抑制作用。

Arrhythmic-Targeting Compound 1 is used for arrhythmic disease, with nitrogen-containing spirocycles.

Compound 2 is used for the research of metabolic bone diseases.

Urinary Incontinence-Targeting Compound 1, used in the research of urinary incontinence, is a sulfonanilide derivative.

Calcium influx inducer compound 634 是一种钙内流诱导剂。Calcium influx inducer compound 634 (10 µM) 增加小鼠骨髓来源树突状细胞 (mBMDCs) 外泌体 (EVs) 的释放，并提升 mBMDCs 表面CD86和CD80的水平，这种效应可被钙释放激活钙通道抑制剂YM-58483 阻断。

A22 is an inhibitor of MreB, an actin-like bacterial protein, and has been proved to be an antibiotic adjuvant. A22 inhibition of MreB disrupts the bacterial actin cytoskeleton, which can cause an increase in cell permeability and altered transport.