hmr

HMR 1556 is a chromanol derivative and is an IKs blocker (IC50s of 10.5 nM and 34 nM in canine and guinea pig left ventricular myocytes, respectively).

HMR-1566 is a potent and selective Iks channel blocker.

HMR1031 is a potent and specific integrin α4ß1 or very late antigen 4 (VLA-4) receptor antagonist which binds to vascular cell adhesion molecule-1 (VCAM-1) and fibronectin.

HMR-1426 is gastric emptying inhibitor. HMR1426 shows an anorectic potential in rats and decreased body weight and fat mass. This was achieved solely by reducing food intake without influencing overall energy expenditure or behavior.

Flavopiridol (Alvocidib) 是一种广谱CDK 竞争型抑制剂， 抑制 CDK1，CDK2，CDK4的IC50分别为30，170，100 nM。

AG-12286 is a pan-CDK inhibitor. AG-012986 may be useful in the treatment of tumors by inhibiting p38 MAPK phosphorylation. Note: many vendors confused the structure of AG-12286 (CAT#573461, CAS# 223784-75-6) with AG-012986 (CAT#406184, CAS# is 486414-35-1).

(E Z)-Teriflunomide (Aubagio) 是一种可口服的嘧啶合成抑制剂，用于治疗复发性多发性硬化症。

Telithromycin（泰利霉素）是一种半合成的14元大环内酯类抗生素和红霉素衍生物，结合到70S细菌核糖体的50S亚基，抑制细菌蛋白合成，对多种革兰氏阳性菌和革兰氏阴性菌具有抗菌活性，治疗轻至中度呼吸道感染。

Flavopiridol hydrochloride (MDL 107826A) 是一种CDK 的广谱抑制剂，与 ATP 竞争性地抑制 CDK1，CDK2 和 CDK4 的活性，IC50值分别为 30, 170, 100 nM。

X 910279 is a leflunomide analog and a malononitrilamide.

Pralnacasan inhibits proinflammatory cytokines IL-18, IL-1β , and IFN-γ. Pralnacasan is an effective, non-peptide, and orally active interleukin-1β converting enzyme inhibitor (Ki: 1.4 nM). Pralnacasan has the potential for osteoarthritis and rheumatoid a

Ataciguat (HMR-1766) 是一种不依赖一氧化氮的可溶性鸟苷酸环化酶 (sGC) 激活剂，具有血管舒张作用。它能够激活 sGC 的铁血红素铁氧化还原形式，刺激 cGMP 的产生。

Clamikalant sodium (HMR 1098) 是 ATP 依赖性钾通道 （KATP) 的心脏选择性阻断剂，可用于研究心律失常。

RU 58841 (PSK-3841) 是一种雄激素受体拮抗剂，能够促进头发再生。

Insulinglulisine (HMR 1964) 是一种速效胰岛素类似物，具有模拟人体生理胰岛素药代动力学和药效学特征。该化合物适用于糖尿病研究。

Aminocandin (HMR 3270) 是一种水溶性的棘白菌素类抗真菌剂 (antifungal)，对 Aspergillus 和 Candidaspp. 具有良好的活性。