fce-2

FCE-27164 is a therapeutic agent that inhibits platelet-derived growth factor beta and IL-7 binding to their receptors.

FCE-27262 is a prostaglandin H2 thromboxane A2 receptor antagonist.

FCE-27837 is a 5-alpha reductase inhibitor and hormone antagonist.

FCE-24265 is a calcium & thromboxane A2 synthase inhibitor.

FCE-24379 is a selective antagonist of vascular serotonin receptors that has been shown to lowers blood pressure in hypertensive rats.

FCE-20635是一种具有抗菌活性的头孢菌素，已被证实可有效治疗小鼠的尿路感染。

FCE-20700是一种具有细胞保护功能的PGE2衍生物。

FCE-28175 is a 5-alpha reductase inhibitor and hormone antagonist.

Romergoline 2HCl 是一种 D1 激动剂和 D2 拮抗剂，可用于研究帕金森病。

BMS-823778 是一种高效的 11β-羟基类固醇脱氢酶 1 型（11β-HSD-1）的抑制剂，可用于研究 2 型糖尿病。

Safinamide mesylate (EMD 1195686 mesylate) 是选择性的、有效的、可逆的单胺氧化酶 B 的抑制剂，对 MAO-A 选择性较低。它能够阻断钠通道和调节谷氨酸释放。它具有神经保护作用，可用于研究帕金森病、缺血脑卒中等疾病。

FCE 28073是一种 Monoamine oxidase B 抑制剂，IC50=0.45 μM。

Tallimustine (FCE 24517)，一种 distamycin-A 衍生物，是一种抗癌剂。

PNU-145156E (FCE26644) a novel angiogenesis inhibitor, has been shown to block circulating angiogenesis promoting growth factor in animal studies and has shown anti-tumor effects in solid tumors in mice.

Fce 22250 is a broad-spectrum antibiotic that is active against Mycobacterium.

(R,R)-Reboxetine mesylate 是一种抗抑郁药，具有良好的生物利用度。(R,R)-Reboxetine 为 Reboxetine 的对映体之一，属于选择性去甲肾上腺素再摄取抑制剂。Reboxetine 本身包含 (R,R) 与 (S,S) 两种对映体，且对 α-肾上腺素能和毒蕈碱受体的亲和力较低，表现出较低的动物毒性。

Cabergoline diphosphate is a dopamine D2 receptor agonist used for prolactinoma treatment. Cabergoline permits rapid and effective hormonal and tumor control by normalizing prolactin-producing pituitary adenomas levels.

Fce 21258 is used to stimulate the adenylate cyclase of synovial fluid macrophages.

FCE 28654 is a water-soluble acyl-CoA inhibitor.

Fce 28260 is a 5 alpha-reductase inhibitor.

XuBP is a potent inhibitor of ribulose-1,5-bisphosphate carboxylase oxygenase (Rubisco).

Rolafagrel is a novel inhibitor of thromboxane synthase.

GR-127935 is a potent and selective 5-HT1B 1D receptor antagonist.

Pibrozelesin is a water-soluble derivative of duocarmycin B2 that alkylates DNA by binding to adenine-thymine (A-T)-rich sequences in the minor groove of DNA, thereby inhibiting DNA replication and inducing apoptosis.