Sulfosuccinimidyl oleate sodium是一种长链脂肪酸，作为有效且不可逆的线粒体呼吸链抑制剂。它通过结合小胶质细胞上的 CD36 受体，阻止脂肪酸转运，具有显著的抗炎作用。该化合物在代谢和炎症相关疾病研究中具有潜在的应用价值。

ABT-737 是一种选择性的 Bcl-2 家族蛋白抑制剂，能够有效抑制 Bcl-2、Bcl-xL 和 Bcl-w 的活性，IC50 值分别为 30.3 nM、78.7 nM 和 197.8 nM。ABT-737 主要用于研究细胞凋亡、抗癌治疗和增强肿瘤对化疗药物的敏感性。

Pinosylvin, a natural product isolated and purified from the herbs of Pinus yunnanensis, can induce autophagy via AMPK activation. Pinosylvin has anti-inflammatory activity, may be utilized as a phytotherapic agent for the prevention of cardiovascular inflammatory diseases.

GSK2578215A is a brain-penetrant, potent and selective LRRK2 inhibitor with IC50 values of 8.9 and 10.1 nM for LRRK2[G2019S] mutant and wild-type LRRK2, respectively.

AC55649 is an agonist of the retinoic acid receptor β (RAR-β).

N-dodecanoyl-L-Homoserine lactone是一种群体感应信号分子，可抑制铜绿假单胞菌 (Pseudomonas aeruginosa) 生物膜的形成，通过阻止细菌的群体感应机制发挥抗菌作用，适用于抗感染及微生物研究。

JGB1741是一种特异性的 SIRT1 抑制剂，IC₅₀ 为 15 μM，通过增加乙酰化 p53 的水平，调节 Bax/Bcl2 比率，诱导细胞凋亡，具有用于乳腺癌等肿瘤研究的潜力。

SU11274 is a selective Met inhibitor with IC50 of 10 nM, no effects on PGDFRβ, EGFR or Tie2.

ZPCK 是吉西他滨的前体，具备口服活性，旨在提高其口服生物利用度。

Peiminine, a natural product isolated and purified from the bulbus of Fritillaria thunbergii Miq., is an effective inhibitor for lung inflammation and pulmonary fibrosis in a rat model of bleomycin-induced lung injury.It induces autophagic cell death thus represses colorectal carcinoma tumor growth.

Tolcapone is a potent, selective and orally active catechol-O-methyltransferase (COMT) inhibitor with Ki of 30 nM.

Danshensu, a herbal preparation used in traditional Chinese medicine, possesses potential antitumor and antiangiogenesis effects.

Oroxin B, a natural product isolated and purified from the roots of Scutellaria baicalensis., can selectively induce tumor-suppressive ER stress and concurrently inhibit tumor-adaptive ER stress in B-lymphoma cells for effective anti-lymphoma therapy.

FTI-277 HCl is an inhibitor of farnesyl transferase (FTase) and a highly potent Ras CAAX peptidomimetic which antagonizes both H- and K-Ras oncogenic signaling.

Deoxypodophyllotoxin, a natural microtube inhibitor isolated and purified from the roots of Dysosma versipellis (Hance) M.Cheng ex Ying, is cytotoxic agent, antineoplastic agent and potent antitumor agent and may be beneficial in regulating the immediate-type allergic reaction.

SBI-0640756是一种 eIF4G1 抑制剂，能够有效破坏 eIF4F 复合体。它在抑制癌细胞增殖和研究翻译调控方面具有潜在的应用价值。

WYC-209 is a RAR agonist which induces apoptosis primarily via the caspase 3 pathway.

Niacin-d4是 Niacin 的氘代物，而 Niacin (烟酸) 是维生素 B 家族的一员。

Rilmenidine Phosphate is an oxazole-derived agonist of adrenergic receptor α2 and Imidazoline receptor, used in trials studying the treatment of hypertension and chronic kidney disease.

SID-852843是一种 WNV NS2B-NS3 蛋白酶抑制剂，能够抑制其活性，IC₅₀ 为 0.105 μM，广泛用于病毒感染的研究。