Others

Gemeprost, an analog of prostaglandin E1, is used for the treatment of obstetric bleeding. It is used to terminate pregnancy up to 24 weeks gestation together with mifepristone.

Metoxuron is a phenylurea herbicide. It is used to control annual gramineous weeds and broadleaf weeds in wheat, barley and carrot fields.

Flunixin is a nonsteroidal anti-inflammatory drug (NSAID), antipyretic, and analgesic used in pigs, horses, and cattle.

Octaethylporphyrin is a stable porphyrin compound used for research.

Fmoc-Dab(Boc)-OH is a chemical intermediate used for chemical synthesis.

M 12325 is used in the production of furosemide; rhinitis and occupational asthma were observed in workers from a lasamide production line.

4A3-SCC-10是一种可降解的离子型脂质（LDIL），其独特的GSH响应性圆锥形结构使其具有优异的内体逃逸能力以及快速释放mRNA的特性。

Lauramide propyl amine oxide is an amphoteric surfactant

Decamethylene glycol is a substance used as a reagent in the biological study of modified oligonucleotide with in vivo antitumoral activity. Also used in the pharmaceutical study on the composition of essential oils obtained from myrrh and frankincense an

Lilopristone is an antagonist of progesterone.

(R)-(–)-Pirlindole 是一种单胺氧化酶A (MAO-A) 的抑制剂，IC50值为0.43 µM。它对MAO-A具有选择性，而非MAO-B。(R)-(–)-Pirlindole 以50 mg/kg的剂量在小鼠强迫游泳实验中可减少不动时间。此外，它在给予25 mg/kg剂量时，可以抑制 reserpine 诱导的小鼠眼睑下垂。

Sodium N-lauroylalanine is an agent of fatty acid.

Ro 25-1553 是由 31 个氨基酸组成的血管活性肠肽 (VIP) 类似物，作为 VIP2 受体 (VPAC2 receptor) 的激动剂。在豚鼠模型中，Ro 25-1553 显示出对神经诱发或 Carbachol 诱发的气管平滑肌收缩的支气管扩张作用。

NSC-672121 is an inhibitor of Cdc25A. It is also a Vitamine K3 analog.

NL3 是细菌胱硫醚 γ-裂解酶抑制剂，IC50 值分别为 0.7 μM (bCSE) 和 3.4 μM (hCSE)。NL3 可用于研究抗菌机制以及克服细菌耐药性。

BVT-2733 hydrochloride 是一种强效、选择性且具有口服活性的非甾体类11β-HSD1抑制剂。其对小鼠11β-HSD1酶的抑制作用(IC50=96 nM)较对人11β-HSD1酶(IC50=3341 nM)更强。BVT-2733 hydrochloride 在研究关节炎和与肥胖相关的疾病方面具有潜在的应用价值。

Glycyltyrosine, a dipeptide composed of tyrosine and glycine, is an incomplete breakdown product of protein catabolism or protein digestion.

Cyclanilide is a plant growth regulator. It is used in cotton at different stages of growth.

The compound is a mechanism-based inhibitor of cytochrome P450 ω-hydroxylase.

5-HT2B receptor agonist

Jmv 167 is an antagonist of the Cholecystokinin receptor.

JNJ-7925476 is an TRI antidepressant agent.

JTE-607 is an inhibitor of cytokine production. It potentially for the treatment of systemic inflammatory response, and induces apoptosis accompanied.

Jmv 179 is an antagonist of the cholecystokinin receptor.

MK-4882 is an effective inhibitor of HCV NS5A.

L 687306 is a partial agonist of muscarinic M1 receptors. It is also a highly competitive antagonist at cardiac M2 receptors and ileal M3 muscarinic receptors.

L 659837 is an antagonist of ANC-2, lactam, and tackykinin.

R1498 is an inhibitor of cyclin-dependent kinase 2. It also acts by targeting angiogenesis and mitosis pathways. It is well-tolerated and orally active for hepatocellular carcinoma and gastric cancer treatment.

L-708906 is the Human Immunodeficiency Virus Type 1 inhibitor.

L 368935 is an antagonist of the cholecystokinin receptor.

L 858051 activates adenylate cyclase. It also inhibits glucose transport in rat adipocytes.

L 738167 is a potent antagonist of the long-acting fibrinogen receptor.

L 731734 is a farnesyltransferase inhibitor.

Fluoroclorgyline is a specific inhibitor of monoamine oxidase A (MAO-A).

Acrihellin is a cardioactive steroid, a cardiotonic drug.

Gallopamil HCl, (-)- is an L-type calcium channel blocker. It is used in the treatment of abnormal heart rhythms.