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Mepixanox is an analeptic drug. It is used for treating respiratory and cardiorespiratory insufficiency.

VEGFR-2/BRAF-IN-1 是一种 VEGFR-2和 BRAF 双重抑制剂，对 VEGFR-2、BRAFV600E 和BRAFWT 的IC50分别为 0.049、0.063 和 0.005 µM。VEGFR-2/BRAF-IN-1 诱导细胞凋亡，在 G1/S 期阻滞细胞周期。

Argireline (Acetyl hexapeptide-3) 是可渗透皮肤的、无毒的抗皱肽。它对神经肌肉接头处依赖 Ca2+的神经递质释放具有显著的抑制作用。它具有抗皱和抗衰老的活性。

3,5,5-Trimethyl-2-cyclohexen-1-ol是一种不饱和环醇，广泛应用于生物化学实验和药物合成研究。

Isothiuronium (AHR 1911) 是一种蛋白合成抑制剂，具有抗菌抗炎活性，可诱导细胞凋亡并减少黑色素瘤细胞的侵袭，可用于研究皮炎。

N-Acetyl-DL-phenylalanine β-naphthyl ester 为一芳香族氨基酸酯，用作糜蛋白酶及微生物丝氨酸蛋白酶（例如枯草杆菌蛋白酶）的显色底物。

N-Ethylpyrrolidine是一种吡咯衍生物，广泛应用于生物化学实验和药物合成研究。

Glycolithocholic acid 3-sulfate (disodium) 是抑制HIV-1复制的化合物，同时它也被用于HIV感染和胆囊疾病的研究。

Boc-NH-PEG2-C2-NH2 (PROTAC Linker 13) is a PEG-based linker utilized for the synthesis of PROTACs. This chemical compound plays a crucial role in connecting the targeted protein and the E3 ubiquitin ligase for selective protein degradation[1].

Emodin-8-glucoside (Anthraglycoside B) 是从芦荟中分离出的蒽醌衍生物，与 DNA 的小沟结合。它具有保护缺血和再灌注引起的局灶性脑损伤的作用。它直接刺激成骨细胞的细胞增殖和分化。

SCH00013 is an agent of cardiotonic that primarily acts via an increase in myofibrillar Ca++ sensitivity. SCH00013 have a significant Ca(2+)sensitizing effect at pH 7.2 to 7.4.

Azaphilone-9 (AZA-9) 通过结合RNA结合蛋白Hu抗原R (HuR) 抑制HuR-ARERNA相互作用的抑制剂(IC50=1.2 μM)。HuR-RNA相互作用稳定了肿瘤中的许多致癌mRNA。因此，Azaphilone-9可能对抑制癌细胞的生长和进展具有潜力。

TIE-2/VEGFR-2 kinase-IN-4，一种苯并咪唑衍生物，作为有效的TIE-2和VEGFR-2酪氨酸激酶受体抑制剂，其IC50值分别为5.2 nM和5.1 nM，适用于血管生成相关研究。

Azido-PEG3-S-PEG4-t-butyl ester is a PEG-based PROTAC linker employed for PROTAC synthesis[1].

Ro-24-0238 is an antagonist of platelet-activating factor and inhibitor of thromboxane synthesis. Ro-24-0238 used for lessening the inflammation and damage resulting from a local release of PAF.

JW 480 是一种有效的丝氨酸水解酶 KIAA1363选择性抑制剂。

(+)-Biotin-PEG12-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Momordicoside L has hypoglycaemic / antihyperglycaemic activities.

Methyl hexacosanoate(二十六酸甲酯)是一种长链脂肪酸酯，可用于有机合成和生化实验。

CCK-B Receptor Antagonist 1 is a cholecystokinin B (CCK-B) receptor agonist and has the potential of reducing the secretion of gastric acid.

carfenazine 靶向多巴胺受体，用于精神分裂症研究。

ZXH-4-137 is a potent and selective CRBN degrader ( PROTAC ).

LDHA-IN-5为新型且有效的GO/LDHA双重抑制剂，旨在治疗原发性高草酸尿。

Boc-Aminoxy-PEG4-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Tubulysin B is an agent of potent microtubule destabilizing and highly cytotoxic peptide isolated from the myxobacteria Archangium geophyra and Angiococcus disciformis.

Nucleoside Derivatives - Didehydro-nucleosides

Benzyl-PEG7-azide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Maltoheptaose hydrate, a maltooligosaccharide composed of seven glucose units, serves as an activator of phosphorylase B for the preparation of heptulose-2-phosphate.

4-Ethyl-1,2-dimethylbenzene是一种芳香烃，广泛应用于生物化学实验和药物合成研究。

Bufrolin，作为Cromoglycate（组胺释放抑制剂）的类似物，是一种高效的GPR35激动剂，能够促进β-arrestin-2与人GPR35a或大鼠GPR35之间的相互作用。此外，Bufrolin亦可作为抗过敏性肥大细胞稳定剂，有效抑制内化肽诱导的抗炎反应，并且在内化肽连接药剂的药物递送研究中，被作为抗炎剂使用。

2'-C-Methyl uridine is a 2'-C-Methyl nucleoside.

PROTACBCR-ABL1 ligand 1，化合物 GMB-475， 是靶向蛋白水解的嵌合体 (PROTAC) 的配体，其以变构方式靶向 BCR-ABL1蛋白并募集 E3 连接酶 Von Hippel-Lindau，从而导致泛素化和随后的 BCR-ABL1 蛋白的降解。

Penta-N-acetylchitopentaose, a chemical compound, elicits the activation of plant defense systems. This compound also functions as a substrate for the Rhizobium leguminosarum nodulation protein NodL.

O-2050 是一种高亲和力的大麻素CB1受体拮抗剂，Ki 为 2.5 nM。O-2050 抑制大麻素 CB2受体，Ki 为 0.2 nM。O-2050 减少了小鼠的食物摄入量，并且引起小鼠运动。

Netupitant N-oxide is a highly selective antagonist of NK1 receptor, is Netupitant metabolite.

KW-8232, an orally active anti-osteoporotic agent, reduces the biosynthesis of PGE2[1].