Others

BoNT-IN-1(compound 8)是一种高效的A型肉毒杆菌神经毒素轻链(Clostridium botulinum neurotoxin serotype A light chain, BoNT/A LC)抑制剂, IC50=0.9 uM。BoNT/A LC是锌依赖性的金属蛋白酶, BoNT-IN-1通过Zn2+螯合基序起到抑制作用。

M2 ion channel blocker ,Antiviral agent, is capable of inhibiting and blocking the activity of M2 ion channel.

Sulfoxone sodium ( Adesulfone Sodium) is an anti-leprosy drug.

5-O-Benzoyl-1,2-O-isopropylidene-alpha-D-xylofuranose is a Carbohydrate; Used for modified nucleoside.

Bis-propargyl-PEG11 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.

STING agonist 1a is an agonist of stimulator of interferon genes (STING).1It induces expression of an IRF-inducible SEAP reporter gene in a cell-based assay (EC50= 16.77 μM). STING agonist 1a (12.5-100 μM) induces expression of IFN-β, IL-6, and chemokine (C-X-C motif) ligand 10 (CXCL10) in THP-1 cells, an effect that can be reversed by STING knockout or the STING inhibitor H-151 . 1.Hou, H., Yang, R., Liu, X., et al.Discovery of triazoloquinoxaline as novel STING agonists via structure-based virtual screeningBioorg. Chem.100103958(2020)

Elobixibat (A 3309) 是回肠胆汁酸转运蛋白的抑制剂(小鼠、人和犬 IBAT 的 IC50：0.13 nM、0.53 nM 和 5.8 nM)。 Elobixibat 可用于慢性特发性便秘的研究。

NH2-UAMC1110 TFA 是 UAMC1110 带有氨基丁氧基的衍生物，用于合成 FAPI-QS。UAMC1110 是一种新型选择性成纤维细胞活化蛋白 (fap) 抑制剂，对相关二肽基肽酶 (dpps) dppiv、dpp9、dppii、和（prep）表现出低纳摩尔抑制力和高选择性。

PI3K-IN-22 是 PI3Kα 和 mTOR 双重激酶抑制剂，IC50s 分别为 0.9、0.6 nM。PI3K-IN-22 可用于癌症研究。

Emoxypine Succinate 是一种抗氧化剂。

BM-1244 is a potent Bcl-xL/Bcl-2 inhibitor with Kis of 134 and 450 nM for Bcl- xL and Bcl-2, respectively. BM-1244 inhibits senescent fibroblasts (SnCs) with an EC50 of 5 nM[1].

Albanol B 是一种芳基苯并呋喃衍生物，可从桑葚中分离得到。Albanol B 具有抗阿尔茨海默病、抗菌和抗氧化活性。Albanol B 抑制癌细胞增殖，下调 CDK1表达。Albanol B 还会诱导细胞周期停滞在 G2/M 期，诱导细胞凋亡 (apoptosis)。Albanol B 诱导线粒体 ROS 产生并增加 AKT 和 ERK1/2的磷酸化水平。

SENP1-IN-4, a distinct inhibitor of the deSUMOylation protease 1 (SENP1), is designed to enhance tumor radiosensitivity.

11-deoxy Prostaglandin E1 是前列腺素 E1类似物，具有支气管扩张活性，可抑制组胺诱导的支气管收缩，引起离体豚鼠的气管条松弛。

UNC3474为小分子配体，与53BP1相结合。该化合物针对53BP1TT的芳香族甲基赖氨酸结合笼展现出1.0 ± 0.3μM的解离常数（Kd）。UNC3474抑制53BP1募集至DSB，其机制为稳定细胞内预存的53BP1自抑制状态。

Trimetazidine是一种无关血流动力学的抗心绞痛剂，能够选择性地抑制mitochondrial enzyme 3-ketoacyl coenzyme A thiolase（LC 3-KAT）从而防止游离脂肪酸的β-氧化，IC50 值为 75 nM。Trimetazidine通过改变心脏代谢防止缺血再灌注损伤，具有抗氧化和抗缺血伤害的作用。

Cichorioside B是一种天然产物，可用于生物化学实验和药物合成研究。

MIR002 是一种有效的、口服具有活力的 DNA polymerase α (POLA1) 和 HDAC 11 双重抑制剂，具有显著的体内抗肿瘤活性。MIR002 能够诱导 p53 乙酰化、激活 p21，将细胞周期阻滞在 G1/S 期，并诱导细胞凋亡。

ZY-444具有潜在的抗癌活性，抑制 PCa 细胞的增殖和转移，抑制皮下肿瘤的生长。

Laminaran 是一种从褐藻中分离出来的 β-1-3-葡聚糖，常作为 Dectin-1 的典型配体，具有抗癌、免疫调节和辐射防护作用。 Laminaran 可被葡糖酶催化。Laminaran 在体内外实验中显示出抗肿瘤活性，可用于预防和治疗癌症。

Levofloxacin sodium is a synthetic fluoroquinolones antibacterial. It inhibits the supercoiling activity of bacterial DNA gyrase, so that halting DNA replication.

Drinidene is a bio-active chemical. Detailed information has not been published.

Nebicapone is a reversible catechol-O-methyltransferase (COMT) inhibitor and is mainly metabolized by glucuronidation. Nebicapone is mainly peripherally acting inhibitor that decreases the biotransformation of L-DOPA to 3-O-methyl-DOPA by inhibition of CO

CL67 is a hypoxia-inducible factor pathway inhibitor. It acts by binding to a G-quadruplex higher-order structure in the HIF promoter sequence in vitro.

EMT inhibitor-2 inhibits CYP3A4 testosteron and CYP2C9 with IC50s of 49.72 and 5.54 μM, respectively. EMT inhibitor-2 inhibits epithelial-mesenchymal transition (EMT) induced by substances such as IL-1β and TGF-β released from the immunocytes.

YKL-5-124 TFA是一种高效、选择性不可逆的CDK7共价抑制剂，具有53.5 nM对CDK7的IC50值和9.7 nM对CDK7/Mat1/CycH的IC50值。此化合物对CDK7的选择性超过CDK9和CDK2 100倍以上，对CDK12和CDK13则无活性。YKL-5-124 TFA能显著诱导细胞周期停滞，抑制E2F驱动的基因表达，对RNA聚合酶II的磷酸化状态影响微乎其微。

Rhein 8-Glucoside 是一种蒽醌糖苷，存在于大黄 (rhubarb) 中，显示出泻下活性。

Sodium 1-heptanesulfonate monohydrate是可用于离子对色谱的试剂，可用于分析多肽和蛋白质等生物分子。

endo-BCN-PEG6-Boc 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.

Vonifimod 是一种免疫调节剂。

N-Benzyl-N-bis-PEG2 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.

3-Ethylbenzoic acid是一种芳香化合物，广泛应用于生物化学实验和药物合成研究。

L-aspartic acid potasium salt（VX-548） 是一种广泛存在于动植物体内的氨基酸。L-aspartic acid potasium salt驱动氮氧化物的产生，从而促进吞噬作用，有助于提高鱼类的成活率。L-aspartic acid potasium salt 可对抗生素产生刺激，刺激作用可能与参与天冬氨酸-4-半醛生物合成的前体有关。

PEG4-bis(phosphonic acid diethyl ester) is a polyethylene glycol (PEG) derivative serving as a linker for PROTAC synthesis. It is specifically designed for the creation of proteolysis-targeting chimeras (PROTACs)[1].

3-Chloro-5-hydroxybenzoic acid 是一种口服具有活力的乳酸受体GPR81选择性激动剂，对人 GPR81 的EC50为 16 μM。肥胖小鼠模型中，它表现出良好的体内脂肪分解作用。