Others

HS-1793 是 resveratrol 类似物，可以诱导细胞凋亡，在多种癌细胞中有抗肿瘤的能力。

TRPC5-IN-1是一种TRPC5抑制剂，在各种慢性肾病动物模型中均具有活性。

(±)-Befunolol is a blocking agent of β-adrenoceptor.

Acotiamide hydrochloride 是选择性的、口服具有活力的、可逆的乙酰胆酶碱酯 (AChE) 抑制剂 (IC50: 1.79 μM)，能够提高胃收缩性，加速胃排空延迟，能够用于研究胃动力障碍的功能性消化不良及肠道炎症。

TH1085是OGG1的增强剂。 TH1085 刺激 DNA 修复并保护细胞免受环境危害百草枯 (PQ) 的侵害。

111-Trifluoroethyl-PEG4-amine is a polyethylene glycol (PEG)-based linker suitable for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

DX2-201 是一种有效的、选择性的氧化磷酸化 (OXPHOS) 复合物 I 抑制剂 (IC50: 312 nM)，表现出抗癌活性。

DL-Isocitric acid trisodium salt (Standard) 是一种可用于分析的标准物质，通常用作 DL-Isocitric acid trisodium salt 的研究和分析中参考的标准样品。DL-Isocitric acid trisodium salt 是内源性代谢产物的一种。

SKI-I 是有效的、选择性的人鞘氨醇激酶 (SK) 抑制剂。SKI-I 抑制ST-hSK 的IC50值为 1.2 μM。SKI-I 也是hERK2的抑制剂(IC50=11 μM)。SKI-I 诱导肿瘤细胞系的凋亡。

Gadodiamide 是一种含钆造影剂，可用于医学成像。

MK-6240 is a tau positron emission tomography (PET) tracer for neurofibrillary tangles (NFTs). MK-6240 exhibits high specificity and selectivity for binding to NFTs.

653-47 是一种增强剂，能显著增强 666-15 的 cAMP 反应元件结合蛋白(CREB)抑制活性。653-47 也是一种非常弱的CREB 抑制剂，IC50值为 26.3 μM。

PPARγ agonist 3, also known as Compound 18a, is a potent and selective agonist of PPARγ. This compound does not exhibit cytotoxicity towards both non-resistant and resistant cells. Notably, PPARγ agonist 3 demonstrates antitumor efficacy exclusively when co-administered with Imatinib [1].

Cathayanon J是一种天然的黄酮，广泛应用于生物化学实验和药物合成研究。

Echinoside B shows anti-tumor activities in vitro and vivo.

D-Glucosyl-β-1,1′-N-palmitoylsphingosine (C16 Glucosyl(β) Ceramide (d18:1/16:0)) 是内源性Mincle配体，具免疫刺激活性。

B10-S 是有效的抗过敏剂，对 P 物质诱导的 LAD2 脱颗粒具有抑制作用。

Proglumide hemicalcium is a antagonist of nonpeptide and orally active cholecystokinin (CCK)-A/B receptors, has antiepileptic and antioxidant activities.

Methylamino-PEG1-acid 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.

Fmoc-His(Trt)-OH为一种人工合成的有机化合物，用于生命科学研究，提供用于肽合成、官能化及化学生物学实验的反应性平台。

Citroside A is a natural product from Cirsium setosum.

m-PEG5-phosphonic acid ethyl ester is a polyethylene glycol (PEG)-derived linker commonly employed in the construction of proteolysis targeting chimeras (PROTACs)[1].

2,5-dimethyl-2,5-hexanediol是一种不饱和醇，可用于生物化学实验和药物合成研究。

LXR (Liver X receptor) agonist 1 是 LXR 的有效激动剂，能够作用于 LXR-α (AC50: 1.5 nM) 和 LXR-β (AC50: 12 nM)。LXR agonist 1 对动脉粥样硬化表现出研究潜力。

(S)-PNU-282987 is the absolute stereochemistry form of PNU-282987. PNU 282987, a potent agonist of α7-containing neuronal nicotinic acetylcholine receptors (nAChRs) with Ki of 26 nM for the rat receptor, has negligible activity against α1β1γδ and α3β4 nAC

p-Tolyl isobutyrate是一种芳香类化合物，广泛应用于生物化学实验和药物合成研究。

Symphytine is a natural inducer of hepatic tumors. Symphytine interacts with DNA in liver endothelial cells and hepatocytes, resulting in DNA damage, mutation induction, and cancer development.

PrPSc-IN-1 is a fluorescent probe, binds to the misfolded protein PrPSc, inhibits its accumulation(IC50 of 1.6 μM), with anti-prion activity.

GPX-100 (13-deoxydoxorubicin) 是蒽环类抗肿瘤抗生素多柔比星的类似物。GPX-100 插入DNA 并与拓扑异构酶II 相互作用，从而抑制DNA 复制和修复以及RNA 和蛋白质合成。

1,2-POPS sodium salt 是一种脂质，可用于合成人工脂质膜和合成运输化合物的脂质体。

5'(R)-C-Methylguanosine is a Nucleoside Derivative - 5'-Modified nucleoside.

Abacavir hydroxyacetate 是一个具有口服活性的核苷类似物逆转录酶抑制剂.具有抗 HIV 和免疫调节活性，在小鼠模型中诱导动脉血栓形成，可用于研究 HIV 感染。

DNP-PEG6-acid 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.

Antibacterial Agent 42 demonstrates potent antibacterial activity by effectively reducing the Minimum Inhibitory Concentration (MIC) of the broad-spectrum antibacterial agent Ceftazidime.

PR-104A is a hypoxia-targeted anticancer agent.

Pelecopan (BCX9930) 是有效的、选择性的口服补体因子D 抑制剂 (IC50= 14.3 nM)。Pelecopan 可以预防PNH 中的血管内和血管外溶血。