Others

SCH-451659 is an 17β-hydroxysteroid dehydrogenases (17β-HSDs) inhibitor.

ADU-S100 (MIW815) enantiomer ammonium salt is the less active enantiomer of ADU-S100, an activator of the stimulator of interferon genes (STING).

(2E)-Hex-2-en-1-yl Hexanoate是一种酯类化合物，广泛应用于生物化学实验和药物合成研究。

Vanitiolide (Vanitiolid) 是一种具有利胆作用的药物。

DAO-IN-2是一个片段分子，CAS号为39793-31-2，可作为分子拼接、扩展和修饰的重要骨架，为新型候选药物的设计与筛选提供结构基础与研究工具，常用于药物发现、药物合成等相关研究。

STING agonist 12b is an agonist of stimulator of interferon genes (STING).1It binds to STING (Kd= 26.4 μM) and induces interferon reporter gene expression in cells expressing human or mouse STING (EC50s = 7.45 and 10.23 μM, respectively). STING agonist 12b (40 μM) induces expression of TNF-a, IL-6, IP-10, and IL-1b in THP-1 cells. 1.Hou, S., Lan, X.-j., Li, W., et al.Design, synthesis and biological evaluation of acridone analogues as novel STING receptor agonistsBioorg. Chem.95103556(2020)

Tubulin polymerization-IN-9 是一种微管蛋白 (tubulin) 的有效抑制剂 (IC50: 1.82 μM)。Tubulin polymerization-IN-9 能够将 K562 细胞的细胞周期停滞在 G2/M 期，并诱导其凋亡 (apoptosis) 及线粒体去极化。Tubulin polymerization-IN-9 表现出强大的抗血管和抗肿瘤作用。

CI-949 is an allergic mediator release inhibitor, which inhibits leukotriene C4/D4 (LTC4/LTD4), histamine, and thromboxane B2 (TXB2) release (IC50s: 0.5 μM, 11.4 μM and 0.1 μM).

L-156,602 在生命科学相关研究中具有广泛的应用。

FTEAA为4-苯乙烯基哌啶类MAO抑制剂，对MAO-A与MAO-B展现出显著的抑制活性，其IC50值分别为0.52 μM与1.02 μM。该类抑制剂在心血管、神经系统及肿瘤相关研究中有广泛应用。

Cbz-N-PEG10-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.

Cholesteryl Laurate是一种胆固醇酯，广泛应用于生物化学实验和药物合成研究。

trans-5-Hydroxyferulic acid 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T126397，CAS号为 110642-42-7。

Antitubercular agent-31 是一种抗结核剂，能够抑制M. tuberculosisH37Rv (MIC: 0.03 μM)，也能够抑制DprE1 (IC50: 1.1 μM)。

NU223612 是一种有效的PROTAC(PROTACs)，可降解吲哚胺 2,3-双加氧酶 1 (IDO1) (Indoleamine 2,3-Dioxygenase (IDO))，Kd 为 640 nM。NU223612 通过CRBN 介导的蛋白酶体降解有效降解IDO1蛋白。NU223612 以 290 nM 的亲和力与 CRBN 结合。NU223612 可以穿过血脑屏障 (BBB)。

Sabcomeline 是一种有效的功能性选择性 M1 毒蕈碱受体受体 (muscarinic M1 receptor) 部分激动剂，可以改善认知功能。Sabcomeline 可用于阿尔茨海默症的研究。

S 17092 (S 17092-1) is a highly effective inhibitor of cerebral prolyl-endopeptidase (PEP), displaying an IC50 value of 1.2 nM. It is utilized in research focused on understanding memory impairment and cognitive disorders associated with cerebral aging [1].

UKI-1 is a urokinase-type plasminogen activator system synthetic inhibitor.

STING-IN-6 (compound 50) 是一种有效的STING 抑制剂，pIC50为 8.9。STING-IN-6 具有免疫研究的潜力。

DBCO-NHCO-PEG2-Biotin 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.

Crocin-4, a carotenoid compound found in saffron, possesses potent antioxidant properties and can penetrate the brain. It effectively inhibits the aggregation and deposition of Aβ fibrils, making it useful for Alzheimer's Disease research. Additionally, Crocin-4 demonstrates antitumor and anti-inflammatory activities.

PIM-447 dihydrochloride is an orally available and selective inhibitor of pan-PIM kinase(Ki values of 6, 18, and 9 pM for PIM1, PIM2, and PIM3, respectively).

Potent NK1 antagonist

DMT-dA(PAc) Phosphoramidite 是一种亚磷酰胺单体，可用于 DNA 或 RNA 的合成。

Carumonam Sodium is a monobactam, penicillin-binding protein inhibitor. It is used as antibacterials.

BMS-502 是一种二酰基甘油激酶 (DGK) α 和 ζ 的强效双重抑制剂， 诱导人和小鼠T细胞的免疫反应，阻断 T 细胞中细胞内检查点信号传导。BMS-502 以剂量依赖的方式刺激免疫反应，可用于研究与免疫相关的疾病。

Diaporthein B 是氧化程度极高的 pimarane 二萜之一。Diaporthein B 表现出抗结核分枝杆菌的活性，MIC 为 3.1 μg/mL。Diaporthein B 显示对 HCT 116 和 LoVo 结肠癌细胞的 IC50为 1.5-3 μM/L。

Nucleoside Derivatives - 8-Modified purine nucleoside; Azido-nucleoside

DMG-PEG 2000 (DMG-PEG2000) 可用于脂质纳米颗粒制备，用于口服质粒 DNA 的体内传递途径，提高纳米颗粒的黏液渗透性和传递效率。DMG-PEG 2000 可用于 siRNA 转染的脂质体的制备，能够提高转染效率。

Cajucarinolide is a clerodane diterpene. It inhibits bee venom phospholipase A2 in vitro. Cajucarinolide possesses anti-inflammatory activity.

Diketone-PEG11-PFP ester serves as a PEG-based PROTAC linker for PROTAC synthesis[1].

Hydroxy-PEG3-PFP ester 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.

Ciwujianoside E 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN3672，CAS号为 114912-36-6。

Sultopride is a compound that an amino on the sulfamide group of sulpiride is replaced by an ethyl group.

KRAS G12C inhibitor 43 是 KRAS G12C 的有效抑制剂，能够抑制 H358 细胞 (IC50: 0.001-1 μM μM)、 A549 细胞 (IC50>1 μM)、 HCC 细胞 (IC50>1 μM) 的迁移和增殖。

Cloprostenol isopropyl ester is a PGF2α agonist and a similar synthetic prostaglandin F2α (PGF2α), which can induce luteal dissolution in mares during the luteal phase without causing clinical side effects or stress responses.