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2′-Deoxy-5-nitrocytidine 是一种 DNA 甲基转移酶(DNMT)的抑制剂，可用于癌症领域研究。

MK-8245 analog 是 MK-8245 的类似物，MK-8245 是一种肝脏靶向的硬脂酰辅酶 A 去饱和酶 (SCD) 抑制剂。它可用于治疗血脂异常和糖尿病。

FTase-IN-1 (compound 17a) is a highly effective inhibitor of fanesyl transferase (FTase), exhibiting a remarkable IC50 value of 0.35 μM. This compound demonstrates significant cytotoxicity potential and exhibits powerful antitumor activity [1].

W1131 是一种有效的STAT3抑制剂，可引发铁死亡。W1131 在胃癌皮下异种移植模型、类器官模型和 PDX 模型中抑制癌症进展。W1131 有效减轻癌细胞对 5-FU 化学耐药性。W1131 调节细胞周期、DNA 损伤反应和氧化磷酸化，包括IL6-JAK-STAT3通路和铁死亡 (ferroptosis) 通路。

Desmorpholinyl Quizartinib-PEG2-COOH is a compound featuring an FLT-3 ligand and a PEG-based PROTAC linker. It is employed in the synthesis of PROTAC FLT-3 degrader 1, which serves as a degrader for the FLT-3 internal tandem duplication (ITD) through PROTAC technology. The degrader exhibits an IC50 of 0.6 nM.

RS 0481 可调节免疫应答，可重建因动物体内肿瘤的生长而受损的淋巴细胞群。

Cholic Acid (Standard) 是一种可用于分析的标准物质，通常用作 Cholic Acid 的研究和分析中参考的标准样品。Cholic Acid (Cholate) 是肝脏产生的主要胆汁酸，与牛磺酸或甘氨酸缀合，有助于脂肪吸收和胆固醇排泄。

Gly-His-Lys acetate 是一种血浆三肽，可促进细胞培养体系中的细胞生长及分化。

RIPK1-IN-3 is a RIPK1 inhibitor, with anti-inflammatory proprieties.

MC-1-F2 是一种 FOXC2 直接抑制剂，具有抗癌活性，抑制癌症干细胞 (CSC) 特性，降低去势抵抗性前列腺癌 (CRPC) 细胞系的侵袭能力。MC-1-F2 可用于研究前列腺癌。

SC144 hydrochloride 是首创的口服活性gp130 (IL6-beta)抑制剂。SC144 hydrochloride 结合 gp130，诱导 gp130 磷酸化(S782) 和去糖基化，消除 Stat3 磷酸化和核易位，进而抑制下游靶基因的表达。SC144 hydrochloride 对 gp130 配体触发的信号转导显示有效的抑制作用。SC144 hydrochloride 诱导人卵巢癌细胞凋亡。

SR8278 是竞争性核血红素受体REV-ERB 合成拮抗剂，能够抑制 REV-ERBα 转录活性(EC50:0.47 μM)。它可用于调节生物体内的代谢和研究生物节律。

Udonitrectag (REC 0559) is a low molecular weight compound developed to emulate the behavior of NGF, with the objective of tackling the challenge of maintaining NGF stability.

7-epi-Isogarcinol 是一种PPAP（多环聚异戊二烯酰基间苯三酚），显示出适度的抗增殖活性。它通过阻断STAT3信号通路，诱导apoptosis（细胞凋亡）并抑制细胞迁移作用。

Cytostatin is a natural antitumor inhibitor of cell adhesion to extracellular matrix, blocking adhesion of B16 melanoma cells to laminin and collagen type IV in vitro (IC50s = 1.3 and 1.4 μg/ml, respectively) and B16 cells metastatic activity in mice. It induces apoptosis of FS3 mouse fibrosarcoma cells (IC50 = 3.1 μg/ml). Cytostatin potently and selectively inhibits protein phosphatase 2A (PP2A; IC50 = 29 nM against the catalytic subunit), while having no effect against PP1, PP2B, or PP5.

Methyltetrazine-PEG5-alkyne, a PEG-based PROTAC linker, is utilized in synthesizing PROTACs[1].

AHR-5333 an antiallergy agent.

Ms-PEG4-Ms 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.

Acid-PEG6-mono-methyl ester is a polyethylene glycol (PEG)-based PROTAC linker appropriate for synthesizing PROTACs. [1]

Piperacillin sodium (Standard) 是一种可用于分析的标准物质，通常用作 Piperacillin sodium 的研究和分析中参考的标准样品。Piperacillin sodium salt(CL227193) )是一种β-内酰胺类广谱抗生素。

Amitriptylinoxide is an antidepressant.

Capecitabine (Standard) 是一种可用于分析的标准物质，通常用作 Capecitabine 的研究和分析中参考的标准样品。Capecitabine (Capecitibine) 是一种可口服的前药，可由胸苷磷酸化酶催化转变为其活性代谢物 Fluorouracil。

Pulcherriminic acid 是环状二肽抗菌剂，对Fe3+有高亲和力，主要在芽孢杆菌和酵母中发现。该化合物通过非酶促反应与铁离子螯合，生成细胞外红色素pulcherrimin，通过竞争铁营养达到抗菌效果。Pulcherriminic acid 在食品、农业和医疗等领域具有广泛应用潜力。

JAK3/BTK-IN-5 是一种 JAK3/BTK 的有效抑制剂。其中 BTK 和 JAK3 是自身免疫性疾病的两个关键的靶点。同时抑制 BTK/JAK3 信号通路具有协同效应。JAK3/BTK-IN-5 对 JAK3 激酶和/或 BTK 相关疾病具有潜在的研究价值。

(R)-Amlodipine 是 Amlodipine 的 R-对映体，作为一种口服活性的二氢吡啶类钙通道阻滞剂，具有抗心绞痛特性。(R)-Amlodipine 通过阻断电压依赖性 L 型钙通道，从而减少细胞内钙离子流入并发挥作用。(R)-Amlodipine 可用于高血压和癌症相关研究，其对钙通道的调控能力为研究心血管疾病和肿瘤相关病理生理学提供了机制基础。

Dipsacoside B 是主要的具有生物活性的皂素，可用作标志物。

3-Aminodihydrofuran-2(3H)-one hydrochloride是一种呋喃衍生物，广泛应用于生物化学实验和药物合成研究。

LmCPB-IN-1 (compound 35) is a highly effective and reversible covalent inhibitor of Leishmania mexicana cysteine protease B (LmCPB). It exhibits a strong binding affinity with a pK i value of 9.7 [1].

Thalidomide-NH-C8-NH2 hydrochloride is a synthetic compound, which functions as an E3 ligase ligand-linker conjugate. It consists of a cereblon ligand derived from Thalidomide, along with a linker commonly used in PROTAC technology.

Alibendol (cebera) 具有促胆汁分泌及抗痉挛的作用。

Hydroxy-PEG4-C2-nitrile is a polyethylene glycol (PEG) based linker commonly employed in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1].

Azido-PEG4-NHS-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.

Ap44mSe is a potent and selective antitumor agent. Ap44mSe effectively depletes cellular Fe, resulting in transferrin receptor-1 up-regulation, ferritin down-regulation, and increased expression of the potent metastasis suppressor, N-myc downstream regula

Benzyl-PEG6-NHBoc 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.

Kauniolide 是从菊芋中分离出来的一种天然化合物。它已被证明通过调节体内的各种信号通路来发挥其作用，具有广泛的生物活性，包括抗炎、抗肿瘤和抗微生物作用。

N-Ethyl-N-methylpropionamide-PEG1-Br is a PEG-derived PROTAC linker suitable for the synthesis of PROTACs.