Others

Deoxythymidine-5'-triphosphate (dTTP) is a nucleoside triphosphate involved in DNA synthesis.

Coenzyme Q0 (CoQ0)，一种从Antrodia cinnamomea提取的口服醌类化合物，具备促进细胞凋亡(apoptosis)与自噬(autophagy)的作用。该化合物通过抑制HER-2/AKT/mTOR信号通路，增强凋亡和自噬机制；同时，调控NFκB/AP-1活化，提升Nrf2稳定性，从而缓解炎症及氧化还原失衡。此外，Coenzyme Q0还表现出抗血管生成特性，通过下降MMP-9/NF-κB并提升HO-1信号路径发挥作用。

UPCDC30245 is an AAA ATPase p97 allosteric inhibitor.

β-catenin-IN-4 是一种β-catenin 抑制剂，Ki 值为 0.64 μM。β-catenin-IN-4 降低 cyclin D1 和c-Myc 的蛋白表达水平。

Norartocarpetin 是一种酪氨酸酶抑制剂。Norartocarpetin 具有较强的酪氨酸酶抑制活性，其抑制活性 IC50值为 0.47 μM。Norartocarpetin 作为一种抗褐变剂可用于食品体系的研究。Norartocarpetin 对肺癌细胞 (NCI-H460) 也具有显著的抗癌活性，其 IC50值为 22 μM。Norartocarpetin 的抗增殖作用是通过靶向 Ras/Raf/MAPK 信号通路、线粒体介导的细胞凋亡、S 期细胞周期阻滞和抑制细胞迁移和侵袭实现的。

(±)9-HEPE is produced by non-enzymatic oxidation of EPA. It contains equal amounts of 9(S)-HEPE and 9(R)-HEPE. The biological activity of (±)9-HEPE has not been clearly documented.

endothelial lipase and lipoprotein lipase inhibitor

m-PEG11-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.

Terbinafine hydrochloride (Standard) 是一种可用于分析的标准物质，通常用作 Terbinafine hydrochloride 的研究和分析中参考的标准样品。Terbinafine hydrochloride (KWD 2019) 具有抗真菌感染活性。它是念珠菌属的角鲨烯环氧化酶的非竞争性抑制剂，Ki 值为 30 nM。它还对某些革兰氏阳性和革兰氏阴性细菌具有抗菌活性。

Iron (III) hexacyanoferrate (II) (Prussian Blue, Berlin blue) 用作吸附剂，用于有效去除水溶液中的重金属（Cu (II)、Co (II)、Ni (II) 和 Pb (II)）。

Hydroxy bosentan (Ro 48-5033) is a primary metabolite of Bosentan (BOS) metabolized by the cytochrome P450 system in the liver, assisting BOS pharmacologically with 10%-20% activity retention.

Bometolol Hydrochloride is a beta-adrenergic blocking compound used for the treatment of cardiovascular disease.

N-(m-PEG4)-N'-hydroxypropyl-Cy5 is a polyethylene glycol (PEG)-based linker for PROTACs synthesis[1].

Herquline A is an alkaloid fungal metabolite originally isolated from P. herquei. It inhibits cell death induced by influenza A strain A/PR/8/34 in MDCK cells with an IC50 value of 10 μg/ml and inhibits viral replication in a plaque assay in a concentration-dependent manner. Herquline A also inhibits platelet aggregation induced by ADP and platelet-activating factor (PAF) in vitro (IC50s = 180 and 240 μM, respectively).

Mal-amido-PEG9-amine 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.

IL-17 modulator 3 (US20200247785A1) is a chemical compound that acts as an IL-17 modulator. It has potential applications in researching inflammation, cancer, and autoimmune diseases.

RUSKI-201 dihydrochloride 是一种有效的、特异性的 Hedgehog 酰基转移酶 (Hhat) 抑制剂 (IC50: 0.20 μM)。RUSKI-201 dihydrochloride 可以阻断 Shh 过表达细胞的 Hh 信号，对 Hh 棕榈酰化具有抑制作用。RUSKI-201 dihydrochloride 是一种有潜力的 Hhat 化学探针，能够用于研究 Hhat 催化功能。

Verilopam 具有镇痛作用，可用于疼痛研究。

Dodecanoic acid ingenol ester, a natural compound, shows moderate cytotoxicity with IC50 values being 35.59 μM (Caco-2), 24.04 μM (MCF-7), and 22.24 μM (MCF-7/ADM).

673-A is an aldehyde dehydrogenase (ALDH1A) inhibitor that depletes CD133+ cancer stem cells (CSC) in ovarian cancer cell lines. 673-A triggers necroptosis in ovarian CSCs and induces expression of mitochondrial uncoupling proteins (UCP). 673-A also overcomes chemotherapy resistance in vivo.

Chamaejasmenin B 是一种从 Stellera chamaejasme L 中分离得到的化合物。Chamaejasmenin B 具有抗癌和抗肿瘤活性，可抑制癌细胞迁移和侵袭，抑制肿瘤转移。Chamaejasmenin B 可用于研究如乳腺癌类的癌症。

KCa1.1 channel activator-2 (化合物 3F) 是一种槲皮素衍生物，是选择性的血管 KCa1.1 channel 刺激剂。KCa1.1 channel activator-2 具有强效的肌肉松弛活性。

Septamycin is a polycyclic, polyether, monocarboxylic acid antibiotic. Septamycin is isolated from strain of Streptomyces albus.

2-Amino-3-hydroxybutanoic acid 是一种苏氨酸的异构体和内源性代谢物，广泛应用于生物化学实验和药物合成研究。

hRSV-IN-1 是一种呼吸道合胞病毒 (hRSV) 抑制剂。

Sulfo-SANPAH Crosslinker (Sulfo-SANPAH Cross linker) 是一种水溶性同双功能蛋白质交联剂。

3-Phenoxyphenol(3-苯氧基苯酚)属于苯酚衍生物类别，是一种有机化合物。

SARS-CoV-2-IN-18 (Compound 26) 是 SARS-CoV-2 3C-样蛋白酶的有效抑制剂 (IC50 = 45 nM)。

AG6033 是潜在的新型 CRBN 调节剂。AG6033 能够调控CRBN 与多种抗肿瘤靶蛋白的相互作用，对多种肿瘤细胞表现出抑制作用。AG6033 能够降解 GSPT1 和 IKZF1，并诱导 CRBN 依赖的细胞毒性作用。

KRAS G12C inhibitor 37 是一种有效的 KRAS G12C 抑制剂。Ras 蛋白家族是一种重要的细胞内信号分子，在生长发育中起重要作用。KRAS G12C inhibitor 37 具有研究 KRAS G12C 介导的癌症的潜力。

N-(Propargyl-PEG2)-N-Boc-PEG3-t-butyl ester is a polyethylene glycol (PEG)-based linker employed for the synthesis of proteolysis-targeting chimeras (PROTACs) [1].

Carboxyaminoimidazole ribotide (CAIR) 为大肠杆菌代谢产物，用于检测大肠杆菌 PurE 活性位点的特征以及合成真菌嘌呤的从头合成。

Ciprofloxacin lactate 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 T66299，CAS号为 97867-33-9。

Olsalazine (Dipentium) 是一种抗炎药，用于治疗炎症性肠病。它也是一种新型的 DNA 去甲基化剂。

RA-V 是一种天然化合物，可作为天然产物对照品。

REDX05358 is a highly selective and potent pan RAF inhibitor with a potential therapeutic for BRAF and RAS mutant tumors. REDX05358 has improved therapeutic potential and predicted safety profile. REDX05358 demonstrates subnanomolar binding affinity for B