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Sulfobromophthalein disodium salt 是一种有机阴离子染料，能够参与药物和代谢物的运输，可用于研究动物组织中表达的多种膜载体。

Genistein 7,4'-di-O-β-D-glucoside是一种天然产物，在MCF-7细胞中具有纳摩尔级别的雌激素增殖作用，可用于研究骨质疏松。

DSPE-PEG5-azide 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.

L-Xylulose is an intermediate in certain metabolic pathways and is classified as a rare sugar. It shows important physiological effects such as acting as an inhibitor of α-glucosidase and decreasing blood glucose, and it can be employed to produce other significant rare sugars, such as L-ribose and L-xylose which contribute to the production of antiviral drugs.

Sel-green is a selective selenol fluorescent probe used for quantifying the selenocysteine (Sec) content in the selenoenzyme thioredoxin reductase, as well as imaging endogenous Sec in live HepG2 cells.

Thiol-PEG10-alcohol 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.

Mitochondria modulator-1为线粒体调节剂，可促进ATP生成。该化合物展现出优良的口服生物利用度、血脑屏障透过性及稳定的血浆稳定性，展现出其研究线粒体疾病的潜力。

ZC0109 是 IDO1和硫氧还蛋白还原酶 1 (TrxR1) 的双抑制剂，IC50分别为 50 nM 和 3.0 μM。ZC0109 诱导活性氧 (ROS) 积累，使细胞周期阻滞于 G1/S 期，导致癌细胞凋亡 (apoptosis)。

Y13g 是白细胞介素 6 (IL-6) 和乙酰胆碱酯酶 (AChE)的有效抑制剂， 这两个靶点阿尔茨海默症 (AD) 进展的有关。Y13g 逆转 STZ 诱导的记忆缺陷，并表现出与正常动物相似的组织病理学。

Mcl-1 antagonist 1 is a Mcl-1 protein antagonist.

Pomalidomide-C6-COOH 是一种合成的 E3 连接酶配体-接头偶联物，它结合了 PROTAC 技术中使用的基于 Pomalidomide 的 CRBN 配体和接头。

Vitamin D4 is the active Vitamin D analog.

11β,13-Dihydrotaraxinic acid 是一种天然存在的小分子代谢物，被鉴定为适用于生命科学和生物化学研究的生物活性化合物。该化合物主要作为参考品或研究级材料，用于天然产物化学、代谢通路分析、生物活性筛选以及药理学、生物化学或分子生物学领域中的实验验证研究，尤其适用于需要结构明确的植物来源化合物的研究体系。

(R)-NVS-ZP7-4 是 NVS-ZP7-4 的 R 型异构体。 NVS-ZP7-4 是一个报道用于探测内质网锌水平影响的化学分子，是一种锌转运体 SLC39A7(ZIP7)的抑制剂，并研究 ZIP7 作为 Notch 通路中的一种新的可成药节点。

5-HT6/5-HT2A receptor ligand-1 (compound 33) is a dual antagonist for the 5-HT6 and 5-HT2A receptors. It exhibits a K i value of 2 nM and 11 nM for the respective receptors. This compound holds promise for research in neurological and psychiatric disorders [1].

Ulifloxacin 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 T65577，CAS号为 112984-60-8。

3'-beta-C-Ethynyluridine is a Nucleoside Derivative - 3'-Modified nucleoside.

HIV-1 integrase inhibitor 3 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 2.7 nM).

Levoprotiline hydrochloride is an antidepressant.

Erythromycin dihyrate dihydrate is a macrolide antibiotic produced by actinomycete Streptomyces erythreus with a broad spectrum of antimicrobial activity. Erythromycin dihyrate acts by binding to bacterial 50S ribosomal subunits and inhibits RNA-dependent protein synthesis by blockage of transpeptidation and/or translocation reactions, without affecting synthesis of nucleic acid.

Propanol-PEG4-CH2OH 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.

Biotin-PEG5-azide 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.

Mal-NH-PEG12-CH2CH2COOPFP ester is a polyethylene glycol (PEG) based linker molecule, designed specifically for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

2,2',3,4,4',5'-PCB in Cyclohexane (Standard)是2.2'3.4.4'5'-六氯联苯溶于环己烷的标准品溶液，可用作分析标准品。

Beloranib is a fumagillin anticancer drug. Beloranib belongs to an angiogenesis inhibitor.

Potent and selective β-secretase (BACE) inhibitor (IC50 values are 10.2 and 20.3 nM for human BACE2 and BACE1, respectively). Displays >5,000-fold selectivity for BACE over other proteases including cathepsin D, pepsin and renin. Inhibits Aβ1-40 and Aβ1-42 production in cells expressing mutated APP. Reduces hippocampal and cortical Aβ and sAPPβ levels in an Alzheimer's disease mouse model.

5'-Azido-5'-deoxy-2'-O-(2-methoxyethyl)uridine is a Nucleoside Derivative - 5'-Modified nucleoside; Azido-nucleoside; 2'-Modified nucleoside.

FXR antagonist 1 是一种选择性的、口服具有活力的肠道 FXR 拮抗剂，其 IC50 值为 2.1 μM。FXR antagonist 1 能够拮抗肠道 FXR，并反馈激活肝脏 FXR，进而选择性地抑制肠道 FXR 信号。FXR antagonist 1 可改善 NASH (非酒精性脂肪性肝炎) 模型中的肝脏脂肪变性、炎症和纤维化，能够用于研究 NASH。

GPVI antagonist 2 (Compound 1) 是一种潜在的 Glycoprotein VI (GPVI) 拮抗剂，能够作用于胶原蛋白 (IC50: 0.35 μM)、CRP (IC50: 0.80 μM)、convulxin (IC50: 195.2 μM)、凝血酶 (IC50: 81.38 μM)。其中糖蛋白 VI (GPVI) 是一种血小板主要胶原受体，是有效的、安全的抗血栓研究靶点。GPVI antagonist 2 是一种很有前途的抗血小板药物。

CB2R probe 1 是一种安全绿色的 CB2R (2 型大麻素受体)荧光探针，Ki 为 130 nM。CB2R probe 1 在癌细胞中显示出低细胞毒性。

5,5-Dimethyldihydrofuran-2(3H)-one是一种呋喃衍生物和内酯，广泛应用于生物化学实验和药物合成研究。

Siomycin A is a thiopeptide antibiotic that selectively inhibits Forkhead box M1 (FOXM1) without affecting other Forkhead box family members, exhibiting anti-tumor properties and promoting apoptosis.

7-Hydroxyneolamellarin A，一种从海绵Dendrilla nigra 提取的天然产物，是高效的缺氧诱导因子 1α (HIF-1α) 抑制剂。该化合物能够减弱HIF-1α蛋白的积累，并抑制血管表皮生长因子 (VEGF) 的转录活性，因而在癌症研究中有应用价值。

11-deoxy PGF1α is a synthetic analog of PGF1α. In whole animal studies, a dose of 32 mg/kg inhibited gastric acid secretion by 35%. 11-deoxy PGF1α is also known to cause rat uterine contractions at a dose 0.3 times that of PGF1α. It also exhibits vasopressor and bronchoconstrictor activities at about half the potency of PGF2α in guinea pigs.

Relzomostat is a MetAP2 inhibitor, specifically targeting methionine aminopeptidase 2. It holds potential in research concerning obesity, type 2 diabetes, and other conditions associated with obesity.

Fischeria A是一种天然产物，属于大戟科大戟属，其产品编号为 TN4059，CAS号为 221456-63-9。Fischeria A可用作对照参考。