Others

TC-E 5008 is a selective inhibitor of mutant isocitrate dehydrogenase 1 (mIDH1).

6-Thioguanosine (6-Mercaptoguanosine) 是一种活性核苷，是 Azathioprine 的代谢物，是低分子量凝胶剂。6-Thioguanosine 具有免疫抑制作用，可用于研究RNA 双螺旋结构的形成。

Gatifloxacin hydrochloride (Standard) 是一种可用于分析的标准物质，通常用作 Gatifloxacin hydrochloride 的研究和分析中参考的标准样品。Gatifloxacin hydrochloride (AM-1155 hydrochloride) 是一种氟喹诺酮类抗生素，有广谱抗菌活性。它可抑制大肠杆菌 DNA 解旋酶 (IC50=0.109 μg/ml)和细菌 II 型拓扑异构酶(IC50=13.8 μg/ml) 。它在动物模型中，可研究细菌性结膜炎。

α-Synuclein(61-95) (human) 是 α-Synuclein 的疏水核心区段，具有诱导神经元死亡的能力。该肽段在神经退行性疾病的研究中有应用，涉及阿尔茨海默病 (AD) 与帕金森病 (PD)。

2-[(2-aminobenzoyl)amino]benzoic acid是一种芳香族化合物，可用于生物化学实验和药物合成研究。

Sch 32615 is an enkephalinase inhibitor with inhibitory action on D-1 and D-2 dopamine receptor-mediated behaviors.

Azido-PEG8-Boc is a polyethylene glycol (PEG) and alkyl/ether-based linker used in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

(S,R,S)-AHPC-PEG5-COOH (VH032-PEG5-COOH) is a synthetic E3 ligase ligand-linker conjugate developed for use in PROTAC technology. It consists of the (S,R,S)-AHPC based VHL ligand and a 5-unit PEG linker [1].

GA-O-02，一种18β-Glycyrrhetinic acid衍生物，具有显著的抗菌和抗炎效果。该化合物通过抑制NO、促炎细胞因子及趋化因子来发挥其抗炎作用，并对革兰氏阳性菌显示出高度的抗菌活性。

CDK6/9-IN-1 (compound 66) is a potent dual inhibitor of CDK 6 and CDK 9 that can be administered orally. It exhibits inhibitory activity with IC 50 values of 40.5 nM and 39.5 nM against CDK6 and CDK9, respectively.

PCSK9-IN-2 is a newly developed small molecule that effectively inhibits the protein-protein interaction (PPI) between PCSK9 and LDLR. It has been found to have a potent inhibitory activity with an IC50 value of 7.57 μM.

Recilisib, also known as ON 01210.Na, is a radioprotectant, which modifys cell cycle distribution patterns in cancer cells subjected to radiation therapy, and it has been identified as a potential candidate for radiation protection studies. It appears tha

DBCO-NHCO-PEG5-NHS ester is a polyethylene glycol (PEG)-based linker utilized in the synthesis of PROTACs[1].

HQL-79 is a selective and orally active human hematopoietic prostaglandin D synthase (H-PGDS) inhibitor. It inhibits the synthesis of PGD2 and acts as an anti-allergic agent (Kd: 0.8 μM and IC50: 6 μM). It also shows no obvious effect on COX-1, COX-2, m-P

Org-12962 hydrochloride is a 5-HT2C receptor agonist.

2-Phenyl-2-propanol (Standard)是2-Phenyl-2-propanol的标准品，适用于定量分析、质量控制及生化实验等相关研究。2-Phenyl-2-propanol是一种醇类和芳香化合物,可用于合成过氧化二异丙苯。

NMS-P515 is an effective, orally active, and stereospecific PARP-1 inhibitor (Kd: 16 nM and an IC50: 27 nM (in Hela cells)). It has anti-tumor activity.

Thalidomide-O-C3-acid is a chemically derived conjugate that combines a cereblon ligand based on Thalidomide and a linker commonly employed in PROTAC technology. This synthesized E3 ligase ligand-linker conjugate serves to facilitate targeted protein degradation.

the primary metabolite of ceftiofur

3,4-Dimethoxystyrene是一种含有甲氧基和乙烯基的芳香化合物，广泛应用于生物化学实验和药物合成研究。

glycogen phosphorylase inhibitor

Bombinin H2, 源自Bombina variegata蛾皮肤的抗菌肽。

Cyanine5.5 amine是一种氨基修饰的Cy5.5和近红外 (NIR) 荧光染料 ，Ex/Em=648/710 nm,具有荧光背景低的优点，可用于基团偶联和活体成像。

1-vinyl-4-dimethoxy-beta-carboline is a natural product from Picrasma javanica.

VEGFR-2-IN-26 (compound 5h) 是一种 VEGFR-2 的高效抑制剂 (IC50: 15.5 nM)。VEGFR-2-IN-26 对白血病、中枢神经系统、非小肺、卵巢、肾、前列腺和乳腺癌细胞表现出良好的抗增殖作用。

Tricine是一种两性离子生物缓冲剂，有效缓冲范围为 pH 7.4至8.8，常用于Tricine-SDS-PAGE系统。

Cbz-NH-PEG24-C2-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.

BDP-13176 是fascin 1抑制剂，Kd=90 nM，IC50=240 nM。它具有成为抗转移剂的潜力。

ST-193 hydrochloride 是有效的广谱arenavirus 抑制剂。ST-193 hydrochloride 抑制Guanarito, Junin, Lassa 和Machupo 病毒，IC50分别为0.44, 0.62, 1.4 和3.1 nM。

Lurbinectedin (PM01183) 是一种 DNA 小沟共价粘合剂，可抑制 RMG1和 RMG2，IC50值分别为1.25和1.16 nM。它具有高效的抗肿瘤活性。

Potassium cinnamate是肉桂酸的钾盐，广泛应用于生物化学实验和药物合成研究。

4-Methylpyrrolidin-2-one是一种吡咯类化合物，广泛应用于生物化学实验和药物合成研究。

Conjugated linoleic acid是一组具有共轭双键的Linoleic acid几何/位置异构体，主要来源于乳制品和牛羊肉，具有抗癌、免疫调节、减肥、减轻肌肉损伤和减轻炎症反应等多种活性。

SR142948A是一种选择性和可逆的非肽的neurotensin receptor（神经紧张素受体）拮抗剂，能够阻断由脑室内注射NT引起的体温过低和镇痛效应，能够浓度和体积依赖性地阻断NMDA诱导的多巴胺释放。

Butriptyline (Butriptylene)，三环抗抑郁剂，具有口服生物活性。

Apigenin 5-O-beta-D-glucopyranoside has inhibitory activity against the enzyme yeast a-glucosidase, withthe IC50 value of 287.12 muM.