tr-β

Tedizolid (DA-7157)是一种新型恶唑烷酮类抗生素，可与核糖体50S 亚基的23S 核糖体 RNA 结合抑制细菌的蛋白质合成。

TR-107 (Anticancer agent 230) 是一种具有选择性和高效性的线粒体蛋白酶 ClpP 激活剂，抑制 MDA-MB-231 异种移植模型中的肿瘤生长。

TR antagonist 1 是一种高效甲状腺激素受体（TR）拮抗剂（对 TRα 和 TRβ 的 IC50 分别为 36 和 22 nM），可用于研究内分泌异常引起的疾病。

Nucleoside Derivatives –Morpholino nucleosides

Dalpiciclib (SHR-6390) 是一种高选择性、口服生物利用度和相当效力的 CDK4 和 CKD6 抑制剂，IC50 分别为 12.4 nM 和 9.9 nM。它通过抑制磷酸化 Rb 蛋白和诱导 G1 细胞周期阻滞在食管鳞状细胞癌中发挥有效的抗肿瘤活性。

Tr-PEG2-OH is a PEG-based PROTAC linker utilized in PROTAC synthesis[1]. It also serves as a non-cleavable 2-unit PEG ADC linker for the synthesis of antibody-drug conjugates (ADCs)[2].

TR4161 is a prostaglandin bronchodilator of low tracheobronchial irritancy.

NASTRp, an inhibitor of CREB-CBP complex, possesses anti-cancer effects along with cell cycle regulation, autophagy suppression, and endoplasmic reticulum stress.

Methoxy-Tr-NH-PEG7 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.

Tr-PEG6-OH is a 6-unit polyethylene glycol (PEG) linker, which is non-cleavable and extensively employed in the synthesis of antibody-drug conjugates (ADCs).

TR-14035 (MDK-1191) 是一种具有口服活性的 α4β7 α4β1整合素双重抑制剂，对 α4β7和 α4β1作用的 IC50值分别为 7 和 87 nM，可用于炎症和自体免疫疾病的研究。

Ganoderic acid TR 是一种从药用灵芝中分离出口来的三萜化合物，是 H5N1 和 H1N1 NAs 抑制剂，具有广谱的抗病毒活性。

Aristolochic acid A (TR 1736) 是植物提取物 Aristolochic acids 的主要成分，主要存在于 Aristolochia 和 Asarum 草本植物中。它降低人细胞中膀胱癌相关BLCAP 基因表达。它显著降低激活蛋白1 (AP-1) 和NF-κB 活性。

Tr-PEG5-OH is a non-cleavable 5-unit PEG ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs).

Tr-PEG4-OH is a non-cleavable tetraethylene glycol ADC linker employed in ADC synthesis for the conjugation of antibodies and drugs.

Tr-PEG3-OH is a non-cleavable, three-unit PEG ADC linker employed for ADC synthesis, specifically in the context of antibody-drug conjugates (ADCs).

Sodium aristolate 1（Aristolochic acid sodium salt）, 作为某些中草药的组成成分，是引起肾脏毒性的主要原因。该化合物作为前体活性分子，通过硝基还原为胺的方式进行活化，进而形成具有细胞毒性的DNA加合物。

Rioprostil is a methyl prostaglandin E1 analog that decreases gastric acid secretion and enhances the gastric mucus-bicarbonate barrier. It is effective in the treatment of gastric ulcers and gives significant protection against NSAID-induced gastric muco

Tedizolid Phosphate (TR-701FA) 是 MAO-A 和 MAO-B 抑制剂，具有抗革兰氏阳性菌的活性。

Ropitoin is a novel drug of antiarrhythmics.

(S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens.

Tedizolid phosphate is a novel antibacterial prodrug. Tedizolid phosphate is a next-generation oxazolidinone with activity against both methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus spp. It also has effective activity a

Xorphanol mesylate is a biochemical.

Xorphanol is a biochemical.