m 6

Cephabacin M6 is a new cephem antibiotic isolated from bacterial.

urolithin M6 (3,8,9,10-tetrahydroxy urolithin) 是一种由肠道微生物群产生的鞣花单宁代谢物，被确定为推定的没食子黄素模拟物。

PD-M6 是一种 mTORPROTAC 降解剂 (DC50: 4.8 μM)，可促进 mTOR 的泛素化和降解。PD-M6 能抑制 HeLa、MCF-7 和 HepG2 癌细胞系的增殖 (IC50值分别为 11.3、2.58 和 3.23 μM)，并诱导自噬。此外，PD-M6 能特异性诱导 mTOR 信号通路中关键蛋白 LAMTOR1 的降解。

Moracin M 6-β-D-glucopyranoside 可在 Morus alba 中发现，是香豆素类化合物的衍生物。

Dasatinib metabolite M6 (Dasatinib carboxylic acid) is an oxidative metabolite of Dasatinib, a potent and orally active inhibitor of both Bcr-Abl and Src family tyrosine kinases[1].

m7Gppm6AmpG 是一种三核苷酸 mRNA 5' 帽类似物，可用于体外 RNA 合成。

m7Gppm6AmpG ammonium 是一种三核苷酸 mRNA 5' 帽类似物，可用于体外 RNA 的合成。

N6-(m-Methoxybenzyl)adenosine 是一种腺嘌呤核苷类似物，也是一种细胞分裂素衍生物，可在农业中研究枝条的生长繁殖。

m-PEG4-(CH2)6-Phosphonic acid is a polyethylene glycol-based linker compound, specifically designed for the synthesis of proteolysis targeting chimeras (PROTACs)[1].

m-PEG6-2-methylacrylate 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.

m-PEG6-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

m-PEG6-amino-Mal 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.

m-PEG6-azide is a six-unit polyethylene glycol linker functionalized with an azide moiety, serving as a non-cleavable linker for the synthesis of antibody-drug conjugates (ADCs).

m-PEG6-Br 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.

m-PEG6-C6-phosphonic acid ethyl ester serves as a PEG-based PROTAC linker for the synthesis of PROTACs[1].

m-PEG6-(CH2)6-Phosphonic acid serves as a PEG-based PROTAC linker for synthesizing PROTACs[1].

m-PEG6-CH2CH2CHO is a non-cleavable ADC linker employed in the synthesis of antibody-drug conjugates (ADCs).

m-PEG6-CH2CH2COOH 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.

m-PEG6-NHS ester is a non-cleavable PEG linker consisting of 5 units, employed in the synthesis of antibody-drug conjugates (ADCs).

m-PEG6-O-CH2COOH 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.

m-PEG6-thiol 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.

m-PEG6-Tos 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.

m-PEG6-Hydrazide 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.

m-PEG6-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.