m 6

urolithin M6 (3,8,9,10-tetrahydroxy urolithin) (UM6) is an ellagitannin metabolite produced by gut microbiota, was identified as a putative galloflavin mimetic

PD-M6 is an mTOR PROTAC degrader with a DC50 of 4.8 μM, which facilitates the ubiquitination and degradation of mTOR. It inhibits the proliferation of cancer cell lines HeLa, MCF-7, and HepG2 with IC50 values of 11.3, 2.58, and 3.23 μM, respectively, and induces autophagy. Additionally, PD-M6 specifically targets the degradation of the key protein LAMTOR1 in the mTOR signaling pathway.

M6 glycan (Man6), 2-AA labelled (Mannose-6 N-linked oligosaccharide, 2-AA labelled; Oligomannose 6 glycan, 2-AA labelled) is a polymeric N-glycoprotein acting as a versatile fluorescent linker. The resulting conjugate exhibits high sensitivity and specificity by mimicking the antennae components of N-glycans.

M6 glycan (Man6) (Mannose-6 N-linked oligosaccharide; Oligomannose 6 glycan) is a polymeric N-linked glycoprotein that serves as a multifunctional fluorescent linker. The resulting conjugates exhibit high sensitivity and specificity by mimicking the antenna elements of N-glycans.

M6 glycan (Man6), procainamide labelled (Mannose-6 N-linked oligosaccharide, procainamide labelled), is a multifunctional fluorescent linker that serves as a polymer of N-glycoprotein. The resulting conjugate mimics the antennal elements of N-glycans, offering high sensitivity and specificity.

M6 glycan (Man6), 2-AB labelled (Mannose-6 N-linked oligosaccharide, 2-AB labelled; Oligomannose 6 glycan, 2-AB labelled) is a polyvalent N-glycoprotein that serves as a multifunctional fluorescent linker. The resulting conjugate, by mimicking the antenna elements of N-glycans, exhibits high sensitivity and specificity.

Moracin M 6-β-D-glucopyranoside is a derivative of coumarin compounds and can be found in Morus alba.

Cephabacin M6 is a new cephem antibiotic isolated from bacterial.

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

m7Gpppm6AmpG, a trinucleotide mRNA 5' cap analog, facilitates RNA synthesis in vitro [1].

M7Gpppm6AmpG ammonium, a trinucleotide mRNA 5' cap analog, facilitates in vitro RNA synthesis [1].

N6-(m-Methoxybenzyl)adenosine is an adenine nucleoside analog and a cytokinin derivative that can be used in agriculture to study branch growth and reproduction.

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

m-PEG6-2-methylacrylate is a PEG-based linker for PROTACs that joins two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation through 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 that connects two essential ligands, facilitating selective protein degradation via 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, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG6-C6-phosphonic acid ethyl ester is a PEG-based PROTAC linker used in the synthesis of PROTACs[1].

m-PEG6-(CH2)6-Phosphonic acid functions as a PEG-based PROTAC linker for PROTAC synthesis [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 that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via 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, facilitating the formation of PROTAC molecules by connecting two essential ligands. It enables selective protein degradation via the ubiquitin-proteasome system within cells.