5″-azido

Framycetin sulfate (Neomycin Sulphate B) 是一种氨基糖苷类抗生素，是 RNase P 裂解活性抑制剂，Ki 为 35 μM。它抑制锤头状核酶，Ki 值为 13.5 μM，可用于肝性脑病和肠致病性大肠杆菌感染的研究。

5-Azido-PEG4-SS-UTP tristriethylamine 是用于点击化学的生化检测试剂.

CG-PEG5-azido 是一种用于合成PROTAC分子的PEG类PROTAC linker。它作为点击化学试剂，含有Azide基团，能够与含有Alkyne基团的分子进行铜催化的叠氮-炔环加成反应（CuAAc）。此外，CG-PEG5-azido 还能与含有DBCO或BCN基团的分子发生环张力驱动的炔-叠氮环加成反应（SPAAC）。

3'-Azido-3'-deoxy-5-methylcytidine 抑制 HIV-1 逆转录酶 (EC50 = 0.06 μM)，是异嗜性鼠白血病相关逆转录病毒 (XMRV, CC50 = 43.5 μM) 的有效抑制剂。

Azido-PEG5-acid is a non-cleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs), such as the conjugate CPT-APO (CPT: Camptothecin.

Azido-PEG5-Ala-Ala-Asn-PAB is a cleavable 5-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].

Azido-PEG5-alcohol, a non-cleavable 5 unit polyethylene glycol (PEG) ADC linker, finds application in the synthesis of antibody-drug conjugates (ADCs)[1]. Additionally, it serves as a PEG-based PROTAC linker for the synthesis of PROTACs[2].

Azido-PEG5-amine 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.

Azido-PEG5-Boc 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.

Azido-PEG5-CH2CO2-NHS 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.

Azido-PEG5-CH2CO2-PFP is a polyethylene glycol (PEG) and Alkyl/ether-based linker compound. It serves as a key component in the synthesis of proteolysis-targeting chimeras (PROTACs), a class of molecules used for targeted protein degradation[1].

Azido-PEG5-CH2CO2H is a cleavable 5-unit PEG ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs)[1].

Azido-PEG5-NHS ester 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.

Azido-PEG5-PFP ester is a Polyethylene Glycol (PEG) and Alkyl/ether-based Proteolysis Targeting Chimera (PROTAC) linker, commonly employed for PROTAC synthesis [1].

Azido-PEG5-succinimidyl carbonate is a polyethylene glycol (PEG) derivative with a linked succinimidyl carbonate and azido group. It serves as a PEG-based PROTAC linker for the synthesis of PROTACs[1].

Azido-PEG5-maleimide 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.

Azido-PEG5-triethoxysilane serves as a PEG-based PROTAC linker for the synthesis of PROTACs[1].

3'-Azido-3'-deoxy-5-fluorocytidine is a cytidine derivative.

L-Lysine, 5'-ester with 3'-azido-3'-deoxythymidine is a bioactive chemical.

Azido-PEG5-S-methyl ethanethioate is a polyethylene glycol (PEG)-based linker utilized for the synthesis of proteolysis targeting chimeras (PROTACs).

Nucleoside Derivatives –Azido-nucleosides, Halo-nucleosides, 3'-Modified nucleosides, 5-Modified pyrimidine nucleosides; Scaffolds and Templates

3'-Azido-3'-deoxy-5-methyuridine is a Azido-nucleoside; 3'-N-Modified nucleoside.

Nucleoside Derivatives - Azido-nucleosides, 3'-Modified nucleosides, 5-Modified pyrimidine nucleosides; Fluoro-modified nucleosides

Nucleoside Derivatives - Azido-nucleosides, 5-Modified pyrimidine nucleosides, 3'-Modified nucleosides; Fluoro-modified nucleosides