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.

Nucleoside Derivatives - Azido-nucleosides, 5'-Modified nucleosides, 2'-Modified nucleosides, Fluoro-modified nucleosides

Nucleoside Derivatives - Azido-nucleosides, 5'-Modified nucleosides, 2'-Modified nucleosides

5'-Azido-5'-deoxy-5-methyluridine is a Nucleoside Derivative - 5'-Modified nucleoside, Azido-nucleoside.

5'-Azido-2',5'-dideoxyuridine is a Nucleoside Derivative - 5'-Modified nucleoside, Azido-nucleoside.

Nucleoside Derivatives - 5'-Modified nucleosides, Azido-nucleosides, 2'-Modified nucleosides

5'-Azido-5'-deoxy-2'-O-(2-methoxyethyl)uridine is a Nucleoside Derivative - 5'-Modified nucleoside; Azido-nucleoside; 2'-Modified nucleoside.

5'-Azido-5'-deoxy-2'-O-(2-methoxyethyl)-5-methyluridine is a Nucleoside Derivative - 5'-Modified nucleoside; Azido-nucleoside; 2'-Modified nucleoside.

Nucleoside Derivatives - Azido nucleosides; 5'-Modified nucleosides

Nucleoside Derivatives - LNA-related nucleosides; 5'-Modified nucleosides; Azido-nucleosides

5'-Azido-2',5'-dideoxyadenosine is a Nucleoside Derivative - 5'-Modified nucleoside; Azido-nucleoside.

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].