dbco acid

DBCO-acid is a cleavable ADC linker utilized in the synthesis of ADC linker DBCO-NHS ester and drug-linker conjugates DBCO-PEG-MMAE[1].

DBCO-C6-acid is a non-cleavable linker utilized for the synthesis of antibody-drug conjugates (ADCs) and carmaphycin analogues[1].

DBCO-Amide-PEG5-acid is a non-cleavable ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs)[1].

DBCO-PEG4-C2-acid 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.

DBCO-NHCO-PEG13-acid 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.

DBCO-NHCO-PEG3-acid 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.

DBCO-NHCO-PEG7-acid 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.

DBCO-PEG1-acid 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.

DBCO-PEG12-acid 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.

DBCO-PEG2-acid 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.

DBCO-PEG8-acid 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.

N-DBCO-N-bis(PEG2-C2-acid) is a polyethylene glycol (PEG) linker commonly employed in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

DBCO-PEG3-C1-acid 作为一种抗体-药物偶联物 (ADC) 连接体，用作细菌促进的叠氮化物-炔烃点击化学反应中的反应手柄。

DBCO-PEG4-acid 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.

DBCO-S-S-acid 是一种点击化学试剂，用于合成可降解（cleavable）的抗体偶联活性分子（ADC）linker。此化合物含有 DBCO 基团，使其能够与含 Azide 基团的分子通过菌株促进的炔-叠氮环加成反应（SPAAC）进行反应。

DBCO-PEG3-acid 作为一种含有三个PEG单元且不可降解 (non-cleavable) 的ADC linker，其主要应用在抗体偶联活性分子 (ADC) 的合成中。该化合物具备DBCO基团，能够通过菌株促进的炔-叠氮环加成反应 (SPAAC) 与含Azide基团的分子进行反应。

DBCO-PEG24-acid 是一种独特的点击化学试剂,作为带有 PEG 连接子的 DBCO-acid 的衍生物,并含有 DBCO 基团.这种 DBCO 基团因其高能量的应变促进特性,常被用于无铜点击化学反应.其亲水性的聚乙二醇链增强了水溶性.此外,该化合物的末端羧酸可在 EDC 或 HATU 等激活剂存在下与伯胺基团反应,形成稳定的酰胺键.产品为试剂级,仅限研究使用.

Sulfo DBCO-PEG3-acid 是一种具备叠氮基团的点化学试剂,是DBCO-acid的衍生物,它包含了一个PEG连接剂和DBCO基团.DBCO基团以其应变促进的高能量特性,经常被应用于无铜点击化学反应中.其亲水性的聚乙二醇链和硫基极大地提高了其水溶性.该化合物的末端羧酸在激活剂(如 EDC 或 HATU)存在下能与伯胺基团发生反应,生成酰胺键.该产品为试剂级,仅限研究使用.

DBCO-PEG2-C2-acid 是一种有效的 ADC 连接子，专门用于制备抗体-药物偶联物 (Antibody-Drug Conjugates (ADCs))。该化合物在 ADC 类偶联物的合成中发挥关键作用。

DBCO-(CH2)3-Acid 是一种用于抗体-药物偶联物的 Click Chemistry 中间体，可用以合成 ADC linker。

DBCO-NHS ester 3 (Compound 12) is a cleavable linker utilized in the synthesis of antibody-drug conjugate (ADC). It is a derivative of Dibenzylcyclooctyne (DBCO) resulting from the activation of N-hydroxysuccinimide by the carboxylic acid moiety of both methyl-oxanorbornadiene (MeOND) and dibenzoazacyclooctyne (DIBAC)[1][2].

3-Azidopropionic Acid Sulfo-NHS Ester is a water-soluble compound containing an azide group and an NHS ester. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The NHS ester can be used to label the p

DBCO-PEG4-acetic-Val-Cit-PAB为含四单元聚乙二醇（PEG）的ADC可分解连接体，适用于合成抗体药物偶联物（ADC）。

11-Azidoundecanoic acid，含有叠氮基团的化合物，兼具疏水性，作为生物偶联剂广泛应用。其叠氮基团可通过Staudinger结扎法或Click-chemistry方法进行修饰，为硫辛酸连接酶(LpIA)的特异性标记底物。此外，11-Azidoundecanoic acid作为点击化学试剂，能与含Alkyne基团的分子发生CuAAc反应，或与DBCO、BCN基团的分子进行SPAAC反应。