dbco-amine

DBCO-amine 是一种可切割的 ADC 接头，用于合成抗体-药物偶联物。

Sulfo DBCO-amine is an alkyl chain-derived PROTAC linker utilized for synthesizing PROTACs[1].

Azido-PEG10-amine是一种不可降解(non-cleavable)的ADC linker和PEG类的PROTAC linker，可用于合成抗体偶联分子(ADC)和PROTAC，可以和含有Alkyne、DBCO或BCN基团的分子发生点击化学反应。

Azido-PEG7-amine是一种不可降解(non-cleavable)的ADC linker和PEG类的PROTAC linker，可用于合成抗体偶联分子(ADC)和PROTAC，可以和含有Alkyne、DBCO或BCN基团的分子发生点击化学反应。

DBCO-NHCO-PEG4-amine is a cleavable ADC linker used to conjugate MMAE and antibody (e.g., DBCO-VCpAB MMAE and DBCO-TRX MMAE with EC50s of 280 nM and 22 nM in SKBR3 cells, respectively) [1].

DBCO-PEG4-amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). DBCO-PEG4-amine can be used in the synthesis of FPM-PEG4-DBCO (a homobifunctional azide-to-azide cross-linker)[1].

Sulfo DBCO-PEG4-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.

DBCO-C2-PEG4-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.

DBCO-C3-PEG4-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.

DBCO-NHCO-PEG12-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.

DBCO-NHCO-PEG2-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.

DBCO-NHCO-PEG6-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.

DBCO-PEG1-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.

DBCO-PEG2-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.

DBCO-PEG6-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.

DBCO-PEG9-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.

DBCO-SS-amine is a cleavable linker vital in ADC synthesis. DBCO-SS-amine joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.

diABZI-V C-DBCO（Compound 3）作为一种高效的STING激动剂，通过组织蛋白酶B的作用释放diABZI-胺，激活STING，从而使干扰素及其他免疫激活分子的生成得以提高，有效增强免疫系统对肿瘤的攻击能力。在THP1-Dual细胞中，diABZI-V C-DBCO与diABZI-胺激活STING的EC50值分别为1.47 nM和0.144 nM；在原代小鼠脾细胞中，这些值分别为7.7 μM和0.17 μM。因此，diABZI-V C-DBCO在癌症免疫研究领域具有重要的应用价值。

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-PEG3-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.

Sulfo DBCO-TFP Ester 是一种水溶性、含有磺基的点击化学试剂，可将磺基 DBCO 部分简单高效地掺入到含胺分子上。

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-PEG4-Val-Cit-PAB-PNP 是一种可裂解的 ADC 连接子，其中 Val-Cit 可以被 Cathepsin B 特异性裂解，而 PNP 可以被含胺的有效载荷取代。DBCO 能与叠氮化物分子通过点击化学反应结合。