dppe

DPPE-mPEG 是一种 PEG- 修饰的脂类。DPPE-mPEG 可以减少蛋白质的非特异性吸附，延长体内循环时间。

DPPE-MPEG(2000) is a polyethylene glycol (PEG) derivative of 1,2-dipalmitoyl-rac-glycero-3-phosphoethanolamine (DPPE), characterized as a PEGylated phospholipid.

DPPE-PEG550 是一种用于设计共轭聚合物纳米颗粒的合成脂质体 (LPs) 的 PEG 脂质功能端基。脂质体纳米颗粒 (LNPs) 通过生物素修饰和羧基端可以进一步与其他生物分子耦合。功能化的纳米颗粒适用于特定细胞蛋白的靶向标记。以链霉亲和素作为连接体，生物素化的 PEG 脂质缀合聚合物纳米颗粒能够与细胞表面受体上的生物素化抗体结合，从而在荧光成像和传感方面具有应用价值。

DPPE-PEG750 是用于合成脂质体的 PEG 脂质功能端基，可设计用于构建共轭聚合物纳米颗粒。脂质体纳米颗粒 (LNPs) 通过生物素修饰和羧基端方便与其他生物分子耦合。功能化的纳米颗粒适用于特定细胞蛋白的靶向标记。利用链霉亲和素作为连接体，生物素化的 PEG 脂质缀合聚合物纳米颗粒能够与细胞表面受体上的生物素化抗体结合，具备基于荧光的成像和传感的应用价值。

DPPE-PEG1000 是一种用于合成脂质体 (LPs) 的 PEG 脂质功能端基，用于设计共轭聚合物纳米颗粒。脂质体纳米颗粒 (LNPs) 通过生物素修饰和羧基端，能够进一步与其他生物分子耦合。功能化的纳米颗粒可实现特定细胞蛋白的靶向标记。借助链霉亲和素连接，生物素化的 PEG 脂质缀合聚合物纳米颗粒能够结合到细胞表面受体上的生物素化抗体，展示了荧光成像和传感的实用性。

DPPE-PEG3000 是一种用于合成脂质体 (LPs) 的 PEG 脂质功能端基，用于设计共轭聚合物纳米颗粒。这些脂质体纳米颗粒 (LNPs) 通过生物素修饰和羧基端，可进一步与其他生物分子耦合。功能化后的纳米颗粒可以用于特定细胞蛋白质的靶向标记。利用链霉亲和素作为连接体，生物素化的 PEG 脂质缀合聚合物纳米颗粒能够结合到细胞表面受体上的生物素化抗体上，从而实现基于荧光的成像和传感应用。

DPPE-PEG5000 是一种用于合成脂质体 (LPs) 的 PEG 脂质功能端基，适合设计共轭聚合物纳米颗粒。脂质体纳米颗粒 (LNPs) 通过生物素修饰和羧基端，便于与其他生物分子进一步耦合。这些功能化的纳米颗粒可用于靶向标记特定细胞蛋白。借助链霉亲和素作为连接体，生物素化的 PEG 脂质缀合聚合物纳米颗粒能够与细胞表面受体上的生物素化抗体结合，从而实现基于荧光的成像和传感应用。

DPPE-PEG-amine (MW 2000) 是一种磷脂，因其良好的生物相容性和显著的两亲性，成为药物配方中的主要剂型或辅料，优化治疗效果。它用于药物递送研究。

m-PEG-DPPE (MW 2000) 是一种 PEG 脂质，用于提高难溶性药物的输送效率和组织特异性，也是药物递送研究的理想选择。

DPPE-PEG350 是一种用于设计共轭聚合物纳米颗粒的 PEG 脂质功能端基，专门用于合成脂质体 (LPs)。脂质体纳米颗粒 (LNPs) 通过生物素修饰和羧基端，能够进一步与其他生物分子进行耦合。功能化的纳米颗粒可用于特定细胞蛋白的靶向标记。当以链霉亲和素作为连接体时，生物素化的 PEG 脂质缀合聚合物纳米颗粒能与细胞表面受体上的生物素化抗体结合，从而实现荧光成像和传感的应用。

Tesmilifene fumarate (DPPE fumarate) 是一种 H1C 受体拮抗剂，可增强化疗的细胞毒性且保护正常细胞。

DPPE-PEG2000 (16:0 PEG2000 PE) 是一种经PEG修饰的脂质，用于降低蛋白质的非特异性吸附并延长体内循环时间。

1,2-Dipalmitoyl-sn-glycero-3-PE-N-(cap biotin) is a biotinylated phospholipid. It has been used in PEGylated polyamidoamine-dendrimer-conjugated supported lipid bilayers (SLB) to isolate circulating tumor cells and tumor cell microembolis from patient-derived blood by antibody-coated microfluidics. [1] It has also been used as a component of SLBs to detect protein-ligand binding with ortho-conjugated Texas Red DHPE. [2] In addition, 1,2-dipalmitoyl-sn-glycero-3-PE-N-(cap biotin) has been used in SLBs partitioned into nanowells to create DNA curtains, which can be used as a high-throughput tool for detection of protein-DNA interactions at the single molecule level.[3]

1,3-Dipalmitoyl glycero-2-phosphatidylethanolamine is a phospholipid incorporating saturated long-chain (16:0) stearic acid at the sn-1 and sn-3 positions, with phosphatidylethanolamine (PE) at the sn-2 position. Phosphatidylethanolamines, critical components of biological membranes, play essential structural and functional roles. Various PE types are instrumental in forming micelles, liposomes, and other synthetic membranes.

SPDP-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.

SPDP-PEG4-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.

SPDP-PEG6-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.

SPDP-PEG12-acid is a cleavable 12-unit polyethylene glycol (PEG) linker utilized for the synthesis of antibody-drug conjugates (ADCs)[1].

SPDP-PEG12-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.

SPDP-PEG24-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.

SPDP-PEG24-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.

SPDP-PEG36-NHS ester is a PEG ADC linker consisting of 36 units, characterized by cleavability. It plays a crucial role in the synthesis of antibody-drug conjugates (ADCs)[1].

SPDP-PEG5-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.

SPDP-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.