Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6741 |
SPDP
SPDP Crosslinker |
Others | Others |
SPDP 是一种短链交联剂,用于通过 NHS 酯和吡啶基二硫醇反应基团与半胱氨酸巯基形成可切割(可还原)的二硫键,实现胺与巯基的共轭。它是一种可降解的 ADC 连接剂,可用于合成抗体偶联药物。 | |||
T38597 |
SPDP-sulfo
|
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SPDP-sulfo is a cleavable linker vital in ADC synthesis. SPDP-sulfo joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness. | |||
T17834 |
DM4-SPDP
|
Others | Others |
DM4-SPDP, a drug-linker conjugate, integrates the antitubulin agent DM4 with the linker SMCC, facilitating the creation of antibody drug conjugates[1]. Additionally, SPDP serves as a short-chain crosslinker enabling amine-to-sulfhydryl conjugation, leveraging NHS-ester and pyridyldithiol groups to establish cleavable (reducible) disulfide bonds with cysteine sulfhydryls[2][3]. | |||
T18535 |
PEG4-SPDP
|
Others | Others |
PEG4-SPDP is a cleavable ADC linker used for the antibody-drug conjugates (ADCs). | |||
T18709 | SPDP-PEG12-acid | Others | Others |
SPDP-PEG12-acid is a cleavable 12-unit polyethylene glycol (PEG) linker utilized for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T18711 |
SPDP-PEG24-acid
|
Others | Others |
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. | |||
T18716 |
SPDP-PEG9-acid
|
Others | Others |
SPDP-PEG9-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. | |||
T16916 |
SPDP-PEG4-acid
|
Others | Others |
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. | |||
T18713 |
SPDP-PEG36-NHS ester
|
Others | Others |
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]. | |||
T18725 |
Sulfo-LC-SPDP
|
Others | Others |
Sulfo-LC-SPDP is a heterobifunctional crosslinker characterized by its thiol-cleavable and membrane impermeable properties. | |||
T15724 |
LC-PEG8-SPDP
|
Others | Others |
LC-PEG8-SPDP is a cleavable ADC linker used for the antibody-drug conjugates (ADCs)[1]. | |||
T18715 |
SPDP-PEG7-acid
|
Others | Others |
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. | |||
T18714 |
SPDP-PEG5-acid
|
Others | Others |
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. | |||
T16915 |
SPDP-C6-NHS ester
|
Others | Others |
SPDP-C6-NHS ester is an alkyl/ether-based linker utilized in the synthesis of PROTACs[1]. | |||
T18710 |
SPDP-PEG12-NHS ester
|
Others | Others |
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. | |||
T18712 |
SPDP-PEG24-NHS ester
|
Others | Others |
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. | |||
T16917 |
SPDP-PEG4-NHS ester
|
Others | Others |
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. | |||
T16918 |
SPDP-PEG6-NHS ester
|
Others | Others |
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. | |||
T18525 | PC SPDP-NHS carbonate ester | Others | Others |
PC SPDP-NHS carbonate ester is a cleavable linker compound utilized in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T18708 |
SPDP-C6-Gly-Leu-NHS ester
|
Others | Others |
SPDP-C6-Gly-Leu-NHS ester is a cleavable linker employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T18733 | Sulfo-SPDP-C6-NHS sodium | Others | Others |
Sulfo-SPDP-C6-NHS sodium is a sodium salt form of a cleavable ADC linker employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T77286 |
DSPE-SPDP
|
||
DSPE-SPDP,一种磷脂分子,能够在水中自行定向并形成脂质双层,适用于多种生化研究。 | |||
T33904 |
PDPH Crosslinker
PDPH Cross linker,SPDP Hydrazide,PDPH Cross-linker |
||
PDPH crosslinker(SPDP Hydrazide) is a lytic heterobisfunctional protein crosslinker. | |||
T18702 |
DBA-DM4
|
Others | Others |
DBA-DM4 is a drug-linker conjugate for antibody-drug conjugate (ADC) synthesis, combining the tubulin inhibitor DM1 with the SPDP linker[1]. |