| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC29215 | NH2-PEG6-CH2CH2COOH | NH2-PEG6-CH2CH2COOH is a cleavable 6 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC29217 | N-Boc-diethanolamine Featured | N-Boc-diethanolamine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC29218 | N-Boc-PEG4-bromide | N-Boc-PEG4-bromide is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC29220 | Propargyl-PEG2-amine | Propargyl-PEG2-amine is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Propargyl-PEG2-amine is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. |
|
| DC29222 | Fmoc-NH-PEG1-CH2COOH | Fmoc-NH-PEG1-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC29223 | Hydroxy-PEG2-(CH2)2-Boc | Hydroxy-PEG2-(CH2)2-Boc is a uncleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Hydroxy-PEG2-(CH2)2-Boc is extracted from patent WO2004008101A2 (compound 196). |
|
| DC29224 | m-PEG3-CH2CH2COOH | m-PEG3-CH2CH2COOH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC29225 | N-Boc-PEG9-alcohol | N-Boc-PEG9-alcohol is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC29226 | N-Boc-PEG6-alcohol | N-Boc-PEG6-alcohol is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC31389 | SGD-1269(MCMMAF) Featured | Mafodotin, also known as mc-MMAF and SGD-1269 or Maleimidocaproyl monomethylauristatin F, is a MMAF derivative having a Maleimidocaproyl linker (MC linker), which is ready to conjugate to antibody or other proteins or biopolymers. Mafodotin is a useful a |
|
| DC31423 | DM-4 Featured | Maytansinoid DM4, a chemical derivative of maytansine, is a potent and selective cytotoxic agent with promising anticancer properties. Anticancer properties of maytansinoids have been attributed to their ability to disrupt microtubule function. Maytansin |
|
| DC32583 | CL2A-SN-38 Featured | CL2A-SN38 is a SN38 derivative with a peptide-linker which can easily react with antibody to form an antibody-drug conjugate (ADC). CL2A-SN-38 is composed of a potent a DNA Topoisomerase I inhibitor SN-38 and a linker CL2A to make antibody drug conjugate |
|
| DC32585 | Paclitaxel succinate NHS ester Featured | DCN10809, also known as Paclitaxel succinate NHS ester, is a paclitaxel derivative with a succinic acid linker, in which the carboxy group is activated with an NHS ester. The NHS ester group is highly reactive to amino group or hydroxy group, and can be used to conjugate with other molecules such as peptides, proteins, antibodies or enzymes, or polymers. Paclitaxel-Succinic acid is a useful agent to make Paclitaxel-conjugate for drug delivery, nanodrug research. |
|
| DC40021 | MC-Val-Ala-OH | MC-Val-Ala-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC40172 | DC41 | DC41 is a DC1 derivative. DC1, a simplified analogue of CC-1065, is an antibody conjugate of cytotoxic DNA alkylators for the targeted treatment of cancer. |
|
| DC40368 | Luisol A | Luisol A, an aromatic tetraol, is a major metabolite of an estuarine marine actinomycete of the genus Streptomyces. Luisol A, anthraquinone antibiotic analog, is an ADC Cytotoxin. |
|
| DC40402 | MAC glucuronide α-hydroxy lactone-linked SN-38 | MAC glucuronide α-hydroxy lactone-linked SN-38 (Topoisomerase I inhibitor) is a stabilized lactone MAC glucuronide α-hydroxy lactone-linked SN-38 drug linker. MAC glucuronide α-hydroxy lactone-linked SN-38 is cytotoxic across L540cy cells and Ramos cells with IC50 values of 99 and 105 ng/mL, respectively. |
|
| DC40434 | Boc-NMe-Val-Val-Dil-Dap-OH | Boc-NMe-Val-Val-Dil-Dap-OH is an ADC Cytotoxin. |
|
| DC40435 | Boc-Val-Dil-Dap-OH | Boc-Val-Dil-Dap-OH is an ADC Cytotoxin. |
|
| DC40436 | Ald-Ph-PEG4-bis-PEG4-propargyl | Ald-Ph-PEG4-bis-PEG4-propargyl is a cleavable 8 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC40437 | Amino-PEG4-bis-PEG3-propargyl | Amino-PEG4-bis-PEG3-propargyl is a cleavable 6 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC40438 | Ald-Ph-PEG4-bis-PEG3-N3 | Ald-Ph-PEG4-bis-PEG3-N3 is a cleavable 6 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC40439 | Amino-PEG4-bis-PEG3-methyltetrazine | Amino-PEG4-bis-PEG3-methyltetrazine is a cleavable 7 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC40440 | Mal-PEG4-bis-PEG3-DBCO | Mal-PEG4-bis-PEG3-DBCO is a cleavable 7 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC40441 | Amino-bis-PEG3-DBCO | Amino-bis-PEG3-DBCO is a cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC40442 | Mal-PEG4-bis-PEG4-propargyl | Mal-PEG4-bis-PEG4-propargyl is a cleavable 8 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC40443 | Ald-Ph-PEG4-bis-PEG3-methyltetrazine | Ald-Ph-PEG4-bis-PEG3-methyltetrazine is a cleavable 7 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC40444 | Boc-Val-Dil-Dap-Phe-OMe | Boc-Val-Dil-Dap-Phe-Ome is an ADC Cytotoxin. |
|
| DC40445 | Tetrazine-PEG4-amine hydrochloride | Tetrazine-PEG4-amine (hydrochloride) is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
|
| DC40451 | Diacetyl Agrochelin | Diacetyl Agrochelin is an acetyl derivative of Agrochelin, which is produced by the fermentation of a marine Agrobacterium sp. Diacetyl Agrochelin has cytotoxic activity in tumor cell lines. |
|
