Inquiry Basket
| Catalog | Product Name | CAS Number |
|---|---|---|
| BADC-01845 | MC-VC-PAB-NH2 TFA | 1616727-21-9 |
| MC-VC-PAB-NH2 TFA is a trifluoroacetate salt form of a cleavable peptide ADC linker with Val-Cit-PABC sequence, enabling enzyme-sensitive payload release in antibody-drug conjugates. Keywords: ADC linker, cleavable linker, Val-Cit, TFA salt, enzyme-sensitive. | Inquiry | |
| BADC-01854 | SCO-PEG7-Maleimide | 2143968-81-2 |
| SCO-PEG7-Maleimide is a strain-promoted cyclooctyne ADC linker with PEG7 spacer and maleimide group, enabling rapid thiol-specific conjugation for stable antibody-drug conjugate formation and improved payload attachment. Keywords: ADC linker, SCO linker, PEG spacer, maleimide, thiol conjugation. | Inquiry | |
| BADC-01863 | Gly-Gly-Gly-PEG4-azide | |
| Gly-Gly-Gly-PEG4-azide is a tri-glycine peptide ADC linker with PEG4 spacer and azide functionality, enabling site-specific click chemistry conjugation for stable payload attachment in antibody-drug conjugates. Keywords: ADC linker, peptide linker, PEG spacer, azide linker, click chemistry. | Inquiry | |
| BADC-01864 | Mal-PEG8-Val-Ala-PABC | |
| Mal-PEG8-Val-Ala-PABC is a maleimide ADC linker featuring a PEG8 spacer and cleavable Val-Ala-PABC sequence, supporting thiol-specific conjugation and enzyme-triggered payload release in antibody-drug conjugates. Keywords: ADC linker, maleimide linker, PEG spacer, cleavable peptide, thiol conjugation. | Inquiry | |
| BADC-01866 | Mal-Val-Ala-PABA-cGAMP | |
| Mal-Val-Ala-PABA-cGAMP is a maleimide-functionalized ADC linker conjugated to cGAMP payload, enabling thiol-specific conjugation and targeted delivery for immune modulation in antibody-drug conjugates. Keywords: ADC linker, maleimide linker, cGAMP payload, thiol conjugation, targeted therapy. | Inquiry | |
| BADC-01867 | Mc-Gly-Gly-Phe-Gly-PAB-OH TFA | |
| Mc-Gly-Gly-Phe-Gly-PAB-OH TFA is a peptide-based cleavable ADC linker with Boc protection and trifluoroacetate salt, designed for enzyme-sensitive payload release and controlled conjugation in antibody-drug conjugates. Keywords: ADC linker, peptide linker, cleavable linker, TFA salt, payload release. | Inquiry | |
| BADC-01869 | NH2-MPAA-NODA | |
| NH2-MPAA-NODA is a nitroveratryl-based photocleavable linker. NH2-MPAA-NODA is also a chelator for Al18F labeling of peptides and antibodies. | Inquiry | |
| BADC-01870 | Tetrazine-PEG7-amine hydrochloride | |
| Tetrazine-PEG7-amine hydrochloride is a cleavable 7 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | Inquiry | |
| BADC-01871 | APN-PEG36-tetrazine | |
| APN-PEG36-tetrazine is a long PEG36 spacer ADC linker with tetrazine functionality, enabling rapid bioorthogonal click conjugation for stable payload attachment in antibody-drug conjugates and enhanced solubility. Keywords: ADC linker, PEG linker, tetrazine linker, bioorthogonal chemistry, payload conjugation. | Inquiry | |
| BADC-01872 | Ala-Ala-Asn-PAB TFA | |
| Ala-Ala-Asn-PAB TFA is a cleavable tripeptide ADC linker intermediate with enzyme-sensitive sequence and trifluoroacetate salt, facilitating targeted drug release in antibody-drug conjugates. Keywords: ADC linker, peptide linker, enzyme-sensitive, TFA salt, controlled release. | Inquiry | |
| BADC-01878 | CbzNH-PEG8-amide-bis(pentayl-5OBz) | |
| CbzNH-PEG8-amide-bis(pentayl-5OBz) is a PEG8-based ADC linker intermediate with multiple protective groups, designed for stable payload conjugation and controlled release in antibody-drug conjugates. Keywords: ADC linker, PEG linker, protective groups, payload conjugation, controlled release. | Inquiry | |
| BADC-01886 | Ala-CO-amide-C4-Boc | |
| Ala-CO-amide-C4-Boc is an alanine-based ADC linker intermediate with amide bond and Boc protection, supporting selective conjugation and controlled drug delivery in antibody-drug conjugates. Keywords: ADC linker, alanine linker, amide bond, Boc protection, payload delivery. | Inquiry | |
| BADC-01888 | Cbz-D-Glu(Bn)-Gly-Gly-Gly-Gly | |
| Cbz-D-Glu(Bn)-Gly-Gly-Gly-Gly is a peptide ADC linker intermediate with protective groups, enabling enzyme-sensitive cleavage and precise payload release in antibody-drug conjugates. Keywords: ADC linker, peptide linker, protective groups, enzyme-sensitive, controlled release. | Inquiry | |
| BADC-01922 | Allyl N-(2-aminoethyl)carbamate | 223741-66-0 |
| Allyl N-(2-aminoethyl)carbamate is an amine-containing ADC intermediate suitable for selective functionalization. Its allyl group enables further click or thiol-ene reactions for modular linker design. | Inquiry | |
| BADC-01930 | (4S)-4-Hydroxy-L-proline hydrochloride | 441067-49-8 |
| (4S)-4-Hydroxy-L-proline hydrochloride is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | Inquiry | |
| BADC-01940 | Fmoc-azetidine-3-carboxylic acid | 193693-64-0 |
| Fmoc-azetidine-3-carboxylic acid is a cyclic amino acid derivative suitable for building constrained linkers in antibody-drug conjugates and peptide-based drug systems. | Inquiry | |
| BADC-01947 | Z-AEVD-FMK | 1135688-47-9 |
| Z-AEVD-FMK is a cell-permeant and irreversible caspase-10 inhibitor. It is a cleavable ADC linker for the synthesis of antibody active molecule conjugates (ADCs). | Inquiry | |
| BADC-01954 | Fmoc-N-amido-PEG6-acetic acid | 437655-96-4 |
| Fmoc-N-amido-PEG6-acetic acid is a PEG linker containing a protected amino group and a carboxylic acid. The carboxylic acid can be reacted with amino groups in the presence of activators. | Inquiry | |
| BADC-01956 | Propargyl-PEG7-acid | 2093154-00-6 |
| Propargyl-PEG7-acid is a heterobifunctional PEG linker containing a propargyl group and a carboxylic acid. The propargyl group can react with azide in various biomolecules via click chemistry, and the carboxylic acid can be reacted with amino groups in the presence of activators. | Inquiry | |
| BADC-01957 | CHO-Ph-CONH-PEG5-azide | 2566404-73-5 |
| CHO-Ph-CONH-PEG5-azide is a PEG reagent containing a benzaldehyde group and a terminal azide group. The benzaldehyde can react with primary amines. The azide can react with alkynes, DBCO and BCN moieties via Click Chemistry reactions. | Inquiry |
