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ADC Linker with Payload

ADC Linker with Payload

货号 产品名 CAS号 信息
CSN23910 VH032-linker 5 2172819-74-6 VH032-ketone-C4-carboxylic acid is a PROTAC block consist of VHL032 linked to alkyl with a carboxylic acid group for conjugation reactions.
CSN20152 Vat-Cit-PAB-Monomethyl Dolastatin 10 1415329-13-3 Vat-Cit-PAB-Monomethyl Dolastatin 10 is an antibody drug conjugate cytotoxin.
CSN20150 Val-Cit-PAB-MMAF 863971-56-6 Val-Cit-PAB-MMAF is an antibody drug conjugate cytotoxin.
CSN18875 Val-Cit-PAB-MMAE 644981-35-1 Val-Cit-PAB-MMAE is a potent tubulin inhibitor (MMAE), Val-Cit-PAB-MMAE is an antibody drug conjugate.
CSN18876 SuO-Val-Cit-PAB-MMAE N/A SuO-Val-Cit-PAB-MMAE consists of the ADCs linker (SuO-Val-Cit-PAB) and potent tubulin inhibitor (MMAE), SuO-Val-Cit-PAB-MMAE is an antibody-drug conjugate.
CSN26869 SuO-Glu-Val-Cit-PAB-MMAE 1895916-24-1 SuO-Glu-Val-Cit-PAB-MMAE consists a cleavable ADC linker (SuO-Glu-Val-Cit-PAB) and a potent tubulin inhibitor (MMAE). SuO-Glu-Val-Cit-PAB-MMAE can be used in the synthesis of antibody-drug conjugates (ADCs)[1].
CSN26878 Vipivotide tetraxetan 1702967-37-0 PSMA-617, also know as vipivotide tetraxetan. It is a ligand used to make 177Lu-PSMA-617, which is a radioactive molecule to fight cancer. PSMA617 possesses a small peptide, which was designed to target prostate-specific membrane antigen (PSMA). PSMA617 demonstrates high radiolytic stability for at least 72 h. PSMA617 has high inhibition potency (equilibrium dissociation constant Ki=2.34±2.94 nM on LNCaP; Ki=0.37±0.21 nM enzymatically determined). 177 Lu-PSMA-617 offers a potential additional life-prolonging treatment option for men with mCRPC.
CSN23909 Thalidomide-NH-PEG3-propionic acid 2138440-82-9 Pomalidomide-PEG3-C2-carboxylic acid is a PROTAC block consist of Pomalidomide linked to PEG with a carboxylic acid functional group for conjugation reactions.
CSN18880 MMAF-OMe 863971-12-4 MMAF-OMe is a synthetic antineoplastic agent and also used as a part of some experimental anti-cancer antibody-drug conjugates such as vorsetuzumab mafodotin and SGN-CD19A.
CSN18878 4-((S)-2-((S)-2-((S)-3-Amino-2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)propanamido)-3-methylbutanamido)-5-ureidopentanamido)benzyl ((S)-1-(((S)-1-(((3R,4S,5S)-1-((S)-2-((1R,2R)-3-(((1S,2R)-1-hydroxy-1-phenylpropan-2-yl)amino)-1-methoxy-2-methyl-3-oxopropyl)pyrrolidin-1-yl)-3-methoxy-5-methyl-1-oxoheptan-4-yl)(methyl)amino)-3-methyl-1-oxobutan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)(methyl)carbamate 1491152-26-1 mDPR-Val-Cit-PAB-MMAE consists the ADCs linker (mDPR-Val-Cit-PAB) and potent tubulin inhibitor (MMAE), mDPR-Val-Cit-PAB-MMAE is an antibody drug conjugate.
CSN26872 MC-VC-PAB-Tubulysin M 1639939-56-2 MC-vc-PAB-Tubulysin M consists a cleavable ADC linker (MC-vc-PAB) and a cytotoxic tubulin inhibitor Tubulysin M (HY-N7053). Tubulysin M is a cytotoxic activity tubulysin which inhibits tubulin polymerization and leads to cell cycle arrest and apoptosis[1].
CSN20149 MC-Val-Cit-PAB-MMAF 863971-17-9 MC-Val-Cit-PAB-MMAF is an antibody drug conjugate cytotoxin.
CSN20151 SGD-1910 1342820-51-2 MC-Val-Ala-PBD is an antibody drug conjugate cytotoxin.
CSN26875 6-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)-N-(4-((S)-7-methoxy-8-(3-(((S)-7-methoxy-2-(4-methoxyphenyl)-5-oxo-5,11a-dihydro-1H-benzo[e]pyrrolo[1,2-a][1,4]diazepin-8-yl)oxy)propoxy)-5-oxo-5,11a-dihydro-1H-benzo[e]pyrrolo[1,2-a][1,4]diazepin-2-yl)phenyl)hexan 1342820-52-3 MC-PBD consists a non-cleavable ADC linker MC and a cytotoxic DNA crosslinking pyrrolobenzodiazepine (PBD). MC-PBD can be used in the synthesis of antibody-drug conjugates (ADCs)[1].
CSN26874 MB-VC-MGBA 932744-62-2 MB-VC-MGBA is a drug-linker conjugate for ADC with potent antitumor activity by using MGBA (minor-groove-binding DNA-alkylating agent), linked via the ADC linker MB-VC[1].
CSN18877 MAL-di-EG-Val-Cit-PAB-MMAE 2746391-62-6 MAL-di-EG-Val-Cit-PAB-MMAE consists the ADCs linker (MAL-di-EG-Val-Cit-PAB) and potent tubulin inhibitor (MMAE), MAL-di-EG-Val-Cit-PAB-MMAE is an antibody drug conjugate.
CSN17728 Fmoc-Val-Cit-PAB-MMAE 1350456-56-2 Fmoc-Val-Cit-PAB-MMAE consists the ADCs linker (Fmoc-Val-Cit-PAB) and potent tubulin inhibitor (MMAE), Fmoc-Val-Cit-PAB-MMAE is an antibody drug conjugate.
CSN20147 DM4-SPDP 2245698-48-8 DM4-SPDP is an antibody drug conjugate cytotoxin.
CSN20148 SPDB-DM4 1626359-62-3 DM4-SPDB is an antibody drug conjugate cytotoxin.
CSN20154 DM4-SMCC 1228105-52-9 DM4-SMCC is an antibody drug conjugate cytotoxin.
CSN20146 SPP-DM1 452072-20-7 DM1-SPP is an antibody drug conjugate cytotoxin.
CSN20153 SMCC-DM1 1228105-51-8 DM1-SMCC is an antibody drug conjugate cytotoxin.
CSN26867 DGN549-C 2058075-34-4 DGN549-C consists a cleavable ADC linker valine-alanine (va) and PBD dimer. DGN549 is a novel DNA-alkylating cytotoxic payload and can be used in the synthesis of antibody-drug conjugates (ADCs)[1].
CSN26873 DBM-MMAF 1810001-93-4 DBM-MMAF is a drug-linker conjugate composed of a potent antitubulin agent MMAF and a linker DBM to make antibody drug conjugate (ADC)[1].
CSN26871 DBCO-PEG4-VC-PAB-MMAE 2129164-91-4 DBCO-PEG4-VC-PAB-MMAE consists a ADC linker (DBCO-PEG4-VC-PAB) and a tubulin polymerization inhibitor MMAE (HY-15162). DBCO-PEG4-VC-PAB-MMAE can be used in the synthesis of antibody-drug conjugates (ADCs). MMAE is a synthetic derivative of dolastatin 10 and functions as a potent mitotic inhibitor by inhibiting tubulin polymerization[1].
CSN26868 DBCO-PEG4-Val-Cit-PAB-MMAF 2244602-23-9 DBCO-PEG4-Val-Cit-PAB-MMAF consists a cleavable 4 unit PEG ADC linker (DBCO-PEG4-Val-Cit-PAB) and a potent tubulin polymerization inhibitor (MMAF). DBCO-PEG4-Val-Cit-PAB-MMAF can be used in the synthesis of antibody-drug conjugates (ADCs)[1].
CSN15788 Ansamitocin P-3' 66547-09-9 Ansamitocin P 3' exhibits antitumour activity, is an antibody drug conjugate cytotoxin.
CSN26866 AcLysValCit-PABC-DMAE-SW-163D 2411007-69-5 AcLysValCit-PABC-DMAE-SW-163D is a drug-linker conjugates for ADC which consists of a natural bis-intercalator, SW-163D, conjugated via an AcLysValCitPABC-DMAE linker[1].
CSN17810 Acetylene-linker-Val-Cit-PABC-MMAE 1411977-95-1 Acetylene-linker-Val-Cit-PABC-MMAE consists the ADCs linker (Acetylene-linker-Val-Cit-PABC) and potent tubulin inhibitor (MMAE), Acetylene-linker-Val-Cit-PABC-MMAE is an antibody drug conjugate.
CSN26870 MC-DM1 1375089-56-7
CSN26865 Mc-VC-PAB-SN38 1801838-28-7
CSN26876 DBCO-PEG4-MMAF 2360411-65-8
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