448 Results for "

ADC molecule

" in MedChemExpress (MCE) Product Catalog:
Products (448)

448 Results for "ADC molecule" in MCE Product Catalog:

Cat. No.: HY-136104
Purity:  97.97%
Target:  

ADC Linkers

Research Areas:  

Cancer

Methyltetrazine-Maleimide is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . Methyltetrazine-Maleimide is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
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Cat. No.: HY-W591408
CAS No.: 2768446-73-5
Research Areas:  

Cancer

DBCO-Val-Cit-PAB-MMAE is a drug-linker conjugate, which can be used for the synthesis of ADC molecules. MMAE (HY-15162) is a tubulin inhibitor, which can be used as an ADC toxin. DBCO-Val-Cit-PAB is the linker with the electrophilic group .
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Cat. No.: HY-138387
CAS No.: 349553-73-7
Purity:  98.69%
Target:  

ADC Linkers

Research Areas:  

Cancer

6-Azido-hexylamine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . 6-Azido-hexylamine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Cat. No.: HY-140313
CAS No.: 1802238-48-7
Purity:  95.22%
Target:  

ADC Linkers

Research Areas:  

Cancer

Methyltetrazine-DBCO is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . Methyltetrazine-DBCO is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups. Methyltetrazine-DBCO also contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
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Cat. No.: HY-140352
CAS No.: 236754-49-7
Purity:  98.49%
Target:  

ADC Linkers

Research Areas:  

Cancer

Azide-PEG5-Tos is a cleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . Azide-PEG5-Tos is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Cat. No.: HY-W250408
CAS No.: 1352202-13-1
Research Areas:  

Cancer

Fmoc-NMe-Val-Val-Dil-Dap-OH is an intermediate for preparing drug-linker conjugate MC-MMAF, which can be used for synthesis of ADC molecule .
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Cat. No.: HY-133412
CAS No.: 2749932-04-3
Purity:  96.02%
Target:  

ADC Linkers

Research Areas:  

Cancer

DBCO-NHCO-S-S-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . DBCO-NHCO-S-S-NHS ester is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
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Cat. No.: HY-136053
CAS No.: 1962919-29-4
Purity:  99.34%
Target:  

ADC Linkers

Research Areas:  

Cancer

Tetrazine-PEG4-biotin is a PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . Tetrazine-PEG4-biotin is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
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Cat. No.: HY-170534
CAS No.: 2921734-44-1
Target:  

ADC Linkers

Research Areas:  

Cancer

Ac-EEVC-OH is a ADC Linker that can be used for the synthesis of ADC molecules .
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Cat. No.: HY-164378
CAS No.: 2694026-68-9
Target:  

ADC Payloads

Research Areas:  

Cancer

Hydrotecan is a Camptothecin (HY-16560) derivative that can be used as an ADC cytotoxin. Hydrotecan can be used to synthesize ADC molecules .
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Cat. No.: HY-169322
CAS No.: 2921735-80-8
Synonyms: Mal-Exo-EVC-MMAE
APL-1081 (Mal-Exo-EVC-MMAE) is part of an antibody-conjugated active molecule (ADC). APL-1081 is conjugated with an ADC linker (peptide Mal-Exo-EEVC) and a potent tubulin polymerization inhibitor, MMAE (HY-15162) .
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Cat. No.: HY-140104
CAS No.: 1807512-40-8
Purity:  ≥98.0%
Target:  

ADC Linkers

Research Areas:  

Cancer

Azidoethyl-SS-ethylamine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . Azidoethyl-SS-ethylamine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Cat. No.: HY-136031
CAS No.: 2123482-78-8
Purity:  96.12%
Target:  

ADC Linkers

Research Areas:  

Cancer

Tetrazine-SS-Biotin is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . Tetrazine-SS-Biotin is a click chemistry reagent, it contains a Tetrazine group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing TCO groups.
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Cat. No.: HY-170400
CAS No.: 2845165-06-0
Research Areas:  

Cancer

LNK4-S is a drug-linker conjugate, that can be used for synthesis of ADC molecule M-VA-EXA and F-VA-EXA .
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Cat. No.: HY-138745
CAS No.: 1802908-01-5
Purity:  97.77%
Target:  

ADC Linkers

Research Areas:  

Cancer

Bis-sulfone-PEG3-Azide is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Bis-sulfone-PEG3-Azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Cat. No.: HY-157275
CAS No.: 2222277-20-3
Purity:  ≥95.0%
Target:  

ADC Linkers

Research Areas:  

Cancer

Gly-Gly-Gly-PEG2-azide is an ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . Gly-Gly-Gly-PEG4-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Cat. No.: HY-170868
CAS No.: 3025194-00-4
Research Areas:  

Cancer

CL2A-FL118 is a drug-linker for synthesis of ADC molecule Sac-CL2A-FL118 .
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Cat. No.: HY-42974
CAS No.: 2754384-59-1
Target:  

ADC Linkers

Research Areas:  

Cancer

DBCO-PEG3-acid is a non-cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). DBCO-PEG3-acid contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups .
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Cat. No.: HY-P99360
CAS No.: 1912423-61-0
Synonyms: Anti-AXL/UFO Reference Antibody (enapotamab)

Research Areas:  

Cancer

Enapotamab (Anti-AXL/UFO Reference Antibody) is an AXL/UFO-related antibody that can be used for synthesis of ADC molecule Enapotamab vedotin (HY-P99921) .
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Cat. No.: HY-148128
CAS No.: 1802498-63-0
Purity:  98.53%
Research Areas:  

Cancer

TAM470 is a novel cytolysin, inhibiting tubulin polymerization and microtubule depolymerization. TAM470 can be used in the synthesis of OMTX705 as payload molecule, OMTX705 is a novel FAP-targeting antibody-drug conjugates (ADCs) with antitumor activity .
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