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D649697-10mgDuostatin 5 is a cytotoxin designed based on dolastatin, can meet the requirement of serving as an effective cytotoxin in ADC , but has the advantages of fewer synthesis steps, easy operation, less difficulty in quality control and more stable
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D649697-1mgDuostatin 5 is a cytotoxin designed based on dolastatin, can meet the requirement of serving as an effective cytotoxin in ADC , but has the advantages of fewer synthesis steps, easy operation, less difficulty in quality control and more stable
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D649697-5mgDuostatin 5 is a cytotoxin designed based on dolastatin, can meet the requirement of serving as an effective cytotoxin in ADC , but has the advantages of fewer synthesis steps, easy operation, less difficulty in quality control and more stable
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D659243-10mgDxd-d 5 is a deuterium labeled Dxd. Dxd is a potent DNA topoisomerase I inhibitor, with an IC50 of 0.31 μM, used as a conjugated drug of HER2-targeting ADC (DS-8201a) .Appearance:SolidIC50&: Target:Topoisomerase I 0.31 μM (IC 50 )In Vitro:Stable
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D659243-1mgDxd-d 5 is a deuterium labeled Dxd. Dxd is a potent DNA topoisomerase I inhibitor, with an IC50 of 0.31 μM, used as a conjugated drug of HER2-targeting ADC (DS-8201a) .Appearance:SolidIC50&: Target:Topoisomerase I 0.31 μM (IC 50 )In Vitro:Stable
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D659243-5mgDxd-d 5 is a deuterium labeled Dxd. Dxd is a potent DNA topoisomerase I inhibitor, with an IC50 of 0.31 μM, used as a conjugated drug of HER2-targeting ADC (DS-8201a) .Appearance:SolidIC50&: Target:Topoisomerase I 0.31 μM (IC 50 )In Vitro:Stable
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D661678-1mlDxd-d 5 is a deuterium labeled Dxd. Dxd is a potent DNA topoisomerase I inhibitor, with an IC50 of 0.31 μM, used as a conjugated drug of HER2-targeting ADC (DS-8201a) .IC50&: Target:Topoisomerase I 0.31 μM (IC 50 )In Vitro:Stable heavy isotopes
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E649126-10mgendo-BCN-PEG4-Val-Cit-PAB-MMAE is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)In VitroADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker. MCE has not
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E649126-1mgendo-BCN-PEG4-Val-Cit-PAB-MMAE is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)In VitroADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker. MCE has not
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E649126-5mgendo-BCN-PEG4-Val-Cit-PAB-MMAE is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)In VitroADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker. MCE has not
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E163650-1gEpoxyl functionctional PEG, EPO PEG is an amino (-NH2) and hydroxyl group reactive PEG derivative that can be used to modify protein, peptide or any other surfaces with available amino or hydroxyl groups. Epoxyl PEGs react readily with amine groups
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E163651-1gEpoxyl functionctional PEG, EPO PEG is an amino (-NH2) and hydroxyl group reactive PEG derivative that can be used to modify protein, peptide or any other surfaces with available amino or hydroxyl groups. Epoxyl PEGs react readily with amine groups