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DMBA-SIL-Mal-MMAE
DMBA-SIL-Mal-MMAE, a cytotoxin-linker conjugate designed for antibody-drug conjugates (ADC), exhibits significant antitumor activity. It incorporates the anti-mitotic agent monomethyl auristatin E (MMAE, a tubulin inhibitor) via the linker DMBA-SIL-Mal [1].
Catalog No. T87862Cas No. 2923885-49-6
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DMBA-SIL-Mal-MMAE
Catalog No. T87862Cas No. 2923885-49-6
DMBA-SIL-Mal-MMAE, a cytotoxin-linker conjugate designed for antibody-drug conjugates (ADC), exhibits significant antitumor activity. It incorporates the anti-mitotic agent monomethyl auristatin E (MMAE, a tubulin inhibitor) via the linker DMBA-SIL-Mal [1].
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose. | Pack Size | Price | Availability | Quantity |
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| 10 mg | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry |
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Product Introduction
Bioactivity
Chemical Properties
| Description | DMBA-SIL-Mal-MMAE, a cytotoxin-linker conjugate designed for antibody-drug conjugates (ADC), exhibits significant antitumor activity. It incorporates the anti-mitotic agent monomethyl auristatin E (MMAE, a tubulin inhibitor) via the linker DMBA-SIL-Mal [1]. |
| Molecular Weight | 1403.65 |
| Formula | C72H106N8O20 |
| Cas No. | 2923885-49-6 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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