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MS023 trihydrochloride
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Catalog No. T77787Cas No. 2108631-19-0
Alias MS023 3HCl
MS023 trihydrochloride (MS023 3HCl) is a selective and potent human type I protein arginine methyltransferase (PRMT) inhibitor with potential anticancer activity against PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8 for cancer research.
MS023 trihydrochloride
😃Good
Catalog No. T77787Alias MS023 3HClCas No. 2108631-19-0
MS023 trihydrochloride (MS023 3HCl) is a selective and potent human type I protein arginine methyltransferase (PRMT) inhibitor with potential anticancer activity against PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8 for cancer research.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $143 | 35 days | |
| 5 mg | $623 | 35 days | |
| 10 mg | $1,090 | 35 days | |
| 25 mg | $2,390 | 35 days |
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Product Introduction
Bioactivity
Chemical Properties
| Description | MS023 trihydrochloride (MS023 3HCl) is a selective and potent human type I protein arginine methyltransferase (PRMT) inhibitor with potential anticancer activity against PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8 for cancer research. |
| Targets&IC50 | PRMT8:5 nM, PRMT4:83 nM, PRMT1:30 nM, PRMT6:4 nM, PRMT3:119 nM |
| In vitro | MS023 trihydrochloride (1-1000 nM; 48 hours) inhibits the activity of PRMT1 methyltransferase in MCF7 cells[2]. MS023 trihydrochloride (1-1000 nM; 20 hours) inhibits the activity of PRMT6 methyltransferase in HEK293 cells[2].' |
| In vivo | Combination administration of MS023 trihydrochloride (160 mg/kg, ip) and PKC412 (100 mg/kg, ig) disrupts the propagation of MLL-r Acute Lymphoblastic Leukemia (ALL) by inhibiting the maintenance of functional MLL-r ALL initiating cells[1]. |
| Alias | MS023 3HCl |
| Molecular Weight | 396.78 |
| Formula | C17H28Cl3N3O |
| Cas No. | 2108631-19-0 |
Storage & Solubility Information
| Storage | Shipping with blue ice. |
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For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (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.
(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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