| Size | Price | Stock |
|---|---|---|
| 5mg | $156 | In-stock |
| 10mg | $252 | In-stock |
| 25mg | $529 | In-stock |
| 50mg | $972 | In-stock |
| 100mg | $1800 | In-stock |
| 200 mg | Get quote | |
| 500 mg | Get quote | |
| We match the lowest price on market. | ||
We offer a substantial discount on larger orders, please inquire via [email protected]
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| Cat. No. : | HY-17493 |
| M.Wt: | 562.50 |
| Formula: | C29H34Cl2FN3O3 |
| Purity: | >98 % |
| Solubility: | DMSO : ≥ 53 mg/mL |
MI-773 is an orally active, selective MDM2-p53 interaction inhibitor with a Ki of 0.88 nM for MDM2. MI-773 blocks the MDM2-TP53 interaction. MI-773 potently activates p53. MI-773 induces Apoptosis. MI-773 causes tumor regression in xenograft models of adenoid cystic carcinoma. MI-773 exhibits anticancer effects in neuroblastoma. MI-773 TFA can be used for the research of adenoid cystic carcinoma[1][2].
In Vivo:MI-773 (10-100 mg/kg; p.o.; daily) induces dose-dependent tumor growth inhibition and regression in the UM-PDX-HACC-5 adenoid cystic carcinoma model, with 100 mg/kg mediating a 127% TGI index and 86% tumor shrinkage via p53-dependent apoptosis[1].
MI-773 (100 mg/kg; p.o.; daily) mediates significant tumor regression in the ACCx6 adenoid cystic carcinoma PDX model[1].
MI-773 (100 mg/kg; p.o.; daily) mediates significant tumor regression in the ACCx9 adenoid cystic carcinoma PDX model[1].
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