ChemicalBook--->CAS DataBase List--->1398568-47-2

1398568-47-2

1398568-47-2 Structure

1398568-47-2 Structure
IdentificationBack Directory
[Name]

Milademetan
[CAS]

1398568-47-2
[Synonyms]

DS-3032
Milademetan
Milademetan (DS-3032)
DS-3032B (Milademetan)
L-erythro-Hexonamide, 2,6-anhydro-5-[[[(3'R,4'S,5'R)-6''-chloro-4'-(2-chloro-3-fluoro-4-pyridinyl)-1'',2''-dihydro-4,4-dimethyl-2''-oxodispiro[cyclohexane-1,2'-pyrrolidine-3',3''-[3H]indol]-5'-yl]carbonyl]amino]-3,4,5-trideoxy-
[Molecular Formula]

C30H34Cl2FN5O4
[MDL Number]

MFCD31692325
[MOL File]

1398568-47-2.mol
[Molecular Weight]

618.53
Chemical PropertiesBack Directory
[Boiling point ]

840.7±65.0 °C(Predicted)
[density ]

1.44±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[pka]

12.43±0.70(Predicted)
[color ]

White to light yellow
Hazard InformationBack Directory
[Uses]

Milademetan (DS-3032) is a specific and orally active MDM2 inhibitor for the research of acute myeloid leukemia (AML) or solid tumors. Milademetan (DS-3032) induces G1 cell cycle arrest, senescence and apoptosis[1][2].
[in vivo]

Milademetan (DS-3032b, 50 mg/kg, oral gavage) delays tumor growth and improves survival in mice xenografted with neuroblastoma cells with functional TP53[4].

Animal Model:SH-SY5Y xenograft tumors in nude mice[4].
Dosage:50 mg/kg.
Administration:Oral gavage for 30 consecutive days with an alternating schedule of 4 days of daily treatment with oral gavages followed by 2 days without treatment (4+2).
Result:Survival in the mouse cohort was significantly prolonged.
Reduced neuroblastoma xenograft tumor growth by activating TP53 signaling.
[storage]

Store at -20°C
[References]

[1] ARYL SULFONOHYDRAZIDES. WO 2017069289 A1.
[2] M.M. Gounder, et al. Milademetan, an oral MDM2 inhibitor, in well-differentiated/dedifferentiated liposarcoma: results from a phase 1 study in patients with solid tumors or lymphomas. European Journal of Cancer 138S2 (2020) S1–S62.
[3] Li, Yangbing, et al. Development of novel PROTAC Small-Molecule Degraders of MDM2 Protein and Peptidomimetic Inhibitors Targeting WDR5-MLL1 Protein-Protein Interaction.
[4] Viktor Arnhold, et al. Reactivating TP53 signaling by the novel MDM2 inhibitor DS-3032b as a therapeutic option for high-risk neuroblastoma. ncotarget. 2018 Jan 5; 9(2): 2304–2319. DOI:10.18632/oncotarget.23409
Spectrum DetailBack Directory
[Spectrum Detail]

Milademetan(1398568-47-2)1HNMR
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