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Chemical Structure| 1398568-47-2 Chemical Structure| 1398568-47-2

Structure of Milademetan
CAS No.: 1398568-47-2

Chemical Structure| 1398568-47-2

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Milademetan is a specific MDM2 inhibitor with oral activity, primarily used in the study of acute myeloid leukemia and various solid tumors. It exerts anti-tumor effects by inducing G1 phase cell cycle arrest, senescence, and apoptosis.

Synonyms: DS-3032

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Product Details of Milademetan

CAS No. :1398568-47-2
Formula : C30H34Cl2FN5O4
M.W : 618.53
SMILES Code : CC1(C)CCC2([C@@]3(C(NC4=CC(Cl)=CC=C43)=O)[C@@H](C5=CC=NC(Cl)=C5F)[C@H](C(N[C@H]6CO[C@H](C(N)=O)CC6)=O)N2)CC1
Synonyms :
DS-3032
MDL No. :MFCD31692325

Safety of Milademetan

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
A549 100nM 48 hours Evaluate the single-agent activity of MDM2 inhibitors and the synergistic effect of combination with MEK inhibitors. Results showed that single-agent milademetan significantly inhibited A549 cell growth (IC50 112-450nM), and combination with trametinib showed synergistic effects, increasing the expression of pro-apoptotic proteins PUMA and BIM. J Thorac Oncol. 2023 Sep;18(9):1165-1183
SW1573 100nM 48 hours Evaluate the single-agent activity of MDM2 inhibitors and the synergistic effect of combination with MEK inhibitors. Results showed that single-agent milademetan significantly inhibited SW1573 cell growth (IC50 112-450nM), and combination with trametinib showed synergistic effects, increasing the expression of pro-apoptotic proteins PUMA and BIM. J Thorac Oncol. 2023 Sep;18(9):1165-1183
LUAD12c 100nM 48 hours Evaluate the single-agent activity of MDM2 inhibitors and the synergistic effect of combination with MEK inhibitors. Results showed that single-agent milademetan significantly inhibited LUAD12c cell growth (IC50 20-40nM), and combination with trametinib showed synergistic effects, increasing the expression of pro-apoptotic proteins PUMA and BIM. J Thorac Oncol. 2023 Sep;18(9):1165-1183
ECLC5-GLx 100nM 48 hours Evaluate the single-agent activity of MDM2 inhibitors and the synergistic effect of combination with MEK inhibitors. Results showed that single-agent milademetan significantly inhibited ECLC5-GLx cell growth (IC50 20-40nM), and combination with trametinib showed synergistic effects, increasing the expression of pro-apoptotic proteins PUMA and BIM. J Thorac Oncol. 2023 Sep;18(9):1165-1183
MCC-336 100 nM 3 days To assess the effect of milademetan on the viability of MCC patient-derived cell lines, results showed that MCC-336 cell line was sensitive to milademetan with an IC50 of 0.0462 μM. JCI Insight. 2022 Jul 8;7(13):e160513
MCC-301 100 nM 3 days To assess the effect of milademetan on the viability of MCC patient-derived cell lines, results showed that MCC-301 cell line was highly sensitive to milademetan with an IC50 of 0.0144 μM. JCI Insight. 2022 Jul 8;7(13):e160513
PeTa 100 nM 3 days To assess the effect of milademetan on the viability of MCC cell lines, results showed that PeTa cell line was sensitive to milademetan with an IC50 of 0.0150 μM. JCI Insight. 2022 Jul 8;7(13):e160513
WaGa 100 nM 3 days To assess the effect of milademetan on the viability of MCC cell lines, results showed that WaGa cell line was highly sensitive to milademetan with an IC50 of 0.0034 μM. JCI Insight. 2022 Jul 8;7(13):e160513
MKL-1 100 nM 3 days To assess the effect of milademetan on the viability of MCC cell lines, results showed that MKL-1 cell line was sensitive to milademetan with an IC50 of 0.1704 μM. JCI Insight. 2022 Jul 8;7(13):e160513
MCF-10A 8.87 ± 1.91 µM 72 hours Evaluate the effect of Milademetan on the viability of non-malignant breast cells, showing a lesser reduction in cell viability compared to triple-negative breast cancer cells. Int J Mol Sci. 2025 Jan 26;26(3):1078
HCT116 p53−/− 8.44 ± 0.67 µM 72 hours Evaluate the effect of Milademetan on the viability of colon cancer cells, showing a significant reduction in cell viability regardless of p53 status. Int J Mol Sci. 2025 Jan 26;26(3):1078
HCT116 p53+/+ 6.42 ± 0.84 µM 72 hours Evaluate the effect of Milademetan on the viability of colon cancer cells, showing a significant reduction in cell viability regardless of p53 status. Int J Mol Sci. 2025 Jan 26;26(3):1078
MDA-MB-468 5.51 ± 0.25 µM 72 hours Evaluate the effect of Milademetan on the viability of triple-negative breast cancer cells, showing a significant reduction in cell viability. Int J Mol Sci. 2025 Jan 26;26(3):1078
MDA-MB-436 7.62 ± 1.52 µM 72 hours Evaluate the effect of Milademetan on the viability of triple-negative breast cancer cells, showing a significant reduction in cell viability. Int J Mol Sci. 2025 Jan 26;26(3):1078
MDA-MB-231 4.04 ± 0.32 µM 72 hours Evaluate the effect of Milademetan on the viability of triple-negative breast cancer cells, showing a significant reduction in cell viability. Int J Mol Sci. 2025 Jan 26;26(3):1078
ECLC5-GLx 100 nM 48 hours Evaluate the combination effect of MDM2 and RET inhibitors, results showed increased p27 expression, increased p21 expression, inhibited CCND1 induction, significantly reduced E2F1 expression, and increased p-p53 and PUMA expression. JCO Precis Oncol. 2024 Sep;8:e2400241

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
NOD scid gamma mouse (NSG) ECLC5-GLx, LX-285, LUAD12c, L13BS1, LU-01-0448, A549 Oral 100 mg/kg milademetan, 1mg/kg trametinib Once daily, 5 days on, 2 days off Evaluate the in vivo antitumor efficacy of MDM2 inhibitors in combination with MEK inhibitors. Results showed that combination therapy was more effective than single-agent therapy in multiple patient-derived xenograft models, significantly inhibiting tumor growth and increasing the expression of pro-apoptotic protein PUMA. J Thorac Oncol. 2023 Sep;18(9):1165-1183
Mice MKL-1 xenograft model Oral 25 mg/kg, 50 mg/kg, 100 mg/kg Once daily for 30 days To evaluate the antitumor activity of milademetan in the MKL-1 xenograft model, results showed that tumor volumes were significantly reduced in the 50 mg/kg and 100 mg/kg dose groups, and survival was significantly prolonged. JCI Insight. 2022 Jul 8;7(13):e160513
NSG mice ECLC5-GLx and LX-285 Oral 100 mg/kg (milademetan) Once daily, 5 days on, 2 days off Evaluate the combination effect of MDM2 and RTK inhibitors, results showed significantly prolonged tumor control compared to single-agent therapy. JCO Precis Oncol. 2024 Sep;8:e2400241

Clinical Trial:

NCT Number Conditions Phases Recruitment Completion Date Locations
NCT03671564 Acute Myeloid Leukemia PHASE1 COMPLETED 2019-09-11 Japanese Red Cross Narita Hosp... More >>ital, Chiba, 286-0041, Japan|Kyusyu University Hospital, Fukuoka, 812-8582, Japan|Gifu Municipal Hospital, Gifu, 500-8513, Japan|Chugoku Central Hospital, Hiroshima, 720-0001, Japan|National Hospital Organization Kumamoto Medical Center, Kumamoto, 860-0008, Japan|Tenri Hospital, Nara, 632-8552, Japan|NTT Medical Center Tokyo, Tokyo, 141-8625, Japan|National Hospital Organization Disaster Medical Center, Tokyo, 190-0014, Japan Less <<

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.62mL

0.32mL

0.16mL

8.08mL

1.62mL

0.81mL

16.17mL

3.23mL

1.62mL

 

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