VTP50469 mesylate
Based on 13 publication(s) in Google Scholar
VTP50469 mesylate is a potent, and selective Menin-MLL1 inhibitor that effectively targets MLL-rearranged and NPM1c+ leukemia. VTP50469 mesylate selectively kills cell lines with MLL rearrangements and NPM1c+ mutations. VTP50469 mesylate displaces Menin from protein complexes and inhibits MLL's chromatin occupancy at specific genes, leading to significant changes in gene expression, differentiation, and apoptosis. VTP50469 demonstrates dramatic reductions in leukemia burden in patient-derived xenograft models of MLL-r acute myeloid leukemia and MLL-r acute lymphoblastic leukemia, with some mice remaining disease-free for over a year post-treatment.
For research use only. We do not sell to patients.
- CAS No.: 2169919-27-9
- Formula: C34H55FN6O10S3
- Molecular Weight:823.03
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications Citing Use of MedChemExpress (MCE) VTP50469 mesylate
More- Blood. 2026 Feb 24:blood.2025031486. [Abstract]
- Blood. 2024 Aug 16:blood.2023023644. [Abstract]
- Nat Cell Biol. 2023 Sep;25(9):1346-1358. [Abstract]
- Nat Commun. 2025 Mar 18;16(1):2641. [Abstract]
- Blood Cancer J. 2022 Jan 11;12(1):5. [Abstract]
- Leukemia. 2026 Mar 25. [Abstract]
- Leukemia. 2025 Jan;39(1):75-86. [Abstract]
- Blood Adv. 2026 Jul 14;10(13):4757-4771. [Abstract]
- Int J Oncol. 2020 Oct;57(4):1057-1071. [Abstract]
- bioRxiv. 2026 Jun 19.
- bioRxiv. 2026 Feb 17.
- bioRxiv. 2025 Nov 12:2025.11.10.687648. [Abstract]
- bioRxiv. 2023 Oct 1.
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Cell Proliferation/Viability Assay
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Cell Proliferation/Viability Assay
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Cell Proliferation/Viability Assay
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Biological Activity
Chemical Information
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CAS No. 2169919-27-9
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Molecular Weight 823.03
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Formula C34H55FN6O10S3
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SMILES
CS(=O)(O)=O.CC(C)N(C(C)C)C(C(C=C(C=C1)F)=C1OC2=CN=CN=C2N(C3)CC3(CC4)CCN4C[C@@H]5CC[C@H](CC5)NS(C)(=O)=O)=O.CS(=O)(O)=O
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Synonyms
SNDX-50469 mesylate
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (13)
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Journal Impact Factor
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Most Recent
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Blood
Overcoming menin inhibitor resistance in AML cells with combinations including BET proteins and a dual BRG1/BRM inhibitor. [Abstract]2026 Feb 24:blood.2025031486. PMID: 41734382 -
Blood
Epigenetic Regulation of Non-canonical Menin Targets Modulates Menin Inhibitor Response in Acute Myeloid Leukemia. [Abstract]2024 Aug 16:blood.2023023644. PMID: 39158067 -
Nat Cell Biol
2023 Sep;25(9):1346-1358. PMID: 37591951
VTP50469 mesylate purchased from MedChemExpress. Usage Cited in: Nat Cell Biol. 2023 Sep;25(9):1346-1358. [Abstract]
Immunoblot analysis of 1014 Kdm6a isogenic cells treated with inhibitors that block the function of epigenetic modifiers that normally maintain gene expression including VTP50469 (500 nM), EPZ-5676 (1 μM), PF-9363 (100 nM), JQAD1 or DMSO for 6 days.
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Nat Commun
Guanine nucleotide biosynthesis blockade impairs MLL complex formation and sensitizes leukemias to menin inhibition. [Abstract]2025 Mar 18;16(1):2641. PMID: 40102405
VTP50469 mesylate purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Mar 18;16(1):2641. [Abstract]
Relative viability of MOLM-13 cells following treatment with different concentrations of VTP50469 (3.91-1000 nM) over 2-7 days.
VTP50469 mesylate purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Mar 18;16(1):2641. [Abstract]
Relative viability of human AML cell lines upon treatment with different concentrations of VTP50469 (3.91-1000 nM) over 5 days.
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Blood Cancer J
Effective Menin inhibitor-based combinations against AML with MLL rearrangement or NPM1 mutation (NPM1c). [Abstract]2022 Jan 11;12(1):5. PMID: 35017466
VTP50469 mesylate purchased from MedChemExpress. Usage Cited in: Blood Cancer J. 2022 Jan 11;12(1):5. [Abstract]
A, B MOLM13 and OCI-AML3 cells were treated with the indicated concentrations of VTP50469 (SNDX-50469; 0, 0.25, 1 μM) for 48 h. Following this, total cell lysates were prepared and immunoblot analyses were conducted. The expression levels of β-Actin in the lysates served as the loading control.
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Leukemia
A Perturb-seq map of a differentiation hub reveals synergistic vulnerabilities in KMT2A-rearranged acute myeloid leukemia. [Abstract]2026 Mar 25. PMID: 41882099 -
Leukemia
NPM1-fusion proteins promote myeloid leukemogenesis through XPO1-dependent HOX activation. [Abstract]2025 Jan;39(1):75-86. PMID: 39443736
VTP50469 mesylate purchased from MedChemExpress. Usage Cited in: Leukemia. 2025 Jan;39(1):75-86. [Abstract]
NPM1::CCDC28A cells and mouse cKit+ bone marrow cells were incubated with selinexor or VTP50469 (0, 0.1, 0.3, 1, 3, 10, and 30 μM) at the indicated concentration for 72 h. Cell viability was assessed using the Cell Counting Kit-8.
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Blood Adv
Combining menin and MEK inhibition to target poor prognosis KMT2A-rearranged RAS pathway-mutant acute myeloid leukemia. [Abstract]2026 Jul 14;10(13):4757-4771. PMID: 42085603 -
Int J Oncol
Menin‑MLL inhibitors induce ferroptosis and enhance the anti‑proliferative activity of auranofin in several types of cancer cells. [Abstract]2020 Oct;57(4):1057-1071. PMID: 32945449 -
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bioRxiv
2025 Nov 12:2025.11.10.687648. PMID: 41292793 -
Purity & Documentation
References
Calculators
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