MEL24

SKU:BHB21901720
Research Validated
Overview
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MEL24 (CAS 642072-48-8) is an inhibitor supplied as a solid. Relevant to PROTAC research. Molecular formula C17H18N4O3, molecular weight 326.35 g/mol.
Purity 98.0%
CAS Number 642072-48-8
Molecular Weight 326.35 g/mol
Form Solid
Storage Powder -20°C; in solvent -80°C
Options selector
Catalog no. Size
HY-153215-5MG 5 mg
HY-153215-10MG 10 mg
HY-153215-25MG 25 mg
HY-153215-50MG 50 mg
HY-153215-100MG 100 mg
HY-153215-200MG 200 mg
HY-153215-500MG 500 mg
HY-153215-1MLX10MM 1 mL x 10 mM (in DMSO)
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg, 500 mg, 1 mL x 10 mM (in DMSO)
  • Lead time: varies by selected option.
  • Storage: Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: transfer to -20°C as soon as possible.
Field Specification
CAS no. 642072-48-8
Applications
  • Functional Assay (In Vitro)
Molecular weight 326.35
Molecular formula C17H18N4O3
Purity 98.0%
SMILES O=C1N(C)C(C(C2NCCC3=C2NC4=C3C=CC=C4)C(N1C)=O)=O
Form Solid
Storage Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-153215
Main SKU BHB21901720
Inhibitors

Compound Overview

MEL24 is an Mdm2 E3 ligase inhibitor that reduces cell survival and increases sensitivity to DNA-damaging agents in a p53-dependent manner, and it has been used in in vitro antitumor studies[1]. It is supplied as a white to off-white solid (C17H18N4O3, MW 326.35) at 98.0% purity.

Physical & Chemical Properties

CAS Number 642072-48-8
Molecular Formula C17H18N4O3
Molecular Weight 326.35 g/mol
Purity 98.0%
Appearance Solid
Color White to off-white
SMILES O=C1N(C)C(C(C2NCCC3=C2NC4=C3C=CC=C4)C(N1C)=O)=O
Signaling Pathway PROTAC
Solubility In Vitro: DMSO: 20 mg/mL (61.28 mM; Requires sonication and warming and heat to 80°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Storage Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Ariel G Herman, et al. Discovery of Mdm2-MdmX E3 ligase inhibitors using a cell-based ubiquitination assay. Cancer Discov. 2011 Sep;1(4):312-25. 

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.

In Vitro

SolventSolubilityNotes
DMSO20 mg/mL (61.28 mM)requires sonication and warming and heat to 80°C; use freshly opened DMSO (absorbed moisture lowers solubility)

Aliquot the stock solution and store it at -80°C (up to 6 months) or -20°C (up to 1 month); avoid repeated freeze-thaw cycles.

In Vivo

Choose the formulation that suits the animal model and route of administration; percentages are volume ratios of the final working solution. Start from a clear DMSO stock (see In Vitro above), add the co-solvents one at a time in the order listed, mixing after each addition, and prepare the working solution fresh on the day of dosing. If precipitation or phase separation occurs, gentle warming or sonication can help.

Protocol 1

Composition10% DMSO + 90% Corn Oil
Result2 mg/mL (6.13 mM); clear solution; requires sonication
How to prepareGives a clear solution at 2 mg/mL. Use with caution if continuous dosing will exceed two weeks. For 1 mL of working solution: add 100 μL DMSO stock (20.0 mg/mL) to 900 μL corn oil.

Data provided by the manufacturer.

In Vitro

MEL24 acts on 293T cells with an ED50 value of 9.2 μM[1]. In HCT116 cells (p53 wild-type), MEL24 (15 μM, 6 h) raises the levels of Mdm2, p53 and MdmX, activates p53, and inhibits degradation of endogenous MdmX[1].

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price on some sizes?
A.Availability and lead time for those sizes are confirmed on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

Can’t find the compound you’re looking for?
Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

LIG1 Loss in TP53-mutant Triple Negative Breast Cancer Rewires DNA Repair and Confers Sensitivity to PARP-ATR Inhibitor Combinations. Mol Cancer Ther 2026 Jul 15:10.1158/1535-7163.MCT-26-0182. PMID: 42456172

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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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