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SMD-3040

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Catalog No. T79820Cas No. 3033109-92-8
Alias SMD3040, SMD 3040

SMD-3040 is a potent and selective SMARCA2 PROTAC degrader that achieves efficient target protein elimination with a DC50 of 12 nM and a Dmax of 91%, leading to robust inhibition of tumor cell proliferation and pronounced antitumor activity, and is enabled by rational assembly of a SMARCA2/4 ligand and a VHL ligand, supporting its application in melanoma and broader oncology research.

SMD-3040

SMD-3040

😃Good
Catalog No. T79820Alias SMD3040, SMD 3040Cas No. 3033109-92-8
SMD-3040 is a potent and selective SMARCA2 PROTAC degrader that achieves efficient target protein elimination with a DC50 of 12 nM and a Dmax of 91%, leading to robust inhibition of tumor cell proliferation and pronounced antitumor activity, and is enabled by rational assembly of a SMARCA2/4 ligand and a VHL ligand, supporting its application in melanoma and broader oncology research.
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
SMD-3040 is a potent and selective SMARCA2 PROTAC degrader that achieves efficient target protein elimination with a DC50 of 12 nM and a Dmax of 91%, leading to robust inhibition of tumor cell proliferation and pronounced antitumor activity, and is enabled by rational assembly of a SMARCA2/4 ligand and a VHL ligand, supporting its application in melanoma and broader oncology research.
In vitro
In proliferation assays utilizing SMARCA4-deficient cancer cell lines (specifically SK-Mel-5, H838, and A549), SMD-3040 was administered over a 7-day treatment period. The compound exhibited potent antiproliferative effects with GI50 values ranging from 8.8 to 119 nM [1].
In vivo
To evaluate antitumor efficacy in a physiological context, a mouse model harboring human melanoma xenografts was employed. SMD-3040 was administered intravenously at dosages ranging from 25 to 50 mg/kg, following a schedule of twice-weekly injections for a duration of two weeks. This treatment regimen led to a significant suppression of tumor growth in the xenograft model [1].
SynonymsSMD3040, SMD 3040
Chemical Properties
Molecular Weight943.21
FormulaC52H66N10O5S
Cas No.3033109-92-8
SmilesC(N1CC2(C1)CCC(CC2)N3C=C(C=N3)C=4C=C(N=NC4N)C5=C(O)C=CC=C5)[C@H]6CC[C@H](C(N[C@H](C(=O)N7[C@H](C(N[C@@H](C)C8=CC=C(C=C8)C9=C(C)N=CS9)=O)C[C@@H](O)C7)C(C)(C)C)=O)CC6
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (84.82 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.0602 mL5.3010 mL10.6021 mL53.0105 mL
5 mM0.2120 mL1.0602 mL2.1204 mL10.6021 mL
10 mM0.1060 mL0.5301 mL1.0602 mL5.3010 mL
20 mM0.0530 mL0.2651 mL0.5301 mL2.6505 mL
50 mM0.0212 mL0.1060 mL0.2120 mL1.0602 mL

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Stock solution preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (stock solution concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
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