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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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| 5 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| 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]. |
| Synonyms | SMD3040, SMD 3040 |
| Molecular Weight | 943.21 |
| Formula | C52H66N10O5S |
| Cas No. | 3033109-92-8 |
| Smiles | C(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 | In 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. | ||||||||||||||||||||||||||||||
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DMSO
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