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Synonyms: ATG7-IN-1


| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $329 | In Stock | In Stock | |
| 5 mg | $798 | In Stock | In Stock | |
| 10 mg | $1,090 | In Stock | In Stock | |
| 25 mg | $1,650 | In Stock | In Stock | |
| 50 mg | $2,230 | In Stock | In Stock | |
| 100 mg | $2,930 | - | In Stock |

| Description | ATG7-IN-1 is a highly potent, selective small-molecule ATG7 inhibitor with an IC₅₀ of 62 nM. ATG7-IN-1 blocks the formation of the ATG12-ATG5 and LC3-PE conjugate system at both the cellular and in vivo levels, thereby inhibiting autophagosome formation. ATG7-IN-1 can be used in research on autophagy mechanisms. |
| Targets & IC50 | SKOV3 cells:3 μM (EC50), NCI-H1650 cells:> 50 μM (EC50), ATG7:62 nM |
| In vitro | Methods: H4 glioma cells were treated with ATG7-IN-1 (0.01, 0.03, 0.1, 0.3, 1, 3 μmol/L) for 6 hours. LC3B spot formation was quantified by immunofluorescence to assess the inhibition of autophagic flux. Results: ATG7-IN-1 significantly reduced the number of LC3B foci and inhibited LC3 phosphorylation downstream of ATG7, with an IC₅₀ as low as the micromolar range. [1] |
| In vivo | Methods: HCT116 colorectal cancer xenograft mice were administered 150 mg/kg of ATG7-IN-1 via subcutaneous injection. Tumor tissue expression of LC3B and NBR1 was assessed 4 hours after dosing. Results: ATG7-IN-1 effectively inhibited autophagy in tumor tissue in vivo, reduced LC3B phosphorylation, and induced NBR1 accumulation, demonstrating good in vivo efficacy. [1] |
| Synonyms | ATG7-IN-1 |
| Molecular Weight | 470.5 |
| Formula | C17H19FN6O5S2 |
| Cas No. | 2226229-87-2 |
| Smiles | S(C=1C=2C(N(N1)[C@@H]3O[C@@H](COS(N)(=O)=O)[C@@H](O)C3)=NC=NC2N)C4=C(F)C=C(C)C=C4 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 255 mg/mL (541.98 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (10.63 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density. | ||||||||||||||||||||||||||||||||||||
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 µL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 µL Tween 80 and mix well until fully clarified.
3) Add 450 µL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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