An autophagy inhibitor
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ROC-325

Item No. 33566

Technical Information
Formal Name
1-[[2-[[2-[(7-chloro-4-quinolinyl)amino]ethyl]methylamino]ethyl]amino]-4-methyl-9H-thioxanthen-9-one
CAS Number
1859141-26-6
Molecular Formula
C28H27ClN4OS
Formula Weight
Purity
≥98%
A solid
Chloroform: 10 mg/mlDMF: slightly solubleDMSO: slightly solubleEthanol: slightly soluble
λmax
220, 257 nm
SMILES
O=C1C2=C(SC3=C1C(NCCN(CCNC4=C5C=CC(Cl)=CC5=NC=C4)C)=CC=C3C)C=CC=C2
InChi Code
InChI=1S/C28H27ClN4OS/c1-18-7-10-23(26-27(34)21-5-3-4-6-25(21)35-28(18)26)32-14-16-33(2)15-13-31-22-11-12-30-24-17-19(29)8-9-20(22)24/h3-12,17,32H,13-16H2,1-2H3,(H,30,31)
InChi Key
HXUYKEGAEIYPKY-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    ROC-325 is an autophagy inhibitor.1 It inhibits autophagic flux and induces lysosomal deacidification and apoptosis in 786-O renal cell carcinoma cells when used at a concentration of 5 µM. ROC-325 decreases viability in a panel of 12 cancer cell lines, including renal, lung, pancreatic, and prostate cancer cells, with IC50 values ranging from 4.9 to 11 µM. It reduces tumor growth in a 786-O mouse xenograft model when administered at a dose of 50 mg/kg. ROC-325 also decreases the cytopathic effect of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in infected Vero E6 cells (EC50 = 3.28 µM).2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Carew, J.S., Espitia, C.M., Zhao, W., et alDisruption of autophagic degradation with ROC-325 antagonizes renal cell carcinoma pathogenesis. Clin. Cancer Res. 23(11), 2869-2879 (2017).

    2. Gorshkov, K., Chen, C.Z., Bostwick, R., et alThe SARS-CoV-2 cytopathic effect is blocked by lysosome alkalizing small molecules. ACS Infect. Dis. (2020).