ROC-325
Based on 4 publication(s) in Google Scholar
ROC-325 is a potent and orally active autophagy inhibitor with a strong anticancer activity. ROC-325 induces the deacidification of lysosomes, accumulation of autophagosomes, and disrupted autophagic flux. ROC-325 also induces renal cell carcinoma apoptosis.
For research use only. We do not sell to patients.
- Purity : 98.73%
- CAS No.: 1859141-26-6
- Formula: C28H27ClN4OS
- Molecular Weight:503.06
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
Publications Citing Use of MedChemExpress (MCE) ROC-325
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WB
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IF
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Histological Imaging/Staining
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In Vivo Efficacy Study
Biological Activity
Description
IC50 & Target
Autophagy[1]
In Vitro
ROC-325 antagonizes renal cell carcinoma (RCC) growth and survival in an ATG5/7-dependent manner, induces apoptosis, and exhibits favorable selectivity. ROC-325 inhibits cells growth with IC50 values of 4.9 μM, 11 μM, 4.6 μM, 5.4 μM, 7.4 μM, 11 μM, 8.2 μM, 5.8 μM, 5.0 μM, 11 μM, 8.4 μM and 6.0 μM for A498, A549, CFPAC-1, COLO-205, DLD-1, IGROV-1, MCF-7, MiaPaCa-2, NCI-H69, PC-3, RL and UACC-62 cells, respectively. ROC-325 induces hallmark features of autophagy inhibition and antagonizes autophagic flux[1].
ROC-325 triggers a highly significant increase in cathepsin D (CTSD) levels. Treatment with 5 μM ROC-325 for 24 hours leads to the formation of LC3B punctae and a robust increase in LC3B levels in both A498 and 786-0 RCC cells. Immunoblotting analysis conducted in both A498 and 786-0 cells demonstrates that ROC-325 promotes a dose-dependent increase in LC3B expression in a manner that correlated with a corresponding increase in the levels of p62 and cathepsin D[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 1859141-26-6
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Appearance Solid
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Molecular Weight 503.06
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Formula C28H27ClN4OS
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Color Light yellow to orange
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SMILES
O=C1C2=C(SC3=C1C=CC=C3)C(C)=CC=C2NCCN(CCNC4=CC=NC5=CC(Cl)=CC=C45)C
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year
Publications (4)
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Journal Impact Factor
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Most Recent
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J Extracell Vesicles
Neuronal Extracellular Vesicles Carrying APOE Downregulate Filament Actin Polymerization Signaling to Inhibit Synapse Formation in Alzheimer's Disease. [Abstract]2026 Mar;15(3):e70248. PMID: 41806350 -
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Eur J Pharmacol
Autophagic inhibitor ROC-325 ameliorates glomerulosclerosis and podocyte injury via inhibiting autophagic flux in experimental FSGS mice. [Abstract]2024 Nov 15:983:177007. PMID: 39307335
ROC-325 purchased from MedChemExpress. Usage Cited in: Eur J Pharmacol. 2024 Nov 15:983:177007. [Abstract]
Western blotting showed the expression of the p62, LC3A/B and GAPDH in MPCs treated with YAP siRNA or added ROC-325 with the concentration of 2.5 μM and 5 μM, respectively.
ROC-325 purchased from MedChemExpress. Usage Cited in: Eur J Pharmacol. 2024 Nov 15:983:177007. [Abstract]
Immunofluorescence staining for mRFP (red puncta) and GFP (green puncta) in the MPCs treated with ROC-325 (5 μM).
ROC-325 purchased from MedChemExpress. Usage Cited in: Eur J Pharmacol. 2024 Nov 15:983:177007. [Abstract]
Representative light microscopy of kidney sections by periodic acid–Schiff (PAS) staining from the mice treated with ROC-325 (50 mg/kg, i.g.).
ROC-325 purchased from MedChemExpress. Usage Cited in: Eur J Pharmacol. 2024 Nov 15:983:177007. [Abstract]
Representative images of the three experimental groups of mice and kidney. Body weight, kidney weight and kidney/body weight treated with ROC-325 (50 mg/kg, i.g.).
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Solvent & Solubility
In Vitro:
DMSO : 4.55 mg/mL (9.04 mM; Need ultrasonic and warming; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
H2O : < 0.1 mg/mL (insoluble)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Purity & Documentation
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Data Sheet (279 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 1.9878 mL | 9.9392 mL | 19.8783 mL | 49.6959 mL |
| 5 mM | 0.3976 mL | 1.9878 mL | 3.9757 mL | 9.9392 mL |