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BioChemicals
ROC-325
tcsc0033428
ROC-325
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$
189.00
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ORDERING INFORMATION
International
TAICLONE BIOTECH CORP.
order@taiclone.com
+886-2-2735-9682
+886-2-2735-9807
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Product Description
ROC-325 is a novel inhibitor of
autophagy
.
IC50 & Target: Autophagy
[1]
In Vitro:
ROC-325 is a novel inhibitor of autophagy. Treatment with ROC-325 results in a significant loss of acridine orange fluorescence. ROC-325 triggers a highly significant increase in cathepsin D (
CTSD
) levels. ROC-325 treatment yields pharmacodynamic effects that are consistent with inhibition of autophagy. 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]
.
In Vivo:
ROC-325 treatment leads to significant, dose-dependent inhibition of disease progression. ROC-325 is well tolerated and no notable toxicities are observed other than a very modest, nonsignificant reduction in mean body weight at the highest dose. Immunohistochemical analysis of specimens collected from animals treated with ROC-325 demonstrates significant, dose-dependent increases in the autophagic markers LC3B and p62 and increases apoptosis
[1]
.
Information
CAS No
1859141-26-6
Formula
C
28
H
27
ClN
4
OS
Clinical Information
clinicalinformation
Pathway
Autophagy
Target
Apoptosis
Autophagy
Specifications
Form
Light yellow to orange (Solid)
Purity / Grade
99.61%
Solubility
DMSO : 32 mg/mL (63.61 mM; Need ultrasonic); H2O : 1 mg/mL (1.99 mM; Need ultrasonic)
Smiles
O=C1C2=C(SC3=C1C=CC=C3)C(C)=CC=C2NCCN(CCNC4=CC=NC5=CC(Cl)=CC=C45)C
Misc Information
Storage Instruction
Storage temp. 2-8°C
Observed Molecular Weight
503.06
References
[1]. Carew JS, et al. Disruption of Autophagic Degradation with ROC-325 Antagonizes Renal Cell Carcinoma Pathogenesis. Clin Cancer Res. 2017 Jun 1;23(11):2869-2879.
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