PeptideDB

HCVcc-IN-2

CAS: F: C32H29BrN2O10S3 W: 777.68

HCVcc-IN-2 is a benzothiazole-2-thiophene S-glycoside derivative with antitumor and antiviral activity. HCVcc-IN-2 has h
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This product is for research use only, not for human use. We do not sell to patients.

Bioactivity HCVcc-IN-2 is a benzothiazole-2-thiophene S-glycoside derivative with antitumor and antiviral activity. HCVcc-IN-2 has high inhibition against the three cell line from CNS cancer (SF-539 and SNB-75), colon cancer (HCT-116), and renal cancer (A498)[1].
Invitro HCVcc-IN-2 (compound 6c) (0.1, 1, 10, and 100 μg/mL; 1 h) shows antiviral activities against a variety of viruses such as coxsackievirus B4 (CBV4), hepatitis A virus HM 175 (HAV), hepatitis C genotype 4 (HCVcc), adenovirus type 7 (HAdV7), and herpes simplex virus 1 (HSV-1) with viral reduction rates of 83.3%, 63.3%, 40%, 63.3%, and 30%, respectively[1]. HCVcc-IN-2 (0.55-1.9 μg/mL; 1 h) inhibits various virus with IC50 of 0.55 μg/mL (herpes simplex virus), 0.76 μg/mL (HCVcc genotype virus), and 0.76 μg/mL (coxsackievirus B4), respectively; or with CC50 of 1.8 μg/mL (herpes simplex virus), 1.9 μg/mL (HCVcc genotype virus), and 1.9 μg/mL (coxsackievirus B4), respectively[1].HCVcc-IN-2 (7.68-16.01 μg/mL; ) inhibits hepatitis C virus NS3/4A and HSV- USP7 protease enzyme with IC50s of 16.01 μg/mL and 7.68 μg/mL[1].HCVcc-IN-2 (0.01 mM; 24 h) has low cytotoxicity, shows high inhibition against two cell lines, SK-MEL-5, OVCAR-4[1]. Cell Cytotoxicity Assay[1] Cell Line:
Name HCVcc-IN-2
Formula C32H29BrN2O10S3
Molar Mass 777.68
Transport Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Reference [1]. Azzam et al. Novel Thiophene Thioglycosides Substituted with the Benzothiazole Moiety: Synthesis, Characterization, Antiviral and Anticancer Evaluations, and NS3/4A and USP7 Enzyme Inhibitions. ACS Omega. 2022 Sep 29;7(40):35656-35667.