6 Results for "

endoribonuclease inhibitor

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "endoribonuclease inhibitor" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-U00460
Target:  

IRE1

Research Areas:  

Cancer

3,6-DMAD hydrochloride, an acridine derivative, is a potent IRE1α-XBP1s pathway inhibitor. 3,6-DMAD hydrochloride promotes IL-6 secretion via the IRE1α-XBP1s pathway. 3,6-DMAD hydrochloride inhibits IRE1α oligomerization and endoribonuclease (RNase) activity. 3,6-DMAD hydrochloride can be used for research of cancer .
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Cat. No.: HY-116999
CAS No.: 452967-14-5
Purity:  99.66%
Target:  

HBV

Research Areas:  

Infection

IR415 is a potent anti-HBV agent and inhibits HBV replication by blocking the HBx activity. IR415 selectively interacts with HBx (Kd=2 nM) and blocks HBV-mediated RNAi suppression, reverses the inhibitory effect of HBx protein on the activity of the dicer endoribonuclease . HBx: hepatitis B virus X protein.
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Cat. No.: HY-U00460B
CAS No.: 2226511-77-7
Target:  

IRE1

Research Areas:  

Cancer

3,6-DMAD dihydrochloride, an acridine derivative, is a potent IRE1α-XBP1s pathway inhibitor. 3,6-DMAD dihydrochloride promotes IL-6 secretion via the IRE1α-XBP1s pathway. 3,6-DMAD dihydrochloride inhibits IRE1α oligomerization and endoribonuclease (RNase) activity. 3,6-DMAD dihydrochloride can be used for research of cancer .
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Cat. No.: HY-171189
CAS No.: 351891-58-2
Target:  

SARS-CoV

Research Areas:  

Infection

C-467929 is an Nsp15 endoribonuclease inhibitor with an IC50 of 8 μM. C-467929 binds to the SARS-CoV Nsp15 protein and can be utilized in infection research .
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Cat. No.: HY-162956
CAS No.: 364338-71-6
Target:  

SARS-CoV

Research Areas:  

Infection

SARS-CoV-2-IN-97 (Compound CO-01) is an inhibitor for SARS-CoV-2 Nsp15 endoribonuclease with an IC50 of 53.5 μM. SARS-CoV-2-IN-97 exhibits low cytotoxicity in A549-AT cell with IC50 of 134 μM .
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Cat. No.: HY-121492
CAS No.: 1414586-62-1
Target:  

Endonuclease

Research Areas:  

Cancer

NSC 45576 is a selective inhibitor of XendoU endoribonuclease and an inhibitor of CREB-CRE interaction, with an IC50 value of 29 μM against Xenopus laevis XendoU. NSC 45576 binds to the active sites of XendoU and PP11, and inhibits CREB-CRE interaction. NSC 45576 can be used in cancer-related research such as breast cancer and gastric cancer .
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