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BB07CA902

Chemical Structure : BB07CA902

CAS No.:

BB07CA902

Catalog No.: PC-25852Not For Human Use, Lab Use Only.

BB07CA902 is a potent, specific, covalent inhibitor of interferon-stimulated gene 15 (ISG15) protease murine USP18 (mUSP18) with IC50 of 35 nM, effectively increases ISGylation levels in cells by inhibiting mUSP18 activity.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

BB07CA902 is a potent, specific, covalent inhibitor of interferon-stimulated gene 15 (ISG15) protease murine USP18 (mUSP18) with IC50 of 35 nM, effectively increases ISGylation levels in cells by inhibiting mUSP18 activity.
showed full mUSP18 specificity amongst a panel of 41 DUBs.
BB07CA902 covalently inhibits mUSP18 with an enzyme inactivation rate (kinact) over inhibition constant (Ki) ratio (kinact/Ki) of 4646 M−1s−1.
BB07CA902 is less potent toward human USP18 with IC50 of 1.2 uM.
BB07CA902 significantly elevated cellular ISGylation in a dose-dependent manner, and a maximum accumulation of ISGylation reached 10 µM.
BB07CA902 does not inhibit human USP18 in cells.
BB07CA902 inhibits in-cell mUSP18/ISG15 interaction in a dose-dependent manner with IC50 of 2.0 uM, does not inhibit the interactions of hUSP18 with ISG15 and STAT2.

Physicochemical Properties

M.Wt 311.43
Formula C19H25N3O
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N-((3aR,5s,6aS)-2-cyanooctahydrocyclopenta[c]pyrrol-5-yl)-4-isopropyl-3-methylbenzamide

References

1. Kooij R, et al. Angew Chem Int Ed Engl. 2025 Oct 7:e202510941.

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