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Cat. No. Product Name Information
PC-70265

RNase L-IN-2

RNase L-IN-2 is a small-molecule activator of RNase L with EC50 of 22 uM.
PC-70260

Compound A5

AP-1 inhibitor

Compound 5431942 (Compound 5431942) is a small molecule that specifically inhibits the clathrin adaptor complex AP-1-dependent traffic, does not significantly affect other pathways through the trans-Golgi network (TGN).
PC-70257

Furin-IN-1d

Furin inhibitor

Furin-IN-1d is a small molecule furin inhibitor with Ki of 22 nM.
PC-70255

INP-0400

INP-0400 is a small-molecule inhibitor of type III secretion in Y. pseudotuberculosis, without affecting in vitro multiplication, causes a dose- and growth phase-dependent inhibition of C. trachomatis RB multiplication.
PC-70254

AUDA

sEH inhibitor

AUDA is a potent inhibitor of sEH (soluble epoxide hydrolase) with IC50 of 18 nM and 69 nM for mouse sEH and human sEH, respectively.
PC-70252

CUDA

sEH inhibitor

CUDA is a potent inhibitor of sEH (soluble epoxide hydrolase) with IC50 of 11.1 nM and 112 nM for mouse sEH and human sEH, respectively.
PC-70251

AUDA-BE

sEH inhibitor

AUDA-BE is the prodrug of AUDA, a potent inhibitor of sEH (soluble epoxide hydrolase) with IC50 of 50 nM and 100 nM for mouse sEH and human sEH, respectively.
PC-70250

Cysmethynil

ICMT inhibitor

Cysmethynil is a selective small-molecule inhibitor of tisoprenylcysteine carboxyl methyltransferase (Icmt) with IC50 <200 nM.
PC-70248

Migrastatin

Cancer migration inhibitor

Migrastatin is a biologically active natural product isolated from Streptomyces that has been shown to inhibit tumor cell migration.
PC-70247

C2-8

polyQ aggregation inhibitor

C2-8 is a small molecule inhibitor of polyglutamine (polyQ) aggregation in Huntington's disease neurons.
PC-70238

NSC 65828

Angiogenin inhibitor

NSC 65828 (NCI65828) is a small-molecule inhibitor of the ribonucleolytic activity of human angiogenin with Ki of 81 uM.
PC-70343

Endosomal trafficking inhibitor EGA

Endosomal trafficking inhibitor

EGA is a potent anthrax lethal toxin entry inhibitor with IC50 of 1.7 uM, inhibits endosomal trafficking pathways exploited by multiple toxins and viruses.

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