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Cat. No. Product Name Information
PC-38447

Fluxapyroxad

Succinate dehydrogenase inhibitor

Fluxapyroxad is a new generation carboxamide funugicide and succinate dehydrogenase (Sdh) inhibitor, exhibits antifungal activities against R. solani with EC50 of 0.033 mg/mL.
PC-73393

1-ECBC

Yak1 inhibitor

1-ECBC is a small molecule inhibiting C. albicans filamentation, 1-ABC targets DYRK1-family kinase Yak1, the sole DYRK-family member expressed in C. albicans.
PC-73392

1-ABC

Yak1 inhibitor

1-ABC is a small molecule inhibiting C. albicans filamentation, 1-ABC targets DYRK1-family kinase Yak1, the sole DYRK-family member expressed in C. albicans.
PC-73162

Aureobasidin A

Antifungal antibiotic

Aureobasidin A (AbA, Basifungin) is a cyclic depsipetide antifungal antibiotic, inhibits the inositolphosphorylceramide synthase AUR1.
PC-72423

GW461484A

Yck2 inhibitor

GW461484A (GW-461484A) is a potent small molecule capable of restoring caspofungin sensitivity, inhibits Yck2 kinase in C. albicans, originally discovered as an inhibitor of human p38α with IC50 of 150 nM.
PC-38031

Rezafungin

Rezafungin (CD101) is a long-acting novel echinocandin possesses potent antibiofilm activity against early and mature candida albicans biofilms.
PC-38016

Echinocandin B

Echinocandin B is a cyclic hexapeptide echinocandin antibiotic isolated from Aspergillus nidulans var. echinulatus with specific anti-yeast activity..
PC-35452

Fosmanogepix

Fosmanogepix (APX001 prodrug) is a novel antifungal agent, the prodrug form of APX001, which inhibits the fungal protein Gwt1..
PC-62607

PC1244

PC1244 is a long acting fungicidal azole that targets A. fumigatus CYP51A and CYP51B, inhibits ergosterol synthesis in A. fumigatus with IC50 of 8 nM.
PC-70346

Filastatin

A small molecule inhibitor that inhibits adhesion of C. albicans to polystyrene.
PC-70282

Cerulenin

An antifungal antibiotic that inhibits fatty acid synthase (FASN), also blocks cellular proliferation of KRAS-associated lung cancer cells.
PC-60335

iKIX1

A small-molecule inhibitor of the interaction of the C. glabrata Pdr1 activation domain with the C. glabrata Gal11A KIX domain with Ki of 18 uM.

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