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Bioactive Products
Inhibitors Compound Library
A unique collection of 267 Inhibitor natural compounds
Catalog No: Bb221 Inhibitors Compound Library
Screening Details
Size: 1mg/well * 267 Compounds
2mg/well * 267 Compounds
Cat. No. Information
CFN90273 Cyclo(Phe-Leu)

Cyclo(Phe-Leu) is a new cell cycle inhibitor.
CFN90295 Ganoderic acid Z

The binding affinities of ganoderic acid DM and ganoderic acid Z (ΔGbind, −16.83 and−10.99 kcal mol−1) are comparable to that of current commercial drug oseltamivir (−23.62 kcal mol−1);Ganoderic acid DM is a potential source of anti-influenza ingredient, with novel binding pattern and advantage over oseltamivir, it has steric hindrance on the 150 cavity of N1 protein, and exerts activities across the H274Y and N294S mutations, is the attractive candidates of novel neuraminidase (NA) inhibitors.Ganoderic acid zeta has cytotoxicity in vitro against Meth-A and LLC cell lines.
CFN90274 Cyclo(Phe-Val)

Cyclo(Phe-Val) is a new cell cycle inhibitor, it shows cyctoxic activity in vitro.
CFN90282 Cyclo(Pro-Ala)

Cyclo(Pro-Ala) is a new cell cycle inhibitor.
CFN97738 Rehmannic acid

Rehmannic acid and oleanolic acetate inhibit succinoxidase activity. Both Rehmannic acid and Icterogenin are potent uncouplers, abolishing the phosphate uptake, the respiration being inhibited by the former and increased by the latter.