Description
A mycotoxin with antiviral activity; it inhibits HIV-1 protease in vitro (IC50 = 161 μM); no observable cytotoxicity at concentrations up to 100 μM in HepG2 cells,
Formal name: (1’R,2’R,4’aS,6’R,8’aS)-3′,4′,4’a,5′,6′,7,7′,8,8′,8’a-decahydro-4,6′-dihydroxy-2′,5′,5′,8’a-tetramethyl-spiro[2H-furo[2,3-e]isoindole-2,1′(2’H)-naphthalen]-6(3H)-one
Synonyms:
Molecular weight: 385.5
CAS: 163391-76-2
Purity: ≥95%
Formulation: A lyophilisate
Product Type|Biochemicals|Antivirals|Protease Inhibitors||Product Type|Biochemicals|Small Molecule Inhibitors|Peptidases & Proteases||Product Type|Biochemicals|Toxins|Mycotoxins||Research Area|Immunology & Inflammation||Research Area|Infectious Disease|Viral Diseases|HIV & AIDS
