149598-70-9
Chemical Structure
Mer-NF5003F
Synonym(s): Stachybotrydial; F 1839M; Stachybotrydial
- CAS. Nr.: 149598-70-9
- Formula:C23H30O5
- Molecular Weight:386.48
IUPAC Name: (2R,2'R,4a'S,6'R,8a'S)-4,6'-dihydroxy-2',5',5',8a'-tetramethyl-3',4',4a',5',6',7',8',8a'-octahydro-2'H,3H-spiro[benzofuran-2,1'-naphthalene]-6,7-dicarbaldehyde
InChIKey: WIGGVNIABVHHCS-QJAXDWLUSA-N
SMILES: O[C@@H]1CC[C@]2([C@]([H])(C1(C)C)CC[C@H]([C@@]23OC4=C(C3)C(O)=CC(C=O)=C4C=O)C)C
Biological Activity: Mer-NF5003F (Stachybotrydial; F 1839M), a sesquiterpene isolated from Stachybotrys, inhibits avian medulloblastoma virus (AMV) protease (IC50=7.8 μM). Mer-NF5003F inhibits sialyltransferase 6N (ST6N), ST3O, and ST3N (IC50=0.61, 6.7, and 10 μg/mL, respectively), and fucosyltransferase (IC50=11.3 μg/mL). Mer-NF5003F has in vitro activity against herpes simplex virus HSV-1 (IC50=4.32 μg/mL) and multidrug-resistant Plasmodium falciparum K1 strain (IC50=0.85 μg/mL).
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Mer-NF5003F | Mer-NF5003F (Stachybotrydial; F 1839M), a sesquiterpene isolated from Stachybotrys, inhibits avian medulloblastoma virus (AMV) protease (IC50=7.8 μM). Mer-NF5003F inhibits sialyltransferase 6N (ST6N), ST3O, and ST3N (IC50=0.61, 6.7, and 10 μg/mL, respectively), and fucosyltransferase (IC50=11.3 μg/mL). Mer-NF5003F has in vitro activity against herpes simplex virus HSV-1 (IC50=4.32 μg/mL) and multidrug-resistant Plasmodium falciparum K1 strain (IC50=0.85 μg/mL). | |||||||||||||||||||||
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