Product Information
- (3'S,6'R)-3',6'-dihydroxy-2',2',4',6'-tetramethyl-2',3'-dihydrospiro[cyclopropane-1,5'-inden]-7'(6'H)-one
- (3′S,6′R)-2′,3′-Dihydro-3′,6′-dihydroxy-2′,2′,4′,6′-tetramethylspiro[cyclopropane-1,5′-[5H]inden]-7′(6′H)-one
- Brn 2286081
- Ccris 3539
- Dr-15977
- Illudine M
- Nsc 400978
- Nsc 626370
- Spiro(cyclopropane-1,5'-(5H)inden)-7'(6'H)-one, 2',3'-dihydro-3'-beta,6'-alpha-dihydroxy-2',24',6'-tetramethyl-
- Spiro[cyclopropane-1,5′-[5H]inden]-7′(6′H)-one, 2′,3′-dihydro-3′,6′-dihydroxy-2′,2′,4′,6′-tetramethyl-, (3′S,6′R)-
- See more synonyms
- Spiro[cyclopropane-1,5′-[5H]inden]-7′(6′H)-one, 2′,3′-dihydro-3′,6′-dihydroxy-2′,2′,4′,6′-tetramethyl-, (3′S-trans)-
- Spiro[cyclopropane-1,5′-[5H]inden]-7′(6′H)-one, 2′,3′-dihydro-3′β,6′α-dihydroxy-2′,2′,4′,6′-tetramethyl-
Illudin M is a cyclic peptide that is isolated from the mushroom Omphalotus olearius. It has been shown to have antitumor activity in vivo and in vitro. Illudin M inhibits the growth of tumor cells by binding to their surface receptors, which blocks the activation of cell signaling pathways that control cell proliferation. Illudin M also induces apoptosis through caspase-3 activation and cytochrome c release. The structure of Illudin M resembles lysine residues found in proteins, and has been shown to inhibit protein synthesis in animal cells.
Chemical properties
Technical inquiry about: 3D-FI178320 Illudin M
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