Illudin M

CAS: 1146-04-9

Ref. 3D-FI178320

Produktinformation

• Name: Illudin M
• Synonyme: (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)-, 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-

Beschreibung

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.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 248.14124
• Formel: C₁₅H₂₀O₃
• Reinheit: Min. 95%
• InChl: InChI=1S/C15H20O3/c1-8-10-9(7-13(2,3)12(10)17)11(16)14(4,18)15(8)5-6-15/h7,12,17-18H,5-6H2,1-4H3/t12-,14+/m1/s1
• InChI Key: InChIKey=QVMDIQLUNODCTG-OCCSQVGLSA-N
• SMILES: CC1=C2C(=CC(C)(C)[C@@H]2O)C(=O)[C@](C)(O)C12CC2