Mrv0541 10161311162D 29 32 0 0 0 0 999 V2000 3.0195 -0.5515 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7343 -0.1379 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7328 0.6900 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.4519 -0.5495 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.4512 -1.3852 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.1182 -1.9029 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.9531 -1.6814 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.4427 -2.3344 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.2523 -2.2353 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.7421 -2.8881 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.5562 -2.7922 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2677 -3.2023 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.3352 -3.5870 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.8786 -2.0375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.3865 -1.3789 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.7106 -0.6169 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.5746 -1.4806 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.0830 -0.8309 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.4060 -0.0684 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.2755 -0.9297 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9164 -0.1879 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.1342 -0.0064 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.9518 0.8012 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.7341 -1.7969 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7327 -2.6250 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0150 -3.0377 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.0173 -1.3818 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2993 -1.7943 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.4466 -3.0387 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 1 2 2 0 0 0 0 2 3 1 0 0 0 0 2 4 1 0 0 0 0 4 5 2 0 0 0 0 5 6 1 0 0 0 0 6 7 1 0 0 0 0 7 8 2 0 0 0 0 8 9 1 0 0 0 0 9 10 1 0 0 0 0 10 11 1 0 0 0 0 11 12 1 0 0 0 0 11 13 1 0 0 0 0 11 14 1 0 0 0 0 14 15 1 0 0 0 0 15 16 2 0 0 0 0 15 17 1 0 0 0 0 17 9 2 0 0 0 0 17 18 1 0 0 0 0 18 19 1 0 0 0 0 18 20 2 0 0 0 0 20 7 1 0 0 0 0 20 21 1 0 0 0 0 21 22 1 0 0 0 0 22 4 1 0 0 0 0 22 23 2 0 0 0 0 5 24 1 0 0 0 0 24 25 1 0 0 0 0 25 26 2 0 0 0 0 24 27 2 0 0 0 0 27 1 1 0 0 0 0 27 28 1 0 0 0 0 25 29 1 0 0 0 0 M END > CHEBI:68801 > mollicellin B > A member of the class of depsidones that is 3,4-dihydro-2H,7H-chromeno[7,6-b][1,4]benzodioxepine substituted by a hydroxy group at position 10, methyl groups at positions 2, 2, 5 and 8, a formyl group at position 11 and oxo groups at positions 4 and 7. Isolated from Chaetomium brasiliense it exhibits antimalarial and cytotoxic activities. > 3 > 10-hydroxy-2,2,5,8-tetramethyl-4,7-dioxo-3,4-dihydro-2H,7H-chromeno[7,6-b][1,4]benzodioxepine-11-carbaldehyde > C21H18O7 > 382.36340 > 382.10525 > 0 > Cc1cc(O)c(C=O)c2Oc3cc4OC(C)(C)CC(=O)c4c(C)c3OC(=O)c12 > InChI=1S/C21H18O7/c1-9-5-12(23)11(8-22)19-16(9)20(25)27-18-10(2)17-13(24)7-21(3,4)28-14(17)6-15(18)26-19/h5-6,8,23H,7H2,1-4H3 > OMOOHFQAZTVBPK-UHFFFAOYSA-N > 19895965 > 19663417 $$$$