Mrv0541 10161309502D 29 31 0 0 0 0 999 V2000 1.7458 -0.9301 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.5623 -0.1258 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.1409 -1.4912 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7739 0.1174 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.3526 -1.2480 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.1691 -0.4437 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4892 -1.2881 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.2325 -0.9302 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.0768 0.5192 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.9018 0.5192 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.4162 -0.1259 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8372 -1.4913 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.6256 -1.2482 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2045 0.1172 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.8092 -0.4439 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5904 0.9218 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.2522 -1.8091 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1.3244 -2.2956 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7196 -2.8566 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.1128 -2.5388 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 1.7188 1.2625 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.3881 0.9215 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2303 -1.8094 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.5975 -0.2008 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.2023 -0.7620 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9906 -0.5189 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.5953 -1.0801 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.1743 0.2854 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7812 0.6035 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3 1 2 0 0 0 0 4 2 2 0 0 0 0 5 3 1 0 0 0 0 6 4 1 0 0 0 0 6 5 2 0 0 0 0 7 1 1 0 0 0 0 2 1 1 0 0 0 0 8 7 1 0 0 0 0 9 2 1 0 0 0 0 10 9 1 0 0 0 0 11 10 1 0 0 0 0 12 8 1 0 0 0 0 11 8 2 0 0 0 0 13 12 2 0 0 0 0 14 11 1 0 0 0 0 15 13 1 0 0 0 0 15 14 2 0 0 0 0 4 16 1 0 0 0 0 5 17 1 0 0 0 0 3 18 1 0 0 0 0 18 19 2 0 0 0 0 18 20 1 0 0 0 0 9 21 2 0 0 0 0 14 22 1 0 0 0 0 13 23 1 0 0 0 0 15 24 1 0 0 0 0 24 25 1 0 0 0 0 25 26 2 0 0 0 0 26 27 1 0 0 0 0 26 28 1 0 0 0 0 24 29 2 0 0 0 0 M END > CHEBI:68724 > mollicellin K > A member of the class of depsidones that is 11H-dibenzo[b,e][1,4]dioxepine substituted by hydroxy groups at positions 3 and 7, methyl groups at positions 1 and 9, a 3-methylbut-2-enoyl group at position 8, a formyl group at position 4 and an oxo group at position 11. Isolated from Chaetomium brasiliense, it exhibits antimalarial, antimycobacterial and cytotoxic activities. > 3 > 3,7-dihydroxy-1,9-dimethyl-8-(3-methylbut-2-enoyl)-11-oxo-11H-dibenzo[b,e][1,4]dioxepine-4-carbaldehyde > C21H18O7 > 382.36340 > 382.10525 > 0 > CC(C)=CC(=O)c1c(O)cc2Oc3c(C=O)c(O)cc(C)c3C(=O)Oc2c1C > InChI=1S/C21H18O7/c1-9(2)5-14(24)18-11(4)19-16(7-15(18)25)27-20-12(8-22)13(23)6-10(3)17(20)21(26)28-19/h5-8,23,25H,1-4H3 > GRJLKDCRKHDXSZ-UHFFFAOYSA-N > 19895966 > 19663417 $$$$