Marvin 06201315252D 29 30 0 0 0 0 999 V2000 16.2228 -10.9702 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.2228 -12.3003 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.0708 -10.3051 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.0708 -12.9654 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.9191 -10.9702 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.9191 -12.3003 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 17.4878 -10.5592 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 18.2695 -11.6353 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 17.4880 -12.7113 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.7673 -10.3051 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.7632 -12.9692 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.7646 -14.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.7634 -16.9608 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.6138 -14.9650 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.6152 -16.2944 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.4198 -16.9341 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.4250 -18.2636 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.4353 -20.9226 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2762 -18.9328 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2813 -20.2623 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.1326 -20.9315 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.1377 -22.2610 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.1481 -24.9200 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9890 -22.9302 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9941 -24.2597 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 17.8989 -9.2943 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 15.0708 -14.2954 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.8453 -24.9289 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.6156 -10.9701 0.0000 C 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 9 8 1 0 0 0 0 10 5 1 0 0 0 0 11 6 1 0 0 0 0 12 11 1 0 0 0 0 14 12 1 0 0 0 0 15 14 2 0 0 0 0 15 13 1 0 0 0 0 16 15 1 0 0 0 0 17 16 1 0 0 0 0 19 17 1 0 0 0 0 20 19 2 0 0 0 0 20 18 1 0 0 0 0 21 20 1 0 0 0 0 22 21 1 0 0 0 0 24 22 1 0 0 0 0 25 23 1 0 0 0 0 25 24 2 0 0 0 0 7 26 2 0 0 0 0 4 27 1 0 0 0 0 25 28 1 0 0 0 0 10 29 1 0 0 0 0 M END > CHEBI:74221 > aspernidine A > A member of the class of isoindoles that is isoindolin-1-one which is substituted at positions 4, 5 and 6 by hydroxy, triprenyloxy and methoxy groups, respectively. The alkaloid was isolated from the model fungus Aspegillus nidulans. > 3 > emeriphenolicin E > 4-hydroxy-6-methoxy-5-{[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]oxy}isoindolin-1-one > C24H33NO4 > 399.52310 > 399.24096 > 0 > COc1cc2C(=O)NCc2c(O)c1OC\C=C(/C)CC\C=C(/C)CCC=C(C)C > InChI=1S/C24H33NO4/c1-16(2)8-6-9-17(3)10-7-11-18(4)12-13-29-23-21(28-5)14-19-20(22(23)26)15-25-24(19)27/h8,10,12,14,26H,6-7,9,11,13,15H2,1-5H3,(H,25,27)/b17-10+,18-12+ > PHOZASLNSDMYGR-VZRGJMDUSA-N > 22085652 > 20661238; 21601895; 23706169 $$$$