Marvin 04191310042D 46 53 0 0 0 0 999 V2000 8.9290 -22.1888 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.1320 -21.9760 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.3462 -22.7726 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1362 -19.9190 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1350 -20.7475 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8509 -21.1610 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8491 -19.5057 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5654 -19.9154 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5643 -20.7450 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2782 -21.1585 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 5.2806 -19.4993 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9991 -19.9174 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9973 -20.7433 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.4238 -19.9147 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.7099 -19.5058 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.4261 -20.7438 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.7117 -21.1536 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.7093 -21.9727 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.4198 -22.3882 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.1383 -21.1531 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.2806 -18.6732 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.8525 -21.9871 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.7080 -18.6797 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.4895 -26.0233 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.6925 -25.8105 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.9067 -26.6071 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6967 -23.7535 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.6955 -24.5820 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4114 -24.9954 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4096 -23.3401 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1259 -23.7499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1248 -24.5794 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.8387 -24.9930 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 3.8411 -23.3337 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5596 -23.7519 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.5579 -24.5778 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9843 -23.7492 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2704 -23.3402 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9866 -24.5783 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2723 -24.9881 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.2698 -25.8071 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.9803 -26.2227 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.6988 -24.9876 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.8411 -22.5076 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.4130 -25.8215 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 5.2685 -22.5141 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9 10 1 0 0 0 0 6 22 1 0 0 0 0 10 13 1 0 0 0 0 15 23 1 0 0 0 0 25 24 1 0 0 0 0 26 25 1 0 0 0 0 12 11 1 0 0 0 0 6 9 2 0 0 0 0 12 13 2 0 0 0 0 13 17 1 0 0 0 0 27 28 2 0 0 0 0 8 7 2 0 0 0 0 28 29 1 0 0 0 0 29 32 2 0 0 0 0 16 14 1 0 0 0 0 31 30 2 0 0 0 0 30 27 1 0 0 0 0 31 32 1 0 0 0 0 7 4 1 0 0 0 0 14 15 2 0 0 0 0 15 12 1 0 0 0 0 16 17 2 0 0 0 0 31 34 1 0 0 0 0 32 33 1 0 0 0 0 33 36 1 0 0 0 0 35 34 1 0 0 0 0 8 9 1 0 0 0 0 2 1 1 0 0 0 0 35 36 2 0 0 0 0 36 40 1 0 0 0 0 4 5 2 0 0 0 0 39 37 1 0 0 0 0 3 2 1 0 0 0 0 37 38 2 0 0 0 0 38 35 1 0 0 0 0 39 40 2 0 0 0 0 5 6 1 0 0 0 0 16 20 1 0 0 0 0 17 18 1 0 0 0 0 18 19 1 0 0 0 0 19 2 1 0 0 0 0 39 43 1 0 0 0 0 40 41 1 0 0 0 0 41 42 1 0 0 0 0 42 25 1 0 0 0 0 25 43 1 0 0 0 0 2 20 1 0 0 0 0 34 44 2 0 0 0 0 8 11 1 0 0 0 0 29 45 1 0 0 0 0 11 21 2 0 0 0 0 38 46 1 0 0 0 0 18 37 1 0 0 0 0 M END > CHEBI:66836 > oriciacridone F > An alkaloid of the class of acridone derivatives isolated from Oriciopsis glaberrima and has been shown to exhibit radical scavenging and α-glucosidase inhibitory activity. > 3 > 5-(6,11-dihydroxy-3,3-dimethyl-7-oxo-2,12-dihydro-1H-pyrano[2,3-c]acridin-1-yl)-6,11-dihydroxy-3,3-dimethyl-2,12-dihydro-1H-pyrano[2,3-c]acridin-7-one; (+)-bis-5-hydroxy-(10H)-hydronoracromycine > 6,6',11,11'-tetrahydroxy-3,3,3',3'-tetramethyl-1,1',2,2',3,3',12,12'-octahydro-7H,7'H-1,5'-bipyrano[2,3-c]acridine-7,7'-dione > C36H32N2O8 > 620.64790 > 620.21587 > 0 > CC1(C)CCc2c(O1)c(C1CC(C)(C)Oc3cc(O)c4c([nH]c5c(O)cccc5c4=O)c13)c(O)c1c2[nH]c2c(O)cccc2c1=O > InChI=1S/C36H32N2O8/c1-35(2)12-11-17-29-26(32(43)16-8-6-9-19(39)27(16)37-29)33(44)24(34(17)46-35)18-14-36(3,4)45-22-13-21(41)25-30(23(18)22)38-28-15(31(25)42)7-5-10-20(28)40/h5-10,13,18,39-41,44H,11-12,14H2,1-4H3,(H,37,43)(H,38,42) > YPOUKZJOAMKOEN-UHFFFAOYSA-N > 10412578 > 16508179 $$$$