Marvin 01281315592D 29 31 0 0 0 0 999 V2000 0.2986 -2.4416 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.2974 -3.2690 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0122 -3.6819 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0104 -2.0289 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7258 -2.4380 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.7292 -3.2711 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4484 -3.6824 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.1688 -3.2652 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.4416 -2.0162 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.1659 -2.4340 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.7871 -1.8743 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 3.4467 -1.1105 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 2.6152 -1.1983 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.8843 -3.6759 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 4.5941 -2.0456 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.0292 -0.3917 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1583 -0.6917 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.8762 -1.0982 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.5872 -0.6798 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.3051 -1.0863 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.4174 -3.6809 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.3120 -1.9113 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.0161 -0.6679 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.7340 -1.0744 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.4450 -0.6560 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.1629 -1.0625 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.1698 -1.8875 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.8739 -0.6441 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.7409 -1.8994 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3 6 2 0 0 0 0 8 14 2 0 0 0 0 1 2 2 0 0 0 0 11 15 1 6 0 0 0 5 9 1 0 0 0 0 12 16 1 1 0 0 0 6 7 1 0 0 0 0 12 17 1 0 0 0 0 7 8 1 0 0 0 0 17 18 1 0 0 0 0 8 10 1 0 0 0 0 18 19 1 0 0 0 0 9 10 2 0 0 0 0 19 20 2 0 0 0 0 5 4 2 0 0 0 0 2 21 1 0 0 0 0 4 1 1 0 0 0 0 20 22 1 0 0 0 0 5 6 1 0 0 0 0 20 23 1 0 0 0 0 23 24 1 0 0 0 0 2 3 1 0 0 0 0 24 25 1 0 0 0 0 10 11 1 0 0 0 0 25 26 2 0 0 0 0 11 12 1 0 0 0 0 26 27 1 0 0 0 0 12 13 1 0 0 0 0 26 28 1 0 0 0 0 13 9 1 0 0 0 0 24 29 2 0 0 0 0 M END > CHEBI:65928 > (2R*,3R*)-2,3-dihydro-7-hydroxy-2,3-dimethyl-2-[4,8-dimethyl-3(E)-7-nonadien-6-onyl]furo[3,2-c]coumarin > A furanocoumarin that is 2,3-dihydrofuro[3,2-c]coumarin substituted by a hydroxy group at position 7, methyl groups at positions 2 and 3 (relatively trans configuration) and a 4,8-dimethyl-3(E)-7-nonadien-6-onyl moiety at position 2. Isolated from the roots of Ferula fukanensis, it exhibits inhibitory effect on the production of nitric oxide (NO). > 3 > (2R*,3R*)-2-[(3E)-4,8-dimethyl-6-oxonona-3,7-dien-1-yl]-7-hydroxy-2,3-dimethyl-2,3-dihydro-4H-furo[3,2-c]chromen-4-one > C24H28O5 > 396.47610 > 396.19367 > 0 > C[C@@H]1c2c(O[C@]1(C)CC\C=C(/C)CC(=O)C=C(C)C)c1ccc(O)cc1oc2=O > InChI=1S/C24H28O5/c1-14(2)11-18(26)12-15(3)7-6-10-24(5)16(4)21-22(29-24)19-9-8-17(25)13-20(19)28-23(21)27/h7-9,11,13,16,25H,6,10,12H2,1-5H3/b15-7+/t16-,24-/m1/s1 > VFFCJVAKVAWFMA-BAFNZYHESA-N > 15043424 $$$$