Marvin 01281310082D 29 30 0 0 0 0 999 V2000 -0.0014 -7.1000 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0026 -7.9273 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7122 -8.3402 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7104 -6.6872 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4258 -7.0963 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4246 -7.9248 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1376 -8.3378 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.8563 -7.9268 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.8574 -7.0983 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1399 -6.6808 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5696 -8.3413 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2.1399 -5.8558 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -0.7174 -8.3393 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.5729 -6.6876 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2864 -7.1018 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.5749 -5.8626 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.2844 -7.9268 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0018 -6.6910 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7153 -7.1053 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.4308 -6.6945 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.1442 -7.1087 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.8597 -6.6980 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.1423 -7.9337 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.5732 -7.1122 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2887 -6.7014 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.5712 -7.9372 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.0021 -7.1156 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.7176 -6.7049 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.0001 -7.9406 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9 14 1 0 0 0 0 1 2 2 0 0 0 0 14 15 1 0 0 0 0 5 4 2 0 0 0 0 14 16 1 0 0 0 0 4 1 1 0 0 0 0 15 17 1 0 0 0 0 5 10 1 0 0 0 0 15 18 2 0 0 0 0 6 7 1 0 0 0 0 18 19 1 0 0 0 0 7 8 1 0 0 0 0 19 20 1 0 0 0 0 8 9 1 0 0 0 0 20 21 2 0 0 0 0 9 10 2 0 0 0 0 21 22 1 0 0 0 0 5 6 1 0 0 0 0 21 23 1 0 0 0 0 8 11 2 0 0 0 0 22 24 1 0 0 0 0 24 25 1 0 0 0 0 10 12 1 0 0 0 0 24 26 2 0 0 0 0 2 3 1 0 0 0 0 25 27 2 0 0 0 0 2 13 1 0 0 0 0 27 28 1 0 0 0 0 3 6 2 0 0 0 0 27 29 1 0 0 0 0 M END > CHEBI:65919 > fukanemarin A > A hydroxycoumarin that is 4,7-dihydroxycoumarin substituted by a 1,2,6,10-tetramethyl-8-oxoundeca-2(E),5(E),9-trienyl moiety at position 3. Isolated from the roots of Ferula fukanensis, it exhibits inhibitory effects on the production of nitric oxide (NO). > 3 > 4,7-dihydroxy-3-(1,2,6,10-tetramethyl-8-oxoundeca-2(E),5(E),9-trienyl)coumarin > 4,7-dihydroxy-3-[(3E,6E)-3,7,11-trimethyl-9-oxododeca-3,6,10-trien-2-yl]-2H-chromen-2-one > C24H28O5 > 396.47610 > 396.19367 > 0 > CC(c1c(O)c2ccc(O)cc2oc1=O)C(\C)=C\C\C=C(/C)CC(=O)C=C(C)C > InChI=1S/C24H28O5/c1-14(2)11-19(26)12-15(3)7-6-8-16(4)17(5)22-23(27)20-10-9-18(25)13-21(20)29-24(22)28/h7-11,13,17,25,27H,6,12H2,1-5H3/b15-7+,16-8+ > PTNBQZMCTYXNSQ-BGPOSVGRSA-N > 10217742 > 15043424 $$$$