Marvin 02061309172D 43 47 0 0 0 0 999 V2000 13.4612 -11.5975 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.1738 -11.1889 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.1738 -10.3632 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.4612 -9.9461 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.7485 -11.1889 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.7511 -10.3650 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.0400 -9.9526 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.3259 -10.3630 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.3273 -11.1900 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.0390 -11.5986 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.8864 -9.9544 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.6006 -10.3712 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.3164 -9.9610 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.3192 -9.1345 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.6004 -8.7196 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.8875 -9.1321 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.0400 -12.4244 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 15.5999 -7.8939 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 17.0300 -10.3764 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 17.0350 -8.7228 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.6109 -9.9500 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.6110 -9.1243 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.8960 -8.7113 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.3261 -8.7115 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.8988 -7.8883 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.1846 -7.4755 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.4684 -7.8882 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.4709 -8.7182 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.1858 -9.1274 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.7529 -7.4762 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.7573 -9.1335 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.1852 -6.6498 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 17.7495 -9.1367 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 18.4652 -8.7251 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 17.7482 -9.9624 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 19.1788 -9.1409 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 19.8941 -8.7299 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 19.8958 -7.9032 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 19.1764 -7.4894 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 18.4641 -7.9028 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 19.1748 -6.6638 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 20.6110 -7.4906 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 20.6083 -9.1442 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9 10 2 0 0 0 0 8 21 1 0 0 0 0 10 5 1 0 0 0 0 21 22 1 0 0 0 0 22 23 1 0 0 0 0 6 4 1 0 0 0 0 22 24 2 0 0 0 0 11 12 2 0 0 0 0 23 25 2 0 0 0 0 5 6 2 0 0 0 0 25 26 1 0 0 0 0 12 13 1 0 0 0 0 26 27 2 0 0 0 0 5 1 1 0 0 0 0 27 28 1 0 0 0 0 13 14 2 0 0 0 0 28 29 2 0 0 0 0 29 23 1 0 0 0 0 6 7 1 0 0 0 0 27 30 1 0 0 0 0 14 15 1 0 0 0 0 28 31 1 0 0 0 0 1 2 1 0 0 0 0 26 32 1 0 0 0 0 15 16 2 0 0 0 0 20 33 1 0 0 0 0 16 11 1 0 0 0 0 33 34 1 0 0 0 0 3 11 1 0 0 0 0 33 35 2 0 0 0 0 7 8 2 0 0 0 0 34 36 2 0 0 0 0 10 17 1 0 0 0 0 36 37 1 0 0 0 0 2 3 1 0 0 0 0 37 38 2 0 0 0 0 15 18 1 0 0 0 0 38 39 1 0 0 0 0 8 9 1 0 0 0 0 39 40 2 0 0 0 0 40 34 1 0 0 0 0 13 19 1 0 0 0 0 39 41 1 0 0 0 0 3 4 1 0 0 0 0 38 42 1 0 0 0 0 14 20 1 0 0 0 0 37 43 1 0 0 0 0 M END > CHEBI:65944 > 7,4'-di-O-galloyltricetiflavan > A diester obtained by the formal condensation of gallic acid with the hydroxy groups at positions 7 and 4' of 3',4',5',5,7-pentahydroxyflavan. Isolated from the leaves of Pithecellobium clypearia, it exhibits antiviral activity. > 3 > tricetiflavan-7,4'-di-O-gallate; 2,6-dihydroxy-4-{5-hydroxy-7-[(3,4,5-trihydroxybenzoyl)oxy]-3,4-dihydro-2H-chromen-2-yl}phenyl 3,4,5-trihydroxybenzoate > C29H22O14 > 594.47660 > 594.10096 > 0 > Oc1cc(cc(O)c1O)C(=O)Oc1cc(O)c2CCC(Oc2c1)c1cc(O)c(OC(=O)c2cc(O)c(O)c(O)c2)c(O)c1 > InChI=1S/C29H22O14/c30-16-9-14(41-28(39)12-5-17(31)25(37)18(32)6-12)10-24-15(16)1-2-23(42-24)11-3-21(35)27(22(36)4-11)43-29(40)13-7-19(33)26(38)20(34)8-13/h3-10,23,30-38H,1-2H2 > LRBYDVJXPROTLX-UHFFFAOYSA-N > 15869678 > 16724853 $$$$