Marvin 12191213332D 46 49 0 0 0 0 999 V2000 12.1254 -8.2817 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.7246 -8.9698 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.1143 -9.6611 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.9164 -9.6604 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.3146 -8.9648 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.9098 -8.2818 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.1396 -8.9684 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.5560 -9.6786 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.3820 -9.6828 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.7950 -8.9627 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.3750 -8.2422 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.5489 -8.2511 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.8975 -8.9698 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.4895 -8.2467 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.6618 -8.2483 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2456 -8.9646 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.6630 -9.6799 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.4850 -9.6818 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.3239 -7.5674 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.9123 -6.8484 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.0879 -6.8505 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.3259 -6.1348 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 16.6221 -8.9626 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.4206 -8.9610 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 13.3274 -10.3781 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.9137 -11.0918 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.0890 -11.0882 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 13.3268 -11.8063 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.1521 -11.8098 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.5651 -12.5240 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.1478 -13.2378 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.5583 -13.9572 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.3874 -13.9538 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.8010 -13.2324 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.3848 -12.5235 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.7160 -7.5696 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.8946 -7.5681 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.4851 -6.8559 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.1797 -7.9731 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 11.7002 -10.3706 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.8788 -10.3667 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.4647 -11.0761 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.8785 -9.5386 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.6433 -11.0723 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2292 -11.7817 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.2359 -10.3591 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 11 12 2 0 0 0 0 12 7 1 0 0 0 0 5 7 1 0 0 0 0 13 14 2 0 0 0 0 14 15 1 0 0 0 0 15 16 2 0 0 0 0 16 17 1 0 0 0 0 17 18 2 0 0 0 0 18 13 1 0 0 0 0 2 13 1 0 0 0 0 6 19 1 0 0 0 0 19 20 1 0 0 0 0 20 21 1 0 0 0 0 20 22 2 0 0 0 0 10 23 1 0 0 0 0 16 24 1 0 0 0 0 4 25 1 0 0 0 0 25 26 1 0 0 0 0 26 27 2 0 0 0 0 26 28 1 0 0 0 0 28 29 1 0 0 0 0 29 30 1 0 0 0 0 30 31 2 0 0 0 0 31 32 1 0 0 0 0 32 33 2 0 0 0 0 33 34 1 0 0 0 0 34 35 2 0 0 0 0 35 30 1 0 0 0 0 1 36 1 0 0 0 0 1 2 2 0 0 0 0 36 37 1 0 0 0 0 2 3 1 0 0 0 0 37 38 1 0 0 0 0 3 4 2 0 0 0 0 37 39 2 0 0 0 0 4 5 1 0 0 0 0 3 40 1 0 0 0 0 5 6 2 0 0 0 0 40 41 1 0 0 0 0 6 1 1 0 0 0 0 41 42 1 0 0 0 0 7 8 2 0 0 0 0 41 43 2 0 0 0 0 8 9 1 0 0 0 0 42 44 1 0 0 0 0 9 10 2 0 0 0 0 44 45 1 0 0 0 0 10 11 1 0 0 0 0 44 46 1 0 0 0 0 M END > CHEBI:65699 > curtisian D > A para-terphenyl that consists of 1,4-diphenylbenzene substituted by acetyloxy groups at positions 5' and 6', hydroxy groups at positions 4 and 4'', a (3-phenylpropanoyl)oxy group at position 3' and a (3-hydroxybutanoyl)oxy group at position 2'. It is isolated from the fruit body of the mushroom Paxillus curtisii and exhibits radical scavenging activity > 3 > 5',6'-bis(acetyloxy)-4,4''-dihydroxy-3'-[(3-phenylpropanoyl)oxy]-1,1':4',1''-terphenyl-2'-yl 3-hydroxybutanoate > C35H32O11 > 628.62200 > 628.19446 > 0 > CC(O)CC(=O)Oc1c(OC(=O)CCc2ccccc2)c(-c2ccc(O)cc2)c(OC(C)=O)c(OC(C)=O)c1-c1ccc(O)cc1 > InChI=1S/C35H32O11/c1-20(36)19-29(42)46-35-31(25-12-16-27(40)17-13-25)33(44-22(3)38)32(43-21(2)37)30(24-10-14-26(39)15-11-24)34(35)45-28(41)18-9-23-7-5-4-6-8-23/h4-8,10-17,20,36,39-40H,9,18-19H2,1-3H3 > PUNBBVSDMLIVQU-UHFFFAOYSA-N > 8601889 > 10805570 $$$$