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0 0 0 0 0 0 0 0 0 8.1679 2.3472 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 8.6749 2.9972 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.3657 3.7599 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.8742 4.4099 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.6011 0.7036 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.2920 1.4676 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.8004 2.1163 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.4912 2.8831 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.9997 3.5318 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.6167 2.0023 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.9818 -1.9445 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.6881 -1.5363 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.4523 -1.9789 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4055 -2.7608 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.1201 -3.1731 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.1201 -3.9950 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.8402 -4.4099 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.8164 1.3152 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.5915 1.0375 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.2210 1.5707 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.9960 1.2932 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.6254 1.8263 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.5480 -3.1690 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.8362 -2.7594 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.8362 -1.9294 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.1174 -1.5144 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.9209 -0.4659 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -6.7386 0.2268 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -7.5150 -0.0522 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.1444 0.4824 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.9208 0.2033 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.5489 0.7366 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.5453 -1.5199 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.4687 -2.0530 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -8.4673 -2.8693 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -9.1888 -3.2858 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.9103 -2.8693 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.6167 -3.2776 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -10.6167 -1.6284 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -9.9103 -2.0366 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.1888 -1.6367 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -9.1888 -0.8054 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.0725 2.3815 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 2 3 1 0 0 0 0 2 33 1 0 0 0 0 3 4 1 0 0 0 0 3 11 1 0 0 0 0 4 5 1 0 0 0 0 4 32 1 0 0 0 0 5 6 1 0 0 0 0 6 7 1 0 0 0 0 6 11 1 0 0 0 0 7 8 1 0 0 0 0 7 13 1 0 0 0 0 8 9 1 0 0 0 0 8 20 1 0 0 0 0 9 10 1 0 0 0 0 10 11 1 0 0 0 0 11 12 1 0 0 0 0 13 14 1 0 0 0 0 14 15 1 0 0 0 0 15 16 1 0 0 0 0 15 20 1 0 0 0 0 16 17 1 0 0 0 0 17 18 1 0 0 0 0 17 22 1 0 0 0 0 18 19 1 0 0 0 0 19 20 1 0 0 0 0 20 21 1 0 0 0 0 22 23 1 0 0 0 0 23 24 1 0 0 0 0 23 29 1 0 0 0 0 24 25 1 0 0 0 0 25 26 1 0 0 0 0 25 52 1 0 0 0 0 26 27 1 0 0 0 0 28 29 1 0 0 0 0 29 30 1 0 0 0 0 30 31 1 0 0 0 0 30 52 1 0 0 0 0 32 33 1 0 0 0 0 33 34 1 0 0 0 0 33 35 1 0 0 0 0 35 36 1 0 0 0 0 36 37 1 0 0 0 0 37 38 1 0 0 0 0 37 39 1 0 0 0 0 39 40 1 0 0 0 0 40 41 1 0 0 0 0 41 42 1 0 0 0 0 41 47 1 0 0 0 0 42 43 1 0 0 0 0 43 44 1 0 0 0 0 43 49 1 0 0 0 0 44 45 1 0 0 0 0 46 47 1 0 0 0 0 47 48 1 0 0 0 0 48 49 1 0 0 0 0 48 51 1 0 0 0 0 49 50 1 0 0 0 0 52 53 1 0 0 0 0 53 54 1 0 0 0 0 54 55 1 0 0 0 0 54 67 1 0 0 0 0 55 56 1 0 0 0 0 56 57 1 0 0 0 0 56 65 1 0 0 0 0 57 58 1 0 0 0 0 59 60 1 0 0 0 0 60 61 1 0 0 0 0 60 69 1 0 0 0 0 61 62 1 0 0 0 0 61 84 1 0 0 0 0 62 63 1 0 0 0 0 62 71 1 0 0 0 0 64 65 1 0 0 0 0 65 66 1 0 0 0 0 66 67 1 0 0 0 0 66 74 1 0 0 0 0 67 68 1 0 0 0 0 68 69 1 0 0 0 0 69 70 1 0 0 0 0 70 71 1 0 0 0 0 71 72 1 0 0 0 0 72 73 1 0 0 0 0 74 75 1 0 0 0 0 75 76 1 0 0 0 0 75 82 1 0 0 0 0 76 77 1 0 0 0 0 77 78 1 0 0 0 0 78 79 1 0 0 0 0 78 81 1 0 0 0 0 80 81 1 0 0 0 0 81 82 1 0 0 0 0 82 83 1 0 0 0 0 M END > <DATABASE_ID> FDB020702 > <DATABASE_NAME> foodb > <SMILES> CC(CCC1(O)OC2CC3C4CCC5CC(CCC5(C)C4CCC3(C)C2C1C)OC1OC(CO)C(OC2OC(CO)C(O)C(OC3OCC(O)C(O)C3O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C1O)COC1OC(CO)C(O)C(O)C1O > <INCHI_IDENTIFIER> InChI=1S/C56H94O28/c1-21(19-74-49-43(70)39(66)36(63)30(15-57)77-49)7-12-56(73)22(2)34-29(84-56)14-27-25-6-5-23-13-24(8-10-54(23,3)26(25)9-11-55(27,34)4)76-51-45(72)41(68)46(33(18-60)80-51)81-53-48(83-52-44(71)40(67)37(64)31(16-58)78-52)47(38(65)32(17-59)79-53)82-50-42(69)35(62)28(61)20-75-50/h21-53,57-73H,5-20H2,1-4H3 > <INCHI_KEY> FJLUJBDSFBGOPL-UHFFFAOYSA-N > <FORMULA> C56H94O28 > <MOLECULAR_WEIGHT> 1215.3288 > <EXACT_MASS> 1214.593162424 > <JCHEM_ACCEPTOR_COUNT> 28 > <JCHEM_AVERAGE_POLARIZABILITY> 127.8777806095912 > <JCHEM_BIOAVAILABILITY> 0 > <JCHEM_DONOR_COUNT> 17 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> 2-({2-[(4,5-dihydroxy-6-{[6-hydroxy-7,9,13-trimethyl-6-(3-methyl-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl)-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-16-yl]oxy}-2-(hydroxymethyl)oxan-3-yl)oxy]-5-hydroxy-6-(hydroxymethyl)-4-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol > <ALOGPS_LOGP> -1.06 > <JCHEM_LOGP> -4.052661923333332 > <ALOGPS_LOGS> -2.67 > <JCHEM_MDDR_LIKE_RULE> 1 > <JCHEM_NUMBER_OF_RINGS> 10 > <JCHEM_PHYSIOLOGICAL_CHARGE> 0 > <JCHEM_PKA> 11.8932055219067 > <JCHEM_PKA_STRONGEST_ACIDIC> 11.463368551765504 > <JCHEM_PKA_STRONGEST_BASIC> -3.6786119366911016 > <JCHEM_POLAR_SURFACE_AREA> 445.44000000000017 > <JCHEM_REFRACTIVITY> 279.03 > <JCHEM_ROTATABLE_BOND_COUNT> 18 > <JCHEM_RULE_OF_FIVE> 0 > <ALOGPS_SOLUBILITY> 2.63e+00 g/l > <JCHEM_TRADITIONAL_IUPAC> 2-({2-[(4,5-dihydroxy-6-{[6-hydroxy-7,9,13-trimethyl-6-(3-methyl-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl)-5-oxapentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan-16-yl]oxy}-2-(hydroxymethyl)oxan-3-yl)oxy]-5-hydroxy-6-(hydroxymethyl)-4-[(3,4,5-trihydroxyoxan-2-yl)oxy]oxan-3-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol > <JCHEM_VEBER_RULE> 0 > <FOODB_ID> FDB020702 > <GENERIC_NAME> Protodegalactotigonin $$$$