60196360 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 11 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 11 -1 1 2 2 3 4 4 5 5 6 7 7 8 8 9 9 10 10 11 12 13 13 14 14 15 15 16 16 17 18 18 18 18 19 19 19 19 20 20 21 21 21 22 22 22 23 23 23 24 24 24 25 25 26 26 27 27 27 28 28 28 29 29 29 30 30 30 31 31 32 32 33 34 34 34 35 35 36 36 36 37 37 37 38 39 39 39 40 40 40 41 41 41 42 42 42 43 43 43 44 44 45 45 45 46 46 46 48 48 49 49 50 50 51 51 51 52 53 53 55 55 56 56 57 57 57 58 11 32 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116 1 1 1 5 255 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 7.755 8.6036 11.3987 7.7434 17.2866 15.7767 6.8678 5.1396 5.1473 5.1357 7.7511 6.0191 6.86 5.1242 3.396 2.5357 3.4075 13.1307 11.3547 12.2647 13.9967 11.3467 13.1468 10.4112 12.2487 13.9967 14.8907 15.7967 14.8907 10.4278 15.7967 9.4716 12.2647 13.7735 9.48 11.3624 14.3389 13.1307 14.8656 16.7405 15.7967 9.9146 10.9146 16.7405 16.6666 15.2868 16.2867 7.7396 6.8716 6.0075 6.8793 6.0114 5.9998 6.8832 5.996 5.128 4.2678 4.2639 3.4037 13.0008 11.349 13.3648 13.7559 11.8514 12.6497 15.6202 14.4861 15.2843 10.8361 10.0379 16.0058 16.4076 9.4704 13.2985 14.172 14.2484 9.2754 8.8683 11.9824 11.3672 10.7424 13.7563 14.551 14.9214 13.1307 14.6431 14.2573 16.9496 17.3514 10.3788 11.2266 11.4503 9.3764 9.6066 10.4527 17.3514 16.9496 16.3607 17.2059 16.9725 15.8201 14.9706 14.7534 7.7372 7.4074 17.5904 5.4718 7.4174 6.0138 6.0022 4.6038 4.6092 6.5341 5.6638 4.2702 4.2615 6.8577 4.586 3.3936 2 3.1703 -1.333 2.2193 0.1703 4.7789 5.6276 -2.3263 -1.3196 0.6803 -2.3196 2.1703 2.177 -4.3263 -5.3196 -4.313 -2.8096 -1.313 0.2193 0.2125 0.7193 0.7193 -0.8291 -0.8222 -1.3788 -1.3499 1.7193 2.254 1.7401 0.1847 0.7766 0.6985 -0.8363 1.7193 -0.5467 0.2486 1.2124 -0.2203 2.2193 3.3387 2.2754 3.8956 -2.2468 -2.2429 3.3604 1.2468 4.7558 4.7674 -0.8297 -1.3263 -0.823 0.6737 0.177 -2.823 1.6736 -3.823 -4.3196 -2.8163 -3.8163 -2.313 1.1443 -1.4491 -1.4026 -0.7067 -1.8259 -1.8228 2.6903 -0.2851 -0.2944 1.2432 1.2586 0.1148 0.8046 -1.4563 -0.9452 -1.0217 -0.1482 0.8339 0.1472 1.2077 1.8324 1.2172 -0.4324 -0.8029 -0.0082 2.8393 3.9174 3.2185 1.6917 2.3815 -2.555 -2.7787 -1.9309 -1.9389 -2.7849 -2.5547 3.2543 3.9441 0.7075 0.941 1.7861 5.072 5.2891 4.4396 -1.4497 -1.6384 5.3194 -0.5109 0.9816 0.797 -2.203 -1.0076 0.3724 -3.515 -4.6317 -2.1963 -4.4363 -4.9463 -5.6276 -4.933 -2.4976 5 5 6 6 3 5 5 5 6 6 6 5 5 6 5 6 5 5 6 18 19 20 21 22 27 28 32 41 48 49 50 51 52 53 55 56 57 58 34 36 60 37 25 66 45 2 46 2 7 8 54 9 7 13 14 59 15 0 Compound Canonicalized 5 2012.05.21 1 Compound Complexity 7 E_COMPLEXITY 3.408 Cactvs xemistry.com 2012.11.26 1740 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.408 Cactvs xemistry.com 2012.11.26 16 Count Hydrogen Bond Donor 5 E_NHDONORS 3.408 Cactvs xemistry.com 2012.11.26 7 Count Rotatable Bond 5 E_NROTBONDS 3.408 Cactvs xemistry.com 2012.11.26 7 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.408 Cactvs xemistry.com 2012.11.26 00000371F07C3E200000000000000000000000000000000000003468C1820000000000C00000001A00000800000F14B080030208000006008802A0D2080200000020000000080140004811101600010422400005A0000F0103CAECFCCF8000000000000000C000060000300000000000000000 IUPAC Name Allowed 1 2.2.0 LexiChem openeye.com 2012.11.26 sodium;(2S,3S,4S,5R,6S)-6-[[(3S,6aR,6bS,8aS,11S,12aR,14aR,14bS)-11-carboxy-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl]oxy]-5-[(2R,3R,4S,5S,6S)-6-carboxy-3,4,5-trihydroxy-tetrahydropyran-2-yl]oxy-3,4-dihydroxy-tetrahydropyran-2-carboxylate IUPAC Name CAS-like Style 1 2.2.0 LexiChem openeye.com 2012.11.26 sodium;(2S,3S,4S,5R,6S)-6-[[(3S,6aR,6bS,8aS,11S,12aR,14aR,14bS)-11-carboxy-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl]oxy]-5-[[(2R,3R,4S,5S,6S)-6-carboxy-3,4,5-trihydroxy-2-oxanyl]oxy]-3,4-dihydroxy-2-oxanecarboxylate IUPAC Name Preferred 1 2.2.0 LexiChem openeye.com 2012.11.26 sodium;(2S,3S,4S,5R,6S)-6-[[(3S,6aR,6bS,8aS,11S,12aR,14aR,14bS)-11-carboxy-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl]oxy]-5-[(2R,3R,4S,5S,6S)-6-carboxy-3,4,5-trihydroxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate IUPAC Name Systematic 1 2.2.0 LexiChem openeye.com 2012.11.26 sodium;(2S,3S,4S,5R,6S)-6-[[(3S,6aR,6bS,8aS,11S,12aR,14aR,14bS)-11-carboxy-4,4,6a,6b,8a,11,14b-heptamethyl-14-oxidanylidene-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl]oxy]-5-[(2R,3R,4S,5S,6S)-6-carboxy-3,4,5-tris(oxidanyl)oxan-2-yl]oxy-3,4-bis(oxidanyl)oxane-2-carboxylate IUPAC Name Traditional 1 2.2.0 LexiChem openeye.com 2012.11.26 sodium;(2S,3S,4S,5R,6S)-6-[[(3S,6aR,6bS,8aS,11S,12aR,14aR,14bS)-11-carboxy-14-keto-4,4,6a,6b,8a,11,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl]oxy]-5-[(2R,3R,4S,5S,6S)-6-carboxy-3,4,5-trihydroxy-tetrahydropyran-2-yl]oxy-3,4-dihydroxy-tetrahydropyran-2-carboxylate InChI Standard 1 1.0.4 InChI iupac.org 2012.11.26 InChI=1S/C42H62O16.Na/c1-37(2)21-8-11-42(7)31(20(43)16-18-19-17-39(4,36(53)54)13-12-38(19,3)14-15-41(18,42)6)40(21,5)10-9-22(37)55-35-30(26(47)25(46)29(57-35)33(51)52)58-34-27(48)23(44)24(45)28(56-34)32(49)50;/h16,19,21-31,34-35,44-48H,8-15,17H2,1-7H3,(H,49,50)(H,51,52)(H,53,54);/q;+1/p-1/t19-,21?,22-,23-,24-,25-,26-,27+,28-,29-,30+,31+,34-,35-,38+,39-,40-,41+,42+;/m0./s1 InChIKey Standard 1 1.0.4 InChI iupac.org 2012.11.26 WRZYGPIFICWRCG-UIAZACTHSA-M Mass Exact 7 2.1 PubChem ncbi.nlm.nih.gov 2012.11.26 844.38573 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2012.11.26 C42H61NaO16 Molecular Weight 7 2.1 PubChem ncbi.nlm.nih.gov 2012.11.26 844.913909 SMILES Canonical 1 1.9.0 OEChem openeye.com 2012.11.26 CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)[O-])O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)C)C(=O)C=C6C3(CCC7(C6CC(CC7)(C)C(=O)O)C)C)C)C.[Na+] SMILES Isomeric 1 1.9.0 OEChem openeye.com 2012.11.26 C[C@]12CC[C@](C[C@H]1C3=CC(=O)[C@@H]4[C@]5(CC[C@@H](C(C5CC[C@]4([C@@]3(CC2)C)C)(C)C)O[C@@H]6[C@@H]([C@H]([C@@H]([C@H](O6)C(=O)[O-])O)O)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)C(=O)O)O)O)O)C)(C)C(=O)O.[Na+] Topological Polar Surface Area 7 E_TPSA 3.408 Cactvs xemistry.com 2012.11.26 270 Weight MonoIsotopic 7 2.1 PubChem ncbi.nlm.nih.gov 2012.11.26 844.38573 59 19 18 1 0 0 0 0 2 5