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1 1 1 2 1 1 1 1 1 2 1 1 1 2 1 2 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 6 7 9 13 17 3 1 7 6 9 14 18 3 1 10 5 8 26 38 3 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 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 5.237 10.6886 2.9975 10.4681 9.0194 7.6606 6.7946 9.0635 6.7944 9.9066 9.4206 7.6767 8.5267 6.7946 8.5267 7.6606 7.6767 5.8846 10.8184 8.289 10.3267 6.7787 9.4206 5.8846 7.3853 10.891 11.0629 7.2736 8.6647 5.2978 10.3267 5.8766 6.7787 5.8766 10.2612 8.2431 6.2345 9.8515 11.6263 6.2784 10.8627 4.8632 8.843 4.3831 7.0559 4.8457 12.414 7.3776 10.5107 4.1033 12.3381 6.4519 8.0602 4.1823 5.0772 9.3402 8.3918 8.2992 3.677 8.2554 11.6676 8.9858 4.3151 7.2967 3.3265 4.1238 3.2404 2.5878 6.2529 3.2989 2.442 2.7197 9.2838 12.1285 4.6771 10.6335 10.3277 12.2096 10.9274 11.242 11.555 11.8998 5.1148 3.6796 11.4706 9.7412 4.5549 3.1197 11.4155 9.6861 3.5574 10.5232 2 3.4351 11.3052 9.5758 6.7771 7.8253 11.455 10.5635 6.5058 9.2983 7.7336 8.5049 12.2867 11.17 8.9209 9.3082 12.7167 11.53 10.4359 11.6464 11.0769 12.4482 5.7332 3.4083 12.0238 9.2222 4.8262 2.5013 11.9345 9.1328 3.9926 3.7065 2.8777 1.9562 1.3816 2.0438 9.8557 9.0226 9.2959 11.6443 11.8242 10.9661 -2.5283 2.1647 0.786 6.1586 0.158 -2.7859 -2.2859 1.157 -3.2864 0.6193 -0.7512 0.2556 -2.2859 -1.2859 -1.2859 -0.7859 -3.8274 -2.7928 0.4986 1.8678 -1.2651 0.7834 -2.8206 -0.7791 -4.1609 0.2385 -0.5199 1.688 -3.9346 -1.5811 -2.3067 0.2625 -4.3552 -3.8344 1.3879 2.8825 -2.4578 1.6177 -2.4794 1.9952 -3.1877 0.5275 -4.9668 -2.0572 -5.3653 -3.8581 -0.6671 3.414 -4.1569 -0.1935 -1.7114 2.996 -5.6628 -3.0686 -4.8736 3.1423 3.5156 -6.7056 -1.1294 -4.7583 -0.4763 -5.8602 1.7712 -6.3794 -3.6157 -5.2236 -5.7637 -2.783 -6.4618 -4.631 -4.763 -3.793 -4.9956 -1.4258 -1.6998 3.1632 -4.8398 -2.4782 -4.0308 -4.3125 -3.2433 -3.4871 -0.8006 -1.7703 3.7102 3.6147 0.028 -0.9417 4.7087 4.6132 -0.0426 5.1602 0.7154 1.6851 6.7056 6.6101 -4.2814 -3.7241 0.4959 -0.2879 -1.9003 1.8977 -5.0931 -4.1907 -0.4433 -0.8462 -5.4982 -4.376 -1.6218 -1.5879 -3.653 -4.7825 -2.8485 -3.7764 -0.7568 -2.3278 3.4303 3.2756 0.5855 -0.9855 5.0478 4.8931 1.4138 2.2426 1.9565 1.3339 0.6717 0.097 7.1634 6.89 6.0569 6.1866 7.0448 7.2247 3 3 3 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 6 7 10 11 11 12 12 13 13 14 14 15 17 17 18 18 19 19 20 20 21 21 22 22 23 23 24 24 27 28 29 30 31 32 33 33 34 35 35 36 39 39 40 40 41 42 43 43 44 44 45 45 46 46 47 47 48 48 49 50 51 52 53 54 55 56 56 57 58 58 59 59 62 63 64 65 66 66 67 68 69 70 71 75 75 76 76 77 77 78 78 79 80 83 84 85 86 87 88 89 90 17 18 38 15 21 16 22 15 23 16 24 16 29 33 30 34 27 35 28 36 27 31 28 32 29 31 30 32 39 40 43 44 41 42 34 45 46 36 47 48 41 51 42 52 49 50 49 53 50 54 53 55 54 55 51 56 52 57 58 59 62 63 64 65 66 57 67 68 62 64 63 65 67 68 69 70 69 70 71 72 71 72 72 83 84 85 86 79 80 81 82 81 82 87 88 89 90 91 91 92 92 0 Compound Canonicalized 5 2010.07.16 0 Compound Complexity 7 E_COMPLEXITY 3.396 Cactvs xemistry.com 2012.02.08 5080 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.396 Cactvs xemistry.com 2012.02.08 4 Count Hydrogen Bond Donor 5 E_NHDONORS 3.396 Cactvs xemistry.com 2012.02.08 0 Count Rotatable Bond 5 E_NROTBONDS 3.396 Cactvs xemistry.com 2012.02.08 6 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.396 Cactvs xemistry.com 2012.02.08 00000371F07F8000000000000000000000001830000183060C103060C1830608000000015400001C00000000000E08C1180432C0C3000000A00234634400820000210200088800286488082022C0919184200860800048C8071080C00FC0008200001000008001040000200001000008000000 InChI Standard 1 1.0.4 InChI nist.gov 2012.02.08 InChI=1S/C92H38N4/c1-95(2)29-17-13-27(14-18-29)93-23-87-21-5-7-25-9-11-26(12-10-25)8-6-22-88(24-94-28-15-19-30(20-16-28)96(3)4)90-81-67-59-48-40-33-31-32-34-39(33)52(59)60-49-41(34)38-43-36(32)45-44-35(31)42-37(40)46-53-61-50(42)55(44)65-66-56(45)51(43)62-54-47(38)58(49)70-74-64(54)76-72(62)80(66)89(87)79(65)71(61)75-63(53)73(69(81)57(46)48)83(90)77-78(86(76)92(87,89)85(75)77)84(74)91(88,90)82(70)68(60)67/h9-20,23-24H,5-8,21-22H2,1-4H3 InChIKey Standard 1 1.0.4 InChI nist.gov 2012.02.08 NKNXMOYVTQATTM-UHFFFAOYSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2012.02.08 17.9 Mass Exact 7 2.1 PubChem ncbi.nlm.nih.gov 2012.02.08 1198.309647 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2012.02.08 C92H38N4 Molecular Weight 7 2.1 PubChem ncbi.nlm.nih.gov 2012.02.08 1199.31292 SMILES Canonical 1 1.7.6 OEChem openeye.com 2012.02.08 CN(C)C1=CC=C(C=C1)N=CC23CCCC4=CC=C(CCCC5(C67C58C9=C1C5=C%10C%11=C%12C5=C5C%13=C%14C%15=C%16C22C33C%14=C%14C%17=C%13C%12=C%12C%17=C%13C%17=C%18C%19=C%20C%21=C%22C(=C%23C%20=C%20C%19=C%19C%17=C%12C%11=C%19C%11=C%20C(=C%236)C9=C%10%11)C7=C(C%16=C8C1=C5%15)C2=C%22C1=C%21C%18=C%13C%14=C31)C=NC1=CC=C(C=C1)N(C)C)C=C4 SMILES Isomeric 1 1.7.6 OEChem openeye.com 2012.02.08 CN(C)C1=CC=C(C=C1)N=CC23CCCC4=CC=C(CCCC5(C67C58C9=C1C5=C%10C%11=C%12C5=C5C%13=C%14C%15=C%16C22C33C%14=C%14C%17=C%13C%12=C%12C%17=C%13C%17=C%18C%19=C%20C%21=C%22C(=C%23C%20=C%20C%19=C%19C%17=C%12C%11=C%19C%11=C%20C(=C%236)C9=C%10%11)C7=C(C%16=C8C1=C5%15)C2=C%22C1=C%21C%18=C%13C%14=C31)C=NC1=CC=C(C=C1)N(C)C)C=C4 Topological Polar Surface Area 7 E_TPSA 3.396 Cactvs xemistry.com 2012.02.08 31.2 Weight MonoIsotopic 7 2.1 PubChem ncbi.nlm.nih.gov 2012.02.08 1198.309647 96 3 0 3 0 0 0 0 1 1