5582251 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 8 8 8 8 7 7 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 2 2 3 4 4 5 5 5 6 6 6 7 7 7 8 8 8 9 9 10 10 11 11 11 12 12 12 13 13 14 14 15 15 16 16 17 18 18 19 19 20 20 22 23 23 24 24 25 25 27 17 21 22 48 21 26 49 7 8 11 9 10 12 9 28 29 10 30 31 32 33 34 35 13 36 37 14 38 39 15 16 18 19 17 20 21 40 22 24 41 25 42 23 43 26 26 44 27 45 27 46 47 1 1 1 1 2 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 2 2 1 2 1 1 1 1 1 1 2 1 2 1 2 1 1 2 1 1 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 6.029 4.269 7.7991 2.5369 6.8776 8.598 7.7493 6.866 8.6095 7.7262 6.0174 9.4581 6.029 9.4466 5.135 6.935 5.135 8.5748 10.3068 4.269 6.935 4.269 3.403 8.5633 10.2952 3.403 9.4234 7.3563 8.1533 6.6472 6.2567 8.8283 9.2188 8.1192 7.3222 5.7986 5.4081 9.6769 10.0674 7.4708 8.0415 10.8472 4.269 2.866 8.0228 10.8285 9.4163 3.732 2 -3.4168 -4.3822 -3.4063 -3.3822 0.1624 1.1824 -0.3275 1.1624 0.1824 1.6723 -0.3476 1.6924 -1.3475 2.6923 -1.8822 -1.8613 -2.8822 3.1822 3.2023 -1.3822 -2.903 -3.3822 -1.8822 4.1822 4.2022 -2.8822 4.6922 -0.8071 -0.7978 1.7425 1.0476 -0.3977 0.2972 2.1518 2.1426 0.2326 -0.4623 1.1122 1.8071 -1.5493 2.8661 2.8985 -0.7622 -1.5722 4.486 4.5184 5.3121 -4.6922 -3.0722 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 1 1 13 13 14 14 15 15 16 17 18 19 20 22 23 24 25 17 21 15 16 18 19 17 20 21 22 24 25 23 26 26 27 27 0 Compound Canonicalized 5 2021.10.14 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 552 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 6 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 2 Count Rotatable Bond 5 E_NROTBONDS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 4 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 00000371E07B38000000000000000000000000000000000000003C6081000000000000814000001E00000800000C04C19804300E83000600880220D208008208002020000888000E8CC80D672286B11B967A2BE5C0158BB907B0F0BE0E20000108000840004000021000108000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 4-[(4-benzylpiperazin-1-yl)methyl]-7,8-dihydroxy-chromen-2-one IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 7,8-dihydroxy-4-[[4-(phenylmethyl)-1-piperazinyl]methyl]-1-benzopyran-2-one IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 4-[(4-benzylpiperazin-1-yl)methyl]-7,8-dihydroxychromen-2-one IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 4-[(4-benzylpiperazin-1-yl)methyl]-7,8-dihydroxychromen-2-one IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 7,8-bis(oxidanyl)-4-[[4-(phenylmethyl)piperazin-1-yl]methyl]chromen-2-one IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 4-[(4-benzylpiperazino)methyl]-7,8-dihydroxy-coumarin InChI Standard 1 1.0.6 InChI iupac.org 2021.10.14 InChI=1S/C21H22N2O4/c24-18-7-6-17-16(12-19(25)27-21(17)20(18)26)14-23-10-8-22(9-11-23)13-15-4-2-1-3-5-15/h1-7,12,24,26H,8-11,13-14H2 InChIKey Standard 1 1.0.6 InChI iupac.org 2021.10.14 ZQONSSLYCOVARI-UHFFFAOYSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2021.10.14 1.9 Mass Exact 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 366.15795719 Molecular Formula 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 C21H22N2O4 Molecular Weight 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 366.4 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 C1CN(CCN1CC2=CC=CC=C2)CC3=CC(=O)OC4=C3C=CC(=C4O)O SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 C1CN(CCN1CC2=CC=CC=C2)CC3=CC(=O)OC4=C3C=CC(=C4O)O Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 73.2 Weight MonoIsotopic 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 366.15795719 27 0 0 0 0 0 0 0 1 -1