data_146
# 
_chem_comp.id                                    146 
_chem_comp.name                                  "[4R-(4ALPHA,5ALPHA,6ALPHA,7ALPHA)]-3,3'-{{TETRAHYDRO-5,6-DIHYDROXY-2-OXO-4,7-BIS(PHENYLMETHYL)-1H-1,3-DIAZEPINE-1,3(2H)-DIYL]BIS(METHYLENE)]BIS[N-1H-BENZIMIDAZOL-2-YLBENZAMIDE]" 
_chem_comp.type                                  NON-POLYMER 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C49 H44 N8 O5" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         SD146 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     1999-07-08 
_chem_comp.pdbx_modified_date                    2008-10-14 
_chem_comp.pdbx_ambiguous_flag                   N 
_chem_comp.pdbx_release_status                   REL 
_chem_comp.pdbx_replaced_by                      ? 
_chem_comp.pdbx_replaces                         ? 
_chem_comp.formula_weight                        824.924 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     146 
_chem_comp.pdbx_model_coordinates_details        ? 
_chem_comp.pdbx_model_coordinates_missing_flag   N 
_chem_comp.pdbx_ideal_coordinates_details        ? 
_chem_comp.pdbx_ideal_coordinates_missing_flag   N 
_chem_comp.pdbx_model_coordinates_db_code        1BWB 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  RCSB 
# 
loop_
_chem_comp_atom.comp_id 
_chem_comp_atom.atom_id 
_chem_comp_atom.alt_atom_id 
_chem_comp_atom.type_symbol 
_chem_comp_atom.charge 
_chem_comp_atom.pdbx_align 
_chem_comp_atom.pdbx_aromatic_flag 
_chem_comp_atom.pdbx_leaving_atom_flag 
_chem_comp_atom.pdbx_stereo_config 
_chem_comp_atom.model_Cartn_x 
_chem_comp_atom.model_Cartn_y 
_chem_comp_atom.model_Cartn_z 
_chem_comp_atom.pdbx_model_Cartn_x_ideal 
_chem_comp_atom.pdbx_model_Cartn_y_ideal 
_chem_comp_atom.pdbx_model_Cartn_z_ideal 
_chem_comp_atom.pdbx_component_atom_id 
_chem_comp_atom.pdbx_component_comp_id 
_chem_comp_atom.pdbx_ordinal 
146 C1   C1   C 0 1 N N N -9.042  15.605 27.839 -2.479 -1.339 0.219  C1   146 1   
146 C2   C2   C 0 1 N N N -9.757  15.070 30.107 -4.063 -0.073 1.484  C2   146 2   
146 C3   C3   C 0 1 N N R -11.039 16.771 28.804 -3.450 0.664  -0.828 C3   146 3   
146 C4   C4   C 0 1 N N S -10.787 18.252 28.595 -2.092 1.034  -1.440 C4   146 4   
146 C5   C5   C 0 1 N N S -10.376 18.493 27.160 -1.656 0.038  -2.504 C5   146 5   
146 C6   C6   C 0 1 N N R -8.989  17.947 26.931 -2.176 -1.357 -2.208 C6   146 6   
146 C7   C7   C 0 1 N N N -8.186  15.972 25.614 -0.673 -2.689 -0.673 C7   146 7   
146 C20  C20  C 0 1 Y N N -9.701  15.825 31.422 -3.274 0.791  2.433  C20  146 8   
146 C21  C21  C 0 1 Y N N -10.415 15.324 32.520 -2.430 0.209  3.355  C21  146 9   
146 C22  C22  C 0 1 Y N N -10.312 15.961 33.770 -1.696 1.012  4.230  C22  146 10  
146 C23  C23  C 0 1 Y N N -9.514  17.104 33.916 -1.830 2.400  4.173  C23  146 11  
146 C24  C24  C 0 1 Y N N -8.803  17.620 32.819 -2.683 2.969  3.250  C24  146 12  
146 C25  C25  C 0 1 Y N N -8.900  16.977 31.572 -3.403 2.168  2.382  C25  146 13  
146 C26  C26  C 0 1 N N N -11.014 15.411 34.969 -0.784 0.394  5.216  C26  146 14  
146 C27  C27  C 0 1 Y N N -11.640 13.239 36.032 0.772  0.594  6.986  C27  146 15  
146 C9   C9   C 0 1 Y N N -12.359 12.412 39.445 2.490  -2.019 8.742  C9   146 16  
146 C11  C11  C 0 1 Y N N -12.565 11.103 39.927 3.393  -1.847 9.771  C11  146 17  
146 C13  C13  C 0 1 Y N N -12.513 9.980  39.069 3.713  -0.574 10.220 C13  146 18  
146 C14  C14  C 0 1 Y N N -12.252 10.124 37.695 3.135  0.535  9.645  C14  146 19  
146 C28  C28  C 0 1 Y N N -12.039 11.412 37.168 2.219  0.378  8.602  C28  146 20  
146 C29  C29  C 0 1 Y N N -12.092 12.598 38.073 1.898  -0.913 8.152  C29  146 21  
146 C31  C31  C 0 1 N N N -12.098 16.131 27.860 -4.330 0.042  -1.914 C31  146 22  
146 C32  C32  C 0 1 Y N N -12.820 14.938 28.454 -5.582 0.865  -2.078 C32  146 23  
146 C33  C33  C 0 1 Y N N -12.475 13.618 28.070 -5.609 1.912  -2.981 C33  146 24  
146 C34  C34  C 0 1 Y N N -13.130 12.515 28.673 -6.757 2.666  -3.131 C34  146 25  
146 C35  C35  C 0 1 Y N N -14.131 12.728 29.655 -7.879 2.374  -2.379 C35  146 26  
146 C36  C36  C 0 1 Y N N -14.478 14.046 30.036 -7.854 1.326  -1.477 C36  146 27  
146 C37  C37  C 0 1 Y N N -13.823 15.149 29.433 -6.707 0.569  -1.330 C37  146 28  
146 C61  C61  C 0 1 N N N -7.909  18.514 27.884 -1.583 -2.341 -3.218 C61  146 29  
146 C62  C62  C 0 1 Y N N -6.491  18.341 27.389 -2.097 -2.017 -4.597 C62  146 30  
146 C63  C63  C 0 1 Y N N -6.029  19.140 26.307 -1.351 -1.218 -5.443 C63  146 31  
146 C64  C64  C 0 1 Y N N -4.737  18.921 25.786 -1.822 -0.920 -6.708 C64  146 32  
146 C65  C65  C 0 1 Y N N -3.919  17.920 26.356 -3.040 -1.423 -7.127 C65  146 33  
146 C66  C66  C 0 1 Y N N -4.374  17.139 27.440 -3.785 -2.223 -6.282 C66  146 34  
146 C67  C67  C 0 1 Y N N -5.662  17.343 27.964 -3.312 -2.524 -5.019 C67  146 35  
146 C70  C70  C 0 1 Y N N -8.858  16.327 24.314 0.569  -1.895 -0.364 C70  146 36  
146 C71  C71  C 0 1 Y N N -8.034  16.624 23.218 1.456  -1.585 -1.374 C71  146 37  
146 C72  C72  C 0 1 Y N N -8.623  16.913 21.966 2.604  -0.844 -1.086 C72  146 38  
146 C73  C73  C 0 1 Y N N -10.027 16.884 21.811 2.852  -0.431 0.223  C73  146 39  
146 C74  C74  C 0 1 Y N N -10.854 16.580 22.912 1.959  -0.753 1.224  C74  146 40  
146 C75  C75  C 0 1 Y N N -10.268 16.312 24.163 0.820  -1.482 0.932  C75  146 41  
146 C76  C76  C 0 1 N N N -7.766  17.293 20.800 3.556  -0.503 -2.164 C76  146 42  
146 C77  C77  C 0 1 Y N N -5.567  16.877 19.707 5.557  0.527  -2.892 C77  146 43  
146 C15  C15  C 0 1 Y N N -4.720  17.243 16.230 8.484  1.962  -4.318 C15  146 44  
146 C8   C8   C 0 1 Y N N -3.662  16.568 15.573 8.871  1.923  -5.639 C8   146 45  
146 C10  C10  C 0 1 Y N N -2.797  15.690 16.277 8.091  1.271  -6.582 C10  146 46  
146 C12  C12  C 0 1 Y N N -2.960  15.459 17.666 6.915  0.652  -6.210 C12  146 47  
146 C78  C78  C 0 1 Y N N -4.017  16.114 18.359 6.509  0.683  -4.884 C78  146 48  
146 C79  C79  C 0 1 Y N N -4.924  17.034 17.609 7.295  1.342  -3.925 C79  146 49  
146 N2   N2   N 0 1 N N N -9.863  15.885 28.886 -3.286 -0.290 0.261  N2   146 50  
146 N7   N7   N 0 1 N N N -8.838  16.474 26.827 -1.803 -1.776 -0.856 N7   146 51  
146 N26  N26  N 0 1 N N N -11.237 14.087 34.902 -0.081 1.172  6.063  N26  146 52  
146 N3   N3   N 0 1 Y N N -11.837 13.688 37.287 0.980  -0.746 7.129  N3   146 53  
146 N27  N27  N 0 1 Y N N -11.756 11.899 35.919 1.504  1.253  7.848  N27  146 54  
146 N76  N76  N 0 1 N N N -6.494  16.845 20.857 4.666  0.208  -1.883 N76  146 55  
146 N1   N1   N 0 1 Y N N -5.844  17.467 18.519 6.659  1.216  -2.731 N1   146 56  
146 N77  N77  N 0 1 Y N N -4.485  16.088 19.658 5.415  0.176  -4.203 N77  146 57  
146 O1   O1   O 0 1 N N N -8.462  14.528 27.808 -2.336 -1.965 1.251  O1   146 58  
146 O4   O4   O 0 1 N N N -12.001 18.905 28.879 -2.186 2.332  -2.029 O4   146 59  
146 O5   O5   O 0 1 N N N -10.307 19.860 26.890 -0.228 0.002  -2.553 O5   146 60  
146 O26  O26  O 0 1 N N N -11.321 16.084 35.937 -0.669 -0.814 5.264  O26  146 61  
146 O76  O76  O 0 1 N N N -8.192  17.934 19.856 3.339  -0.863 -3.304 O76  146 62  
146 H21A 1H2  H 0 0 N N N -8.878  14.388 30.028 -5.001 0.422  1.235  H21A 146 63  
146 H22  2H2  H 0 1 N N N -10.588 14.327 30.135 -4.273 -1.032 1.956  H22  146 64  
146 H3   H3   H 0 1 N N N -11.462 16.824 29.834 -3.932 1.564  -0.447 H3   146 65  
146 H4   H4   H 0 1 N N N -9.970  18.632 29.252 -1.342 1.057  -0.649 H4   146 66  
146 H5   H5   H 0 1 N N N -11.130 17.996 26.506 -2.037 0.363  -3.473 H5   146 67  
146 H6   H6   H 0 1 N N N -8.811  18.336 25.901 -3.263 -1.362 -2.299 H6   146 68  
146 H71A 1H7  H 0 0 N N N -8.053  14.867 25.683 -0.884 -3.369 0.152  H71A 146 69  
146 H72  2H7  H 0 1 N N N -7.120  16.299 25.592 -0.519 -3.265 -1.586 H72  146 70  
146 H21  H21  H 0 1 N N N -11.054 14.433 32.401 -2.330 -0.865 3.394  H21  146 71  
146 H23  H23  H 0 1 N N N -9.445  17.599 34.898 -1.268 3.026  4.850  H23  146 72  
146 H24  H24  H 0 1 N N N -8.175  18.519 32.935 -2.788 4.043  3.204  H24  146 73  
146 H25  H25  H 0 1 N N N -8.345  17.378 30.707 -4.068 2.619  1.661  H25  146 74  
146 H9   H9   H 0 1 N N N -12.405 13.275 40.129 2.244  -3.012 8.398  H9   146 75  
146 H11  H11  H 0 1 N N N -12.771 10.954 41.000 3.853  -2.709 10.231 H11  146 76  
146 H13  H13  H 0 1 N N N -12.679 8.970  39.480 4.421  -0.452 11.026 H13  146 77  
146 H14  H14  H 0 1 N N N -12.214 9.238  37.039 3.388  1.523  10.000 H14  146 78  
146 H311 1H31 H 0 0 N N N -12.830 16.899 27.517 -3.784 0.021  -2.857 H311 146 79  
146 H312 2H31 H 0 0 N N N -11.635 15.860 26.882 -4.599 -0.973 -1.627 H312 146 80  
146 H33  H33  H 0 1 N N N -11.699 13.449 27.304 -4.732 2.140  -3.568 H33  146 81  
146 H34  H34  H 0 1 N N N -12.859 11.487 28.377 -6.777 3.484  -3.836 H34  146 82  
146 H35  H35  H 0 1 N N N -14.639 11.868 30.122 -8.777 2.964  -2.496 H35  146 83  
146 H36  H36  H 0 1 N N N -15.255 14.212 30.799 -8.730 1.098  -0.889 H36  146 84  
146 H37  H37  H 0 1 N N N -14.095 16.176 29.727 -6.686 -0.248 -0.625 H37  146 85  
146 H611 1H61 H 0 0 N N N -8.114  19.586 28.111 -0.496 -2.261 -3.208 H611 146 86  
146 H612 2H61 H 0 0 N N N -8.021  18.078 28.904 -1.875 -3.357 -2.951 H612 146 87  
146 H63  H63  H 0 1 N N N -6.670  19.926 25.873 -0.400 -0.825 -5.115 H63  146 88  
146 H64  H64  H 0 1 N N N -4.369  19.526 24.940 -1.240 -0.295 -7.368 H64  146 89  
146 H65  H65  H 0 1 N N N -2.909  17.745 25.948 -3.409 -1.190 -8.115 H65  146 90  
146 H66  H66  H 0 1 N N N -3.720  16.366 27.879 -4.737 -2.616 -6.609 H66  146 91  
146 H67  H67  H 0 1 N N N -6.015  16.731 28.810 -3.894 -3.150 -4.358 H67  146 92  
146 H71  H71  H 0 1 N N N -6.937  16.630 23.339 1.259  -1.908 -2.385 H71  146 93  
146 H73  H73  H 0 1 N N N -10.478 17.099 20.828 3.740  0.138  0.453  H73  146 94  
146 H74  H74  H 0 1 N N N -11.950 16.552 22.795 2.149  -0.434 2.239  H74  146 95  
146 H75  H75  H 0 1 N N N -10.915 16.089 25.027 0.124  -1.731 1.719  H75  146 96  
146 H15  H15  H 0 1 N N N -5.380  17.927 15.671 9.097  2.471  -3.589 H15  146 97  
146 H8   H8   H 0 1 N N N -3.508  16.729 14.492 9.790  2.402  -5.942 H8   146 98  
146 H10  H10  H 0 1 N N N -1.983  15.178 15.735 8.406  1.247  -7.615 H10  146 99  
146 H12  H12  H 0 1 N N N -2.274  14.779 18.199 6.312  0.146  -6.949 H12  146 100 
146 HN6  HN6  H 0 1 N N N -11.095 13.713 33.963 -0.173 2.137  6.025  HN6  146 101 
146 HN3  HN3  H 0 1 N N N -11.800 14.663 37.584 0.563  -1.452 6.610  HN3  146 102 
146 HN7  HN7  H 0 1 N N N -6.232  16.480 21.773 4.840  0.496  -0.973 HN7  146 103 
146 HN77 7HN7 H 0 0 N N N -4.096  15.572 20.448 4.684  -0.332 -4.587 HN77 146 104 
146 HO4  HO4  H 0 1 N N N -11.843 19.832 28.748 -1.311 2.541  -2.386 HO4  146 105 
146 HO5  HO5  H 0 1 N N N -10.048 20.011 25.988 0.066  0.896  -2.774 HO5  146 106 
# 
loop_
_chem_comp_bond.comp_id 
_chem_comp_bond.atom_id_1 
_chem_comp_bond.atom_id_2 
_chem_comp_bond.value_order 
_chem_comp_bond.pdbx_aromatic_flag 
_chem_comp_bond.pdbx_stereo_config 
_chem_comp_bond.pdbx_ordinal 
146 C1  N2   SING N N 1   
146 C1  N7   SING N N 2   
146 C1  O1   DOUB N N 3   
146 C2  C20  SING N N 4   
146 C2  N2   SING N N 5   
146 C2  H21A SING N N 6   
146 C2  H22  SING N N 7   
146 C3  C4   SING N N 8   
146 C3  C31  SING N N 9   
146 C3  N2   SING N N 10  
146 C3  H3   SING N N 11  
146 C4  C5   SING N N 12  
146 C4  O4   SING N N 13  
146 C4  H4   SING N N 14  
146 C5  C6   SING N N 15  
146 C5  O5   SING N N 16  
146 C5  H5   SING N N 17  
146 C6  C61  SING N N 18  
146 C6  N7   SING N N 19  
146 C6  H6   SING N N 20  
146 C7  C70  SING N N 21  
146 C7  N7   SING N N 22  
146 C7  H71A SING N N 23  
146 C7  H72  SING N N 24  
146 C20 C21  DOUB Y N 25  
146 C20 C25  SING Y N 26  
146 C21 C22  SING Y N 27  
146 C21 H21  SING N N 28  
146 C22 C23  DOUB Y N 29  
146 C22 C26  SING N N 30  
146 C23 C24  SING Y N 31  
146 C23 H23  SING N N 32  
146 C24 C25  DOUB Y N 33  
146 C24 H24  SING N N 34  
146 C25 H25  SING N N 35  
146 C26 N26  SING N N 36  
146 C26 O26  DOUB N N 37  
146 C27 N26  SING N N 38  
146 C27 N3   SING Y N 39  
146 C27 N27  DOUB Y N 40  
146 C9  C11  SING Y N 41  
146 C9  C29  DOUB Y N 42  
146 C9  H9   SING N N 43  
146 C11 C13  DOUB Y N 44  
146 C11 H11  SING N N 45  
146 C13 C14  SING Y N 46  
146 C13 H13  SING N N 47  
146 C14 C28  DOUB Y N 48  
146 C14 H14  SING N N 49  
146 C28 C29  SING Y N 50  
146 C28 N27  SING Y N 51  
146 C29 N3   SING Y N 52  
146 C31 C32  SING N N 53  
146 C31 H311 SING N N 54  
146 C31 H312 SING N N 55  
146 C32 C33  DOUB Y N 56  
146 C32 C37  SING Y N 57  
146 C33 C34  SING Y N 58  
146 C33 H33  SING N N 59  
146 C34 C35  DOUB Y N 60  
146 C34 H34  SING N N 61  
146 C35 C36  SING Y N 62  
146 C35 H35  SING N N 63  
146 C36 C37  DOUB Y N 64  
146 C36 H36  SING N N 65  
146 C37 H37  SING N N 66  
146 C61 C62  SING N N 67  
146 C61 H611 SING N N 68  
146 C61 H612 SING N N 69  
146 C62 C63  DOUB Y N 70  
146 C62 C67  SING Y N 71  
146 C63 C64  SING Y N 72  
146 C63 H63  SING N N 73  
146 C64 C65  DOUB Y N 74  
146 C64 H64  SING N N 75  
146 C65 C66  SING Y N 76  
146 C65 H65  SING N N 77  
146 C66 C67  DOUB Y N 78  
146 C66 H66  SING N N 79  
146 C67 H67  SING N N 80  
146 C70 C71  DOUB Y N 81  
146 C70 C75  SING Y N 82  
146 C71 C72  SING Y N 83  
146 C71 H71  SING N N 84  
146 C72 C73  DOUB Y N 85  
146 C72 C76  SING N N 86  
146 C73 C74  SING Y N 87  
146 C73 H73  SING N N 88  
146 C74 C75  DOUB Y N 89  
146 C74 H74  SING N N 90  
146 C75 H75  SING N N 91  
146 C76 N76  SING N N 92  
146 C76 O76  DOUB N N 93  
146 C77 N76  SING N N 94  
146 C77 N1   DOUB Y N 95  
146 C77 N77  SING Y N 96  
146 C15 C8   DOUB Y N 97  
146 C15 C79  SING Y N 98  
146 C15 H15  SING N N 99  
146 C8  C10  SING Y N 100 
146 C8  H8   SING N N 101 
146 C10 C12  DOUB Y N 102 
146 C10 H10  SING N N 103 
146 C12 C78  SING Y N 104 
146 C12 H12  SING N N 105 
146 C78 C79  DOUB Y N 106 
146 C78 N77  SING Y N 107 
146 C79 N1   SING Y N 108 
146 N26 HN6  SING N N 109 
146 N3  HN3  SING N N 110 
146 N76 HN7  SING N N 111 
146 N77 HN77 SING N N 112 
146 O4  HO4  SING N N 113 
146 O5  HO5  SING N N 114 
# 
loop_
_pdbx_chem_comp_descriptor.comp_id 
_pdbx_chem_comp_descriptor.type 
_pdbx_chem_comp_descriptor.program 
_pdbx_chem_comp_descriptor.program_version 
_pdbx_chem_comp_descriptor.descriptor 
146 SMILES           ACDLabs              10.04 O=C(Nc1nc2ccccc2n1)c3cc(ccc3)CN5C(=O)N(C(Cc4ccccc4)C(O)C(O)C5Cc6ccccc6)Cc7cccc(c7)C(=O)Nc9nc8ccccc8n9 
146 InChI            InChI                1.02b 
;InChI=1/C49H44N8O5/c58-43-41(27-31-13-3-1-4-14-31)56(29-33-17-11-19-35(25-33)45(60)54-47-50-37-21-7-8-22-38(37)51-47)49(62)57(42(44(43)59)28-32-15-5-2-6-16-32)30-34-18-12-20-36(26-34)46(61)55-48-52-39-23-9-10-24-40(39)53-48/h1-26,41-44,58-59H,27-30H2,(H2,50,51,54,60)(H2,52,53,55,61)/t41-,42-,43+,44+/m1/s1/f/h50,52,54-55H
;
146 InChIKey         InChI                1.02b UWSVAGUSMAEUKO-BQOIFOEADR 
146 SMILES_CANONICAL CACTVS               3.341 O[C@@H]1[C@@H](O)[C@@H](Cc2ccccc2)N(Cc3cccc(c3)C(=O)Nc4[nH]c5ccccc5n4)C(=O)N(Cc6cccc(c6)C(=O)Nc7[nH]c8ccccc8n7)[C@@H]1Cc9ccccc9 
146 SMILES           CACTVS               3.341 O[CH]1[CH](O)[CH](Cc2ccccc2)N(Cc3cccc(c3)C(=O)Nc4[nH]c5ccccc5n4)C(=O)N(Cc6cccc(c6)C(=O)Nc7[nH]c8ccccc8n7)[CH]1Cc9ccccc9 
146 SMILES_CANONICAL "OpenEye OEToolkits" 1.5.0 c1ccc(cc1)C[C@@H]2[C@@H]([C@H]([C@H](N(C(=O)N2Cc3cccc(c3)C(=O)Nc4[nH]c5ccccc5n4)Cc6cccc(c6)C(=O)Nc7[nH]c8ccccc8n7)Cc9ccccc9)O)O 
146 SMILES           "OpenEye OEToolkits" 1.5.0 c1ccc(cc1)CC2C(C(C(N(C(=O)N2Cc3cccc(c3)C(=O)Nc4[nH]c5ccccc5n4)Cc6cccc(c6)C(=O)Nc7[nH]c8ccccc8n7)Cc9ccccc9)O)O 
# 
loop_
_pdbx_chem_comp_identifier.comp_id 
_pdbx_chem_comp_identifier.type 
_pdbx_chem_comp_identifier.program 
_pdbx_chem_comp_identifier.program_version 
_pdbx_chem_comp_identifier.identifier 
146 "SYSTEMATIC NAME" ACDLabs              10.04 "3,3'-{[(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-2-oxo-1,3-diazepane-1,3-diyl]dimethanediyl}bis(N-1H-benzimidazol-2-ylbenzamide)"                                           
146 "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.5.0 N-(1H-benzimidazol-2-yl)-3-[[(4R,5S,6S,7R)-3-[[3-(1H-benzimidazol-2-ylcarbamoyl)phenyl]methyl]-5,6-dihydroxy-2-oxo-4,7-bis(phenylmethyl)-1,3-diazepan-1-yl]methyl]benzamide 
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