data_DRR
# 
_chem_comp.id                                    DRR 
_chem_comp.name                                  
(9S,12S)-9-(1-methylethyl)-N-[(8S,11S)-8-[(1S)-1-methylpropyl]-7,10-dioxo-2-oxa-6,9-diazabicyclo[11.2.2]heptadeca-1(15),13,16-trien-11-yl]-7,10-dioxo-2-oxa-8,11-diazabicyclo[12.2.2]octadeca-1(16),14,17-triene-12-carboxamide 
_chem_comp.type                                  NON-POLYMER 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C37 H51 N5 O7" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2008-01-15 
_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                        677.830 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     DRR 
_chem_comp.pdbx_model_coordinates_details        ? 
_chem_comp.pdbx_model_coordinates_missing_flag   N 
_chem_comp.pdbx_ideal_coordinates_details        Corina 
_chem_comp.pdbx_ideal_coordinates_missing_flag   N 
_chem_comp.pdbx_model_coordinates_db_code        3BXR 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  PDBJ 
# 
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 
DRR CBR  CBR  C 0 1 N N N 10.294 -3.093  15.292 -1.772 3.694  -3.543 CBR  DRR 1   
DRR CBQ  CBQ  C 0 1 N N N 8.904  -3.721  15.179 -1.587 3.090  -2.150 CBQ  DRR 2   
DRR CBO  CBO  C 0 1 N N S 8.605  -4.675  16.339 -2.955 2.895  -1.492 CBO  DRR 3   
DRR CBP  CBP  C 0 1 N N N 9.562  -5.870  16.304 -3.607 4.259  -1.258 CBP  DRR 4   
DRR CBN  CBN  C 0 1 N N S 7.150  -5.148  16.270 -2.779 2.177  -0.153 CBN  DRR 5   
DRR NBM  NBM  N 0 1 N N N 6.190  -4.037  16.363 -2.008 0.932  -0.358 NBM  DRR 6   
DRR CBK  CBK  C 0 1 N N N 5.643  -3.470  15.291 -2.569 0.012  -1.194 CBK  DRR 7   
DRR OBL  OBL  O 0 1 N N N 5.958  -3.746  14.134 -3.659 0.214  -1.686 OBL  DRR 8   
DRR CBS  CBS  C 0 1 N N N 6.819  -6.112  17.411 -4.133 1.840  0.418  CBS  DRR 9   
DRR OBT  OBT  O 0 1 N N N 6.887  -5.744  18.584 -5.109 1.781  -0.299 OBT  DRR 10  
DRR NBU  NBU  N 0 1 N N N 6.429  -7.324  17.025 -4.238 1.601  1.758  NBU  DRR 11  
DRR CBV  CBV  C 0 1 N N N 6.060  -8.367  17.994 -5.604 1.383  2.281  CBV  DRR 12  
DRR CBW  CBW  C 0 1 N N N 5.402  -9.550  17.277 -6.428 0.638  1.232  CBW  DRR 13  
DRR CBJ  CBJ  C 0 1 N N N 4.223  -9.119  16.401 -7.464 -0.245 1.935  CBJ  DRR 14  
DRR OBI  OBI  O 0 1 N N N 3.268  -8.353  17.155 -7.336 -1.585 1.442  OBI  DRR 15  
DRR CBH  CBH  C 0 1 Y N N 3.196  -7.056  16.745 -6.257 -1.816 0.646  CBH  DRR 16  
DRR CBG  CBG  C 0 1 Y N N 3.198  -6.721  15.393 -5.047 -2.189 1.213  CBG  DRR 17  
DRR CBF  CBF  C 0 1 Y N N 3.144  -5.386  15.001 -3.940 -2.386 0.411  CBF  DRR 18  
DRR CBE  CBE  C 0 1 Y N N 3.121  -6.045  17.699 -6.364 -1.685 -0.731 CBE  DRR 19  
DRR CBD  CBD  C 0 1 Y N N 3.067  -4.708  17.308 -5.253 -1.884 -1.528 CBD  DRR 20  
DRR CBC  CBC  C 0 1 Y N N 3.090  -4.377  15.957 -4.038 -2.216 -0.958 CBC  DRR 21  
DRR CBB  CBB  C 0 1 N N N 3.193  -2.917  15.498 -2.817 -2.372 -1.826 CBB  DRR 22  
DRR CBA  CBA  C 0 1 N N S 4.621  -2.365  15.574 -1.818 -1.259 -1.500 CBA  DRR 23  
DRR NAZ  NAZ  N 0 1 N N N 4.831  -1.347  14.536 -1.018 -1.646 -0.335 NAZ  DRR 24  
DRR CAX  CAX  C 0 1 N N N 5.909  -0.567  14.565 0.209  -1.117 -0.154 CAX  DRR 25  
DRR OAY  OAY  O 0 1 N N N 6.730  -0.586  15.481 0.650  -0.321 -0.956 OAY  DRR 26  
DRR CAN  CAN  C 0 1 N N S 6.066  0.379   13.372 1.032  -1.515 1.043  CAN  DRR 27  
DRR CAO  CAO  C 0 1 N N N 7.279  1.298   13.534 0.929  -0.432 2.120  CAO  DRR 28  
DRR CAP  CAP  C 0 1 Y N N 7.517  2.093   12.248 2.141  0.462  2.041  CAP  DRR 29  
DRR CAR  CAR  C 0 1 Y N N 7.355  3.474   12.258 2.204  1.455  1.081  CAR  DRR 30  
DRR CAT  CAT  C 0 1 Y N N 7.485  4.195   11.075 3.316  2.271  1.002  CAT  DRR 31  
DRR CAQ  CAQ  C 0 1 Y N N 7.825  1.433   11.061 3.187  0.286  2.928  CAQ  DRR 32  
DRR CAS  CAS  C 0 1 Y N N 7.954  2.157   9.878  4.301  1.100  2.854  CAS  DRR 33  
DRR CAU  CAU  C 0 1 Y N N 7.776  3.539   9.883  4.369  2.094  1.888  CAU  DRR 34  
DRR OAV  OAV  O 0 1 N N N 7.833  4.273   8.737  5.467  2.891  1.808  OAV  DRR 35  
DRR CAW  CAW  C 0 1 N N N 7.079  3.704   7.652  6.601  2.364  1.115  CAW  DRR 36  
DRR CAC  CAC  C 0 1 N N N 5.630  3.444   8.074  6.271  2.233  -0.374 CAC  DRR 37  
DRR CAB  CAB  C 0 1 N N N 5.013  4.709   8.671  7.245  1.250  -1.027 CAB  DRR 38  
DRR CAA  CAA  C 0 1 N N N 3.571  4.474   9.123  6.524  0.481  -2.136 CAA  DRR 39  
DRR CAD  CAD  C 0 1 N N N 3.419  3.854   10.514 5.933  -0.784 -1.569 CAD  DRR 40  
DRR OAE  OAE  O 0 1 N N N 3.521  4.547   11.525 6.639  -1.611 -1.031 OAE  DRR 41  
DRR N    N    N 0 1 N N N 3.180  2.543   10.535 4.581  -0.978 -1.673 N    DRR 42  
DRR CA   CA   C 0 1 N N S 2.923  1.815   11.786 4.098  -2.256 -1.094 CA   DRR 43  
DRR CB   CB   C 0 1 N N N 1.557  1.136   11.635 4.978  -2.646 0.096  CB   DRR 44  
DRR CG1  CG1  C 0 1 N N N 0.488  2.164   11.256 5.080  -1.465 1.063  CG1  DRR 45  
DRR CG2  CG2  C 0 1 N N N 1.133  0.380   12.896 4.359  -3.845 0.817  CG2  DRR 46  
DRR C    C    C 0 1 N N N 4.018  0.795   12.111 2.676  -2.067 -0.631 C    DRR 47  
DRR O    O    O 0 1 N N N 4.077  -0.287  11.529 1.750  -2.279 -1.384 O    DRR 48  
DRR NAM  NAM  N 0 1 N N N 4.841  1.144   13.099 2.449  -1.655 0.647  NAM  DRR 49  
DRR HBR  HBR  H 0 1 N N N 10.712 -2.942  14.286 -2.376 3.023  -4.153 HBR  DRR 50  
DRR HBRA HBRA H 0 0 N N N 10.217 -2.124  15.806 -2.274 4.658  -3.457 HBRA DRR 51  
DRR HBRB HBRB H 0 0 N N N 10.953 -3.762  15.866 -0.797 3.833  -4.011 HBRB DRR 52  
DRR HBQ  HBQ  H 0 1 N N N 8.154  -2.916  15.185 -1.084 2.126  -2.235 HBQ  DRR 53  
DRR HBQA HBQA H 0 0 N N N 8.868  -4.301  14.245 -0.983 3.761  -1.539 HBQA DRR 54  
DRR HBO  HBO  H 0 1 N N N 8.754  -4.139  17.288 -3.589 2.296  -2.145 HBO  DRR 55  
DRR HBP  HBP  H 0 1 N N N 9.791  -6.126  15.259 -2.975 4.856  -0.601 HBP  DRR 56  
DRR HBPA HBPA H 0 0 N N N 10.492 -5.610  16.830 -3.727 4.773  -2.212 HBPA DRR 57  
DRR HBPB HBPB H 0 0 N N N 9.090  -6.732  16.797 -4.584 4.120  -0.795 HBPB DRR 58  
DRR HBN  HBN  H 0 1 N N N 7.057  -5.644  15.293 -2.244 2.826  0.540  HBN  DRR 59  
DRR HNBM HNBM H 0 0 N N N 5.939  -3.694  17.268 -1.155 0.779  0.076  HNBM DRR 60  
DRR HNBU HNBU H 0 0 N N N 6.386  -7.532  16.048 -3.459 1.576  2.335  HNBU DRR 61  
DRR HBV  HBV  H 0 1 N N N 6.965  -8.716  18.512 -5.554 0.790  3.194  HBV  DRR 62  
DRR HBVA HBVA H 0 0 N N N 5.348  -7.946  18.719 -6.070 2.345  2.495  HBVA DRR 63  
DRR HBW  HBW  H 0 1 N N N 6.155  -10.032 16.636 -6.938 1.358  0.592  HBW  DRR 64  
DRR HBWA HBWA H 0 0 N N N 5.018  -10.238 18.045 -5.769 0.015  0.627  HBWA DRR 65  
DRR HBJ  HBJ  H 0 1 N N N 4.601  -8.501  15.573 -7.286 -0.232 3.010  HBJ  DRR 66  
DRR HBJA HBJA H 0 0 N N N 3.723  -10.021 16.019 -8.466 0.128  1.724  HBJA DRR 67  
DRR HBG  HBG  H 0 1 N N N 3.242  -7.500  14.646 -4.971 -2.326 2.282  HBG  DRR 68  
DRR HBF  HBF  H 0 1 N N N 3.144  -5.133  13.951 -2.997 -2.672 0.853  HBF  DRR 69  
DRR HBE  HBE  H 0 1 N N N 3.105  -6.298  18.749 -7.313 -1.430 -1.178 HBE  DRR 70  
DRR HBD  HBD  H 0 1 N N N 3.007  -3.929  18.054 -5.334 -1.779 -2.600 HBD  DRR 71  
DRR HBB  HBB  H 0 1 N N N 2.855  -2.859  14.453 -2.356 -3.342 -1.635 HBB  DRR 72  
DRR HBBA HBBA H 0 0 N N N 2.568  -2.313  16.172 -3.106 -2.306 -2.875 HBBA DRR 73  
DRR HBA  HBA  H 0 1 N N N 4.751  -1.948  16.584 -1.162 -1.096 -2.355 HBA  DRR 74  
DRR HNAZ HNAZ H 0 0 N N N 4.160  -1.239  13.803 -1.371 -2.282 0.306  HNAZ DRR 75  
DRR HAN  HAN  H 0 1 N N N 6.247  -0.254  12.491 0.665  -2.461 1.441  HAN  DRR 76  
DRR HAO  HAO  H 0 1 N N N 7.095  1.997   14.363 0.029  0.161  1.957  HAO  DRR 77  
DRR HAOA HAOA H 0 0 N N N 8.167  0.685   13.747 0.885  -0.899 3.104  HAOA DRR 78  
DRR HAR  HAR  H 0 1 N N N 7.129  3.986   13.182 1.384  1.592  0.393  HAR  DRR 79  
DRR HAT  HAT  H 0 1 N N N 7.360  5.268   11.082 3.365  3.046  0.252  HAT  DRR 80  
DRR HAQ  HAQ  H 0 1 N N N 7.964  0.362   11.058 3.134  -0.488 3.679  HAQ  DRR 81  
DRR HAS  HAS  H 0 1 N N N 8.192  1.647   8.956  5.118  0.963  3.547  HAS  DRR 82  
DRR HAW  HAW  H 0 1 N N N 7.085  4.405   6.804  7.449  3.036  1.241  HAW  DRR 83  
DRR HAWA HAWA H 0 0 N N N 7.540  2.748   7.365  6.851  1.383  1.519  HAWA DRR 84  
DRR HAC  HAC  H 0 1 N N N 5.047  3.139   7.193  5.252  1.865  -0.489 HAC  DRR 85  
DRR HACA HACA H 0 0 N N N 5.616  2.648   8.833  6.363  3.207  -0.853 HACA DRR 86  
DRR HAB  HAB  H 0 1 N N N 5.611  5.017   9.542  8.085  1.799  -1.453 HAB  DRR 87  
DRR HABA HABA H 0 0 N N N 5.008  5.489   7.896  7.611  0.549  -0.278 HABA DRR 88  
DRR HAA  HAA  H 0 1 N N N 3.063  5.449   9.136  5.727  1.100  -2.549 HAA  DRR 89  
DRR HAAA HAAA H 0 0 N N N 3.138  3.753   8.414  7.234  0.229  -2.924 HAAA DRR 90  
DRR HN   HN   H 0 1 N N N 3.175  2.038   9.672  3.988  -0.334 -2.091 HN   DRR 91  
DRR HA   HA   H 0 1 N N N 2.924  2.519   12.631 4.138  -3.039 -1.851 HA   DRR 92  
DRR HB   HB   H 0 1 N N N 1.658  0.395   10.829 5.973  -2.911 -0.260 HB   DRR 93  
DRR HG1  HG1  H 0 1 N N N -0.115 2.411   12.142 4.348  -1.586 1.862  HG1  DRR 94  
DRR HG1A HG1A H 0 0 N N N 0.974  3.076   10.878 6.082  -1.431 1.491  HG1A DRR 95  
DRR HG1B HG1B H 0 0 N N N -0.163 1.744   10.475 4.882  -0.537 0.527  HG1B DRR 96  
DRR HG2  HG2  H 0 1 N N N 1.031  -0.691  12.665 4.161  -4.639 0.098  HG2  DRR 97  
DRR HG2A HG2A H 0 0 N N N 1.894  0.516   13.678 5.049  -4.207 1.579  HG2A DRR 98  
DRR HG2B HG2B H 0 0 N N N 0.168  0.772   13.251 3.424  -3.541 1.289  HG2B DRR 99  
DRR HNAM HNAM H 0 0 N N N 4.622  1.939   13.664 3.175  -1.464 1.262  HNAM DRR 100 
# 
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 
DRR CBR CBQ  SING N N 1   
DRR CBQ CBO  SING N N 2   
DRR CBO CBP  SING N N 3   
DRR CBO CBN  SING N N 4   
DRR CBN NBM  SING N N 5   
DRR CBN CBS  SING N N 6   
DRR NBM CBK  SING N N 7   
DRR CBK OBL  DOUB N N 8   
DRR CBK CBA  SING N N 9   
DRR CBS OBT  DOUB N N 10  
DRR CBS NBU  SING N N 11  
DRR NBU CBV  SING N N 12  
DRR CBV CBW  SING N N 13  
DRR CBW CBJ  SING N N 14  
DRR CBJ OBI  SING N N 15  
DRR OBI CBH  SING N N 16  
DRR CBH CBG  DOUB N N 17  
DRR CBH CBE  SING N N 18  
DRR CBG CBF  SING N N 19  
DRR CBF CBC  DOUB N N 20  
DRR CBE CBD  DOUB N N 21  
DRR CBD CBC  SING N N 22  
DRR CBC CBB  SING N N 23  
DRR CBB CBA  SING N N 24  
DRR CBA NAZ  SING N N 25  
DRR NAZ CAX  SING N N 26  
DRR CAX OAY  DOUB N N 27  
DRR CAX CAN  SING N N 28  
DRR CAN CAO  SING N N 29  
DRR CAN NAM  SING N N 30  
DRR CAO CAP  SING N N 31  
DRR CAP CAR  DOUB N N 32  
DRR CAP CAQ  SING N N 33  
DRR CAR CAT  SING N N 34  
DRR CAT CAU  DOUB Y N 35  
DRR CAQ CAS  DOUB Y N 36  
DRR CAS CAU  SING Y N 37  
DRR CAU OAV  SING N N 38  
DRR OAV CAW  SING Y N 39  
DRR CAW CAC  SING N N 40  
DRR CAC CAB  SING Y N 41  
DRR CAB CAA  SING N N 42  
DRR CAA CAD  SING Y N 43  
DRR CAD OAE  DOUB N N 44  
DRR CAD N    SING N N 45  
DRR N   CA   SING N N 46  
DRR CA  CB   SING N N 47  
DRR CA  C    SING N N 48  
DRR CB  CG1  SING N N 49  
DRR CB  CG2  SING N N 50  
DRR C   O    DOUB N N 51  
DRR C   NAM  SING N N 52  
DRR CBR HBR  SING N N 53  
DRR CBR HBRA SING N N 54  
DRR CBR HBRB SING N N 55  
DRR CBQ HBQ  SING N N 56  
DRR CBQ HBQA SING N N 57  
DRR CBO HBO  SING N N 58  
DRR CBP HBP  SING N N 59  
DRR CBP HBPA SING N N 60  
DRR CBP HBPB SING Y N 61  
DRR CBN HBN  SING Y N 62  
DRR NBM HNBM SING Y N 63  
DRR NBU HNBU SING N N 64  
DRR CBV HBV  SING Y N 65  
DRR CBV HBVA SING N N 66  
DRR CBW HBW  SING Y N 67  
DRR CBW HBWA SING N N 68  
DRR CBJ HBJ  SING Y N 69  
DRR CBJ HBJA SING N N 70  
DRR CBG HBG  SING N N 71  
DRR CBF HBF  SING N N 72  
DRR CBE HBE  SING N N 73  
DRR CBD HBD  SING N N 74  
DRR CBB HBB  SING N N 75  
DRR CBB HBBA SING N N 76  
DRR CBA HBA  SING N N 77  
DRR NAZ HNAZ SING N N 78  
DRR CAN HAN  SING N N 79  
DRR CAO HAO  SING N N 80  
DRR CAO HAOA SING N N 81  
DRR CAR HAR  SING N N 82  
DRR CAT HAT  SING N N 83  
DRR CAQ HAQ  SING N N 84  
DRR CAS HAS  SING N N 85  
DRR CAW HAW  SING N N 86  
DRR CAW HAWA SING N N 87  
DRR CAC HAC  SING N N 88  
DRR CAC HACA SING N N 89  
DRR CAB HAB  SING N N 90  
DRR CAB HABA SING N N 91  
DRR CAA HAA  SING N N 92  
DRR CAA HAAA SING N N 93  
DRR N   HN   SING N N 94  
DRR CA  HA   SING N N 95  
DRR CB  HB   SING N N 96  
DRR CG1 HG1  SING N N 97  
DRR CG1 HG1A SING N N 98  
DRR CG1 HG1B SING N N 99  
DRR CG2 HG2  SING N N 100 
DRR CG2 HG2A SING N N 101 
DRR CG2 HG2B SING N N 102 
DRR NAM HNAM SING N N 103 
# 
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 
DRR SMILES           ACDLabs              10.04 O=C3NC(C(=O)NC(C(=O)NC2C(=O)NC(C(=O)NCCCOc1ccc(cc1)C2)C(C)CC)Cc4ccc(OCCCC3)cc4)C(C)C 
DRR InChI            InChI                1.02b 
;InChI=1/C37H51N5O7/c1-5-24(4)33-36(46)38-18-8-20-49-28-16-12-26(13-17-28)22-30(35(45)42-33)39-34(44)29-21-25-10-14-27(15-11-25)48-19-7-6-9-31(43)41-32(23(2)3)37(47)40-29/h10-17,23-24,29-30,32-33H,5-9,18-22H2,1-4H3,(H,38,46)(H,39,44)(H,40,47)(H,41,43)(H,42,45)/t24-,29-,30-,32-,33-/m0/s1/f/h38-42H
;
DRR InChIKey         InChI                1.02b LMXVYRBJYYRIPR-BVSJEUDODZ 
DRR SMILES_CANONICAL CACTVS               3.341 CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(OCCCNC1=O)cc2)NC(=O)[C@@H]3Cc4ccc(OCCCCC(=O)N[C@@H](C(C)C)C(=O)N3)cc4 
DRR SMILES           CACTVS               3.341 CC[CH](C)[CH]1NC(=O)[CH](Cc2ccc(OCCCNC1=O)cc2)NC(=O)[CH]3Cc4ccc(OCCCCC(=O)N[CH](C(C)C)C(=O)N3)cc4 
DRR SMILES_CANONICAL "OpenEye OEToolkits" 1.5.0 CC[C@H](C)[C@H]1C(=O)NCCCOc2ccc(cc2)C[C@@H](C(=O)N1)NC(=O)[C@@H]3Cc4ccc(cc4)OCCCCC(=O)N[C@H](C(=O)N3)C(C)C 
DRR SMILES           "OpenEye OEToolkits" 1.5.0 CCC(C)C1C(=O)NCCCOc2ccc(cc2)CC(C(=O)N1)NC(=O)C3Cc4ccc(cc4)OCCCCC(=O)NC(C(=O)N3)C(C)C 
# 
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 
DRR "SYSTEMATIC NAME" ACDLabs              10.04 
(9S,12S)-9-(1-methylethyl)-N-[(8S,11S)-8-[(1S)-1-methylpropyl]-7,10-dioxo-2-oxa-6,9-diazabicyclo[11.2.2]heptadeca-1(15),13,16-trien-11-yl]-7,10-dioxo-2-oxa-8,11-diazabicyclo[12.2.2]octadeca-1(16),14,17-triene-12-carboxamide 
DRR "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.5.0 
(3S,6S)-N-[(8S,11S)-8-[(2S)-butan-2-yl]-7,10-dioxo-2-oxa-6,9-diazabicyclo[11.2.2]heptadeca-1(16),13(17),14-trien-11-yl]-5,8-dioxo-6-propan-2-yl-13-oxa-4,7-diazabicyclo[12.2.2]octadeca-1(17),14(18),15-triene-3-carboxamide    
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