data_2Z3
#

_chem_comp.id                                   2Z3
_chem_comp.name                                 "N-(morpholin-4-ylcarbonyl)-L-phenylalanyl-N-[(1R)-1-(cyclohexylmethyl)-3,3-difluoro-2,2-dihydroxy-4-(methylamino)-4-oxobutyl]-L-norleucinamide"
_chem_comp.type                                 peptide-like
_chem_comp.pdbx_type                            HETAIN
_chem_comp.formula                              "C32 H49 F2 N5 O7"
_chem_comp.mon_nstd_parent_comp_id              ?
_chem_comp.pdbx_synonyms                        "CP-81,282"
_chem_comp.pdbx_formal_charge                   0
_chem_comp.pdbx_initial_date                    2008-08-28
_chem_comp.pdbx_modified_date                   2021-03-13
_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                       653.758
_chem_comp.one_letter_code                      ?
_chem_comp.three_letter_code                    2Z3
_chem_comp.pdbx_model_coordinates_details       "not provided"
_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       1epo
_chem_comp.pdbx_subcomponent_list               "MOR PHE NLE CHF NME"
_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
2Z3  O1    O1   O  0  1  N  N  N  30.972   -7.322  -7.567    8.821   0.787   2.043  O1    MOR   1  
2Z3  C2    C1   C  0  1  N  N  N  30.777   -6.553  -6.356    8.802   1.353   0.731  C2    MOR   2  
2Z3  C3    C2   C  0  1  N  N  N  32.009   -6.310  -5.715    8.007   0.435  -0.204  C3    MOR   3  
2Z3  N4    N1   N  0  1  N  N  N  32.837   -7.466  -5.629    6.697   0.167   0.411  N4    MOR   4  
2Z3  C5    C3   C  0  1  N  N  N  32.862   -8.465  -6.683    6.670  -0.290   1.809  C5    MOR   5  
2Z3  C6    C4   C  0  1  N  N  N  31.486   -8.641  -7.188    7.530   0.664   2.646  C6    MOR   6  
2Z3  C     C5   C  0  1  N  N  N  33.637   -7.620  -4.527    5.556   0.336  -0.286  C     MOR   7  
2Z3  O     O2   O  0  1  N  N  N  34.359   -8.599  -4.453    5.594   0.787  -1.414  O     MOR   8  
2Z3  N     N2   N  0  1  N  N  N  33.617   -6.707  -3.578    4.373   0.004   0.268  N     PHE   9  
2Z3  CA    C6   C  0  1  N  N  S  34.432   -6.805  -2.325    3.138   0.132  -0.510  CA    PHE  10  
2Z3  C1    C7   C  0  1  N  N  N  33.858   -7.898  -1.378    1.971   0.308   0.426  C     PHE  11  
2Z3  O2    O3   O  0  1  N  N  N  32.732   -8.185  -1.268    2.152   0.326   1.625  O     PHE  12  
2Z3  CB    C8   C  0  1  N  N  N  34.226   -5.456  -1.528    2.932  -1.130  -1.351  CB    PHE  13  
2Z3  CG    C9   C  0  1  Y  N  N  35.045   -4.395  -2.262    4.037  -1.240  -2.370  CG    PHE  14  
2Z3  CD1   C10  C  0  1  Y  N  N  36.383   -4.538  -2.441    5.200  -1.918  -2.058  CD1   PHE  15  
2Z3  CD2   C11  C  0  1  Y  N  N  34.363   -3.267  -2.811    3.884  -0.669  -3.620  CD2   PHE  16  
2Z3  CE1   C12  C  0  1  Y  N  N  37.165   -3.605  -3.106    6.213  -2.019  -2.993  CE1   PHE  17  
2Z3  CE2   C13  C  0  1  Y  N  N  35.144   -2.349  -3.473    4.896  -0.770  -4.555  CE2   PHE  18  
2Z3  CZ    C14  C  0  1  Y  N  N  36.499   -2.473  -3.638    6.062  -1.443  -4.241  CZ    PHE  19  
2Z3  N1    N3   N  0  1  N  N  N  34.824   -8.526  -0.640    0.725   0.447  -0.070  N     NLE  20  
2Z3  CA1   C15  C  0  1  N  N  S  34.424   -9.612   0.295   -0.410   0.618   0.840  CA    NLE  21  
2Z3  C4    C16  C  0  1  N  N  N  35.527   -9.638   1.414   -1.672   0.148   0.164  C     NLE  22  
2Z3  O3    O5   O  0  1  N  N  N  36.596  -10.145   1.175   -1.627  -0.288  -0.967  O     NLE  23  
2Z3  CB1   C17  C  0  1  N  N  N  34.511  -10.962  -0.472   -0.550   2.097   1.208  CB    NLE  24  
2Z3  CG1   C18  C  0  1  N  N  N  34.202  -12.149   0.411    0.678   2.543   2.005  CG    NLE  25  
2Z3  CD    C19  C  0  1  N  N  N  33.471  -13.318  -0.194    0.538   4.021   2.373  CD    NLE  26  
2Z3  CE    C20  C  0  1  N  N  N  34.033  -13.821  -1.467    1.766   4.467   3.169  CE    NLE  27  
2Z3  N2    N4   N  0  1  N  N  N  35.196   -9.045   2.509   -2.850   0.211   0.816  N     CHF  28  
2Z3  CA2   C21  C  0  1  N  N  S  36.207   -8.756   3.586   -4.065  -0.311   0.185  CA    CHF  29  
2Z3  CB2   C22  C  0  1  N  N  N  36.666   -7.354   3.636   -4.727  -1.328   1.117  CB    CHF  30  
2Z3  CG2   C23  C  0  1  N  N  N  36.975   -6.604   2.370   -3.867  -2.591   1.187  CG    CHF  31  
2Z3  CD11  C24  C  0  0  N  N  N  38.207   -7.016   1.690   -4.622  -3.681   1.951  CD1   CHF  32  
2Z3  CD21  C25  C  0  0  N  N  N  36.810   -5.114   2.484   -2.556  -2.276   1.912  CD2   CHF  33  
2Z3  CE11  C26  C  0  0  N  N  N  38.676   -6.270   0.453   -3.762  -4.944   2.021  CE1   CHF  34  
2Z3  CE21  C27  C  0  0  N  N  N  37.310   -4.343   1.273   -1.696  -3.540   1.982  CE2   CHF  35  
2Z3  CZ1   C28  C  0  1  N  N  N  38.602   -4.758   0.724   -2.452  -4.629   2.745  CZ    CHF  36  
2Z3  CH    C29  C  0  1  N  N  N  35.675   -9.317   4.905   -5.035   0.841  -0.085  CH    CHF  37  
2Z3  OH1   O7   O  0  1  N  N  N  34.364   -8.757   5.247   -5.493   1.378   1.158  OH1   CHF  38  
2Z3  OH2   O8   O  0  1  N  N  N  36.507   -8.924   5.936   -4.367   1.862  -0.828  OH2   CHF  39  
2Z3  CM    C30  C  0  1  N  N  N  35.591  -10.848   4.937   -6.230   0.324  -0.889  CM    CHF  40  
2Z3  F1    F1   F  0  1  N  N  N  35.104  -11.296   3.841   -5.778  -0.539  -1.893  F1    CHF  41  
2Z3  F2    F2   F  0  1  N  N  N  34.710  -11.281   5.853   -7.101  -0.365  -0.038  F2    CHF  42  
2Z3  C7    C31  C  0  1  N  N  N  36.910  -11.465   5.260   -6.955   1.487  -1.515  C     CHF  43  
2Z3  O4    O9   O  0  1  N  N  N  37.781  -11.821   4.416   -6.363   2.522  -1.737  O     CHF  44  
2Z3  N3    N5   N  0  1  N  N  N  37.172  -11.783   6.555   -8.261   1.377  -1.829  N     NME  45  
2Z3  C8    C32  C  0  1  N  N  N  38.509  -12.419   6.812   -8.965   2.508  -2.438  C     NME  46  
2Z3  H21   H1   H  0  1  N  N  N  30.310   -5.591  -6.613    8.329   2.335   0.765  H21   MOR  47  
2Z3  H22   H2   H  0  1  N  N  N  30.130   -7.125  -5.674    9.823   1.453   0.363  H22   MOR  48  
2Z3  H31   H3   H  0  1  N  N  N  32.549   -5.542  -6.288    7.867   0.924  -1.168  H31   MOR  49  
2Z3  H32   H4   H  0  1  N  N  N  31.786   -5.989  -4.687    8.546  -0.503  -0.343  H32   MOR  50  
2Z3  H51   H5   H  0  1  N  N  N  33.520   -8.131  -7.499    5.645  -0.280   2.179  H51   MOR  51  
2Z3  H52   H6   H  0  1  N  N  N  33.246   -9.418  -6.291    7.075  -1.300   1.873  H52   MOR  52  
2Z3  H61   H7   H  0  1  N  N  N  30.851   -9.081  -6.405    7.636   0.268   3.656  H61   MOR  53  
2Z3  H62   H8   H  0  1  N  N  N  31.481   -9.317  -8.056    7.053   1.643   2.687  H62   MOR  54  
2Z3  H     H10  H  0  1  N  N  N  33.028   -5.908  -3.700    4.339  -0.319   1.182  H     PHE  55  
2Z3  HA    H12  H  0  1  N  N  N  35.475   -7.021  -2.601    3.211   0.998  -1.168  HA    PHE  56  
2Z3  HB2   H13  H  0  1  N  N  N  33.162   -5.178  -1.509    2.948  -2.005  -0.702  HB2   PHE  57  
2Z3  HB3   H14  H  0  1  N  N  N  34.551   -5.557  -0.482    1.971  -1.073  -1.861  HB3   PHE  58  
2Z3  HD1   H15  H  0  1  N  N  N  36.862   -5.422  -2.046    5.318  -2.368  -1.083  HD1   PHE  59  
2Z3  HD2   H16  H  0  1  N  N  N  33.295   -3.142  -2.712    2.972  -0.144  -3.865  HD2   PHE  60  
2Z3  HE1   H17  H  0  1  N  N  N  38.232   -3.735  -3.213    7.123  -2.548  -2.749  HE1   PHE  61  
2Z3  HE2   H18  H  0  1  N  N  N  34.660   -1.477  -3.888    4.777  -0.324  -5.531  HE2   PHE  62  
2Z3  HZ    H19  H  0  1  N  N  N  37.055   -1.714  -4.169    6.854  -1.522  -4.971  HZ    PHE  63  
2Z3  H1    H21  H  0  1  N  N  N  35.784   -8.259  -0.728    0.580   0.433  -1.029  H     NLE  64  
2Z3  HA1   H23  H  0  1  N  N  N  33.412   -9.460   0.699   -0.243   0.033   1.745  HA    NLE  65  
2Z3  HB21  H25  H  0  0  N  N  N  33.783  -10.942  -1.297   -0.629   2.692   0.298  HB2   NLE  66  
2Z3  HB31  H26  H  0  0  N  N  N  35.542  -11.075  -0.839   -1.446   2.238   1.813  HB3   NLE  67  
2Z3  HG2   H27  H  0  1  N  N  N  35.168  -12.534   0.771    0.756   1.948   2.914  HG2   NLE  68  
2Z3  HG3   H28  H  0  1  N  N  N  33.513  -11.755   1.172    1.574   2.402   1.400  HG3   NLE  69  
2Z3  HD21  H29  H  0  0  N  N  N  33.503  -14.143   0.533    0.459   4.616   1.463  HD2   NLE  70  
2Z3  HD3   H30  H  0  1  N  N  N  32.456  -12.962  -0.424   -0.358   4.162   2.977  HD3   NLE  71  
2Z3  HE11  H31  H  0  0  N  N  N  33.224  -13.946  -2.202    2.662   4.326   2.564  HE1   NLE  72  
2Z3  HE21  H32  H  0  0  N  N  N  34.770  -13.101  -1.852    1.666   5.520   3.431  HE2   NLE  73  
2Z3  HE3   H33  H  0  1  N  N  N  34.523  -14.790  -1.293    1.845   3.872   4.079  HE3   NLE  74  
2Z3  H2    H34  H  0  1  N  N  N  34.244   -8.770   2.647   -2.893   0.602   1.702  H     CHF  75  
2Z3  HA2   H36  H  0  1  N  N  N  37.147   -9.274   3.346   -3.806  -0.796  -0.756  HA    CHF  76  
2Z3  HB22  H37  H  0  0  N  N  N  35.862   -6.791   4.132   -4.823  -0.898   2.114  HB2   CHF  77  
2Z3  HB32  H38  H  0  0  N  N  N  37.645   -7.425   4.133   -5.715  -1.582   0.734  HB3   CHF  78  
2Z3  HG    H39  H  0  1  N  N  N  36.179   -6.924   1.682   -3.649  -2.939   0.178  HG    CHF  79  
2Z3  HD12  H40  H  0  0  N  N  N  39.013   -6.915   2.431   -4.840  -3.333   2.960  HD12  CHF  80  
2Z3  HD13  H41  H  0  0  N  N  N  37.972   -8.022   1.313   -5.556  -3.905   1.435  HD13  CHF  81  
2Z3  HD23  H42  H  0  0  N  N  N  35.738   -4.899   2.605   -2.018  -1.500   1.368  HD23  CHF  82  
2Z3  HD22  H43  H  0  0  N  N  N  37.414   -4.789   3.344   -2.774  -1.928   2.922  HD22  CHF  83  
2Z3  HE12  H44  H  0  0  N  N  N  39.713   -6.554   0.221   -4.301  -5.720   2.565  HE12  CHF  84  
2Z3  HE13  H45  H  0  0  N  N  N  38.033   -6.527  -0.402   -3.545  -5.292   1.011  HE13  CHF  85  
2Z3  HE23  H46  H  0  0  N  N  N  36.562   -4.468   0.476   -1.479  -3.888   0.972  HE23  CHF  86  
2Z3  HE22  H47  H  0  0  N  N  N  37.454   -3.309   1.619   -0.763  -3.315   2.498  HE22  CHF  87  
2Z3  HZ2   H48  H  0  1  N  N  N  39.387   -4.497   1.449   -2.670  -4.281   3.755  HZ2   CHF  88  
2Z3  HZ3   H49  H  0  1  N  N  N  38.737   -4.240  -0.237   -1.839  -5.529   2.795  HZ3   CHF  89  
2Z3  HH1   H50  H  0  1  N  N  N  34.306   -8.636   6.187   -5.957   0.739   1.715  HH1   CHF  90  
2Z3  HH2   H51  H  0  1  N  N  N  37.395   -8.834   5.610   -4.028   1.568  -1.685  HH2   CHF  91  
2Z3  HN1   H53  H  0  1  N  N  N  36.517  -11.605   7.290   -8.734   0.549  -1.652  HN1   NME  92  
2Z3  H11   H55  H  0  1  N  N  N  39.031  -12.574   5.857   -8.927   3.365  -1.765  H1    NME  93  
2Z3  H23   H56  H  0  1  N  N  N  39.111  -11.760   7.456   -8.488   2.767  -3.383  H2    NME  94  
2Z3  H3    H57  H  0  1  N  N  N  38.364  -13.388   7.312  -10.005   2.234  -2.619  H3    NME  95  
#   #
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
2Z3  O1    C2    SING  N  N   1  
2Z3  O1    C6    SING  N  N   2  
2Z3  C2    C3    SING  N  N   3  
2Z3  C2    H21   SING  N  N   4  
2Z3  C2    H22   SING  N  N   5  
2Z3  C3    N4    SING  N  N   6  
2Z3  C3    H31   SING  N  N   7  
2Z3  C3    H32   SING  N  N   8  
2Z3  N4    C5    SING  N  N   9  
2Z3  N4    C     SING  N  N  10  
2Z3  C5    C6    SING  N  N  11  
2Z3  C5    H51   SING  N  N  12  
2Z3  C5    H52   SING  N  N  13  
2Z3  C6    H61   SING  N  N  14  
2Z3  C6    H62   SING  N  N  15  
2Z3  C     O     DOUB  N  N  16  
2Z3  N     CA    SING  N  N  17  
2Z3  N     H     SING  N  N  18  
2Z3  CA    C1    SING  N  N  19  
2Z3  CA    CB    SING  N  N  20  
2Z3  CA    HA    SING  N  N  21  
2Z3  C1    O2    DOUB  N  N  22  
2Z3  CB    CG    SING  N  N  23  
2Z3  CB    HB2   SING  N  N  24  
2Z3  CB    HB3   SING  N  N  25  
2Z3  CG    CD1   DOUB  Y  N  26  
2Z3  CG    CD2   SING  Y  N  27  
2Z3  CD1   CE1   SING  Y  N  28  
2Z3  CD1   HD1   SING  N  N  29  
2Z3  CD2   CE2   DOUB  Y  N  30  
2Z3  CD2   HD2   SING  N  N  31  
2Z3  CE1   CZ    DOUB  Y  N  32  
2Z3  CE1   HE1   SING  N  N  33  
2Z3  CE2   CZ    SING  Y  N  34  
2Z3  CE2   HE2   SING  N  N  35  
2Z3  CZ    HZ    SING  N  N  36  
2Z3  N1    CA1   SING  N  N  37  
2Z3  N1    H1    SING  N  N  38  
2Z3  CA1   C4    SING  N  N  39  
2Z3  CA1   CB1   SING  N  N  40  
2Z3  CA1   HA1   SING  N  N  41  
2Z3  C4    O3    DOUB  N  N  42  
2Z3  CB1   CG1   SING  N  N  43  
2Z3  CB1   HB21  SING  N  N  44  
2Z3  CB1   HB31  SING  N  N  45  
2Z3  CG1   CD    SING  N  N  46  
2Z3  CG1   HG2   SING  N  N  47  
2Z3  CG1   HG3   SING  N  N  48  
2Z3  CD    CE    SING  N  N  49  
2Z3  CD    HD21  SING  N  N  50  
2Z3  CD    HD3   SING  N  N  51  
2Z3  CE    HE11  SING  N  N  52  
2Z3  CE    HE21  SING  N  N  53  
2Z3  CE    HE3   SING  N  N  54  
2Z3  N2    CA2   SING  N  N  55  
2Z3  N2    H2    SING  N  N  56  
2Z3  CA2   CB2   SING  N  N  57  
2Z3  CA2   CH    SING  N  N  58  
2Z3  CA2   HA2   SING  N  N  59  
2Z3  CB2   CG2   SING  N  N  60  
2Z3  CB2   HB22  SING  N  N  61  
2Z3  CB2   HB32  SING  N  N  62  
2Z3  CG2   CD11  SING  N  N  63  
2Z3  CG2   CD21  SING  N  N  64  
2Z3  CG2   HG    SING  N  N  65  
2Z3  CD11  CE11  SING  N  N  66  
2Z3  CD11  HD12  SING  N  N  67  
2Z3  CD11  HD13  SING  N  N  68  
2Z3  CD21  CE21  SING  N  N  69  
2Z3  CD21  HD23  SING  N  N  70  
2Z3  CD21  HD22  SING  N  N  71  
2Z3  CE11  CZ1   SING  N  N  72  
2Z3  CE11  HE12  SING  N  N  73  
2Z3  CE11  HE13  SING  N  N  74  
2Z3  CE21  CZ1   SING  N  N  75  
2Z3  CE21  HE23  SING  N  N  76  
2Z3  CE21  HE22  SING  N  N  77  
2Z3  CZ1   HZ2   SING  N  N  78  
2Z3  CZ1   HZ3   SING  N  N  79  
2Z3  CH    OH1   SING  N  N  80  
2Z3  CH    OH2   SING  N  N  81  
2Z3  CH    CM    SING  N  N  82  
2Z3  OH1   HH1   SING  N  N  83  
2Z3  OH2   HH2   SING  N  N  84  
2Z3  CM    F1    SING  N  N  85  
2Z3  CM    F2    SING  N  N  86  
2Z3  CM    C7    SING  N  N  87  
2Z3  C7    O4    DOUB  N  N  88  
2Z3  N3    C8    SING  N  N  89  
2Z3  N3    HN1   SING  N  N  90  
2Z3  C8    H11   SING  N  N  91  
2Z3  C8    H23   SING  N  N  92  
2Z3  C8    H3    SING  N  N  93  
2Z3  C     N     SING  N  N  94  
2Z3  C1    N1    SING  N  N  95  
2Z3  C4    N2    SING  N  N  96  
2Z3  C7    N3    SING  N  N  97  
#   #
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
2Z3  SMILES            ACDLabs  10.04  "O=C(NC(C(=O)NC(C(=O)NC(CC1CCCCC1)C(O)(O)C(F)(F)C(=O)NC)CCCC)Cc2ccccc2)N3CCOCC3"  
2Z3  SMILES_CANONICAL  CACTVS   3.341  "CCCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)N2CCOCC2)C(=O)N[C@@H](CC3CCCCC3)C(O)(O)C(F)(F)C(=O)NC"  
2Z3  SMILES            CACTVS   3.341  "CCCC[CH](NC(=O)[CH](Cc1ccccc1)NC(=O)N2CCOCC2)C(=O)N[CH](CC3CCCCC3)C(O)(O)C(F)(F)C(=O)NC"  
2Z3  InChI             InChI     1.03  "InChI=1S/C32H49F2N5O7/c1-3-4-15-24(27(40)38-26(21-23-13-9-6-10-14-23)32(44,45)31(33,34)29(42)35-2)36-28(41)25(20-22-11-7-5-8-12-22)37-30(43)39-16-18-46-19-17-39/h5,7-8,11-12,23-26,44-45H,3-4,6,9-10,13-21H2,1-2H3,(H,35,42)(H,36,41)(H,37,43)(H,38,40)/t24-,25-,26-/m0/s1"  
2Z3  InChIKey          InChI     1.03  IPZOKQNUWWOCTK-GSDHBNRESA-N  
#   #
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
2Z3  "SYSTEMATIC NAME"  ACDLabs               10.04  "N-(morpholin-4-ylcarbonyl)-L-phenylalanyl-N-[(1R)-1-(cyclohexylmethyl)-3,3-difluoro-2,2-dihydroxy-4-(methylamino)-4-oxobutyl]-L-norleucinamide"  
2Z3  "SYSTEMATIC NAME"  "OpenEye OEToolkits"  1.5.0  "N-[(2S)-1-[[(2S)-1-[[(2S)-1-cyclohexyl-4,4-difluoro-3,3-dihydroxy-5-methylamino-5-oxo-pentan-2-yl]amino]-1-oxo-hexan-2-yl]amino]-1-oxo-3-phenyl-propan-2-yl]morpholine-4-carboxamide"  
#   #
loop_
_pdbx_chem_comp_audit.comp_id
_pdbx_chem_comp_audit.action_type
_pdbx_chem_comp_audit.date
_pdbx_chem_comp_audit.processing_site
2Z3  "Create component"      2008-08-28  RCSB  
2Z3  "Modify aromatic_flag"  2011-06-04  RCSB  
2Z3  "Modify descriptor"     2011-06-04  RCSB  
2Z3  "Modify synonyms"       2021-03-13  RCSB  
#
_pdbx_chem_comp_synonyms.ordinal     1
_pdbx_chem_comp_synonyms.comp_id     2Z3
_pdbx_chem_comp_synonyms.name        "CP-81,282"
_pdbx_chem_comp_synonyms.provenance  PDB
_pdbx_chem_comp_synonyms.type        ?
##
