data_XN1
#

_chem_comp.id                                   XN1
_chem_comp.name                                 
;N-[2-HYDROXY-1-INDANYL]-5-[(2-TERTIARYBUTYLAMINOCARBONYL)-4(3-PYRIDYLMETHYL)PIPERAZINO]-4-HYDROXY-2-(1-PHENYLETHYL)-PEN
TANAMIDE
;

_chem_comp.type                                 NON-POLYMER
_chem_comp.pdbx_type                            HETAIN
_chem_comp.formula                              "C37 H49 N5 O4"
_chem_comp.mon_nstd_parent_comp_id              ?
_chem_comp.pdbx_synonyms                        "ANALOGUE OF INDINAVIR"
_chem_comp.pdbx_formal_charge                   0
_chem_comp.pdbx_initial_date                    2001-11-05
_chem_comp.pdbx_modified_date                   2020-06-17
_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                       627.816
_chem_comp.one_letter_code                      ?
_chem_comp.three_letter_code                    XN1
_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       1K6T
_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
XN1  N1    N1    N  0  1  N  N  N   3.182   -5.332  16.303   0.509   2.365  -4.638  N1    XN1   1  
XN1  C1    C1    C  0  1  N  N  N   4.602   -5.146  15.800  -0.058   1.023  -4.814  C1    XN1   2  
XN1  C2    C2    C  0  1  N  N  S   5.403   -3.997  16.407  -1.151   0.787  -3.771  C2    XN1   3  
XN1  C3    C3    C  0  1  N  N  N   6.737   -4.025  15.740  -1.780  -0.562  -4.001  C3    XN1   4  
XN1  O1    O1    O  0  1  N  N  N   6.850   -3.583  14.580  -1.742  -1.406  -3.130  O1    XN1   5  
XN1  N2    N2    N  0  1  N  N  N   7.760   -4.533  16.439  -2.386  -0.832  -5.174  N2    XN1   6  
XN1  C4    C4    C  0  1  N  N  N   9.173   -4.700  16.090  -2.998  -2.145  -5.398  C4    XN1   7  
XN1  C5    C5    C  0  1  N  N  N   9.907   -5.365  17.282  -3.611  -2.189  -6.799  C5    XN1   8  
XN1  C6    C6    C  0  1  N  N  N   9.829   -3.480  15.872  -1.930  -3.233  -5.274  C6    XN1   9  
XN1  C7    C7    C  0  1  N  N  N   9.411   -5.586  14.916  -4.091  -2.382  -4.354  C7    XN1  10  
XN1  N3    N3    N  0  1  N  N  N   4.490   -2.776  16.122  -0.566   0.829  -2.425  N3    XN1  11  
XN1  C8    C8    C  0  1  N  N  N   3.061   -2.859  16.566   0.001   2.172  -2.249  C8    XN1  12  
XN1  C9    C9    C  0  1  N  N  N   2.439   -4.142  16.032   1.093   2.408  -3.292  C9    XN1  13  
XN1  C10   C10   C  0  1  N  N  N   5.012   -1.489  16.657  -1.682   0.715  -1.476  C10   XN1  14  
XN1  C11   C11   C  0  1  N  N  S   4.997   -0.437  15.604  -1.164   0.926  -0.052  C11   XN1  15  
XN1  O2    O2    O  0  1  N  N  N   5.122    0.614  16.527  -0.787   2.294   0.119  O2    XN1  16  
XN1  C12   C12   C  0  1  N  N  N   6.166   -0.263  14.636  -2.265   0.571   0.948  C12   XN1  17  
XN1  C13   C13   C  0  1  N  N  S   6.137    0.819  13.537  -1.711   0.668   2.371  C13   XN1  18  
XN1  C14   C14   C  0  1  N  N  S   7.494    0.777  12.692  -2.853   0.499   3.376  C14   XN1  19  
XN1  C15   C15   C  0  1  Y  N  N   7.493    1.843  11.587  -2.341   0.764   4.768  C15   XN1  20  
XN1  C16   C16   C  0  1  Y  N  N   7.326    3.273  11.893  -2.413  -0.225   5.730  C16   XN1  21  
XN1  C17   C17   C  0  1  Y  N  N   7.318    4.233  10.823  -1.943   0.017   7.008  C17   XN1  22  
XN1  C18   C18   C  0  1  Y  N  N   7.481    3.766   9.441  -1.401   1.249   7.322  C18   XN1  23  
XN1  C19   C19   C  0  1  Y  N  N   7.648    2.351   9.153  -1.328   2.238   6.360  C19   XN1  24  
XN1  C20   C20   C  0  1  Y  N  N   7.653    1.404  10.220  -1.794   1.994   5.081  C20   XN1  25  
XN1  C21   C21   C  0  1  N  N  N   4.951    0.612  12.533  -0.687  -0.415   2.587  C21   XN1  26  
XN1  O3    O3    O  0  1  N  N  N   4.483   -0.537  12.198  -0.426  -1.190   1.691  O3    XN1  27  
XN1  N4    N4    N  0  1  N  N  N   4.516    1.759  12.058  -0.062  -0.524   3.776  N4    XN1  28  
XN1  C22   C22   C  0  1  N  N  S   3.453    1.892  11.081   0.932  -1.579   3.986  C22   XN1  29  
XN1  C23   C23   C  0  1  N  N  R   3.415    3.282  10.476   0.980  -1.982   5.475  C23   XN1  30  
XN1  O4    O4    O  0  1  N  N  N   3.703    4.274  11.447   0.568  -0.896   6.309  O4    XN1  31  
XN1  C24   C24   C  0  1  N  N  N   2.050    3.398   9.854   2.475  -2.303   5.684  C24   XN1  32  
XN1  C25   C25   C  0  1  Y  N  N   1.053    2.685  10.729   3.206  -1.478   4.647  C25   XN1  33  
XN1  C26   C26   C  0  1  Y  N  N  -0.321    2.701  10.957   4.541  -1.120   4.563  C26   XN1  34  
XN1  C27   C27   C  0  1  Y  N  N  -0.856    1.797  11.936   4.989  -0.349   3.509  C27   XN1  35  
XN1  C28   C28   C  0  1  Y  N  N   0.003    0.888  12.675   4.103   0.067   2.533  C28   XN1  36  
XN1  C29   C29   C  0  1  Y  N  N   1.394    0.860  12.457   2.771  -0.289   2.615  C29   XN1  37  
XN1  C30   C30   C  0  1  Y  N  N   1.999    1.696  11.532   2.320  -1.062   3.669  C30   XN1  38  
XN1  C31   C31   C  0  1  N  N  N   2.496   -6.492  15.704   1.624   2.479  -5.587  C31   XN1  39  
XN1  C32   C32   C  0  1  Y  N  N   3.118   -7.880  15.876   2.497   1.254  -5.486  C32   XN1  40  
XN1  C33   C33   C  0  1  Y  N  N   3.268   -8.508  17.162   3.562   1.225  -4.606  C33   XN1  41  
XN1  N5    N5    N  0  1  Y  N  N   3.858   -9.824  17.371   4.326   0.154  -4.508  N5    XN1  42  
XN1  C34   C34   C  0  1  Y  N  N   4.294  -10.471  16.149   4.115  -0.917  -5.246  C34   XN1  43  
XN1  C35   C35   C  0  1  Y  N  N   4.172   -9.899  14.836   3.072  -0.958  -6.152  C35   XN1  44  
XN1  C36   C36   C  0  1  Y  N  N   3.575   -8.582  14.706   2.244   0.145  -6.279  C36   XN1  45  
XN1  C37   C37   C  0  1  N  N  N   8.885    0.784  13.310  -3.972   1.490   3.047  C37   XN1  46  
XN1  H11A  1H1   H  0  0  N  N  N   4.595   -5.050  14.689  -0.486   0.938  -5.813  H11A  XN1  47  
XN1  H12   2H1   H  0  1  N  N  N   5.168   -6.099  15.920   0.727   0.278  -4.691  H12   XN1  48  
XN1  H2    H2    H  0  1  N  N  N   5.635   -4.014  17.497  -1.912   1.562  -3.860  H2    XN1  49  
XN1  HN2   HN2   H  0  1  N  N  N   7.420   -4.830  17.353  -2.417  -0.158  -5.871  HN2   XN1  50  
XN1  H51   1H5   H  0  1  N  N  N   9.430   -6.323  17.595  -4.067  -3.166  -6.965  H51   XN1  51  
XN1  H52   2H5   H  0  1  N  N  N  10.982   -5.492  17.016  -4.372  -1.414  -6.887  H52   XN1  52  
XN1  H53   3H5   H  0  1  N  N  N   9.767   -4.803  18.235  -2.832  -2.020  -7.542  H53   XN1  53  
XN1  H61   1H6   H  0  1  N  N  N   9.713   -2.802  16.750  -1.151  -3.064  -6.017  H61   XN1  54  
XN1  H62   2H6   H  0  1  N  N  N  10.904   -3.607  15.606  -1.493  -3.201  -4.276  H62   XN1  55  
XN1  H63   3H6   H  0  1  N  N  N   9.297   -2.873  15.102  -2.385  -4.209  -5.440  H63   XN1  56  
XN1  H71   1H7   H  0  1  N  N  N   8.831   -5.229  14.034  -4.852  -1.606  -4.443  H71   XN1  57  
XN1  H72   2H7   H  0  1  N  N  N  10.486   -5.713  14.650  -4.547  -3.358  -4.521  H72   XN1  58  
XN1  H73   3H7   H  0  1  N  N  N   8.928   -6.579  15.072  -3.654  -2.350  -3.356  H73   XN1  59  
XN1  H81   1H8   H  0  1  N  N  N   2.476   -1.955  16.277  -0.784   2.917  -2.372  H81   XN1  60  
XN1  H82   2H8   H  0  1  N  N  N   2.957   -2.768  17.673   0.428   2.257  -1.250  H82   XN1  61  
XN1  H91   1H9   H  0  1  N  N  N   1.394   -4.247  16.406   1.549   3.384  -3.126  H91   XN1  62  
XN1  H92   2H9   H  0  1  N  N  N   2.246   -4.050  14.938   1.855   1.633  -3.203  H92   XN1  63  
XN1  H101  1H10  H  0  0  N  N  N   6.025   -1.609  17.107  -2.128  -0.275  -1.557  H101  XN1  64  
XN1  H102  2H10  H  0  0  N  N  N   4.460   -1.167  17.571  -2.433   1.472  -1.705  H102  XN1  65  
XN1  H11   H11   H  0  1  N  N  N   4.154   -0.589  14.891  -0.298   0.287   0.117  H11   XN1  66  
XN1  HO2   HO2   H  0  1  N  N  N   5.112    1.285  15.855  -1.595   2.819   0.040  HO2   XN1  67  
XN1  H121  1H12  H  0  0  N  N  N   6.359   -1.246  14.147  -2.611  -0.445   0.762  H121  XN1  68  
XN1  H122  2H12  H  0  0  N  N  N   7.094   -0.120  15.237  -3.098   1.265   0.834  H122  XN1  69  
XN1  H13   H13   H  0  1  N  N  N   6.011    1.798  14.056  -1.244   1.643   2.513  H13   XN1  70  
XN1  H141  1H14  H  0  0  N  N  N   7.399   -0.288  12.377  -3.240  -0.517   3.318  H141  XN1  71  
XN1  H16   H16   H  0  1  N  N  N   7.206    3.627  12.931  -2.836  -1.188   5.485  H16   XN1  72  
XN1  H17   H17   H  0  1  N  N  N   7.190    5.303  11.057  -1.999  -0.756   7.760  H17   XN1  73  
XN1  H18   H18   H  0  1  N  N  N   7.478    4.488   8.607  -1.034   1.438   8.320  H18   XN1  74  
XN1  H19   H19   H  0  1  N  N  N   7.772    1.993   8.117  -0.905   3.201   6.605  H19   XN1  75  
XN1  H20   H20   H  0  1  N  N  N   7.781    0.333   9.988  -1.737   2.767   4.329  H20   XN1  76  
XN1  HN4   HN4   H  0  1  N  N  N   5.011    2.558  12.454  -0.271   0.094   4.493  HN4   XN1  77  
XN1  H22   H22   H  0  1  N  N  N   3.740    1.057  10.400   0.701  -2.445   3.367  H22   XN1  78  
XN1  H23   H23   H  0  1  N  N  N   4.200    3.444   9.701   0.365  -2.863   5.658  H23   XN1  79  
XN1  HO4   HO4   H  0  1  N  N  N   3.679    5.145  11.068   0.619  -1.210   7.222  HO4   XN1  80  
XN1  H241  1H24  H  0  0  N  N  N   2.030    3.032   8.801   2.788  -2.013   6.687  H241  XN1  81  
XN1  H242  2H24  H  0  0  N  N  N   1.762    4.457   9.656   2.660  -3.365   5.522  H242  XN1  82  
XN1  H26   H26   H  0  1  N  N  N  -0.957    3.399  10.387   5.234  -1.444   5.325  H26   XN1  83  
XN1  H27   H27   H  0  1  N  N  N  -1.943    1.801  12.123   6.031  -0.071   3.447  H27   XN1  84  
XN1  H28   H28   H  0  1  N  N  N  -0.414    0.197  13.426   4.451   0.670   1.708  H28   XN1  85  
XN1  H29   H29   H  0  1  N  N  N   2.029    0.162  13.028   2.079   0.036   1.852  H29   XN1  86  
XN1  H311  1H31  H  0  0  N  N  N   2.340   -6.298  14.617   1.232   2.563  -6.601  H311  XN1  87  
XN1  H312  2H31  H  0  0  N  N  N   1.444   -6.519  16.072   2.214   3.365  -5.351  H312  XN1  88  
XN1  H33   H33   H  0  1  N  N  N   2.909   -7.947  18.041   3.766   2.085  -3.986  H33   XN1  89  
XN1  H34   H34   H  0  1  N  N  N   4.752  -11.472  16.224   4.765  -1.774  -5.141  H34   XN1  90  
XN1  H35   H35   H  0  1  N  N  N   4.527  -10.455  13.952   2.904  -1.840  -6.753  H35   XN1  91  
XN1  H36   H36   H  0  1  N  N  N   3.468   -8.113  13.714   1.421   0.141  -6.978  H36   XN1  92  
XN1  H371  1H37  H  0  0  N  N  N   8.925   -0.063  14.034  -3.601   2.508   3.163  H371  XN1  93  
XN1  H372  2H37  H  0  0  N  N  N   9.831    0.755  12.721  -4.302   1.337   2.020  H372  XN1  94  
XN1  H373  3H37  H  0  0  N  N  N   8.942    1.677  13.975  -4.810   1.329   3.725  H373  XN1  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
XN1  N1   C1    SING  N  N   1  
XN1  N1   C9    SING  N  N   2  
XN1  N1   C31   SING  N  N   3  
XN1  C1   C2    SING  N  N   4  
XN1  C1   H11A  SING  N  N   5  
XN1  C1   H12   SING  N  N   6  
XN1  C2   C3    SING  N  N   7  
XN1  C2   N3    SING  N  N   8  
XN1  C2   H2    SING  N  N   9  
XN1  C3   O1    DOUB  N  N  10  
XN1  C3   N2    SING  N  N  11  
XN1  N2   C4    SING  N  N  12  
XN1  N2   HN2   SING  N  N  13  
XN1  C4   C5    SING  N  N  14  
XN1  C4   C6    SING  N  N  15  
XN1  C4   C7    SING  N  N  16  
XN1  C5   H51   SING  N  N  17  
XN1  C5   H52   SING  N  N  18  
XN1  C5   H53   SING  N  N  19  
XN1  C6   H61   SING  N  N  20  
XN1  C6   H62   SING  N  N  21  
XN1  C6   H63   SING  N  N  22  
XN1  C7   H71   SING  N  N  23  
XN1  C7   H72   SING  N  N  24  
XN1  C7   H73   SING  N  N  25  
XN1  N3   C8    SING  N  N  26  
XN1  N3   C10   SING  N  N  27  
XN1  C8   C9    SING  N  N  28  
XN1  C8   H81   SING  N  N  29  
XN1  C8   H82   SING  N  N  30  
XN1  C9   H91   SING  N  N  31  
XN1  C9   H92   SING  N  N  32  
XN1  C10  C11   SING  N  N  33  
XN1  C10  H101  SING  N  N  34  
XN1  C10  H102  SING  N  N  35  
XN1  C11  O2    SING  N  N  36  
XN1  C11  C12   SING  N  N  37  
XN1  C11  H11   SING  N  N  38  
XN1  O2   HO2   SING  N  N  39  
XN1  C12  C13   SING  N  N  40  
XN1  C12  H121  SING  N  N  41  
XN1  C12  H122  SING  N  N  42  
XN1  C13  C14   SING  N  N  43  
XN1  C13  C21   SING  N  N  44  
XN1  C13  H13   SING  N  N  45  
XN1  C14  C15   SING  N  N  46  
XN1  C14  C37   SING  N  N  47  
XN1  C14  H141  SING  N  N  48  
XN1  C15  C16   DOUB  Y  N  49  
XN1  C15  C20   SING  Y  N  50  
XN1  C16  C17   SING  Y  N  51  
XN1  C16  H16   SING  N  N  52  
XN1  C17  C18   DOUB  Y  N  53  
XN1  C17  H17   SING  N  N  54  
XN1  C18  C19   SING  Y  N  55  
XN1  C18  H18   SING  N  N  56  
XN1  C19  C20   DOUB  Y  N  57  
XN1  C19  H19   SING  N  N  58  
XN1  C20  H20   SING  N  N  59  
XN1  C21  O3    DOUB  N  N  60  
XN1  C21  N4    SING  N  N  61  
XN1  N4   C22   SING  N  N  62  
XN1  N4   HN4   SING  N  N  63  
XN1  C22  C23   SING  N  N  64  
XN1  C22  C30   SING  N  N  65  
XN1  C22  H22   SING  N  N  66  
XN1  C23  O4    SING  N  N  67  
XN1  C23  C24   SING  N  N  68  
XN1  C23  H23   SING  N  N  69  
XN1  O4   HO4   SING  N  N  70  
XN1  C24  C25   SING  N  N  71  
XN1  C24  H241  SING  N  N  72  
XN1  C24  H242  SING  N  N  73  
XN1  C25  C26   DOUB  Y  N  74  
XN1  C25  C30   SING  Y  N  75  
XN1  C26  C27   SING  Y  N  76  
XN1  C26  H26   SING  N  N  77  
XN1  C27  C28   DOUB  Y  N  78  
XN1  C27  H27   SING  N  N  79  
XN1  C28  C29   SING  Y  N  80  
XN1  C28  H28   SING  N  N  81  
XN1  C29  C30   DOUB  Y  N  82  
XN1  C29  H29   SING  N  N  83  
XN1  C31  C32   SING  N  N  84  
XN1  C31  H311  SING  N  N  85  
XN1  C31  H312  SING  N  N  86  
XN1  C32  C33   DOUB  Y  N  87  
XN1  C32  C36   SING  Y  N  88  
XN1  C33  N5    SING  Y  N  89  
XN1  C33  H33   SING  N  N  90  
XN1  N5   C34   DOUB  Y  N  91  
XN1  C34  C35   SING  Y  N  92  
XN1  C34  H34   SING  N  N  93  
XN1  C35  C36   DOUB  Y  N  94  
XN1  C35  H35   SING  N  N  95  
XN1  C36  H36   SING  N  N  96  
XN1  C37  H371  SING  N  N  97  
XN1  C37  H372  SING  N  N  98  
XN1  C37  H373  SING  N  N  99  
#   #
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
XN1  SMILES            ACDLabs               10.04  "O=C(NC2c1ccccc1CC2O)C(C(c3ccccc3)C)CC(O)CN5C(C(=O)NC(C)(C)C)CN(Cc4cnccc4)CC5"  
XN1  SMILES_CANONICAL  CACTVS                3.341  "C[C@@H]([C@H](C[C@H](O)CN1CCN(C[C@H]1C(=O)NC(C)(C)C)Cc2cccnc2)C(=O)N[C@@H]3[C@H](O)Cc4ccccc34)c5ccccc5"  
XN1  SMILES            CACTVS                3.341  "C[CH]([CH](C[CH](O)CN1CCN(C[CH]1C(=O)NC(C)(C)C)Cc2cccnc2)C(=O)N[CH]3[CH](O)Cc4ccccc34)c5ccccc5"  
XN1  SMILES_CANONICAL  "OpenEye OEToolkits"  1.5.0  "C[C@H](c1ccccc1)[C@H](C[C@@H](C[N@@]2CC[N@](C[C@H]2C(=O)NC(C)(C)C)Cc3cccnc3)O)C(=O)N[C@H]4c5ccccc5C[C@H]4O"  
XN1  SMILES            "OpenEye OEToolkits"  1.5.0  "CC(c1ccccc1)C(CC(CN2CCN(CC2C(=O)NC(C)(C)C)Cc3cccnc3)O)C(=O)NC4c5ccccc5CC4O"  
XN1  InChI             InChI                 1.03   "InChI=1S/C37H49N5O4/c1-25(27-12-6-5-7-13-27)31(35(45)39-34-30-15-9-8-14-28(30)19-33(34)44)20-29(43)23-42-18-17-41(22-26-11-10-16-38-21-26)24-32(42)36(46)40-37(2,3)4/h5-16,21,25,29,31-34,43-44H,17-20,22-24H2,1-4H3,(H,39,45)(H,40,46)/t25-,29+,31+,32+,33-,34+/m1/s1"  
XN1  InChIKey          InChI                 1.03   AITMPVIQUIXEST-FGUNTGOFSA-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
XN1  "SYSTEMATIC NAME"  ACDLabs               10.04  "(2S)-N-tert-butyl-1-[(2S,4S,5S)-2-hydroxy-4-{[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]carbamoyl}-5-phenylhexyl]-4-(pyridin-3-ylmethyl)piperazine-2-carboxamide (non-preferred name)"  
XN1  "SYSTEMATIC NAME"  "OpenEye OEToolkits"  1.5.0  "(1S,2S,4R)-N-tert-butyl-1-[(2S,4S,5S)-2-hydroxy-4-[[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]carbamoyl]-5-phenyl-hexyl]-4-(pyridin-3-ylmethyl)piperazine-2-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
XN1  "Create component"   2001-11-05  RCSB  
XN1  "Modify descriptor"  2011-06-04  RCSB  
XN1  "Modify synonyms"    2020-06-05  PDBE  
#
_pdbx_chem_comp_synonyms.ordinal     1
_pdbx_chem_comp_synonyms.comp_id     XN1
_pdbx_chem_comp_synonyms.name        "ANALOGUE OF INDINAVIR"
_pdbx_chem_comp_synonyms.provenance  ?
_pdbx_chem_comp_synonyms.type        ?
##
