data_PHW
# 
_chem_comp.id                                    PHW 
_chem_comp.name                                  "BETA-PHENYL-N-{[(PHENYLMETHYL)OXY]CARBONYL}-D-PHENYLALANYL-N- [(1S,3E)-1-[DIHYDROXY(METHYLOXY)(PHENYLOXY)-LAMBDA5-PHOSPHANYL]-4- (METHYLOXY)BUT-3-ENYL]-D-PROLINAMIDE" 
_chem_comp.type                                  NON-POLYMER 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C40 H46 N3 O9 P" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         "PHENYLMETHYL (1R)-2-[(2R)-2-({[(1S,3E)-1-[DIHYDROXY(METHYLOXY)(PHENYLOXY)- LAMBDA5-PHOSPHANYL]-4-(METHYLOXY)BUT-3-ENYL]AMINO}CARBONYL)PYRROLIDIN-1-YL]- 1-(DIPHENYLMETHYL)-2-OXOETHYLCARBAMATE" 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2001-02-07 
_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                        743.782 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     PHW 
_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        1H8D 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  EBI 
# 
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 
PHW O1A  O1A  O 0 1 N N N 16.380 -10.791 17.838 0.345  2.091  3.954  O1A  PHW 1  
PHW O1D  O1D  O 0 1 N N N 15.717 -12.261 16.734 -1.541 0.711  3.279  O1D  PHW 2  
PHW C1   C1   C 0 1 N N N 15.637 -18.668 17.761 2.345  -1.393 8.572  C1   PHW 3  
PHW C2   C2   C 0 1 N N N 15.840 -16.468 18.561 1.135  -1.841 6.745  C2   PHW 4  
PHW C3   C3   C 0 1 N N N 16.735 -15.863 18.111 0.838  -2.388 5.584  C3   PHW 5  
PHW C4   C4   C 0 1 N N N 16.844 -14.487 17.689 -0.472 -2.068 4.914  C4   PHW 6  
PHW C5   C5   C 0 1 N N S 16.181 -13.763 18.653 -0.205 -1.433 3.548  C5   PHW 7  
PHW C7   C7   C 0 1 N N N 18.612 -13.553 19.375 -1.186 -1.774 1.344  C7   PHW 8  
PHW C8   C8   C 0 1 N N S 19.524 -13.768 20.597 -2.376 -1.996 0.445  C8   PHW 9  
PHW C10  C10  C 0 1 N N N 17.989 -14.961 22.284 -1.336 -0.467 -1.254 C10  PHW 10 
PHW C11  C11  C 0 1 N N R 17.831 -16.123 23.258 -1.001 -0.196 -2.698 C11  PHW 11 
PHW C12  C12  C 0 1 N N N 18.271 -15.748 24.682 -1.652 1.117  -3.136 C12  PHW 12 
PHW C14  C14  C 0 1 N N N 15.903 -17.706 22.703 1.034  -0.454 -4.012 C14  PHW 13 
PHW C16  C16  C 0 1 N N N 14.066 -19.001 22.099 2.997  -0.748 -5.404 C16  PHW 14 
PHW O2   O2   O 0 1 N N N 15.764 -17.858 18.633 2.316  -2.129 7.348  O2   PHW 15 
PHW P    P    P 0 1 N N N 15.390 -12.177 18.342 0.081  0.402  3.759  P    PHW 16 
PHW O1C  O1C  O 0 1 N N N 13.838 -12.144 17.955 1.331  0.343  2.580  O1C  PHW 17 
PHW C61  C61  C 0 1 N N N 16.914 -12.976 15.907 -2.380 0.263  4.345  C61  PHW 18 
PHW O1B  O1B  O 0 1 N N N 15.053 -11.907 19.931 0.453  0.153  5.420  O1B  PHW 19 
PHW C51  C51  C 0 1 Y N N 13.756 -12.085 20.424 0.863  1.350  5.915  C51  PHW 20 
PHW C52  C52  C 0 1 Y N N 12.864 -11.013 20.483 -0.059 2.231  6.458  C52  PHW 21 
PHW C53  C53  C 0 1 Y N N 11.694 -11.106 21.235 0.360  3.447  6.960  C53  PHW 22 
PHW C54  C54  C 0 1 Y N N 11.393 -12.273 21.943 1.699  3.787  6.922  C54  PHW 23 
PHW C55  C55  C 0 1 Y N N 12.285 -13.344 21.887 2.622  2.911  6.381  C55  PHW 24 
PHW C56  C56  C 0 1 Y N N 13.455 -13.250 21.137 2.208  1.691  5.883  C56  PHW 25 
PHW N6   N6   N 0 1 N N N 17.179 -13.485 19.674 -1.361 -1.649 2.674  N6   PHW 26 
PHW O7   O7   O 0 1 N N N 19.067 -13.414 18.258 -0.072 -1.707 0.870  O7   PHW 27 
PHW C8A  C8A  C 0 1 N N N 20.984 -14.075 20.364 -2.674 -3.510 0.311  C8A  PHW 28 
PHW C8B  C8B  C 0 1 N N N 21.038 -15.585 20.143 -3.424 -3.560 -1.046 C8B  PHW 29 
PHW C8C  C8C  C 0 1 N N N 19.940 -16.147 21.040 -2.712 -2.471 -1.875 C8C  PHW 30 
PHW N9   N9   N 0 1 N N N 19.066 -14.994 21.293 -2.074 -1.545 -0.925 N9   PHW 31 
PHW O10  O10  O 0 1 N N N 17.308 -13.946 22.440 -0.942 0.285  -0.389 O10  PHW 32 
PHW C21  C21  C 0 1 Y N N 19.724 -15.270 24.760 -1.391 1.343  -4.603 C21  PHW 33 
PHW C22  C22  C 0 1 Y N N 19.991 -14.001 25.252 -0.679 2.454  -5.014 C22  PHW 34 
PHW C23  C23  C 0 1 Y N N 21.287 -13.475 25.291 -0.439 2.662  -6.360 C23  PHW 35 
PHW C24  C24  C 0 1 Y N N 22.343 -14.254 24.812 -0.911 1.758  -7.293 C24  PHW 36 
PHW C25  C25  C 0 1 Y N N 22.067 -15.530 24.316 -1.622 0.647  -6.882 C25  PHW 37 
PHW C26  C26  C 0 1 Y N N 20.778 -16.063 24.276 -1.858 0.437  -5.536 C26  PHW 38 
PHW C31  C31  C 0 1 Y N N 17.965 -16.903 25.632 -3.138 1.044  -2.896 C31  PHW 39 
PHW C32  C32  C 0 1 Y N N 18.155 -18.234 25.261 -3.765 2.018  -2.140 C32  PHW 40 
PHW C33  C33  C 0 1 Y N N 17.980 -19.265 26.190 -5.128 1.952  -1.920 C33  PHW 41 
PHW C34  C34  C 0 1 Y N N 17.610 -18.976 27.507 -5.865 0.912  -2.456 C34  PHW 42 
PHW C35  C35  C 0 1 Y N N 17.419 -17.646 27.885 -5.238 -0.061 -3.212 C35  PHW 43 
PHW C36  C36  C 0 1 Y N N 17.594 -16.624 26.950 -3.876 0.007  -3.436 C36  PHW 44 
PHW N13  N13  N 0 1 N N N 16.398 -16.452 23.275 0.452  -0.094 -2.851 N13  PHW 45 
PHW O14  O14  O 0 1 N N N 16.683 -18.521 22.207 0.354  -0.862 -4.932 O14  PHW 46 
PHW O15  O15  O 0 1 N N N 14.557 -17.987 22.967 2.370  -0.360 -4.153 O15  PHW 47 
PHW C41  C41  C 0 1 Y N N 12.971 -18.390 21.215 4.488  -0.549 -5.301 C41  PHW 48 
PHW C42  C42  C 0 1 Y N N 12.902 -16.996 21.114 5.292  -1.577 -4.847 C42  PHW 49 
PHW C43  C43  C 0 1 Y N N 11.926 -16.409 20.311 6.659  -1.395 -4.752 C43  PHW 50 
PHW C44  C44  C 0 1 Y N N 11.020 -17.208 19.612 7.222  -0.185 -5.113 C44  PHW 51 
PHW C45  C45  C 0 1 Y N N 11.092 -18.600 19.710 6.417  0.842  -5.568 C45  PHW 52 
PHW C46  C46  C 0 1 Y N N 12.067 -19.184 20.518 5.051  0.658  -5.666 C46  PHW 53 
PHW HOA1 1HOA H 0 0 N N N 16.190 -10.742 18.767 1.302  2.228  3.934  HOA1 PHW 54 
PHW HC11 1HC1 H 0 0 N N N 15.576 -19.779 17.818 3.280  -1.594 9.095  HC11 PHW 55 
PHW HC12 2HC1 H 0 0 N N N 14.721 -18.356 17.206 2.270  -0.327 8.357  HC12 PHW 56 
PHW HC13 3HC1 H 0 0 N N N 16.469 -18.459 17.048 1.506  -1.697 9.199  HC13 PHW 57 
PHW H2   H2   H 0 1 N N N 15.084 -15.743 18.909 0.439  -1.163 7.216  H2   PHW 58 
PHW H3   H3   H 0 1 N N N 17.522 -16.635 18.083 1.534  -3.066 5.113  H3   PHW 59 
PHW HC41 1HC4 H 0 0 N N N 17.892 -14.150 17.513 -1.046 -2.985 4.782  HC41 PHW 60 
PHW HC42 2HC4 H 0 0 N N N 16.475 -14.302 16.653 -1.037 -1.372 5.534  HC42 PHW 61 
PHW HC5  HC5  H 0 1 N N N 15.304 -14.420 18.859 0.677  -1.889 3.101  HC5  PHW 62 
PHW H8C  H8C  H 0 1 N N N 19.451 -12.787 21.123 -3.248 -1.470 0.834  H8C  PHW 63 
PHW H11  H11  H 0 1 N N N 18.469 -16.977 22.931 -1.375 -1.011 -3.317 H11  PHW 64 
PHW H12  H12  H 0 1 N N N 17.676 -14.862 25.007 -1.231 1.941  -2.560 H12  PHW 65 
PHW H161 1H16 H 0 0 N N N 14.875 -19.487 21.505 2.784  -1.797 -5.608 H161 PHW 66 
PHW H162 2H16 H 0 0 N N N 13.717 -19.905 22.649 2.604  -0.133 -6.213 H162 PHW 67 
PHW HOC1 1HOC H 0 0 N N N 13.308 -12.885 18.224 1.676  1.242  2.493  HOC1 PHW 68 
PHW H611 1H61 H 0 0 N N N 17.135 -13.033 14.815 -3.273 0.886  4.390  H611 PHW 69 
PHW H612 2H61 H 0 0 N N N 17.847 -12.566 16.359 -2.668 -0.773 4.169  H612 PHW 70 
PHW H613 3H61 H 0 0 N N N 16.885 -14.039 16.240 -1.838 0.334  5.288  H613 PHW 71 
PHW H52  H52  H 0 1 N N N 13.085 -10.084 19.930 -1.106 1.966  6.488  H52  PHW 72 
PHW H53  H53  H 0 1 N N N 11.000 -10.249 21.270 -0.358 4.134  7.383  H53  PHW 73 
PHW H54  H54  H 0 1 N N N 10.466 -12.347 22.536 2.026  4.739  7.315  H54  PHW 74 
PHW H55  H55  H 0 1 N N N 12.063 -14.272 22.440 3.668  3.179  6.351  H55  PHW 75 
PHW H56  H56  H 0 1 N N N 14.149 -14.106 21.107 2.929  1.007  5.460  H56  PHW 76 
PHW HN6  HN6  H 0 1 N N N 16.869 -13.238 20.614 -2.252 -1.702 3.054  HN6  PHW 77 
PHW H8A1 1H8A H 0 0 N N N 21.445 -13.480 19.540 -1.751 -4.088 0.269  H8A1 PHW 78 
PHW H8A2 2H8A H 0 0 N N N 21.657 -13.712 21.175 -3.313 -3.856 1.123  H8A2 PHW 79 
PHW H8B1 1H8B H 0 0 N N N 20.951 -15.890 19.074 -3.309 -4.538 -1.514 H8B1 PHW 80 
PHW H8B2 2H8B H 0 0 N N N 22.043 -16.033 20.320 -4.478 -3.316 -0.913 H8B2 PHW 81 
PHW H8C1 1H8C H 0 0 N N N 19.415 -17.037 20.620 -1.956 -2.927 -2.514 H8C1 PHW 82 
PHW H8C2 2H8C H 0 0 N N N 20.313 -16.651 21.961 -3.439 -1.933 -2.483 H8C2 PHW 83 
PHW H22  H22  H 0 1 N N N 19.148 -13.392 25.622 -0.310 3.160  -4.285 H22  PHW 84 
PHW H23  H23  H 0 1 N N N 21.472 -12.464 25.692 0.116  3.530  -6.681 H23  PHW 85 
PHW H24  H24  H 0 1 N N N 23.376 -13.868 24.825 -0.724 1.921  -8.345 H24  PHW 86 
PHW H25  H25  H 0 1 N N N 22.903 -16.143 23.939 -1.991 -0.058 -7.611 H25  PHW 87 
PHW H26  H26  H 0 1 N N N 20.598 -17.075 23.876 -2.414 -0.431 -5.214 H26  PHW 88 
PHW H32  H32  H 0 1 N N N 18.446 -18.473 24.224 -3.189 2.830  -1.722 H32  PHW 89 
PHW H33  H33  H 0 1 N N N 18.134 -20.312 25.882 -5.617 2.712  -1.330 H33  PHW 90 
PHW H34  H34  H 0 1 N N N 17.470 -19.788 28.239 -6.929 0.859  -2.283 H34  PHW 91 
PHW H35  H35  H 0 1 N N N 17.130 -17.402 28.921 -5.814 -0.873 -3.630 H35  PHW 92 
PHW H36  H36  H 0 1 N N N 17.436 -15.576 27.258 -3.387 -0.752 -4.026 H36  PHW 93 
PHW HN31 1HN3 H 0 0 N N N 15.735 -15.798 23.691 0.995  0.231  -2.117 HN31 PHW 94 
PHW H42  H42  H 0 1 N N N 13.615 -16.361 21.666 4.853  -2.523 -4.565 H42  PHW 95 
PHW H43  H43  H 0 1 N N N 11.870 -15.310 20.228 7.288  -2.198 -4.397 H43  PHW 96 
PHW H44  H44  H 0 1 N N N 10.246 -16.738 18.981 8.290  -0.043 -5.039 H44  PHW 97 
PHW H45  H45  H 0 1 N N N 10.382 -19.234 19.152 6.857  1.788  -5.849 H45  PHW 98 
PHW H46  H46  H 0 1 N N N 12.123 -20.282 20.606 4.422  1.461  -6.022 H46  PHW 99 
# 
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 
PHW O1A P    SING N N 1   
PHW O1A HOA1 SING N N 2   
PHW O1D P    SING N N 3   
PHW O1D C61  SING N N 4   
PHW C1  O2   SING N N 5   
PHW C1  HC11 SING N N 6   
PHW C1  HC12 SING N N 7   
PHW C1  HC13 SING N N 8   
PHW C2  C3   DOUB N E 9   
PHW C2  O2   SING N N 10  
PHW C2  H2   SING N N 11  
PHW C3  C4   SING N N 12  
PHW C3  H3   SING N N 13  
PHW C4  C5   SING N N 14  
PHW C4  HC41 SING N N 15  
PHW C4  HC42 SING N N 16  
PHW C5  P    SING N N 17  
PHW C5  N6   SING N N 18  
PHW C5  HC5  SING N N 19  
PHW C7  C8   SING N N 20  
PHW C7  N6   SING N N 21  
PHW C7  O7   DOUB N N 22  
PHW C8  C8A  SING N N 23  
PHW C8  N9   SING N N 24  
PHW C8  H8C  SING N N 25  
PHW C10 C11  SING N N 26  
PHW C10 N9   SING N N 27  
PHW C10 O10  DOUB N N 28  
PHW C11 C12  SING N N 29  
PHW C11 N13  SING N N 30  
PHW C11 H11  SING N N 31  
PHW C12 C21  SING N N 32  
PHW C12 C31  SING N N 33  
PHW C12 H12  SING N N 34  
PHW C14 N13  SING N N 35  
PHW C14 O14  DOUB N N 36  
PHW C14 O15  SING N N 37  
PHW C16 O15  SING N N 38  
PHW C16 C41  SING N N 39  
PHW C16 H161 SING N N 40  
PHW C16 H162 SING N N 41  
PHW P   O1C  SING N N 42  
PHW P   O1B  SING N N 43  
PHW O1C HOC1 SING N N 44  
PHW C61 H611 SING N N 45  
PHW C61 H612 SING N N 46  
PHW C61 H613 SING N N 47  
PHW O1B C51  SING N N 48  
PHW C51 C52  DOUB Y N 49  
PHW C51 C56  SING Y N 50  
PHW C52 C53  SING Y N 51  
PHW C52 H52  SING N N 52  
PHW C53 C54  DOUB Y N 53  
PHW C53 H53  SING N N 54  
PHW C54 C55  SING Y N 55  
PHW C54 H54  SING N N 56  
PHW C55 C56  DOUB Y N 57  
PHW C55 H55  SING N N 58  
PHW C56 H56  SING N N 59  
PHW N6  HN6  SING N N 60  
PHW C8A C8B  SING N N 61  
PHW C8A H8A1 SING N N 62  
PHW C8A H8A2 SING N N 63  
PHW C8B C8C  SING N N 64  
PHW C8B H8B1 SING N N 65  
PHW C8B H8B2 SING N N 66  
PHW C8C N9   SING N N 67  
PHW C8C H8C1 SING N N 68  
PHW C8C H8C2 SING N N 69  
PHW C21 C22  DOUB Y N 70  
PHW C21 C26  SING Y N 71  
PHW C22 C23  SING Y N 72  
PHW C22 H22  SING N N 73  
PHW C23 C24  DOUB Y N 74  
PHW C23 H23  SING N N 75  
PHW C24 C25  SING Y N 76  
PHW C24 H24  SING N N 77  
PHW C25 C26  DOUB Y N 78  
PHW C25 H25  SING N N 79  
PHW C26 H26  SING N N 80  
PHW C31 C32  DOUB Y N 81  
PHW C31 C36  SING Y N 82  
PHW C32 C33  SING Y N 83  
PHW C32 H32  SING N N 84  
PHW C33 C34  DOUB Y N 85  
PHW C33 H33  SING N N 86  
PHW C34 C35  SING Y N 87  
PHW C34 H34  SING N N 88  
PHW C35 C36  DOUB Y N 89  
PHW C35 H35  SING N N 90  
PHW C36 H36  SING N N 91  
PHW N13 HN31 SING N N 92  
PHW C41 C42  DOUB Y N 93  
PHW C41 C46  SING Y N 94  
PHW C42 C43  SING Y N 95  
PHW C42 H42  SING N N 96  
PHW C43 C44  DOUB Y N 97  
PHW C43 H43  SING N N 98  
PHW C44 C45  SING Y N 99  
PHW C44 H44  SING N N 100 
PHW C45 C46  DOUB Y N 101 
PHW C45 H45  SING N N 102 
PHW C46 H46  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 
PHW SMILES           ACDLabs              10.04 O=C(NC(C\C=C\OC)P(Oc1ccccc1)(OC)(O)O)C5N(C(=O)C(NC(=O)OCc2ccccc2)C(c3ccccc3)c4ccccc4)CCC5 
PHW InChI            InChI                1.02b 
;InChI=1/C40H46N3O9P/c1-49-28-16-26-35(53(47,48,50-2)52-33-23-13-6-14-24-33)41-38(44)34-25-15-27-43(34)39(45)37(42-40(46)51-29-30-17-7-3-8-18-30)36(31-19-9-4-10-20-31)32-21-11-5-12-22-32/h3-14,16-24,28,34-37,47-48H,15,25-27,29H2,1-2H3,(H,41,44)(H,42,46)/b28-16+/t34-,35-,37+/m0/s1/f/h41-42H
;
PHW InChIKey         InChI                1.02b QSFRPIRTVOLCSO-SQPFTZABDA 
PHW SMILES_CANONICAL CACTVS               3.341 CO\C=C\C[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](NC(=O)OCc2ccccc2)C(c3ccccc3)c4ccccc4)[P](O)(O)(OC)Oc5ccccc5 
PHW SMILES           CACTVS               3.341 COC=CC[CH](NC(=O)[CH]1CCCN1C(=O)[CH](NC(=O)OCc2ccccc2)C(c3ccccc3)c4ccccc4)[P](O)(O)(OC)Oc5ccccc5 
PHW SMILES_CANONICAL "OpenEye OEToolkits" 1.5.0 COC=CC[C@@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H](C(c2ccccc2)c3ccccc3)NC(=O)OCc4ccccc4)P(O)(O)(OC)Oc5ccccc5 
PHW SMILES           "OpenEye OEToolkits" 1.5.0 COC=CCC(NC(=O)C1CCCN1C(=O)C(C(c2ccccc2)c3ccccc3)NC(=O)OCc4ccccc4)P(O)(O)(OC)Oc5ccccc5 
# 
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 
PHW "SYSTEMATIC NAME" ACDLabs              10.04 N-[(benzyloxy)carbonyl]-beta-phenyl-D-phenylalanyl-N-{(1S,3E)-1-[dihydroxy(methoxy)phenoxy-lambda~5~-phosphanyl]-4-methoxybut-3-en-1-yl}-L-prolinamide                      
PHW "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.5.0 "phenylmethyl N-[(2R)-1-[(2S)-2-[[(1S)-1-(dihydroxy-methoxy-phenoxy-phosphoranyl)-4-methoxy-but-3-enyl]carbamoyl]pyrrolidin-1-yl]-1-oxo-3,3-diphenyl-propan-2-yl]carbamate" 
# 
