data_A1CM6
# 
_chem_comp.id                                    A1CM6 
_chem_comp.name                                  "(3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl {(2S,3R)-1-(3,5-difluorophenyl)-4-[(2-ethylbutyl){4-[(1S)-1-hydroxyethyl]benzene-1-sulfonyl}amino]-3-hydroxybutan-2-yl}carbamate" 
_chem_comp.type                                  non-polymer 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C31 H42 F2 N2 O8 S" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2025-08-11 
_chem_comp.pdbx_modified_date                    2025-12-19 
_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                        640.736 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     A1CM6 
_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        9PZ1 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  RCSB 
_chem_comp.pdbx_pcm                              ? 
# 
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.pdbx_n_terminal_atom_flag 
_chem_comp_atom.pdbx_backbone_atom_flag 
_chem_comp_atom.pdbx_c_terminal_atom_flag 
_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 
A1CM6 C10 C1  C 0 1 Y N N N N N -17.822 0.392  -7.950  -4.715 0.415  0.993  C10 A1CM6 1  
A1CM6 C13 C2  C 0 1 N N N N N N -18.244 2.532  -5.514  -2.631 2.793  -0.864 C13 A1CM6 2  
A1CM6 C15 C3  C 0 1 N N N N N N -17.343 3.299  -3.237  -3.984 3.668  -2.773 C15 A1CM6 3  
A1CM6 C17 C4  C 0 1 N N S N N N -19.203 -0.916 -3.097  1.024  0.161  -0.025 C17 A1CM6 4  
A1CM6 C20 C5  C 0 1 N N N N N N -18.595 -3.796 1.320   7.999  1.874  1.983  C20 A1CM6 5  
A1CM6 C21 C6  C 0 1 N N N N N N -19.640 -2.311 -3.558  0.762  -1.184 0.657  C21 A1CM6 6  
A1CM6 C22 C7  C 0 1 Y N N N N N -18.702 -3.402 -3.094  1.778  -2.192 0.184  C22 A1CM6 7  
A1CM6 C24 C8  C 0 1 Y N N N N N -16.546 -4.437 -3.068  3.905  -3.268 0.433  C24 A1CM6 8  
A1CM6 C26 C9  C 0 1 Y N N N N N -18.289 -5.396 -1.820  2.445  -3.899 -1.360 C26 A1CM6 9  
A1CM6 C28 C10 C 0 1 N N S N N N -18.638 1.086  -12.142 -7.865 -2.297 0.006  C28 A1CM6 10 
A1CM6 C01 C11 C 0 1 N N N N N N -18.515 4.930  -4.907  -3.436 1.234  -2.642 C01 A1CM6 11 
A1CM6 C02 C12 C 0 1 N N N N N N -19.874 0.747  -5.010  -1.417 0.664  -0.205 C02 A1CM6 12 
A1CM6 C03 C13 C 0 1 N N N N N N -18.182 -0.553 -0.840  3.449  0.294  -0.216 C03 A1CM6 13 
A1CM6 C04 C14 C 0 1 N N N N N N -18.278 0.010  2.681   6.139  1.261  -1.710 C04 A1CM6 14 
A1CM6 C05 C15 C 0 1 N N S N N N -17.212 -2.022 2.161   7.063  0.385  0.364  C05 A1CM6 15 
A1CM6 C06 C16 C 0 1 N N N N N N -17.333 -3.007 0.996   6.692  1.097  1.689  C06 A1CM6 16 
A1CM6 C07 C17 C 0 1 Y N N N N N -18.323 0.879  -10.660 -6.755 -1.340 0.358  C07 A1CM6 17 
A1CM6 C08 C18 C 0 1 Y N N N N N -18.934 -0.193 -9.994  -6.918 0.016  0.142  C08 A1CM6 18 
A1CM6 C09 C19 C 0 1 Y N N N N N -18.690 -0.444 -8.649  -5.900 0.894  0.465  C09 A1CM6 19 
A1CM6 C11 C20 C 0 1 Y N N N N N -17.204 1.464  -8.589  -4.548 -0.942 1.197  C11 A1CM6 20 
A1CM6 C12 C21 C 0 1 Y N N N N N -17.459 1.703  -9.938  -5.569 -1.819 0.880  C12 A1CM6 21 
A1CM6 C14 C22 C 0 1 N N N N N N -18.423 3.490  -4.321  -3.778 2.483  -1.827 C14 A1CM6 22 
A1CM6 C16 C23 C 0 1 N N R N N N -20.111 0.232  -3.584  -0.079 1.150  0.358  C16 A1CM6 23 
A1CM6 C18 C24 C 0 1 N N R N N N -17.502 -0.634 1.555   5.814  0.312  -0.536 C18 A1CM6 24 
A1CM6 C19 C25 C 0 1 N N R N N N -18.375 -2.301 3.149   7.977  1.435  -0.329 C19 A1CM6 25 
A1CM6 C23 C26 C 0 1 Y N N N N N -17.368 -3.420 -3.518  2.971  -2.341 0.865  C23 A1CM6 26 
A1CM6 C25 C27 C 0 1 Y N N N N N -16.967 -5.447 -2.217  3.642  -4.045 -0.682 C25 A1CM6 27 
A1CM6 C27 C28 C 0 1 Y N N N N N -19.163 -4.403 -2.234  1.513  -2.971 -0.926 C27 A1CM6 28 
A1CM6 C29 C29 C 0 1 N N N N N N -17.502 0.810  -13.136 -8.715 -2.572 1.249  C29 A1CM6 29 
A1CM6 C30 C30 C 0 1 N N N N N N -17.324 4.432  -2.192  -4.348 4.912  -1.960 C30 A1CM6 30 
A1CM6 C31 C31 C 0 1 N N N N N N -17.179 5.688  -5.072  -3.760 -0.015 -1.821 C31 A1CM6 31 
A1CM6 F01 F1  F 0 1 N N N N N N -15.258 -4.461 -3.473  5.074  -3.409 1.095  F01 A1CM6 32 
A1CM6 F02 F2  F 0 1 N N N N N N -18.753 -6.356 -0.990  2.185  -4.660 -2.446 F02 A1CM6 33 
A1CM6 N01 N1  N 0 1 N N N N N N -18.462 1.098  -5.262  -2.450 1.668  0.058  N01 A1CM6 34 
A1CM6 N02 N2  N 0 1 N N N N N N -19.251 -0.898 -1.621  2.321  0.684  0.410  N02 A1CM6 35 
A1CM6 O01 O1  O 0 1 N N N N N N -16.122 0.522  -5.960  -4.023 2.804  1.584  O01 A1CM6 36 
A1CM6 O02 O2  O 0 1 N N N N N N -17.895 -1.293 -5.920  -2.630 0.892  2.394  O02 A1CM6 37 
A1CM6 O03 O3  O 0 1 N N N N N N -21.495 -0.124 -3.538  -0.166 1.240  1.781  O03 A1CM6 38 
A1CM6 O04 O4  O 0 1 N N N N N N -17.085 -0.260 -1.245  3.391  -0.492 -1.140 O04 A1CM6 39 
A1CM6 O05 O5  O 0 1 N N N N N N -18.503 -0.659 0.487   4.642  0.775  0.184  O05 A1CM6 40 
A1CM6 O06 O6  O 0 1 N N N N N N -19.122 -1.068 3.135   7.089  2.202  -1.170 O06 A1CM6 41 
A1CM6 O07 O7  O 0 1 N N N N N N -18.975 -3.474 2.682   8.482  2.297  0.699  O07 A1CM6 42 
A1CM6 O08 O8  O 0 1 N N N N N N -19.146 2.408  -12.373 -7.304 -3.523 -0.468 O08 A1CM6 43 
A1CM6 S01 S1  S 0 1 N N N N N N -17.490 0.086  -6.202  -3.415 1.533  1.397  S01 A1CM6 44 
A1CM6 H14 H1  H 0 1 N N N N N N -18.952 2.842  -6.297  -1.713 2.949  -1.430 H14 A1CM6 45 
A1CM6 H15 H2  H 0 1 N N N N N N -17.214 2.651  -5.883  -2.866 3.694  -0.297 H15 A1CM6 46 
A1CM6 H18 H3  H 0 1 N N N N N N -17.533 2.348  -2.718  -3.065 3.854  -3.329 H18 A1CM6 47 
A1CM6 H17 H4  H 0 1 N N N N N N -16.359 3.259  -3.727  -4.790 3.441  -3.470 H17 A1CM6 48 
A1CM6 H20 H5  H 0 1 N N N N N N -18.175 -0.729 -3.440  1.031  0.025  -1.106 H20 A1CM6 49 
A1CM6 H24 H6  H 0 1 N N N N N N -19.402 -3.513 0.628   7.792  2.740  2.613  H24 A1CM6 50 
A1CM6 H23 H7  H 0 1 N N N N N N -18.397 -4.874 1.231   8.728  1.223  2.465  H23 A1CM6 51 
A1CM6 H25 H8  H 0 1 N N N N N N -20.643 -2.516 -3.156  0.843  -1.065 1.737  H25 A1CM6 52 
A1CM6 H26 H9  H 0 1 N N N N N N -19.676 -2.323 -4.657  -0.239 -1.531 0.403  H26 A1CM6 53 
A1CM6 H30 H10 H 0 1 N N N N N N -19.442 0.377  -12.389 -8.490 -1.858 -0.771 H30 A1CM6 54 
A1CM6 H01 H11 H 0 1 N N N N N N -18.985 4.859  -5.899  -4.024 1.227  -3.560 H01 A1CM6 55 
A1CM6 H02 H12 H 0 1 N N N N N N -19.157 5.523  -4.239  -2.375 1.241  -2.890 H02 A1CM6 56 
A1CM6 H04 H13 H 0 1 N N N N N N -20.174 -0.036 -5.721  -1.324 0.511  -1.280 H04 A1CM6 57 
A1CM6 H03 H14 H 0 1 N N N N N N -20.493 1.643  -5.168  -1.693 -0.275 0.274  H03 A1CM6 58 
A1CM6 H06 H15 H 0 1 N N N N N N -17.606 0.353  3.482   6.583  0.705  -2.536 H06 A1CM6 59 
A1CM6 H05 H16 H 0 1 N N N N N N -18.877 0.858  2.317   5.238  1.778  -2.040 H05 A1CM6 60 
A1CM6 H07 H17 H 0 1 N N N N N N -16.229 -2.068 2.652   7.538  -0.584 0.516  H07 A1CM6 61 
A1CM6 H09 H18 H 0 1 N N N N N N -17.439 -2.473 0.040   6.479  0.374  2.477  H09 A1CM6 62 
A1CM6 H08 H19 H 0 1 N N N N N N -16.457 -3.670 0.950   5.853  1.778  1.547  H08 A1CM6 63 
A1CM6 H10 H20 H 0 1 N N N N N N -19.609 -0.837 -10.538 -7.845 0.391  -0.265 H10 A1CM6 64 
A1CM6 H11 H21 H 0 1 N N N N N N -19.167 -1.276 -8.152  -6.030 1.954  0.306  H11 A1CM6 65 
A1CM6 H12 H22 H 0 1 N N N N N N -16.530 2.107  -8.042  -3.621 -1.317 1.605  H12 A1CM6 66 
A1CM6 H13 H23 H 0 1 N N N N N N -16.982 2.537  -10.431 -5.442 -2.879 1.048  H13 A1CM6 67 
A1CM6 H16 H24 H 0 1 N N N N N N -19.396 3.263  -3.860  -4.692 2.308  -1.260 H16 A1CM6 68 
A1CM6 H19 H25 H 0 1 N N N N N N -19.949 1.081  -2.903  0.154  2.131  -0.055 H19 A1CM6 69 
A1CM6 H21 H26 H 0 1 N N N N N N -16.585 -0.086 1.294   5.664  -0.705 -0.898 H21 A1CM6 70 
A1CM6 H22 H27 H 0 1 N N N N N N -17.946 -2.463 4.149   8.773  0.963  -0.905 H22 A1CM6 71 
A1CM6 H27 H28 H 0 1 N N N N N N -16.989 -2.657 -4.182  3.176  -1.735 1.735  H27 A1CM6 72 
A1CM6 H28 H29 H 0 1 N N N N N N -16.300 -6.228 -1.884  4.372  -4.765 -1.023 H28 A1CM6 73 
A1CM6 H29 H30 H 0 1 N N N N N N -20.189 -4.403 -1.896  0.578  -2.857 -1.454 H29 A1CM6 74 
A1CM6 H31 H31 H 0 1 N N N N N N -17.857 0.995  -14.160 -9.142 -1.637 1.611  H31 A1CM6 75 
A1CM6 H33 H32 H 0 1 N N N N N N -16.653 1.475  -12.916 -9.517 -3.264 0.994  H33 A1CM6 76 
A1CM6 H32 H33 H 0 1 N N N N N N -17.181 -0.238 -13.044 -8.089 -3.010 2.026  H32 A1CM6 77 
A1CM6 H36 H34 H 0 1 N N N N N N -16.535 4.235  -1.451  -4.442 5.768  -2.628 H36 A1CM6 78 
A1CM6 H35 H35 H 0 1 N N N N N N -17.125 5.390  -2.694  -5.295 4.746  -1.446 H35 A1CM6 79 
A1CM6 H34 H36 H 0 1 N N N N N N -18.299 4.479  -1.685  -3.566 5.108  -1.226 H34 A1CM6 80 
A1CM6 H38 H37 H 0 1 N N N N N N -17.373 6.686  -5.492  -4.838 -0.084 -1.673 H38 A1CM6 81 
A1CM6 H39 H38 H 0 1 N N N N N N -16.692 5.791  -4.091  -3.409 -0.900 -2.351 H39 A1CM6 82 
A1CM6 H37 H39 H 0 1 N N N N N N -16.520 5.126  -5.751  -3.264 0.048  -0.852 H37 A1CM6 83 
A1CM6 H40 H40 H 0 1 N N N N N N -20.107 -1.150 -1.170  2.368  1.312  1.148  H40 A1CM6 84 
A1CM6 H41 H41 H 0 1 N N N N N N -21.709 -0.454 -2.673  -0.371 0.401  2.217  H41 A1CM6 85 
A1CM6 H42 H42 H 0 1 N N N N N N -19.336 2.518  -13.297 -7.962 -4.187 -0.714 H42 A1CM6 86 
# 
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 
A1CM6 C01 C14 SING N N 1  
A1CM6 C01 C31 SING N N 2  
A1CM6 C02 C16 SING N N 3  
A1CM6 C02 N01 SING N N 4  
A1CM6 C03 N02 SING N N 5  
A1CM6 C03 O04 DOUB N N 6  
A1CM6 C03 O05 SING N N 7  
A1CM6 C04 C18 SING N N 8  
A1CM6 C04 O06 SING N N 9  
A1CM6 C05 C06 SING N N 10 
A1CM6 C05 C18 SING N N 11 
A1CM6 C05 C19 SING N N 12 
A1CM6 C06 C20 SING N N 13 
A1CM6 C07 C08 DOUB Y N 14 
A1CM6 C07 C12 SING Y N 15 
A1CM6 C07 C28 SING N N 16 
A1CM6 C08 C09 SING Y N 17 
A1CM6 C09 C10 DOUB Y N 18 
A1CM6 C10 C11 SING Y N 19 
A1CM6 C10 S01 SING N N 20 
A1CM6 C11 C12 DOUB Y N 21 
A1CM6 C13 C14 SING N N 22 
A1CM6 C13 N01 SING N N 23 
A1CM6 C14 C15 SING N N 24 
A1CM6 C15 C30 SING N N 25 
A1CM6 C16 C17 SING N N 26 
A1CM6 C16 O03 SING N N 27 
A1CM6 C17 C21 SING N N 28 
A1CM6 C17 N02 SING N N 29 
A1CM6 C18 O05 SING N N 30 
A1CM6 C19 O06 SING N N 31 
A1CM6 C19 O07 SING N N 32 
A1CM6 C20 O07 SING N N 33 
A1CM6 C21 C22 SING N N 34 
A1CM6 C22 C23 DOUB Y N 35 
A1CM6 C22 C27 SING Y N 36 
A1CM6 C23 C24 SING Y N 37 
A1CM6 C24 C25 DOUB Y N 38 
A1CM6 C24 F01 SING N N 39 
A1CM6 C25 C26 SING Y N 40 
A1CM6 C26 C27 DOUB Y N 41 
A1CM6 C26 F02 SING N N 42 
A1CM6 C28 C29 SING N N 43 
A1CM6 C28 O08 SING N N 44 
A1CM6 N01 S01 SING N N 45 
A1CM6 O01 S01 DOUB N N 46 
A1CM6 O02 S01 DOUB N N 47 
A1CM6 C13 H14 SING N N 48 
A1CM6 C13 H15 SING N N 49 
A1CM6 C15 H18 SING N N 50 
A1CM6 C15 H17 SING N N 51 
A1CM6 C17 H20 SING N N 52 
A1CM6 C20 H24 SING N N 53 
A1CM6 C20 H23 SING N N 54 
A1CM6 C21 H25 SING N N 55 
A1CM6 C21 H26 SING N N 56 
A1CM6 C28 H30 SING N N 57 
A1CM6 C01 H01 SING N N 58 
A1CM6 C01 H02 SING N N 59 
A1CM6 C02 H04 SING N N 60 
A1CM6 C02 H03 SING N N 61 
A1CM6 C04 H06 SING N N 62 
A1CM6 C04 H05 SING N N 63 
A1CM6 C05 H07 SING N N 64 
A1CM6 C06 H09 SING N N 65 
A1CM6 C06 H08 SING N N 66 
A1CM6 C08 H10 SING N N 67 
A1CM6 C09 H11 SING N N 68 
A1CM6 C11 H12 SING N N 69 
A1CM6 C12 H13 SING N N 70 
A1CM6 C14 H16 SING N N 71 
A1CM6 C16 H19 SING N N 72 
A1CM6 C18 H21 SING N N 73 
A1CM6 C19 H22 SING N N 74 
A1CM6 C23 H27 SING N N 75 
A1CM6 C25 H28 SING N N 76 
A1CM6 C27 H29 SING N N 77 
A1CM6 C29 H31 SING N N 78 
A1CM6 C29 H33 SING N N 79 
A1CM6 C29 H32 SING N N 80 
A1CM6 C30 H36 SING N N 81 
A1CM6 C30 H35 SING N N 82 
A1CM6 C30 H34 SING N N 83 
A1CM6 C31 H38 SING N N 84 
A1CM6 C31 H39 SING N N 85 
A1CM6 C31 H37 SING N N 86 
A1CM6 N02 H40 SING N N 87 
A1CM6 O03 H41 SING N N 88 
A1CM6 O08 H42 SING N N 89 
# 
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 
A1CM6 SMILES           ACDLabs              14.52   "CC(O)c1ccc(cc1)S(=O)(=O)N(CC(CC)CC)CC(O)C(Cc1cc(F)cc(F)c1)NC(=O)OC1COC2OCCC12"                                                                                                                                                                                       
A1CM6 InChI            InChI                1.06    "InChI=1S/C31H42F2N2O8S/c1-4-20(5-2)16-35(44(39,40)25-8-6-22(7-9-25)19(3)36)17-28(37)27(14-21-12-23(32)15-24(33)13-21)34-31(38)43-29-18-42-30-26(29)10-11-41-30/h6-9,12-13,15,19-20,26-30,36-37H,4-5,10-11,14,16-18H2,1-3H3,(H,34,38)/t19-,26-,27-,28+,29-,30+/m0/s1" 
A1CM6 InChIKey         InChI                1.06    QSTWKEAHGIUFAI-CYJVAZRPSA-N                                                                                                                                                                                                                                           
A1CM6 SMILES_CANONICAL CACTVS               3.385   "CCC(CC)CN(C[C@@H](O)[C@H](Cc1cc(F)cc(F)c1)NC(=O)O[C@H]2CO[C@H]3OCC[C@@H]23)[S](=O)(=O)c4ccc(cc4)[C@H](C)O"                                                                                                                                                           
A1CM6 SMILES           CACTVS               3.385   "CCC(CC)CN(C[CH](O)[CH](Cc1cc(F)cc(F)c1)NC(=O)O[CH]2CO[CH]3OCC[CH]23)[S](=O)(=O)c4ccc(cc4)[CH](C)O"                                                                                                                                                                   
A1CM6 SMILES_CANONICAL "OpenEye OEToolkits" 3.1.0.0 "CCC(CC)CN(C[C@H]([C@H](Cc1cc(cc(c1)F)F)NC(=O)O[C@H]2CO[C@@H]3[C@H]2CCO3)O)S(=O)(=O)c4ccc(cc4)[C@H](C)O"                                                                                                                                                              
A1CM6 SMILES           "OpenEye OEToolkits" 3.1.0.0 "CCC(CC)CN(CC(C(Cc1cc(cc(c1)F)F)NC(=O)OC2COC3C2CCO3)O)S(=O)(=O)c4ccc(cc4)C(C)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 
A1CM6 "SYSTEMATIC NAME" ACDLabs              14.52   "(3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl {(2S,3R)-1-(3,5-difluorophenyl)-4-[(2-ethylbutyl){4-[(1S)-1-hydroxyethyl]benzene-1-sulfonyl}amino]-3-hydroxybutan-2-yl}carbamate"                                                         
A1CM6 "SYSTEMATIC NAME" "OpenEye OEToolkits" 3.1.0.0 "[(3~{a}~{S},4~{R},6~{a}~{R})-2,3,3~{a},4,5,6~{a}-hexahydrofuro[2,3-b]furan-4-yl] ~{N}-[(2~{S},3~{R})-1-[3,5-bis(fluoranyl)phenyl]-4-[2-ethylbutyl-[4-[(1~{S})-1-oxidanylethyl]phenyl]sulfonyl-amino]-3-oxidanyl-butan-2-yl]carbamate" 
# 
loop_
_pdbx_chem_comp_audit.comp_id 
_pdbx_chem_comp_audit.action_type 
_pdbx_chem_comp_audit.date 
_pdbx_chem_comp_audit.processing_site 
A1CM6 "Create component" 2025-08-11 RCSB 
A1CM6 "Initial release"  2025-12-24 RCSB 
# 
