data_A1CM5
# 
_chem_comp.id                                    A1CM5 
_chem_comp.name                                  "(3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl {(2S,3R)-1-(3,5-difluorophenyl)-4-[(2-ethylbutyl){4-[(1R)-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                     A1CM5 
_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        9PYX 
_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 
A1CM5 C10 C1  C 0 1 Y N N N N N -17.688 -0.303 -0.434  -4.716 0.434  1.053  C10 A1CM5 1  
A1CM5 C13 C2  C 0 1 N N N N N N -18.535 -2.367 -2.676  -2.646 2.788  -0.850 C13 A1CM5 2  
A1CM5 C15 C3  C 0 1 N N N N N N -17.514 -3.062 -4.915  -4.016 3.643  -2.756 C15 A1CM5 3  
A1CM5 C17 C4  C 0 1 N N S N N N -19.145 1.037  -5.187  1.014  0.163  -0.013 C17 A1CM5 4  
A1CM5 C20 C5  C 0 1 N N N N N N -18.770 3.605  -9.487  8.008  1.894  1.912  C20 A1CM5 5  
A1CM5 C21 C6  C 0 1 N N N N N N -19.570 2.454  -4.775  0.757  -1.173 0.687  C21 A1CM5 6  
A1CM5 C22 C7  C 0 1 Y N N N N N -18.634 3.525  -5.282  1.768  -2.188 0.217  C22 A1CM5 7  
A1CM5 C24 C8  C 0 1 Y N N N N N -16.447 4.560  -5.337  3.896  -3.262 0.459  C24 A1CM5 8  
A1CM5 C26 C9  C 0 1 Y N N N N N -18.203 5.477  -6.639  2.419  -3.913 -1.314 C26 A1CM5 9  
A1CM5 C28 C10 C 0 1 N N R N N N -18.177 -1.175 3.783   -7.876 -2.286 0.127  C28 A1CM5 10 
A1CM5 C01 C11 C 0 1 N N N N N N -18.874 -4.757 -3.471  -3.469 1.210  -2.602 C01 A1CM5 11 
A1CM5 C02 C12 C 0 1 N N N N N N -19.904 -0.276 -3.172  -1.428 0.667  -0.177 C02 A1CM5 12 
A1CM5 C03 C13 C 0 1 N N N N N N -18.066 0.646  -7.386  3.438  0.292  -0.227 C03 A1CM5 13 
A1CM5 C04 C14 C 0 1 N N N N N N -18.140 -0.053 -10.838 6.114  1.239  -1.757 C04 A1CM5 14 
A1CM5 C05 C15 C 0 1 N N S N N N -17.094 2.021  -10.178 7.057  0.387  0.318  C05 A1CM5 15 
A1CM5 C06 C16 C 0 1 N N N N N N -17.284 3.289  -9.302  6.698  1.115  1.639  C06 A1CM5 16 
A1CM5 C07 C17 C 0 1 Y N N N N N -17.914 -0.934 2.276   -6.763 -1.326 0.458  C07 A1CM5 17 
A1CM5 C08 C18 C 0 1 Y N N N N N -18.815 -0.036 1.659   -6.926 0.027  0.228  C08 A1CM5 18 
A1CM5 C09 C19 C 0 1 Y N N N N N -18.716 0.292  0.317   -5.905 0.908  0.531  C09 A1CM5 19 
A1CM5 C11 C20 C 0 1 Y N N N N N -16.790 -1.210 0.125   -4.548 -0.920 1.272  C11 A1CM5 20 
A1CM5 C12 C21 C 0 1 Y N N N N N -16.905 -1.529 1.473   -5.572 -1.801 0.974  C12 A1CM5 21 
A1CM5 C14 C22 C 0 1 N N N N N N -18.671 -3.280 -3.918  -3.803 2.468  -1.799 C14 A1CM5 22 
A1CM5 C16 C23 C 0 1 N N R N N N -20.102 -0.036 -4.669  -0.085 1.158  0.368  C16 A1CM5 23 
A1CM5 C18 C24 C 0 1 N N R N N N -17.436 0.611  -9.667  5.800  0.304  -0.569 C18 A1CM5 24 
A1CM5 C19 C25 C 0 1 N N R N N N -18.147 2.252  -11.278 7.964  1.428  -0.394 C19 A1CM5 25 
A1CM5 C23 C26 C 0 1 Y N N N N N -17.294 3.562  -4.859  2.967  -2.330 0.889  C23 A1CM5 26 
A1CM5 C25 C27 C 0 1 Y N N N N N -16.873 5.534  -6.233  3.623  -4.052 -0.645 C25 A1CM5 27 
A1CM5 C27 C28 C 0 1 Y N N N N N -19.085 4.503  -6.189  1.492  -2.980 -0.882 C27 A1CM5 28 
A1CM5 C29 C29 C 0 1 N N N N N N -18.446 0.087  4.608   -7.586 -2.961 -1.215 C29 A1CM5 29 
A1CM5 C30 C30 C 0 1 N N N N N N -17.565 -3.986 -6.141  -4.372 4.896  -1.954 C30 A1CM5 30 
A1CM5 C31 C31 C 0 1 N N N N N N -17.590 -5.513 -3.126  -3.786 -0.030 -1.763 C31 A1CM5 31 
A1CM5 F01 F1  F 0 1 N N N N N N -15.155 4.604  -4.934  5.071  -3.397 1.112  F01 A1CM5 32 
A1CM5 F02 F2  F 0 1 N N N N N N -18.664 6.402  -7.503  2.149  -4.686 -2.388 F02 A1CM5 33 
A1CM5 N01 N1  N 0 1 N N N N N N -18.596 -0.901 -2.928  -2.458 1.675  0.084  N01 A1CM5 34 
A1CM5 N02 N2  N 0 1 N N N N N N -19.147 0.985  -6.647  2.315  0.691  0.404  N02 A1CM5 35 
A1CM5 O01 O1  O 0 1 N N N N N N -16.132 -0.454 -2.534  -4.016 2.829  1.611  O01 A1CM5 36 
A1CM5 O02 O2  O 0 1 N N N N N N -17.881 1.460  -2.363  -2.618 0.926  2.430  O02 A1CM5 37 
A1CM5 O03 O3  O 0 1 N N N N N N -21.451 0.277  -4.849  -0.159 1.264  1.791  O03 A1CM5 38 
A1CM5 O04 O4  O 0 1 N N N N N N -16.952 0.405  -7.005  3.370  -0.504 -1.142 O04 A1CM5 39 
A1CM5 O05 O5  O 0 1 N N N N N N -18.469 0.627  -8.671  4.634  0.777  0.156  O05 A1CM5 40 
A1CM5 O06 O6  O 0 1 N N N N N N -18.862 1.011  -11.430 7.069  2.186  -1.237 O06 A1CM5 41 
A1CM5 O07 O7  O 0 1 N N N N N N -18.975 3.315  -10.884 8.480  2.302  0.618  O07 A1CM5 42 
A1CM5 O08 O8  O 0 1 N N N N N N -19.136 -2.214 3.791   -7.968 -3.280 1.150  O08 A1CM5 43 
A1CM5 S01 S1  S 0 1 N N N N N N -17.449 0.058  -2.186  -3.411 1.556  1.433  S01 A1CM5 44 
A1CM5 H14 H1  H 0 1 N N N N N N -19.349 -2.622 -1.981  -1.733 2.937  -1.426 H14 A1CM5 45 
A1CM5 H15 H2  H 0 1 N N N N N N -17.566 -2.586 -2.203  -2.875 3.696  -0.291 H15 A1CM5 46 
A1CM5 H18 H3  H 0 1 N N N N N N -17.551 -2.020 -5.265  -3.102 3.821  -3.322 H18 A1CM5 47 
A1CM5 H17 H4  H 0 1 N N N N N N -16.565 -3.239 -4.388  -4.829 3.408  -3.444 H17 A1CM5 48 
A1CM5 H20 H5  H 0 1 N N N N N N -18.134 0.837  -4.802  1.011  0.015  -1.093 H20 A1CM5 49 
A1CM5 H24 H6  H 0 1 N N N N N N -19.396 2.962  -8.851  7.807  2.767  2.533  H24 A1CM5 50 
A1CM5 H23 H7  H 0 1 N N N N N N -18.983 4.661  -9.264  8.741  1.248  2.395  H23 A1CM5 51 
A1CM5 H26 H8  H 0 1 N N N N N N -20.575 2.649  -5.177  0.848  -1.042 1.765  H26 A1CM5 52 
A1CM5 H25 H9  H 0 1 N N N N N N -19.598 2.505  -3.677  -0.247 -1.522 0.446  H25 A1CM5 53 
A1CM5 H30 H10 H 0 1 N N N N N N -17.242 -1.597 4.181   -8.819 -1.742 0.064  H30 A1CM5 54 
A1CM5 H02 H11 H 0 1 N N N N N N -19.520 -4.758 -2.580  -4.065 1.193  -3.515 H02 A1CM5 55 
A1CM5 H01 H12 H 0 1 N N N N N N -19.377 -5.294 -4.289  -2.410 1.213  -2.860 H01 A1CM5 56 
A1CM5 H03 H13 H 0 1 N N N N N N -19.952 0.686  -2.640  -1.345 0.501  -1.251 H03 A1CM5 57 
A1CM5 H04 H14 H 0 1 N N N N N N -20.699 -0.940 -2.802  -1.700 -0.267 0.316  H04 A1CM5 58 
A1CM5 H06 H15 H 0 1 N N N N N N -17.413 -0.477 -11.546 6.550  0.674  -2.580 H06 A1CM5 59 
A1CM5 H05 H16 H 0 1 N N N N N N -18.820 -0.845 -10.491 5.211  1.753  -2.085 H05 A1CM5 60 
A1CM5 H07 H17 H 0 1 N N N N N N -16.087 2.024  -10.620 7.532  -0.581 0.478  H07 A1CM5 61 
A1CM5 H08 H18 H 0 1 N N N N N N -17.051 3.081  -8.247  6.492  0.401  2.437  H08 A1CM5 62 
A1CM5 H09 H19 H 0 1 N N N N N N -16.655 4.117  -9.660  5.858  1.795  1.496  H09 A1CM5 63 
A1CM5 H10 H20 H 0 1 N N N N N N -19.603 0.407  2.251   -7.857 0.398  -0.176 H10 A1CM5 64 
A1CM5 H11 H21 H 0 1 N N N N N N -19.408 0.984  -0.139  -6.036 1.966  0.360  H11 A1CM5 65 
A1CM5 H12 H22 H 0 1 N N N N N N -16.016 -1.659 -0.480  -3.618 -1.291 1.676  H12 A1CM5 66 
A1CM5 H13 H23 H 0 1 N N N N N N -16.219 -2.237 1.915   -5.444 -2.858 1.154  H13 A1CM5 67 
A1CM5 H16 H24 H 0 1 N N N N N N -19.595 -2.978 -4.433  -4.711 2.301  -1.221 H16 A1CM5 68 
A1CM5 H19 H25 H 0 1 N N N N N N -19.869 -0.975 -5.193  0.145  2.134  -0.058 H19 A1CM5 69 
A1CM5 H21 H26 H 0 1 N N N N N N -16.537 0.059  -9.357  5.645  -0.717 -0.918 H21 A1CM5 70 
A1CM5 H22 H27 H 0 1 N N N N N N -17.625 2.499  -12.214 8.755  0.948  -0.972 H22 A1CM5 71 
A1CM5 H27 H28 H 0 1 N N N N N N -16.923 2.821  -4.167  3.180  -1.713 1.750  H27 A1CM5 72 
A1CM5 H28 H29 H 0 1 N N N N N N -16.203 6.299  -6.597  4.349  -4.777 -0.984 H28 A1CM5 73 
A1CM5 H29 H30 H 0 1 N N N N N N -20.109 4.496  -6.532  0.552  -2.871 -1.403 H29 A1CM5 74 
A1CM5 H31 H31 H 0 1 N N N N N N -18.619 -0.191 5.658   -8.391 -3.656 -1.454 H31 A1CM5 75 
A1CM5 H33 H32 H 0 1 N N N N N N -17.577 0.758  4.545   -7.516 -2.204 -1.995 H33 A1CM5 76 
A1CM5 H32 H33 H 0 1 N N N N N N -19.335 0.600  4.213   -6.644 -3.506 -1.151 H32 A1CM5 77 
A1CM5 H35 H34 H 0 1 N N N N N N -16.711 -3.770 -6.800  -4.471 5.745  -2.632 H35 A1CM5 78 
A1CM5 H36 H35 H 0 1 N N N N N N -17.518 -5.035 -5.812  -5.314 4.737  -1.431 H36 A1CM5 79 
A1CM5 H34 H36 H 0 1 N N N N N N -18.503 -3.816 -6.689  -3.583 5.100  -1.230 H34 A1CM5 80 
A1CM5 H37 H37 H 0 1 N N N N N N -17.839 -6.541 -2.824  -4.863 -0.096 -1.606 H37 A1CM5 81 
A1CM5 H39 H38 H 0 1 N N N N N N -16.932 -5.539 -4.007  -3.441 -0.921 -2.287 H39 A1CM5 82 
A1CM5 H38 H39 H 0 1 N N N N N N -17.075 -5.002 -2.299  -3.282 0.045  -0.800 H38 A1CM5 83 
A1CM5 H40 H40 H 0 1 N N N N N N -19.994 1.213  -7.127  2.370  1.327  1.135  H40 A1CM5 84 
A1CM5 H41 H41 H 0 1 N N N N N N -21.620 0.435  -5.770  -0.360 0.431  2.238  H41 A1CM5 85 
A1CM5 H42 H42 H 0 1 N N N N N N -19.361 -2.431 4.688   -8.666 -3.933 1.003  H42 A1CM5 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 
A1CM5 C01 C14 SING N N 1  
A1CM5 C01 C31 SING N N 2  
A1CM5 C02 C16 SING N N 3  
A1CM5 C02 N01 SING N N 4  
A1CM5 C03 N02 SING N N 5  
A1CM5 C03 O04 DOUB N N 6  
A1CM5 C03 O05 SING N N 7  
A1CM5 C04 C18 SING N N 8  
A1CM5 C04 O06 SING N N 9  
A1CM5 C05 C06 SING N N 10 
A1CM5 C05 C18 SING N N 11 
A1CM5 C05 C19 SING N N 12 
A1CM5 C06 C20 SING N N 13 
A1CM5 C07 C08 DOUB Y N 14 
A1CM5 C07 C12 SING Y N 15 
A1CM5 C07 C28 SING N N 16 
A1CM5 C08 C09 SING Y N 17 
A1CM5 C09 C10 DOUB Y N 18 
A1CM5 C10 C11 SING Y N 19 
A1CM5 C10 S01 SING N N 20 
A1CM5 C11 C12 DOUB Y N 21 
A1CM5 C13 C14 SING N N 22 
A1CM5 C13 N01 SING N N 23 
A1CM5 C14 C15 SING N N 24 
A1CM5 C15 C30 SING N N 25 
A1CM5 C16 C17 SING N N 26 
A1CM5 C16 O03 SING N N 27 
A1CM5 C17 C21 SING N N 28 
A1CM5 C17 N02 SING N N 29 
A1CM5 C18 O05 SING N N 30 
A1CM5 C19 O06 SING N N 31 
A1CM5 C19 O07 SING N N 32 
A1CM5 C20 O07 SING N N 33 
A1CM5 C21 C22 SING N N 34 
A1CM5 C22 C23 DOUB Y N 35 
A1CM5 C22 C27 SING Y N 36 
A1CM5 C23 C24 SING Y N 37 
A1CM5 C24 C25 DOUB Y N 38 
A1CM5 C24 F01 SING N N 39 
A1CM5 C25 C26 SING Y N 40 
A1CM5 C26 C27 DOUB Y N 41 
A1CM5 C26 F02 SING N N 42 
A1CM5 C28 C29 SING N N 43 
A1CM5 C28 O08 SING N N 44 
A1CM5 N01 S01 SING N N 45 
A1CM5 O01 S01 DOUB N N 46 
A1CM5 O02 S01 DOUB N N 47 
A1CM5 C13 H14 SING N N 48 
A1CM5 C13 H15 SING N N 49 
A1CM5 C15 H18 SING N N 50 
A1CM5 C15 H17 SING N N 51 
A1CM5 C17 H20 SING N N 52 
A1CM5 C20 H24 SING N N 53 
A1CM5 C20 H23 SING N N 54 
A1CM5 C21 H26 SING N N 55 
A1CM5 C21 H25 SING N N 56 
A1CM5 C28 H30 SING N N 57 
A1CM5 C01 H02 SING N N 58 
A1CM5 C01 H01 SING N N 59 
A1CM5 C02 H03 SING N N 60 
A1CM5 C02 H04 SING N N 61 
A1CM5 C04 H06 SING N N 62 
A1CM5 C04 H05 SING N N 63 
A1CM5 C05 H07 SING N N 64 
A1CM5 C06 H08 SING N N 65 
A1CM5 C06 H09 SING N N 66 
A1CM5 C08 H10 SING N N 67 
A1CM5 C09 H11 SING N N 68 
A1CM5 C11 H12 SING N N 69 
A1CM5 C12 H13 SING N N 70 
A1CM5 C14 H16 SING N N 71 
A1CM5 C16 H19 SING N N 72 
A1CM5 C18 H21 SING N N 73 
A1CM5 C19 H22 SING N N 74 
A1CM5 C23 H27 SING N N 75 
A1CM5 C25 H28 SING N N 76 
A1CM5 C27 H29 SING N N 77 
A1CM5 C29 H31 SING N N 78 
A1CM5 C29 H33 SING N N 79 
A1CM5 C29 H32 SING N N 80 
A1CM5 C30 H35 SING N N 81 
A1CM5 C30 H36 SING N N 82 
A1CM5 C30 H34 SING N N 83 
A1CM5 C31 H37 SING N N 84 
A1CM5 C31 H39 SING N N 85 
A1CM5 C31 H38 SING N N 86 
A1CM5 N02 H40 SING N N 87 
A1CM5 O03 H41 SING N N 88 
A1CM5 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 
A1CM5 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"                                                                                                                                                                                       
A1CM5 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-/m1/s1" 
A1CM5 InChIKey         InChI                1.06    QSTWKEAHGIUFAI-KKWHVFEBSA-N                                                                                                                                                                                                                                           
A1CM5 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"                                                                                                                                                          
A1CM5 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"                                                                                                                                                                   
A1CM5 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"                                                                                                                                                             
A1CM5 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 
A1CM5 "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-[(1R)-1-hydroxyethyl]benzene-1-sulfonyl}amino]-3-hydroxybutan-2-yl}carbamate"                                                         
A1CM5 "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~{R})-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 
A1CM5 "Create component" 2025-08-11 RCSB 
A1CM5 "Initial release"  2025-12-24 RCSB 
# 
