data_A1BH6
# 
_chem_comp.id                                    A1BH6 
_chem_comp.name                                  "(3S)-N,5-dimethyl-3-({4-[3-(morpholin-4-yl)phenyl]-6-(2-propanoyl-2,6-diazaspiro[3.4]octan-6-yl)-1,3,5-triazin-2-yl}amino)hexanamide" 
_chem_comp.type                                  non-polymer 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C30 H44 N8 O3" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2024-11-21 
_chem_comp.pdbx_modified_date                    2025-02-21 
_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                        564.722 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     A1BH6 
_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        9E9H 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  RCSB 
_chem_comp.pdbx_pcm                              Y 
# 
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 
A1BH6 C26 C1  C 0 1 N N N N N N -7.838  -14.751 30.427 -5.572 -0.203 1.258  C26 A1BH6 1  
A1BH6 C27 C2  C 0 1 N N N N N N -8.005  -15.206 31.881 -6.780 0.689  1.555  C27 A1BH6 2  
A1BH6 O3  O1  O 0 1 N N N N N N -7.243  -16.401 32.146 -7.980 -0.075 1.403  O3  A1BH6 3  
A1BH6 C28 C3  C 0 1 N N N N N N -7.662  -17.462 31.262 -8.142 -0.638 0.098  C28 A1BH6 4  
A1BH6 C29 C4  C 0 1 N N N N N N -7.424  -17.035 29.809 -6.947 -1.544 -0.213 C29 A1BH6 5  
A1BH6 N7  N1  N 0 1 N N N N N N -8.268  -15.849 29.535 -5.705 -0.766 -0.093 N7  A1BH6 6  
A1BH6 C25 C5  C 0 1 Y N N N N N -8.403  -15.517 28.230 -4.593 -1.545 -0.422 C25 A1BH6 7  
A1BH6 C30 C6  C 0 1 Y N N N N N -7.866  -16.273 27.189 -3.322 -0.995 -0.372 C30 A1BH6 8  
A1BH6 C24 C7  C 0 1 Y N N N N N -9.169  -14.406 27.896 -4.761 -2.874 -0.795 C24 A1BH6 9  
A1BH6 C23 C8  C 0 1 Y N N N N N -9.355  -14.051 26.562 -3.664 -3.648 -1.121 C23 A1BH6 10 
A1BH6 C22 C9  C 0 1 Y N N N N N -8.800  -14.822 25.547 -2.394 -3.106 -1.079 C22 A1BH6 11 
A1BH6 C21 C10 C 0 1 Y N N N N N -8.038  -15.952 25.845 -2.216 -1.776 -0.701 C21 A1BH6 12 
A1BH6 C20 C11 C 0 1 Y N N N N N -7.484  -16.730 24.817 -0.853 -1.192 -0.655 C20 A1BH6 13 
A1BH6 N6  N2  N 0 1 Y N N N N N -8.166  -16.986 23.692 0.199  -1.933 -0.990 N6  A1BH6 14 
A1BH6 N8  N3  N 0 1 Y N N N N N -6.256  -17.260 24.950 -0.684 0.074  -0.285 N8  A1BH6 15 
A1BH6 C9  C12 C 0 1 Y N N N N N -5.725  -18.014 23.973 0.538  0.596  -0.244 C9  A1BH6 16 
A1BH6 N2  N4  N 0 1 N N N N N N -4.515  -18.522 24.149 0.713  1.910  0.140  N2  A1BH6 17 
A1BH6 C5  C13 C 0 1 N N S N N N -3.790  -19.309 23.150 -0.443 2.720  0.531  C5  A1BH6 18 
A1BH6 C4  C14 C 0 1 N N N N N N -2.623  -18.478 22.605 -0.457 2.889  2.052  C4  A1BH6 19 
A1BH6 C2  C15 C 0 1 N N N N N N -3.083  -17.149 21.978 -0.704 1.531  2.713  C2  A1BH6 20 
A1BH6 C3  C16 C 0 1 N N N N N N -1.876  -16.235 21.724 -0.602 1.679  4.233  C3  A1BH6 21 
A1BH6 C1  C17 C 0 1 N N N N N N -3.887  -17.351 20.685 -2.101 1.030  2.342  C1  A1BH6 22 
A1BH6 C6  C18 C 0 1 N N N N N N -3.265  -20.567 23.868 -0.351 4.095  -0.134 C6  A1BH6 23 
A1BH6 C7  C19 C 0 1 N N N N N N -2.650  -21.616 22.931 -0.461 3.938  -1.628 C7  A1BH6 24 
A1BH6 O1  O2  O 0 1 N N N N N N -3.336  -22.189 22.087 -0.599 2.836  -2.114 O1  A1BH6 25 
A1BH6 N1  N5  N 0 1 N N N N N N -1.368  -21.879 23.170 -0.406 5.024  -2.425 N1  A1BH6 26 
A1BH6 C8  C20 C 0 1 N N N N N N -0.697  -22.883 22.337 -0.512 4.872  -3.879 C8  A1BH6 27 
A1BH6 N3  N6  N 0 1 Y N N N N N -6.418  -18.238 22.849 1.590  -0.146 -0.573 N3  A1BH6 28 
A1BH6 C10 C21 C 0 1 Y N N N N N -7.649  -17.724 22.707 1.420  -1.408 -0.954 C10 A1BH6 29 
A1BH6 N4  N7  N 0 1 N N N N N N -8.316  -17.963 21.579 2.513  -2.179 -1.295 N4  A1BH6 30 
A1BH6 C11 C22 C 0 1 N N N N N N -9.714  -17.550 21.315 3.766  -1.407 -1.167 C11 A1BH6 31 
A1BH6 C19 C23 C 0 1 N N N N N N -7.720  -18.690 20.438 2.608  -3.377 -0.431 C19 A1BH6 32 
A1BH6 C18 C24 C 0 1 N N N N N N -8.949  -19.340 19.806 4.129  -3.631 -0.265 C18 A1BH6 33 
A1BH6 C12 C25 C 0 1 N N N N N N -9.999  -18.234 19.976 4.677  -2.194 -0.222 C12 A1BH6 34 
A1BH6 C17 C26 C 0 1 N N N N N N -10.023 -17.278 18.782 4.888  -1.602 1.168  C17 A1BH6 35 
A1BH6 C13 C27 C 0 1 N N N N N N -11.439 -18.648 19.685 6.179  -2.046 -0.447 C13 A1BH6 36 
A1BH6 N5  N8  N 0 1 N N N N N N -11.310 -17.903 18.416 6.120  -1.009 0.605  N5  A1BH6 37 
A1BH6 C14 C28 C 0 1 N N N N N N -12.067 -17.811 17.344 6.885  0.054  0.924  C14 A1BH6 38 
A1BH6 O2  O3  O 0 1 N N N N N N -11.769 -17.097 16.392 6.588  0.753  1.870  O2  A1BH6 39 
A1BH6 C15 C29 C 0 1 N N N N N N -13.367 -18.614 17.309 8.109  0.374  0.105  C15 A1BH6 40 
A1BH6 C16 C30 C 0 1 N N N N N N -14.705 -17.875 17.358 8.792  1.619  0.675  C16 A1BH6 41 
A1BH6 H1  H1  H 0 1 N N N N N N -6.783  -14.509 30.234 -4.659 0.390  1.317  H1  A1BH6 42 
A1BH6 H2  H2  H 0 1 N N N N N N -8.458  -13.861 30.244 -5.529 -1.011 1.988  H2  A1BH6 43 
A1BH6 H3  H3  H 0 1 N N N N N N -7.658  -14.404 32.550 -6.715 1.064  2.576  H3  A1BH6 44 
A1BH6 H4  H4  H 0 1 N N N N N N -9.069  -15.409 32.073 -6.793 1.528  0.859  H4  A1BH6 45 
A1BH6 H5  H5  H 0 1 N N N N N N -8.732  -17.666 31.414 -9.061 -1.224 0.066  H5  A1BH6 46 
A1BH6 H6  H6  H 0 1 N N N N N N -7.081  -18.371 31.478 -8.195 0.162  -0.640 H6  A1BH6 47 
A1BH6 H7  H7  H 0 1 N N N N N N -7.700  -17.855 29.129 -6.927 -2.374 0.493  H7  A1BH6 48 
A1BH6 H8  H8  H 0 1 N N N N N N -6.364  -16.780 29.664 -7.039 -1.931 -1.228 H8  A1BH6 49 
A1BH6 H9  H9  H 0 1 N N N N N N -7.288  -17.151 27.437 -3.189 0.036  -0.079 H9  A1BH6 50 
A1BH6 H10 H10 H 0 1 N N N N N N -9.623  -13.814 28.677 -5.752 -3.303 -0.829 H10 A1BH6 51 
A1BH6 H11 H11 H 0 1 N N N N N N -9.933  -13.173 26.315 -3.799 -4.679 -1.410 H11 A1BH6 52 
A1BH6 H12 H12 H 0 1 N N N N N N -8.961  -14.543 24.516 -1.539 -3.714 -1.335 H12 A1BH6 53 
A1BH6 H13 H13 H 0 1 N N N N N N -4.586  -19.110 24.954 1.603  2.297  0.152  H13 A1BH6 54 
A1BH6 H14 H14 H 0 1 N N N N N N -4.456  -19.603 22.325 -1.359 2.223  0.213  H14 A1BH6 55 
A1BH6 H15 H15 H 0 1 N N N N N N -2.100  -19.067 21.837 0.503  3.285  2.382  H15 A1BH6 56 
A1BH6 H16 H16 H 0 1 N N N N N N -1.932  -18.257 23.432 -1.252 3.580  2.333  H16 A1BH6 57 
A1BH6 H17 H17 H 0 1 N N N N N N -3.738  -16.646 22.705 0.043  0.817  2.367  H17 A1BH6 58 
A1BH6 H18 H18 H 0 1 N N N N N N -1.313  -16.102 22.660 -1.349 2.393  4.580  H18 A1BH6 59 
A1BH6 H19 H19 H 0 1 N N N N N N -1.224  -16.692 20.965 -0.778 0.712  4.704  H19 A1BH6 60 
A1BH6 H20 H20 H 0 1 N N N N N N -2.227  -15.256 21.365 0.393  2.036  4.497  H20 A1BH6 61 
A1BH6 H21 H21 H 0 1 N N N N N N -4.747  -18.007 20.886 -2.844 1.770  2.639  H21 A1BH6 62 
A1BH6 H22 H22 H 0 1 N N N N N N -4.247  -16.377 20.321 -2.156 0.872  1.265  H22 A1BH6 63 
A1BH6 H23 H23 H 0 1 N N N N N N -3.244  -17.813 19.922 -2.298 0.089  2.857  H23 A1BH6 64 
A1BH6 H24 H24 H 0 1 N N N N N N -4.104  -21.034 24.404 -1.163 4.728  0.226  H24 A1BH6 65 
A1BH6 H25 H25 H 0 1 N N N N N N -2.496  -20.256 24.590 0.605  4.555  0.114  H25 A1BH6 66 
A1BH6 H26 H26 H 0 1 N N N N N N -0.874  -21.404 23.899 -0.295 5.906  -2.037 H26 A1BH6 67 
A1BH6 H27 H27 H 0 1 N N N N N N 0.350   -22.985 22.657 -0.447 5.851  -4.352 H27 A1BH6 68 
A1BH6 H28 H28 H 0 1 N N N N N N -1.209  -23.850 22.445 0.299  4.239  -4.238 H28 A1BH6 69 
A1BH6 H29 H29 H 0 1 N N N N N N -0.729  -22.567 21.284 -1.469 4.411  -4.127 H29 A1BH6 70 
A1BH6 H30 H30 H 0 1 N N N N N N -9.799  -16.456 21.232 4.241  -1.303 -2.142 H30 A1BH6 71 
A1BH6 H31 H31 H 0 1 N N N N N N -10.393 -17.912 22.101 3.556  -0.422 -0.748 H31 A1BH6 72 
A1BH6 H32 H32 H 0 1 N N N N N N -6.997  -19.446 20.778 2.147  -3.182 0.537  H32 A1BH6 73 
A1BH6 H33 H33 H 0 1 N N N N N N -7.227  -18.000 19.737 2.130  -4.230 -0.913 H33 A1BH6 74 
A1BH6 H34 H34 H 0 1 N N N N N N -9.240  -20.256 20.341 4.337  -4.157 0.667  H34 A1BH6 75 
A1BH6 H35 H35 H 0 1 N N N N N N -8.779  -19.574 18.745 4.530  -4.178 -1.118 H35 A1BH6 76 
A1BH6 H36 H36 H 0 1 N N N N N N -9.213  -17.429 18.053 4.136  -0.867 1.453  H36 A1BH6 77 
A1BH6 H37 H37 H 0 1 N N N N N N -10.086 -16.212 19.045 5.070  -2.348 1.941  H37 A1BH6 78 
A1BH6 H38 H38 H 0 1 N N N N N N -12.186 -18.243 20.384 6.755  -2.928 -0.164 H38 A1BH6 79 
A1BH6 H39 H39 H 0 1 N N N N N N -11.593 -19.731 19.570 6.442  -1.663 -1.433 H39 A1BH6 80 
A1BH6 H40 H40 H 0 1 N N N N N N -13.358 -19.199 16.378 8.800  -0.468 0.141  H40 A1BH6 81 
A1BH6 H41 H41 H 0 1 N N N N N N -13.346 -19.297 18.171 7.817  0.561  -0.928 H41 A1BH6 82 
A1BH6 H44 H44 H 0 1 N Y N N N N -15.528 -18.604 17.324 9.085  1.433  1.708  H44 A1BH6 83 
A1BH6 H43 H43 H 0 1 N N N N N N -14.769 -17.293 18.289 9.678  1.851  0.083  H43 A1BH6 84 
A1BH6 H42 H42 H 0 1 N N N N N N -14.780 -17.196 16.496 8.101  2.461  0.639  H42 A1BH6 85 
# 
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 
A1BH6 O2  C14 DOUB N N 1  
A1BH6 C15 C14 SING N N 2  
A1BH6 C15 C16 SING N N 3  
A1BH6 C14 N5  SING N N 4  
A1BH6 N5  C17 SING N N 5  
A1BH6 N5  C13 SING N N 6  
A1BH6 C17 C12 SING N N 7  
A1BH6 C13 C12 SING N N 8  
A1BH6 C18 C12 SING N N 9  
A1BH6 C18 C19 SING N N 10 
A1BH6 C12 C11 SING N N 11 
A1BH6 C19 N4  SING N N 12 
A1BH6 C1  C2  SING N N 13 
A1BH6 C11 N4  SING N N 14 
A1BH6 N4  C10 SING N N 15 
A1BH6 C3  C2  SING N N 16 
A1BH6 C2  C4  SING N N 17 
A1BH6 O1  C7  DOUB N N 18 
A1BH6 C8  N1  SING N N 19 
A1BH6 C4  C5  SING N N 20 
A1BH6 C10 N3  DOUB Y N 21 
A1BH6 C10 N6  SING Y N 22 
A1BH6 N3  C9  SING Y N 23 
A1BH6 C7  N1  SING N N 24 
A1BH6 C7  C6  SING N N 25 
A1BH6 C5  C6  SING N N 26 
A1BH6 C5  N2  SING N N 27 
A1BH6 N6  C20 DOUB Y N 28 
A1BH6 C9  N2  SING N N 29 
A1BH6 C9  N8  DOUB Y N 30 
A1BH6 C20 N8  SING Y N 31 
A1BH6 C20 C21 SING N N 32 
A1BH6 C22 C21 DOUB Y N 33 
A1BH6 C22 C23 SING Y N 34 
A1BH6 C21 C30 SING Y N 35 
A1BH6 C23 C24 DOUB Y N 36 
A1BH6 C30 C25 DOUB Y N 37 
A1BH6 C24 C25 SING Y N 38 
A1BH6 C25 N7  SING N N 39 
A1BH6 N7  C29 SING N N 40 
A1BH6 N7  C26 SING N N 41 
A1BH6 C29 C28 SING N N 42 
A1BH6 C26 C27 SING N N 43 
A1BH6 C28 O3  SING N N 44 
A1BH6 C27 O3  SING N N 45 
A1BH6 C26 H1  SING N N 46 
A1BH6 C26 H2  SING N N 47 
A1BH6 C27 H3  SING N N 48 
A1BH6 C27 H4  SING N N 49 
A1BH6 C28 H5  SING N N 50 
A1BH6 C28 H6  SING N N 51 
A1BH6 C29 H7  SING N N 52 
A1BH6 C29 H8  SING N N 53 
A1BH6 C30 H9  SING N N 54 
A1BH6 C24 H10 SING N N 55 
A1BH6 C23 H11 SING N N 56 
A1BH6 C22 H12 SING N N 57 
A1BH6 N2  H13 SING N N 58 
A1BH6 C5  H14 SING N N 59 
A1BH6 C4  H15 SING N N 60 
A1BH6 C4  H16 SING N N 61 
A1BH6 C2  H17 SING N N 62 
A1BH6 C3  H18 SING N N 63 
A1BH6 C3  H19 SING N N 64 
A1BH6 C3  H20 SING N N 65 
A1BH6 C1  H21 SING N N 66 
A1BH6 C1  H22 SING N N 67 
A1BH6 C1  H23 SING N N 68 
A1BH6 C6  H24 SING N N 69 
A1BH6 C6  H25 SING N N 70 
A1BH6 N1  H26 SING N N 71 
A1BH6 C8  H27 SING N N 72 
A1BH6 C8  H28 SING N N 73 
A1BH6 C8  H29 SING N N 74 
A1BH6 C11 H30 SING N N 75 
A1BH6 C11 H31 SING N N 76 
A1BH6 C19 H32 SING N N 77 
A1BH6 C19 H33 SING N N 78 
A1BH6 C18 H34 SING N N 79 
A1BH6 C18 H35 SING N N 80 
A1BH6 C17 H36 SING N N 81 
A1BH6 C17 H37 SING N N 82 
A1BH6 C13 H38 SING N N 83 
A1BH6 C13 H39 SING N N 84 
A1BH6 C15 H40 SING N N 85 
A1BH6 C15 H41 SING N N 86 
A1BH6 C16 H44 SING N N 87 
A1BH6 C16 H43 SING N N 88 
A1BH6 C16 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 
A1BH6 SMILES           ACDLabs              14.52   "CNC(=O)CC(CC(C)C)Nc1nc(nc(n1)N1CCC2(CN(C2)C(=O)CC)C1)c1cc(ccc1)N1CCOCC1"                                                                                                                                                       
A1BH6 InChI            InChI                1.06    "InChI=1S/C30H44N8O3/c1-5-26(40)38-19-30(20-38)9-10-37(18-30)29-34-27(22-7-6-8-24(16-22)36-11-13-41-14-12-36)33-28(35-29)32-23(15-21(2)3)17-25(39)31-4/h6-8,16,21,23H,5,9-15,17-20H2,1-4H3,(H,31,39)(H,32,33,34,35)/t23-/m0/s1" 
A1BH6 InChIKey         InChI                1.06    DLRWVWTVIJRPNB-QHCPKHFHSA-N                                                                                                                                                                                                     
A1BH6 SMILES_CANONICAL CACTVS               3.385   "CCC(=O)N1CC2(CCN(C2)c3nc(N[C@@H](CC(C)C)CC(=O)NC)nc(n3)c4cccc(c4)N5CCOCC5)C1"                                                                                                                                                  
A1BH6 SMILES           CACTVS               3.385   "CCC(=O)N1CC2(CCN(C2)c3nc(N[CH](CC(C)C)CC(=O)NC)nc(n3)c4cccc(c4)N5CCOCC5)C1"                                                                                                                                                    
A1BH6 SMILES_CANONICAL "OpenEye OEToolkits" 3.1.0.0 "CCC(=O)N1CC2(C1)CCN(C2)c3nc(nc(n3)N[C@@H](CC(C)C)CC(=O)NC)c4cccc(c4)N5CCOCC5"                                                                                                                                                  
A1BH6 SMILES           "OpenEye OEToolkits" 3.1.0.0 "CCC(=O)N1CC2(C1)CCN(C2)c3nc(nc(n3)NC(CC(C)C)CC(=O)NC)c4cccc(c4)N5CCOCC5"                                                                                                                                                       
# 
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 
A1BH6 "SYSTEMATIC NAME" ACDLabs              14.52   "(3S)-N,5-dimethyl-3-({4-[3-(morpholin-4-yl)phenyl]-6-(2-propanoyl-2,6-diazaspiro[3.4]octan-6-yl)-1,3,5-triazin-2-yl}amino)hexanamide"     
A1BH6 "SYSTEMATIC NAME" "OpenEye OEToolkits" 3.1.0.0 "(3~{S})-~{N},5-dimethyl-3-[[4-(3-morpholin-4-ylphenyl)-6-(2-propanoyl-2,7-diazaspiro[3.4]octan-7-yl)-1,3,5-triazin-2-yl]amino]hexanamide" 
# 
_pdbx_chem_comp_pcm.pcm_id                             1 
_pdbx_chem_comp_pcm.comp_id                            A1BH6 
_pdbx_chem_comp_pcm.modified_residue_id                CYS 
_pdbx_chem_comp_pcm.type                               None 
_pdbx_chem_comp_pcm.category                           "Covalent chemical modification" 
_pdbx_chem_comp_pcm.position                           "Amino-acid side chain" 
_pdbx_chem_comp_pcm.polypeptide_position               "Any position" 
_pdbx_chem_comp_pcm.comp_id_linking_atom               C16 
_pdbx_chem_comp_pcm.modified_residue_id_linking_atom   SG 
_pdbx_chem_comp_pcm.uniprot_specific_ptm_accession     ? 
_pdbx_chem_comp_pcm.uniprot_generic_ptm_accession      ? 
# 
loop_
_pdbx_chem_comp_audit.comp_id 
_pdbx_chem_comp_audit.action_type 
_pdbx_chem_comp_audit.date 
_pdbx_chem_comp_audit.processing_site 
A1BH6 "Create component" 2024-11-21 RCSB 
A1BH6 "Modify PCM"       2024-11-25 RCSB 
A1BH6 "Initial release"  2025-02-26 RCSB 
# 
