data_UT3
# 
_chem_comp.id                                    UT3 
_chem_comp.name                                  "(4Z,6E,8S,9S,10R,11R,12R,13R,14R,15S,16S,17Z,22R,23S)-4,8,10,12,14,16,18,22-octamethyl-9,11,13,15,23,26,28-heptakis(oxidanyl)-2-azabicyclo[22.3.1]octacosa-1(27),4,6,17,24(28),25-hexaene-3,19,21-trione" 
_chem_comp.type                                  non-polymer 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C35 H51 N O10" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2023-09-11 
_chem_comp.pdbx_modified_date                    2026-06-05 
_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                        645.780 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     UT3 
_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        8WAH 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  PDBC 
_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_backbone_atom_flag 
_chem_comp_atom.pdbx_n_terminal_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 
UT3 C02 C1  C 0 1 N N N N N N 20.018 -4.030  19.610 20.018 -4.030  19.610 C02 UT3 1  
UT3 C03 C2  C 0 1 N N N N N N 20.753 -5.194  20.257 20.753 -5.194  20.257 C03 UT3 2  
UT3 C04 C3  C 0 1 N N N N N N 22.195 -4.970  20.686 22.195 -4.970  20.686 C04 UT3 3  
UT3 C05 C4  C 0 1 N N N N N N 20.199 -6.354  20.518 20.199 -6.354  20.518 C05 UT3 4  
UT3 C06 C5  C 0 1 N N N N N N 18.771 -6.703  20.134 18.771 -6.703  20.134 C06 UT3 5  
UT3 C07 C6  C 0 1 N N N N N N 18.315 -7.910  20.358 18.315 -7.910  20.358 C07 UT3 6  
UT3 C08 C7  C 0 1 N N S N N N 16.908 -8.218  19.887 16.908 -8.218  19.887 C08 UT3 7  
UT3 C09 C8  C 0 1 N N S N N N 17.118 -8.927  18.554 17.118 -8.927  18.554 C09 UT3 8  
UT3 C11 C9  C 0 1 N N R N N N 17.310 -7.955  17.395 17.310 -7.955  17.395 C11 UT3 9  
UT3 C12 C10 C 0 1 N N N N N N 18.776 -7.869  16.979 18.776 -7.869  16.979 C12 UT3 10 
UT3 C13 C11 C 0 1 N N R N N N 16.546 -8.595  16.256 16.546 -8.595  16.256 C13 UT3 11 
UT3 C15 C12 C 0 1 N N R N N N 16.196 -7.591  15.182 16.196 -7.591  15.182 C15 UT3 12 
UT3 C16 C13 C 0 1 N N R N N N 15.345 -6.560  15.952 15.345 -6.560  15.952 C16 UT3 13 
UT3 C18 C14 C 0 1 N N R N N N 14.960 -5.225  15.273 14.960 -5.225  15.273 C18 UT3 14 
UT3 C19 C15 C 0 1 N N N N N N 14.609 -5.319  13.777 14.609 -5.319  13.777 C19 UT3 15 
UT3 C20 C16 C 0 1 N N S N N N 15.941 -4.086  15.665 15.941 -4.086  15.665 C20 UT3 16 
UT3 C22 C17 C 0 1 N N N N N N 15.489 -8.441  14.119 15.489 -8.441  14.119 C22 UT3 17 
UT3 C23 C18 C 0 1 N N N N N N 16.235 -9.193  20.837 16.235 -9.193  20.837 C23 UT3 18 
UT3 C25 C19 C 0 1 Y N N N N N 20.173 -1.480  19.362 20.173 -1.480  19.362 C25 UT3 19 
UT3 C26 C20 C 0 1 Y N N N N N 19.788 -1.271  18.032 19.788 -1.271  18.032 C26 UT3 20 
UT3 C28 C21 C 0 1 Y N N N N N 19.332 0.011   17.660 19.332 0.011   17.660 C28 UT3 21 
UT3 C29 C22 C 0 1 N N S N N N 18.824 0.488   16.285 18.824 0.488   16.285 C29 UT3 22 
UT3 C31 C23 C 0 1 N N R N N N 19.703 0.444   15.017 19.703 0.444   15.017 C31 UT3 23 
UT3 C32 C24 C 0 1 N N N N N N 20.658 -0.748  14.878 20.658 -0.748  14.878 C32 UT3 24 
UT3 C33 C25 C 0 1 N N N N N N 18.728 0.480   13.826 18.728 0.480   13.826 C33 UT3 25 
UT3 C34 C26 C 0 1 N N N N N N 17.212 0.440   14.070 17.212 0.440   14.070 C34 UT3 26 
UT3 C35 C27 C 0 1 N N N N N N 16.594 -0.933  14.370 16.594 -0.933  14.370 C35 UT3 27 
UT3 C36 C28 C 0 1 N N N N N N 16.641 -1.998  13.268 16.641 -1.998  13.268 C36 UT3 28 
UT3 C37 C29 C 0 1 N N N N N N 16.359 -1.598  11.826 16.359 -1.598  11.826 C37 UT3 29 
UT3 C38 C30 C 0 1 N N N N N N 16.949 -3.257  13.486 16.949 -3.257  13.486 C38 UT3 30 
UT3 C39 C31 C 0 1 N N S N N N 17.257 -3.833  14.868 17.257 -3.833  14.868 C39 UT3 31 
UT3 C40 C32 C 0 1 N N N N N N 18.231 -5.007  14.701 18.231 -5.007  14.701 C40 UT3 32 
UT3 C43 C33 C 0 1 Y N N N N N 19.246 1.006   18.625 19.246 1.006   18.625 C43 UT3 33 
UT3 C44 C34 C 0 1 Y N N N N N 19.625 0.790   19.935 19.625 0.790   19.935 C44 UT3 34 
UT3 C46 C35 C 0 1 Y N N N N N 20.085 -0.462  20.310 20.085 -0.462  20.310 C46 UT3 35 
UT3 N24 N1  N 0 1 N N N N N N 20.676 -2.759  19.832 20.676 -2.759  19.832 N24 UT3 36 
UT3 O01 O1  O 0 1 N N N N N N 19.000 -4.134  18.983 19.000 -4.134  18.983 O01 UT3 37 
UT3 O10 O2  O 0 1 N N N N N N 18.261 -9.733  18.636 18.261 -9.733  18.636 O10 UT3 38 
UT3 O14 O3  O 0 1 N N N N N N 15.337 -9.054  16.792 15.337 -9.054  16.792 O14 UT3 39 
UT3 O17 O4  O 0 1 N N N N N N 14.179 -7.170  16.446 14.179 -7.170  16.446 O17 UT3 40 
UT3 O21 O5  O 0 1 N N N N N N 16.232 -4.196  17.037 16.232 -4.196  17.037 O21 UT3 41 
UT3 O27 O6  O 0 1 N N N N N N 19.888 -2.354  17.139 19.888 -2.354  17.139 O27 UT3 42 
UT3 O30 O7  O 0 1 N N N N N N 18.485 1.849   16.456 18.485 1.849   16.456 O30 UT3 43 
UT3 O41 O8  O 0 1 N N N N N N 16.084 -1.120  15.435 16.084 -1.120  15.435 O41 UT3 44 
UT3 O42 O9  O 0 1 N N N N N N 19.136 0.565   12.713 19.136 0.565   12.713 O42 UT3 45 
UT3 O45 O10 O 0 1 N N N N N N 19.532 1.851   20.853 19.532 1.851   20.853 O45 UT3 46 
UT3 H1  H1  H 0 1 N N N N N N 22.592 -5.893  21.134 22.592 -5.893  21.134 H1  UT3 47 
UT3 H2  H2  H 0 1 N N N N N N 22.800 -4.698  19.809 22.800 -4.698  19.809 H2  UT3 48 
UT3 H3  H3  H 0 1 N N N N N N 22.235 -4.157  21.425 22.235 -4.157  21.425 H3  UT3 49 
UT3 H4  H4  H 0 1 N N N N N N 20.788 -7.099  21.032 20.788 -7.099  21.032 H4  UT3 50 
UT3 H5  H5  H 0 1 N N N N N N 18.135 -5.959  19.678 18.135 -5.959  19.678 H5  UT3 51 
UT3 H6  H6  H 0 1 N N N N N N 18.917 -8.655  20.858 18.917 -8.655  20.858 H6  UT3 52 
UT3 H7  H7  H 0 1 N N N N N N 16.314 -7.301  19.764 16.314 -7.300  19.764 H7  UT3 53 
UT3 H8  H8  H 0 1 N N N N N N 16.233 -9.546  18.346 16.233 -9.546  18.346 H8  UT3 54 
UT3 H9  H9  H 0 1 N N N N N N 16.907 -6.961  17.639 16.907 -6.961  17.639 H9  UT3 55 
UT3 H10 H10 H 0 1 N N N N N N 19.361 -7.407  17.788 19.361 -7.407  17.788 H10 UT3 56 
UT3 H11 H11 H 0 1 N N N N N N 19.161 -8.880  16.780 19.161 -8.880  16.781 H11 UT3 57 
UT3 H12 H12 H 0 1 N N N N N N 18.863 -7.258  16.068 18.863 -7.258  16.068 H12 UT3 58 
UT3 H13 H13 H 0 1 N N N N N N 17.136 -9.417  15.824 17.136 -9.417  15.824 H13 UT3 59 
UT3 H14 H14 H 0 1 N N N N N N 17.100 -7.119  14.769 17.100 -7.119  14.769 H14 UT3 60 
UT3 H15 H15 H 0 1 N N N N N N 15.951 -6.277  16.825 15.951 -6.277  16.825 H15 UT3 61 
UT3 H16 H16 H 0 1 N N N N N N 14.013 -4.941  15.755 14.013 -4.941  15.755 H16 UT3 62 
UT3 H17 H17 H 0 1 N N N N N N 13.912 -6.155  13.615 13.912 -6.155  13.615 H17 UT3 63 
UT3 H18 H18 H 0 1 N N N N N N 14.137 -4.380  13.452 14.137 -4.380  13.451 H18 UT3 64 
UT3 H19 H19 H 0 1 N N N N N N 15.527 -5.489  13.195 15.527 -5.489  13.195 H19 UT3 65 
UT3 H20 H20 H 0 1 N N N N N N 15.359 -3.160  15.545 15.359 -3.160  15.545 H20 UT3 66 
UT3 H21 H21 H 0 1 N N N N N N 16.214 -9.126  13.655 16.214 -9.127  13.655 H21 UT3 67 
UT3 H22 H22 H 0 1 N N N N N N 14.684 -9.023  14.591 14.684 -9.023  14.591 H22 UT3 68 
UT3 H23 H23 H 0 1 N N N N N N 15.062 -7.783  13.348 15.062 -7.783  13.348 H23 UT3 69 
UT3 H24 H24 H 0 1 N N N N N N 16.072 -8.705  21.809 16.072 -8.705  21.809 H24 UT3 70 
UT3 H25 H25 H 0 1 N N N N N N 15.268 -9.506  20.417 15.268 -9.506  20.417 H25 UT3 71 
UT3 H26 H26 H 0 1 N N N N N N 16.878 -10.075 20.973 16.878 -10.075 20.973 H26 UT3 72 
UT3 H27 H27 H 0 1 N N N N N N 17.908 -0.079  16.063 17.908 -0.079  16.063 H27 UT3 73 
UT3 H28 H28 H 0 1 N N N N N N 20.304 1.365   14.991 20.304 1.365   14.991 H28 UT3 74 
UT3 H29 H29 H 0 1 N N N N N N 21.350 -0.766  15.733 21.350 -0.766  15.733 H29 UT3 75 
UT3 H30 H30 H 0 1 N N N N N N 20.078 -1.682  14.857 20.078 -1.682  14.857 H30 UT3 76 
UT3 H31 H31 H 0 1 N N N N N N 21.231 -0.652  13.944 21.231 -0.651  13.944 H31 UT3 77 
UT3 H32 H32 H 0 1 N N N N N N 16.995 1.096   14.926 16.996 1.096   14.926 H32 UT3 78 
UT3 H33 H33 H 0 1 N N N N N N 16.720 0.837   13.170 16.720 0.837   13.170 H33 UT3 79 
UT3 H34 H34 H 0 1 N N N N N N 16.116 -0.526  11.783 16.116 -0.526  11.783 H34 UT3 80 
UT3 H35 H35 H 0 1 N N N N N N 17.248 -1.797  11.210 17.248 -1.797  11.210 H35 UT3 81 
UT3 H36 H36 H 0 1 N N N N N N 15.509 -2.182  11.443 15.509 -2.182  11.443 H36 UT3 82 
UT3 H37 H37 H 0 1 N N N N N N 16.987 -3.925  12.638 16.987 -3.925  12.638 H37 UT3 83 
UT3 H38 H38 H 0 1 N N N N N N 17.803 -3.052  15.418 17.803 -3.052  15.418 H38 UT3 84 
UT3 H39 H39 H 0 1 N N N N N N 18.464 -5.434  15.688 18.464 -5.434  15.688 H39 UT3 85 
UT3 H40 H40 H 0 1 N N N N N N 17.770 -5.779  14.067 17.770 -5.779  14.067 H40 UT3 86 
UT3 H41 H41 H 0 1 N N N N N N 19.158 -4.650  14.228 19.158 -4.650  14.228 H41 UT3 87 
UT3 H42 H42 H 0 1 N N N N N N 18.871 1.979   18.342 18.871 1.979   18.342 H42 UT3 88 
UT3 H43 H43 H 0 1 N N N N N N 20.374 -0.649  21.334 20.375 -0.649  21.334 H43 UT3 89 
UT3 H44 H44 H 0 1 N N N N N N 21.535 -2.762  20.344 21.535 -2.762  20.344 H44 UT3 90 
UT3 H45 H45 H 0 1 N N N N N N 18.164 -10.348 19.353 18.164 -10.349 19.353 H45 UT3 91 
UT3 H46 H46 H 0 1 N N N N N N 15.514 -9.691  17.475 15.514 -9.691  17.475 H46 UT3 92 
UT3 H47 H47 H 0 1 N N N N N N 13.661 -6.529  16.918 13.661 -6.529  16.918 H47 UT3 93 
UT3 H48 H48 H 0 1 N N N N N N 15.429 -4.350  17.520 15.429 -4.350  17.520 H48 UT3 94 
UT3 H49 H49 H 0 1 N N N N N N 19.614 -3.152  17.576 19.614 -3.152  17.576 H49 UT3 95 
UT3 H50 H50 H 0 1 N N N N N N 17.939 1.945   17.227 17.939 1.945   17.227 H50 UT3 96 
UT3 H51 H51 H 0 1 N N N N N N 19.824 1.557   21.708 19.824 1.557   21.708 H51 UT3 97 
# 
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 
UT3 C37 C36 SING N N 1  
UT3 O42 C33 DOUB N N 2  
UT3 C36 C38 DOUB N Z 3  
UT3 C36 C35 SING N N 4  
UT3 C38 C39 SING N N 5  
UT3 C19 C18 SING N N 6  
UT3 C33 C34 SING N N 7  
UT3 C33 C31 SING N N 8  
UT3 C34 C35 SING N N 9  
UT3 C22 C15 SING N N 10 
UT3 C35 O41 DOUB N N 11 
UT3 C40 C39 SING N N 12 
UT3 C39 C20 SING N N 13 
UT3 C32 C31 SING N N 14 
UT3 C31 C29 SING N N 15 
UT3 C15 C16 SING N N 16 
UT3 C15 C13 SING N N 17 
UT3 C18 C20 SING N N 18 
UT3 C18 C16 SING N N 19 
UT3 C20 O21 SING N N 20 
UT3 C16 O17 SING N N 21 
UT3 C13 O14 SING N N 22 
UT3 C13 C11 SING N N 23 
UT3 C29 O30 SING N N 24 
UT3 C29 C28 SING N N 25 
UT3 C12 C11 SING N N 26 
UT3 O27 C26 SING N N 27 
UT3 C11 C09 SING N N 28 
UT3 C28 C26 DOUB Y N 29 
UT3 C28 C43 SING Y N 30 
UT3 C26 C25 SING Y N 31 
UT3 C09 O10 SING N N 32 
UT3 C09 C08 SING N N 33 
UT3 C43 C44 DOUB Y N 34 
UT3 O01 C02 DOUB N N 35 
UT3 C25 N24 SING N N 36 
UT3 C25 C46 DOUB Y N 37 
UT3 C02 N24 SING N N 38 
UT3 C02 C03 SING N N 39 
UT3 C08 C07 SING N N 40 
UT3 C08 C23 SING N N 41 
UT3 C44 C46 SING Y N 42 
UT3 C44 O45 SING N N 43 
UT3 C06 C07 DOUB N E 44 
UT3 C06 C05 SING N N 45 
UT3 C03 C05 DOUB N Z 46 
UT3 C03 C04 SING N N 47 
UT3 C04 H1  SING N N 48 
UT3 C04 H2  SING N N 49 
UT3 C04 H3  SING N N 50 
UT3 C05 H4  SING N N 51 
UT3 C06 H5  SING N N 52 
UT3 C07 H6  SING N N 53 
UT3 C08 H7  SING N N 54 
UT3 C09 H8  SING N N 55 
UT3 C11 H9  SING N N 56 
UT3 C12 H10 SING N N 57 
UT3 C12 H11 SING N N 58 
UT3 C12 H12 SING N N 59 
UT3 C13 H13 SING N N 60 
UT3 C15 H14 SING N N 61 
UT3 C16 H15 SING N N 62 
UT3 C18 H16 SING N N 63 
UT3 C19 H17 SING N N 64 
UT3 C19 H18 SING N N 65 
UT3 C19 H19 SING N N 66 
UT3 C20 H20 SING N N 67 
UT3 C22 H21 SING N N 68 
UT3 C22 H22 SING N N 69 
UT3 C22 H23 SING N N 70 
UT3 C23 H24 SING N N 71 
UT3 C23 H25 SING N N 72 
UT3 C23 H26 SING N N 73 
UT3 C29 H27 SING N N 74 
UT3 C31 H28 SING N N 75 
UT3 C32 H29 SING N N 76 
UT3 C32 H30 SING N N 77 
UT3 C32 H31 SING N N 78 
UT3 C34 H32 SING N N 79 
UT3 C34 H33 SING N N 80 
UT3 C37 H34 SING N N 81 
UT3 C37 H35 SING N N 82 
UT3 C37 H36 SING N N 83 
UT3 C38 H37 SING N N 84 
UT3 C39 H38 SING N N 85 
UT3 C40 H39 SING N N 86 
UT3 C40 H40 SING N N 87 
UT3 C40 H41 SING N N 88 
UT3 C43 H42 SING N N 89 
UT3 C46 H43 SING N N 90 
UT3 N24 H44 SING N N 91 
UT3 O10 H45 SING N N 92 
UT3 O14 H46 SING N N 93 
UT3 O17 H47 SING N N 94 
UT3 O21 H48 SING N N 95 
UT3 O27 H49 SING N N 96 
UT3 O30 H50 SING N N 97 
UT3 O45 H51 SING N N 98 
# 
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 
UT3 InChI            InChI                1.06  "InChI=1S/C35H51NO10/c1-16-10-9-11-17(2)35(46)36-26-14-24(37)13-25(34(26)45)33(44)20(5)28(39)15-27(38)18(3)12-19(4)30(41)22(7)32(43)23(8)31(42)21(6)29(16)40/h9-14,16,19-23,29-33,37,40-45H,15H2,1-8H3,(H,36,46)/b10-9+,17-11-,18-12-/t16-,19-,20-,21+,22+,23+,29-,30-,31+,32+,33-/m0/s1" 
UT3 InChIKey         InChI                1.06  DCAQDNOEKBBUAJ-BIVYTFGRSA-N                                                                                                                                                                                                                                                               
UT3 SMILES_CANONICAL CACTVS               3.385 "C[C@H]1\C=C\C=C(C)/C(=O)Nc2cc(O)cc([C@@H](O)[C@@H](C)C(=O)CC(=O)\C(=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@H](C)[C@H](O)[C@H](C)[C@H]1O)C)c2O"                                                                                                                                           
UT3 SMILES           CACTVS               3.385 "C[CH]1C=CC=C(C)C(=O)Nc2cc(O)cc([CH](O)[CH](C)C(=O)CC(=O)C(=C[CH](C)[CH](O)[CH](C)[CH](O)[CH](C)[CH](O)[CH](C)[CH]1O)C)c2O"                                                                                                                                                               
UT3 SMILES_CANONICAL "OpenEye OEToolkits" 2.0.7 "C[C@H]1/C=C/C=C(\C(=O)Nc2cc(cc(c2O)[C@H]([C@H](C(=O)CC(=O)/C(=C\[C@@H]([C@@H]([C@H]([C@H]([C@@H]([C@@H]([C@@H]([C@H]1O)C)O)C)O)C)O)C)/C)C)O)O)/C"                                                                                                                                        
UT3 SMILES           "OpenEye OEToolkits" 2.0.7 "CC1C=CC=C(C(=O)Nc2cc(cc(c2O)C(C(C(=O)CC(=O)C(=CC(C(C(C(C(C(C(C1O)C)O)C)O)C)O)C)C)C)O)O)C"                                                                                                                                                                                                
# 
_pdbx_chem_comp_identifier.comp_id           UT3 
_pdbx_chem_comp_identifier.type              "SYSTEMATIC NAME" 
_pdbx_chem_comp_identifier.program           "OpenEye OEToolkits" 
_pdbx_chem_comp_identifier.program_version   2.0.7 
_pdbx_chem_comp_identifier.identifier        "(4~{Z},6~{E},8~{S},9~{S},10~{R},11~{R},12~{R},13~{R},14~{R},15~{S},16~{S},17~{Z},22~{R},23~{S})-4,8,10,12,14,16,18,22-octamethyl-9,11,13,15,23,26,28-heptakis(oxidanyl)-2-azabicyclo[22.3.1]octacosa-1(27),4,6,17,24(28),25-hexaene-3,19,21-trione" 
# 
loop_
_pdbx_chem_comp_audit.comp_id 
_pdbx_chem_comp_audit.action_type 
_pdbx_chem_comp_audit.date 
_pdbx_chem_comp_audit.processing_site 
UT3 "Create component" 2023-09-11 PDBC 
UT3 "Initial release"  2026-06-10 RCSB 
# 
