data_A1H75
# 
_chem_comp.id                                    A1H75 
_chem_comp.name                                  "(1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(1~{R},3~{a}~{S},7~{a}~{R})-7~{a}-methyl-1-[(1~{R})-5-methyl-1-[(1~{S},2~{S})-2-(3-methyl-3-oxidanyl-butyl)cyclopropyl]-5-oxidanyl-hexyl]-2,3,3~{a},5,6,7-hexahydro-1~{H}-inden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol" 
_chem_comp.type                                  non-polymer 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C34 H56 O4" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2024-04-10 
_chem_comp.pdbx_modified_date                    2024-06-14 
_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                        528.806 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     A1H75 
_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        9EYR 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  PDBE 
# 
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 
A1H75 C4   C1  C 0 1 N N S N N N 28.178 -17.048 -4.846  0.140  -0.363 1.755  C4   A1H75 1  
A1H75 C5   C2  C 0 1 N N R N N N 27.386 -16.701 -6.132  1.200  -0.096 0.649  C5   A1H75 2  
A1H75 C6   C3  C 0 1 N N N N N N 27.882 -15.310 -6.569  2.095  -1.312 0.570  C6   A1H75 3  
A1H75 C7   C4  C 0 1 N N N N N N 27.452 -18.286 -4.286  -0.528 1.009  1.866  C7   A1H75 4  
A1H75 C8   C5  C 0 1 N N N N N N 25.981 -18.116 -4.740  0.681  1.985  1.807  C8   A1H75 5  
A1H75 C10  C6  C 0 1 N N N N N N 27.712 -17.760 -7.200  0.490  0.096  -0.693 C10  A1H75 6  
A1H75 C13  C7  C 0 1 N N S N N N 23.598 -15.838 -5.930  3.233  1.162  -0.986 C13  A1H75 7  
A1H75 C15  C8  C 0 1 N N N N N N 23.758 -16.509 -8.895  0.070  3.195  -0.161 C15  A1H75 8  
A1H75 C17  C9  C 0 1 N N N N N N 22.447 -18.119 -10.454 -1.804 4.845  -0.242 C17  A1H75 9  
A1H75 C21  C10 C 0 1 N N R N N N 23.151 -15.799 -4.500  4.589  0.817  -0.365 C21  A1H75 10 
A1H75 C22  C11 C 0 1 N N N N N N 22.703 -14.477 -3.871  5.182  -0.557 -0.682 C22  A1H75 11 
A1H75 C24  C12 C 0 1 N N N N N N 20.376 -14.490 -2.700  7.078  -2.117 -0.218 C24  A1H75 12 
A1H75 C26  C13 C 0 1 N N N N N N 19.979 -13.166 -3.332  6.036  -3.200 0.067  C26  A1H75 13 
A1H75 C28  C14 C 0 1 N N N N N N 31.836 -18.215 -5.303  -2.805 -2.498 0.560  C28  A1H75 14 
A1H75 C1   C15 C 0 1 N N N N N N 29.399 -15.235 -6.736  1.251  -2.473 0.018  C1   A1H75 15 
A1H75 C11  C16 C 0 1 N N N N N N 30.436 -18.146 -5.029  -2.026 -1.368 1.072  C11  A1H75 16 
A1H75 C12  C17 C 0 1 N N R N N N 24.691 -16.716 -6.482  2.274  2.018  -0.157 C12  A1H75 17 
A1H75 C14  C18 C 0 1 N N N N N N 24.961 -16.401 -7.962  1.056  2.387  -1.007 C14  A1H75 18 
A1H75 C16  C19 C 0 1 N N N N N N 23.388 -17.947 -9.258  -0.903 3.936  -1.080 C16  A1H75 19 
A1H75 C18  C20 C 0 1 N N N N N N 22.343 -19.575 -10.876 -2.809 5.549  -1.156 C18  A1H75 20 
A1H75 C19  C21 C 0 1 N N N N N N 22.877 -17.246 -11.622 -2.557 4.005  0.792  C19  A1H75 21 
A1H75 C2   C22 C 0 1 N N N N N N 30.144 -15.673 -5.470  0.043  -2.768 0.905  C2   A1H75 22 
A1H75 C23  C23 C 0 1 N N N N N N 21.894 -14.616 -2.577  6.484  -0.743 0.099  C23  A1H75 23 
A1H75 C25  C24 C 0 1 N N N N N N 19.703 -14.668 -1.349  8.311  -2.353 0.656  C25  A1H75 24 
A1H75 C29  C25 C 0 1 N N N N N N 32.602 -19.321 -5.541  -4.138 -2.380 0.396  C29  A1H75 25 
A1H75 C3   C26 C 0 1 N N N N N N 29.670 -17.042 -5.075  -0.708 -1.486 1.235  C3   A1H75 26 
A1H75 C30  C27 C 0 1 N N N N N N 34.092 -19.180 -5.755  -4.979 -3.525 -0.131 C30  A1H75 27 
A1H75 C31  C28 C 0 1 N N R N N N 34.957 -20.297 -5.198  -5.914 -2.979 -1.215 C31  A1H75 28 
A1H75 C32  C29 C 0 1 N N N N N N 34.416 -21.641 -5.642  -6.780 -1.860 -0.636 C32  A1H75 29 
A1H75 C33  C30 C 0 1 N N S N N N 32.972 -21.805 -5.198  -5.901 -0.661 -0.266 C33  A1H75 30 
A1H75 C34  C31 C 0 1 N N N N N N 32.114 -20.681 -5.728  -4.851 -1.128 0.728  C34  A1H75 31 
A1H75 C35  C32 C 0 1 N N N N N N 30.987 -20.954 -6.359  -4.583 -0.446 1.841  C35  A1H75 32 
A1H75 C38  C33 C 0 1 N N N N N N 22.273 -16.421 -5.543  4.506  1.832  -1.508 C38  A1H75 33 
A1H75 C9   C34 C 0 1 N N R N N N 25.949 -16.807 -5.558  1.817  1.228  1.071  C9   A1H75 34 
A1H75 O20  O1  O 0 1 N N N N N N 21.132 -17.690 -10.051 -1.005 5.821  0.428  O20  A1H75 35 
A1H75 O27  O2  O 0 1 N N N N N N 19.907 -15.544 -3.561  7.453  -2.167 -1.595 O27  A1H75 36 
A1H75 O36  O3  O 0 1 N N N N N N 32.458 -23.045 -5.674  -5.266 -0.150 -1.439 O36  A1H75 37 
A1H75 O37  O4  O 0 1 N N N N N N 34.971 -20.243 -3.769  -6.754 -4.032 -1.692 O37  A1H75 38 
A1H75 H4   H1  H 0 1 N N N N N N 27.972 -16.232 -4.138  0.619  -0.637 2.695  H4   A1H75 39 
A1H75 H6B  H2  H 0 1 N N N N N N 27.578 -14.576 -5.809  2.932  -1.112 -0.098 H6B  A1H75 40 
A1H75 H6A  H3  H 0 1 N N N N N N 27.412 -15.058 -7.531  2.466  -1.562 1.564  H6A  A1H75 41 
A1H75 H7A  H4  H 0 1 N N N N N N 27.882 -19.209 -4.701  -1.202 1.179  1.027  H7A  A1H75 42 
A1H75 H7B  H5  H 0 1 N N N N N N 27.519 -18.312 -3.188  -1.057 1.105  2.814  H7B  A1H75 43 
A1H75 H8A  H6  H 0 1 N N N N N N 25.671 -18.967 -5.364  0.410  2.884  1.253  H8A  A1H75 44 
A1H75 H8B  H7  H 0 1 N N N N N N 25.316 -18.040 -3.867  0.999  2.248  2.816  H8B  A1H75 45 
A1H75 H10C H8  H 0 0 N N N N N N 27.159 -17.533 -8.123  -0.253 0.888  -0.600 H10C A1H75 46 
A1H75 H10A H9  H 0 0 N N N N N N 28.792 -17.751 -7.408  1.220  0.371  -1.454 H10A A1H75 47 
A1H75 H10B H10 H 0 0 N N N N N N 27.418 -18.754 -6.832  -0.002 -0.832 -0.980 H10B A1H75 48 
A1H75 H13  H11 H 0 1 N N N N N N 23.518 -14.867 -6.441  2.764  0.410  -1.620 H13  A1H75 49 
A1H75 H15B H12 H 0 0 N N N N N N 22.893 -16.042 -8.401  -0.487 2.521  0.491  H15B A1H75 50 
A1H75 H15A H13 H 0 0 N N N N N N 23.988 -15.965 -9.823  0.617  3.916  0.446  H15A A1H75 51 
A1H75 H21  H14 H 0 1 N N N N N N 23.658 -16.498 -3.818  4.796  1.200  0.634  H21  A1H75 52 
A1H75 H22A H15 H 0 0 N N N N N N 23.602 -13.883 -3.649  4.473  -1.334 -0.396 H22A A1H75 53 
A1H75 H22B H16 H 0 0 N N N N N N 22.082 -13.943 -4.606  5.386  -0.627 -1.750 H22B A1H75 54 
A1H75 H26B H17 H 0 0 N N N N N N 18.883 -13.108 -3.405  5.749  -3.161 1.118  H26B A1H75 55 
A1H75 H26A H18 H 0 0 N N N N N N 20.349 -12.337 -2.710  5.157  -3.032 -0.555 H26A A1H75 56 
A1H75 H26C H19 H 0 0 N N N N N N 20.418 -13.094 -4.338  6.458  -4.179 -0.158 H26C A1H75 57 
A1H75 H28  H20 H 0 1 N N N N N N 32.357 -17.269 -5.325  -2.311 -3.427 0.314  H28  A1H75 58 
A1H75 H1B  H21 H 0 1 N N N N N N 29.679 -14.197 -6.970  0.903  -2.215 -0.982 H1B  A1H75 59 
A1H75 H1A  H22 H 0 1 N N N N N N 29.697 -15.891 -7.567  1.873  -3.366 -0.043 H1A  A1H75 60 
A1H75 H11  H23 H 0 1 N N N N N N 29.945 -19.069 -4.759  -2.520 -0.440 1.319  H11  A1H75 61 
A1H75 H12  H24 H 0 1 N N N N N N 24.272 -17.733 -6.481  2.782  2.927  0.164  H12  A1H75 62 
A1H75 H14B H25 H 0 0 N N N N N N 25.344 -15.372 -8.023  0.571  1.478  -1.361 H14B A1H75 63 
A1H75 H14A H26 H 0 0 N N N N N N 25.730 -17.101 -8.321  1.377  2.985  -1.860 H14A A1H75 64 
A1H75 H16A H27 H 0 0 N N N N N N 24.319 -18.487 -9.483  -0.342 4.538  -1.794 H16A A1H75 65 
A1H75 H16B H28 H 0 0 N N N N N N 22.903 -18.401 -8.381  -1.516 3.213  -1.618 H16B A1H75 66 
A1H75 H18C H29 H 0 0 N N N N N N 21.661 -19.661 -11.735 -3.451 6.197  -0.559 H18C A1H75 67 
A1H75 H18B H30 H 0 0 N N N N N N 23.339 -19.946 -11.160 -2.273 6.148  -1.893 H18B A1H75 68 
A1H75 H18A H31 H 0 0 N N N N N N 21.954 -20.173 -10.038 -3.419 4.805  -1.667 H18A A1H75 69 
A1H75 H19C H32 H 0 0 N N N N N N 22.184 -17.391 -12.464 -3.093 3.202  0.287  H19C A1H75 70 
A1H75 H19A H33 H 0 0 N N N N N N 22.864 -16.190 -11.314 -1.847 3.579  1.500  H19A A1H75 71 
A1H75 H19B H34 H 0 0 N N N N N N 23.895 -17.525 -11.933 -3.267 4.636  1.325  H19B A1H75 72 
A1H75 H2A  H35 H 0 1 N N N N N N 31.226 -15.700 -5.669  -0.627 -3.452 0.384  H2A  A1H75 73 
A1H75 H2B  H36 H 0 1 N N N N N N 29.938 -14.962 -4.656  0.382  -3.233 1.830  H2B  A1H75 74 
A1H75 H23A H37 H 0 0 N N N N N N 22.113 -15.607 -2.152  7.194  0.034  -0.187 H23A A1H75 75 
A1H75 H23B H38 H 0 0 N N N N N N 22.238 -13.835 -1.883  6.280  -0.672 1.168  H23B A1H75 76 
A1H75 H25B H39 H 0 0 N N N N N N 18.613 -14.573 -1.466  8.734  -3.332 0.430  H25B A1H75 77 
A1H75 H25C H40 H 0 0 N N N N N N 19.943 -15.664 -0.948  9.054  -1.581 0.453  H25C A1H75 78 
A1H75 H25A H41 H 0 0 N N N N N N 20.066 -13.896 -0.654  8.025  -2.315 1.707  H25A A1H75 79 
A1H75 H30A H42 H 0 0 N N N N N N 34.272 -19.125 -6.839  -4.330 -4.291 -0.558 H30A A1H75 80 
A1H75 H30B H43 H 0 0 N N N N N N 34.412 -18.240 -5.282  -5.568 -3.953 0.680  H30B A1H75 81 
A1H75 H31  H44 H 0 1 N N N N N N 35.979 -20.180 -5.588  -5.321 -2.587 -2.041 H31  A1H75 82 
A1H75 H33  H47 H 0 1 N N N N N N 32.939 -21.785 -4.099  -6.514 0.117  0.189  H33  A1H75 83 
A1H75 H35A H48 H 0 0 N N N N N N 30.680 -21.980 -6.496  -3.829 -0.804 2.526  H35A A1H75 84 
A1H75 H35B H49 H 0 0 N N N N N N 30.372 -20.151 -6.739  -5.120 0.466  2.057  H35B A1H75 85 
A1H75 H38B H50 H 0 0 N N N N N N 21.342 -15.921 -5.848  4.875  1.520  -2.485 H38B A1H75 86 
A1H75 H38A H51 H 0 0 N N N N N N 22.126 -17.511 -5.559  4.660  2.882  -1.260 H38A A1H75 87 
A1H75 H9   H52 H 0 1 N N N N N N 25.850 -15.990 -4.828  2.657  1.056  1.745  H9   A1H75 88 
A1H75 H20  H53 H 0 1 N N N N N N 20.530 -17.788 -10.779 -1.511 6.433  0.979  H20  A1H75 89 
A1H75 H27  H54 H 0 1 N N N N N N 18.963 -15.484 -3.651  8.112  -1.507 -1.848 H27  A1H75 90 
A1H75 H36  H55 H 0 1 N N N N N N 31.556 -23.143 -5.394  -4.693 0.612  -1.276 H36  A1H75 91 
A1H75 H37  H56 H 0 1 N N N N N N 35.514 -20.945 -3.430  -6.272 -4.775 -2.079 H37  A1H75 92 
A1H75 H1   H55 H 0 1 N N N N N N 34.468 -21.708 -6.739  -7.518 -1.553 -1.377 H1   A1H75 93 
A1H75 H2   H56 H 0 1 N N N N N N 35.025 -22.442 -5.197  -7.292 -2.223 0.255  H2   A1H75 94 
# 
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 
A1H75 C1  C2   SING N N 1  
A1H75 C1  C6   SING N N 2  
A1H75 C2  C3   SING N N 3  
A1H75 C3  C4   SING N N 4  
A1H75 C3  C11  DOUB N E 5  
A1H75 C4  C5   SING N N 6  
A1H75 C4  C7   SING N N 7  
A1H75 C5  C6   SING N N 8  
A1H75 C5  C9   SING N N 9  
A1H75 C5  C10  SING N N 10 
A1H75 C7  C8   SING N N 11 
A1H75 C8  C9   SING N N 12 
A1H75 C9  C12  SING N N 13 
A1H75 C11 C28  SING N N 14 
A1H75 C12 C13  SING N N 15 
A1H75 C12 C14  SING N N 16 
A1H75 C13 C21  SING N N 17 
A1H75 C13 C38  SING N N 18 
A1H75 C14 C15  SING N N 19 
A1H75 C15 C16  SING N N 20 
A1H75 C16 C17  SING N N 21 
A1H75 C17 C18  SING N N 22 
A1H75 C17 C19  SING N N 23 
A1H75 C17 O20  SING N N 24 
A1H75 C21 C22  SING N N 25 
A1H75 C21 C38  SING N N 26 
A1H75 C22 C23  SING N N 27 
A1H75 C23 C24  SING N N 28 
A1H75 C24 C25  SING N N 29 
A1H75 C24 C26  SING N N 30 
A1H75 C24 O27  SING N N 31 
A1H75 C28 C29  DOUB N Z 32 
A1H75 C29 C30  SING N N 33 
A1H75 C29 C34  SING N N 34 
A1H75 C30 C31  SING N N 35 
A1H75 C31 C32  SING N N 36 
A1H75 C31 O37  SING N N 37 
A1H75 C32 C33  SING N N 38 
A1H75 C33 C34  SING N N 39 
A1H75 C33 O36  SING N N 40 
A1H75 C34 C35  DOUB N N 41 
A1H75 C4  H4   SING N N 42 
A1H75 C6  H6B  SING N N 43 
A1H75 C6  H6A  SING N N 44 
A1H75 C7  H7A  SING N N 45 
A1H75 C7  H7B  SING N N 46 
A1H75 C8  H8A  SING N N 47 
A1H75 C8  H8B  SING N N 48 
A1H75 C10 H10C SING N N 49 
A1H75 C10 H10A SING N N 50 
A1H75 C10 H10B SING N N 51 
A1H75 C13 H13  SING N N 52 
A1H75 C15 H15B SING N N 53 
A1H75 C15 H15A SING N N 54 
A1H75 C21 H21  SING N N 55 
A1H75 C22 H22A SING N N 56 
A1H75 C22 H22B SING N N 57 
A1H75 C26 H26B SING N N 58 
A1H75 C26 H26A SING N N 59 
A1H75 C26 H26C SING N N 60 
A1H75 C28 H28  SING N N 61 
A1H75 C1  H1B  SING N N 62 
A1H75 C1  H1A  SING N N 63 
A1H75 C11 H11  SING N N 64 
A1H75 C12 H12  SING N N 65 
A1H75 C14 H14B SING N N 66 
A1H75 C14 H14A SING N N 67 
A1H75 C16 H16A SING N N 68 
A1H75 C16 H16B SING N N 69 
A1H75 C18 H18C SING N N 70 
A1H75 C18 H18B SING N N 71 
A1H75 C18 H18A SING N N 72 
A1H75 C19 H19C SING N N 73 
A1H75 C19 H19A SING N N 74 
A1H75 C19 H19B SING N N 75 
A1H75 C2  H2A  SING N N 76 
A1H75 C2  H2B  SING N N 77 
A1H75 C23 H23A SING N N 78 
A1H75 C23 H23B SING N N 79 
A1H75 C25 H25B SING N N 80 
A1H75 C25 H25C SING N N 81 
A1H75 C25 H25A SING N N 82 
A1H75 C30 H30A SING N N 83 
A1H75 C30 H30B SING N N 84 
A1H75 C31 H31  SING N N 85 
A1H75 C33 H33  SING N N 86 
A1H75 C35 H35A SING N N 87 
A1H75 C35 H35B SING N N 88 
A1H75 C38 H38B SING N N 89 
A1H75 C38 H38A SING N N 90 
A1H75 C9  H9   SING N N 91 
A1H75 O20 H20  SING N N 92 
A1H75 O27 H27  SING N N 93 
A1H75 O36 H36  SING N N 94 
A1H75 O37 H37  SING N N 95 
A1H75 C32 H1   SING N N 96 
A1H75 C32 H2   SING N N 97 
# 
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 
A1H75 InChI            InChI                1.06  "InChI=1S/C34H56O4/c1-22-24(19-26(35)21-31(22)36)12-11-23-9-7-17-34(6)29(23)13-14-30(34)27(10-8-16-32(2,3)37)28-20-25(28)15-18-33(4,5)38/h11-12,25-31,35-38H,1,7-10,13-21H2,2-6H3/b23-11+,24-12-/t25-,26+,27-,28+,29+,30-,31+,34+/m1/s1" 
A1H75 InChIKey         InChI                1.06  IKZQBCYVSWLJFE-OZUXJOQISA-N                                                                                                                                                                                                              
A1H75 SMILES_CANONICAL CACTVS               3.385 "CC(C)(O)CCC[C@H]([C@H]1C[C@@H]1CCC(C)(C)O)[C@H]2CC[C@H]3\C(CCC[C@]23C)=C\C=C4\C[C@@H](O)C[C@H](O)C4=C"                                                                                                                                  
A1H75 SMILES           CACTVS               3.385 "CC(C)(O)CCC[CH]([CH]1C[CH]1CCC(C)(C)O)[CH]2CC[CH]3C(CCC[C]23C)=CC=C4C[CH](O)C[CH](O)C4=C"                                                                                                                                               
A1H75 SMILES_CANONICAL "OpenEye OEToolkits" 2.0.7 "C[C@]12CCC/C(=C\C=C/3\C[C@H](C[C@@H](C3=C)O)O)/[C@@H]1CC[C@@H]2[C@H](CCCC(C)(C)O)[C@H]4C[C@@H]4CCC(C)(C)O"                                                                                                                              
A1H75 SMILES           "OpenEye OEToolkits" 2.0.7 "CC12CCCC(=CC=C3CC(CC(C3=C)O)O)C1CCC2C(CCCC(C)(C)O)C4CC4CCC(C)(C)O"                                                                                                                                                                      
# 
_pdbx_chem_comp_identifier.comp_id           A1H75 
_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        "(1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(1~{R},3~{a}~{S},7~{a}~{R})-7~{a}-methyl-1-[(1~{R})-5-methyl-1-[(1~{S},2~{S})-2-(3-methyl-3-oxidanyl-butyl)cyclopropyl]-5-oxidanyl-hexyl]-2,3,3~{a},5,6,7-hexahydro-1~{H}-inden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol" 
# 
loop_
_pdbx_chem_comp_audit.comp_id 
_pdbx_chem_comp_audit.action_type 
_pdbx_chem_comp_audit.date 
_pdbx_chem_comp_audit.processing_site 
A1H75 "Create component" 2024-04-10 PDBE 
A1H75 "Initial release"  2024-06-19 RCSB 
# 
