data_A1L1G
# 
_chem_comp.id                                    A1L1G 
_chem_comp.name                                  "(1~{R},3~{S})-6-[(3~{E},5~{E},7~{E},9~{E},11~{E},13~{E},15~{Z},17~{E})-16-(hydroxymethyl)-3,7,12-trimethyl-18-[(1~{S},4~{S},6~{R})-2,2,6-trimethyl-4-oxidanyl-7-oxabicyclo[4.1.0]heptan-1-yl]octadeca-1,3,5,7,9,11,13,15,17-nonaenylidene]-1,5,5-trimethyl-cyclohexane-1,3-diol" 
_chem_comp.type                                  non-polymer 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C40 H56 O5" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2024-05-03 
_chem_comp.pdbx_modified_date                    2025-08-22 
_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                        616.870 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     A1L1G 
_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        ? 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  PDBJ 
_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 
A1L1G C1  C1  C 0 1 N N N N N N ? ? ? 11.536  0.057  -0.043 C1  A1L1G 1   
A1L1G C5  C2  C 0 1 N N N N N N ? ? ? 12.228  0.871  -2.289 C5  A1L1G 2   
A1L1G C4  C3  C 0 1 N N N N N N ? ? ? 13.661  0.589  1.103  C4  A1L1G 3   
A1L1G C3  C4  C 0 1 N N N N N N ? ? ? 13.663  -0.741 -1.018 C3  A1L1G 4   
A1L1G C2  C5  C 0 1 N N N N N N ? ? ? 9.222   -0.973 0.601  C2  A1L1G 5   
A1L1G C10 C6  C 0 1 N N N N N N ? ? ? 11.477  1.129  2.200  C10 A1L1G 6   
A1L1G C11 C7  C 0 1 N N R N N N ? ? ? 12.221  1.055  0.864  C11 A1L1G 7   
A1L1G C12 C8  C 0 1 N N N N N N ? ? ? 11.482  -1.496 -1.985 C12 A1L1G 8   
A1L1G C14 C9  C 0 1 N N N N N N ? ? ? -9.934  -0.294 0.229  C14 A1L1G 9   
A1L1G C17 C10 C 0 1 N N N N N N ? ? ? -11.714 -2.096 -1.172 C17 A1L1G 10  
A1L1G C18 C11 C 0 1 N N N N N N ? ? ? -10.910 1.725  1.694  C18 A1L1G 11  
A1L1G C19 C12 C 0 1 N N N N N N ? ? ? -11.581 2.762  -0.476 C19 A1L1G 12  
A1L1G C20 C13 C 0 1 N N R N N N ? ? ? -12.161 -0.638 -1.046 C20 A1L1G 13  
A1L1G C21 C14 C 0 1 N N N N N N ? ? ? -13.662 -0.439 -0.906 C21 A1L1G 14  
A1L1G C22 C15 C 0 1 N N S N N N ? ? ? -13.976 1.001  -0.502 C22 A1L1G 15  
A1L1G C23 C16 C 0 1 N N N N N N ? ? ? -13.198 1.332  0.777  C23 A1L1G 16  
A1L1G C24 C17 C 0 1 N N N N N N ? ? ? -11.725 1.526  0.414  C24 A1L1G 17  
A1L1G C25 C18 C 0 1 N N S N N N ? ? ? -11.211 0.296  -0.312 C25 A1L1G 18  
A1L1G C26 C19 C 0 1 N N N N N N ? ? ? -7.608  -1.498 1.331  C26 A1L1G 19  
A1L1G C27 C20 C 0 1 N N N N N N ? ? ? -2.823  -1.901 1.158  C27 A1L1G 20  
A1L1G C28 C21 C 0 1 N N N N N N ? ? ? 3.339   1.035  -0.679 C28 A1L1G 21  
A1L1G C29 C22 C 0 1 N N N N N N ? ? ? -8.752  0.172  -0.189 C29 A1L1G 22  
A1L1G C30 C23 C 0 1 N N N N N N ? ? ? -7.553  -0.383 0.319  C30 A1L1G 23  
A1L1G C31 C24 C 0 1 N N N N N N ? ? ? -6.348  0.092  -0.107 C31 A1L1G 24  
A1L1G C32 C25 C 0 1 N N N N N N ? ? ? -5.164  -0.541 0.295  C32 A1L1G 25  
A1L1G C33 C26 C 0 1 N N N N N N ? ? ? -3.941  0.002  -0.045 C33 A1L1G 26  
A1L1G C34 C27 C 0 1 N N N N N N ? ? ? -2.762  -0.627 0.355  C34 A1L1G 27  
A1L1G C35 C28 C 0 1 N N N N N N ? ? ? -1.535  -0.082 0.014  C35 A1L1G 28  
A1L1G C36 C29 C 0 1 N N N N N N ? ? ? -0.360  -0.710 0.412  C36 A1L1G 29  
A1L1G C37 C30 C 0 1 N N N N N N ? ? ? 0.871   -0.162 0.070  C37 A1L1G 30  
A1L1G C38 C31 C 0 1 N N N N N N ? ? ? 2.042   -0.788 0.467  C38 A1L1G 31  
A1L1G C39 C32 C 0 1 N N N N N N ? ? ? 3.277   -0.239 0.124  C39 A1L1G 32  
A1L1G C40 C33 C 0 1 N N N N N N ? ? ? 4.444   -0.862 0.520  C40 A1L1G 33  
A1L1G C41 C34 C 0 1 N N N N N N ? ? ? 5.685   -0.310 0.175  C41 A1L1G 34  
A1L1G C42 C35 C 0 1 N N N N N N ? ? ? 6.837   -0.926 0.565  C42 A1L1G 35  
A1L1G C43 C36 C 0 1 N N N N N N ? ? ? 8.152   0.905  -0.586 C43 A1L1G 36  
A1L1G C44 C37 C 0 1 N N N N N N ? ? ? 8.090   -0.368 0.217  C44 A1L1G 37  
A1L1G C45 C38 C 0 1 N N S N N N ? ? ? 10.379  -0.458 0.279  C45 A1L1G 38  
A1L1G C6  C39 C 0 1 N N N N N N ? ? ? 12.223  -0.326 -1.336 C6  A1L1G 39  
A1L1G C8  C40 C 0 1 N N S N N N ? ? ? 14.357  0.381  -0.244 C8  A1L1G 40  
A1L1G O13 O1  O 0 1 N N N N N N ? ? ? -8.226  -2.645 0.743  O13 A1L1G 41  
A1L1G O15 O2  O 0 1 N N N N N N ? ? ? -11.376 0.323  -1.739 O15 A1L1G 42  
A1L1G O16 O3  O 0 1 N N N N N N ? ? ? -15.378 1.135  -0.258 O16 A1L1G 43  
A1L1G O7  O4  O 0 1 N N N N N N ? ? ? 15.724  0.030  -0.022 O7  A1L1G 44  
A1L1G O9  O5  O 0 1 N N N N N N ? ? ? 12.225  2.343  0.245  O9  A1L1G 45  
A1L1G H1  H1  H 0 1 N N N N N N ? ? ? 12.762  1.701  -1.827 H1  A1L1G 46  
A1L1G H2  H2  H 0 1 N N N N N N ? ? ? 12.723  0.593  -3.219 H2  A1L1G 47  
A1L1G H3  H3  H 0 1 N N N N N N ? ? ? 11.201  1.172  -2.499 H3  A1L1G 48  
A1L1G H4  H4  H 0 1 N N N N N N ? ? ? 14.198  1.345  1.676  H4  A1L1G 49  
A1L1G H5  H5  H 0 1 N N N N N N ? ? ? 13.653  -0.349 1.657  H5  A1L1G 50  
A1L1G H6  H6  H 0 1 N N N N N N ? ? ? 13.655  -1.648 -0.414 H6  A1L1G 51  
A1L1G H7  H7  H 0 1 N N N N N N ? ? ? 14.201  -0.928 -1.947 H7  A1L1G 52  
A1L1G H8  H8  H 0 1 N N N N N N ? ? ? 9.178   -1.885 1.176  H8  A1L1G 53  
A1L1G H9  H9  H 0 1 N N N N N N ? ? ? 11.482  0.147  2.673  H9  A1L1G 54  
A1L1G H10 H10 H 0 1 N N N N N N ? ? ? 11.973  1.849  2.852  H10 A1L1G 55  
A1L1G H11 H11 H 0 1 N N N N N N ? ? ? 10.449  1.444  2.026  H11 A1L1G 56  
A1L1G H12 H12 H 0 1 N N N N N N ? ? ? 10.453  -1.203 -2.194 H12 A1L1G 57  
A1L1G H13 H13 H 0 1 N N N N N N ? ? ? 11.978  -1.770 -2.915 H13 A1L1G 58  
A1L1G H14 H14 H 0 1 N N N N N N ? ? ? 11.486  -2.349 -1.306 H14 A1L1G 59  
A1L1G H15 H15 H 0 1 N N N N N N ? ? ? -9.974  -1.093 0.955  H15 A1L1G 60  
A1L1G H16 H16 H 0 1 N N N N N N ? ? ? -10.746 -2.138 -1.671 H16 A1L1G 61  
A1L1G H17 H17 H 0 1 N N N N N N ? ? ? -11.630 -2.537 -0.179 H17 A1L1G 62  
A1L1G H18 H18 H 0 1 N N N N N N ? ? ? -12.448 -2.652 -1.755 H18 A1L1G 63  
A1L1G H19 H19 H 0 1 N N N N N N ? ? ? -11.016 0.847  2.332  H19 A1L1G 64  
A1L1G H20 H20 H 0 1 N N N N N N ? ? ? -9.860  1.863  1.438  H20 A1L1G 65  
A1L1G H21 H21 H 0 1 N N N N N N ? ? ? -11.274 2.605  2.224  H21 A1L1G 66  
A1L1G H22 H22 H 0 1 N N N N N N ? ? ? -11.943 3.639  0.059  H22 A1L1G 67  
A1L1G H23 H23 H 0 1 N N N N N N ? ? ? -10.532 2.902  -0.735 H23 A1L1G 68  
A1L1G H24 H24 H 0 1 N N N N N N ? ? ? -12.165 2.624  -1.386 H24 A1L1G 69  
A1L1G H25 H25 H 0 1 N N N N N N ? ? ? -14.144 -0.659 -1.859 H25 A1L1G 70  
A1L1G H26 H26 H 0 1 N N N N N N ? ? ? -14.045 -1.119 -0.145 H26 A1L1G 71  
A1L1G H27 H27 H 0 1 N N N N N N ? ? ? -13.675 1.679  -1.300 H27 A1L1G 72  
A1L1G H28 H28 H 0 1 N N N N N N ? ? ? -13.590 2.248  1.217  H28 A1L1G 73  
A1L1G H29 H29 H 0 1 N N N N N N ? ? ? -13.295 0.511  1.487  H29 A1L1G 74  
A1L1G H30 H30 H 0 1 N N N N N N ? ? ? -6.596  -1.752 1.647  H30 A1L1G 75  
A1L1G H31 H31 H 0 1 N N N N N N ? ? ? -8.188  -1.175 2.196  H31 A1L1G 76  
A1L1G H32 H32 H 0 1 N N N N N N ? ? ? -2.836  -2.756 0.482  H32 A1L1G 77  
A1L1G H33 H33 H 0 1 N N N N N N ? ? ? -1.950  -1.964 1.807  H33 A1L1G 78  
A1L1G H34 H34 H 0 1 N N N N N N ? ? ? -3.728  -1.905 1.765  H34 A1L1G 79  
A1L1G H35 H35 H 0 1 N N N N N N ? ? ? 3.351   1.890  -0.003 H35 A1L1G 80  
A1L1G H36 H36 H 0 1 N N N N N N ? ? ? 4.244   1.038  -1.287 H36 A1L1G 81  
A1L1G H37 H37 H 0 1 N N N N N N ? ? ? 2.465   1.098  -1.328 H37 A1L1G 82  
A1L1G H38 H38 H 0 1 N N N N N N ? ? ? -8.712  0.971  -0.915 H38 A1L1G 83  
A1L1G H39 H39 H 0 1 N N N N N N ? ? ? -6.307  0.955  -0.754 H39 A1L1G 84  
A1L1G H40 H40 H 0 1 N N N N N N ? ? ? -5.208  -1.454 0.870  H40 A1L1G 85  
A1L1G H41 H41 H 0 1 N N N N N N ? ? ? -3.898  0.915  -0.621 H41 A1L1G 86  
A1L1G H42 H42 H 0 1 N N N N N N ? ? ? -1.491  0.831  -0.562 H42 A1L1G 87  
A1L1G H43 H43 H 0 1 N N N N N N ? ? ? -0.404  -1.622 0.988  H43 A1L1G 88  
A1L1G H44 H44 H 0 1 N N N N N N ? ? ? 0.915   0.751  -0.506 H44 A1L1G 89  
A1L1G H45 H45 H 0 1 N N N N N N ? ? ? 1.999   -1.701 1.043  H45 A1L1G 90  
A1L1G H46 H46 H 0 1 N N N N N N ? ? ? 4.401   -1.775 1.095  H46 A1L1G 91  
A1L1G H47 H47 H 0 1 N N N N N N ? ? ? 5.729   0.603  -0.401 H47 A1L1G 92  
A1L1G H48 H48 H 0 1 N N N N N N ? ? ? 6.793   -1.839 1.141  H48 A1L1G 93  
A1L1G H49 H49 H 0 1 N N N N N N ? ? ? 8.164   1.761  0.090  H49 A1L1G 94  
A1L1G H50 H50 H 0 1 N N N N N N ? ? ? 9.057   0.909  -1.194 H50 A1L1G 95  
A1L1G H51 H51 H 0 1 N N N N N N ? ? ? 7.278   0.968  -1.235 H51 A1L1G 96  
A1L1G H52 H52 H 0 1 N N N N N N ? ? ? 14.310  1.303  -0.822 H52 A1L1G 97  
A1L1G H53 H53 H 0 1 N N N N N N ? ? ? -8.295  -3.403 1.340  H53 A1L1G 98  
A1L1G H54 H54 H 0 1 N N N N N N ? ? ? -15.932 0.928  -1.023 H54 A1L1G 99  
A1L1G H55 H55 H 0 1 N N N N N N ? ? ? 16.229  0.700  0.460  H55 A1L1G 100 
A1L1G H56 H56 H 0 1 N N N N N N ? ? ? 12.650  3.032  0.774  H56 A1L1G 101 
# 
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 
A1L1G O16 C22 SING N N 1   
A1L1G C21 C22 SING N N 2   
A1L1G C21 C20 SING N N 3   
A1L1G C22 C23 SING N N 4   
A1L1G C17 C20 SING N N 5   
A1L1G C20 O15 SING N N 6   
A1L1G C20 C25 SING N N 7   
A1L1G C23 C24 SING N N 8   
A1L1G O15 C25 SING N N 9   
A1L1G C25 C24 SING N N 10  
A1L1G C25 C14 SING N N 11  
A1L1G C24 C19 SING N N 12  
A1L1G C24 C18 SING N N 13  
A1L1G C14 C29 DOUB N E 14  
A1L1G C29 C30 SING N N 15  
A1L1G C30 C31 DOUB N Z 16  
A1L1G C30 C26 SING N N 17  
A1L1G O13 C26 SING N N 18  
A1L1G C31 C32 SING N N 19  
A1L1G C32 C33 DOUB N E 20  
A1L1G C33 C34 SING N N 21  
A1L1G C34 C35 DOUB N E 22  
A1L1G C34 C27 SING N N 23  
A1L1G C35 C36 SING N N 24  
A1L1G C28 C39 SING N N 25  
A1L1G C37 C36 DOUB N E 26  
A1L1G C37 C38 SING N N 27  
A1L1G C38 C39 DOUB N E 28  
A1L1G C39 C40 SING N N 29  
A1L1G C40 C41 DOUB N E 30  
A1L1G C41 C42 SING N N 31  
A1L1G C43 C44 SING N N 32  
A1L1G C42 C44 DOUB N E 33  
A1L1G C44 C2  SING N N 34  
A1L1G C2  C45 DOUB N N 35  
A1L1G C45 C1  DOUB N N 36  
A1L1G C10 C11 SING N N 37  
A1L1G C1  C11 SING N N 38  
A1L1G C1  C6  SING N N 39  
A1L1G C12 C6  SING N N 40  
A1L1G C11 O9  SING N N 41  
A1L1G C11 C4  SING N N 42  
A1L1G C6  C5  SING N N 43  
A1L1G C6  C3  SING N N 44  
A1L1G C4  C8  SING N N 45  
A1L1G C3  C8  SING N N 46  
A1L1G C8  O7  SING N N 47  
A1L1G C5  H1  SING N N 48  
A1L1G C5  H2  SING N N 49  
A1L1G C5  H3  SING N N 50  
A1L1G C4  H4  SING N N 51  
A1L1G C4  H5  SING N N 52  
A1L1G C3  H6  SING N N 53  
A1L1G C3  H7  SING N N 54  
A1L1G C2  H8  SING N N 55  
A1L1G C10 H9  SING N N 56  
A1L1G C10 H10 SING N N 57  
A1L1G C10 H11 SING N N 58  
A1L1G C12 H12 SING N N 59  
A1L1G C12 H13 SING N N 60  
A1L1G C12 H14 SING N N 61  
A1L1G C14 H15 SING N N 62  
A1L1G C17 H16 SING N N 63  
A1L1G C17 H17 SING N N 64  
A1L1G C17 H18 SING N N 65  
A1L1G C18 H19 SING N N 66  
A1L1G C18 H20 SING N N 67  
A1L1G C18 H21 SING N N 68  
A1L1G C19 H22 SING N N 69  
A1L1G C19 H23 SING N N 70  
A1L1G C19 H24 SING N N 71  
A1L1G C21 H25 SING N N 72  
A1L1G C21 H26 SING N N 73  
A1L1G C22 H27 SING N N 74  
A1L1G C23 H28 SING N N 75  
A1L1G C23 H29 SING N N 76  
A1L1G C26 H30 SING N N 77  
A1L1G C26 H31 SING N N 78  
A1L1G C27 H32 SING N N 79  
A1L1G C27 H33 SING N N 80  
A1L1G C27 H34 SING N N 81  
A1L1G C28 H35 SING N N 82  
A1L1G C28 H36 SING N N 83  
A1L1G C28 H37 SING N N 84  
A1L1G C29 H38 SING N N 85  
A1L1G C31 H39 SING N N 86  
A1L1G C32 H40 SING N N 87  
A1L1G C33 H41 SING N N 88  
A1L1G C35 H42 SING N N 89  
A1L1G C36 H43 SING N N 90  
A1L1G C37 H44 SING N N 91  
A1L1G C38 H45 SING N N 92  
A1L1G C40 H46 SING N N 93  
A1L1G C41 H47 SING N N 94  
A1L1G C42 H48 SING N N 95  
A1L1G C43 H49 SING N N 96  
A1L1G C43 H50 SING N N 97  
A1L1G C43 H51 SING N N 98  
A1L1G C8  H52 SING N N 99  
A1L1G O13 H53 SING N N 100 
A1L1G O16 H54 SING N N 101 
A1L1G O7  H55 SING N N 102 
A1L1G O9  H56 SING N N 103 
# 
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 
A1L1G InChI            InChI                1.06  "InChI=1S/C40H56O5/c1-29(16-12-17-31(3)20-21-35-36(4,5)24-33(42)26-38(35,8)44)14-10-11-15-30(2)18-13-19-32(28-41)22-23-40-37(6,7)25-34(43)27-39(40,9)45-40/h10-20,22-23,33-34,41-44H,24-28H2,1-9H3/b11-10+,16-12+,18-13+,23-22+,29-14+,30-15+,31-17+,32-19-/t21-,33+,34+,38-,39-,40+/m1/s1" 
A1L1G InChIKey         InChI                1.06  OWWSPDNLRSCPIS-XZHZJERWSA-N                                                                                                                                                                                                                                                                 
A1L1G SMILES_CANONICAL CACTVS               3.385 "CC(=C/C=C/C=C(C)/C=C/C=C(CO)/C=C/[C@@]12O[C@]1(C)C[C@@H](O)CC2(C)C)\C=C\C=C(C)\[CH]=[C@@]=[C]3C(C)(C)C[C@H](O)C[C@@]3(C)O"                                                                                                                                                                 
A1L1G SMILES           CACTVS               3.385 "CC(=CC=CC=C(C)C=CC=C(CO)C=C[C]12O[C]1(C)C[CH](O)CC2(C)C)C=CC=C(C)[CH]=[C]=[C]3C(C)(C)C[CH](O)C[C]3(C)O"                                                                                                                                                                                    
A1L1G SMILES_CANONICAL "OpenEye OEToolkits" 2.0.7 "C/C(=C\C=C\C=C(/C)\C=C\C=C(/CO)\C=C\[C@]12[C@](O1)(C[C@H](CC2(C)C)O)C)/C=C/C=C(\C)/C=C=C3[C@](C[C@H](CC3(C)C)O)(C)O"                                                                                                                                                                       
A1L1G SMILES           "OpenEye OEToolkits" 2.0.7 "CC(=CC=CC=C(C)C=CC=C(CO)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=C=C3C(CC(CC3(C)O)O)(C)C"                                                                                                                                                                                                     
# 
_pdbx_chem_comp_identifier.comp_id           A1L1G 
_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})-6-[(3~{E},5~{E},7~{E},9~{E},11~{E},13~{E},15~{Z},17~{E})-16-(hydroxymethyl)-3,7,12-trimethyl-18-[(1~{S},4~{S},6~{R})-2,2,6-trimethyl-4-oxidanyl-7-oxabicyclo[4.1.0]heptan-1-yl]octadeca-1,3,5,7,9,11,13,15,17-nonaenylidene]-1,5,5-trimethyl-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 
A1L1G "Create component"   2024-05-03 PDBJ 
A1L1G "Modify coordinates" 2025-08-18 RCSB 
A1L1G "Initial release"    2025-08-27 RCSB 
# 
