data_A1L6D
# 
_chem_comp.id                                    A1L6D 
_chem_comp.name                                  "[(1~{R},5~{S})-3,3,5-trimethyl-5-oxidanyl-4-[(3~{E},5~{E},7~{E},9~{E},11~{E},13~{E},15~{E},17~{Z})-3,7,12,16-tetramethyl-17-oxidanyl-19-oxidanylidene-19-[(1~{R},4~{S})-1,2,2-trimethyl-4-oxidanyl-cyclopentyl]nonadeca-1,3,5,7,9,11,13,15,17-nonaenylidene]cyclohexyl] ethanoate" 
_chem_comp.type                                  non-polymer 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C42 H58 O6" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         ? 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2024-11-26 
_chem_comp.pdbx_modified_date                    2026-01-23 
_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                        658.906 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     A1L6D 
_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 
A1L6D C1  C1  C 0 1 N N N N N N ? ? ? 2.408   0.730  0.104  C1  A1L6D 1   
A1L6D C2  C2  C 0 1 N N N N N N ? ? ? 1.135   1.291  0.025  C2  A1L6D 2   
A1L6D C3  C3  C 0 1 N N N N N N ? ? ? 0.014   0.496  0.206  C3  A1L6D 3   
A1L6D C4  C4  C 0 1 N N N N N N ? ? ? -1.256  1.056  0.127  C4  A1L6D 4   
A1L6D C5  C5  C 0 1 N N N N N N ? ? ? -2.380  0.258  0.309  C5  A1L6D 5   
A1L6D C6  C6  C 0 1 N N N N N N ? ? ? -3.647  0.817  0.230  C6  A1L6D 6   
A1L6D O5  O1  O 0 1 N N N N N N ? ? ? 14.979  -1.893 -0.803 O5  A1L6D 7   
A1L6D C38 C7  C 0 1 N N N N N N ? ? ? 14.409  -2.709 -0.117 C38 A1L6D 8   
A1L6D C39 C8  C 0 1 N N N N N N ? ? ? 15.017  -4.072 0.094  C39 A1L6D 9   
A1L6D O4  O2  O 0 1 N N N N N N ? ? ? 13.236  -2.402 0.457  O4  A1L6D 10  
A1L6D C34 C9  C 0 1 N N R N N N ? ? ? 12.710  -1.071 0.211  C34 A1L6D 11  
A1L6D C33 C10 C 0 1 N N N N N N ? ? ? 11.887  -0.618 1.417  C33 A1L6D 12  
A1L6D C32 C11 C 0 1 N N N N N N ? ? ? 11.409  0.821  1.197  C32 A1L6D 13  
A1L6D C41 C12 C 0 1 N N N N N N ? ? ? 12.615  1.762  1.157  C41 A1L6D 14  
A1L6D C40 C13 C 0 1 N N N N N N ? ? ? 10.470  1.231  2.333  C40 A1L6D 15  
A1L6D C35 C14 C 0 1 N N N N N N ? ? ? 11.828  -1.096 -1.039 C35 A1L6D 16  
A1L6D C36 C15 C 0 1 N N S N N N ? ? ? 11.349  0.325  -1.352 C36 A1L6D 17  
A1L6D C37 C16 C 0 1 N N N N N N ? ? ? 10.354  0.288  -2.515 C37 A1L6D 18  
A1L6D O3  O3  O 0 1 N N N N N N ? ? ? 12.467  1.143  -1.703 O3  A1L6D 19  
A1L6D C31 C17 C 0 1 N N N N N N ? ? ? 10.670  0.886  -0.122 C31 A1L6D 20  
A1L6D C30 C18 C 0 1 N N R N N N ? ? ? 9.476   1.412  -0.196 C30 A1L6D 21  
A1L6D C29 C19 C 0 1 N N N N N N ? ? ? 8.282   1.939  -0.270 C29 A1L6D 22  
A1L6D C27 C20 C 0 1 N N N N N N ? ? ? 7.200   1.171  -0.095 C27 A1L6D 23  
A1L6D C28 C21 C 0 1 N N N N N N ? ? ? 7.358   -0.301 0.187  C28 A1L6D 24  
A1L6D C26 C22 C 0 1 N N N N N N ? ? ? 5.907   1.741  -0.175 C26 A1L6D 25  
A1L6D C25 C23 C 0 1 N N N N N N ? ? ? 4.805   0.958  0.003  C25 A1L6D 26  
A1L6D C24 C24 C 0 1 N N N N N N ? ? ? 3.525   1.522  -0.076 C24 A1L6D 27  
A1L6D C   C25 C 0 1 N N N N N N ? ? ? 2.567   -0.741 0.393  C   A1L6D 28  
A1L6D C7  C26 C 0 1 N N N N N N ? ? ? -3.806  2.289  -0.052 C7  A1L6D 29  
A1L6D C9  C27 C 0 1 N N N N N N ? ? ? -8.428  0.330  0.438  C9  A1L6D 30  
A1L6D C10 C28 C 0 1 N N N N N N ? ? ? -9.562  -0.475 0.621  C10 A1L6D 31  
A1L6D C11 C29 C 0 1 N N N N N N ? ? ? -10.833 0.085  0.543  C11 A1L6D 32  
A1L6D C13 C30 C 0 1 N N N N N N ? ? ? -11.957 -0.729 0.615  C13 A1L6D 33  
A1L6D O   O4  O 0 1 N N N N N N ? ? ? -11.834 -1.917 0.853  O   A1L6D 34  
A1L6D C15 C31 C 0 1 N N R N N N ? ? ? -13.328 -0.142 0.398  C15 A1L6D 35  
A1L6D C19 C32 C 0 1 N N N N N N ? ? ? -14.408 -1.210 0.663  C19 A1L6D 36  
A1L6D C18 C33 C 0 1 N N S N N N ? ? ? -14.728 -1.783 -0.739 C18 A1L6D 37  
A1L6D O2  O5  O 0 1 N N N N N N ? ? ? -16.036 -2.358 -0.765 O2  A1L6D 38  
A1L6D C17 C34 C 0 1 N N N N N N ? ? ? -14.663 -0.528 -1.645 C17 A1L6D 39  
A1L6D C16 C35 C 0 1 N N N N N N ? ? ? -13.489 0.293  -1.069 C16 A1L6D 40  
A1L6D C23 C36 C 0 1 N N N N N N ? ? ? -13.809 1.787  -1.142 C23 A1L6D 41  
A1L6D C22 C37 C 0 1 N N N N N N ? ? ? -12.207 -0.007 -1.849 C22 A1L6D 42  
A1L6D O1  O6  O 0 1 N N N N N N ? ? ? -9.420  -1.798 0.875  O1  A1L6D 43  
A1L6D C12 C38 C 0 1 N N N N N N ? ? ? -8.586  1.802  0.156  C12 A1L6D 44  
A1L6D C8  C39 C 0 1 N N N N N N ? ? ? -7.167  -0.226 0.516  C8  A1L6D 45  
A1L6D C42 C40 C 0 1 N N N N N N ? ? ? -6.038  0.575  0.334  C42 A1L6D 46  
A1L6D C43 C41 C 0 1 N N N N N N ? ? ? -4.773  0.017  0.412  C43 A1L6D 47  
A1L6D C21 C42 C 0 1 N N N N N N ? ? ? -13.537 1.056  1.326  C21 A1L6D 48  
A1L6D H1  H1  H 0 1 N N N N N N ? ? ? 1.021   2.346  -0.177 H1  A1L6D 49  
A1L6D H2  H2  H 0 1 N N N N N N ? ? ? 0.127   -0.559 0.408  H2  A1L6D 50  
A1L6D H3  H3  H 0 1 N N N N N N ? ? ? -1.370  2.110  -0.075 H3  A1L6D 51  
A1L6D H4  H4  H 0 1 N N N N N N ? ? ? -2.267  -0.797 0.511  H4  A1L6D 52  
A1L6D H5  H5  H 0 1 N N N N N N ? ? ? 15.661  -4.051 0.973  H5  A1L6D 53  
A1L6D H6  H6  H 0 1 N N N N N N ? ? ? 14.224  -4.805 0.242  H6  A1L6D 54  
A1L6D H7  H7  H 0 1 N N N N N N ? ? ? 15.607  -4.346 -0.781 H7  A1L6D 55  
A1L6D H8  H8  H 0 1 N N N N N N ? ? ? 13.537  -0.377 0.057  H8  A1L6D 56  
A1L6D H9  H9  H 0 1 N N N N N N ? ? ? 11.024  -1.273 1.535  H9  A1L6D 57  
A1L6D H10 H10 H 0 1 N N N N N N ? ? ? 12.503  -0.663 2.315  H10 A1L6D 58  
A1L6D H11 H11 H 0 1 N N N N N N ? ? ? 13.276  1.471  0.341  H11 A1L6D 59  
A1L6D H12 H12 H 0 1 N N N N N N ? ? ? 12.272  2.785  1.000  H12 A1L6D 60  
A1L6D H13 H13 H 0 1 N N N N N N ? ? ? 13.155  1.701  2.102  H13 A1L6D 61  
A1L6D H14 H14 H 0 1 N N N N N N ? ? ? 10.999  1.167  3.283  H14 A1L6D 62  
A1L6D H15 H15 H 0 1 N N N N N N ? ? ? 10.131  2.255  2.173  H15 A1L6D 63  
A1L6D H16 H16 H 0 1 N N N N N N ? ? ? 9.609   0.563  2.351  H16 A1L6D 64  
A1L6D H17 H17 H 0 1 N N N N N N ? ? ? 12.403  -1.479 -1.882 H17 A1L6D 65  
A1L6D H18 H18 H 0 1 N N N N N N ? ? ? 10.967  -1.740 -0.863 H18 A1L6D 66  
A1L6D H19 H19 H 0 1 N N N N N N ? ? ? 9.500   -0.331 -2.242 H19 A1L6D 67  
A1L6D H20 H20 H 0 1 N N N N N N ? ? ? 10.015  1.300  -2.735 H20 A1L6D 68  
A1L6D H21 H21 H 0 1 N N N N N N ? ? ? 10.841  -0.132 -3.395 H21 A1L6D 69  
A1L6D H22 H22 H 0 1 N N N N N N ? ? ? 12.955  0.831  -2.477 H22 A1L6D 70  
A1L6D H23 H23 H 0 1 N N N N N N ? ? ? 8.169   2.994  -0.472 H23 A1L6D 71  
A1L6D H24 H24 H 0 1 N N N N N N ? ? ? 7.420   -0.460 1.264  H24 A1L6D 72  
A1L6D H25 H25 H 0 1 N N N N N N ? ? ? 6.500   -0.842 -0.211 H25 A1L6D 73  
A1L6D H26 H26 H 0 1 N N N N N N ? ? ? 8.269   -0.666 -0.287 H26 A1L6D 74  
A1L6D H27 H27 H 0 1 N N N N N N ? ? ? 5.794   2.795  -0.377 H27 A1L6D 75  
A1L6D H28 H28 H 0 1 N N N N N N ? ? ? 4.918   -0.097 0.205  H28 A1L6D 76  
A1L6D H29 H29 H 0 1 N N N N N N ? ? ? 3.412   2.577  -0.279 H29 A1L6D 77  
A1L6D H30 H30 H 0 1 N N N N N N ? ? ? 2.579   -1.296 -0.545 H30 A1L6D 78  
A1L6D H31 H31 H 0 1 N N N N N N ? ? ? 3.503   -0.908 0.926  H31 A1L6D 79  
A1L6D H32 H32 H 0 1 N N N N N N ? ? ? 1.733   -1.083 1.006  H32 A1L6D 80  
A1L6D H33 H33 H 0 1 N N N N N N ? ? ? -3.868  2.447  -1.128 H33 A1L6D 81  
A1L6D H34 H34 H 0 1 N N N N N N ? ? ? -4.717  2.653  0.422  H34 A1L6D 82  
A1L6D H35 H35 H 0 1 N N N N N N ? ? ? -2.947  2.829  0.346  H35 A1L6D 83  
A1L6D H36 H36 H 0 1 N N N N N N ? ? ? -10.946 1.153  0.425  H36 A1L6D 84  
A1L6D H37 H37 H 0 1 N N N N N N ? ? ? -14.019 -1.993 1.315  H37 A1L6D 85  
A1L6D H38 H38 H 0 1 N N N N N N ? ? ? -15.295 -0.755 1.103  H38 A1L6D 86  
A1L6D H39 H39 H 0 1 N N N N N N ? ? ? -13.980 -2.517 -1.037 H39 A1L6D 87  
A1L6D H40 H40 H 0 1 N N N N N N ? ? ? -16.153 -3.099 -0.154 H40 A1L6D 88  
A1L6D H41 H41 H 0 1 N N N N N N ? ? ? -14.459 -0.812 -2.677 H41 A1L6D 89  
A1L6D H42 H42 H 0 1 N N N N N N ? ? ? -15.592 0.037  -1.579 H42 A1L6D 90  
A1L6D H43 H43 H 0 1 N N N N N N ? ? ? -14.724 1.990  -0.585 H43 A1L6D 91  
A1L6D H44 H44 H 0 1 N N N N N N ? ? ? -12.986 2.357  -0.710 H44 A1L6D 92  
A1L6D H45 H45 H 0 1 N N N N N N ? ? ? -13.946 2.079  -2.183 H45 A1L6D 93  
A1L6D H46 H46 H 0 1 N N N N N N ? ? ? -12.368 0.206  -2.906 H46 A1L6D 94  
A1L6D H47 H47 H 0 1 N N N N N N ? ? ? -11.398 0.618  -1.472 H47 A1L6D 95  
A1L6D H48 H48 H 0 1 N N N N N N ? ? ? -11.944 -1.057 -1.726 H48 A1L6D 96  
A1L6D H49 H49 H 0 1 N N N N N N ? ? ? -10.255 -2.283 0.915  H49 A1L6D 97  
A1L6D H50 H50 H 0 1 N N N N N N ? ? ? -8.601  2.352  1.096  H50 A1L6D 98  
A1L6D H51 H51 H 0 1 N N N N N N ? ? ? -7.751  2.146  -0.455 H51 A1L6D 99  
A1L6D H52 H52 H 0 1 N N N N N N ? ? ? -9.521  1.971  -0.379 H52 A1L6D 100 
A1L6D H53 H53 H 0 1 N N N N N N ? ? ? -7.053  -1.281 0.719  H53 A1L6D 101 
A1L6D H54 H54 H 0 1 N N N N N N ? ? ? -6.152  1.630  0.132  H54 A1L6D 102 
A1L6D H55 H55 H 0 1 N N N N N N ? ? ? -4.660  -1.038 0.615  H55 A1L6D 103 
A1L6D H56 H56 H 0 1 N N N N N N ? ? ? -12.792 1.821  1.105  H56 A1L6D 104 
A1L6D H57 H57 H 0 1 N N N N N N ? ? ? -14.535 1.466  1.171  H57 A1L6D 105 
A1L6D H58 H58 H 0 1 N N N N N N ? ? ? -13.432 0.736  2.362  H58 A1L6D 106 
# 
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 
A1L6D C39 C38 SING N N 1   
A1L6D O5  C38 DOUB N N 2   
A1L6D C38 O4  SING N N 3   
A1L6D O4  C34 SING N N 4   
A1L6D C34 C35 SING N N 5   
A1L6D C34 C33 SING N N 6   
A1L6D C35 C36 SING N N 7   
A1L6D C33 C32 SING N N 8   
A1L6D C41 C32 SING N N 9   
A1L6D C32 C31 SING N N 10  
A1L6D C32 C40 SING N N 11  
A1L6D C36 C37 SING N N 12  
A1L6D C36 C31 SING N N 13  
A1L6D C36 O3  SING N N 14  
A1L6D C31 C30 DOUB N N 15  
A1L6D C30 C29 DOUB N N 16  
A1L6D C28 C27 SING N N 17  
A1L6D C29 C27 SING N N 18  
A1L6D C27 C26 DOUB N E 19  
A1L6D C26 C25 SING N N 20  
A1L6D C25 C24 DOUB N E 21  
A1L6D C   C1  SING N N 22  
A1L6D C24 C1  SING N N 23  
A1L6D C1  C2  DOUB N E 24  
A1L6D C2  C3  SING N N 25  
A1L6D C3  C4  DOUB N E 26  
A1L6D C4  C5  SING N N 27  
A1L6D C5  C6  DOUB N E 28  
A1L6D C6  C43 SING N N 29  
A1L6D C6  C7  SING N N 30  
A1L6D C43 C42 DOUB N E 31  
A1L6D C42 C8  SING N N 32  
A1L6D C8  C9  DOUB N E 33  
A1L6D C22 C16 SING N N 34  
A1L6D C9  C10 SING N N 35  
A1L6D C9  C12 SING N N 36  
A1L6D O1  C10 SING N N 37  
A1L6D C10 C11 DOUB N Z 38  
A1L6D C17 C16 SING N N 39  
A1L6D C17 C18 SING N N 40  
A1L6D C16 C23 SING N N 41  
A1L6D C16 C15 SING N N 42  
A1L6D C11 C13 SING N N 43  
A1L6D C13 O   DOUB N N 44  
A1L6D C13 C15 SING N N 45  
A1L6D C15 C21 SING N N 46  
A1L6D C15 C19 SING N N 47  
A1L6D C18 O2  SING N N 48  
A1L6D C18 C19 SING N N 49  
A1L6D C2  H1  SING N N 50  
A1L6D C3  H2  SING N N 51  
A1L6D C4  H3  SING N N 52  
A1L6D C5  H4  SING N N 53  
A1L6D C39 H5  SING N N 54  
A1L6D C39 H6  SING N N 55  
A1L6D C39 H7  SING N N 56  
A1L6D C34 H8  SING N N 57  
A1L6D C33 H9  SING N N 58  
A1L6D C33 H10 SING N N 59  
A1L6D C41 H11 SING N N 60  
A1L6D C41 H12 SING N N 61  
A1L6D C41 H13 SING N N 62  
A1L6D C40 H14 SING N N 63  
A1L6D C40 H15 SING N N 64  
A1L6D C40 H16 SING N N 65  
A1L6D C35 H17 SING N N 66  
A1L6D C35 H18 SING N N 67  
A1L6D C37 H19 SING N N 68  
A1L6D C37 H20 SING N N 69  
A1L6D C37 H21 SING N N 70  
A1L6D O3  H22 SING N N 71  
A1L6D C29 H23 SING N N 72  
A1L6D C28 H24 SING N N 73  
A1L6D C28 H25 SING N N 74  
A1L6D C28 H26 SING N N 75  
A1L6D C26 H27 SING N N 76  
A1L6D C25 H28 SING N N 77  
A1L6D C24 H29 SING N N 78  
A1L6D C   H30 SING N N 79  
A1L6D C   H31 SING N N 80  
A1L6D C   H32 SING N N 81  
A1L6D C7  H33 SING N N 82  
A1L6D C7  H34 SING N N 83  
A1L6D C7  H35 SING N N 84  
A1L6D C11 H36 SING N N 85  
A1L6D C19 H37 SING N N 86  
A1L6D C19 H38 SING N N 87  
A1L6D C18 H39 SING N N 88  
A1L6D O2  H40 SING N N 89  
A1L6D C17 H41 SING N N 90  
A1L6D C17 H42 SING N N 91  
A1L6D C23 H43 SING N N 92  
A1L6D C23 H44 SING N N 93  
A1L6D C23 H45 SING N N 94  
A1L6D C22 H46 SING N N 95  
A1L6D C22 H47 SING N N 96  
A1L6D C22 H48 SING N N 97  
A1L6D O1  H49 SING N N 98  
A1L6D C12 H50 SING N N 99  
A1L6D C12 H51 SING N N 100 
A1L6D C12 H52 SING N N 101 
A1L6D C8  H53 SING N N 102 
A1L6D C42 H54 SING N N 103 
A1L6D C43 H55 SING N N 104 
A1L6D C21 H56 SING N N 105 
A1L6D C21 H57 SING N N 106 
A1L6D C21 H58 SING N N 107 
# 
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 
A1L6D InChI            InChI                1.06  "InChI=1S/C42H58O6/c1-29(18-14-19-31(3)22-23-37-39(6,7)27-35(48-33(5)43)28-42(37,11)47)16-12-13-17-30(2)20-15-21-32(4)36(45)24-38(46)41(10)26-34(44)25-40(41,8)9/h12-22,24,34-35,44-45,47H,25-28H2,1-11H3/b13-12+,18-14+,20-15+,29-16+,30-17+,31-19+,32-21+,36-24-/t23-,34-,35+,41-,42-/m0/s1" 
A1L6D InChIKey         InChI                1.06  LUDSIBUOXLKVSG-BDVOIICUSA-N                                                                                                                                                                                                                                                                    
A1L6D SMILES_CANONICAL CACTVS               3.385 "CC(=O)O[C@@H]1CC(C)(C)[C](=[C@@]=[CH]\C(C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(C)\C(O)=C\C(=O)[C@]2(C)C[C@@H](O)CC2(C)C)[C@@](C)(O)C1"                                                                                                                                                            
A1L6D SMILES           CACTVS               3.385 "CC(=O)O[CH]1CC(C)(C)[C](=[C]=[CH]C(C)=CC=CC(C)=CC=CC=C(C)C=CC=C(C)C(O)=CC(=O)[C]2(C)C[CH](O)CC2(C)C)[C](C)(O)C1"                                                                                                                                                                              
A1L6D SMILES_CANONICAL "OpenEye OEToolkits" 2.0.7 "C/C(=C\C=C\C=C(/C)\C=C\C=C(/C)\C(=C\C(=O)[C@@]1(C[C@H](CC1(C)C)O)C)\O)/C=C/C=C(\C)/C=C=C2[C@@](C[C@@H](CC2(C)C)OC(=O)C)(C)O"                                                                                                                                                                  
A1L6D SMILES           "OpenEye OEToolkits" 2.0.7 "CC(=CC=CC=C(C)C=CC=C(C)C(=CC(=O)C1(CC(CC1(C)C)O)C)O)C=CC=C(C)C=C=C2C(CC(CC2(C)O)OC(=O)C)(C)C"                                                                                                                                                                                                 
# 
_pdbx_chem_comp_identifier.comp_id           A1L6D 
_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},5~{S})-3,3,5-trimethyl-5-oxidanyl-4-[(3~{E},5~{E},7~{E},9~{E},11~{E},13~{E},15~{E},17~{Z})-3,7,12,16-tetramethyl-17-oxidanyl-19-oxidanylidene-19-[(1~{R},4~{S})-1,2,2-trimethyl-4-oxidanyl-cyclopentyl]nonadeca-1,3,5,7,9,11,13,15,17-nonaenylidene]cyclohexyl] ethanoate" 
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loop_
_pdbx_chem_comp_audit.comp_id 
_pdbx_chem_comp_audit.action_type 
_pdbx_chem_comp_audit.date 
_pdbx_chem_comp_audit.processing_site 
A1L6D "Create component"   2024-11-26 PDBJ 
A1L6D "Modify coordinates" 2026-01-20 RCSB 
A1L6D "Initial release"    2026-01-28 RCSB 
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