data_MOU
# 
_chem_comp.id                                    MOU 
_chem_comp.name                                  
"(1S,4R,5R,9S,11S)-2-({[(2S,5R,6R,7R,9S,10R)-2-(7-CARBOXYHEPTYL)-6-HYDROXY-10-METHOXY-9-METHYL-3-OXO-1,4,8-TRIOXASPIRO[4.5]DEC-7-YL]OXY}METHYL)-9-FORMYL-13-ISOPROPYL-5-METHYLTETRACYCLO[7.4.0.02,11.04.8]TRIDEC-12-ENE-1-CARBOXYLIC ACID" 
_chem_comp.type                                  NON-POLYMER 
_chem_comp.pdbx_type                             HETAIN 
_chem_comp.formula                               "C37 H54 O12" 
_chem_comp.mon_nstd_parent_comp_id               ? 
_chem_comp.pdbx_synonyms                         MORINIAFUNGIN 
_chem_comp.pdbx_formal_charge                    0 
_chem_comp.pdbx_initial_date                     2006-11-02 
_chem_comp.pdbx_modified_date                    2008-10-14 
_chem_comp.pdbx_ambiguous_flag                   ? 
_chem_comp.pdbx_release_status                   REL 
_chem_comp.pdbx_replaced_by                      ? 
_chem_comp.pdbx_replaces                         ? 
_chem_comp.formula_weight                        690.817 
_chem_comp.one_letter_code                       ? 
_chem_comp.three_letter_code                     MOU 
_chem_comp.pdbx_model_coordinates_details        ? 
_chem_comp.pdbx_model_coordinates_missing_flag   N 
_chem_comp.pdbx_ideal_coordinates_details        ? 
_chem_comp.pdbx_ideal_coordinates_missing_flag   N 
_chem_comp.pdbx_model_coordinates_db_code        2NPF 
_chem_comp.pdbx_subcomponent_list                ? 
_chem_comp.pdbx_processing_site                  RCSB 
# 
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.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 
MOU C    C    C 0 1 N N R 3.286  12.144 39.147 1.895  -0.912  -0.511 C    MOU 1   
MOU O    O    O 0 1 N N N 3.315  10.750 39.203 2.443  0.356   -0.849 O    MOU 2   
MOU C1   C1   C 0 1 N N N 4.584  10.314 39.191 3.754  0.350   -0.501 C1   MOU 3   
MOU C2   C2   C 0 1 N N S 5.536  11.465 39.367 4.089  -0.945  0.175  C2   MOU 4   
MOU O3   O3   O 0 1 N N N 4.627  12.606 39.279 2.892  -1.708  0.131  O3   MOU 5   
MOU C4   C4   C 0 1 N N N 2.134  18.225 43.477 -0.244 -7.601  -3.187 C4   MOU 6   
MOU C5   C5   C 0 1 N N N 2.135  16.952 44.128 0.882  -7.034  -3.654 C5   MOU 7   
MOU C6   C6   C 0 1 N N R 0.729  16.368 43.777 0.457  -5.896  -4.565 C6   MOU 8   
MOU C7   C7   C 0 1 N N N -0.292 17.061 44.769 -0.108 -6.647  -5.802 C7   MOU 9   
MOU C8   C8   C 0 1 N N R -0.577 18.376 43.898 -1.536 -7.068  -5.307 C8   MOU 10  
MOU C9   C9   C 0 1 N N R 0.671  18.231 42.757 -1.410 -6.798  -3.754 C9   MOU 11  
MOU C10  C10  C 0 1 N N S 0.534  16.796 42.268 -0.786 -5.366  -3.775 C10  MOU 12  
MOU C11  C11  C 0 1 N N N -0.482 19.635 44.798 -1.826 -8.507  -5.626 C11  MOU 13  
MOU O12  O12  O 0 1 N N N 0.266  19.805 45.769 -1.034 -9.245  -6.203 O12  MOU 14  
MOU C13  C13  C 0 1 N N N -0.884 16.450 41.543 -1.703 -4.302  -4.465 C13  MOU 15  
MOU C14  C14  C 0 1 N N R -1.928 18.355 43.078 -2.631 -6.157  -5.884 C14  MOU 16  
MOU C15  C15  C 0 1 N N S -2.146 16.934 42.386 -2.199 -4.691  -5.845 C15  MOU 17  
MOU C16  C16  C 0 1 N N R -3.494 17.149 41.663 -3.367 -3.963  -6.522 C16  MOU 18  
MOU C17  C17  C 0 1 N N N -4.270 18.004 42.691 -3.824 -4.980  -7.603 C17  MOU 19  
MOU C18  C18  C 0 1 N N N -3.271 18.459 43.769 -3.050 -6.288  -7.343 C18  MOU 20  
MOU C19  C19  C 0 1 N N N -3.393 17.921 40.325 -4.514 -3.570  -5.595 C19  MOU 21  
MOU C20  C20  C 0 1 N N N 3.217  19.284 43.444 -0.372 -8.806  -2.333 C20  MOU 22  
MOU C21  C21  C 0 1 N N N 3.856  19.522 44.831 0.198  -10.038 -3.041 C21  MOU 23  
MOU C22  C22  C 0 1 N N N 4.316  18.905 42.421 0.317  -8.606  -0.979 C22  MOU 24  
MOU C23  C23  C 0 1 N N N 0.620  19.442 41.677 -2.657 -6.925  -2.927 C23  MOU 25  
MOU O24  O24  O 0 1 N N N 0.729  20.626 42.151 -3.723 -7.366  -3.328 O24  MOU 26  
MOU O25  O25  O 0 1 N N N 0.478  19.153 40.439 -2.442 -6.478  -1.665 O25  MOU 27  
MOU C26  C26  C 0 1 N N N 1.479  16.189 41.178 -0.405 -4.761  -2.398 C26  MOU 28  
MOU O27  O27  O 0 1 N N N 1.494  14.756 41.251 0.282  -3.557  -2.639 O27  MOU 29  
MOU C28  C28  C 0 1 N N S 2.355  14.206 40.210 0.712  -2.935  -1.431 C28  MOU 30  
MOU O29  O29  O 0 1 N N N 1.904  14.618 38.846 -0.406 -2.652  -0.587 O29  MOU 31  
MOU C30  C30  C 0 1 N N S 2.694  14.137 37.766 -0.025 -2.067  0.664  C30  MOU 32  
MOU C31  C31  C 0 1 N N S 2.695  12.614 37.793 0.696  -0.730  0.434  C31  MOU 33  
MOU C32  C32  C 0 1 N N S 2.391  12.678 40.293 1.447  -1.637  -1.786 C32  MOU 34  
MOU O33  O33  O 0 1 N N N 1.063  12.215 40.172 0.562  -0.785  -2.519 O33  MOU 35  
MOU C34  C34  C 0 1 N N N 2.123  14.656 36.468 -1.295 -1.886  1.489  C34  MOU 36  
MOU O35  O35  O 0 1 N N N 3.510  12.123 36.707 1.131  -0.205  1.685  O35  MOU 37  
MOU C36  C36  C 0 1 N N N 2.943  11.067 35.926 1.804  1.034   1.520  C36  MOU 38  
MOU O37  O37  O 0 1 N N N 4.859  9.151  39.025 4.531  1.269   -0.706 O37  MOU 39  
MOU C38  C38  C 0 1 N N N 6.127  11.374 40.746 5.191  -1.692  -0.547 C38  MOU 40  
MOU C39  C39  C 0 1 N N N 7.091  12.416 41.215 5.579  -3.020  0.116  C39  MOU 41  
MOU C40  C40  C 0 1 N N N 7.358  12.015 42.646 6.717  -3.745  -0.607 C40  MOU 42  
MOU C41  C41  C 0 1 N N N 8.232  12.924 43.403 7.109  -5.073  0.051  C41  MOU 43  
MOU C42  C42  C 0 1 N N N 8.344  12.386 44.802 8.230  -5.810  -0.687 C42  MOU 44  
MOU C43  C43  C 0 1 N N N 9.191  13.304 45.657 8.625  -7.138  -0.027 C43  MOU 45  
MOU C44  C44  C 0 1 N N N 10.227 12.582 46.535 9.759  -7.892  -0.715 C44  MOU 46  
MOU C45  C45  C 0 1 N N N 11.584 13.287 46.718 9.417  -8.291  -2.128 C45  MOU 47  
MOU O46  O46  O 0 1 N N N 12.370 12.631 47.460 10.501 -8.311  -2.943 O46  MOU 48  
MOU O47  O47  O 0 1 N N N 11.798 14.423 46.137 8.287  -8.574  -2.503 O47  MOU 49  
MOU H46  H46  H 0 1 N N N 13.191 13.101 47.547 10.320 -8.571  -3.871 H46  MOU 50  
MOU H441 1H44 H 0 0 N N N 9.783  12.468 47.535 10.007 -8.800  -0.152 H441 MOU 51  
MOU H442 2H44 H 0 0 N N N 10.452 11.640 46.013 10.680 -7.299  -0.736 H442 MOU 52  
MOU H431 1H43 H 0 0 N N N 9.735  13.984 44.985 7.735  -7.777  0.008  H431 MOU 53  
MOU H432 2H43 H 0 0 N N N 8.503  13.822 46.342 8.911  -6.947  1.015  H432 MOU 54  
MOU H421 1H42 H 0 0 N N N 7.338  12.311 45.241 7.909  -6.037  -1.709 H421 MOU 55  
MOU H422 2H42 H 0 0 N N N 8.819  11.395 44.765 9.108  -5.159  -0.773 H422 MOU 56  
MOU H411 1H41 H 0 0 N N N 9.226  12.970 42.935 7.431  -4.849  1.074  H411 MOU 57  
MOU H412 2H41 H 0 0 N N N 7.814  13.941 43.413 6.227  -5.720  0.130  H412 MOU 58  
MOU H401 1H40 H 0 0 N N N 6.389  11.977 43.166 7.607  -3.106  -0.616 H401 MOU 59  
MOU H402 2H40 H 0 0 N N N 7.884  11.050 42.601 6.441  -3.920  -1.654 H402 MOU 60  
MOU H391 1H39 H 0 0 N N N 8.013  12.416 40.615 4.688  -3.657  0.133  H391 MOU 61  
MOU H392 2H39 H 0 0 N N N 6.698  13.439 41.121 5.859  -2.838  1.160  H392 MOU 62  
MOU H381 1H38 H 0 0 N N N 5.278  11.407 41.445 4.859  -1.907  -1.572 H381 MOU 63  
MOU H382 2H38 H 0 0 N N N 6.733  10.457 40.709 6.079  -1.051  -0.636 H382 MOU 64  
MOU H2   H2   H 0 1 N N N 6.370  11.509 38.651 4.345  -0.760  1.222  H2   MOU 65  
MOU H32  H32  H 0 1 N N N 2.810  12.325 41.247 2.297  -1.850  -2.444 H32  MOU 66  
MOU H33  H33  H 0 1 N N N 0.683  12.111 41.037 0.937  -0.703  -3.408 H33  MOU 67  
MOU H28  H28  H 0 1 N N N 3.365  14.608 40.378 1.376  -3.643  -0.923 H28  MOU 68  
MOU H261 1H26 H 0 0 N N N 1.119  16.493 40.184 0.233  -5.462  -1.877 H261 MOU 69  
MOU H262 2H26 H 0 0 N N N 2.500  16.560 41.352 -1.312 -4.573  -1.840 H262 MOU 70  
MOU H131 1H13 H 0 0 N N N -0.906 16.955 40.566 -1.167 -3.347  -4.540 H131 MOU 71  
MOU H132 2H13 H 0 0 N N N -0.949 15.356 41.446 -2.563 -4.123  -3.809 H132 MOU 72  
MOU H15  H15  H 0 1 N N N -2.213 16.067 43.059 -1.356 -4.518  -6.526 H15  MOU 73  
MOU H16  H16  H 0 1 N N N -3.952 16.190 41.381 -3.004 -3.049  -7.008 H16  MOU 74  
MOU H191 1H19 H 0 0 N N N -3.369 19.002 40.526 -4.675 -2.489  -5.620 H191 MOU 75  
MOU H192 2H19 H 0 0 N N N -2.473 17.625 39.800 -5.441 -4.064  -5.901 H192 MOU 76  
MOU H193 3H19 H 0 0 N N N -4.266 17.684 39.698 -4.292 -3.862  -4.565 H193 MOU 77  
MOU H171 1H17 H 0 0 N N N -4.715 18.879 42.195 -3.602 -4.608  -8.610 H171 MOU 78  
MOU H172 2H17 H 0 0 N N N -5.083 17.418 43.143 -4.903 -5.161  -7.553 H172 MOU 79  
MOU H181 1H18 H 0 0 N N N -3.317 17.814 44.659 -3.675 -7.167  -7.524 H181 MOU 80  
MOU H182 2H18 H 0 0 N N N -3.480 19.473 44.140 -2.180 -6.349  -8.007 H182 MOU 81  
MOU H14  H14  H 0 1 N N N -1.740 19.256 42.475 -3.543 -6.299  -5.286 H14  MOU 82  
MOU H11  H11  H 0 1 N N N -1.141 20.454 44.550 -2.816 -8.876  -5.308 H11  MOU 83  
MOU H71  1H7  H 0 1 N N N -1.192 16.460 44.966 -0.111 -6.023  -6.698 H71  MOU 84  
MOU H72  2H7  H 0 1 N N N 0.071  17.231 45.793 0.510  -7.517  -6.064 H72  MOU 85  
MOU H6   H6   H 0 1 N N N 0.597  15.281 43.881 1.242  -5.166  -4.766 H6   MOU 86  
MOU H5   H5   H 0 1 N N N 2.919  16.502 44.720 1.894  -7.369  -3.488 H5   MOU 87  
MOU H20  H20  H 0 1 N N N 2.732  20.222 43.137 -1.440 -8.989  -2.139 H20  MOU 88  
MOU H211 1H21 H 0 0 N N N 4.950  19.579 44.727 1.266  -9.918  -3.252 H211 MOU 89  
MOU H212 2H21 H 0 0 N N N 3.479  20.466 45.251 -0.315 -10.210 -3.995 H212 MOU 90  
MOU H213 3H21 H 0 0 N N N 3.595  18.691 45.502 0.074  -10.939 -2.431 H213 MOU 91  
MOU H221 1H22 H 0 0 N N N 3.870  18.815 41.419 -0.099 -7.737  -0.457 H221 MOU 92  
MOU H222 2H22 H 0 0 N N N 5.090  19.686 42.409 1.394  -8.443  -1.099 H222 MOU 93  
MOU H223 3H22 H 0 0 N N N 4.768  17.944 42.708 0.179  -9.480  -0.333 H223 MOU 94  
MOU H25  H25  H 0 1 N N N 0.466  19.953 39.926 -3.247 -6.550  -1.109 H25  MOU 95  
MOU H30  H30  H 0 1 N N N 3.732  14.490 37.858 0.619  -2.767  1.209  H30  MOU 96  
MOU H341 1H34 H 0 0 N N N 1.035  14.782 36.570 -1.086 -1.309  2.395  H341 MOU 97  
MOU H342 2H34 H 0 0 N N N 2.583  15.625 36.227 -2.057 -1.355  0.910  H342 MOU 98  
MOU H343 3H34 H 0 0 N N N 2.335  13.938 35.662 -1.702 -2.857  1.786  H343 MOU 99  
MOU H31  H31  H 0 1 N N N 1.671  12.228 37.681 0.003  0.002   0.001  H31  MOU 100 
MOU H361 1H36 H 0 0 N N N 2.797  11.413 34.892 1.539  1.706   2.340  H361 MOU 101 
MOU H362 2H36 H 0 0 N N N 3.622  10.202 35.931 1.520  1.479   0.563  H362 MOU 102 
MOU H363 3H36 H 0 0 N N N 1.973  10.775 36.355 2.882  0.857   1.531  H363 MOU 103 
# 
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 
MOU C   O3   SING N N 1   
MOU C   O    SING N N 2   
MOU C   C32  SING N N 3   
MOU C   C31  SING N N 4   
MOU O   C1   SING N N 5   
MOU C1  C2   SING N N 6   
MOU C1  O37  DOUB N N 7   
MOU C2  C38  SING N N 8   
MOU C2  H2   SING N N 9   
MOU C2  O3   SING N N 10  
MOU C4  C5   DOUB N N 11  
MOU C4  C20  SING N N 12  
MOU C4  C9   SING N N 13  
MOU C5  C6   SING N N 14  
MOU C5  H5   SING N N 15  
MOU C6  C7   SING N N 16  
MOU C6  C10  SING N N 17  
MOU C6  H6   SING N N 18  
MOU C7  C8   SING N N 19  
MOU C7  H71  SING N N 20  
MOU C7  H72  SING N N 21  
MOU C8  C14  SING N N 22  
MOU C8  C11  SING N N 23  
MOU C8  C9   SING N N 24  
MOU C9  C10  SING N N 25  
MOU C9  C23  SING N N 26  
MOU C10 C26  SING N N 27  
MOU C10 C13  SING N N 28  
MOU C11 H11  SING N N 29  
MOU C11 O12  DOUB N N 30  
MOU C13 H131 SING N N 31  
MOU C13 H132 SING N N 32  
MOU C13 C15  SING N N 33  
MOU C14 C18  SING N N 34  
MOU C14 C15  SING N N 35  
MOU C14 H14  SING N N 36  
MOU C15 H15  SING N N 37  
MOU C15 C16  SING N N 38  
MOU C16 H16  SING N N 39  
MOU C16 C19  SING N N 40  
MOU C16 C17  SING N N 41  
MOU C17 H171 SING N N 42  
MOU C17 H172 SING N N 43  
MOU C17 C18  SING N N 44  
MOU C18 H181 SING N N 45  
MOU C18 H182 SING N N 46  
MOU C19 H191 SING N N 47  
MOU C19 H192 SING N N 48  
MOU C19 H193 SING N N 49  
MOU C20 H20  SING N N 50  
MOU C20 C21  SING N N 51  
MOU C20 C22  SING N N 52  
MOU C21 H211 SING N N 53  
MOU C21 H212 SING N N 54  
MOU C21 H213 SING N N 55  
MOU C22 H221 SING N N 56  
MOU C22 H222 SING N N 57  
MOU C22 H223 SING N N 58  
MOU C23 O24  DOUB N N 59  
MOU C23 O25  SING N N 60  
MOU O25 H25  SING N N 61  
MOU C26 O27  SING N N 62  
MOU C26 H261 SING N N 63  
MOU C26 H262 SING N N 64  
MOU O27 C28  SING N N 65  
MOU C28 C32  SING N N 66  
MOU C28 H28  SING N N 67  
MOU C28 O29  SING N N 68  
MOU O29 C30  SING N N 69  
MOU C30 H30  SING N N 70  
MOU C30 C34  SING N N 71  
MOU C30 C31  SING N N 72  
MOU C31 H31  SING N N 73  
MOU C31 O35  SING N N 74  
MOU C32 H32  SING N N 75  
MOU C32 O33  SING N N 76  
MOU O33 H33  SING N N 77  
MOU C34 H341 SING N N 78  
MOU C34 H342 SING N N 79  
MOU C34 H343 SING N N 80  
MOU O35 C36  SING N N 81  
MOU C36 H361 SING N N 82  
MOU C36 H362 SING N N 83  
MOU C36 H363 SING N N 84  
MOU C38 C39  SING N N 85  
MOU C38 H381 SING N N 86  
MOU C38 H382 SING N N 87  
MOU C39 C40  SING N N 88  
MOU C39 H391 SING N N 89  
MOU C39 H392 SING N N 90  
MOU C40 C41  SING N N 91  
MOU C40 H401 SING N N 92  
MOU C40 H402 SING N N 93  
MOU C41 C42  SING N N 94  
MOU C41 H411 SING N N 95  
MOU C41 H412 SING N N 96  
MOU C42 C43  SING N N 97  
MOU C42 H421 SING N N 98  
MOU C42 H422 SING N N 99  
MOU C43 C44  SING N N 100 
MOU C43 H431 SING N N 101 
MOU C43 H432 SING N N 102 
MOU C44 C45  SING N N 103 
MOU C44 H441 SING N N 104 
MOU C44 H442 SING N N 105 
MOU C45 O46  SING N N 106 
MOU C45 O47  DOUB N N 107 
MOU O46 H46  SING N N 108 
# 
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 
MOU SMILES           ACDLabs              10.04 O=CC41CC2C=C(C(C)C)C1(C(=O)O)C2(CC3C(C)CCC34)COC6OC(C)C(OC)C5(OC(=O)C(O5)CCCCCCCC(=O)O)C6O 
MOU InChI            InChI                1.02b 
;InChI=1/C37H54O12/c1-20(2)26-15-23-16-34(18-38)25-14-13-21(3)24(25)17-35(23,36(26,34)33(43)44)19-46-32-29(41)37(30(45-5)22(4)47-32)48-27(31(42)49-37)11-9-7-6-8-10-12-28(39)40/h15,18,20-25,27,29-30,32,41H,6-14,16-17,19H2,1-5H3,(H,39,40)(H,43,44)/t21-,22-,23+,24-,25-,27+,29-,30-,32-,34+,35+,36+,37-/m1/s1/f/h39,43H
;
MOU InChIKey         InChI                1.02b UDEBDAZBOLNLCQ-KHUWRTSNDM 
MOU SMILES_CANONICAL CACTVS               3.341 CO[C@@H]1[C@@H](C)O[C@@H](OC[C@@]23C[C@@H]4[C@H](C)CC[C@H]4[C@]5(C[C@@H]2C=C(C(C)C)[C@@]35C(O)=O)C=O)[C@@H](O)[C@]16O[C@@H](CCCCCCCC(O)=O)C(=O)O6 
MOU SMILES           CACTVS               3.341 CO[CH]1[CH](C)O[CH](OC[C]23C[CH]4[CH](C)CC[CH]4[C]5(C[CH]2C=C(C(C)C)[C]35C(O)=O)C=O)[CH](O)[C]16O[CH](CCCCCCCC(O)=O)C(=O)O6 
MOU SMILES_CANONICAL "OpenEye OEToolkits" 1.5.0 C[C@@H]1CC[C@@H]2[C@@H]1C[C@@]3([C@@H]4C[C@]2([C@]3(C(=C4)C(C)C)C(=O)O)C=O)CO[C@H]5[C@H]([C@@]6([C@@H]([C@H](O5)C)OC)O[C@H](C(=O)O6)CCCCCCCC(=O)O)O 
MOU SMILES           "OpenEye OEToolkits" 1.5.0 CC1CCC2C1CC3(C4CC2(C3(C(=C4)C(C)C)C(=O)O)C=O)COC5C(C6(C(C(O5)C)OC)OC(C(=O)O6)CCCCCCCC(=O)O)O 
# 
_pdbx_chem_comp_identifier.comp_id           MOU 
_pdbx_chem_comp_identifier.type              "SYSTEMATIC NAME" 
_pdbx_chem_comp_identifier.program           ACDLabs 
_pdbx_chem_comp_identifier.program_version   10.04 
_pdbx_chem_comp_identifier.identifier        
;(1R,2S,4R,5R,8R,9S,11R)-2-({[(2S,5R,6R,7R,9R,10R)-2-(7-carboxyheptyl)-6-hydroxy-10-methoxy-9-methyl-3-oxo-1,4,8-trioxaspiro[4.5]dec-7-yl]oxy}methyl)-9-formyl-5-methyl-13-(1-methylethyl)tetracyclo[7.4.0.0~2,11~.0~4,8~]tridec-12-ene-1-carboxylic acid (non-preferred name)
;
# 
