data_5BG # _chem_comp.id 5BG _chem_comp.name "{3-[(1R)-1-[({(2S)-1-[(2S)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetyl]piperidin-2-yl}carbonyl)amino]-3-(3,4-dimethoxyphenyl)propyl]phenoxy}acetic acid" _chem_comp.type NON-POLYMER _chem_comp.pdbx_type HETAIN _chem_comp.formula "C42 H54 N2 O10" _chem_comp.mon_nstd_parent_comp_id ? _chem_comp.pdbx_synonyms ? _chem_comp.pdbx_formal_charge 0 _chem_comp.pdbx_initial_date 2015-09-02 _chem_comp.pdbx_modified_date 2016-03-18 _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 746.886 _chem_comp.one_letter_code ? _chem_comp.three_letter_code 5BG _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 5DIU _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 5BG CAC C1 C 0 1 N N N 17.123 -4.518 -8.295 -7.335 3.551 -0.727 CAC 5BG 1 5BG OBH O1 O 0 1 N N N 16.450 -5.220 -7.252 -7.303 2.727 0.440 OBH 5BG 2 5BG CBU C2 C 0 1 Y N N 15.324 -5.877 -7.543 -6.248 1.879 0.568 CBU 5BG 3 5BG CAQ C3 C 0 1 Y N N 14.731 -5.833 -8.828 -5.262 1.845 -0.407 CAQ 5BG 4 5BG CBW C4 C 0 1 Y N N 14.749 -6.636 -6.588 -6.154 1.048 1.678 CBW 5BG 5 5BG OBJ O2 O 0 1 N N N 15.286 -6.643 -5.255 -7.117 1.082 2.639 OBJ 5BG 6 5BG CAE C5 C 0 1 N N N 16.358 -7.546 -5.145 -8.226 0.196 2.478 CAE 5BG 7 5BG CBV C6 C 0 1 Y N N 13.608 -7.325 -6.799 -5.074 0.183 1.804 CBV 5BG 8 5BG OBI O3 O 0 1 N N N 13.057 -8.064 -5.739 -4.977 -0.632 2.889 OBI 5BG 9 5BG CAD C7 C 0 1 N N N 11.723 -8.634 -5.837 -3.840 -1.495 2.952 CAD 5BG 10 5BG CAR C8 C 0 1 Y N N 12.978 -7.331 -8.045 -4.095 0.151 0.823 CAR 5BG 11 5BG CBR C9 C 0 1 Y N N 13.548 -6.553 -9.041 -4.189 0.983 -0.278 CBR 5BG 12 5BG CCA C10 C 0 1 N N S 12.858 -6.523 -10.419 -3.120 0.949 -1.339 CCA 5BG 13 5BG CBY C11 C 0 1 N N N 13.689 -7.178 -11.544 -3.043 -0.455 -1.941 CBY 5BG 14 5BG CAY C12 C 0 1 N N N 14.255 -8.506 -11.141 -4.430 -0.877 -2.430 CAY 5BG 15 5BG CAT C13 C 0 1 N N N 15.008 -9.257 -12.255 -4.353 -2.282 -3.032 CAT 5BG 16 5BG CAS C14 C 0 1 N N N 14.134 -9.318 -13.555 -3.377 -2.279 -4.210 CAS 5BG 17 5BG CAU C15 C 0 1 N N N 13.663 -7.977 -13.979 -1.990 -1.856 -3.721 CAU 5BG 18 5BG CAZ C16 C 0 1 N N N 12.905 -7.278 -12.823 -2.067 -0.452 -3.119 CAZ 5BG 19 5BG CBN C17 C 0 1 N N N 12.554 -5.078 -10.764 -1.791 1.306 -0.725 CBN 5BG 20 5BG OAH O4 O 0 1 N N N 13.252 -4.397 -11.492 -1.058 0.431 -0.316 OAH 5BG 21 5BG N N1 N 0 1 N N N 11.450 -4.488 -10.165 -1.418 2.598 -0.629 N 5BG 22 5BG CBD C18 C 0 1 N N N 10.597 -5.172 -9.139 -2.326 3.673 -1.052 CBD 5BG 23 5BG CAW C19 C 0 1 N N N 9.147 -4.857 -9.314 -2.484 4.667 0.102 CAW 5BG 24 5BG CAV C20 C 0 1 N N N 8.842 -3.348 -9.466 -1.102 5.151 0.547 CAV 5BG 25 5BG CB C21 C 0 1 N N N 9.697 -2.804 -10.592 -0.279 3.960 1.044 CB 5BG 26 5BG CA C22 C 0 1 N N S 11.210 -3.067 -10.386 -0.098 2.958 -0.094 CA 5BG 27 5BG C C23 C 0 1 N N N 11.670 -2.153 -9.213 0.592 1.723 0.425 C 5BG 28 5BG O O5 O 0 1 N N N 11.244 -1.035 -9.150 0.120 1.112 1.360 O 5BG 29 5BG NBE N2 N 0 1 N N N 12.559 -2.707 -8.373 1.735 1.298 -0.149 NBE 5BG 30 5BG CBX C24 C 0 1 N N R 12.947 -1.962 -7.120 2.407 0.098 0.356 CBX 5BG 31 5BG CBQ C25 C 0 1 Y N N 12.185 -2.568 -6.025 1.800 -1.124 -0.285 CBQ 5BG 32 5BG CAP C26 C 0 1 Y N N 11.151 -1.858 -5.464 1.581 -2.261 0.468 CAP 5BG 33 5BG CAL C27 C 0 1 Y N N 12.318 -3.893 -5.722 1.459 -1.104 -1.624 CAL 5BG 34 5BG CAJ C28 C 0 1 Y N N 11.543 -4.582 -4.809 0.901 -2.223 -2.215 CAJ 5BG 35 5BG CAK C29 C 0 1 Y N N 10.526 -3.833 -4.213 0.684 -3.364 -1.468 CAK 5BG 36 5BG CBP C30 C 0 1 Y N N 10.311 -2.506 -4.497 1.022 -3.385 -0.122 CBP 5BG 37 5BG OBK O6 O 0 1 N N N 9.282 -1.715 -3.978 0.806 -4.506 0.616 OBK 5BG 38 5BG CBC C31 C 0 1 N N N 8.353 -2.315 -3.073 0.228 -5.625 -0.058 CBC 5BG 39 5BG CBL C32 C 0 1 N N N 8.997 -2.608 -1.710 0.064 -6.766 0.913 CBL 5BG 40 5BG OAI O7 O 0 1 N N N 8.367 -3.433 -1.060 -0.464 -7.929 0.500 OAI 5BG 41 5BG OAF O8 O 0 1 N N N 10.068 -2.072 -1.419 0.407 -6.634 2.064 OAF 5BG 42 5BG CBA C33 C 0 1 N N N 14.440 -2.007 -6.938 3.897 0.166 0.016 CBA 5BG 43 5BG CAX C34 C 0 1 N N N 14.871 -0.873 -5.937 4.538 1.334 0.767 CAX 5BG 44 5BG CBO C35 C 0 1 Y N N 14.746 0.444 -6.466 6.006 1.401 0.432 CBO 5BG 45 5BG CAO C36 C 0 1 Y N N 15.601 0.870 -7.495 6.921 0.701 1.197 CAO 5BG 46 5BG CAM C37 C 0 1 Y N N 13.741 1.355 -6.067 6.435 2.157 -0.643 CAM 5BG 47 5BG CAN C38 C 0 1 Y N N 13.596 2.610 -6.578 7.780 2.221 -0.955 CAN 5BG 48 5BG CBS C39 C 0 1 Y N N 14.473 3.052 -7.614 8.703 1.527 -0.189 CBS 5BG 49 5BG OBF O9 O 0 1 N N N 14.415 4.298 -8.191 10.026 1.590 -0.494 OBF 5BG 50 5BG CAA C40 C 0 1 N N N 13.515 5.276 -7.712 10.396 2.390 -1.618 CAA 5BG 51 5BG CBT C41 C 0 1 Y N N 15.403 2.153 -8.011 8.270 0.757 0.887 CBT 5BG 52 5BG OBG O10 O 0 1 N N N 16.084 2.717 -9.110 9.172 0.074 1.642 OBG 5BG 53 5BG CAB C42 C 0 1 N N N 17.221 1.974 -9.525 8.656 -0.695 2.730 CAB 5BG 54 5BG H1 H1 H 0 1 N N N 18.025 -4.035 -7.890 -6.447 4.183 -0.751 H1 5BG 55 5BG H2 H2 H 0 1 N N N 17.410 -5.225 -9.087 -7.357 2.921 -1.617 H2 5BG 56 5BG H3 H3 H 0 1 N N N 16.453 -3.752 -8.713 -8.226 4.179 -0.705 H3 5BG 57 5BG H4 H4 H 0 1 N N N 15.180 -5.258 -9.625 -5.333 2.493 -1.268 H4 5BG 58 5BG H5 H5 H 0 1 N N N 16.748 -7.530 -4.116 -7.868 -0.834 2.458 H5 5BG 59 5BG H6 H6 H 0 1 N N N 16.009 -8.560 -5.389 -8.918 0.324 3.311 H6 5BG 60 5BG H7 H7 H 0 1 N N N 17.156 -7.255 -5.844 -8.738 0.421 1.542 H7 5BG 61 5BG H8 H8 H 0 1 N N N 11.483 -9.170 -4.907 -2.929 -0.897 2.954 H8 5BG 62 5BG H9 H9 H 0 1 N N N 10.991 -7.828 -5.995 -3.885 -2.089 3.865 H9 5BG 63 5BG H10 H10 H 0 1 N N N 11.685 -9.335 -6.684 -3.838 -2.158 2.087 H10 5BG 64 5BG H11 H11 H 0 1 N N N 12.087 -7.915 -8.225 -3.255 -0.521 0.920 H11 5BG 65 5BG H12 H12 H 0 1 N N N 11.906 -7.068 -10.337 -3.363 1.668 -2.122 H12 5BG 66 5BG H13 H13 H 0 1 N N N 14.540 -6.508 -11.738 -2.696 -1.157 -1.183 H13 5BG 67 5BG H14 H14 H 0 1 N N N 13.424 -9.142 -10.802 -5.126 -0.880 -1.590 H14 5BG 68 5BG H15 H15 H 0 1 N N N 14.954 -8.341 -10.308 -4.778 -0.176 -3.188 H15 5BG 69 5BG H16 H16 H 0 1 N N N 15.229 -10.280 -11.918 -4.006 -2.984 -2.274 H16 5BG 70 5BG H17 H17 H 0 1 N N N 15.949 -8.732 -12.475 -5.341 -2.583 -3.380 H17 5BG 71 5BG H18 H18 H 0 1 N N N 13.259 -9.956 -13.363 -3.322 -3.279 -4.639 H18 5BG 72 5BG H19 H19 H 0 1 N N N 14.736 -9.754 -14.366 -3.724 -1.577 -4.968 H19 5BG 73 5BG H20 H20 H 0 1 N N N 14.529 -7.363 -14.267 -1.642 -2.558 -2.963 H20 5BG 74 5BG H21 H21 H 0 1 N N N 12.988 -8.086 -14.841 -1.294 -1.854 -4.560 H21 5BG 75 5BG H22 H22 H 0 1 N N N 12.643 -6.260 -13.148 -2.414 0.250 -3.877 H22 5BG 76 5BG H23 H23 H 0 1 N N N 11.985 -7.846 -12.620 -1.079 -0.151 -2.771 H23 5BG 77 5BG H24 H24 H 0 1 N N N 10.737 -6.259 -9.229 -1.908 4.183 -1.920 H24 5BG 78 5BG H25 H25 H 0 1 N N N 10.913 -4.843 -8.138 -3.297 3.250 -1.309 H25 5BG 79 5BG H26 H26 H 0 1 N N N 8.603 -5.232 -8.434 -3.078 5.519 -0.231 H26 5BG 80 5BG H27 H27 H 0 1 N N N 8.787 -5.375 -10.216 -2.985 4.179 0.937 H27 5BG 81 5BG H28 H28 H 0 1 N N N 9.082 -2.823 -8.529 -0.592 5.618 -0.296 H28 5BG 82 5BG H29 H29 H 0 1 N N N 7.778 -3.205 -9.704 -1.213 5.877 1.352 H29 5BG 83 5BG H30 H30 H 0 1 N N N 9.536 -1.718 -10.661 0.697 4.306 1.383 H30 5BG 84 5BG H31 H31 H 0 1 N N N 9.383 -3.281 -11.532 -0.803 3.481 1.871 H31 5BG 85 5BG H32 H32 H 0 1 N N N 11.740 -2.746 -11.295 0.501 3.408 -0.886 H32 5BG 86 5BG H33 H33 H 0 1 N N N 12.958 -3.601 -8.575 2.114 1.787 -0.896 H33 5BG 87 5BG H34 H34 H 0 1 N N N 12.641 -0.911 -7.231 2.283 0.040 1.438 H34 5BG 88 5BG H35 H35 H 0 1 N N N 10.973 -0.831 -5.746 1.844 -2.275 1.515 H35 5BG 89 5BG H36 H36 H 0 1 N N N 13.090 -4.446 -6.237 1.627 -0.212 -2.210 H36 5BG 90 5BG H37 H37 H 0 1 N N N 11.711 -5.623 -4.574 0.635 -2.204 -3.261 H37 5BG 91 5BG H38 H38 H 0 1 N N N 9.880 -4.319 -3.497 0.248 -4.238 -1.929 H38 5BG 92 5BG H39 H39 H 0 1 N N N 7.505 -1.630 -2.927 -0.747 -5.345 -0.457 H39 5BG 93 5BG H40 H40 H 0 1 N N N 7.992 -3.259 -3.507 0.880 -5.934 -0.874 H40 5BG 94 5BG H41 H41 H 0 1 N N N 8.831 -3.623 -0.253 -0.549 -8.631 1.158 H41 5BG 95 5BG H42 H42 H 0 1 N N N 14.732 -2.987 -6.532 4.380 -0.766 0.312 H42 5BG 96 5BG H43 H43 H 0 1 N N N 14.934 -1.849 -7.908 4.018 0.313 -1.057 H43 5BG 97 5BG H44 H44 H 0 1 N N N 14.240 -0.946 -5.039 4.056 2.266 0.470 H44 5BG 98 5BG H45 H45 H 0 1 N N N 15.923 -1.037 -5.661 4.417 1.187 1.840 H45 5BG 99 5BG H46 H46 H 0 1 N N N 16.383 0.229 -7.874 6.584 0.112 2.036 H46 5BG 100 5BG H47 H47 H 0 1 N N N 13.043 1.035 -5.308 5.717 2.699 -1.241 H47 5BG 101 5BG H48 H48 H 0 1 N N N 12.824 3.265 -6.202 8.112 2.812 -1.796 H48 5BG 102 5BG H49 H49 H 0 1 N N N 13.624 6.197 -8.304 9.907 2.007 -2.514 H49 5BG 103 5BG H50 H50 H 0 1 N N N 12.485 4.902 -7.803 10.086 3.421 -1.447 H50 5BG 104 5BG H51 H51 H 0 1 N N N 13.735 5.491 -6.656 11.477 2.353 -1.750 H51 5BG 105 5BG H52 H52 H 0 1 N N N 17.695 2.476 -10.382 9.478 -1.188 3.248 H52 5BG 106 5BG H53 H53 H 0 1 N N N 17.940 1.909 -8.695 8.131 -0.038 3.423 H53 5BG 107 5BG H54 H54 H 0 1 N N N 16.909 0.961 -9.820 7.965 -1.447 2.348 H54 5BG 108 # 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 5BG CAU CAS SING N N 1 5BG CAU CAZ SING N N 2 5BG CAS CAT SING N N 3 5BG CAZ CBY SING N N 4 5BG CAT CAY SING N N 5 5BG CBY CAY SING N N 6 5BG CBY CCA SING N N 7 5BG OAH CBN DOUB N N 8 5BG CBN CCA SING N N 9 5BG CBN N SING N N 10 5BG CB CA SING N N 11 5BG CB CAV SING N N 12 5BG CCA CBR SING N N 13 5BG CA N SING N N 14 5BG CA C SING N N 15 5BG N CBD SING N N 16 5BG CAB OBG SING N N 17 5BG CAV CAW SING N N 18 5BG CAW CBD SING N N 19 5BG C O DOUB N N 20 5BG C NBE SING N N 21 5BG OBG CBT SING N N 22 5BG CBR CAQ DOUB Y N 23 5BG CBR CAR SING Y N 24 5BG CAQ CBU SING Y N 25 5BG NBE CBX SING N N 26 5BG CAC OBH SING N N 27 5BG OBF CAA SING N N 28 5BG OBF CBS SING N N 29 5BG CAR CBV DOUB Y N 30 5BG CBT CBS DOUB Y N 31 5BG CBT CAO SING Y N 32 5BG CBS CAN SING Y N 33 5BG CBU OBH SING N N 34 5BG CBU CBW DOUB Y N 35 5BG CAO CBO DOUB Y N 36 5BG CBX CBA SING N N 37 5BG CBX CBQ SING N N 38 5BG CBA CAX SING N N 39 5BG CBV CBW SING Y N 40 5BG CBV OBI SING N N 41 5BG CBW OBJ SING N N 42 5BG CAN CAM DOUB Y N 43 5BG CBO CAM SING Y N 44 5BG CBO CAX SING N N 45 5BG CBQ CAL DOUB Y N 46 5BG CBQ CAP SING Y N 47 5BG CAD OBI SING N N 48 5BG CAL CAJ SING Y N 49 5BG CAP CBP DOUB Y N 50 5BG OBJ CAE SING N N 51 5BG CAJ CAK DOUB Y N 52 5BG CBP CAK SING Y N 53 5BG CBP OBK SING N N 54 5BG OBK CBC SING N N 55 5BG CBC CBL SING N N 56 5BG CBL OAF DOUB N N 57 5BG CBL OAI SING N N 58 5BG CAC H1 SING N N 59 5BG CAC H2 SING N N 60 5BG CAC H3 SING N N 61 5BG CAQ H4 SING N N 62 5BG CAE H5 SING N N 63 5BG CAE H6 SING N N 64 5BG CAE H7 SING N N 65 5BG CAD H8 SING N N 66 5BG CAD H9 SING N N 67 5BG CAD H10 SING N N 68 5BG CAR H11 SING N N 69 5BG CCA H12 SING N N 70 5BG CBY H13 SING N N 71 5BG CAY H14 SING N N 72 5BG CAY H15 SING N N 73 5BG CAT H16 SING N N 74 5BG CAT H17 SING N N 75 5BG CAS H18 SING N N 76 5BG CAS H19 SING N N 77 5BG CAU H20 SING N N 78 5BG CAU H21 SING N N 79 5BG CAZ H22 SING N N 80 5BG CAZ H23 SING N N 81 5BG CBD H24 SING N N 82 5BG CBD H25 SING N N 83 5BG CAW H26 SING N N 84 5BG CAW H27 SING N N 85 5BG CAV H28 SING N N 86 5BG CAV H29 SING N N 87 5BG CB H30 SING N N 88 5BG CB H31 SING N N 89 5BG CA H32 SING N N 90 5BG NBE H33 SING N N 91 5BG CBX H34 SING N N 92 5BG CAP H35 SING N N 93 5BG CAL H36 SING N N 94 5BG CAJ H37 SING N N 95 5BG CAK H38 SING N N 96 5BG CBC H39 SING N N 97 5BG CBC H40 SING N N 98 5BG OAI H41 SING N N 99 5BG CBA H42 SING N N 100 5BG CBA H43 SING N N 101 5BG CAX H44 SING N N 102 5BG CAX H45 SING N N 103 5BG CAO H46 SING N N 104 5BG CAM H47 SING N N 105 5BG CAN H48 SING N N 106 5BG CAA H49 SING N N 107 5BG CAA H50 SING N N 108 5BG CAA H51 SING N N 109 5BG CAB H52 SING N N 110 5BG CAB H53 SING N N 111 5BG CAB H54 SING N N 112 # 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 5BG SMILES ACDLabs 12.01 "COc1c(OC)c(OC)cc(c1)C(C2CCCCC2)C(N3CCCCC3C(=O)NC(CCc4ccc(OC)c(c4)OC)c5cccc(c5)OCC(=O)O)=O" 5BG InChI InChI 1.03 ;InChI=1S/C42H54N2O10/c1-49-34-20-18-27(22-35(34)50-2)17-19-32(29-14-11-15-31(23-29)54-26-38(45)46)43-41(47)33-16-9-10-21-44(33)42(48)39(28-12-7-6-8-13-28)30-24-36(51-3)40(53-5)37(25-30)52-4/h11,14-15,18,20,22-25,28,32-33,39H,6-10,12-13,16-17,19,21,26H2,1-5H3,(H,43,47)(H,45,46)/t32-,33+,39+/m1/s1 ; 5BG InChIKey InChI 1.03 HVSNNDISDMAIJE-XEAFTEEUSA-N 5BG SMILES_CANONICAL CACTVS 3.385 "COc1ccc(CC[C@@H](NC(=O)[C@@H]2CCCCN2C(=O)[C@@H](C3CCCCC3)c4cc(OC)c(OC)c(OC)c4)c5cccc(OCC(O)=O)c5)cc1OC" 5BG SMILES CACTVS 3.385 "COc1ccc(CC[CH](NC(=O)[CH]2CCCCN2C(=O)[CH](C3CCCCC3)c4cc(OC)c(OC)c(OC)c4)c5cccc(OCC(O)=O)c5)cc1OC" 5BG SMILES_CANONICAL "OpenEye OEToolkits" 1.9.2 "COc1ccc(cc1OC)CC[C@H](c2cccc(c2)OCC(=O)O)NC(=O)[C@@H]3CCCCN3C(=O)[C@H](c4cc(c(c(c4)OC)OC)OC)C5CCCCC5" 5BG SMILES "OpenEye OEToolkits" 1.9.2 "COc1ccc(cc1OC)CCC(c2cccc(c2)OCC(=O)O)NC(=O)C3CCCCN3C(=O)C(c4cc(c(c(c4)OC)OC)OC)C5CCCCC5" # loop_ _pdbx_chem_comp_identifier.comp_id _pdbx_chem_comp_identifier.type _pdbx_chem_comp_identifier.program _pdbx_chem_comp_identifier.program_version _pdbx_chem_comp_identifier.identifier 5BG "SYSTEMATIC NAME" ACDLabs 12.01 "{3-[(1R)-1-[({(2S)-1-[(2S)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetyl]piperidin-2-yl}carbonyl)amino]-3-(3,4-dimethoxyphenyl)propyl]phenoxy}acetic acid" 5BG "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.9.2 "2-[3-[(1R)-1-[[(2S)-1-[(2S)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)ethanoyl]piperidin-2-yl]carbonylamino]-3-(3,4-dimethoxyphenyl)propyl]phenoxy]ethanoic acid" # loop_ _pdbx_chem_comp_audit.comp_id _pdbx_chem_comp_audit.action_type _pdbx_chem_comp_audit.date _pdbx_chem_comp_audit.processing_site 5BG "Create component" 2015-09-02 RCSB 5BG "Initial release" 2016-03-23 RCSB #