data_RR6 # _chem_comp.id RR6 _chem_comp.name "3-HYDROXY-7-(4-{1-[2-HYDROXY-3-(2-HYDROXY-5-SULFO-PHENYLAZO)-BENZYL]-2-SULFO-ETHYLAMINO}-[1,2,5]TRIAZIN-2-YLAMINO)-2-(2-HYDROXY-5-SULFO-PHENYLAZO)-NAPTHALENE-1,8-DISULFONIC ACID" _chem_comp.type NON-POLYMER _chem_comp.pdbx_type HETAIN _chem_comp.formula "C35 H25 N9 O22 S6" _chem_comp.mon_nstd_parent_comp_id ? _chem_comp.pdbx_synonyms "AZO-DYE RR6 HAPTEN" _chem_comp.pdbx_formal_charge 0 _chem_comp.pdbx_initial_date 2000-07-14 _chem_comp.pdbx_modified_date 2021-03-01 _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 1116.010 _chem_comp.one_letter_code ? _chem_comp.three_letter_code RR6 _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 1QD0 _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 RR6 C60 C60 C 0 1 Y N N -9.732 25.600 -12.939 4.169 -0.466 10.859 C60 RR6 1 RR6 C61 C61 C 0 1 Y N N -9.458 26.597 -12.016 4.824 -0.282 12.065 C61 RR6 2 RR6 C62 C62 C 0 1 Y N N -8.828 26.256 -10.810 4.141 0.224 13.154 C62 RR6 3 RR6 C63 C63 C 0 1 Y N N -8.490 24.928 -10.553 2.801 0.557 13.048 C63 RR6 4 RR6 C64 C64 C 0 1 Y N N -8.782 23.964 -11.493 2.134 0.385 11.853 C64 RR6 5 RR6 C54 C54 C 0 1 Y N N -9.390 24.296 -12.682 2.814 -0.126 10.744 C54 RR6 6 RR6 O79 O79 O 0 1 N N N -10.357 25.889 -14.126 4.840 -0.965 9.788 O79 RR6 7 RR6 O82 O82 O 0 1 N N N -6.103 24.605 -9.243 2.944 1.748 15.294 O82 RR6 8 RR6 O83 O83 O 0 1 N N N -7.886 25.301 -7.912 1.356 0.022 15.204 O83 RR6 9 RR6 O84 O84 O 0 1 N N N -7.773 23.099 -8.660 0.832 1.917 13.920 O84 RR6 10 RR6 S81 S81 S 0 1 N N N -7.503 24.461 -8.992 1.944 1.203 14.445 S81 RR6 11 RR6 C55 C55 C 0 1 Y N N -10.282 21.048 -15.528 0.944 -0.674 7.174 C55 RR6 12 RR6 C53 C53 C 0 1 Y N N -9.579 20.916 -14.350 0.259 -0.163 8.275 C53 RR6 13 RR6 C59 C59 C 0 1 Y N N -9.153 19.663 -13.919 -1.103 0.176 8.171 C59 RR6 14 RR6 C58 C58 C 0 1 Y N N -9.426 18.556 -14.699 -1.773 0.013 7.004 C58 RR6 15 RR6 C57 C57 C 0 1 Y N N -10.127 18.691 -15.889 -1.111 -0.501 5.872 C57 RR6 16 RR6 C56 C56 C 0 1 Y N N -10.556 19.941 -16.304 0.260 -0.849 5.956 C56 RR6 17 RR6 C65 C65 C 0 1 Y N N -11.132 20.097 -17.562 0.918 -1.361 4.824 C65 RR6 18 RR6 C66 C66 C 0 1 Y N N -11.268 18.997 -18.407 0.237 -1.520 3.658 C66 RR6 19 RR6 C67 C67 C 0 1 Y N N -10.827 17.753 -17.983 -1.117 -1.180 3.565 C67 RR6 20 RR6 C68 C68 C 0 1 Y N N -10.267 17.599 -16.728 -1.790 -0.670 4.655 C68 RR6 21 RR6 O78 O78 O 0 1 N N N -10.720 22.275 -15.916 2.257 -1.000 7.274 O78 RR6 22 RR6 O87 O87 O 0 1 N N N -8.501 15.787 -15.663 -3.773 -0.192 3.131 O87 RR6 23 RR6 O88 O88 O 0 1 N N N -10.121 14.884 -17.092 -3.692 0.830 5.438 O88 RR6 24 RR6 O91 O91 O 0 1 N N N -10.711 15.600 -14.943 -4.302 -1.406 5.069 O91 RR6 25 RR6 S86 S86 S 0 1 N N N -9.875 15.858 -16.066 -3.493 -0.238 4.523 S86 RR6 26 RR6 O89 O89 O 0 1 N N N -8.012 18.086 -11.985 -3.327 0.562 9.350 O89 RR6 27 RR6 O90 O90 O 0 1 N N N -7.296 20.303 -11.994 -1.800 2.335 9.541 O90 RR6 28 RR6 O92 O92 O 0 1 N N N -9.416 19.763 -11.185 -1.205 0.386 10.707 O92 RR6 29 RR6 S85 S85 S 0 1 N N N -8.427 19.441 -12.160 -1.948 0.820 9.576 S85 RR6 30 RR6 N51 N51 N 0 1 N N N -9.262 22.080 -13.546 0.911 0.009 9.459 N51 RR6 31 RR6 N52 N52 N 0 1 N N N -9.478 23.269 -13.734 2.160 -0.299 9.558 N52 RR6 32 RR6 C10 C10 C 0 1 Y N N -20.142 24.009 -15.765 4.189 -0.461 -10.795 C10 RR6 33 RR6 C11 C11 C 0 1 Y N N -21.097 24.719 -15.063 4.854 -0.325 -12.003 C11 RR6 34 RR6 C12 C12 C 0 1 Y N N -22.437 24.543 -15.358 4.179 0.132 -13.118 C12 RR6 35 RR6 C13 C13 C 0 1 Y N N -22.833 23.661 -16.355 2.835 0.458 -13.039 C13 RR6 36 RR6 C14 C14 C 0 1 Y N N -21.869 22.951 -17.061 2.157 0.328 -11.846 C14 RR6 37 RR6 C4 C4 C 0 1 Y N N -20.518 23.118 -16.771 2.827 -0.138 -10.711 C4 RR6 38 RR6 O29 O29 O 0 1 N N N -18.825 24.201 -15.430 4.852 -0.911 -9.699 O29 RR6 39 RR6 O32 O32 O 0 1 N N N -25.431 23.361 -15.551 2.995 1.561 -15.329 O32 RR6 40 RR6 O33 O33 O 0 1 N N N -25.126 24.588 -17.523 0.866 1.766 -13.986 O33 RR6 41 RR6 O34 O34 O 0 1 N N N -24.871 22.262 -17.538 1.418 -0.172 -15.188 O34 RR6 42 RR6 S31 S31 S 0 1 N N N -24.682 23.455 -16.770 1.989 1.041 -14.470 S31 RR6 43 RR6 C5 C5 C 0 1 Y N N -17.182 21.227 -19.264 0.923 -0.559 -7.142 C5 RR6 44 RR6 C3 C3 C 0 1 Y N N -18.533 21.394 -19.558 0.247 -0.092 -8.269 C3 RR6 45 RR6 C9 C9 C 0 1 Y N N -19.101 20.718 -20.638 -1.115 0.249 -8.190 C9 RR6 46 RR6 C8 C8 C 0 1 Y N N -18.314 19.894 -21.415 -1.799 0.121 -7.026 C8 RR6 47 RR6 C7 C7 C 0 1 Y N N -16.972 19.732 -21.127 -1.146 -0.346 -5.868 C7 RR6 48 RR6 C6 C6 C 0 1 Y N N -16.407 20.394 -20.046 0.227 -0.690 -5.925 C6 RR6 49 RR6 C15 C15 C 0 1 Y N N -15.105 20.106 -19.664 0.875 -1.157 -4.768 C15 RR6 50 RR6 C16 C16 C 0 1 Y N N -14.370 19.165 -20.363 0.183 -1.275 -3.604 C16 RR6 51 RR6 C17 C17 C 0 1 Y N N -14.938 18.511 -21.442 -1.173 -0.938 -3.538 C17 RR6 52 RR6 C18 C18 C 0 1 Y N N -16.239 18.798 -21.824 -1.838 -0.477 -4.655 C18 RR6 53 RR6 O28 O28 O 0 1 N N N -16.589 22.018 -18.324 2.238 -0.883 -7.217 O28 RR6 54 RR6 O37 O37 O 0 1 N N N -18.012 17.072 -22.956 -4.339 -1.243 -5.082 O37 RR6 55 RR6 O38 O38 O 0 1 N N N -15.984 17.288 -24.101 -3.845 0.028 -3.171 O38 RR6 56 RR6 O41 O41 O 0 1 N N N -17.575 18.997 -24.199 -3.740 0.986 -5.505 O41 RR6 57 RR6 S36 S36 S 0 1 N N N -16.998 17.986 -23.368 -3.546 -0.054 -4.558 S36 RR6 58 RR6 O39 O39 O 0 1 N N N -21.171 20.590 -22.424 -1.814 2.352 -9.643 O39 RR6 59 RR6 O40 O40 O 0 1 N N N -21.726 20.072 -20.215 -1.188 0.370 -10.733 O40 RR6 60 RR6 O42 O42 O 0 1 N N N -21.333 22.290 -20.832 -3.328 0.573 -9.408 O42 RR6 61 RR6 S35 S35 S 0 1 N N N -20.950 20.929 -21.053 -1.949 0.836 -9.627 S35 RR6 62 RR6 N1 N1 N 0 1 N N N -19.523 22.316 -17.524 2.162 -0.269 -9.526 N1 RR6 63 RR6 N2 N2 N 0 1 N N N -19.375 22.308 -18.742 0.911 0.038 -9.451 N2 RR6 64 RR6 N19 N19 N 0 1 N N N -14.173 17.677 -22.225 -1.860 -1.069 -2.330 N19 RR6 65 RR6 N26 N26 N 0 1 N N N -10.870 16.635 -18.782 -1.792 -1.354 2.355 N26 RR6 66 RR6 C20 C20 C 0 1 Y N N -13.195 16.748 -21.733 -1.179 -0.960 -1.133 C20 RR6 67 RR6 N21 N21 N 0 1 Y N N -12.540 17.071 -20.504 -1.806 -1.201 0.013 N21 RR6 68 RR6 C22 C22 C 0 1 Y N N -11.526 16.235 -19.986 -1.146 -1.100 1.161 C22 RR6 69 RR6 N23 N23 N 0 1 Y N N -11.154 15.042 -20.700 0.137 -0.747 1.160 N23 RR6 70 RR6 C24 C24 C 0 1 Y N N -11.803 14.701 -21.952 0.756 -0.504 0.018 C24 RR6 71 RR6 N25 N25 N 0 1 Y N N -12.830 15.566 -22.460 0.104 -0.608 -1.126 N25 RR6 72 RR6 H61 H61 H 0 1 N N N -9.735 27.641 -12.236 5.869 -0.538 12.157 H61 RR6 73 RR6 H62 H62 H 0 1 N N N -8.597 27.033 -10.062 4.655 0.362 14.094 H62 RR6 74 RR6 H64 H64 H 0 1 N N N -8.525 22.910 -11.290 1.089 0.646 11.774 H64 RR6 75 RR6 H79 H79 H 0 1 N N N -10.544 25.205 -14.758 4.748 -1.927 9.824 H79 RR6 76 RR6 H83 H83 H 0 1 N N N -7.393 25.068 -7.133 0.888 0.386 15.968 H83 RR6 77 RR6 H58 H58 H 0 1 N N N -9.083 17.560 -14.370 -2.818 0.278 6.942 H58 RR6 78 RR6 H65 H65 H 0 1 N N N -11.480 21.091 -17.888 1.963 -1.628 4.881 H65 RR6 79 RR6 H66 H66 H 0 1 N N N -11.722 19.110 -19.405 0.748 -1.915 2.792 H66 RR6 80 RR6 H78 H78 H 0 1 N N N -11.204 22.366 -16.728 2.760 -0.208 7.041 H78 RR6 81 RR6 H91 H91 H 0 1 N N N -10.515 14.731 -14.612 -5.234 -1.160 4.993 H91 RR6 82 RR6 H90 H90 H 0 1 N N N -6.936 20.192 -11.121 -2.266 2.679 10.315 H90 RR6 83 RR6 H11 H11 H 0 1 N N N -20.791 25.423 -14.270 5.902 -0.577 -12.073 H11 RR6 84 RR6 H12 H12 H 0 1 N N N -23.195 25.110 -14.793 4.702 0.236 -14.057 H12 RR6 85 RR6 H14 H14 H 0 1 N N N -22.177 22.251 -17.855 1.110 0.584 -11.788 H14 RR6 86 RR6 H29 H29 H 0 1 N N N -18.168 23.712 -15.912 5.213 -0.133 -9.251 H29 RR6 87 RR6 H34 H34 H 0 1 N N N -25.792 22.159 -17.744 0.956 0.156 -15.971 H34 RR6 88 RR6 H8 H8 H 0 1 N N N -18.760 19.361 -22.271 -2.845 0.384 -6.984 H8 RR6 89 RR6 H15 H15 H 0 1 N N N -14.653 20.626 -18.802 1.922 -1.421 -4.804 H15 RR6 90 RR6 H16 H16 H 0 1 N N N -13.334 18.936 -20.060 0.686 -1.635 -2.719 H16 RR6 91 RR6 H28 H28 H 0 1 N N N -15.667 21.904 -18.123 2.736 -0.080 -7.008 H28 RR6 92 RR6 H37 H37 H 0 1 N N N -18.391 16.666 -23.727 -5.274 -1.002 -5.025 H37 RR6 93 RR6 H39 H39 H 0 1 N N N -22.092 20.695 -22.630 -2.274 2.665 -10.434 H39 RR6 94 RR6 H19 H19 H 0 1 N N N -13.697 18.269 -22.905 -2.815 -1.237 -2.330 H19 RR6 95 RR6 H26 H26 H 0 1 N N N -11.132 15.898 -18.126 -2.715 -1.653 2.354 H26 RR6 96 RR6 H24 H24 H 0 1 N N N -11.518 13.794 -22.511 1.798 -0.218 0.020 H24 RR6 97 # # 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 RR6 C60 C61 DOUB Y N 1 RR6 C60 C54 SING Y N 2 RR6 C60 O79 SING N N 3 RR6 C61 C62 SING Y N 4 RR6 C61 H61 SING N N 5 RR6 C62 C63 DOUB Y N 6 RR6 C62 H62 SING N N 7 RR6 C63 C64 SING Y N 8 RR6 C63 S81 SING N N 9 RR6 C64 C54 DOUB Y N 10 RR6 C64 H64 SING N N 11 RR6 C54 N52 SING N N 12 RR6 O79 H79 SING N N 13 RR6 O82 S81 DOUB N N 14 RR6 O83 S81 SING N N 15 RR6 O83 H83 SING N N 16 RR6 O84 S81 DOUB N N 17 RR6 C55 C53 DOUB Y N 18 RR6 C55 C56 SING Y N 19 RR6 C55 O78 SING N N 20 RR6 C53 C59 SING Y N 21 RR6 C53 N51 SING N N 22 RR6 C59 C58 DOUB Y N 23 RR6 C59 S85 SING N N 24 RR6 C58 C57 SING Y N 25 RR6 C58 H58 SING N N 26 RR6 C57 C56 DOUB Y N 27 RR6 C57 C68 SING Y N 28 RR6 C56 C65 SING Y N 29 RR6 C65 C66 DOUB Y N 30 RR6 C65 H65 SING N N 31 RR6 C66 C67 SING Y N 32 RR6 C66 H66 SING N N 33 RR6 C67 C68 DOUB Y N 34 RR6 C67 N26 SING N N 35 RR6 C68 S86 SING N N 36 RR6 O78 H78 SING N N 37 RR6 O87 S86 DOUB N N 38 RR6 O88 S86 DOUB N N 39 RR6 O91 S86 SING N N 40 RR6 O91 H91 SING N N 41 RR6 O89 S85 DOUB N N 42 RR6 O90 S85 SING N N 43 RR6 O90 H90 SING N N 44 RR6 O92 S85 DOUB N N 45 RR6 N51 N52 DOUB N N 46 RR6 C10 C11 DOUB Y N 47 RR6 C10 C4 SING Y N 48 RR6 C10 O29 SING N N 49 RR6 C11 C12 SING Y N 50 RR6 C11 H11 SING N N 51 RR6 C12 C13 DOUB Y N 52 RR6 C12 H12 SING N N 53 RR6 C13 C14 SING Y N 54 RR6 C13 S31 SING N N 55 RR6 C14 C4 DOUB Y N 56 RR6 C14 H14 SING N N 57 RR6 C4 N1 SING N N 58 RR6 O29 H29 SING N N 59 RR6 O32 S31 DOUB N N 60 RR6 O33 S31 DOUB N N 61 RR6 O34 S31 SING N N 62 RR6 O34 H34 SING N N 63 RR6 C5 C3 DOUB Y N 64 RR6 C5 C6 SING Y N 65 RR6 C5 O28 SING N N 66 RR6 C3 C9 SING Y N 67 RR6 C3 N2 SING N N 68 RR6 C9 C8 DOUB Y N 69 RR6 C9 S35 SING N N 70 RR6 C8 C7 SING Y N 71 RR6 C8 H8 SING N N 72 RR6 C7 C6 DOUB Y N 73 RR6 C7 C18 SING Y N 74 RR6 C6 C15 SING Y N 75 RR6 C15 C16 DOUB Y N 76 RR6 C15 H15 SING N N 77 RR6 C16 C17 SING Y N 78 RR6 C16 H16 SING N N 79 RR6 C17 C18 DOUB Y N 80 RR6 C17 N19 SING N N 81 RR6 C18 S36 SING N N 82 RR6 O28 H28 SING N N 83 RR6 O37 S36 SING N N 84 RR6 O37 H37 SING N N 85 RR6 O38 S36 DOUB N N 86 RR6 O41 S36 DOUB N N 87 RR6 O39 S35 SING N N 88 RR6 O39 H39 SING N N 89 RR6 O40 S35 DOUB N N 90 RR6 O42 S35 DOUB N N 91 RR6 N1 N2 DOUB N E 92 RR6 N19 C20 SING N N 93 RR6 N19 H19 SING N N 94 RR6 N26 C22 SING N N 95 RR6 N26 H26 SING N N 96 RR6 C20 N21 DOUB Y N 97 RR6 C20 N25 SING Y N 98 RR6 N21 C22 SING Y N 99 RR6 C22 N23 DOUB Y N 100 RR6 N23 C24 SING Y N 101 RR6 C24 N25 DOUB Y N 102 RR6 C24 H24 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 RR6 SMILES ACDLabs 10.04 "O=S(=O)(O)c7cc(/N=N/c2c(O)c1ccc(c(c1cc2S(=O)(=O)O)S(=O)(=O)O)Nc3ncnc(n3)Nc4c(c6c(cc4)c(O)c(/N=N/c5cc(ccc5O)S(=O)(=O)O)c(c6)S(=O)(=O)O)S(=O)(=O)O)c(O)cc7" RR6 SMILES_CANONICAL CACTVS 3.341 "Oc1ccc(cc1N=Nc2c(O)c3ccc(Nc4ncnc(Nc5ccc6c(O)c(N=Nc7cc(ccc7O)[S](O)(=O)=O)c(cc6c5[S](O)(=O)=O)[S](O)(=O)=O)n4)c(c3cc2[S](O)(=O)=O)[S](O)(=O)=O)[S](O)(=O)=O" RR6 SMILES CACTVS 3.341 "Oc1ccc(cc1N=Nc2c(O)c3ccc(Nc4ncnc(Nc5ccc6c(O)c(N=Nc7cc(ccc7O)[S](O)(=O)=O)c(cc6c5[S](O)(=O)=O)[S](O)(=O)=O)n4)c(c3cc2[S](O)(=O)=O)[S](O)(=O)=O)[S](O)(=O)=O" RR6 SMILES_CANONICAL "OpenEye OEToolkits" 1.5.0 "c1cc(c(cc1S(=O)(=O)O)N=Nc2c(cc3c(c2O)ccc(c3S(=O)(=O)O)Nc4ncnc(n4)Nc5ccc6c(c5S(=O)(=O)O)cc(c(c6O)/N=N/c7cc(ccc7O)S(=O)(=O)O)S(=O)(=O)O)S(=O)(=O)O)O" RR6 SMILES "OpenEye OEToolkits" 1.5.0 "c1cc(c(cc1S(=O)(=O)O)N=Nc2c(cc3c(c2O)ccc(c3S(=O)(=O)O)Nc4ncnc(n4)Nc5ccc6c(c5S(=O)(=O)O)cc(c(c6O)N=Nc7cc(ccc7O)S(=O)(=O)O)S(=O)(=O)O)S(=O)(=O)O)O" RR6 InChI InChI 1.03 "InChI=1S/C35H25N9O22S6/c45-24-7-1-14(67(49,50)51)9-22(24)41-43-28-26(69(55,56)57)11-18-16(30(28)47)3-5-20(32(18)71(61,62)63)38-34-36-13-37-35(40-34)39-21-6-4-17-19(33(21)72(64,65)66)12-27(70(58,59)60)29(31(17)48)44-42-23-10-15(68(52,53)54)2-8-25(23)46/h1-13,45-48H,(H,49,50,51)(H,52,53,54)(H,55,56,57)(H,58,59,60)(H,61,62,63)(H,64,65,66)(H2,36,37,38,39,40)/b43-41+,44-42+" RR6 InChIKey InChI 1.03 PJONDRDKCIFXDA-CHQNLTHESA-N # # 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 RR6 "SYSTEMATIC NAME" ACDLabs 10.04 "2,2'-(1,3,5-triazine-2,4-diyldiimino)bis{5-hydroxy-6-[(E)-(2-hydroxy-5-sulfophenyl)diazenyl]naphthalene-1,7-disulfonic acid}" RR6 "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.5.0 "5-hydroxy-2-[[4-[[5-hydroxy-6-(2-hydroxy-5-sulfo-phenyl)diazenyl-1,7-disulfo-naphthalen-2-yl]amino]-1,3,5-triazin-2-yl]amino]-6-(2-hydroxy-5-sulfo-phenyl)diazenyl-naphthalene-1,7-disulfonic 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 RR6 "Create component" 2000-07-14 RCSB RR6 "Modify descriptor" 2011-06-04 RCSB RR6 "Modify synonyms" 2021-03-01 PDBE # _pdbx_chem_comp_synonyms.ordinal 1 _pdbx_chem_comp_synonyms.comp_id RR6 _pdbx_chem_comp_synonyms.name "AZO-DYE RR6 HAPTEN" _pdbx_chem_comp_synonyms.provenance ? _pdbx_chem_comp_synonyms.type ? ##