data_SV6 # _chem_comp.id SV6 _chem_comp.name "(1S,3aR,6aS)-2-[(2S)-2-({(2S)-2-cyclohexyl-2-[(pyrazin-2-ylcarbonyl)amino]acetyl}amino)-3,3-dimethylbutanoyl]-N-[(2R,3S)-1-(cyclopropylamino)-2-hydroxy-1-oxohexan-3-yl]octahydrocyclopenta[c]pyrrole-1-carboxamide" _chem_comp.type PEPTIDE-LIKE _chem_comp.pdbx_type HETAIN _chem_comp.formula "C36 H55 N7 O6" _chem_comp.mon_nstd_parent_comp_id ? _chem_comp.pdbx_synonyms "TELAPREVIR, bound form" _chem_comp.pdbx_formal_charge 0 _chem_comp.pdbx_initial_date 2011-08-08 _chem_comp.pdbx_modified_date 2021-03-13 _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 681.865 _chem_comp.one_letter_code ? _chem_comp.three_letter_code SV6 _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 3SV6 _chem_comp.pdbx_subcomponent_list "VGL CHG TBG 037 03A" _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 SV6 CBN CBN C 0 1 Y N N -23.817 -9.539 13.465 7.909 -0.215 0.760 C1 VGL 1 SV6 CBO CBO C 0 1 Y N N -25.768 -8.730 12.537 8.997 -2.231 0.832 C3 VGL 2 SV6 CBP CBP C 0 1 Y N N -26.147 -10.036 12.219 10.194 -1.574 1.078 C4 VGL 3 SV6 CBB CBB C 0 1 N N N -22.483 -9.269 14.180 6.660 0.563 0.588 C2 VGL 4 SV6 CBQ CBQ C 0 1 Y N N -24.207 -10.841 13.141 9.112 0.442 1.012 C6 VGL 5 SV6 OBW OBW O 0 1 N N N -22.121 -8.124 14.428 6.683 1.775 0.667 O1 VGL 6 SV6 NAF NAF N 0 1 Y N N -24.615 -8.505 13.155 7.884 -1.543 0.679 N2 VGL 7 SV6 NAG NAG N 0 1 Y N N -25.363 -11.060 12.525 10.223 -0.256 1.165 N5 VGL 8 SV6 NAD NAD N 0 1 N N N -21.799 -10.352 14.496 5.497 -0.074 0.344 N CHG 9 SV6 CAY CAY C 0 1 N N S -20.502 -10.262 15.186 4.262 0.695 0.174 CA CHG 10 SV6 CAX CAX C 0 1 N N N -19.394 -10.161 14.147 3.079 -0.171 0.523 C CHG 11 SV6 OBU OBU O 0 1 N N N -19.280 -11.013 13.262 3.251 -1.318 0.879 O CHG 12 SV6 CBH CBH C 0 1 N N N -20.311 -11.490 16.067 4.145 1.157 -1.280 C1 CHG 13 SV6 CBI CBI C 0 1 N N N -21.424 -11.561 17.125 4.116 -0.064 -2.202 C2 CHG 14 SV6 CBJ CBJ C 0 1 N N N -21.223 -12.757 18.053 3.999 0.398 -3.656 C3 CHG 15 SV6 CBK CBK C 0 1 N N N -19.835 -12.723 18.712 5.200 1.277 -4.010 C4 CHG 16 SV6 CBL CBL C 0 1 N N N -18.728 -12.644 17.656 5.228 2.498 -3.088 C5 CHG 17 SV6 CBM CBM C 0 1 N N N -18.935 -11.434 16.740 5.346 2.036 -1.634 C6 CHG 18 SV6 NAC NAC N 0 1 N N N -18.643 -9.074 14.263 1.830 0.329 0.440 N TBG 19 SV6 CAW CAW C 0 1 N N S -17.530 -8.803 13.343 0.680 -0.513 0.779 CA TBG 20 SV6 CAZ CAZ C 0 1 N N N -17.691 -7.434 12.656 0.441 -0.465 2.290 CB TBG 21 SV6 CBC CBC C 0 1 N N N -17.812 -6.256 13.620 0.261 0.989 2.732 CG1 TBG 22 SV6 CBD CBD C 0 1 N N N -18.945 -7.456 11.766 -0.819 -1.262 2.632 CG2 TBG 23 SV6 CBA CBA C 0 1 N N N -16.473 -7.182 11.743 1.643 -1.073 3.016 CG3 TBG 24 SV6 CAV CAV C 0 1 N N N -16.201 -8.933 14.117 -0.544 -0.005 0.061 C TBG 25 SV6 OBT OBT O 0 1 N N N -15.957 -8.199 15.093 -0.698 1.186 -0.106 O TBG 26 SV6 C C C 0 1 N N N -13.112 -8.882 14.031 -3.562 0.313 -0.045 C 037 27 SV6 N N N 0 1 N N N -15.317 -9.856 13.746 -1.466 -0.875 -0.396 N 037 28 SV6 O O O 0 1 N N N -13.089 -8.531 12.850 -3.292 0.305 1.138 O 037 29 SV6 CA CA C 0 1 N N S -14.021 -10.027 14.437 -2.752 -0.515 -1.008 CA 037 30 SV6 CB CB C 0 1 N N S -13.457 -11.366 13.971 -3.500 -1.823 -1.331 CB 037 31 SV6 CG CG C 0 1 N N R -14.143 -11.661 12.629 -2.803 -2.867 -0.404 CG 037 32 SV6 CBE CBE C 0 1 N N N -13.815 -12.508 14.902 -3.093 -2.283 -2.749 CBE 037 33 SV6 CBF CBF C 0 1 N N N -13.861 -13.725 13.980 -3.057 -3.821 -2.672 CBF 037 34 SV6 CD1 CD1 C 0 1 N N N -15.440 -10.818 12.611 -1.348 -2.343 -0.370 CD 037 35 SV6 CD2 CD2 C 0 1 N N N -14.425 -13.168 12.665 -2.847 -4.184 -1.194 CD2 037 36 SV6 NAA NAA N 0 1 N N N -9.164 -6.143 13.099 -7.759 -0.009 0.694 NAA 03A 37 SV6 NAE NAE N 0 1 N N N -12.438 -8.272 15.009 -4.588 1.062 -0.496 NAE 03A 38 SV6 CAH CAH C 0 1 N N S -11.659 -7.055 14.701 -5.376 1.866 0.441 CAH 03A 39 SV6 CAI CAI C 0 1 N N R -10.164 -7.184 14.997 -6.773 2.101 -0.138 CAI 03A 40 SV6 CAJ CAJ C 0 1 N N N -12.291 -5.861 15.443 -4.684 3.212 0.665 CAJ 03A 41 SV6 CAK CAK C 0 1 N N N -13.562 -5.422 14.676 -3.339 2.985 1.358 CAK 03A 42 SV6 CAL CAL C 0 1 N N N -14.246 -4.237 15.340 -2.647 4.331 1.582 CAL 03A 43 SV6 CAM CAM C 0 1 N N N -9.398 -6.015 14.398 -7.454 0.775 -0.359 CAM 03A 44 SV6 CAN CAN C 0 1 N N N -8.484 -5.093 12.345 -8.422 -1.298 0.479 CAN 03A 45 SV6 CAO CAO C 0 1 N N N -7.037 -5.401 12.027 -8.232 -2.376 1.548 CAO 03A 46 SV6 CAP CAP C 0 1 N N N -8.100 -5.489 10.926 -9.578 -1.661 1.413 CAP 03A 47 SV6 OBR OBR O 0 1 N N N -9.632 -8.378 14.454 -6.662 2.793 -1.384 OBR 03A 48 SV6 OBS OBS O 0 1 N N N -9.087 -5.046 15.081 -7.729 0.414 -1.484 OBS 03A 49 SV6 HBQ HBQ H 0 1 N N N -23.566 -11.673 13.393 9.136 1.519 1.083 H6 VGL 50 SV6 HBO HBO H 0 1 N N N -26.413 -7.903 12.280 8.977 -3.309 0.766 H3 VGL 51 SV6 HBP HBP H 0 1 N N N -27.088 -10.213 11.719 11.104 -2.142 1.203 H4 VGL 52 SV6 HNAD HNAD H 0 0 N N N -22.169 -11.251 14.262 5.478 -1.042 0.281 HN CHG 53 SV6 HAY HAY H 0 1 N N N -20.471 -9.368 15.826 4.282 1.564 0.831 HA CHG 54 SV6 HBH HBH H 0 1 N N N -20.366 -12.395 15.444 3.226 1.729 -1.406 H1 CHG 55 SV6 HBI HBI H 0 1 N N N -21.408 -10.638 17.723 5.035 -0.636 -2.076 H2 CHG 56 SV6 HBIA HBIA H 0 0 N N N -22.394 -11.662 16.617 3.261 -0.690 -1.950 H2A CHG 57 SV6 HBJ HBJ H 0 1 N N N -21.991 -12.730 18.840 3.979 -0.471 -4.313 H3 CHG 58 SV6 HBJA HBJA H 0 0 N N N -21.316 -13.683 17.466 3.080 0.970 -3.782 H3A CHG 59 SV6 HBK HBK H 0 1 N N N -19.770 -11.840 19.364 6.119 0.705 -3.884 H4 CHG 60 SV6 HBKA HBKA H 0 0 N N N -19.698 -13.639 19.305 5.116 1.606 -5.046 H4A CHG 61 SV6 HBL HBL H 0 1 N N N -17.756 -12.549 18.162 6.084 3.124 -3.341 H5 CHG 62 SV6 HBLA HBLA H 0 0 N N N -18.746 -13.561 17.049 4.309 3.070 -3.214 H5A CHG 63 SV6 HBM HBM H 0 1 N N N -18.156 -11.434 15.964 5.366 2.905 -0.977 H6 CHG 64 SV6 HBMA HBMA H 0 0 N N N -18.866 -10.514 17.340 6.265 1.464 -1.508 H6A CHG 65 SV6 HNAC HNAC H 0 0 N N N -18.839 -8.422 14.995 1.693 1.246 0.156 H TBG 66 SV6 HAW HAW H 0 1 N N N -17.529 -9.543 12.529 0.880 -1.540 0.475 HA TBG 67 SV6 HBC HBC H 0 1 N N N -17.923 -5.323 13.048 -0.595 1.422 2.215 HG11 TBG 68 SV6 HBCA HBCA H 0 0 N N N -18.693 -6.398 14.264 0.090 1.023 3.808 HG12 TBG 69 SV6 HBCB HBCB H 0 0 N N N -16.908 -6.198 14.243 1.158 1.557 2.488 HG13 TBG 70 SV6 HBD HBD H 0 1 N N N -19.063 -6.479 11.274 -0.660 -2.314 2.394 HG21 TBG 71 SV6 HBDA HBDA H 0 0 N N N -18.839 -8.241 11.003 -1.036 -1.160 3.695 HG22 TBG 72 SV6 HBDB HBDB H 0 0 N N N -19.830 -7.664 12.385 -1.659 -0.881 2.052 HG23 TBG 73 SV6 HBA HBA H 0 1 N N N -16.581 -6.205 11.248 2.540 -0.505 2.772 HG31 TBG 74 SV6 HBAA HBAA H 0 0 N N N -15.554 -7.187 12.348 1.472 -1.039 4.092 HG32 TBG 75 SV6 HBAB HBAB H 0 0 N N N -16.415 -7.974 10.982 1.771 -2.109 2.701 HG33 TBG 76 SV6 HA HA H 0 1 N N N -14.118 -10.019 15.533 -2.579 0.049 -1.925 HA 037 77 SV6 HB HB H 0 1 N N N -12.360 -11.295 13.923 -4.578 -1.749 -1.193 HB2 037 78 SV6 HG HG H 0 1 N N N -13.559 -11.412 11.731 -3.266 -2.945 0.580 HG2 037 79 SV6 HBE HBE H 0 1 N N N -13.062 -12.632 15.694 -3.834 -1.957 -3.480 HBE 037 80 SV6 HBEA HBEA H 0 0 N N N -14.785 -12.338 15.393 -2.109 -1.891 -3.007 HBEA 037 81 SV6 HBF HBF H 0 1 N N N -12.860 -14.158 13.836 -4.000 -4.235 -3.028 HBF 037 82 SV6 HBFA HBFA H 0 0 N N N -14.506 -14.515 14.391 -2.232 -4.205 -3.272 HBFA 037 83 SV6 HD1 HD1 H 0 1 N N N -16.323 -11.461 12.740 -0.797 -2.693 -1.243 HD2 037 84 SV6 HD1A HD1A H 0 0 N N N -15.542 -10.282 11.656 -0.852 -2.665 0.545 HD3 037 85 SV6 HD2 HD2 H 0 1 N N N -15.509 -13.349 12.615 -1.906 -4.721 -1.073 H1 037 86 SV6 HD2A HD2A H 0 0 N N N -13.940 -13.661 11.810 -3.675 -4.800 -0.842 HD2A 037 87 SV6 HNAA HNAA H 0 0 N N N -9.459 -6.974 12.627 -7.540 0.280 1.594 HNAA 03A 88 SV6 HNAE HNAE H 0 0 N N N -12.460 -8.635 15.940 -4.804 1.068 -1.442 HNAE 03A 89 SV6 HAH HAH H 0 1 N N N -11.708 -6.891 13.614 -5.460 1.339 1.391 HAH 03A 90 SV6 HAI HAI H 0 1 N N N -10.054 -7.195 16.091 -7.359 2.700 0.559 HAI 03A 91 SV6 HAJ HAJ H 0 1 N N N -12.559 -6.159 16.468 -4.519 3.701 -0.296 HAJ 03A 92 SV6 HAJA HAJA H 0 0 N N N -11.575 -5.027 15.485 -5.313 3.845 1.291 HAJA 03A 93 SV6 HAK HAK H 0 1 N N N -13.274 -5.135 13.654 -3.503 2.497 2.319 HAK 03A 94 SV6 HAKA HAKA H 0 0 N N N -14.267 -6.266 14.651 -2.710 2.353 0.732 HAKA 03A 95 SV6 HAL HAL H 0 1 N N N -15.141 -3.960 14.764 -3.276 4.964 2.208 HAL 03A 96 SV6 HALA HALA H 0 0 N N N -14.540 -4.510 16.364 -1.689 4.169 2.076 HALA 03A 97 SV6 HALB HALB H 0 0 N N N -13.552 -3.384 15.372 -2.482 4.819 0.621 HALB 03A 98 SV6 HAN HAN H 0 1 N N N -9.018 -4.243 12.795 -8.491 -1.624 -0.558 HAN 03A 99 SV6 HAO HAO H 0 1 N N N -6.133 -4.779 12.108 -8.176 -3.412 1.213 HAO 03A 100 SV6 HAOA HAOA H 0 0 N N N -6.357 -6.163 12.434 -7.613 -2.127 2.410 HAOA 03A 101 SV6 HAP HAP H 0 1 N N N -8.423 -6.330 10.295 -9.846 -0.942 2.186 HAP 03A 102 SV6 HAPA HAPA H 0 0 N N N -8.201 -4.953 9.971 -10.408 -2.227 0.989 HAPA 03A 103 SV6 HOBR HOBR H 0 0 N N N -8.705 -8.431 14.653 -6.152 2.318 -2.054 HOBR 03A 104 # # 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 SV6 O C DOUB N N 1 SV6 C CA SING N N 2 SV6 C NAE SING N N 3 SV6 CD1 N SING N N 4 SV6 N CAV SING N N 5 SV6 N CA SING N N 6 SV6 CB CA SING N N 7 SV6 CA HA SING N N 8 SV6 CG CB SING N N 9 SV6 CB CBE SING N N 10 SV6 CB HB SING N N 11 SV6 CD1 CG SING N N 12 SV6 CG CD2 SING N N 13 SV6 CG HG SING N N 14 SV6 CAN NAA SING N N 15 SV6 NAA CAM SING N N 16 SV6 NAA HNAA SING N N 17 SV6 CAW NAC SING N N 18 SV6 CAX NAC SING N N 19 SV6 NAC HNAC SING N N 20 SV6 CBB NAD SING N N 21 SV6 NAD CAY SING N N 22 SV6 NAD HNAD SING N N 23 SV6 CAH NAE SING N N 24 SV6 NAE HNAE SING N N 25 SV6 CBO NAF DOUB Y N 26 SV6 NAF CBN SING Y N 27 SV6 CBP NAG DOUB Y N 28 SV6 NAG CBQ SING Y N 29 SV6 CAH CAI SING N N 30 SV6 CAH CAJ SING N N 31 SV6 CAH HAH SING N N 32 SV6 CAM CAI SING N N 33 SV6 OBR CAI SING N N 34 SV6 CAI HAI SING N N 35 SV6 CAK CAJ SING N N 36 SV6 CAJ HAJ SING N N 37 SV6 CAJ HAJA SING N N 38 SV6 CAK CAL SING N N 39 SV6 CAK HAK SING N N 40 SV6 CAK HAKA SING N N 41 SV6 CAL HAL SING N N 42 SV6 CAL HALA SING N N 43 SV6 CAL HALB SING N N 44 SV6 CAM OBS DOUB N N 45 SV6 CAP CAN SING N N 46 SV6 CAO CAN SING N N 47 SV6 CAN HAN SING N N 48 SV6 CAP CAO SING N N 49 SV6 CAO HAO SING N N 50 SV6 CAO HAOA SING N N 51 SV6 CAP HAP SING N N 52 SV6 CAP HAPA SING N N 53 SV6 CAW CAV SING N N 54 SV6 CAV OBT DOUB N N 55 SV6 CAZ CAW SING N N 56 SV6 CAW HAW SING N N 57 SV6 OBU CAX DOUB N N 58 SV6 CAX CAY SING N N 59 SV6 CAY CBH SING N N 60 SV6 CAY HAY SING N N 61 SV6 CBA CAZ SING N N 62 SV6 CBD CAZ SING N N 63 SV6 CAZ CBC SING N N 64 SV6 CBA HBA SING N N 65 SV6 CBA HBAA SING N N 66 SV6 CBA HBAB SING N N 67 SV6 CBN CBB SING N N 68 SV6 CBB OBW DOUB N N 69 SV6 CBC HBC SING N N 70 SV6 CBC HBCA SING N N 71 SV6 CBC HBCB SING N N 72 SV6 CBD HBD SING N N 73 SV6 CBD HBDA SING N N 74 SV6 CBD HBDB SING N N 75 SV6 CBF CBE SING N N 76 SV6 CBE HBE SING N N 77 SV6 CBE HBEA SING N N 78 SV6 CD2 CBF SING N N 79 SV6 CBF HBF SING N N 80 SV6 CBF HBFA SING N N 81 SV6 CBH CBM SING N N 82 SV6 CBH CBI SING N N 83 SV6 CBH HBH SING N N 84 SV6 CBI CBJ SING N N 85 SV6 CBI HBI SING N N 86 SV6 CBI HBIA SING N N 87 SV6 CBJ CBK SING N N 88 SV6 CBJ HBJ SING N N 89 SV6 CBJ HBJA SING N N 90 SV6 CBL CBK SING N N 91 SV6 CBK HBK SING N N 92 SV6 CBK HBKA SING N N 93 SV6 CBM CBL SING N N 94 SV6 CBL HBL SING N N 95 SV6 CBL HBLA SING N N 96 SV6 CBM HBM SING N N 97 SV6 CBM HBMA SING N N 98 SV6 CBQ CBN DOUB Y N 99 SV6 CBP CBO SING Y N 100 SV6 CBO HBO SING N N 101 SV6 CBP HBP SING N N 102 SV6 CBQ HBQ SING N N 103 SV6 OBR HOBR SING N N 104 SV6 CD1 HD1 SING N N 105 SV6 CD1 HD1A SING N N 106 SV6 CD2 HD2 SING N N 107 SV6 CD2 HD2A 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 SV6 SMILES ACDLabs 12.01 "O=C(NC1CC1)C(O)C(NC(=O)C4N(C(=O)C(NC(=O)C(NC(=O)c2nccnc2)C3CCCCC3)C(C)(C)C)CC5CCCC45)CCC" SV6 InChI InChI 1.03 "InChI=1S/C36H55N7O6/c1-5-10-25(29(44)34(48)39-23-15-16-23)40-33(47)28-24-14-9-13-22(24)20-43(28)35(49)30(36(2,3)4)42-32(46)27(21-11-7-6-8-12-21)41-31(45)26-19-37-17-18-38-26/h17-19,21-25,27-30,44H,5-16,20H2,1-4H3,(H,39,48)(H,40,47)(H,41,45)(H,42,46)/t22-,24-,25-,27-,28-,29+,30+/m0/s1" SV6 InChIKey InChI 1.03 FTZGWEAUHOMNIG-FJRGXGLZSA-N SV6 SMILES_CANONICAL CACTVS 3.370 "CCC[C@H](NC(=O)[C@@H]1[C@H]2CCC[C@H]2CN1C(=O)[C@@H](NC(=O)[C@@H](NC(=O)c3cnccn3)C4CCCCC4)C(C)(C)C)[C@@H](O)C(=O)NC5CC5" SV6 SMILES CACTVS 3.370 "CCC[CH](NC(=O)[CH]1[CH]2CCC[CH]2CN1C(=O)[CH](NC(=O)[CH](NC(=O)c3cnccn3)C4CCCCC4)C(C)(C)C)[CH](O)C(=O)NC5CC5" SV6 SMILES_CANONICAL "OpenEye OEToolkits" 1.7.2 "CCC[C@@H]([C@H](C(=O)NC1CC1)O)NC(=O)[C@@H]2[C@H]3CCC[C@H]3CN2C(=O)[C@H](C(C)(C)C)NC(=O)[C@H](C4CCCCC4)NC(=O)c5cnccn5" SV6 SMILES "OpenEye OEToolkits" 1.7.2 "CCCC(C(C(=O)NC1CC1)O)NC(=O)C2C3CCCC3CN2C(=O)C(C(C)(C)C)NC(=O)C(C4CCCCC4)NC(=O)c5cnccn5" # # 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 SV6 "SYSTEMATIC NAME" ACDLabs 12.01 "(1S,3aR,6aS)-2-[(2S)-2-({(2S)-2-cyclohexyl-2-[(pyrazin-2-ylcarbonyl)amino]acetyl}amino)-3,3-dimethylbutanoyl]-N-[(2R,3S)-1-(cyclopropylamino)-2-hydroxy-1-oxohexan-3-yl]octahydrocyclopenta[c]pyrrole-1-carboxamide (non-preferred name)" SV6 "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.7.2 "(3S,3aS,6aR)-2-[(2S)-2-[[(2S)-2-cyclohexyl-2-(pyrazin-2-ylcarbonylamino)ethanoyl]amino]-3,3-dimethyl-butanoyl]-N-[(2R,3S)-1-(cyclopropylamino)-2-oxidanyl-1-oxidanylidene-hexan-3-yl]-3,3a,4,5,6,6a-hexahydro-1H-cyclopenta[c]pyrrole-3-carboxamide" # # loop_ _pdbx_chem_comp_audit.comp_id _pdbx_chem_comp_audit.action_type _pdbx_chem_comp_audit.date _pdbx_chem_comp_audit.processing_site SV6 "Create component" 2011-08-08 RCSB SV6 "Modify synonyms" 2011-08-10 RCSB SV6 "Modify synonyms" 2011-09-19 RCSB SV6 "Initial release" 2012-08-31 RCSB SV6 "Modify synonyms" 2021-03-13 RCSB # _pdbx_chem_comp_synonyms.ordinal 1 _pdbx_chem_comp_synonyms.comp_id SV6 _pdbx_chem_comp_synonyms.name "TELAPREVIR, bound form" _pdbx_chem_comp_synonyms.provenance PDB _pdbx_chem_comp_synonyms.type ? ##