data_OMS # _chem_comp.id OMS _chem_comp.name "1-methylcyclobutyl [(2R,6S,12Z,13aS,14aR,16aS)-2-[(7-methoxy-3-methylquinoxalin-2-yl)oxy]-14a-{[(1-methylcyclopropyl)sulfonyl]carbamoyl}-5,16-dioxo-1,2,3,5,6,7,8,9,10,11,13a,14,14a,15,16,16a-hexadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecin-6-yl]carbamate" _chem_comp.type NON-POLYMER _chem_comp.pdbx_type HETAIN _chem_comp.formula "C38 H50 N6 O9 S" _chem_comp.mon_nstd_parent_comp_id ? _chem_comp.pdbx_synonyms "P4-2 (NR02-61)" _chem_comp.pdbx_formal_charge 0 _chem_comp.pdbx_initial_date 2019-06-28 _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 766.903 _chem_comp.one_letter_code ? _chem_comp.three_letter_code OMS _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 6PIY _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 OMS C10 C1 C 0 1 N N N -15.791 -20.455 15.610 -0.595 2.082 -0.521 C10 OMS 1 OMS C17 C2 C 0 1 N N N -19.664 -17.379 13.345 4.947 4.076 0.654 C17 OMS 2 OMS C21 C3 C 0 1 Y N N -13.569 -15.731 15.623 3.342 -1.821 -1.932 C21 OMS 3 OMS C24 C4 C 0 1 Y N N -12.154 -13.339 14.953 5.630 -2.867 -0.969 C24 OMS 4 OMS C26 C5 C 0 1 Y N N -13.835 -15.036 14.290 4.433 -2.102 -2.769 C26 OMS 5 OMS C28 C6 C 0 1 Y N N -10.192 -12.214 16.946 5.799 -3.381 1.758 C28 OMS 6 OMS C01 C7 C 0 1 N N S -13.262 -19.482 15.736 -0.932 0.177 -2.100 C01 OMS 7 OMS C02 C8 C 0 1 N N N -12.692 -18.489 16.767 -0.213 -1.165 -2.273 C02 OMS 8 OMS C03 C9 C 0 1 N N R -13.724 -17.677 17.014 1.137 -1.025 -1.553 C03 OMS 9 OMS C04 C10 C 0 1 N N N -15.022 -18.650 17.223 1.205 0.430 -1.069 C04 OMS 10 OMS C06 C11 C 0 1 N N N -12.927 -20.871 15.733 -2.303 -0.045 -1.517 C06 OMS 11 OMS C09 C12 C 0 1 N N R -12.063 -22.723 14.161 -4.683 0.161 -1.535 C09 OMS 12 OMS C11 C13 C 0 1 N N S -17.205 -20.472 16.183 0.296 2.826 0.438 C11 OMS 13 OMS C14 C14 C 0 1 N N N -18.404 -18.833 14.798 2.648 3.465 0.462 C14 OMS 14 OMS C18 C15 C 0 1 N N N -17.464 -21.894 16.707 -0.425 4.075 0.945 C18 OMS 15 OMS C19 C16 C 0 1 N N N -16.441 -22.260 17.825 -1.836 3.704 1.407 C19 OMS 16 OMS C23 C17 C 0 1 Y N N -11.942 -14.032 16.252 4.532 -2.580 -0.120 C23 OMS 17 OMS C27 C18 C 0 1 Y N N -10.957 -13.494 17.276 4.635 -2.846 1.255 C27 OMS 18 OMS C29 C19 C 0 1 Y N N -10.399 -11.522 15.629 6.878 -3.662 0.914 C29 OMS 19 OMS C30 C20 C 0 1 Y N N -11.371 -12.059 14.615 6.804 -3.413 -0.421 C30 OMS 20 OMS C32 C21 C 0 1 N N N -9.298 -12.387 19.132 7.134 -4.194 3.548 C32 OMS 21 OMS C33 C22 C 0 1 N N N -14.811 -15.593 13.269 4.334 -1.816 -4.246 C33 OMS 22 OMS C34 C23 C 0 1 N N N -10.924 -23.418 14.813 -4.645 -0.682 -0.291 C34 OMS 23 OMS C40 C24 C 0 1 N N N -8.207 -22.223 17.657 -5.950 -3.208 1.249 C40 OMS 24 OMS C41 C25 C 0 1 N N N -7.091 -21.328 17.128 -6.616 -2.588 2.478 C41 OMS 25 OMS C42 C26 C 0 1 N N N -6.764 -22.476 18.097 -6.355 -4.095 2.428 C42 OMS 26 OMS C43 C27 C 0 1 N N N -9.173 -21.650 18.738 -6.784 -3.310 -0.030 C43 OMS 27 OMS C44 C28 C 0 1 N N S -13.281 -23.678 14.102 -5.553 1.419 -1.527 C44 OMS 28 OMS C45 C29 C 0 1 N N N -13.533 -25.135 14.516 -6.304 1.730 -0.259 C45 OMS 29 OMS C46 C30 C 0 1 N N N -14.534 -25.529 15.329 -5.858 2.670 0.541 C46 OMS 30 OMS C47 C31 C 0 1 N N N -15.587 -24.575 15.928 -4.604 3.423 0.179 C47 OMS 31 OMS C48 C32 C 0 1 N N N -15.475 -24.613 17.463 -4.236 4.394 1.301 C48 OMS 32 OMS C49 C33 C 0 1 N N N -12.494 -23.363 12.828 -5.978 0.198 -2.344 C49 OMS 33 OMS C50 C34 C 0 1 N N N -16.612 -23.777 18.171 -2.791 4.862 1.111 C50 OMS 34 OMS C51 C35 C 0 1 N N N -20.614 -16.729 14.264 4.799 5.154 1.730 C51 OMS 35 OMS C52 C36 C 0 1 N N N -18.490 -16.494 12.943 5.505 2.746 1.188 C52 OMS 36 OMS C53 C37 C 0 1 N N N -19.087 -16.273 11.568 6.906 3.305 0.891 C53 OMS 37 OMS C54 C38 C 0 1 N N N -20.135 -17.340 11.900 6.239 4.200 -0.170 C54 OMS 38 OMS N05 N1 N 0 1 N N N -14.802 -19.557 16.194 -0.143 0.993 -1.172 N05 OMS 39 OMS N08 N2 N 0 1 N N N -12.332 -21.336 14.531 -3.404 0.254 -2.276 N08 OMS 40 OMS N13 N3 N 0 1 N N N -18.194 -20.182 15.209 1.529 3.219 -0.249 N13 OMS 41 OMS N22 N4 N 0 1 Y N N -12.673 -15.216 16.603 3.412 -2.060 -0.638 N22 OMS 42 OMS N25 N5 N 0 1 Y N N -13.102 -13.848 13.970 5.538 -2.611 -2.280 N25 OMS 43 OMS N35 N6 N 0 1 N N N -10.147 -22.617 15.701 -4.113 -1.920 -0.332 N35 OMS 44 OMS O07 O1 O 0 1 N N N -13.109 -21.625 16.619 -2.431 -0.482 -0.393 O07 OMS 45 OMS O12 O2 O 0 1 N N N -15.477 -21.176 14.701 -1.732 2.462 -0.703 O12 OMS 46 OMS O15 O3 O 0 1 N N N -19.309 -18.712 13.750 3.752 3.922 -0.157 O15 OMS 47 OMS O16 O4 O 0 1 N N N -17.908 -17.911 15.379 2.659 3.273 1.662 O16 OMS 48 OMS O20 O5 O 0 1 N N N -14.273 -16.871 15.941 2.209 -1.294 -2.459 O20 OMS 49 OMS O31 O6 O 0 1 N N N -9.298 -11.738 17.884 5.900 -3.639 3.087 O31 OMS 50 OMS O36 O7 O 0 1 N N N -10.563 -24.510 14.548 -5.092 -0.248 0.750 O36 OMS 51 OMS O38 O8 O 0 1 N N N -7.836 -23.810 15.438 -3.669 -2.084 2.055 O38 OMS 52 OMS O39 O9 O 0 1 N N N -9.343 -24.498 17.173 -3.513 -4.084 0.607 O39 OMS 53 OMS S37 S1 S 0 1 N N N -8.846 -23.358 16.403 -4.180 -2.894 1.006 S37 OMS 54 OMS H011 H1 H 0 0 N N N -13.207 -19.049 14.726 -1.015 0.685 -3.060 H011 OMS 55 OMS H022 H2 H 0 0 N N N -12.373 -19.010 17.682 -0.799 -1.965 -1.820 H022 OMS 56 OMS H021 H3 H 0 0 N N N -11.842 -17.930 16.348 -0.054 -1.371 -3.331 H021 OMS 57 OMS H031 H4 H 0 0 N N N -13.587 -17.077 17.926 1.182 -1.706 -0.703 H031 OMS 58 OMS H042 H5 H 0 0 N N N -15.968 -18.104 17.093 1.540 0.460 -0.033 H042 OMS 59 OMS H041 H6 H 0 0 N N N -15.013 -19.139 18.209 1.892 0.997 -1.697 H041 OMS 60 OMS H111 H7 H 0 0 N N N -17.264 -19.763 17.022 0.541 2.181 1.281 H111 OMS 61 OMS H181 H8 H 0 0 N N N -18.483 -21.948 17.117 0.131 4.501 1.781 H181 OMS 62 OMS H182 H9 H 0 0 N N N -17.364 -22.609 15.877 -0.488 4.809 0.141 H182 OMS 63 OMS H191 H10 H 0 0 N N N -15.417 -22.073 17.468 -2.170 2.813 0.875 H191 OMS 64 OMS H192 H11 H 0 0 N N N -16.634 -21.650 18.720 -1.827 3.505 2.478 H192 OMS 65 OMS H271 H12 H 0 0 N N N -10.801 -14.005 18.215 3.806 -2.633 1.913 H271 OMS 66 OMS H291 H13 H 0 0 N N N -9.841 -10.624 15.407 7.783 -4.081 1.328 H291 OMS 67 OMS H301 H14 H 0 0 N N N -11.516 -11.557 13.670 7.646 -3.635 -1.060 H301 OMS 68 OMS H322 H15 H 0 0 N N N -8.549 -11.921 19.788 7.312 -5.148 3.050 H322 OMS 69 OMS H323 H16 H 0 0 N N N -10.294 -12.298 19.591 7.949 -3.508 3.320 H323 OMS 70 OMS H321 H17 H 0 0 N N N -9.052 -13.450 18.992 7.082 -4.351 4.626 H321 OMS 71 OMS H332 H18 H 0 0 N N N -14.809 -14.955 12.373 4.676 -0.800 -4.443 H332 OMS 72 OMS H333 H19 H 0 0 N N N -14.510 -16.614 12.993 4.956 -2.522 -4.795 H333 OMS 73 OMS H331 H20 H 0 0 N N N -15.822 -15.613 13.702 3.297 -1.919 -4.567 H331 OMS 74 OMS H411 H21 H 0 0 N N N -6.786 -21.394 16.073 -5.991 -1.991 3.142 H411 OMS 75 OMS H412 H22 H 0 0 N N N -7.016 -20.284 17.466 -7.648 -2.253 2.377 H412 OMS 76 OMS H422 H23 H 0 0 N N N -6.226 -23.365 17.736 -7.215 -4.751 2.293 H422 OMS 77 OMS H421 H24 H 0 0 N N N -6.456 -22.255 19.130 -5.558 -4.489 3.059 H421 OMS 78 OMS H432 H25 H 0 0 N N N -8.616 -20.983 19.412 -7.818 -3.044 0.188 H432 OMS 79 OMS H433 H26 H 0 0 N N N -9.979 -21.085 18.247 -6.384 -2.628 -0.780 H433 OMS 80 OMS H431 H27 H 0 0 N N N -9.607 -22.478 19.318 -6.744 -4.331 -0.410 H431 OMS 81 OMS H441 H28 H 0 0 N N N -14.218 -23.103 14.129 -5.185 2.287 -2.077 H441 OMS 82 OMS H451 H29 H 0 0 N N N -12.866 -25.892 14.132 -7.200 1.185 -0.009 H451 OMS 83 OMS H461 H30 H 0 0 N N N -14.602 -26.578 15.576 -6.385 2.900 1.454 H461 OMS 84 OMS H471 H31 H 0 0 N N N -15.405 -23.551 15.569 -3.788 2.717 0.029 H471 OMS 85 OMS H472 H32 H 0 0 N N N -16.594 -24.897 15.623 -4.771 3.981 -0.742 H472 OMS 86 OMS H481 H33 H 0 0 N N N -15.546 -25.659 17.796 -4.904 5.254 1.271 H481 OMS 87 OMS H482 H34 H 0 0 N N N -14.498 -24.200 17.756 -4.332 3.891 2.263 H482 OMS 88 OMS H491 H35 H 0 0 N N N -11.867 -24.139 12.364 -5.893 0.263 -3.428 H491 OMS 89 OMS H492 H36 H 0 0 N N N -12.948 -22.741 12.043 -6.820 -0.387 -1.973 H492 OMS 90 OMS H501 H37 H 0 0 N N N -17.595 -24.124 17.819 -2.584 5.687 1.794 H501 OMS 91 OMS H502 H38 H 0 0 N N N -16.543 -23.914 19.260 -2.649 5.197 0.084 H502 OMS 92 OMS H513 H39 H 0 0 N N N -20.227 -16.785 15.292 4.003 4.873 2.418 H513 OMS 93 OMS H511 H40 H 0 0 N N N -20.739 -15.675 13.976 5.736 5.250 2.278 H511 OMS 94 OMS H512 H41 H 0 0 N N N -21.586 -17.242 14.210 4.555 6.106 1.259 H512 OMS 95 OMS H522 H42 H 0 0 N N N -17.523 -17.018 12.929 5.314 2.586 2.249 H522 OMS 96 OMS H521 H43 H 0 0 N N N -18.400 -15.575 13.542 5.239 1.884 0.575 H521 OMS 97 OMS H531 H44 H 0 0 N N N -18.419 -16.535 10.734 7.338 3.862 1.723 H531 OMS 98 OMS H532 H45 H 0 0 N N N -19.498 -15.266 11.406 7.592 2.569 0.472 H532 OMS 99 OMS H541 H46 H 0 0 N N N -21.174 -16.999 11.778 6.175 3.736 -1.154 H541 OMS 100 OMS H542 H47 H 0 0 N N N -19.994 -18.287 11.359 6.642 5.212 -0.203 H542 OMS 101 OMS H081 H48 H 0 0 N N N -12.068 -20.638 13.865 -3.351 0.504 -3.211 H081 OMS 102 OMS H131 H49 H 0 0 N N N -18.741 -20.919 14.813 1.541 3.303 -1.215 H131 OMS 103 OMS H351 H50 H 0 0 N N N -10.376 -21.662 15.888 -3.692 -2.240 -1.144 H351 OMS 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 OMS C53 C54 SING N N 1 OMS C53 C52 SING N N 2 OMS C54 C17 SING N N 3 OMS C49 C44 SING N N 4 OMS C49 C09 SING N N 5 OMS C52 C17 SING N N 6 OMS C33 C26 SING N N 7 OMS C17 O15 SING N N 8 OMS C17 C51 SING N N 9 OMS O15 C14 SING N N 10 OMS N25 C26 DOUB Y N 11 OMS N25 C24 SING Y N 12 OMS C44 C09 SING N N 13 OMS C44 C45 SING N N 14 OMS C09 N08 SING N N 15 OMS C09 C34 SING N N 16 OMS C26 C21 SING Y N 17 OMS C45 C46 DOUB N Z 18 OMS N08 C06 SING N N 19 OMS O36 C34 DOUB N N 20 OMS C30 C24 DOUB Y N 21 OMS C30 C29 SING Y N 22 OMS O12 C10 DOUB N N 23 OMS C14 N13 SING N N 24 OMS C14 O16 DOUB N N 25 OMS C34 N35 SING N N 26 OMS C24 C23 SING Y N 27 OMS N13 C11 SING N N 28 OMS C46 C47 SING N N 29 OMS O38 S37 DOUB N N 30 OMS C10 C11 SING N N 31 OMS C10 N05 SING N N 32 OMS C21 O20 SING N N 33 OMS C21 N22 DOUB Y N 34 OMS C29 C28 DOUB Y N 35 OMS N35 S37 SING N N 36 OMS C06 C01 SING N N 37 OMS C06 O07 DOUB N N 38 OMS C01 N05 SING N N 39 OMS C01 C02 SING N N 40 OMS C47 C48 SING N N 41 OMS O20 C03 SING N N 42 OMS C11 C18 SING N N 43 OMS N05 C04 SING N N 44 OMS C23 N22 SING Y N 45 OMS C23 C27 DOUB Y N 46 OMS S37 O39 DOUB N N 47 OMS S37 C40 SING N N 48 OMS C18 C19 SING N N 49 OMS C02 C03 SING N N 50 OMS C28 C27 SING Y N 51 OMS C28 O31 SING N N 52 OMS C03 C04 SING N N 53 OMS C41 C40 SING N N 54 OMS C41 C42 SING N N 55 OMS C48 C50 SING N N 56 OMS C40 C42 SING N N 57 OMS C40 C43 SING N N 58 OMS C19 C50 SING N N 59 OMS O31 C32 SING N N 60 OMS C01 H011 SING N N 61 OMS C02 H022 SING N N 62 OMS C02 H021 SING N N 63 OMS C03 H031 SING N N 64 OMS C04 H042 SING N N 65 OMS C04 H041 SING N N 66 OMS C11 H111 SING N N 67 OMS C18 H181 SING N N 68 OMS C18 H182 SING N N 69 OMS C19 H191 SING N N 70 OMS C19 H192 SING N N 71 OMS C27 H271 SING N N 72 OMS C29 H291 SING N N 73 OMS C30 H301 SING N N 74 OMS C32 H322 SING N N 75 OMS C32 H323 SING N N 76 OMS C32 H321 SING N N 77 OMS C33 H332 SING N N 78 OMS C33 H333 SING N N 79 OMS C33 H331 SING N N 80 OMS C41 H411 SING N N 81 OMS C41 H412 SING N N 82 OMS C42 H422 SING N N 83 OMS C42 H421 SING N N 84 OMS C43 H432 SING N N 85 OMS C43 H433 SING N N 86 OMS C43 H431 SING N N 87 OMS C44 H441 SING N N 88 OMS C45 H451 SING N N 89 OMS C46 H461 SING N N 90 OMS C47 H471 SING N N 91 OMS C47 H472 SING N N 92 OMS C48 H481 SING N N 93 OMS C48 H482 SING N N 94 OMS C49 H491 SING N N 95 OMS C49 H492 SING N N 96 OMS C50 H501 SING N N 97 OMS C50 H502 SING N N 98 OMS C51 H513 SING N N 99 OMS C51 H511 SING N N 100 OMS C51 H512 SING N N 101 OMS C52 H522 SING N N 102 OMS C52 H521 SING N N 103 OMS C53 H531 SING N N 104 OMS C53 H532 SING N N 105 OMS C54 H541 SING N N 106 OMS C54 H542 SING N N 107 OMS N08 H081 SING N N 108 OMS N13 H131 SING N N 109 OMS N35 H351 SING N N 110 # # 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 OMS SMILES ACDLabs 12.01 "C1(C(CCCCCC=CC6C(NC(C2N1CC(C2)Oc4nc3c(ccc(c3)OC)nc4C)=O)(C(NS(C5(CC5)C)(=O)=O)=O)C6)NC(=O)OC7(C)CCC7)=O" OMS InChI InChI 1.03 "InChI=1S/C38H50N6O9S/c1-23-32(40-29-19-25(51-4)13-14-27(29)39-23)52-26-20-30-31(45)42-38(34(47)43-54(49,50)37(3)17-18-37)21-24(38)11-8-6-5-7-9-12-28(33(46)44(30)22-26)41-35(48)53-36(2)15-10-16-36/h8,11,13-14,19,24,26,28,30H,5-7,9-10,12,15-18,20-22H2,1-4H3,(H,41,48)(H,42,45)(H,43,47)/b11-8-/t24-,26-,28+,30+,38-/m1/s1" OMS InChIKey InChI 1.03 PDBMENIRROXLPP-AJUMDJHNSA-N OMS SMILES_CANONICAL CACTVS 3.385 "COc1ccc2nc(C)c(O[C@@H]3C[C@@H]4N(C3)C(=O)[C@H](CCCCC\C=C/[C@@H]5C[C@]5(NC4=O)C(=O)N[S](=O)(=O)C6(C)CC6)NC(=O)OC7(C)CCC7)nc2c1" OMS SMILES CACTVS 3.385 "COc1ccc2nc(C)c(O[CH]3C[CH]4N(C3)C(=O)[CH](CCCCCC=C[CH]5C[C]5(NC4=O)C(=O)N[S](=O)(=O)C6(C)CC6)NC(=O)OC7(C)CCC7)nc2c1" OMS SMILES_CANONICAL "OpenEye OEToolkits" 2.0.7 "Cc1c(nc2cc(ccc2n1)OC)O[C@@H]3C[C@H]4C(=O)N[C@@]5(C[C@H]5/C=C\CCCCC[C@@H](C(=O)N4C3)NC(=O)OC6(CCC6)C)C(=O)NS(=O)(=O)C7(CC7)C" OMS SMILES "OpenEye OEToolkits" 2.0.7 "Cc1c(nc2cc(ccc2n1)OC)OC3CC4C(=O)NC5(CC5C=CCCCCCC(C(=O)N4C3)NC(=O)OC6(CCC6)C)C(=O)NS(=O)(=O)C7(CC7)C" # # 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 OMS "SYSTEMATIC NAME" ACDLabs 12.01 "1-methylcyclobutyl [(2R,6S,12Z,13aS,14aR,16aS)-2-[(7-methoxy-3-methylquinoxalin-2-yl)oxy]-14a-{[(1-methylcyclopropyl)sulfonyl]carbamoyl}-5,16-dioxo-1,2,3,5,6,7,8,9,10,11,13a,14,14a,15,16,16a-hexadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecin-6-yl]carbamate" OMS "SYSTEMATIC NAME" "OpenEye OEToolkits" 2.0.7 "(1-methylcyclobutyl) ~{N}-[(1~{S},4~{R},6~{S},7~{Z},14~{S},18~{R})-18-(7-methoxy-3-methyl-quinoxalin-2-yl)oxy-4-[(1-methylcyclopropyl)sulfonylcarbamoyl]-2,15-bis(oxidanylidene)-3,16-diazatricyclo[14.3.0.0^{4,6}]nonadec-7-en-14-yl]carbamate" # # loop_ _pdbx_chem_comp_audit.comp_id _pdbx_chem_comp_audit.action_type _pdbx_chem_comp_audit.date _pdbx_chem_comp_audit.processing_site OMS "Create component" 2019-06-28 RCSB OMS "Initial release" 2020-03-04 RCSB OMS "Modify synonyms" 2021-03-01 PDBE # _pdbx_chem_comp_synonyms.ordinal 1 _pdbx_chem_comp_synonyms.comp_id OMS _pdbx_chem_comp_synonyms.name "P4-2 (NR02-61)" _pdbx_chem_comp_synonyms.provenance ? _pdbx_chem_comp_synonyms.type ? ##