data_bmse011343 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse011343 _Entry.Title ; NMR quality control of fragment libraries for screening ; _Entry.Type 'compound library' _Entry.Version_type original _Entry.Submission_date 2020-09-15 _Entry.Accession_date 2020-09-15 _Entry.Last_release_date 2020-09-15 _Entry.Original_release_date 2020-09-15 _Entry.Origination author _Entry.NMR_STAR_version 3.2.0.16 _Entry.Original_NMR_STAR_version 3.2.0.16 _Entry.Experimental_method NMR _Entry.Experimental_method_subtype solution _Entry.DOI 10.12018/bmse011343 loop_ _Entry_experimental_methods.ID _Entry_experimental_methods.Method _Entry_experimental_methods.Subtype _Entry_experimental_methods.Entry_ID 1 NMR solution bmse011343 stop_ loop_ _Entry_author.Ordinal _Entry_author.Given_name _Entry_author.Family_name _Entry_author.First_initial _Entry_author.Middle_initials _Entry_author.Entry_ID 1 Sridhar Sreeramulu S. . bmse011343 2 Christian Richter C. . bmse011343 3 Till Kuehn T. . bmse011343 4 Kamal Azzaoui K. . bmse011343 5 Marcel Blommers M. J.J. bmse011343 6 Rebecca 'Del Conte' R. . bmse011343 7 Marco Fragai M. . bmse011343 8 Nils Trieloff N. . bmse011343 9 Peter Schmieder P. . bmse011343 10 Marc Nazare M. . bmse011343 11 Edgar Specker E. . bmse011343 12 Vladimir Ivanov V. . bmse011343 13 Hartmut Oschkinat H. . bmse011343 14 Lucia Banci L. . bmse011343 15 Harald Schwalbe H. . bmse011343 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Entry_ID 1 iNEXT 'Infrastructure for NMR' bmse011343 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID spectral_peak_list 1 bmse011343 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 6 bmse011343 stop_ loop_ _Release.Release_number _Release.Format_type _Release.Format_version _Release.Date _Release.Type _Release.Author _Release.Entry_ID 1 NMR-STAR 3.2.11.4 2020-09-15 original author bmse011343 stop_ loop_ _Auxiliary_files.ID _Auxiliary_files.Name _Auxiliary_files.Format _Auxiliary_files.URI _Auxiliary_files.Details _Auxiliary_files.Entry_ID 3 bmse011343.sdf sdf na 'Structure Definition File' bmse011343 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID bmse011343 _Citation.ID 1 _Citation.Class 'entry citation' _Citation.DOI 10.1007/s10858-020-00327-9 _Citation.Title ; NMR quality control of fragment libraries for screening ; _Citation.Status published _Citation.Type 'open access' _Citation.Journal_abbrev 'J. Biomol. NMR' _Citation.Year 2020 loop_ _Citation_author.Ordinal _Citation_author.Given_name _Citation_author.Family_name _Citation_author.First_initial _Citation_author.Middle_initials _Citation_author.Entry_ID _Citation_author.Citation_ID 1 Sridhar Sreeramulu S. . bmse011343 1 2 Christian Richter C. . bmse011343 1 3 Till Kuehn T. . bmse011343 1 4 Kamal Azzaoui K. . bmse011343 1 5 Marcel Blommers M. J.J. bmse011343 1 6 Rebecca 'Del Conte' R. . bmse011343 1 7 Marco Fragai M. . bmse011343 1 8 Nils Trieloff N. . bmse011343 1 9 Peter Schmieder P. . bmse011343 1 10 Marc Nazare M. . bmse011343 1 11 Edgar Specker E. . bmse011343 1 12 Vladimir Ivanov V. . bmse011343 1 13 Hartmut Oschkinat H. . bmse011343 1 14 Lucia Banci L. . bmse011343 1 15 Harald Schwalbe H. . bmse011343 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly_1 _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly_1 _Assembly.Entry_ID bmse011343 _Assembly.ID 1 _Assembly.Name 1-tert-butyl-3-(4-ethoxyphenyl)urea _Assembly.Number_of_components 1 _Assembly.Paramagnetic no _Assembly.Thiol_state na loop_ _Entity_assembly.ID _Entity_assembly.Entity_assembly_name _Entity_assembly.Entity_ID _Entity_assembly.Entity_label _Entity_assembly.Experimental_data_reported _Entity_assembly.Physical_state _Entity_assembly.Conformational_isomer _Entity_assembly.Chemical_exchange_state _Entity_assembly.Entry_ID _Entity_assembly.Assembly_ID 1 Z44586802 1 $entity_1 yes native no no bmse011343 1 stop_ loop_ _Atom.Assembly_atom_ID _Atom.Entity_assembly_ID _Atom.Entity_ID _Atom.Comp_index_ID _Atom.Seq_ID _Atom.Comp_ID _Atom.Atom_ID _Atom.Type_symbol _Atom.Entry_ID _Atom.Assembly_ID 1 1 1 1 1 Z44586802 C1 C bmse011343 1 2 1 1 1 1 Z44586802 C2 C bmse011343 1 3 1 1 1 1 Z44586802 C3 C bmse011343 1 4 1 1 1 1 Z44586802 C4 C bmse011343 1 5 1 1 1 1 Z44586802 C5 C bmse011343 1 6 1 1 1 1 Z44586802 C6 C bmse011343 1 7 1 1 1 1 Z44586802 C7 C bmse011343 1 8 1 1 1 1 Z44586802 C8 C bmse011343 1 9 1 1 1 1 Z44586802 C9 C bmse011343 1 10 1 1 1 1 Z44586802 C10 C bmse011343 1 11 1 1 1 1 Z44586802 C11 C bmse011343 1 12 1 1 1 1 Z44586802 C12 C bmse011343 1 13 1 1 1 1 Z44586802 C13 C bmse011343 1 14 1 1 1 1 Z44586802 N14 N bmse011343 1 15 1 1 1 1 Z44586802 N15 N bmse011343 1 16 1 1 1 1 Z44586802 O16 O bmse011343 1 17 1 1 1 1 Z44586802 O17 O bmse011343 1 18 1 1 1 1 Z44586802 H18 H bmse011343 1 19 1 1 1 1 Z44586802 H19 H bmse011343 1 20 1 1 1 1 Z44586802 H20 H bmse011343 1 21 1 1 1 1 Z44586802 H21 H bmse011343 1 22 1 1 1 1 Z44586802 H22 H bmse011343 1 23 1 1 1 1 Z44586802 H23 H bmse011343 1 24 1 1 1 1 Z44586802 H24 H bmse011343 1 25 1 1 1 1 Z44586802 H25 H bmse011343 1 26 1 1 1 1 Z44586802 H26 H bmse011343 1 27 1 1 1 1 Z44586802 H27 H bmse011343 1 28 1 1 1 1 Z44586802 H28 H bmse011343 1 29 1 1 1 1 Z44586802 H29 H bmse011343 1 30 1 1 1 1 Z44586802 H30 H bmse011343 1 31 1 1 1 1 Z44586802 H31 H bmse011343 1 32 1 1 1 1 Z44586802 H32 H bmse011343 1 33 1 1 1 1 Z44586802 H33 H bmse011343 1 34 1 1 1 1 Z44586802 H34 H bmse011343 1 35 1 1 1 1 Z44586802 H35 H bmse011343 1 36 1 1 1 1 Z44586802 H36 H bmse011343 1 37 1 1 1 1 Z44586802 H37 H bmse011343 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_entity_1 _Entity.Sf_category entity _Entity.Sf_framecode entity_1 _Entity.Entry_ID bmse011343 _Entity.ID 1 _Entity.Name 1-tert-butyl-3-(4-ethoxyphenyl)urea _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID Z44586802 _Entity.Nonpolymer_comp_label $chem_comp_1 _Entity.Number_of_monomers 1 _Entity.Number_of_nonpolymer_components 1 _Entity.Paramagnetic no _Entity.Thiol_state 'not present' _Entity.Formula_weight 236.3100999999998 loop_ _Entity_comp_index.ID _Entity_comp_index.Auth_seq_ID _Entity_comp_index.Comp_ID _Entity_comp_index.Comp_label _Entity_comp_index.Entry_ID _Entity_comp_index.Entity_ID 1 1 Z44586802 $chem_comp_1 bmse011343 1 stop_ save_ #################### # Natural source # #################### save_natural_source _Entity_natural_src_list.Sf_category natural_source _Entity_natural_src_list.Sf_framecode natural_source _Entity_natural_src_list.Entry_ID bmse011343 _Entity_natural_src_list.ID 1 loop_ _Entity_natural_src.ID _Entity_natural_src.Entity_ID _Entity_natural_src.Entity_label _Entity_natural_src.NCBI_taxonomy_ID _Entity_natural_src.Type _Entity_natural_src.Common _Entity_natural_src.Organism_name_scientific _Entity_natural_src.Organism_name_common _Entity_natural_src.Superkingdom _Entity_natural_src.Genus _Entity_natural_src.Species _Entity_natural_src.Entry_ID _Entity_natural_src.Entity_natural_src_list_ID 1 1 $entity_1 na na yes na na na na na bmse011343 1 stop_ save_ ######################### # Experimental source # ######################### save_experimental_source _Entity_experimental_src_list.Sf_category experimental_source _Entity_experimental_src_list.Sf_framecode experimental_source _Entity_experimental_src_list.Entry_ID bmse011343 _Entity_experimental_src_list.ID 1 loop_ _Entity_experimental_src.ID _Entity_experimental_src.Entity_ID _Entity_experimental_src.Entity_label _Entity_experimental_src.Production_method _Entity_experimental_src.Entry_ID _Entity_experimental_src.Entity_experimental_src_list_ID 1 1 $entity_1 'chemical synthesis' bmse011343 1 stop_ save_ ################################# # Polymer residues and ligands # ################################# save_chem_comp_1 _Chem_comp.Sf_category chem_comp _Chem_comp.Sf_framecode chem_comp_1 _Chem_comp.Entry_ID bmse011343 _Chem_comp.ID Z44586802 _Chem_comp.Provenance iNEXT _Chem_comp.Name 1-tert-butyl-3-(4-ethoxyphenyl)urea _Chem_comp.Type non-polymer _Chem_comp.Number_atoms_all 37 _Chem_comp.Number_atoms_nh 17 _Chem_comp.InChI_code InChI=1S/C13H20N2O2/c1-5-17-11-8-6-10(7-9-11)14-12(16)15-13(2,3)4/h6-9H,5H2,1-4H3,(H2,14,15,16) _Chem_comp.Synonyms P4_G07 _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic no _Chem_comp.Formula C13H20N2O2 _Chem_comp.Formula_weight 236.3100999999998 _Chem_comp.Formula_mono_iso_wt_nat 236.15247789 _Chem_comp.Formula_mono_iso_wt_13C 249.19609078400006 _Chem_comp.Formula_mono_iso_wt_15N 238.146547676 _Chem_comp.Formula_mono_iso_wt_13C_15N 251.19016057000007 _Chem_comp.Image_file_name bmse011343.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse011343.sdf _Chem_comp.Struct_file_format sdf loop_ _Chem_comp_descriptor.Descriptor _Chem_comp_descriptor.Type _Chem_comp_descriptor.Program _Chem_comp_descriptor.Program_version _Chem_comp_descriptor.Entry_ID _Chem_comp_descriptor.Comp_ID O=C(NC1=CC=C(OCC)C=C1)NC(C)(C)C SMILES Bruker_TopSpin_FBS na bmse011343 Z44586802 CCOc1ccc(NC(=O)NC(C)(C)C)cc1 SMILES_CANONICAL RDKit 2017.09.3 bmse011343 Z44586802 CCOc1ccc(NC(=O)NC(C)(C)C)cc1 SMILES_ISOMERIC RDKit 2017.09.3 bmse011343 Z44586802 CCOc1ccc(NC(=O)NC(C)(C)C)cc1 SMILES RDKit 2017.09.3 bmse011343 Z44586802 CCOc1ccc(cc1)NC(=O)NC(C)(C)C SMILES_CANONICAL OpenBabel 2.3.2 bmse011343 Z44586802 CCOc1ccc(cc1)NC(=O)NC(C)(C)C SMILES OpenBabel 2.3.2 bmse011343 Z44586802 InChI=1S/C13H20N2O2/c1-5-17-11-8-6-10(7-9-11)14-12(16)15-13(2,3)4/h6-9H,5H2,1-4H3,(H2,14,15,16) InChI OpenBabel 2.3.2 bmse011343 Z44586802 GIFYSRSYORMVRS-UHFFFAOYSA-N InChI_KEY OpenBabel 2.3.2 bmse011343 Z44586802 InChI=1S/C13H20N2O2/c1-5-17-11-8-6-10(7-9-11)14-12(16)15-13(2,3)4/h6-9H,5H2,1-4H3,(H2,14,15,16) InChI ALATIS na bmse011343 Z44586802 stop_ loop_ _Chem_comp_atom.Atom_ID _Chem_comp_atom.Type_symbol _Chem_comp_atom.Stereo_config _Chem_comp_atom.Charge _Chem_comp_atom.Aromatic_flag _Chem_comp_atom.PDBX_ordinal _Chem_comp_atom.Entry_ID _Chem_comp_atom.Comp_ID C1 C N 0 no 1 bmse011343 Z44586802 C2 C N 0 no 2 bmse011343 Z44586802 C3 C N 0 no 3 bmse011343 Z44586802 C4 C N 0 no 4 bmse011343 Z44586802 C5 C N 0 no 5 bmse011343 Z44586802 C6 C N 0 yes 6 bmse011343 Z44586802 C7 C N 0 yes 7 bmse011343 Z44586802 C8 C N 0 yes 8 bmse011343 Z44586802 C9 C N 0 yes 9 bmse011343 Z44586802 C10 C N 0 yes 10 bmse011343 Z44586802 C11 C N 0 yes 11 bmse011343 Z44586802 C12 C N 0 no 12 bmse011343 Z44586802 C13 C N 0 no 13 bmse011343 Z44586802 N14 N N 0 no 14 bmse011343 Z44586802 N15 N N 0 no 15 bmse011343 Z44586802 O16 O N 0 no 16 bmse011343 Z44586802 O17 O N 0 no 17 bmse011343 Z44586802 H18 H N 0 no 18 bmse011343 Z44586802 H19 H N 0 no 19 bmse011343 Z44586802 H20 H N 0 no 20 bmse011343 Z44586802 H21 H N 0 no 21 bmse011343 Z44586802 H22 H N 0 no 22 bmse011343 Z44586802 H23 H N 0 no 23 bmse011343 Z44586802 H24 H N 0 no 24 bmse011343 Z44586802 H25 H N 0 no 25 bmse011343 Z44586802 H26 H N 0 no 26 bmse011343 Z44586802 H27 H N 0 no 27 bmse011343 Z44586802 H28 H N 0 no 28 bmse011343 Z44586802 H29 H N 0 no 29 bmse011343 Z44586802 H30 H N 0 no 30 bmse011343 Z44586802 H31 H N 0 no 31 bmse011343 Z44586802 H32 H N 0 no 32 bmse011343 Z44586802 H33 H N 0 no 33 bmse011343 Z44586802 H34 H N 0 no 34 bmse011343 Z44586802 H35 H N 0 no 35 bmse011343 Z44586802 H36 H N 0 no 36 bmse011343 Z44586802 H37 H N 0 no 37 bmse011343 Z44586802 stop_ loop_ _Atom_nomenclature.Naming_system _Atom_nomenclature.Atom_name _Atom_nomenclature.Atom_ID _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID author C17 C1 bmse011343 Z44586802 author C13 C2 bmse011343 Z44586802 author C14 C3 bmse011343 Z44586802 author C15 C4 bmse011343 Z44586802 author C16 C5 bmse011343 Z44586802 author C8 C6 bmse011343 Z44586802 author C9 C7 bmse011343 Z44586802 author C10 C8 bmse011343 Z44586802 author C11 C9 bmse011343 Z44586802 author C6 C10 bmse011343 Z44586802 author C7 C11 bmse011343 Z44586802 author C1 C12 bmse011343 Z44586802 author C5 C13 bmse011343 Z44586802 author N3 N14 bmse011343 Z44586802 author N2 N15 bmse011343 Z44586802 author O4 O16 bmse011343 Z44586802 author O12 O17 bmse011343 Z44586802 author H36 H18 bmse011343 Z44586802 author H35 H19 bmse011343 Z44586802 author H37 H20 bmse011343 Z44586802 author H25 H21 bmse011343 Z44586802 author H24 H22 bmse011343 Z44586802 author H26 H23 bmse011343 Z44586802 author H28 H24 bmse011343 Z44586802 author H27 H25 bmse011343 Z44586802 author H29 H26 bmse011343 Z44586802 author H31 H27 bmse011343 Z44586802 author H30 H28 bmse011343 Z44586802 author H32 H29 bmse011343 Z44586802 author H33 H30 bmse011343 Z44586802 author H34 H31 bmse011343 Z44586802 author H20 H32 bmse011343 Z44586802 author H21 H33 bmse011343 Z44586802 author H22 H34 bmse011343 Z44586802 author H23 H35 bmse011343 Z44586802 author H19 H36 bmse011343 Z44586802 author H18 H37 bmse011343 Z44586802 ALATIS C1 C1 bmse011343 Z44586802 ALATIS C2 C2 bmse011343 Z44586802 ALATIS C3 C3 bmse011343 Z44586802 ALATIS C4 C4 bmse011343 Z44586802 ALATIS C5 C5 bmse011343 Z44586802 ALATIS C6 C6 bmse011343 Z44586802 ALATIS C7 C7 bmse011343 Z44586802 ALATIS C8 C8 bmse011343 Z44586802 ALATIS C9 C9 bmse011343 Z44586802 ALATIS C10 C10 bmse011343 Z44586802 ALATIS C11 C11 bmse011343 Z44586802 ALATIS C12 C12 bmse011343 Z44586802 ALATIS C13 C13 bmse011343 Z44586802 ALATIS N14 N14 bmse011343 Z44586802 ALATIS N15 N15 bmse011343 Z44586802 ALATIS O16 O16 bmse011343 Z44586802 ALATIS O17 O17 bmse011343 Z44586802 ALATIS H18 H18 bmse011343 Z44586802 ALATIS H19 H19 bmse011343 Z44586802 ALATIS H20 H20 bmse011343 Z44586802 ALATIS H21 H21 bmse011343 Z44586802 ALATIS H22 H22 bmse011343 Z44586802 ALATIS H23 H23 bmse011343 Z44586802 ALATIS H24 H24 bmse011343 Z44586802 ALATIS H25 H25 bmse011343 Z44586802 ALATIS H26 H26 bmse011343 Z44586802 ALATIS H27 H27 bmse011343 Z44586802 ALATIS H28 H28 bmse011343 Z44586802 ALATIS H29 H29 bmse011343 Z44586802 ALATIS H30 H30 bmse011343 Z44586802 ALATIS H31 H31 bmse011343 Z44586802 ALATIS H32 H32 bmse011343 Z44586802 ALATIS H33 H33 bmse011343 Z44586802 ALATIS H34 H34 bmse011343 Z44586802 ALATIS H35 H35 bmse011343 Z44586802 ALATIS H36 H36 bmse011343 Z44586802 ALATIS H37 H37 bmse011343 Z44586802 stop_ loop_ _Chem_comp_bond.ID _Chem_comp_bond.Type _Chem_comp_bond.Value_order _Chem_comp_bond.Atom_ID_1 _Chem_comp_bond.Atom_ID_2 _Chem_comp_bond.Aromatic_flag _Chem_comp_bond.Stereo_config _Chem_comp_bond.Ordinal _Chem_comp_bond.Entry_ID _Chem_comp_bond.Comp_ID 1 covalent AROM C6 C10 yes N 1 bmse011343 Z44586802 2 covalent AROM C7 C10 yes N 2 bmse011343 Z44586802 3 covalent AROM C8 C6 yes N 3 bmse011343 Z44586802 4 covalent AROM C8 C11 yes N 4 bmse011343 Z44586802 5 covalent AROM C9 C7 yes N 5 bmse011343 Z44586802 6 covalent AROM C11 C9 yes N 6 bmse011343 Z44586802 7 carbonyl DOUB O16 C12 no N 7 bmse011343 Z44586802 8 covalent SING C1 C5 no N 8 bmse011343 Z44586802 9 covalent SING C1 H18 no N 9 bmse011343 Z44586802 10 covalent SING C1 H19 no N 10 bmse011343 Z44586802 11 covalent SING C1 H20 no N 11 bmse011343 Z44586802 12 covalent SING C2 C13 no N 12 bmse011343 Z44586802 13 covalent SING C2 H21 no N 13 bmse011343 Z44586802 14 covalent SING C2 H22 no N 14 bmse011343 Z44586802 15 covalent SING C2 H23 no N 15 bmse011343 Z44586802 16 covalent SING C3 C13 no N 16 bmse011343 Z44586802 17 covalent SING C3 H24 no N 17 bmse011343 Z44586802 18 covalent SING C3 H25 no N 18 bmse011343 Z44586802 19 covalent SING C3 H26 no N 19 bmse011343 Z44586802 20 covalent SING C4 C13 no N 20 bmse011343 Z44586802 21 covalent SING C4 H27 no N 21 bmse011343 Z44586802 22 covalent SING C4 H28 no N 22 bmse011343 Z44586802 23 covalent SING C4 H29 no N 23 bmse011343 Z44586802 24 covalent SING C5 O17 no N 24 bmse011343 Z44586802 25 covalent SING C5 H30 no N 25 bmse011343 Z44586802 26 covalent SING C5 H31 no N 26 bmse011343 Z44586802 27 covalent SING C6 H32 no N 27 bmse011343 Z44586802 28 covalent SING C7 H33 no N 28 bmse011343 Z44586802 29 covalent SING C8 H34 no N 29 bmse011343 Z44586802 30 covalent SING C9 H35 no N 30 bmse011343 Z44586802 31 covalent SING C10 N14 no N 31 bmse011343 Z44586802 32 covalent SING C13 N15 no N 32 bmse011343 Z44586802 33 amide SING N14 C12 no N 33 bmse011343 Z44586802 34 covalent SING N14 H36 no N 34 bmse011343 Z44586802 35 amide SING N15 C12 no N 35 bmse011343 Z44586802 36 covalent SING N15 H37 no N 36 bmse011343 Z44586802 37 covalent SING O17 C11 no N 37 bmse011343 Z44586802 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse011343 _Sample.ID 1 _Sample.Type solution loop_ _Sample_component.ID _Sample_component.Mol_common_name _Sample_component.Isotopic_labeling _Sample_component.Assembly_ID _Sample_component.Assembly_label _Sample_component.Entity_ID _Sample_component.Entity_label _Sample_component.Type _Sample_component.Concentration_val _Sample_component.Concentration_val_units _Sample_component.Entry_ID _Sample_component.Sample_ID 1 Z44586802 'natural abundance' 1 $assembly_1 1 $entity_1 solute 1 mM bmse011343 1 2 'Potassium phosphate' 'natural abundance' . . . . buffer 25 mM bmse011343 1 3 'Potassium chloride' 'natural abundance' . . . . salt 50 mM bmse011343 1 4 'Magnesium chloride' 'natural abundance' . . . . salt 5 mM bmse011343 1 5 D2O 'natural abundance' . . . . solvent 9 % bmse011343 1 6 H2O 'natural abundance' . . . . solvent 90 % bmse011343 1 7 DMSO '[2H U-100%]' . . . . solvent 1 % bmse011343 1 stop_ save_ ####################### # Sample conditions # ####################### save_sample_conditions_1 _Sample_condition_list.Sf_category sample_conditions _Sample_condition_list.Sf_framecode sample_conditions_1 _Sample_condition_list.Entry_ID bmse011343 _Sample_condition_list.ID 1 loop_ _Sample_condition_variable.Type _Sample_condition_variable.Val _Sample_condition_variable.Val_err _Sample_condition_variable.Val_units _Sample_condition_variable.Entry_ID _Sample_condition_variable.Sample_condition_list_ID pH 6.0 ? pH bmse011343 1 pressure 1 . atm bmse011343 1 temperature 298 0.1 K bmse011343 1 stop_ save_ ############################ # Computer software used # ############################ save_software_topspin _Software.Sf_category software _Software.Sf_framecode software_topspin _Software.Entry_ID bmse011343 _Software.ID 1 _Software.Name TopSpin _Software.Version 4.0.3 loop_ _Vendor.Name _Vendor.Electronic_address _Vendor.Entry_ID _Vendor.Software_ID 'Bruker Biospin' http://www.bruker.com/products/mr/nmr/nmr-software/software/topspin/ bmse011343 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'data analysis' bmse011343 1 'peak picking' bmse011343 1 processing bmse011343 1 stop_ save_ ######################### # Experimental detail # ######################### ################################## # NMR Spectrometer definitions # ################################## save_spectrometer_Bruker _NMR_spectrometer.Sf_category NMR_spectrometer _NMR_spectrometer.Sf_framecode spectrometer_Bruker _NMR_spectrometer.Entry_ID bmse011343 _NMR_spectrometer.ID 1 _NMR_spectrometer.Manufacturer Bruker _NMR_spectrometer.Model Avance _NMR_spectrometer.Field_strength 600 save_ ############################# # NMR applied experiments # ############################# save_experiment_list _Experiment_list.Sf_category experiment_list _Experiment_list.Sf_framecode experiment_list _Experiment_list.Entry_ID bmse011343 _Experiment_list.ID 1 loop_ _Experiment.ID _Experiment.Name _Experiment.Raw_data_flag _Experiment.Sample_ID _Experiment.Sample_label _Experiment.Sample_state _Experiment.Sample_condition_list_ID _Experiment.Sample_condition_list_label _Experiment.NMR_spectrometer_ID _Experiment.NMR_spectrometer_label _Experiment.Entry_ID _Experiment.Experiment_list_ID 1 '1D 1H' yes 1 $sample_1 isotropic 1 $sample_conditions_1 1 $spectrometer_Bruker bmse011343 1 stop_ loop_ _Experiment_file.Experiment_ID _Experiment_file.Name _Experiment_file.Type _Experiment_file.Content _Experiment_file.Directory_path _Experiment_file.Entry_ID _Experiment_file.Experiment_list_ID 1 1 text/directory 'NMR experiment directory' nmr/set01/ bmse011343 1 1 cmcproject.xml text/xml 'spectrum analysis' nmr/set01/1/pdata/1/ bmse011343 1 1 multiplet.txt text 'Peak list' nmr/set01/1/pdata/1/ bmse011343 1 1 spectrum_overview.pdf pdf 'Spectrum image' nmr/set01/1/pdata/1/ bmse011343 1 1 spectrum_overview.png image/png 'Spectral image' nmr/set01/1/pdata/1/ bmse011343 1 stop_ save_ #################### # NMR parameters # #################### ############################## # Assigned chemical shifts # ############################## ################################ # Chemical shift referencing # ################################ save_chem_shift_ref_set _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chem_shift_ref_set _Chem_shift_reference.Entry_ID bmse011343 _Chem_shift_reference.ID 1 loop_ _Chem_shift_ref.Atom_type _Chem_shift_ref.Atom_isotope_number _Chem_shift_ref.Mol_common_name _Chem_shift_ref.Atom_group _Chem_shift_ref.Chem_shift_units _Chem_shift_ref.Chem_shift_val _Chem_shift_ref.Ref_method _Chem_shift_ref.Ref_type _Chem_shift_ref.Indirect_shift_ratio _Chem_shift_ref.Entry_ID _Chem_shift_ref.Chem_shift_reference_ID H 1 TSP 'methyl protons' ppm 0.0 internal direct 1.0 bmse011343 1 stop_ save_ ######################### # Spectral peak lists # ######################### save_spectral_peaks_1D_1H _Spectral_peak_list.Sf_category spectral_peak_list _Spectral_peak_list.Sf_framecode spectral_peaks_1D_1H _Spectral_peak_list.Entry_ID bmse011343 _Spectral_peak_list.ID 1 _Spectral_peak_list.Sample_ID 1 _Spectral_peak_list.Sample_label $sample_1 _Spectral_peak_list.Sample_condition_list_ID 1 _Spectral_peak_list.Sample_condition_list_label $sample_conditions_1 _Spectral_peak_list.Experiment_ID 1 _Spectral_peak_list.Experiment_name '1D 1H' _Spectral_peak_list.Number_of_spectral_dimensions 1 _Spectral_peak_list.Assigned_chem_shift_list_ID 1 _Spectral_peak_list.Details 'F1: 1H' loop_ _Spectral_dim.ID _Spectral_dim.Spectrometer_frequency _Spectral_dim.Atom_type _Spectral_dim.Atom_isotope_number _Spectral_dim.Spectral_region _Spectral_dim.Sweep_width _Spectral_dim.Sweep_width_units _Spectral_dim.Entry_ID _Spectral_dim.Spectral_peak_list_ID 1 600.1728185 H 1 'Full H' 12.0157698570257 ppm bmse011343 1 stop_ loop_ _Spectral_peak_software.Software_ID _Spectral_peak_software.Software_label _Spectral_peak_software.Entry_ID _Spectral_peak_software.Spectral_peak_list_ID 1 $software_topspin bmse011343 1 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse011343 1 2 bmse011343 1 3 bmse011343 1 4 bmse011343 1 5 bmse011343 1 6 bmse011343 1 stop_ loop_ _Peak_char.Peak_ID _Peak_char.Spectral_dim_ID _Peak_char.Chem_shift_val _Peak_char.Details _Peak_char.Entry_ID _Peak_char.Spectral_peak_list_ID 1 1 1.2362 m_6H bmse011343 1 2 1 2.6032 DMSO bmse011343 1 3 1 1.2826 t_2H bmse011343 1 4 1 4.0227 q_1H bmse011343 1 5 1 6.8873 m_1H bmse011343 1 6 1 7.1151 m_1H_Q1 bmse011343 1 stop_ loop_ _Peak_coupling.ID _Peak_coupling.Peak_ID _Peak_coupling.Spectral_dim_ID _Peak_coupling.Coupling_val _Peak_coupling.Entry_ID _Peak_coupling.Spectral_peak_list_ID 1 1 1 0.0000 bmse011343 1 2 2 1 1.8982 bmse011343 1 3 3 1 7.0425 bmse011343 1 4 4 1 7.0425 bmse011343 1 5 5 1 2.9344 bmse011343 1 6 6 1 4.4016 bmse011343 1 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse011343 1 2 bmse011343 1 3 bmse011343 1 4 bmse011343 1 5 bmse011343 1 6 bmse011343 1 7 bmse011343 1 8 bmse011343 1 9 bmse011343 1 10 bmse011343 1 11 bmse011343 1 12 bmse011343 1 13 bmse011343 1 14 bmse011343 1 15 bmse011343 1 16 bmse011343 1 17 bmse011343 1 18 bmse011343 1 19 bmse011343 1 20 bmse011343 1 stop_ loop_ _Spectral_transition_char.Spectral_transition_ID _Spectral_transition_char.Spectral_dim_ID _Spectral_transition_char.Chem_shift_val _Spectral_transition_char.Entry_ID _Spectral_transition_char.Spectral_peak_list_ID 1 1 1.2362 bmse011343 1 2 1 2.5968 bmse011343 1 3 1 2.6000 bmse011343 1 4 1 2.6031 bmse011343 1 5 1 2.6062 bmse011343 1 6 1 2.6095 bmse011343 1 7 1 1.2709 bmse011343 1 8 1 1.2826 bmse011343 1 9 1 1.2943 bmse011343 1 10 1 4.0051 bmse011343 1 11 1 4.0169 bmse011343 1 12 1 4.0286 bmse011343 1 13 1 4.0403 bmse011343 1 14 1 6.8947 bmse011343 1 15 1 6.8912 bmse011343 1 16 1 6.8833 bmse011343 1 17 1 6.8800 bmse011343 1 18 1 7.1224 bmse011343 1 19 1 7.1189 bmse011343 1 20 1 7.1077 bmse011343 1 stop_ save_