data_bmse011584 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse011584 _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/bmse011584 loop_ _Entry_experimental_methods.ID _Entry_experimental_methods.Method _Entry_experimental_methods.Subtype _Entry_experimental_methods.Entry_ID 1 NMR solution bmse011584 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. . bmse011584 2 Christian Richter C. . bmse011584 3 Till Kuehn T. . bmse011584 4 Kamal Azzaoui K. . bmse011584 5 Marcel Blommers M. J.J. bmse011584 6 Rebecca 'Del Conte' R. . bmse011584 7 Marco Fragai M. . bmse011584 8 Nils Trieloff N. . bmse011584 9 Peter Schmieder P. . bmse011584 10 Marc Nazare M. . bmse011584 11 Edgar Specker E. . bmse011584 12 Vladimir Ivanov V. . bmse011584 13 Hartmut Oschkinat H. . bmse011584 14 Lucia Banci L. . bmse011584 15 Harald Schwalbe H. . bmse011584 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Entry_ID 1 iNEXT 'Infrastructure for NMR' bmse011584 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID spectral_peak_list 1 bmse011584 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 10 bmse011584 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 bmse011584 stop_ loop_ _Auxiliary_files.ID _Auxiliary_files.Name _Auxiliary_files.Format _Auxiliary_files.URI _Auxiliary_files.Details _Auxiliary_files.Entry_ID 3 bmse011584.sdf sdf na 'Structure Definition File' bmse011584 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID bmse011584 _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. . bmse011584 1 2 Christian Richter C. . bmse011584 1 3 Till Kuehn T. . bmse011584 1 4 Kamal Azzaoui K. . bmse011584 1 5 Marcel Blommers M. J.J. bmse011584 1 6 Rebecca 'Del Conte' R. . bmse011584 1 7 Marco Fragai M. . bmse011584 1 8 Nils Trieloff N. . bmse011584 1 9 Peter Schmieder P. . bmse011584 1 10 Marc Nazare M. . bmse011584 1 11 Edgar Specker E. . bmse011584 1 12 Vladimir Ivanov V. . bmse011584 1 13 Hartmut Oschkinat H. . bmse011584 1 14 Lucia Banci L. . bmse011584 1 15 Harald Schwalbe H. . bmse011584 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly_1 _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly_1 _Assembly.Entry_ID bmse011584 _Assembly.ID 1 _Assembly.Name [2-(trifluoromethoxy)phenyl]methanamine _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 Z2856434776 1 $entity_1 yes native no no bmse011584 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 Z2856434776 C1 C bmse011584 1 2 1 1 1 1 Z2856434776 C2 C bmse011584 1 3 1 1 1 1 Z2856434776 C3 C bmse011584 1 4 1 1 1 1 Z2856434776 C4 C bmse011584 1 5 1 1 1 1 Z2856434776 C5 C bmse011584 1 6 1 1 1 1 Z2856434776 C6 C bmse011584 1 7 1 1 1 1 Z2856434776 C7 C bmse011584 1 8 1 1 1 1 Z2856434776 C8 C bmse011584 1 9 1 1 1 1 Z2856434776 F9 F bmse011584 1 10 1 1 1 1 Z2856434776 F10 F bmse011584 1 11 1 1 1 1 Z2856434776 F11 F bmse011584 1 12 1 1 1 1 Z2856434776 N12 N bmse011584 1 13 1 1 1 1 Z2856434776 O13 O bmse011584 1 14 1 1 1 1 Z2856434776 H14 H bmse011584 1 15 1 1 1 1 Z2856434776 H15 H bmse011584 1 16 1 1 1 1 Z2856434776 H16 H bmse011584 1 17 1 1 1 1 Z2856434776 H17 H bmse011584 1 18 1 1 1 1 Z2856434776 H18 H bmse011584 1 19 1 1 1 1 Z2856434776 H19 H bmse011584 1 20 1 1 1 1 Z2856434776 H20 H bmse011584 1 21 1 1 1 1 Z2856434776 H21 H bmse011584 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_entity_1 _Entity.Sf_category entity _Entity.Sf_framecode entity_1 _Entity.Entry_ID bmse011584 _Entity.ID 1 _Entity.Name [2-(trifluoromethoxy)phenyl]methanamine _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID Z2856434776 _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 191.15042959999994 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 Z2856434776 $chem_comp_1 bmse011584 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 bmse011584 _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 bmse011584 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 bmse011584 _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' bmse011584 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 bmse011584 _Chem_comp.ID Z2856434776 _Chem_comp.Provenance iNEXT _Chem_comp.Name [2-(trifluoromethoxy)phenyl]methanamine _Chem_comp.Type non-polymer _Chem_comp.Number_atoms_all 21 _Chem_comp.Number_atoms_nh 13 _Chem_comp.InChI_code InChI=1S/C8H8F3NO/c9-8(10,11)13-7-4-2-1-3-6(7)5-12/h1-4H,5,12H2 _Chem_comp.Synonyms P7_H01 _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic no _Chem_comp.Formula C8H8F3NO _Chem_comp.Formula_weight 191.15042959999994 _Chem_comp.Formula_mono_iso_wt_nat 191.055798541 _Chem_comp.Formula_mono_iso_wt_13C 199.08263724500003 _Chem_comp.Formula_mono_iso_wt_15N 192.052833434 _Chem_comp.Formula_mono_iso_wt_13C_15N 200.07967213800003 _Chem_comp.Image_file_name bmse011584.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse011584.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 FC(F)(F)OC=1C=CC=CC1CN SMILES Bruker_TopSpin_FBS na bmse011584 Z2856434776 NCc1ccccc1OC(F)(F)F SMILES_CANONICAL RDKit 2017.09.3 bmse011584 Z2856434776 NCc1ccccc1OC(F)(F)F SMILES_ISOMERIC RDKit 2017.09.3 bmse011584 Z2856434776 NCc1ccccc1OC(F)(F)F SMILES RDKit 2017.09.3 bmse011584 Z2856434776 NCc1ccccc1OC(F)(F)F SMILES_CANONICAL OpenBabel 2.3.2 bmse011584 Z2856434776 NCc1ccccc1OC(F)(F)F SMILES OpenBabel 2.3.2 bmse011584 Z2856434776 InChI=1S/C8H8F3NO/c9-8(10,11)13-7-4-2-1-3-6(7)5-12/h1-4H,5,12H2 InChI OpenBabel 2.3.2 bmse011584 Z2856434776 FYXMMFFZMQMXCQ-UHFFFAOYSA-N InChI_KEY OpenBabel 2.3.2 bmse011584 Z2856434776 InChI=1S/C8H8F3NO/c9-8(10,11)13-7-4-2-1-3-6(7)5-12/h1-4H,5,12H2 InChI ALATIS na bmse011584 Z2856434776 stop_ loop_ _Chem_comp_identifier.Identifier _Chem_comp_identifier.Type _Chem_comp_identifier.Program _Chem_comp_identifier.Program_version _Chem_comp_identifier.Entry_ID _Chem_comp_identifier.Comp_ID [2-(trifluoromethoxy)phenyl]methanamine 'IUPAC NAME' http://cactus.nci.nih.gov/chemical/structure na bmse011584 Z2856434776 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 yes 1 bmse011584 Z2856434776 C2 C N 0 yes 2 bmse011584 Z2856434776 C3 C N 0 yes 3 bmse011584 Z2856434776 C4 C N 0 yes 4 bmse011584 Z2856434776 C5 C N 0 no 5 bmse011584 Z2856434776 C6 C N 0 yes 6 bmse011584 Z2856434776 C7 C N 0 yes 7 bmse011584 Z2856434776 C8 C N 0 no 8 bmse011584 Z2856434776 F9 F N 0 no 9 bmse011584 Z2856434776 F10 F N 0 no 10 bmse011584 Z2856434776 F11 F N 0 no 11 bmse011584 Z2856434776 N12 N N 0 no 12 bmse011584 Z2856434776 O13 O N 0 no 13 bmse011584 Z2856434776 H14 H N 0 no 14 bmse011584 Z2856434776 H15 H N 0 no 15 bmse011584 Z2856434776 H16 H N 0 no 16 bmse011584 Z2856434776 H17 H N 0 no 17 bmse011584 Z2856434776 H18 H N 0 no 18 bmse011584 Z2856434776 H19 H N 0 no 19 bmse011584 Z2856434776 H20 H N 0 no 20 bmse011584 Z2856434776 H21 H N 0 no 21 bmse011584 Z2856434776 stop_ loop_ _Atom_nomenclature.Naming_system _Atom_nomenclature.Atom_name _Atom_nomenclature.Atom_ID _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID author C12 C1 bmse011584 Z2856434776 author C13 C2 bmse011584 Z2856434776 author C11 C3 bmse011584 Z2856434776 author C10 C4 bmse011584 Z2856434776 author C9 C5 bmse011584 Z2856434776 author C4 C6 bmse011584 Z2856434776 author C3 C7 bmse011584 Z2856434776 author C1 C8 bmse011584 Z2856434776 author F5 F9 bmse011584 Z2856434776 author F6 F10 bmse011584 Z2856434776 author F7 F11 bmse011584 Z2856434776 author N8 N12 bmse011584 Z2856434776 author O2 O13 bmse011584 Z2856434776 author H20 H14 bmse011584 Z2856434776 author H21 H15 bmse011584 Z2856434776 author H19 H16 bmse011584 Z2856434776 author H18 H17 bmse011584 Z2856434776 author H16 H18 bmse011584 Z2856434776 author H17 H19 bmse011584 Z2856434776 author H14 H20 bmse011584 Z2856434776 author H15 H21 bmse011584 Z2856434776 ALATIS C1 C1 bmse011584 Z2856434776 ALATIS C2 C2 bmse011584 Z2856434776 ALATIS C3 C3 bmse011584 Z2856434776 ALATIS C4 C4 bmse011584 Z2856434776 ALATIS C5 C5 bmse011584 Z2856434776 ALATIS C6 C6 bmse011584 Z2856434776 ALATIS C7 C7 bmse011584 Z2856434776 ALATIS C8 C8 bmse011584 Z2856434776 ALATIS F9 F9 bmse011584 Z2856434776 ALATIS F10 F10 bmse011584 Z2856434776 ALATIS F11 F11 bmse011584 Z2856434776 ALATIS N12 N12 bmse011584 Z2856434776 ALATIS O13 O13 bmse011584 Z2856434776 ALATIS H14 H14 bmse011584 Z2856434776 ALATIS H15 H15 bmse011584 Z2856434776 ALATIS H16 H16 bmse011584 Z2856434776 ALATIS H17 H17 bmse011584 Z2856434776 ALATIS H18 H18 bmse011584 Z2856434776 ALATIS H19 H19 bmse011584 Z2856434776 ALATIS H20 H20 bmse011584 Z2856434776 ALATIS H21 H21 bmse011584 Z2856434776 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 C1 C3 yes N 1 bmse011584 Z2856434776 2 covalent AROM C2 C1 yes N 2 bmse011584 Z2856434776 3 covalent AROM C2 C4 yes N 3 bmse011584 Z2856434776 4 covalent AROM C3 C6 yes N 4 bmse011584 Z2856434776 5 covalent AROM C4 C7 yes N 5 bmse011584 Z2856434776 6 covalent AROM C6 C7 yes N 6 bmse011584 Z2856434776 7 covalent SING C1 H14 no N 7 bmse011584 Z2856434776 8 covalent SING C2 H15 no N 8 bmse011584 Z2856434776 9 covalent SING C3 H16 no N 9 bmse011584 Z2856434776 10 covalent SING C4 H17 no N 10 bmse011584 Z2856434776 11 covalent SING C5 C6 no N 11 bmse011584 Z2856434776 12 covalent SING C5 H18 no N 12 bmse011584 Z2856434776 13 covalent SING C5 H19 no N 13 bmse011584 Z2856434776 14 covalent SING C7 O13 no N 14 bmse011584 Z2856434776 15 covalent SING F9 C8 no N 15 bmse011584 Z2856434776 16 covalent SING F10 C8 no N 16 bmse011584 Z2856434776 17 covalent SING F11 C8 no N 17 bmse011584 Z2856434776 18 covalent SING N12 C5 no N 18 bmse011584 Z2856434776 19 covalent SING N12 H20 no N 19 bmse011584 Z2856434776 20 covalent SING N12 H21 no N 20 bmse011584 Z2856434776 21 covalent SING O13 C8 no N 21 bmse011584 Z2856434776 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse011584 _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 Z2856434776 'natural abundance' 1 $assembly_1 1 $entity_1 solute 1 mM bmse011584 1 2 'Potassium phosphate' 'natural abundance' . . . . buffer 25 mM bmse011584 1 3 'Potassium chloride' 'natural abundance' . . . . salt 50 mM bmse011584 1 4 'Magnesium chloride' 'natural abundance' . . . . salt 5 mM bmse011584 1 5 D2O 'natural abundance' . . . . solvent 9 % bmse011584 1 6 H2O 'natural abundance' . . . . solvent 90 % bmse011584 1 7 DMSO '[2H U-100%]' . . . . solvent 1 % bmse011584 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 bmse011584 _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 bmse011584 1 pressure 1 . atm bmse011584 1 temperature 298 0.1 K bmse011584 1 stop_ save_ ############################ # Computer software used # ############################ save_software_topspin _Software.Sf_category software _Software.Sf_framecode software_topspin _Software.Entry_ID bmse011584 _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/ bmse011584 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'data analysis' bmse011584 1 'peak picking' bmse011584 1 processing bmse011584 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 bmse011584 _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 bmse011584 _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 bmse011584 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/ bmse011584 1 1 cmcproject.xml text/xml 'spectrum analysis' nmr/set01/1/pdata/1/ bmse011584 1 1 multiplet.txt text 'Peak list' nmr/set01/1/pdata/1/ bmse011584 1 1 spectrum_overview.pdf pdf 'Spectrum image' nmr/set01/1/pdata/1/ bmse011584 1 1 spectrum_overview.png image/png 'Spectral image' nmr/set01/1/pdata/1/ bmse011584 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 bmse011584 _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 bmse011584 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 bmse011584 _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 bmse011584 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 bmse011584 1 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse011584 1 2 bmse011584 1 3 bmse011584 1 4 bmse011584 1 5 bmse011584 1 6 bmse011584 1 7 bmse011584 1 9 bmse011584 1 10 bmse011584 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 7.3807 m_6H bmse011584 1 2 1 4.2191 s_2H bmse011584 1 3 1 2.4876 Imp1 bmse011584 1 4 1 7.7411 m_1H bmse011584 1 5 1 2.7206 Imp2 bmse011584 1 6 1 7.4851 m_6H bmse011584 1 7 1 7.9006 dd_1H_Q1 bmse011584 1 8 1 2.6027 DMSO bmse011584 1 9 1 10.1940 s_1H bmse011584 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 7.9779 bmse011584 1 2 2 1 0.0000 bmse011584 1 3 3 1 0.0000 bmse011584 1 4 4 1 3.5029 bmse011584 1 5 5 1 0.0000 bmse011584 1 6 6 1 6.6574 bmse011584 1 7 7 1 7.8128 bmse011584 1 8 7 1 1.3205 bmse011584 1 9 8 1 1.9807 bmse011584 1 10 9 1 0.0000 bmse011584 1 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse011584 1 2 bmse011584 1 3 bmse011584 1 4 bmse011584 1 5 bmse011584 1 6 bmse011584 1 7 bmse011584 1 8 bmse011584 1 9 bmse011584 1 10 bmse011584 1 11 bmse011584 1 12 bmse011584 1 13 bmse011584 1 14 bmse011584 1 15 bmse011584 1 16 bmse011584 1 17 bmse011584 1 18 bmse011584 1 19 bmse011584 1 20 bmse011584 1 21 bmse011584 1 22 bmse011584 1 23 bmse011584 1 24 bmse011584 1 25 bmse011584 1 26 bmse011584 1 27 bmse011584 1 28 bmse011584 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 7.4073 bmse011584 1 2 1 7.3939 bmse011584 1 3 1 7.3794 bmse011584 1 4 1 7.3668 bmse011584 1 5 1 7.3541 bmse011584 1 6 1 4.2191 bmse011584 1 7 1 2.4876 bmse011584 1 8 1 7.7586 bmse011584 1 9 1 7.7526 bmse011584 1 10 1 7.7509 bmse011584 1 11 1 7.7441 bmse011584 1 12 1 7.7381 bmse011584 1 13 1 7.7267 bmse011584 1 14 1 7.7236 bmse011584 1 15 1 2.7206 bmse011584 1 16 1 7.4962 bmse011584 1 17 1 7.4863 bmse011584 1 18 1 7.4741 bmse011584 1 19 1 7.9082 bmse011584 1 20 1 7.9058 bmse011584 1 21 1 7.8950 bmse011584 1 22 1 7.8930 bmse011584 1 23 1 2.5961 bmse011584 1 24 1 2.6000 bmse011584 1 25 1 2.6027 bmse011584 1 26 1 2.6055 bmse011584 1 27 1 2.6093 bmse011584 1 28 1 10.1940 bmse011584 1 stop_ save_