data_bmse011017 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse011017 _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/bmse011017 loop_ _Entry_experimental_methods.ID _Entry_experimental_methods.Method _Entry_experimental_methods.Subtype _Entry_experimental_methods.Entry_ID 1 NMR solution bmse011017 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. . bmse011017 2 Christian Richter C. . bmse011017 3 Till Kuehn T. . bmse011017 4 Kamal Azzaoui K. . bmse011017 5 Marcel Blommers M. J.J. bmse011017 6 Rebecca 'Del Conte' R. . bmse011017 7 Marco Fragai M. . bmse011017 8 Nils Trieloff N. . bmse011017 9 Peter Schmieder P. . bmse011017 10 Marc Nazare M. . bmse011017 11 Edgar Specker E. . bmse011017 12 Vladimir Ivanov V. . bmse011017 13 Hartmut Oschkinat H. . bmse011017 14 Lucia Banci L. . bmse011017 15 Harald Schwalbe H. . bmse011017 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Entry_ID 1 iNEXT 'Infrastructure for NMR' bmse011017 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID spectral_peak_list 1 bmse011017 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 15 bmse011017 stop_ loop_ _Release.Release_number _Release.Format_type _Release.Format_version _Release.Date _Release.Submission_date _Release.Type _Release.Author _Release.Detail _Release.Entry_ID 1 NMR-STAR 3.2.11.4 2020-09-15 . original author . bmse011017 stop_ loop_ _Auxiliary_files.ID _Auxiliary_files.Name _Auxiliary_files.Format _Auxiliary_files.URI _Auxiliary_files.Details _Auxiliary_files.Entry_ID 3 bmse011017.sdf sdf na 'Structure Definition File' bmse011017 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID bmse011017 _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. . bmse011017 1 2 Christian Richter C. . bmse011017 1 3 Till Kuehn T. . bmse011017 1 4 Kamal Azzaoui K. . bmse011017 1 5 Marcel Blommers M. J.J. bmse011017 1 6 Rebecca 'Del Conte' R. . bmse011017 1 7 Marco Fragai M. . bmse011017 1 8 Nils Trieloff N. . bmse011017 1 9 Peter Schmieder P. . bmse011017 1 10 Marc Nazare M. . bmse011017 1 11 Edgar Specker E. . bmse011017 1 12 Vladimir Ivanov V. . bmse011017 1 13 Hartmut Oschkinat H. . bmse011017 1 14 Lucia Banci L. . bmse011017 1 15 Harald Schwalbe H. . bmse011017 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly_1 _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly_1 _Assembly.Entry_ID bmse011017 _Assembly.ID 1 _Assembly.Name N-(4-carbamoylphenyl)pyrazine-2-carboxamide _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 Z30242120 1 $entity_1 yes native no no bmse011017 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 Z30242120 C1 C bmse011017 1 2 1 1 1 1 Z30242120 C2 C bmse011017 1 3 1 1 1 1 Z30242120 C3 C bmse011017 1 4 1 1 1 1 Z30242120 C4 C bmse011017 1 5 1 1 1 1 Z30242120 C5 C bmse011017 1 6 1 1 1 1 Z30242120 C6 C bmse011017 1 7 1 1 1 1 Z30242120 C7 C bmse011017 1 8 1 1 1 1 Z30242120 C8 C bmse011017 1 9 1 1 1 1 Z30242120 C9 C bmse011017 1 10 1 1 1 1 Z30242120 C10 C bmse011017 1 11 1 1 1 1 Z30242120 C11 C bmse011017 1 12 1 1 1 1 Z30242120 C12 C bmse011017 1 13 1 1 1 1 Z30242120 N13 N bmse011017 1 14 1 1 1 1 Z30242120 N14 N bmse011017 1 15 1 1 1 1 Z30242120 N15 N bmse011017 1 16 1 1 1 1 Z30242120 N16 N bmse011017 1 17 1 1 1 1 Z30242120 O17 O bmse011017 1 18 1 1 1 1 Z30242120 O18 O bmse011017 1 19 1 1 1 1 Z30242120 H19 H bmse011017 1 20 1 1 1 1 Z30242120 H20 H bmse011017 1 21 1 1 1 1 Z30242120 H21 H bmse011017 1 22 1 1 1 1 Z30242120 H22 H bmse011017 1 23 1 1 1 1 Z30242120 H23 H bmse011017 1 24 1 1 1 1 Z30242120 H24 H bmse011017 1 25 1 1 1 1 Z30242120 H25 H bmse011017 1 26 1 1 1 1 Z30242120 H26 H bmse011017 1 27 1 1 1 1 Z30242120 H27 H bmse011017 1 28 1 1 1 1 Z30242120 H28 H bmse011017 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_entity_1 _Entity.Sf_category entity _Entity.Sf_framecode entity_1 _Entity.Entry_ID bmse011017 _Entity.ID 1 _Entity.Name N-(4-carbamoylphenyl)pyrazine-2-carboxamide _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID Z30242120 _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 242.2333999999999 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 Z30242120 $chem_comp_1 bmse011017 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 bmse011017 _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 bmse011017 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 bmse011017 _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' bmse011017 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 bmse011017 _Chem_comp.ID Z30242120 _Chem_comp.Provenance iNEXT _Chem_comp.Name N-(4-carbamoylphenyl)pyrazine-2-carboxamide _Chem_comp.Type non-polymer _Chem_comp.Number_atoms_all 28 _Chem_comp.Number_atoms_nh 18 _Chem_comp.InChI_code InChI=1S/C12H10N4O2/c13-11(17)8-1-3-9(4-2-8)16-12(18)10-7-14-5-6-15-10/h1-7H,(H2,13,17)(H,16,18) _Chem_comp.Synonyms P1_A03 _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic no _Chem_comp.Formula C12H10N4O2 _Chem_comp.Formula_weight 242.2333999999999 _Chem_comp.Formula_mono_iso_wt_nat 242.08037558 _Chem_comp.Formula_mono_iso_wt_13C 254.12063363600006 _Chem_comp.Formula_mono_iso_wt_15N 246.06851515200003 _Chem_comp.Formula_mono_iso_wt_13C_15N 258.1087732080002 _Chem_comp.Image_file_name bmse011017.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse011017.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(N)C1=CC=C(C=C1)NC(=O)C2=NC=CN=C2 SMILES Bruker_TopSpin_FBS na bmse011017 Z30242120 NC(=O)c1ccc(NC(=O)c2cnccn2)cc1 SMILES_CANONICAL RDKit 2017.09.3 bmse011017 Z30242120 NC(=O)c1ccc(NC(=O)c2cnccn2)cc1 SMILES_ISOMERIC RDKit 2017.09.3 bmse011017 Z30242120 NC(=O)c1ccc(NC(=O)c2cnccn2)cc1 SMILES RDKit 2017.09.3 bmse011017 Z30242120 O=C(c1nccnc1)Nc1ccc(cc1)C(=O)N SMILES_CANONICAL OpenBabel 2.3.2 bmse011017 Z30242120 O=C(c1nccnc1)Nc1ccc(cc1)C(=O)N SMILES OpenBabel 2.3.2 bmse011017 Z30242120 InChI=1S/C12H10N4O2/c13-11(17)8-1-3-9(4-2-8)16-12(18)10-7-14-5-6-15-10/h1-7H,(H2,13,17)(H,16,18) InChI OpenBabel 2.3.2 bmse011017 Z30242120 PXSAWLVHALLJDY-UHFFFAOYSA-N InChI_KEY OpenBabel 2.3.2 bmse011017 Z30242120 InChI=1S/C12H10N4O2/c13-11(17)8-1-3-9(4-2-8)16-12(18)10-7-14-5-6-15-10/h1-7H,(H2,13,17)(H,16,18) InChI ALATIS na bmse011017 Z30242120 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 N-(4-carbamoylphenyl)pyrazine-2-carboxamide 'IUPAC NAME' http://cactus.nci.nih.gov/chemical/structure na bmse011017 Z30242120 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 bmse011017 Z30242120 C2 C N 0 yes 2 bmse011017 Z30242120 C3 C N 0 yes 3 bmse011017 Z30242120 C4 C N 0 yes 4 bmse011017 Z30242120 C5 C N 0 yes 5 bmse011017 Z30242120 C6 C N 0 yes 6 bmse011017 Z30242120 C7 C N 0 yes 7 bmse011017 Z30242120 C8 C N 0 yes 8 bmse011017 Z30242120 C9 C N 0 yes 9 bmse011017 Z30242120 C10 C N 0 yes 10 bmse011017 Z30242120 C11 C N 0 no 11 bmse011017 Z30242120 C12 C N 0 no 12 bmse011017 Z30242120 N13 N N 0 no 13 bmse011017 Z30242120 N14 N N 0 yes 14 bmse011017 Z30242120 N15 N N 0 yes 15 bmse011017 Z30242120 N16 N N 0 no 16 bmse011017 Z30242120 O17 O N 0 no 17 bmse011017 Z30242120 O18 O N 0 no 18 bmse011017 Z30242120 H19 H N 0 no 19 bmse011017 Z30242120 H20 H N 0 no 20 bmse011017 Z30242120 H21 H N 0 no 21 bmse011017 Z30242120 H22 H N 0 no 22 bmse011017 Z30242120 H23 H N 0 no 23 bmse011017 Z30242120 H24 H N 0 no 24 bmse011017 Z30242120 H25 H N 0 no 25 bmse011017 Z30242120 H26 H N 0 no 26 bmse011017 Z30242120 H27 H N 0 no 27 bmse011017 Z30242120 H28 H N 0 no 28 bmse011017 Z30242120 stop_ loop_ _Atom_nomenclature.Naming_system _Atom_nomenclature.Atom_name _Atom_nomenclature.Atom_ID _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID author C11 C1 bmse011017 Z30242120 author C12 C2 bmse011017 Z30242120 author C16 C3 bmse011017 Z30242120 author C15 C4 bmse011017 Z30242120 author C18 C5 bmse011017 Z30242120 author C17 C6 bmse011017 Z30242120 author C14 C7 bmse011017 Z30242120 author C6 C8 bmse011017 Z30242120 author C10 C9 bmse011017 Z30242120 author C2 C10 bmse011017 Z30242120 author C4 C11 bmse011017 Z30242120 author C1 C12 bmse011017 Z30242120 author N13 N13 bmse011017 Z30242120 author N9 N14 bmse011017 Z30242120 author N5 N15 bmse011017 Z30242120 author N3 N16 bmse011017 Z30242120 author O8 O17 bmse011017 Z30242120 author O7 O18 bmse011017 Z30242120 author H20 H19 bmse011017 Z30242120 author H21 H20 bmse011017 Z30242120 author H26 H21 bmse011017 Z30242120 author H25 H22 bmse011017 Z30242120 author H28 H23 bmse011017 Z30242120 author H27 H24 bmse011017 Z30242120 author H24 H25 bmse011017 Z30242120 author H22 H26 bmse011017 Z30242120 author H23 H27 bmse011017 Z30242120 author H19 H28 bmse011017 Z30242120 ALATIS C1 C1 bmse011017 Z30242120 ALATIS C2 C2 bmse011017 Z30242120 ALATIS C3 C3 bmse011017 Z30242120 ALATIS C4 C4 bmse011017 Z30242120 ALATIS C5 C5 bmse011017 Z30242120 ALATIS C6 C6 bmse011017 Z30242120 ALATIS C7 C7 bmse011017 Z30242120 ALATIS C8 C8 bmse011017 Z30242120 ALATIS C9 C9 bmse011017 Z30242120 ALATIS C10 C10 bmse011017 Z30242120 ALATIS C11 C11 bmse011017 Z30242120 ALATIS C12 C12 bmse011017 Z30242120 ALATIS N13 N13 bmse011017 Z30242120 ALATIS N14 N14 bmse011017 Z30242120 ALATIS N15 N15 bmse011017 Z30242120 ALATIS N16 N16 bmse011017 Z30242120 ALATIS O17 O17 bmse011017 Z30242120 ALATIS O18 O18 bmse011017 Z30242120 ALATIS H19 H19 bmse011017 Z30242120 ALATIS H20 H20 bmse011017 Z30242120 ALATIS H21 H21 bmse011017 Z30242120 ALATIS H22 H22 bmse011017 Z30242120 ALATIS H23 H23 bmse011017 Z30242120 ALATIS H24 H24 bmse011017 Z30242120 ALATIS H25 H25 bmse011017 Z30242120 ALATIS H26 H26 bmse011017 Z30242120 ALATIS H27 H27 bmse011017 Z30242120 ALATIS H28 H28 bmse011017 Z30242120 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 bmse011017 Z30242120 2 covalent AROM C1 C8 yes N 2 bmse011017 Z30242120 3 covalent AROM C2 C4 yes N 3 bmse011017 Z30242120 4 covalent AROM C3 C9 yes N 4 bmse011017 Z30242120 5 covalent AROM C4 C9 yes N 5 bmse011017 Z30242120 6 covalent AROM C5 C6 yes N 6 bmse011017 Z30242120 7 covalent AROM C5 N14 yes N 7 bmse011017 Z30242120 8 covalent AROM C6 N15 yes N 8 bmse011017 Z30242120 9 covalent AROM C7 C10 yes N 9 bmse011017 Z30242120 10 covalent AROM C8 C2 yes N 10 bmse011017 Z30242120 11 covalent AROM N14 C7 yes N 11 bmse011017 Z30242120 12 covalent AROM N15 C10 yes N 12 bmse011017 Z30242120 13 carbonyl DOUB O17 C11 no N 13 bmse011017 Z30242120 14 carbonyl DOUB O18 C12 no N 14 bmse011017 Z30242120 15 covalent SING C1 H19 no N 15 bmse011017 Z30242120 16 covalent SING C2 H20 no N 16 bmse011017 Z30242120 17 covalent SING C3 H21 no N 17 bmse011017 Z30242120 18 covalent SING C4 H22 no N 18 bmse011017 Z30242120 19 covalent SING C5 H23 no N 19 bmse011017 Z30242120 20 covalent SING C6 H24 no N 20 bmse011017 Z30242120 21 covalent SING C7 H25 no N 21 bmse011017 Z30242120 22 covalent SING C9 N16 no N 22 bmse011017 Z30242120 23 covalent SING C10 C12 no N 23 bmse011017 Z30242120 24 covalent SING C11 C8 no N 24 bmse011017 Z30242120 25 amide SING N13 C11 no N 25 bmse011017 Z30242120 26 covalent SING N13 H26 no N 26 bmse011017 Z30242120 27 covalent SING N13 H27 no N 27 bmse011017 Z30242120 28 amide SING N16 C12 no N 28 bmse011017 Z30242120 29 covalent SING N16 H28 no N 29 bmse011017 Z30242120 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse011017 _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 Z30242120 'natural abundance' 1 $assembly_1 1 $entity_1 solute 1 mM bmse011017 1 2 'Potassium phosphate' 'natural abundance' . . . . buffer 25 mM bmse011017 1 3 'Potassium chloride' 'natural abundance' . . . . salt 50 mM bmse011017 1 4 'Magnesium chloride' 'natural abundance' . . . . salt 5 mM bmse011017 1 5 D2O 'natural abundance' . . . . solvent 9 % bmse011017 1 6 H2O 'natural abundance' . . . . solvent 90 % bmse011017 1 7 DMSO '[2H U-100%]' . . . . solvent 1 % bmse011017 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 bmse011017 _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 bmse011017 1 pressure 1 . atm bmse011017 1 temperature 298 0.1 K bmse011017 1 stop_ save_ ############################ # Computer software used # ############################ save_software_topspin _Software.Sf_category software _Software.Sf_framecode software_topspin _Software.Entry_ID bmse011017 _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/ bmse011017 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'data analysis' bmse011017 1 'peak picking' bmse011017 1 processing bmse011017 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 bmse011017 _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 bmse011017 _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 bmse011017 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/ bmse011017 1 1 cmcproject.xml text/xml 'spectrum analysis' nmr/set01/1/pdata/1/ bmse011017 1 1 multiplet.txt text 'Peak list' nmr/set01/1/pdata/1/ bmse011017 1 1 spectrum_overview.pdf pdf 'Spectrum image' nmr/set01/1/pdata/1/ bmse011017 1 1 spectrum_overview.png image/png 'Spectral image' nmr/set01/1/pdata/1/ bmse011017 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 bmse011017 _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 bmse011017 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 bmse011017 _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 bmse011017 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 bmse011017 1 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse011017 1 2 bmse011017 1 3 bmse011017 1 4 bmse011017 1 5 bmse011017 1 6 bmse011017 1 7 bmse011017 1 8 bmse011017 1 9 bmse011017 1 10 bmse011017 1 11 bmse011017 1 12 bmse011017 1 13 bmse011017 1 14 bmse011017 1 15 bmse011017 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 2.6031 DMSO bmse011017 1 2 1 3.5679 q_2H bmse011017 1 3 1 1.0906 m_3H bmse011017 1 4 1 3.5123 s_3H bmse011017 1 5 1 7.7640 m_4H bmse011017 1 6 1 1.2510 m_15H bmse011017 1 7 1 7.8406 m_4H bmse011017 1 8 1 3.1098 t_2H bmse011017 1 9 1 8.6009 m_1H bmse011017 1 10 1 8.7571 m_3H_Q1 bmse011017 1 11 1 3.2694 s_2H bmse011017 1 12 1 6.5718 s_1H bmse011017 1 13 1 7.5921 m_2H bmse011017 1 14 1 9.2300 s_1H bmse011017 1 15 1 3.6294 m_2H bmse011017 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 bmse011017 1 2 2 1 7.0058 bmse011017 1 3 3 1 4.0715 bmse011017 1 4 4 1 0.0000 bmse011017 1 5 5 1 8.4730 bmse011017 1 6 6 1 5.7771 bmse011017 1 7 7 1 8.5831 bmse011017 1 8 8 1 7.4277 bmse011017 1 9 9 1 8.5831 bmse011017 1 10 10 1 12.1043 bmse011017 1 11 11 1 0.0000 bmse011017 1 12 12 1 0.0000 bmse011017 1 13 13 1 3.0811 bmse011017 1 14 14 1 0.0000 bmse011017 1 15 15 1 4.4383 bmse011017 1 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse011017 1 2 bmse011017 1 3 bmse011017 1 4 bmse011017 1 5 bmse011017 1 6 bmse011017 1 7 bmse011017 1 8 bmse011017 1 9 bmse011017 1 10 bmse011017 1 11 bmse011017 1 12 bmse011017 1 13 bmse011017 1 14 bmse011017 1 15 bmse011017 1 16 bmse011017 1 17 bmse011017 1 18 bmse011017 1 19 bmse011017 1 20 bmse011017 1 21 bmse011017 1 22 bmse011017 1 23 bmse011017 1 24 bmse011017 1 25 bmse011017 1 26 bmse011017 1 27 bmse011017 1 28 bmse011017 1 29 bmse011017 1 30 bmse011017 1 31 bmse011017 1 32 bmse011017 1 33 bmse011017 1 34 bmse011017 1 35 bmse011017 1 36 bmse011017 1 37 bmse011017 1 38 bmse011017 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 2.6031 bmse011017 1 2 1 3.5504 bmse011017 1 3 1 3.5618 bmse011017 1 4 1 3.5737 bmse011017 1 5 1 3.5855 bmse011017 1 6 1 1.1042 bmse011017 1 7 1 1.0925 bmse011017 1 8 1 1.0877 bmse011017 1 9 1 1.0806 bmse011017 1 10 1 1.0771 bmse011017 1 11 1 3.5123 bmse011017 1 12 1 7.7570 bmse011017 1 13 1 7.7711 bmse011017 1 14 1 1.2606 bmse011017 1 15 1 1.2494 bmse011017 1 16 1 1.2414 bmse011017 1 17 1 7.8477 bmse011017 1 18 1 7.8334 bmse011017 1 19 1 3.0974 bmse011017 1 20 1 3.1098 bmse011017 1 21 1 3.1221 bmse011017 1 22 1 8.5938 bmse011017 1 23 1 8.6081 bmse011017 1 24 1 8.7773 bmse011017 1 25 1 8.7733 bmse011017 1 26 1 8.7370 bmse011017 1 27 1 3.2694 bmse011017 1 28 1 6.5718 bmse011017 1 29 1 7.6024 bmse011017 1 30 1 7.5996 bmse011017 1 31 1 7.5930 bmse011017 1 32 1 7.5897 bmse011017 1 33 1 7.5819 bmse011017 1 34 1 9.2300 bmse011017 1 35 1 3.6405 bmse011017 1 36 1 3.6291 bmse011017 1 37 1 3.6230 bmse011017 1 38 1 3.6183 bmse011017 1 stop_ save_