data_bmse011015 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse011015 _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/bmse011015 loop_ _Entry_experimental_methods.ID _Entry_experimental_methods.Method _Entry_experimental_methods.Subtype _Entry_experimental_methods.Entry_ID 1 NMR solution bmse011015 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. . bmse011015 2 Christian Richter C. . bmse011015 3 Till Kuehn T. . bmse011015 4 Kamal Azzaoui K. . bmse011015 5 Marcel Blommers M. J.J. bmse011015 6 Rebecca 'Del Conte' R. . bmse011015 7 Marco Fragai M. . bmse011015 8 Nils Trieloff N. . bmse011015 9 Peter Schmieder P. . bmse011015 10 Marc Nazare M. . bmse011015 11 Edgar Specker E. . bmse011015 12 Vladimir Ivanov V. . bmse011015 13 Hartmut Oschkinat H. . bmse011015 14 Lucia Banci L. . bmse011015 15 Harald Schwalbe H. . bmse011015 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Entry_ID 1 iNEXT 'Infrastructure for NMR' bmse011015 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID spectral_peak_list 1 bmse011015 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 7 bmse011015 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 . bmse011015 stop_ loop_ _Auxiliary_files.ID _Auxiliary_files.Name _Auxiliary_files.Format _Auxiliary_files.URI _Auxiliary_files.Details _Auxiliary_files.Entry_ID 3 bmse011015.sdf sdf na 'Structure Definition File' bmse011015 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID bmse011015 _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. . bmse011015 1 2 Christian Richter C. . bmse011015 1 3 Till Kuehn T. . bmse011015 1 4 Kamal Azzaoui K. . bmse011015 1 5 Marcel Blommers M. J.J. bmse011015 1 6 Rebecca 'Del Conte' R. . bmse011015 1 7 Marco Fragai M. . bmse011015 1 8 Nils Trieloff N. . bmse011015 1 9 Peter Schmieder P. . bmse011015 1 10 Marc Nazare M. . bmse011015 1 11 Edgar Specker E. . bmse011015 1 12 Vladimir Ivanov V. . bmse011015 1 13 Hartmut Oschkinat H. . bmse011015 1 14 Lucia Banci L. . bmse011015 1 15 Harald Schwalbe H. . bmse011015 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly_1 _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly_1 _Assembly.Entry_ID bmse011015 _Assembly.ID 1 _Assembly.Name N-(2-fluorophenyl)-3-methoxybenzamide _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 Z28290384 1 $entity_1 yes native no no bmse011015 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 Z28290384 C1 C bmse011015 1 2 1 1 1 1 Z28290384 C2 C bmse011015 1 3 1 1 1 1 Z28290384 C3 C bmse011015 1 4 1 1 1 1 Z28290384 C4 C bmse011015 1 5 1 1 1 1 Z28290384 C5 C bmse011015 1 6 1 1 1 1 Z28290384 C6 C bmse011015 1 7 1 1 1 1 Z28290384 C7 C bmse011015 1 8 1 1 1 1 Z28290384 C8 C bmse011015 1 9 1 1 1 1 Z28290384 C9 C bmse011015 1 10 1 1 1 1 Z28290384 C10 C bmse011015 1 11 1 1 1 1 Z28290384 C11 C bmse011015 1 12 1 1 1 1 Z28290384 C12 C bmse011015 1 13 1 1 1 1 Z28290384 C13 C bmse011015 1 14 1 1 1 1 Z28290384 C14 C bmse011015 1 15 1 1 1 1 Z28290384 F15 F bmse011015 1 16 1 1 1 1 Z28290384 N16 N bmse011015 1 17 1 1 1 1 Z28290384 O17 O bmse011015 1 18 1 1 1 1 Z28290384 O18 O bmse011015 1 19 1 1 1 1 Z28290384 H19 H bmse011015 1 20 1 1 1 1 Z28290384 H20 H bmse011015 1 21 1 1 1 1 Z28290384 H21 H bmse011015 1 22 1 1 1 1 Z28290384 H22 H bmse011015 1 23 1 1 1 1 Z28290384 H23 H bmse011015 1 24 1 1 1 1 Z28290384 H24 H bmse011015 1 25 1 1 1 1 Z28290384 H25 H bmse011015 1 26 1 1 1 1 Z28290384 H26 H bmse011015 1 27 1 1 1 1 Z28290384 H27 H bmse011015 1 28 1 1 1 1 Z28290384 H28 H bmse011015 1 29 1 1 1 1 Z28290384 H29 H bmse011015 1 30 1 1 1 1 Z28290384 H30 H bmse011015 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_entity_1 _Entity.Sf_category entity _Entity.Sf_framecode entity_1 _Entity.Entry_ID bmse011015 _Entity.ID 1 _Entity.Name N-(2-fluorophenyl)-3-methoxybenzamide _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID Z28290384 _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 245.24898319999986 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 Z28290384 $chem_comp_1 bmse011015 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 bmse011015 _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 bmse011015 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 bmse011015 _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' bmse011015 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 bmse011015 _Chem_comp.ID Z28290384 _Chem_comp.Provenance iNEXT _Chem_comp.Name N-(2-fluorophenyl)-3-methoxybenzamide _Chem_comp.Type non-polymer _Chem_comp.Number_atoms_all 30 _Chem_comp.Number_atoms_nh 18 _Chem_comp.InChI_code InChI=1S/C14H12FNO2/c1-18-11-6-4-5-10(9-11)14(17)16-13-8-3-2-7-12(13)15/h2-9H,1H3,(H,16,17) _Chem_comp.Synonyms P1_G02 _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic no _Chem_comp.Formula C14H12FNO2 _Chem_comp.Formula_weight 245.24898319999986 _Chem_comp.Formula_mono_iso_wt_nat 245.085206849 _Chem_comp.Formula_mono_iso_wt_13C 259.1321745810002 _Chem_comp.Formula_mono_iso_wt_15N 246.082241742 _Chem_comp.Formula_mono_iso_wt_13C_15N 260.1292094740002 _Chem_comp.Image_file_name bmse011015.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse011015.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(NC=1C=CC=CC1F)C=2C=CC=C(OC)C2 SMILES Bruker_TopSpin_FBS na bmse011015 Z28290384 COc1cccc(C(=O)Nc2ccccc2F)c1 SMILES_CANONICAL RDKit 2017.09.3 bmse011015 Z28290384 COc1cccc(C(=O)Nc2ccccc2F)c1 SMILES_ISOMERIC RDKit 2017.09.3 bmse011015 Z28290384 COc1cccc(C(=O)Nc2ccccc2F)c1 SMILES RDKit 2017.09.3 bmse011015 Z28290384 COc1cccc(c1)C(=O)Nc1ccccc1F SMILES_CANONICAL OpenBabel 2.3.2 bmse011015 Z28290384 COc1cccc(c1)C(=O)Nc1ccccc1F SMILES OpenBabel 2.3.2 bmse011015 Z28290384 InChI=1S/C14H12FNO2/c1-18-11-6-4-5-10(9-11)14(17)16-13-8-3-2-7-12(13)15/h2-9H,1H3,(H,16,17) InChI OpenBabel 2.3.2 bmse011015 Z28290384 GIUMGIOTJZLCCG-UHFFFAOYSA-N InChI_KEY OpenBabel 2.3.2 bmse011015 Z28290384 InChI=1S/C14H12FNO2/c1-18-11-6-4-5-10(9-11)14(17)16-13-8-3-2-7-12(13)15/h2-9H,1H3,(H,16,17) InChI ALATIS na bmse011015 Z28290384 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 bmse011015 Z28290384 C2 C N 0 yes 2 bmse011015 Z28290384 C3 C N 0 yes 3 bmse011015 Z28290384 C4 C N 0 yes 4 bmse011015 Z28290384 C5 C N 0 yes 5 bmse011015 Z28290384 C6 C N 0 yes 6 bmse011015 Z28290384 C7 C N 0 yes 7 bmse011015 Z28290384 C8 C N 0 yes 8 bmse011015 Z28290384 C9 C N 0 yes 9 bmse011015 Z28290384 C10 C N 0 yes 10 bmse011015 Z28290384 C11 C N 0 yes 11 bmse011015 Z28290384 C12 C N 0 yes 12 bmse011015 Z28290384 C13 C N 0 yes 13 bmse011015 Z28290384 C14 C N 0 no 14 bmse011015 Z28290384 F15 F N 0 no 15 bmse011015 Z28290384 N16 N N 0 no 16 bmse011015 Z28290384 O17 O N 0 no 17 bmse011015 Z28290384 O18 O N 0 no 18 bmse011015 Z28290384 H19 H N 0 no 19 bmse011015 Z28290384 H20 H N 0 no 20 bmse011015 Z28290384 H21 H N 0 no 21 bmse011015 Z28290384 H22 H N 0 no 22 bmse011015 Z28290384 H23 H N 0 no 23 bmse011015 Z28290384 H24 H N 0 no 24 bmse011015 Z28290384 H25 H N 0 no 25 bmse011015 Z28290384 H26 H N 0 no 26 bmse011015 Z28290384 H27 H N 0 no 27 bmse011015 Z28290384 H28 H N 0 no 28 bmse011015 Z28290384 H29 H N 0 no 29 bmse011015 Z28290384 H30 H N 0 no 30 bmse011015 Z28290384 stop_ loop_ _Atom_nomenclature.Naming_system _Atom_nomenclature.Atom_name _Atom_nomenclature.Atom_ID _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID author C16 C1 bmse011015 Z28290384 author C18 C2 bmse011015 Z28290384 author C17 C3 bmse011015 Z28290384 author C12 C4 bmse011015 Z28290384 author C11 C5 bmse011015 Z28290384 author C15 C6 bmse011015 Z28290384 author C14 C7 bmse011015 Z28290384 author C13 C8 bmse011015 Z28290384 author C6 C9 bmse011015 Z28290384 author C3 C10 bmse011015 Z28290384 author C8 C11 bmse011015 Z28290384 author C7 C12 bmse011015 Z28290384 author C4 C13 bmse011015 Z28290384 author C1 C14 bmse011015 Z28290384 author F9 F15 bmse011015 Z28290384 author N2 N16 bmse011015 Z28290384 author O5 O17 bmse011015 Z28290384 author O10 O18 bmse011015 Z28290384 author H26 H19 bmse011015 Z28290384 author H27 H20 bmse011015 Z28290384 author H28 H21 bmse011015 Z28290384 author H30 H22 bmse011015 Z28290384 author H29 H23 bmse011015 Z28290384 author H22 H24 bmse011015 Z28290384 author H21 H25 bmse011015 Z28290384 author H25 H26 bmse011015 Z28290384 author H24 H27 bmse011015 Z28290384 author H23 H28 bmse011015 Z28290384 author H20 H29 bmse011015 Z28290384 author H19 H30 bmse011015 Z28290384 ALATIS C1 C1 bmse011015 Z28290384 ALATIS C2 C2 bmse011015 Z28290384 ALATIS C3 C3 bmse011015 Z28290384 ALATIS C4 C4 bmse011015 Z28290384 ALATIS C5 C5 bmse011015 Z28290384 ALATIS C6 C6 bmse011015 Z28290384 ALATIS C7 C7 bmse011015 Z28290384 ALATIS C8 C8 bmse011015 Z28290384 ALATIS C9 C9 bmse011015 Z28290384 ALATIS C10 C10 bmse011015 Z28290384 ALATIS C11 C11 bmse011015 Z28290384 ALATIS C12 C12 bmse011015 Z28290384 ALATIS C13 C13 bmse011015 Z28290384 ALATIS C14 C14 bmse011015 Z28290384 ALATIS F15 F15 bmse011015 Z28290384 ALATIS N16 N16 bmse011015 Z28290384 ALATIS O17 O17 bmse011015 Z28290384 ALATIS O18 O18 bmse011015 Z28290384 ALATIS H19 H19 bmse011015 Z28290384 ALATIS H20 H20 bmse011015 Z28290384 ALATIS H21 H21 bmse011015 Z28290384 ALATIS H22 H22 bmse011015 Z28290384 ALATIS H23 H23 bmse011015 Z28290384 ALATIS H24 H24 bmse011015 Z28290384 ALATIS H25 H25 bmse011015 Z28290384 ALATIS H26 H26 bmse011015 Z28290384 ALATIS H27 H27 bmse011015 Z28290384 ALATIS H28 H28 bmse011015 Z28290384 ALATIS H29 H29 bmse011015 Z28290384 ALATIS H30 H30 bmse011015 Z28290384 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 C2 C3 yes N 1 bmse011015 Z28290384 2 covalent AROM C2 C7 yes N 2 bmse011015 Z28290384 3 covalent AROM C3 C8 yes N 3 bmse011015 Z28290384 4 covalent AROM C4 C5 yes N 4 bmse011015 Z28290384 5 covalent AROM C4 C6 yes N 5 bmse011015 Z28290384 6 covalent AROM C5 C10 yes N 6 bmse011015 Z28290384 7 covalent AROM C6 C11 yes N 7 bmse011015 Z28290384 8 covalent AROM C7 C12 yes N 8 bmse011015 Z28290384 9 covalent AROM C8 C13 yes N 9 bmse011015 Z28290384 10 covalent AROM C9 C10 yes N 10 bmse011015 Z28290384 11 covalent AROM C11 C9 yes N 11 bmse011015 Z28290384 12 covalent AROM C12 C13 yes N 12 bmse011015 Z28290384 13 carbonyl DOUB O17 C14 no N 13 bmse011015 Z28290384 14 covalent SING C1 O18 no N 14 bmse011015 Z28290384 15 covalent SING C1 H19 no N 15 bmse011015 Z28290384 16 covalent SING C1 H20 no N 16 bmse011015 Z28290384 17 covalent SING C1 H21 no N 17 bmse011015 Z28290384 18 covalent SING C2 H22 no N 18 bmse011015 Z28290384 19 covalent SING C3 H23 no N 19 bmse011015 Z28290384 20 covalent SING C4 H24 no N 20 bmse011015 Z28290384 21 covalent SING C5 H25 no N 21 bmse011015 Z28290384 22 covalent SING C6 H26 no N 22 bmse011015 Z28290384 23 covalent SING C7 H27 no N 23 bmse011015 Z28290384 24 covalent SING C8 H28 no N 24 bmse011015 Z28290384 25 covalent SING C9 H29 no N 25 bmse011015 Z28290384 26 covalent SING C10 C14 no N 26 bmse011015 Z28290384 27 covalent SING C13 N16 no N 27 bmse011015 Z28290384 28 covalent SING F15 C12 no N 28 bmse011015 Z28290384 29 amide SING N16 C14 no N 29 bmse011015 Z28290384 30 covalent SING N16 H30 no N 30 bmse011015 Z28290384 31 covalent SING O18 C11 no N 31 bmse011015 Z28290384 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse011015 _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 Z28290384 'natural abundance' 1 $assembly_1 1 $entity_1 solute 1 mM bmse011015 1 2 'Potassium phosphate' 'natural abundance' . . . . buffer 25 mM bmse011015 1 3 'Potassium chloride' 'natural abundance' . . . . salt 50 mM bmse011015 1 4 'Magnesium chloride' 'natural abundance' . . . . salt 5 mM bmse011015 1 5 D2O 'natural abundance' . . . . solvent 9 % bmse011015 1 6 H2O 'natural abundance' . . . . solvent 90 % bmse011015 1 7 DMSO '[2H U-100%]' . . . . solvent 1 % bmse011015 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 bmse011015 _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 bmse011015 1 pressure 1 . atm bmse011015 1 temperature 298 0.1 K bmse011015 1 stop_ save_ ############################ # Computer software used # ############################ save_software_topspin _Software.Sf_category software _Software.Sf_framecode software_topspin _Software.Entry_ID bmse011015 _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/ bmse011015 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'data analysis' bmse011015 1 'peak picking' bmse011015 1 processing bmse011015 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 bmse011015 _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 bmse011015 _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 bmse011015 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/ bmse011015 1 1 cmcproject.xml text/xml 'spectrum analysis' nmr/set01/1/pdata/1/ bmse011015 1 1 multiplet.txt text 'Peak list' nmr/set01/1/pdata/1/ bmse011015 1 1 spectrum_overview.pdf pdf 'Spectrum image' nmr/set01/1/pdata/1/ bmse011015 1 1 spectrum_overview.png image/png 'Spectral image' nmr/set01/1/pdata/1/ bmse011015 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 bmse011015 _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 bmse011015 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 bmse011015 _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 bmse011015 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 bmse011015 1 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse011015 1 2 bmse011015 1 3 bmse011015 1 4 bmse011015 1 5 bmse011015 1 6 bmse011015 1 7 bmse011015 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 7.4044 11_s_Q3 bmse011015 1 2 1 4.6500 SUP bmse011015 1 3 1 7.4952 6,12,13_m bmse011015 1 4 1 3.8273 16_s bmse011015 1 5 1 7.3116 14_m_Q2 bmse011015 1 6 1 2.6028 DMSO bmse011015 1 7 1 7.2070 15,17,18_Q1 bmse011015 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 bmse011015 1 2 2 1 0.0000 bmse011015 1 3 3 1 82.4790 bmse011015 1 4 4 1 0.0000 bmse011015 1 5 5 1 4.1375 bmse011015 1 6 6 1 1.9532 bmse011015 1 7 7 1 73.4333 bmse011015 1 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse011015 1 2 bmse011015 1 3 bmse011015 1 4 bmse011015 1 5 bmse011015 1 6 bmse011015 1 7 bmse011015 1 8 bmse011015 1 9 bmse011015 1 10 bmse011015 1 11 bmse011015 1 12 bmse011015 1 13 bmse011015 1 14 bmse011015 1 15 bmse011015 1 16 bmse011015 1 17 bmse011015 1 18 bmse011015 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 7.4044 bmse011015 1 2 1 4.6500 bmse011015 1 3 1 7.5639 bmse011015 1 4 1 7.4265 bmse011015 1 5 1 3.8273 bmse011015 1 6 1 7.3288 bmse011015 1 7 1 7.3167 bmse011015 1 8 1 7.3098 bmse011015 1 9 1 7.3057 bmse011015 1 10 1 7.2969 bmse011015 1 11 1 7.2944 bmse011015 1 12 1 2.5963 bmse011015 1 13 1 2.5998 bmse011015 1 14 1 2.6029 bmse011015 1 15 1 2.6058 bmse011015 1 16 1 2.6093 bmse011015 1 17 1 7.2682 bmse011015 1 18 1 7.1459 bmse011015 1 stop_ save_