data_bmse011200 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse011200 _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/bmse011200 loop_ _Entry_experimental_methods.ID _Entry_experimental_methods.Method _Entry_experimental_methods.Subtype _Entry_experimental_methods.Entry_ID 1 NMR solution bmse011200 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. . bmse011200 2 Christian Richter C. . bmse011200 3 Till Kuehn T. . bmse011200 4 Kamal Azzaoui K. . bmse011200 5 Marcel Blommers M. J.J. bmse011200 6 Rebecca 'Del Conte' R. . bmse011200 7 Marco Fragai M. . bmse011200 8 Nils Trieloff N. . bmse011200 9 Peter Schmieder P. . bmse011200 10 Marc Nazare M. . bmse011200 11 Edgar Specker E. . bmse011200 12 Vladimir Ivanov V. . bmse011200 13 Hartmut Oschkinat H. . bmse011200 14 Lucia Banci L. . bmse011200 15 Harald Schwalbe H. . bmse011200 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Entry_ID 1 iNEXT 'Infrastructure for NMR' bmse011200 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID spectral_peak_list 1 bmse011200 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 11 bmse011200 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 . bmse011200 stop_ loop_ _Auxiliary_files.ID _Auxiliary_files.Name _Auxiliary_files.Format _Auxiliary_files.URI _Auxiliary_files.Details _Auxiliary_files.Entry_ID 3 bmse011200.sdf sdf na 'Structure Definition File' bmse011200 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID bmse011200 _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. . bmse011200 1 2 Christian Richter C. . bmse011200 1 3 Till Kuehn T. . bmse011200 1 4 Kamal Azzaoui K. . bmse011200 1 5 Marcel Blommers M. J.J. bmse011200 1 6 Rebecca 'Del Conte' R. . bmse011200 1 7 Marco Fragai M. . bmse011200 1 8 Nils Trieloff N. . bmse011200 1 9 Peter Schmieder P. . bmse011200 1 10 Marc Nazare M. . bmse011200 1 11 Edgar Specker E. . bmse011200 1 12 Vladimir Ivanov V. . bmse011200 1 13 Hartmut Oschkinat H. . bmse011200 1 14 Lucia Banci L. . bmse011200 1 15 Harald Schwalbe H. . bmse011200 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly_1 _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly_1 _Assembly.Entry_ID bmse011200 _Assembly.ID 1 _Assembly.Name '3-piperidin-1-ylpropanoic acid;hydrochloride' _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 Z53115945 1 $entity_1 yes native no no bmse011200 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 Z53115945 C1 C bmse011200 1 2 1 1 1 1 Z53115945 C2 C bmse011200 1 3 1 1 1 1 Z53115945 C3 C bmse011200 1 4 1 1 1 1 Z53115945 C4 C bmse011200 1 5 1 1 1 1 Z53115945 C5 C bmse011200 1 6 1 1 1 1 Z53115945 C6 C bmse011200 1 7 1 1 1 1 Z53115945 C7 C bmse011200 1 8 1 1 1 1 Z53115945 C8 C bmse011200 1 9 1 1 1 1 Z53115945 N9 N bmse011200 1 10 1 1 1 1 Z53115945 O10 O bmse011200 1 11 1 1 1 1 Z53115945 O11 O bmse011200 1 12 1 1 1 1 Z53115945 H12 H bmse011200 1 13 1 1 1 1 Z53115945 H13 H bmse011200 1 14 1 1 1 1 Z53115945 H14 H bmse011200 1 15 1 1 1 1 Z53115945 H15 H bmse011200 1 16 1 1 1 1 Z53115945 H16 H bmse011200 1 17 1 1 1 1 Z53115945 H17 H bmse011200 1 18 1 1 1 1 Z53115945 H18 H bmse011200 1 19 1 1 1 1 Z53115945 H19 H bmse011200 1 20 1 1 1 1 Z53115945 H20 H bmse011200 1 21 1 1 1 1 Z53115945 H21 H bmse011200 1 22 1 1 1 1 Z53115945 H22 H bmse011200 1 23 1 1 1 1 Z53115945 H23 H bmse011200 1 24 1 1 1 1 Z53115945 H24 H bmse011200 1 25 1 1 1 1 Z53115945 H25 H bmse011200 1 26 1 1 1 1 Z53115945 H26 H bmse011200 1 27 1 1 1 1 Z53115945 Cl27 Cl bmse011200 1 28 1 1 1 1 Z53115945 H28 H bmse011200 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_entity_1 _Entity.Sf_category entity _Entity.Sf_framecode entity_1 _Entity.Entry_ID bmse011200 _Entity.ID 1 _Entity.Name '3-piperidin-1-ylpropanoic acid;hydrochloride' _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID Z53115945 _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 193.67113999999984 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 Z53115945 $chem_comp_1 bmse011200 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 bmse011200 _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 bmse011200 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 bmse011200 _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' bmse011200 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 bmse011200 _Chem_comp.ID Z53115945 _Chem_comp.Provenance iNEXT _Chem_comp.Name '3-piperidin-1-ylpropanoic acid;hydrochloride' _Chem_comp.Type non-polymer _Chem_comp.Number_atoms_all 28 _Chem_comp.Number_atoms_nh 12 _Chem_comp.InChI_code InChI=1S/C8H15NO2.ClH/c10-8(11)4-7-9-5-2-1-3-6-9;/h1-7H2,(H,10,11);1H _Chem_comp.Synonyms P3_H01 _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic no _Chem_comp.Formula C8H16ClNO2 _Chem_comp.Formula_weight 193.67113999999984 _Chem_comp.Formula_mono_iso_wt_nat 193.086956437 _Chem_comp.Formula_mono_iso_wt_13C 201.11379514100003 _Chem_comp.Formula_mono_iso_wt_15N 194.08399133 _Chem_comp.Formula_mono_iso_wt_13C_15N 202.11083003400003 _Chem_comp.Image_file_name bmse011200.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse011200.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 Cl.O=C(O)CCN1CCCCC1 SMILES Bruker_TopSpin_FBS na bmse011200 Z53115945 Cl.O=C(O)CCN1CCCCC1 SMILES_CANONICAL RDKit 2017.09.3 bmse011200 Z53115945 Cl.O=C(O)CCN1CCCCC1 SMILES_ISOMERIC RDKit 2017.09.3 bmse011200 Z53115945 Cl.O=C(O)CCN1CCCCC1 SMILES RDKit 2017.09.3 bmse011200 Z53115945 OC(=O)CCN1CCCCC1.Cl SMILES_CANONICAL OpenBabel 2.3.2 bmse011200 Z53115945 OC(=O)CCN1CCCCC1.Cl SMILES OpenBabel 2.3.2 bmse011200 Z53115945 InChI=1S/C8H15NO2.ClH/c10-8(11)4-7-9-5-2-1-3-6-9;/h1-7H2,(H,10,11);1H InChI OpenBabel 2.3.2 bmse011200 Z53115945 ZBTNZXCCWPOONU-UHFFFAOYSA-N InChI_KEY OpenBabel 2.3.2 bmse011200 Z53115945 InChI=1S/C8H15NO2.ClH/c10-8(11)4-7-9-5-2-1-3-6-9;/h1-7H2,(H,10,11);1H InChI ALATIS na bmse011200 Z53115945 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 bmse011200 Z53115945 C2 C N 0 no 2 bmse011200 Z53115945 C3 C N 0 no 3 bmse011200 Z53115945 C4 C N 0 no 4 bmse011200 Z53115945 C5 C N 0 no 5 bmse011200 Z53115945 C6 C N 0 no 6 bmse011200 Z53115945 C7 C N 0 no 7 bmse011200 Z53115945 C8 C N 0 no 8 bmse011200 Z53115945 N9 N N 0 no 9 bmse011200 Z53115945 O10 O N 0 no 10 bmse011200 Z53115945 O11 O N 0 no 11 bmse011200 Z53115945 H12 H N 0 no 12 bmse011200 Z53115945 H13 H N 0 no 13 bmse011200 Z53115945 H14 H N 0 no 14 bmse011200 Z53115945 H15 H N 0 no 15 bmse011200 Z53115945 H16 H N 0 no 16 bmse011200 Z53115945 H17 H N 0 no 17 bmse011200 Z53115945 H18 H N 0 no 18 bmse011200 Z53115945 H19 H N 0 no 19 bmse011200 Z53115945 H20 H N 0 no 20 bmse011200 Z53115945 H21 H N 0 no 21 bmse011200 Z53115945 H22 H N 0 no 22 bmse011200 Z53115945 H23 H N 0 no 23 bmse011200 Z53115945 H24 H N 0 no 24 bmse011200 Z53115945 H25 H N 0 no 25 bmse011200 Z53115945 H26 H N 0 no 26 bmse011200 Z53115945 Cl27 Cl N 0 no 27 bmse011200 Z53115945 H28 H N 0 no 28 bmse011200 Z53115945 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 bmse011200 Z53115945 author C10 C2 bmse011200 Z53115945 author C11 C3 bmse011200 Z53115945 author C3 C4 bmse011200 Z53115945 author C9 C5 bmse011200 Z53115945 author C8 C6 bmse011200 Z53115945 author C5 C7 bmse011200 Z53115945 author C1 C8 bmse011200 Z53115945 author N2 N9 bmse011200 Z53115945 author O4 O10 bmse011200 Z53115945 author O6 O11 bmse011200 Z53115945 author H27 H12 bmse011200 Z53115945 author H28 H13 bmse011200 Z53115945 author H23 H14 bmse011200 Z53115945 author H24 H15 bmse011200 Z53115945 author H25 H16 bmse011200 Z53115945 author H26 H17 bmse011200 Z53115945 author H13 H18 bmse011200 Z53115945 author H14 H19 bmse011200 Z53115945 author H21 H20 bmse011200 Z53115945 author H22 H21 bmse011200 Z53115945 author H19 H22 bmse011200 Z53115945 author H20 H23 bmse011200 Z53115945 author H15 H24 bmse011200 Z53115945 author H16 H25 bmse011200 Z53115945 author H17 H26 bmse011200 Z53115945 author Cl7 Cl27 bmse011200 Z53115945 author H18 H28 bmse011200 Z53115945 ALATIS C1 C1 bmse011200 Z53115945 ALATIS C2 C2 bmse011200 Z53115945 ALATIS C3 C3 bmse011200 Z53115945 ALATIS C4 C4 bmse011200 Z53115945 ALATIS C5 C5 bmse011200 Z53115945 ALATIS C6 C6 bmse011200 Z53115945 ALATIS C7 C7 bmse011200 Z53115945 ALATIS C8 C8 bmse011200 Z53115945 ALATIS N9 N9 bmse011200 Z53115945 ALATIS O10 O10 bmse011200 Z53115945 ALATIS O11 O11 bmse011200 Z53115945 ALATIS H12 H12 bmse011200 Z53115945 ALATIS H13 H13 bmse011200 Z53115945 ALATIS H14 H14 bmse011200 Z53115945 ALATIS H15 H15 bmse011200 Z53115945 ALATIS H16 H16 bmse011200 Z53115945 ALATIS H17 H17 bmse011200 Z53115945 ALATIS H18 H18 bmse011200 Z53115945 ALATIS H19 H19 bmse011200 Z53115945 ALATIS H20 H20 bmse011200 Z53115945 ALATIS H21 H21 bmse011200 Z53115945 ALATIS H22 H22 bmse011200 Z53115945 ALATIS H23 H23 bmse011200 Z53115945 ALATIS H24 H24 bmse011200 Z53115945 ALATIS H25 H25 bmse011200 Z53115945 ALATIS H26 H26 bmse011200 Z53115945 ALATIS Cl27 Cl27 bmse011200 Z53115945 ALATIS H28 H28 bmse011200 Z53115945 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 carbonyl DOUB O10 C8 no N 1 bmse011200 Z53115945 2 covalent SING C1 C2 no N 2 bmse011200 Z53115945 3 covalent SING C1 C3 no N 3 bmse011200 Z53115945 4 covalent SING C1 H12 no N 4 bmse011200 Z53115945 5 covalent SING C1 H13 no N 5 bmse011200 Z53115945 6 covalent SING C2 C5 no N 6 bmse011200 Z53115945 7 covalent SING C2 H14 no N 7 bmse011200 Z53115945 8 covalent SING C2 H15 no N 8 bmse011200 Z53115945 9 covalent SING C3 C6 no N 9 bmse011200 Z53115945 10 covalent SING C3 H16 no N 10 bmse011200 Z53115945 11 covalent SING C3 H17 no N 11 bmse011200 Z53115945 12 covalent SING C4 C8 no N 12 bmse011200 Z53115945 13 covalent SING C4 H18 no N 13 bmse011200 Z53115945 14 covalent SING C4 H19 no N 14 bmse011200 Z53115945 15 covalent SING C5 N9 no N 15 bmse011200 Z53115945 16 covalent SING C5 H20 no N 16 bmse011200 Z53115945 17 covalent SING C5 H21 no N 17 bmse011200 Z53115945 18 covalent SING C6 N9 no N 18 bmse011200 Z53115945 19 covalent SING C6 H22 no N 19 bmse011200 Z53115945 20 covalent SING C6 H23 no N 20 bmse011200 Z53115945 21 covalent SING C7 C4 no N 21 bmse011200 Z53115945 22 covalent SING C7 H24 no N 22 bmse011200 Z53115945 23 covalent SING C7 H25 no N 23 bmse011200 Z53115945 24 covalent SING N9 C7 no N 24 bmse011200 Z53115945 25 ester SING O11 C8 no N 25 bmse011200 Z53115945 26 covalent SING O11 H26 no N 26 bmse011200 Z53115945 27 covalent SING Cl27 H28 no N 27 bmse011200 Z53115945 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse011200 _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 Z53115945 'natural abundance' 1 $assembly_1 1 $entity_1 solute 1 mM bmse011200 1 2 'Potassium phosphate' 'natural abundance' . . . . buffer 25 mM bmse011200 1 3 'Potassium chloride' 'natural abundance' . . . . salt 50 mM bmse011200 1 4 'Magnesium chloride' 'natural abundance' . . . . salt 5 mM bmse011200 1 5 D2O 'natural abundance' . . . . solvent 9 % bmse011200 1 6 H2O 'natural abundance' . . . . solvent 90 % bmse011200 1 7 DMSO '[2H U-100%]' . . . . solvent 1 % bmse011200 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 bmse011200 _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 bmse011200 1 pressure 1 . atm bmse011200 1 temperature 298 0.1 K bmse011200 1 stop_ save_ ############################ # Computer software used # ############################ save_software_topspin _Software.Sf_category software _Software.Sf_framecode software_topspin _Software.Entry_ID bmse011200 _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/ bmse011200 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'data analysis' bmse011200 1 'peak picking' bmse011200 1 processing bmse011200 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 bmse011200 _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 bmse011200 _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 bmse011200 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/ bmse011200 1 1 cmcproject.xml text/xml 'spectrum analysis' nmr/set01/1/pdata/1/ bmse011200 1 1 multiplet.txt text 'Peak list' nmr/set01/1/pdata/1/ bmse011200 1 1 spectrum_overview.pdf pdf 'Spectrum image' nmr/set01/1/pdata/1/ bmse011200 1 1 spectrum_overview.png image/png 'Spectral image' nmr/set01/1/pdata/1/ bmse011200 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 bmse011200 _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 bmse011200 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 bmse011200 _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 bmse011200 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 bmse011200 1 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse011200 1 2 bmse011200 1 3 bmse011200 1 4 bmse011200 1 6 bmse011200 1 7 bmse011200 1 8 bmse011200 1 9 bmse011200 1 10 bmse011200 1 11 bmse011200 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 2.8386 8,9_m_Q3 bmse011200 1 2 1 4.6500 SUP bmse011200 1 3 1 1.6249 10,11_m bmse011200 1 4 1 2.5307 3_dd bmse011200 1 5 1 1.3970 12_m_Q1 bmse011200 1 6 1 1.8615 10,11_d_Q2 bmse011200 1 7 1 2.6030 DMSO bmse011200 1 8 1 3.4365 8,9_d bmse011200 1 9 1 1.7236 12_m bmse011200 1 10 1 3.2102 5_t bmse011200 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 6.9050 bmse011200 1 2 2 1 0.0000 bmse011200 1 3 3 1 6.7596 bmse011200 1 4 4 1 7.0975 bmse011200 1 5 4 1 7.0975 bmse011200 1 6 5 1 6.0050 bmse011200 1 7 6 1 14.6352 bmse011200 1 8 7 1 1.9532 bmse011200 1 9 8 1 12.4344 bmse011200 1 10 9 1 6.8224 bmse011200 1 11 10 1 7.0975 bmse011200 1 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse011200 1 2 bmse011200 1 3 bmse011200 1 4 bmse011200 1 5 bmse011200 1 6 bmse011200 1 7 bmse011200 1 8 bmse011200 1 9 bmse011200 1 10 bmse011200 1 11 bmse011200 1 12 bmse011200 1 13 bmse011200 1 14 bmse011200 1 15 bmse011200 1 16 bmse011200 1 17 bmse011200 1 18 bmse011200 1 19 bmse011200 1 20 bmse011200 1 21 bmse011200 1 22 bmse011200 1 23 bmse011200 1 24 bmse011200 1 25 bmse011200 1 26 bmse011200 1 27 bmse011200 1 28 bmse011200 1 29 bmse011200 1 30 bmse011200 1 31 bmse011200 1 32 bmse011200 1 33 bmse011200 1 34 bmse011200 1 35 bmse011200 1 36 bmse011200 1 37 bmse011200 1 38 bmse011200 1 39 bmse011200 1 40 bmse011200 1 41 bmse011200 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 2.8616 bmse011200 1 2 1 2.8401 bmse011200 1 3 1 2.8368 bmse011200 1 4 1 2.8191 bmse011200 1 5 1 2.8156 bmse011200 1 6 1 4.6500 bmse011200 1 7 1 1.6643 bmse011200 1 8 1 1.6579 bmse011200 1 9 1 1.6521 bmse011200 1 10 1 1.6367 bmse011200 1 11 1 1.6148 bmse011200 1 12 1 1.5963 bmse011200 1 13 1 1.5910 bmse011200 1 14 1 1.5855 bmse011200 1 15 1 2.5426 bmse011200 1 16 1 2.5307 bmse011200 1 17 1 2.5307 bmse011200 1 18 1 2.5189 bmse011200 1 19 1 1.4320 bmse011200 1 20 1 1.4256 bmse011200 1 21 1 1.4194 bmse011200 1 22 1 1.4042 bmse011200 1 23 1 1.3981 bmse011200 1 24 1 1.3890 bmse011200 1 25 1 1.3825 bmse011200 1 26 1 1.3620 bmse011200 1 27 1 1.8493 bmse011200 1 28 1 1.8737 bmse011200 1 29 1 2.5965 bmse011200 1 30 1 2.6001 bmse011200 1 31 1 2.6031 bmse011200 1 32 1 2.6060 bmse011200 1 33 1 2.6095 bmse011200 1 34 1 3.4261 bmse011200 1 35 1 3.4468 bmse011200 1 36 1 1.7349 bmse011200 1 37 1 1.7156 bmse011200 1 38 1 1.7122 bmse011200 1 39 1 3.1984 bmse011200 1 40 1 3.2101 bmse011200 1 41 1 3.2221 bmse011200 1 stop_ save_