data_bmse011541 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse011541 _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/bmse011541 loop_ _Entry_experimental_methods.ID _Entry_experimental_methods.Method _Entry_experimental_methods.Subtype _Entry_experimental_methods.Entry_ID 1 NMR solution bmse011541 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. . bmse011541 2 Christian Richter C. . bmse011541 3 Till Kuehn T. . bmse011541 4 Kamal Azzaoui K. . bmse011541 5 Marcel Blommers M. J.J. bmse011541 6 Rebecca 'Del Conte' R. . bmse011541 7 Marco Fragai M. . bmse011541 8 Nils Trieloff N. . bmse011541 9 Peter Schmieder P. . bmse011541 10 Marc Nazare M. . bmse011541 11 Edgar Specker E. . bmse011541 12 Vladimir Ivanov V. . bmse011541 13 Hartmut Oschkinat H. . bmse011541 14 Lucia Banci L. . bmse011541 15 Harald Schwalbe H. . bmse011541 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Entry_ID 1 iNEXT 'Infrastructure for NMR' bmse011541 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID spectral_peak_list 1 bmse011541 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 16 bmse011541 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 . bmse011541 stop_ loop_ _Auxiliary_files.ID _Auxiliary_files.Name _Auxiliary_files.Format _Auxiliary_files.URI _Auxiliary_files.Details _Auxiliary_files.Entry_ID 3 bmse011541.sdf sdf na 'Structure Definition File' bmse011541 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID bmse011541 _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. . bmse011541 1 2 Christian Richter C. . bmse011541 1 3 Till Kuehn T. . bmse011541 1 4 Kamal Azzaoui K. . bmse011541 1 5 Marcel Blommers M. J.J. bmse011541 1 6 Rebecca 'Del Conte' R. . bmse011541 1 7 Marco Fragai M. . bmse011541 1 8 Nils Trieloff N. . bmse011541 1 9 Peter Schmieder P. . bmse011541 1 10 Marc Nazare M. . bmse011541 1 11 Edgar Specker E. . bmse011541 1 12 Vladimir Ivanov V. . bmse011541 1 13 Hartmut Oschkinat H. . bmse011541 1 14 Lucia Banci L. . bmse011541 1 15 Harald Schwalbe H. . bmse011541 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly_1 _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly_1 _Assembly.Entry_ID bmse011541 _Assembly.ID 1 _Assembly.Name N-[[(2R)-oxolan-2-yl]methyl]pyridin-4-amine _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 Z1267882044 1 $entity_1 yes native no no bmse011541 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 Z1267882044 C1 C bmse011541 1 2 1 1 1 1 Z1267882044 C2 C bmse011541 1 3 1 1 1 1 Z1267882044 C3 C bmse011541 1 4 1 1 1 1 Z1267882044 C4 C bmse011541 1 5 1 1 1 1 Z1267882044 C5 C bmse011541 1 6 1 1 1 1 Z1267882044 C6 C bmse011541 1 7 1 1 1 1 Z1267882044 C7 C bmse011541 1 8 1 1 1 1 Z1267882044 C8 C bmse011541 1 9 1 1 1 1 Z1267882044 C9 C bmse011541 1 10 1 1 1 1 Z1267882044 C10 C bmse011541 1 11 1 1 1 1 Z1267882044 N11 N bmse011541 1 12 1 1 1 1 Z1267882044 N12 N bmse011541 1 13 1 1 1 1 Z1267882044 O13 O bmse011541 1 14 1 1 1 1 Z1267882044 H14 H bmse011541 1 15 1 1 1 1 Z1267882044 H15 H bmse011541 1 16 1 1 1 1 Z1267882044 H16 H bmse011541 1 17 1 1 1 1 Z1267882044 H17 H bmse011541 1 18 1 1 1 1 Z1267882044 H18 H bmse011541 1 19 1 1 1 1 Z1267882044 H19 H bmse011541 1 20 1 1 1 1 Z1267882044 H20 H bmse011541 1 21 1 1 1 1 Z1267882044 H21 H bmse011541 1 22 1 1 1 1 Z1267882044 H22 H bmse011541 1 23 1 1 1 1 Z1267882044 H23 H bmse011541 1 24 1 1 1 1 Z1267882044 H24 H bmse011541 1 25 1 1 1 1 Z1267882044 H25 H bmse011541 1 26 1 1 1 1 Z1267882044 H26 H bmse011541 1 27 1 1 1 1 Z1267882044 H27 H bmse011541 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_entity_1 _Entity.Sf_category entity _Entity.Sf_framecode entity_1 _Entity.Entry_ID bmse011541 _Entity.ID 1 _Entity.Name N-[[(2R)-oxolan-2-yl]methyl]pyridin-4-amine _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID Z1267882044 _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 178.23095999999987 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 Z1267882044 $chem_comp_1 bmse011541 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 bmse011541 _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 bmse011541 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 bmse011541 _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' bmse011541 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 bmse011541 _Chem_comp.ID Z1267882044 _Chem_comp.Provenance iNEXT _Chem_comp.Name N-[[(2R)-oxolan-2-yl]methyl]pyridin-4-amine _Chem_comp.Type non-polymer _Chem_comp.Number_atoms_all 27 _Chem_comp.Number_atoms_nh 13 _Chem_comp.InChI_code InChI=1S/C10H14N2O/c1-2-10(13-7-1)8-12-9-3-5-11-6-4-9/h3-6,10H,1-2,7-8H2,(H,11,12)/t10-/m1/s1 _Chem_comp.Synonyms P6_E08 _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic no _Chem_comp.Formula C10H14N2O _Chem_comp.Formula_weight 178.23095999999987 _Chem_comp.Formula_mono_iso_wt_nat 178.110613078 _Chem_comp.Formula_mono_iso_wt_13C 188.14416145800004 _Chem_comp.Formula_mono_iso_wt_15N 180.104682864 _Chem_comp.Formula_mono_iso_wt_13C_15N 190.13823124400005 _Chem_comp.Image_file_name bmse011541.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse011541.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 N=1C=CC(=CC1)NCC2OCCC2 SMILES Bruker_TopSpin_FBS na bmse011541 Z1267882044 c1cc(NCC2CCCO2)ccn1 SMILES_CANONICAL RDKit 2017.09.3 bmse011541 Z1267882044 c1cc(NCC2CCCO2)ccn1 SMILES_ISOMERIC RDKit 2017.09.3 bmse011541 Z1267882044 c1cc(NCC2CCCO2)ccn1 SMILES RDKit 2017.09.3 bmse011541 Z1267882044 C1CO[C@H](C1)CNc1ccncc1 SMILES_CANONICAL OpenBabel 2.3.2 bmse011541 Z1267882044 C1CO[C@H](C1)CNc1ccncc1 SMILES OpenBabel 2.3.2 bmse011541 Z1267882044 InChI=1S/C10H14N2O/c1-2-10(13-7-1)8-12-9-3-5-11-6-4-9/h3-6,10H,1-2,7-8H2,(H,11,12)/t10-/m1/s1 InChI OpenBabel 2.3.2 bmse011541 Z1267882044 CRFFHQRTZREWOJ-SNVBAGLBSA-N InChI_KEY OpenBabel 2.3.2 bmse011541 Z1267882044 InChI=1S/C10H14N2O/c1-2-10(13-7-1)8-12-9-3-5-11-6-4-9/h3-6,10H,1-2,7-8H2,(H,11,12)/t10-/m1/s1 InChI ALATIS na bmse011541 Z1267882044 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 bmse011541 Z1267882044 C2 C N 0 no 2 bmse011541 Z1267882044 C3 C N 0 yes 3 bmse011541 Z1267882044 C4 C N 0 yes 4 bmse011541 Z1267882044 C5 C N 0 yes 5 bmse011541 Z1267882044 C6 C N 0 yes 6 bmse011541 Z1267882044 C7 C N 0 no 7 bmse011541 Z1267882044 C8 C N 0 no 8 bmse011541 Z1267882044 C9 C N 0 yes 9 bmse011541 Z1267882044 C10 C N 0 no 10 bmse011541 Z1267882044 N11 N N 0 yes 11 bmse011541 Z1267882044 N12 N N 0 no 12 bmse011541 Z1267882044 O13 O N 0 no 13 bmse011541 Z1267882044 H14 H N 0 no 14 bmse011541 Z1267882044 H15 H N 0 no 15 bmse011541 Z1267882044 H16 H N 0 no 16 bmse011541 Z1267882044 H17 H N 0 no 17 bmse011541 Z1267882044 H18 H N 0 no 18 bmse011541 Z1267882044 H19 H N 0 no 19 bmse011541 Z1267882044 H20 H N 0 no 20 bmse011541 Z1267882044 H21 H N 0 no 21 bmse011541 Z1267882044 H22 H N 0 no 22 bmse011541 Z1267882044 H23 H N 0 no 23 bmse011541 Z1267882044 H24 H N 0 no 24 bmse011541 Z1267882044 H25 H N 0 no 25 bmse011541 Z1267882044 H26 H N 0 no 26 bmse011541 Z1267882044 H27 H N 0 no 27 bmse011541 Z1267882044 stop_ loop_ _Atom_nomenclature.Naming_system _Atom_nomenclature.Atom_name _Atom_nomenclature.Atom_ID _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID author C13 C1 bmse011541 Z1267882044 author C12 C2 bmse011541 Z1267882044 author C7 C3 bmse011541 Z1267882044 author C8 C4 bmse011541 Z1267882044 author C10 C5 bmse011541 Z1267882044 author C9 C6 bmse011541 Z1267882044 author C11 C7 bmse011541 Z1267882044 author C5 C8 bmse011541 Z1267882044 author C4 C9 bmse011541 Z1267882044 author C6 C10 bmse011541 Z1267882044 author N1 N11 bmse011541 Z1267882044 author N2 N12 bmse011541 Z1267882044 author O3 O13 bmse011541 Z1267882044 author H26 H14 bmse011541 Z1267882044 author H27 H15 bmse011541 Z1267882044 author H24 H16 bmse011541 Z1267882044 author H25 H17 bmse011541 Z1267882044 author H18 H18 bmse011541 Z1267882044 author H19 H19 bmse011541 Z1267882044 author H21 H20 bmse011541 Z1267882044 author H20 H21 bmse011541 Z1267882044 author H22 H22 bmse011541 Z1267882044 author H23 H23 bmse011541 Z1267882044 author H15 H24 bmse011541 Z1267882044 author H16 H25 bmse011541 Z1267882044 author H17 H26 bmse011541 Z1267882044 author H14 H27 bmse011541 Z1267882044 ALATIS C1 C1 bmse011541 Z1267882044 ALATIS C2 C2 bmse011541 Z1267882044 ALATIS C3 C3 bmse011541 Z1267882044 ALATIS C4 C4 bmse011541 Z1267882044 ALATIS C5 C5 bmse011541 Z1267882044 ALATIS C6 C6 bmse011541 Z1267882044 ALATIS C7 C7 bmse011541 Z1267882044 ALATIS C8 C8 bmse011541 Z1267882044 ALATIS C9 C9 bmse011541 Z1267882044 ALATIS C10 C10 bmse011541 Z1267882044 ALATIS N11 N11 bmse011541 Z1267882044 ALATIS N12 N12 bmse011541 Z1267882044 ALATIS O13 O13 bmse011541 Z1267882044 ALATIS H14 H14 bmse011541 Z1267882044 ALATIS H15 H15 bmse011541 Z1267882044 ALATIS H16 H16 bmse011541 Z1267882044 ALATIS H17 H17 bmse011541 Z1267882044 ALATIS H18 H18 bmse011541 Z1267882044 ALATIS H19 H19 bmse011541 Z1267882044 ALATIS H20 H20 bmse011541 Z1267882044 ALATIS H21 H21 bmse011541 Z1267882044 ALATIS H22 H22 bmse011541 Z1267882044 ALATIS H23 H23 bmse011541 Z1267882044 ALATIS H24 H24 bmse011541 Z1267882044 ALATIS H25 H25 bmse011541 Z1267882044 ALATIS H26 H26 bmse011541 Z1267882044 ALATIS H27 H27 bmse011541 Z1267882044 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 C3 C5 yes N 1 bmse011541 Z1267882044 2 covalent AROM C3 C9 yes N 2 bmse011541 Z1267882044 3 covalent AROM C4 C6 yes N 3 bmse011541 Z1267882044 4 covalent AROM C5 N11 yes N 4 bmse011541 Z1267882044 5 covalent AROM C6 N11 yes N 5 bmse011541 Z1267882044 6 covalent AROM C9 C4 yes N 6 bmse011541 Z1267882044 7 covalent SING C1 C2 no N 7 bmse011541 Z1267882044 8 covalent SING C1 H14 no N 8 bmse011541 Z1267882044 9 covalent SING C1 H15 no N 9 bmse011541 Z1267882044 10 covalent SING C2 C10 no N 10 bmse011541 Z1267882044 11 covalent SING C2 H16 no N 11 bmse011541 Z1267882044 12 covalent SING C2 H17 no N 12 bmse011541 Z1267882044 13 covalent SING C3 H18 no N 13 bmse011541 Z1267882044 14 covalent SING C4 H19 no N 14 bmse011541 Z1267882044 15 covalent SING C5 H20 no N 15 bmse011541 Z1267882044 16 covalent SING C6 H21 no N 16 bmse011541 Z1267882044 17 covalent SING C7 C1 no N 17 bmse011541 Z1267882044 18 covalent SING C7 O13 no N 18 bmse011541 Z1267882044 19 covalent SING C7 H22 no N 19 bmse011541 Z1267882044 20 covalent SING C7 H23 no N 20 bmse011541 Z1267882044 21 covalent SING C8 N12 no N 21 bmse011541 Z1267882044 22 covalent SING C8 H24 no N 22 bmse011541 Z1267882044 23 covalent SING C8 H25 no N 23 bmse011541 Z1267882044 24 covalent SING C10 C8 no N 24 bmse011541 Z1267882044 25 covalent SING C10 H26 no N 25 bmse011541 Z1267882044 26 covalent SING N12 C9 no N 26 bmse011541 Z1267882044 27 covalent SING N12 H27 no N 27 bmse011541 Z1267882044 28 covalent SING O13 C10 no N 28 bmse011541 Z1267882044 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse011541 _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 Z1267882044 'natural abundance' 1 $assembly_1 1 $entity_1 solute 1 mM bmse011541 1 2 'Potassium phosphate' 'natural abundance' . . . . buffer 25 mM bmse011541 1 3 'Potassium chloride' 'natural abundance' . . . . salt 50 mM bmse011541 1 4 'Magnesium chloride' 'natural abundance' . . . . salt 5 mM bmse011541 1 5 D2O 'natural abundance' . . . . solvent 9 % bmse011541 1 6 H2O 'natural abundance' . . . . solvent 90 % bmse011541 1 7 DMSO '[2H U-100%]' . . . . solvent 1 % bmse011541 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 bmse011541 _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 bmse011541 1 pressure 1 . atm bmse011541 1 temperature 298 0.1 K bmse011541 1 stop_ save_ ############################ # Computer software used # ############################ save_software_topspin _Software.Sf_category software _Software.Sf_framecode software_topspin _Software.Entry_ID bmse011541 _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/ bmse011541 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'data analysis' bmse011541 1 'peak picking' bmse011541 1 processing bmse011541 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 bmse011541 _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 bmse011541 _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 bmse011541 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/ bmse011541 1 1 cmcproject.xml text/xml 'spectrum analysis' nmr/set01/1/pdata/1/ bmse011541 1 1 multiplet.txt text 'Peak list' nmr/set01/1/pdata/1/ bmse011541 1 1 spectrum_overview.pdf pdf 'Spectrum image' nmr/set01/1/pdata/1/ bmse011541 1 1 spectrum_overview.png image/png 'Spectral image' nmr/set01/1/pdata/1/ bmse011541 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 bmse011541 _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 bmse011541 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 bmse011541 _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 bmse011541 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 bmse011541 1 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse011541 1 2 bmse011541 1 3 bmse011541 1 4 bmse011541 1 5 bmse011541 1 6 bmse011541 1 9 bmse011541 1 10 bmse011541 1 11 bmse011541 1 12 bmse011541 1 13 bmse011541 1 14 bmse011541 1 15 bmse011541 1 16 bmse011541 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 2.7166 Imp2 bmse011541 1 2 1 3.4228 m_2H bmse011541 1 3 1 4.1168 m_1H bmse011541 1 4 1 6.7962 d_4H bmse011541 1 5 1 7.7524 s_1H bmse011541 1 6 1 1.6024 ddd_2H bmse011541 1 7 1 2.6029 DMSO bmse011541 1 8 1 1.8639 m_4H bmse011541 1 9 1 3.7394 m_4H bmse011541 1 10 1 3.3408 m_2H bmse011541 1 11 1 7.8994 m_2H bmse011541 1 12 1 4.6500 SUP bmse011541 1 13 1 2.4852 Imp1 bmse011541 1 14 1 2.0147 m_2H_Q1 bmse011541 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 bmse011541 1 2 2 1 3.9247 bmse011541 1 3 3 1 3.5841 bmse011541 1 4 4 1 5.2819 bmse011541 1 5 5 1 0.0000 bmse011541 1 6 6 1 15.3505 bmse011541 1 7 6 1 12.7646 bmse011541 1 8 6 1 7.2626 bmse011541 1 9 7 1 1.9807 bmse011541 1 10 8 1 3.9549 bmse011541 1 11 9 1 7.9916 bmse011541 1 12 10 1 7.0150 bmse011541 1 13 11 1 15.0754 bmse011541 1 14 12 1 0.0000 bmse011541 1 15 13 1 0.0000 bmse011541 1 16 14 1 3.3452 bmse011541 1 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse011541 1 2 bmse011541 1 3 bmse011541 1 4 bmse011541 1 5 bmse011541 1 6 bmse011541 1 7 bmse011541 1 8 bmse011541 1 9 bmse011541 1 10 bmse011541 1 11 bmse011541 1 12 bmse011541 1 13 bmse011541 1 14 bmse011541 1 15 bmse011541 1 16 bmse011541 1 17 bmse011541 1 18 bmse011541 1 19 bmse011541 1 20 bmse011541 1 21 bmse011541 1 22 bmse011541 1 23 bmse011541 1 24 bmse011541 1 25 bmse011541 1 26 bmse011541 1 27 bmse011541 1 28 bmse011541 1 29 bmse011541 1 30 bmse011541 1 31 bmse011541 1 32 bmse011541 1 33 bmse011541 1 34 bmse011541 1 35 bmse011541 1 36 bmse011541 1 37 bmse011541 1 38 bmse011541 1 39 bmse011541 1 40 bmse011541 1 41 bmse011541 1 42 bmse011541 1 43 bmse011541 1 44 bmse011541 1 45 bmse011541 1 46 bmse011541 1 47 bmse011541 1 48 bmse011541 1 49 bmse011541 1 50 bmse011541 1 51 bmse011541 1 52 bmse011541 1 53 bmse011541 1 54 bmse011541 1 55 bmse011541 1 56 bmse011541 1 57 bmse011541 1 58 bmse011541 1 59 bmse011541 1 60 bmse011541 1 61 bmse011541 1 62 bmse011541 1 63 bmse011541 1 64 bmse011541 1 65 bmse011541 1 66 bmse011541 1 67 bmse011541 1 68 bmse011541 1 69 bmse011541 1 70 bmse011541 1 71 bmse011541 1 72 bmse011541 1 73 bmse011541 1 74 bmse011541 1 75 bmse011541 1 76 bmse011541 1 77 bmse011541 1 78 bmse011541 1 79 bmse011541 1 80 bmse011541 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 2.7166 bmse011541 1 2 1 3.4424 bmse011541 1 3 1 3.4351 bmse011541 1 4 1 3.4338 bmse011541 1 5 1 3.4270 bmse011541 1 6 1 3.4188 bmse011541 1 7 1 3.4116 bmse011541 1 8 1 3.4032 bmse011541 1 9 1 4.1377 bmse011541 1 10 1 4.1315 bmse011541 1 11 1 4.1258 bmse011541 1 12 1 4.1195 bmse011541 1 13 1 4.1139 bmse011541 1 14 1 4.1076 bmse011541 1 15 1 4.1021 bmse011541 1 16 1 4.0959 bmse011541 1 17 1 6.7918 bmse011541 1 18 1 6.8006 bmse011541 1 19 1 7.7524 bmse011541 1 20 1 1.6319 bmse011541 1 21 1 1.6198 bmse011541 1 22 1 1.6103 bmse011541 1 23 1 1.5985 bmse011541 1 24 1 1.6062 bmse011541 1 25 1 1.5939 bmse011541 1 26 1 1.5851 bmse011541 1 27 1 1.5729 bmse011541 1 28 1 2.5963 bmse011541 1 29 1 2.6000 bmse011541 1 30 1 2.6029 bmse011541 1 31 1 2.6060 bmse011541 1 32 1 2.6095 bmse011541 1 33 1 1.9199 bmse011541 1 34 1 1.9093 bmse011541 1 35 1 1.9062 bmse011541 1 36 1 1.8994 bmse011541 1 37 1 1.8897 bmse011541 1 38 1 1.8862 bmse011541 1 39 1 1.8856 bmse011541 1 40 1 1.8776 bmse011541 1 41 1 1.8754 bmse011541 1 42 1 1.8657 bmse011541 1 43 1 1.8541 bmse011541 1 44 1 1.8451 bmse011541 1 45 1 1.8413 bmse011541 1 46 1 1.8327 bmse011541 1 47 1 1.8288 bmse011541 1 48 1 1.8283 bmse011541 1 49 1 1.8204 bmse011541 1 50 1 1.8079 bmse011541 1 51 1 3.7926 bmse011541 1 52 1 3.7807 bmse011541 1 53 1 3.7675 bmse011541 1 54 1 3.7558 bmse011541 1 55 1 3.7224 bmse011541 1 56 1 3.7098 bmse011541 1 57 1 3.6995 bmse011541 1 58 1 3.6960 bmse011541 1 59 1 3.6861 bmse011541 1 60 1 3.3642 bmse011541 1 61 1 3.3528 bmse011541 1 62 1 3.3410 bmse011541 1 63 1 3.3291 bmse011541 1 64 1 3.3174 bmse011541 1 65 1 7.9245 bmse011541 1 66 1 7.8778 bmse011541 1 67 1 7.8743 bmse011541 1 68 1 4.6500 bmse011541 1 69 1 2.4852 bmse011541 1 70 1 2.0426 bmse011541 1 71 1 2.0334 bmse011541 1 72 1 2.0331 bmse011541 1 73 1 2.0298 bmse011541 1 74 1 2.0211 bmse011541 1 75 1 2.0175 bmse011541 1 76 1 2.0167 bmse011541 1 77 1 2.0123 bmse011541 1 78 1 2.0081 bmse011541 1 79 1 1.9988 bmse011541 1 80 1 1.9868 bmse011541 1 stop_ save_