data_bmse011614 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse011614 _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/bmse011614 loop_ _Entry_experimental_methods.ID _Entry_experimental_methods.Method _Entry_experimental_methods.Subtype _Entry_experimental_methods.Entry_ID 1 NMR solution bmse011614 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. . bmse011614 2 Christian Richter C. . bmse011614 3 Till Kuehn T. . bmse011614 4 Kamal Azzaoui K. . bmse011614 5 Marcel Blommers M. J.J. bmse011614 6 Rebecca 'Del Conte' R. . bmse011614 7 Marco Fragai M. . bmse011614 8 Nils Trieloff N. . bmse011614 9 Peter Schmieder P. . bmse011614 10 Marc Nazare M. . bmse011614 11 Edgar Specker E. . bmse011614 12 Vladimir Ivanov V. . bmse011614 13 Hartmut Oschkinat H. . bmse011614 14 Lucia Banci L. . bmse011614 15 Harald Schwalbe H. . bmse011614 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Entry_ID 1 iNEXT 'Infrastructure for NMR' bmse011614 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID spectral_peak_list 1 bmse011614 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 9 bmse011614 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 . bmse011614 stop_ loop_ _Auxiliary_files.ID _Auxiliary_files.Name _Auxiliary_files.Format _Auxiliary_files.URI _Auxiliary_files.Details _Auxiliary_files.Entry_ID 3 bmse011614.sdf sdf na 'Structure Definition File' bmse011614 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID bmse011614 _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. . bmse011614 1 2 Christian Richter C. . bmse011614 1 3 Till Kuehn T. . bmse011614 1 4 Kamal Azzaoui K. . bmse011614 1 5 Marcel Blommers M. J.J. bmse011614 1 6 Rebecca 'Del Conte' R. . bmse011614 1 7 Marco Fragai M. . bmse011614 1 8 Nils Trieloff N. . bmse011614 1 9 Peter Schmieder P. . bmse011614 1 10 Marc Nazare M. . bmse011614 1 11 Edgar Specker E. . bmse011614 1 12 Vladimir Ivanov V. . bmse011614 1 13 Hartmut Oschkinat H. . bmse011614 1 14 Lucia Banci L. . bmse011614 1 15 Harald Schwalbe H. . bmse011614 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly_1 _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly_1 _Assembly.Entry_ID bmse011614 _Assembly.ID 1 _Assembly.Name 5-fluoro-1-(1-methylcyclopropyl)sulfonyl-3,6-dihydro-2H-pyridine _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 Z2277255954 1 $entity_1 yes native no no bmse011614 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 Z2277255954 C1 C bmse011614 1 2 1 1 1 1 Z2277255954 C2 C bmse011614 1 3 1 1 1 1 Z2277255954 C3 C bmse011614 1 4 1 1 1 1 Z2277255954 C4 C bmse011614 1 5 1 1 1 1 Z2277255954 C5 C bmse011614 1 6 1 1 1 1 Z2277255954 C6 C bmse011614 1 7 1 1 1 1 Z2277255954 C7 C bmse011614 1 8 1 1 1 1 Z2277255954 C8 C bmse011614 1 9 1 1 1 1 Z2277255954 C9 C bmse011614 1 10 1 1 1 1 Z2277255954 F10 F bmse011614 1 11 1 1 1 1 Z2277255954 N11 N bmse011614 1 12 1 1 1 1 Z2277255954 O12 O bmse011614 1 13 1 1 1 1 Z2277255954 O13 O bmse011614 1 14 1 1 1 1 Z2277255954 S14 S bmse011614 1 15 1 1 1 1 Z2277255954 H15 H bmse011614 1 16 1 1 1 1 Z2277255954 H16 H bmse011614 1 17 1 1 1 1 Z2277255954 H17 H bmse011614 1 18 1 1 1 1 Z2277255954 H18 H bmse011614 1 19 1 1 1 1 Z2277255954 H19 H bmse011614 1 20 1 1 1 1 Z2277255954 H20 H bmse011614 1 21 1 1 1 1 Z2277255954 H21 H bmse011614 1 22 1 1 1 1 Z2277255954 H22 H bmse011614 1 23 1 1 1 1 Z2277255954 H23 H bmse011614 1 24 1 1 1 1 Z2277255954 H24 H bmse011614 1 25 1 1 1 1 Z2277255954 H25 H bmse011614 1 26 1 1 1 1 Z2277255954 H26 H bmse011614 1 27 1 1 1 1 Z2277255954 H27 H bmse011614 1 28 1 1 1 1 Z2277255954 H28 H bmse011614 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_entity_1 _Entity.Sf_category entity _Entity.Sf_framecode entity_1 _Entity.Entry_ID bmse011614 _Entity.ID 1 _Entity.Name 5-fluoro-1-(1-methylcyclopropyl)sulfonyl-3,6-dihydro-2H-pyridine _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID Z2277255954 _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 219.27636319999988 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 Z2277255954 $chem_comp_1 bmse011614 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 bmse011614 _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 bmse011614 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 bmse011614 _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' bmse011614 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 bmse011614 _Chem_comp.ID Z2277255954 _Chem_comp.Provenance iNEXT _Chem_comp.Name 5-fluoro-1-(1-methylcyclopropyl)sulfonyl-3,6-dihydro-2H-pyridine _Chem_comp.Type non-polymer _Chem_comp.Number_atoms_all 28 _Chem_comp.Number_atoms_nh 14 _Chem_comp.InChI_code InChI=1S/C9H14FNO2S/c1-9(4-5-9)14(12,13)11-6-2-3-8(10)7-11/h3H,2,4-7H2,1H3 _Chem_comp.Synonyms P7_F05 _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic no _Chem_comp.Formula C9H14FNO2S _Chem_comp.Formula_weight 219.27636319999988 _Chem_comp.Formula_mono_iso_wt_nat 219.072927913 _Chem_comp.Formula_mono_iso_wt_13C 228.10312145500004 _Chem_comp.Formula_mono_iso_wt_15N 220.069962806 _Chem_comp.Formula_mono_iso_wt_13C_15N 229.10015634800004 _Chem_comp.Image_file_name bmse011614.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse011614.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=S(=O)(N1CC(F)=CCC1)C2(C)CC2 SMILES Bruker_TopSpin_FBS na bmse011614 Z2277255954 CC1(S(=O)(=O)N2CCC=C(F)C2)CC1 SMILES_CANONICAL RDKit 2017.09.3 bmse011614 Z2277255954 CC1(S(=O)(=O)N2CCC=C(F)C2)CC1 SMILES_ISOMERIC RDKit 2017.09.3 bmse011614 Z2277255954 CC1(S(=O)(=O)N2CCC=C(F)C2)CC1 SMILES RDKit 2017.09.3 bmse011614 Z2277255954 FC1=CCCN(C1)S(=O)(=O)C1(C)CC1 SMILES_CANONICAL OpenBabel 2.3.2 bmse011614 Z2277255954 FC1=CCCN(C1)S(=O)(=O)C1(C)CC1 SMILES OpenBabel 2.3.2 bmse011614 Z2277255954 InChI=1S/C9H14FNO2S/c1-9(4-5-9)14(12,13)11-6-2-3-8(10)7-11/h3H,2,4-7H2,1H3 InChI OpenBabel 2.3.2 bmse011614 Z2277255954 USHLSOPQTSXCNW-UHFFFAOYSA-N InChI_KEY OpenBabel 2.3.2 bmse011614 Z2277255954 InChI=1S/C9H14FNO2S/c1-9(4-5-9)14(12,13)11-6-2-3-8(10)7-11/h3H,2,4-7H2,1H3 InChI ALATIS na bmse011614 Z2277255954 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 bmse011614 Z2277255954 C2 C N 0 no 2 bmse011614 Z2277255954 C3 C N 0 no 3 bmse011614 Z2277255954 C4 C N 0 no 4 bmse011614 Z2277255954 C5 C N 0 no 5 bmse011614 Z2277255954 C6 C N 0 no 6 bmse011614 Z2277255954 C7 C N 0 no 7 bmse011614 Z2277255954 C8 C N 0 no 8 bmse011614 Z2277255954 C9 C N 0 no 9 bmse011614 Z2277255954 F10 F N 0 no 10 bmse011614 Z2277255954 N11 N N 0 no 11 bmse011614 Z2277255954 O12 O N 0 no 12 bmse011614 Z2277255954 O13 O N 0 no 13 bmse011614 Z2277255954 S14 S N 0 no 14 bmse011614 Z2277255954 H15 H N 0 no 15 bmse011614 Z2277255954 H16 H N 0 no 16 bmse011614 Z2277255954 H17 H N 0 no 17 bmse011614 Z2277255954 H18 H N 0 no 18 bmse011614 Z2277255954 H19 H N 0 no 19 bmse011614 Z2277255954 H20 H N 0 no 20 bmse011614 Z2277255954 H21 H N 0 no 21 bmse011614 Z2277255954 H22 H N 0 no 22 bmse011614 Z2277255954 H23 H N 0 no 23 bmse011614 Z2277255954 H24 H N 0 no 24 bmse011614 Z2277255954 H25 H N 0 no 25 bmse011614 Z2277255954 H26 H N 0 no 26 bmse011614 Z2277255954 H27 H N 0 no 27 bmse011614 Z2277255954 H28 H N 0 no 28 bmse011614 Z2277255954 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 bmse011614 Z2277255954 author C14 C2 bmse011614 Z2277255954 author C10 C3 bmse011614 Z2277255954 author C5 C4 bmse011614 Z2277255954 author C6 C5 bmse011614 Z2277255954 author C11 C6 bmse011614 Z2277255954 author C4 C7 bmse011614 Z2277255954 author C9 C8 bmse011614 Z2277255954 author C3 C9 bmse011614 Z2277255954 author F12 F10 bmse011614 Z2277255954 author N2 N11 bmse011614 Z2277255954 author O7 O12 bmse011614 Z2277255954 author O8 O13 bmse011614 Z2277255954 author S1 S14 bmse011614 Z2277255954 author H25 H15 bmse011614 Z2277255954 author H26 H16 bmse011614 Z2277255954 author H24 H17 bmse011614 Z2277255954 author H27 H18 bmse011614 Z2277255954 author H28 H19 bmse011614 Z2277255954 author H21 H20 bmse011614 Z2277255954 author H17 H21 bmse011614 Z2277255954 author H18 H22 bmse011614 Z2277255954 author H19 H23 bmse011614 Z2277255954 author H20 H24 bmse011614 Z2277255954 author H22 H25 bmse011614 Z2277255954 author H23 H26 bmse011614 Z2277255954 author H15 H27 bmse011614 Z2277255954 author H16 H28 bmse011614 Z2277255954 ALATIS C1 C1 bmse011614 Z2277255954 ALATIS C2 C2 bmse011614 Z2277255954 ALATIS C3 C3 bmse011614 Z2277255954 ALATIS C4 C4 bmse011614 Z2277255954 ALATIS C5 C5 bmse011614 Z2277255954 ALATIS C6 C6 bmse011614 Z2277255954 ALATIS C7 C7 bmse011614 Z2277255954 ALATIS C8 C8 bmse011614 Z2277255954 ALATIS C9 C9 bmse011614 Z2277255954 ALATIS F10 F10 bmse011614 Z2277255954 ALATIS N11 N11 bmse011614 Z2277255954 ALATIS O12 O12 bmse011614 Z2277255954 ALATIS O13 O13 bmse011614 Z2277255954 ALATIS S14 S14 bmse011614 Z2277255954 ALATIS H15 H15 bmse011614 Z2277255954 ALATIS H16 H16 bmse011614 Z2277255954 ALATIS H17 H17 bmse011614 Z2277255954 ALATIS H18 H18 bmse011614 Z2277255954 ALATIS H19 H19 bmse011614 Z2277255954 ALATIS H20 H20 bmse011614 Z2277255954 ALATIS H21 H21 bmse011614 Z2277255954 ALATIS H22 H22 bmse011614 Z2277255954 ALATIS H23 H23 bmse011614 Z2277255954 ALATIS H24 H24 bmse011614 Z2277255954 ALATIS H25 H25 bmse011614 Z2277255954 ALATIS H26 H26 bmse011614 Z2277255954 ALATIS H27 H27 bmse011614 Z2277255954 ALATIS H28 H28 bmse011614 Z2277255954 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 DOUB C3 C8 no N 1 bmse011614 Z2277255954 2 covalent DOUB O12 S14 no N 2 bmse011614 Z2277255954 3 covalent DOUB O13 S14 no N 3 bmse011614 Z2277255954 4 covalent SING C1 C9 no N 4 bmse011614 Z2277255954 5 covalent SING C1 H15 no N 5 bmse011614 Z2277255954 6 covalent SING C1 H16 no N 6 bmse011614 Z2277255954 7 covalent SING C1 H17 no N 7 bmse011614 Z2277255954 8 covalent SING C2 C6 no N 8 bmse011614 Z2277255954 9 covalent SING C2 H18 no N 9 bmse011614 Z2277255954 10 covalent SING C2 H19 no N 10 bmse011614 Z2277255954 11 covalent SING C3 C2 no N 11 bmse011614 Z2277255954 12 covalent SING C3 H20 no N 12 bmse011614 Z2277255954 13 covalent SING C4 C5 no N 13 bmse011614 Z2277255954 14 covalent SING C4 C9 no N 14 bmse011614 Z2277255954 15 covalent SING C4 H21 no N 15 bmse011614 Z2277255954 16 covalent SING C4 H22 no N 16 bmse011614 Z2277255954 17 covalent SING C5 C9 no N 17 bmse011614 Z2277255954 18 covalent SING C5 H23 no N 18 bmse011614 Z2277255954 19 covalent SING C5 H24 no N 19 bmse011614 Z2277255954 20 covalent SING C6 N11 no N 20 bmse011614 Z2277255954 21 covalent SING C6 H25 no N 21 bmse011614 Z2277255954 22 covalent SING C6 H26 no N 22 bmse011614 Z2277255954 23 covalent SING C7 N11 no N 23 bmse011614 Z2277255954 24 covalent SING C7 H27 no N 24 bmse011614 Z2277255954 25 covalent SING C7 H28 no N 25 bmse011614 Z2277255954 26 covalent SING C8 C7 no N 26 bmse011614 Z2277255954 27 covalent SING C9 S14 no N 27 bmse011614 Z2277255954 28 covalent SING F10 C8 no N 28 bmse011614 Z2277255954 29 covalent SING N11 S14 no N 29 bmse011614 Z2277255954 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse011614 _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 Z2277255954 'natural abundance' 1 $assembly_1 1 $entity_1 solute 1 mM bmse011614 1 2 'Potassium phosphate' 'natural abundance' . . . . buffer 25 mM bmse011614 1 3 'Potassium chloride' 'natural abundance' . . . . salt 50 mM bmse011614 1 4 'Magnesium chloride' 'natural abundance' . . . . salt 5 mM bmse011614 1 5 D2O 'natural abundance' . . . . solvent 9 % bmse011614 1 6 H2O 'natural abundance' . . . . solvent 90 % bmse011614 1 7 DMSO '[2H U-100%]' . . . . solvent 1 % bmse011614 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 bmse011614 _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 bmse011614 1 pressure 1 . atm bmse011614 1 temperature 298 0.1 K bmse011614 1 stop_ save_ ############################ # Computer software used # ############################ save_software_topspin _Software.Sf_category software _Software.Sf_framecode software_topspin _Software.Entry_ID bmse011614 _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/ bmse011614 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'data analysis' bmse011614 1 'peak picking' bmse011614 1 processing bmse011614 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 bmse011614 _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 bmse011614 _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 bmse011614 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/ bmse011614 1 1 cmcproject.xml text/xml 'spectrum analysis' nmr/set01/1/pdata/1/ bmse011614 1 1 multiplet.txt text 'Peak list' nmr/set01/1/pdata/1/ bmse011614 1 1 spectrum_overview.pdf pdf 'Spectrum image' nmr/set01/1/pdata/1/ bmse011614 1 1 spectrum_overview.png image/png 'Spectral image' nmr/set01/1/pdata/1/ bmse011614 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 bmse011614 _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 bmse011614 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 bmse011614 _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 bmse011614 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 bmse011614 1 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse011614 1 2 bmse011614 1 3 bmse011614 1 4 bmse011614 1 5 bmse011614 1 7 bmse011614 1 8 bmse011614 1 9 bmse011614 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 3.3758 11_t_Q3 bmse011614 1 2 1 3.8991 4_d bmse011614 1 3 1 1.3886 13_m_Q1 bmse011614 1 4 1 0.8916 5,6_m bmse011614 1 5 1 1.2648 5,6_dd bmse011614 1 6 1 2.1862 14_m_Q2 bmse011614 1 7 1 2.6029 DMSO bmse011614 1 8 1 4.6500 SUP bmse011614 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 5.6670 bmse011614 1 2 2 1 1.6506 bmse011614 1 3 3 1 0.0000 bmse011614 1 4 4 1 3.7780 bmse011614 1 5 5 1 5.9421 bmse011614 1 6 5 1 5.9421 bmse011614 1 7 6 1 2.2833 bmse011614 1 8 7 1 1.9807 bmse011614 1 9 8 1 0.0000 bmse011614 1 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse011614 1 2 bmse011614 1 3 bmse011614 1 4 bmse011614 1 5 bmse011614 1 6 bmse011614 1 7 bmse011614 1 8 bmse011614 1 9 bmse011614 1 10 bmse011614 1 11 bmse011614 1 12 bmse011614 1 13 bmse011614 1 14 bmse011614 1 15 bmse011614 1 16 bmse011614 1 17 bmse011614 1 18 bmse011614 1 19 bmse011614 1 20 bmse011614 1 21 bmse011614 1 22 bmse011614 1 23 bmse011614 1 24 bmse011614 1 25 bmse011614 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 3.3664 bmse011614 1 2 1 3.3759 bmse011614 1 3 1 3.3852 bmse011614 1 4 1 3.8977 bmse011614 1 5 1 3.9004 bmse011614 1 6 1 1.3886 bmse011614 1 7 1 0.9011 bmse011614 1 8 1 0.8930 bmse011614 1 9 1 0.8904 bmse011614 1 10 1 0.8822 bmse011614 1 11 1 1.2747 bmse011614 1 12 1 1.2652 bmse011614 1 13 1 1.2652 bmse011614 1 14 1 1.2549 bmse011614 1 15 1 2.1938 bmse011614 1 16 1 2.1896 bmse011614 1 17 1 2.1863 bmse011614 1 18 1 2.1828 bmse011614 1 19 1 2.1786 bmse011614 1 20 1 2.5963 bmse011614 1 21 1 2.6001 bmse011614 1 22 1 2.6029 bmse011614 1 23 1 2.6056 bmse011614 1 24 1 2.6095 bmse011614 1 25 1 4.6500 bmse011614 1 stop_ save_