data_bmse011047 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse011047 _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/bmse011047 loop_ _Entry_experimental_methods.ID _Entry_experimental_methods.Method _Entry_experimental_methods.Subtype _Entry_experimental_methods.Entry_ID 1 NMR solution bmse011047 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. . bmse011047 2 Christian Richter C. . bmse011047 3 Till Kuehn T. . bmse011047 4 Kamal Azzaoui K. . bmse011047 5 Marcel Blommers M. J.J. bmse011047 6 Rebecca 'Del Conte' R. . bmse011047 7 Marco Fragai M. . bmse011047 8 Nils Trieloff N. . bmse011047 9 Peter Schmieder P. . bmse011047 10 Marc Nazare M. . bmse011047 11 Edgar Specker E. . bmse011047 12 Vladimir Ivanov V. . bmse011047 13 Hartmut Oschkinat H. . bmse011047 14 Lucia Banci L. . bmse011047 15 Harald Schwalbe H. . bmse011047 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Entry_ID 1 iNEXT 'Infrastructure for NMR' bmse011047 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID spectral_peak_list 1 bmse011047 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 8 bmse011047 stop_ loop_ _Release.Release_number _Release.Format_type _Release.Format_version _Release.Date _Release.Type _Release.Author _Release.Entry_ID 1 NMR-STAR 3.2.11.4 2020-09-15 original author bmse011047 stop_ loop_ _Auxiliary_files.ID _Auxiliary_files.Name _Auxiliary_files.Format _Auxiliary_files.URI _Auxiliary_files.Details _Auxiliary_files.Entry_ID 3 bmse011047.sdf sdf na 'Structure Definition File' bmse011047 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID bmse011047 _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. . bmse011047 1 2 Christian Richter C. . bmse011047 1 3 Till Kuehn T. . bmse011047 1 4 Kamal Azzaoui K. . bmse011047 1 5 Marcel Blommers M. J.J. bmse011047 1 6 Rebecca 'Del Conte' R. . bmse011047 1 7 Marco Fragai M. . bmse011047 1 8 Nils Trieloff N. . bmse011047 1 9 Peter Schmieder P. . bmse011047 1 10 Marc Nazare M. . bmse011047 1 11 Edgar Specker E. . bmse011047 1 12 Vladimir Ivanov V. . bmse011047 1 13 Hartmut Oschkinat H. . bmse011047 1 14 Lucia Banci L. . bmse011047 1 15 Harald Schwalbe H. . bmse011047 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly_1 _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly_1 _Assembly.Entry_ID bmse011047 _Assembly.ID 1 _Assembly.Name N-(1H-benzimidazol-2-ylmethyl)furan-2-carboxamide _Assembly.Number_of_components 1 _Assembly.Paramagnetic no _Assembly.Thiol_state na loop_ _Entity_assembly.ID _Entity_assembly.Entity_assembly_name _Entity_assembly.Entity_ID _Entity_assembly.Entity_label _Entity_assembly.Experimental_data_reported _Entity_assembly.Physical_state _Entity_assembly.Conformational_isomer _Entity_assembly.Chemical_exchange_state _Entity_assembly.Entry_ID _Entity_assembly.Assembly_ID 1 Z26781964 1 $entity_1 yes native no no bmse011047 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 Z26781964 C1 C bmse011047 1 2 1 1 1 1 Z26781964 C2 C bmse011047 1 3 1 1 1 1 Z26781964 C3 C bmse011047 1 4 1 1 1 1 Z26781964 C4 C bmse011047 1 5 1 1 1 1 Z26781964 C5 C bmse011047 1 6 1 1 1 1 Z26781964 C6 C bmse011047 1 7 1 1 1 1 Z26781964 C7 C bmse011047 1 8 1 1 1 1 Z26781964 C8 C bmse011047 1 9 1 1 1 1 Z26781964 C9 C bmse011047 1 10 1 1 1 1 Z26781964 C10 C bmse011047 1 11 1 1 1 1 Z26781964 C11 C bmse011047 1 12 1 1 1 1 Z26781964 C12 C bmse011047 1 13 1 1 1 1 Z26781964 C13 C bmse011047 1 14 1 1 1 1 Z26781964 N14 N bmse011047 1 15 1 1 1 1 Z26781964 N15 N bmse011047 1 16 1 1 1 1 Z26781964 N16 N bmse011047 1 17 1 1 1 1 Z26781964 O17 O bmse011047 1 18 1 1 1 1 Z26781964 O18 O bmse011047 1 19 1 1 1 1 Z26781964 H19 H bmse011047 1 20 1 1 1 1 Z26781964 H20 H bmse011047 1 21 1 1 1 1 Z26781964 H21 H bmse011047 1 22 1 1 1 1 Z26781964 H22 H bmse011047 1 23 1 1 1 1 Z26781964 H23 H bmse011047 1 24 1 1 1 1 Z26781964 H24 H bmse011047 1 25 1 1 1 1 Z26781964 H25 H bmse011047 1 26 1 1 1 1 Z26781964 H26 H bmse011047 1 27 1 1 1 1 Z26781964 H27 H bmse011047 1 28 1 1 1 1 Z26781964 H28 H bmse011047 1 29 1 1 1 1 Z26781964 H29 H bmse011047 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_entity_1 _Entity.Sf_category entity _Entity.Sf_framecode entity_1 _Entity.Entry_ID bmse011047 _Entity.ID 1 _Entity.Name N-(1H-benzimidazol-2-ylmethyl)furan-2-carboxamide _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID Z26781964 _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 241.24533999999989 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 Z26781964 $chem_comp_1 bmse011047 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 bmse011047 _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 bmse011047 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 bmse011047 _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' bmse011047 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 bmse011047 _Chem_comp.ID Z26781964 _Chem_comp.Provenance iNEXT _Chem_comp.Name N-(1H-benzimidazol-2-ylmethyl)furan-2-carboxamide _Chem_comp.Type non-polymer _Chem_comp.Number_atoms_all 29 _Chem_comp.Number_atoms_nh 18 _Chem_comp.InChI_code InChI=1S/C13H11N3O2/c17-13(11-6-3-7-18-11)14-8-12-15-9-4-1-2-5-10(9)16-12/h1-7H,8H2,(H,14,17)(H,15,16) _Chem_comp.Synonyms P1_G06 _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic no _Chem_comp.Formula C13H11N3O2 _Chem_comp.Formula_weight 241.24533999999989 _Chem_comp.Formula_mono_iso_wt_nat 241.085126607 _Chem_comp.Formula_mono_iso_wt_13C 254.12873950100007 _Chem_comp.Formula_mono_iso_wt_15N 244.07623128600002 _Chem_comp.Formula_mono_iso_wt_13C_15N 257.11984418000014 _Chem_comp.Image_file_name bmse011047.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse011047.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(NCC1=NC=2C=CC=CC2N1)C=3OC=CC3 SMILES Bruker_TopSpin_FBS na bmse011047 Z26781964 O=C(NCc1nc2ccccc2[nH]1)c1ccco1 SMILES_CANONICAL RDKit 2017.09.3 bmse011047 Z26781964 O=C(NCc1nc2ccccc2[nH]1)c1ccco1 SMILES_ISOMERIC RDKit 2017.09.3 bmse011047 Z26781964 O=C(NCc1nc2ccccc2[nH]1)c1ccco1 SMILES RDKit 2017.09.3 bmse011047 Z26781964 O=C(c1ccco1)NCc1nc2c([nH]1)cccc2 SMILES_CANONICAL OpenBabel 2.3.2 bmse011047 Z26781964 O=C(c1ccco1)NCc1nc2c([nH]1)cccc2 SMILES OpenBabel 2.3.2 bmse011047 Z26781964 InChI=1S/C13H11N3O2/c17-13(11-6-3-7-18-11)14-8-12-15-9-4-1-2-5-10(9)16-12/h1-7H,8H2,(H,14,17)(H,15,16) InChI OpenBabel 2.3.2 bmse011047 Z26781964 WFEIYWNIMQWEHE-UHFFFAOYSA-N InChI_KEY OpenBabel 2.3.2 bmse011047 Z26781964 InChI=1S/C13H11N3O2/c17-13(11-6-3-7-18-11)14-8-12-15-9-4-1-2-5-10(9)16-12/h1-7H,8H2,(H,14,17)(H,15,16) InChI ALATIS na bmse011047 Z26781964 stop_ loop_ _Chem_comp_identifier.Identifier _Chem_comp_identifier.Type _Chem_comp_identifier.Program _Chem_comp_identifier.Program_version _Chem_comp_identifier.Entry_ID _Chem_comp_identifier.Comp_ID N-(1H-benzimidazol-2-ylmethyl)furan-2-carboxamide 'IUPAC NAME' http://cactus.nci.nih.gov/chemical/structure na bmse011047 Z26781964 stop_ loop_ _Chem_comp_atom.Atom_ID _Chem_comp_atom.Type_symbol _Chem_comp_atom.Stereo_config _Chem_comp_atom.Charge _Chem_comp_atom.Aromatic_flag _Chem_comp_atom.PDBX_ordinal _Chem_comp_atom.Entry_ID _Chem_comp_atom.Comp_ID C1 C N 0 yes 1 bmse011047 Z26781964 C2 C N 0 yes 2 bmse011047 Z26781964 C3 C N 0 yes 3 bmse011047 Z26781964 C4 C N 0 yes 4 bmse011047 Z26781964 C5 C N 0 yes 5 bmse011047 Z26781964 C6 C N 0 yes 6 bmse011047 Z26781964 C7 C N 0 yes 7 bmse011047 Z26781964 C8 C N 0 no 8 bmse011047 Z26781964 C9 C N 0 yes 9 bmse011047 Z26781964 C10 C N 0 yes 10 bmse011047 Z26781964 C11 C N 0 yes 11 bmse011047 Z26781964 C12 C N 0 yes 12 bmse011047 Z26781964 C13 C N 0 no 13 bmse011047 Z26781964 N14 N N 0 no 14 bmse011047 Z26781964 N15 N N 0 yes 15 bmse011047 Z26781964 N16 N N 0 yes 16 bmse011047 Z26781964 O17 O N 0 no 17 bmse011047 Z26781964 O18 O N 0 yes 18 bmse011047 Z26781964 H19 H N 0 no 19 bmse011047 Z26781964 H20 H N 0 no 20 bmse011047 Z26781964 H21 H N 0 no 21 bmse011047 Z26781964 H22 H N 0 no 22 bmse011047 Z26781964 H23 H N 0 no 23 bmse011047 Z26781964 H24 H N 0 no 24 bmse011047 Z26781964 H25 H N 0 no 25 bmse011047 Z26781964 H26 H N 0 no 26 bmse011047 Z26781964 H27 H N 0 no 27 bmse011047 Z26781964 H28 H N 0 no 28 bmse011047 Z26781964 H29 H N 0 no 29 bmse011047 Z26781964 stop_ loop_ _Atom_nomenclature.Naming_system _Atom_nomenclature.Atom_name _Atom_nomenclature.Atom_ID _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID author C17 C1 bmse011047 Z26781964 author C18 C2 bmse011047 Z26781964 author C14 C3 bmse011047 Z26781964 author C15 C4 bmse011047 Z26781964 author C16 C5 bmse011047 Z26781964 author C10 C6 bmse011047 Z26781964 author C12 C7 bmse011047 Z26781964 author C13 C8 bmse011047 Z26781964 author C6 C9 bmse011047 Z26781964 author C7 C10 bmse011047 Z26781964 author C5 C11 bmse011047 Z26781964 author C2 C12 bmse011047 Z26781964 author C4 C13 bmse011047 Z26781964 author N8 N14 bmse011047 Z26781964 author N1 N15 bmse011047 Z26781964 author N3 N16 bmse011047 Z26781964 author O11 O17 bmse011047 Z26781964 author O9 O18 bmse011047 Z26781964 author H28 H19 bmse011047 Z26781964 author H29 H20 bmse011047 Z26781964 author H25 H21 bmse011047 Z26781964 author H26 H22 bmse011047 Z26781964 author H27 H23 bmse011047 Z26781964 author H21 H24 bmse011047 Z26781964 author H22 H25 bmse011047 Z26781964 author H23 H26 bmse011047 Z26781964 author H24 H27 bmse011047 Z26781964 author H20 H28 bmse011047 Z26781964 author H19 H29 bmse011047 Z26781964 ALATIS C1 C1 bmse011047 Z26781964 ALATIS C2 C2 bmse011047 Z26781964 ALATIS C3 C3 bmse011047 Z26781964 ALATIS C4 C4 bmse011047 Z26781964 ALATIS C5 C5 bmse011047 Z26781964 ALATIS C6 C6 bmse011047 Z26781964 ALATIS C7 C7 bmse011047 Z26781964 ALATIS C8 C8 bmse011047 Z26781964 ALATIS C9 C9 bmse011047 Z26781964 ALATIS C10 C10 bmse011047 Z26781964 ALATIS C11 C11 bmse011047 Z26781964 ALATIS C12 C12 bmse011047 Z26781964 ALATIS C13 C13 bmse011047 Z26781964 ALATIS N14 N14 bmse011047 Z26781964 ALATIS N15 N15 bmse011047 Z26781964 ALATIS N16 N16 bmse011047 Z26781964 ALATIS O17 O17 bmse011047 Z26781964 ALATIS O18 O18 bmse011047 Z26781964 ALATIS H19 H19 bmse011047 Z26781964 ALATIS H20 H20 bmse011047 Z26781964 ALATIS H21 H21 bmse011047 Z26781964 ALATIS H22 H22 bmse011047 Z26781964 ALATIS H23 H23 bmse011047 Z26781964 ALATIS H24 H24 bmse011047 Z26781964 ALATIS H25 H25 bmse011047 Z26781964 ALATIS H26 H26 bmse011047 Z26781964 ALATIS H27 H27 bmse011047 Z26781964 ALATIS H28 H28 bmse011047 Z26781964 ALATIS H29 H29 bmse011047 Z26781964 stop_ loop_ _Chem_comp_bond.ID _Chem_comp_bond.Type _Chem_comp_bond.Value_order _Chem_comp_bond.Atom_ID_1 _Chem_comp_bond.Atom_ID_2 _Chem_comp_bond.Aromatic_flag _Chem_comp_bond.Stereo_config _Chem_comp_bond.Ordinal _Chem_comp_bond.Entry_ID _Chem_comp_bond.Comp_ID 1 covalent AROM C1 C4 yes N 1 bmse011047 Z26781964 2 covalent AROM C2 C1 yes N 2 bmse011047 Z26781964 3 covalent AROM C2 C5 yes N 3 bmse011047 Z26781964 4 covalent AROM C3 C6 yes N 4 bmse011047 Z26781964 5 covalent AROM C4 C9 yes N 5 bmse011047 Z26781964 6 covalent AROM C5 C10 yes N 6 bmse011047 Z26781964 7 covalent AROM C6 C11 yes N 7 bmse011047 Z26781964 8 covalent AROM C7 C3 yes N 8 bmse011047 Z26781964 9 covalent AROM C7 O18 yes N 9 bmse011047 Z26781964 10 covalent AROM C9 N15 yes N 10 bmse011047 Z26781964 11 covalent AROM C10 C9 yes N 11 bmse011047 Z26781964 12 covalent AROM C12 N15 yes N 12 bmse011047 Z26781964 13 covalent AROM N16 C10 yes N 13 bmse011047 Z26781964 14 covalent AROM N16 C12 yes N 14 bmse011047 Z26781964 15 covalent AROM O18 C11 yes N 15 bmse011047 Z26781964 16 carbonyl DOUB O17 C13 no N 16 bmse011047 Z26781964 17 covalent SING C1 H19 no N 17 bmse011047 Z26781964 18 covalent SING C2 H20 no N 18 bmse011047 Z26781964 19 covalent SING C3 H21 no N 19 bmse011047 Z26781964 20 covalent SING C4 H22 no N 20 bmse011047 Z26781964 21 covalent SING C5 H23 no N 21 bmse011047 Z26781964 22 covalent SING C6 H24 no N 22 bmse011047 Z26781964 23 covalent SING C7 H25 no N 23 bmse011047 Z26781964 24 covalent SING C8 C12 no N 24 bmse011047 Z26781964 25 covalent SING C8 H26 no N 25 bmse011047 Z26781964 26 covalent SING C8 H27 no N 26 bmse011047 Z26781964 27 covalent SING C11 C13 no N 27 bmse011047 Z26781964 28 amide SING C13 N14 no N 28 bmse011047 Z26781964 29 covalent SING N14 C8 no N 29 bmse011047 Z26781964 30 covalent SING N14 H28 no N 30 bmse011047 Z26781964 31 covalent SING N16 H29 no N 31 bmse011047 Z26781964 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse011047 _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 Z26781964 'natural abundance' 1 $assembly_1 1 $entity_1 solute 1 mM bmse011047 1 2 'Potassium phosphate' 'natural abundance' . . . . buffer 25 mM bmse011047 1 3 'Potassium chloride' 'natural abundance' . . . . salt 50 mM bmse011047 1 4 'Magnesium chloride' 'natural abundance' . . . . salt 5 mM bmse011047 1 5 D2O 'natural abundance' . . . . solvent 9 % bmse011047 1 6 H2O 'natural abundance' . . . . solvent 90 % bmse011047 1 7 DMSO '[2H U-100%]' . . . . solvent 1 % bmse011047 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 bmse011047 _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 bmse011047 1 pressure 1 . atm bmse011047 1 temperature 298 0.1 K bmse011047 1 stop_ save_ ############################ # Computer software used # ############################ save_software_topspin _Software.Sf_category software _Software.Sf_framecode software_topspin _Software.Entry_ID bmse011047 _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/ bmse011047 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'data analysis' bmse011047 1 'peak picking' bmse011047 1 processing bmse011047 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 bmse011047 _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 bmse011047 _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 bmse011047 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/ bmse011047 1 1 cmcproject.xml text/xml 'spectrum analysis' nmr/set01/1/pdata/1/ bmse011047 1 1 multiplet.txt text 'Peak list' nmr/set01/1/pdata/1/ bmse011047 1 1 spectrum_overview.pdf pdf 'Spectrum image' nmr/set01/1/pdata/1/ bmse011047 1 1 spectrum_overview.png image/png 'Spectral image' nmr/set01/1/pdata/1/ bmse011047 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 bmse011047 _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 bmse011047 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 bmse011047 _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 bmse011047 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 bmse011047 1 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse011047 1 2 bmse011047 1 3 bmse011047 1 4 bmse011047 1 5 bmse011047 1 6 bmse011047 1 8 bmse011047 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 7.1568 10_d_Q2 bmse011047 1 2 1 7.2704 17,18_m bmse011047 1 3 1 7.6427 12_s_Q3 bmse011047 1 4 1 7.5574 15,16_m bmse011047 1 5 1 2.6024 DMSO bmse011047 1 6 1 6.5805 14_dd_Q1 bmse011047 1 7 1 4.6500 SUP bmse011047 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 3.6313 bmse011047 1 2 2 1 56.3441 bmse011047 1 3 3 1 0.0000 bmse011047 1 4 4 1 45.4000 bmse011047 1 5 5 1 1.7056 bmse011047 1 6 6 1 3.4662 bmse011047 1 7 6 1 1.7056 bmse011047 1 8 7 1 0.0000 bmse011047 1 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse011047 1 2 bmse011047 1 3 bmse011047 1 4 bmse011047 1 5 bmse011047 1 6 bmse011047 1 7 bmse011047 1 8 bmse011047 1 9 bmse011047 1 10 bmse011047 1 11 bmse011047 1 12 bmse011047 1 13 bmse011047 1 14 bmse011047 1 15 bmse011047 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 7.1537 bmse011047 1 2 1 7.1598 bmse011047 1 3 1 7.3174 bmse011047 1 4 1 7.2235 bmse011047 1 5 1 7.6427 bmse011047 1 6 1 7.5952 bmse011047 1 7 1 7.5196 bmse011047 1 8 1 2.6053 bmse011047 1 9 1 2.6023 bmse011047 1 10 1 2.5996 bmse011047 1 11 1 6.5848 bmse011047 1 12 1 6.5819 bmse011047 1 13 1 6.5790 bmse011047 1 14 1 6.5762 bmse011047 1 15 1 4.6500 bmse011047 1 stop_ save_