data_bmse011656 ####################### # Entry information # ####################### save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmse011656 _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/bmse011656 loop_ _Entry_experimental_methods.ID _Entry_experimental_methods.Method _Entry_experimental_methods.Subtype _Entry_experimental_methods.Entry_ID 1 NMR solution bmse011656 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. . bmse011656 2 Christian Richter C. . bmse011656 3 Till Kuehn T. . bmse011656 4 Kamal Azzaoui K. . bmse011656 5 Marcel Blommers M. J.J. bmse011656 6 Rebecca 'Del Conte' R. . bmse011656 7 Marco Fragai M. . bmse011656 8 Nils Trieloff N. . bmse011656 9 Peter Schmieder P. . bmse011656 10 Marc Nazare M. . bmse011656 11 Edgar Specker E. . bmse011656 12 Vladimir Ivanov V. . bmse011656 13 Hartmut Oschkinat H. . bmse011656 14 Lucia Banci L. . bmse011656 15 Harald Schwalbe H. . bmse011656 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Entry_ID 1 iNEXT 'Infrastructure for NMR' bmse011656 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID spectral_peak_list 1 bmse011656 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID '1H chemical shifts' 9 bmse011656 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 bmse011656 stop_ loop_ _Auxiliary_files.ID _Auxiliary_files.Name _Auxiliary_files.Format _Auxiliary_files.URI _Auxiliary_files.Details _Auxiliary_files.Entry_ID 3 bmse011656.sdf sdf na 'Structure Definition File' bmse011656 stop_ save_ ############### # Citations # ############### save_entry_citation _Citation.Sf_category citations _Citation.Sf_framecode entry_citation _Citation.Entry_ID bmse011656 _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. . bmse011656 1 2 Christian Richter C. . bmse011656 1 3 Till Kuehn T. . bmse011656 1 4 Kamal Azzaoui K. . bmse011656 1 5 Marcel Blommers M. J.J. bmse011656 1 6 Rebecca 'Del Conte' R. . bmse011656 1 7 Marco Fragai M. . bmse011656 1 8 Nils Trieloff N. . bmse011656 1 9 Peter Schmieder P. . bmse011656 1 10 Marc Nazare M. . bmse011656 1 11 Edgar Specker E. . bmse011656 1 12 Vladimir Ivanov V. . bmse011656 1 13 Hartmut Oschkinat H. . bmse011656 1 14 Lucia Banci L. . bmse011656 1 15 Harald Schwalbe H. . bmse011656 1 stop_ save_ ############################################# # Molecular system (assembly) description # ############################################# save_assembly_1 _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly_1 _Assembly.Entry_ID bmse011656 _Assembly.ID 1 _Assembly.Name cyclopropyl-[4-(4-fluorophenyl)piperazin-1-yl]methanone _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 Z30620520 1 $entity_1 yes native no no bmse011656 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 Z30620520 C1 C bmse011656 1 2 1 1 1 1 Z30620520 C2 C bmse011656 1 3 1 1 1 1 Z30620520 C3 C bmse011656 1 4 1 1 1 1 Z30620520 C4 C bmse011656 1 5 1 1 1 1 Z30620520 C5 C bmse011656 1 6 1 1 1 1 Z30620520 C6 C bmse011656 1 7 1 1 1 1 Z30620520 C7 C bmse011656 1 8 1 1 1 1 Z30620520 C8 C bmse011656 1 9 1 1 1 1 Z30620520 C9 C bmse011656 1 10 1 1 1 1 Z30620520 C10 C bmse011656 1 11 1 1 1 1 Z30620520 C11 C bmse011656 1 12 1 1 1 1 Z30620520 C12 C bmse011656 1 13 1 1 1 1 Z30620520 C13 C bmse011656 1 14 1 1 1 1 Z30620520 C14 C bmse011656 1 15 1 1 1 1 Z30620520 F15 F bmse011656 1 16 1 1 1 1 Z30620520 N16 N bmse011656 1 17 1 1 1 1 Z30620520 N17 N bmse011656 1 18 1 1 1 1 Z30620520 O18 O bmse011656 1 19 1 1 1 1 Z30620520 H19 H bmse011656 1 20 1 1 1 1 Z30620520 H20 H bmse011656 1 21 1 1 1 1 Z30620520 H21 H bmse011656 1 22 1 1 1 1 Z30620520 H22 H bmse011656 1 23 1 1 1 1 Z30620520 H23 H bmse011656 1 24 1 1 1 1 Z30620520 H24 H bmse011656 1 25 1 1 1 1 Z30620520 H25 H bmse011656 1 26 1 1 1 1 Z30620520 H26 H bmse011656 1 27 1 1 1 1 Z30620520 H27 H bmse011656 1 28 1 1 1 1 Z30620520 H28 H bmse011656 1 29 1 1 1 1 Z30620520 H29 H bmse011656 1 30 1 1 1 1 Z30620520 H30 H bmse011656 1 31 1 1 1 1 Z30620520 H31 H bmse011656 1 32 1 1 1 1 Z30620520 H32 H bmse011656 1 33 1 1 1 1 Z30620520 H33 H bmse011656 1 34 1 1 1 1 Z30620520 H34 H bmse011656 1 35 1 1 1 1 Z30620520 H35 H bmse011656 1 stop_ save_ #################################### # Biological polymers and ligands # #################################### save_entity_1 _Entity.Sf_category entity _Entity.Sf_framecode entity_1 _Entity.Entry_ID bmse011656 _Entity.ID 1 _Entity.Name cyclopropyl-[4-(4-fluorophenyl)piperazin-1-yl]methanone _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_linkage no _Entity.Nonpolymer_comp_ID Z30620520 _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 248.2959831999998 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 Z30620520 $chem_comp_1 bmse011656 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 bmse011656 _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 bmse011656 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 bmse011656 _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' bmse011656 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 bmse011656 _Chem_comp.ID Z30620520 _Chem_comp.Provenance iNEXT _Chem_comp.Name cyclopropyl-[4-(4-fluorophenyl)piperazin-1-yl]methanone _Chem_comp.Type non-polymer _Chem_comp.Number_atoms_all 35 _Chem_comp.Number_atoms_nh 18 _Chem_comp.InChI_code InChI=1S/C14H17FN2O/c15-12-3-5-13(6-4-12)16-7-9-17(10-8-16)14(18)11-1-2-11/h3-6,11H,1-2,7-10H2 _Chem_comp.Synonyms P7_H10 _Chem_comp.Formal_charge 0 _Chem_comp.Paramagnetic no _Chem_comp.Formula C14H17FN2O _Chem_comp.Formula_weight 248.2959831999998 _Chem_comp.Formula_mono_iso_wt_nat 248.132491394 _Chem_comp.Formula_mono_iso_wt_13C 262.17945912600027 _Chem_comp.Formula_mono_iso_wt_15N 250.12656118 _Chem_comp.Formula_mono_iso_wt_13C_15N 264.17352891200034 _Chem_comp.Image_file_name bmse011656.png _Chem_comp.Image_file_format png _Chem_comp.Struct_file_name bmse011656.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(N1CCN(C2=CC=C(F)C=C2)CC1)C3CC3 SMILES Bruker_TopSpin_FBS na bmse011656 Z30620520 O=C(C1CC1)N1CCN(c2ccc(F)cc2)CC1 SMILES_CANONICAL RDKit 2017.09.3 bmse011656 Z30620520 O=C(C1CC1)N1CCN(c2ccc(F)cc2)CC1 SMILES_ISOMERIC RDKit 2017.09.3 bmse011656 Z30620520 O=C(C1CC1)N1CCN(c2ccc(F)cc2)CC1 SMILES RDKit 2017.09.3 bmse011656 Z30620520 O=C(C1CC1)N1CCN(CC1)c1ccc(cc1)F SMILES_CANONICAL OpenBabel 2.3.2 bmse011656 Z30620520 O=C(C1CC1)N1CCN(CC1)c1ccc(cc1)F SMILES OpenBabel 2.3.2 bmse011656 Z30620520 InChI=1S/C14H17FN2O/c15-12-3-5-13(6-4-12)16-7-9-17(10-8-16)14(18)11-1-2-11/h3-6,11H,1-2,7-10H2 InChI OpenBabel 2.3.2 bmse011656 Z30620520 FYCKRJKFEXRNGG-UHFFFAOYSA-N InChI_KEY OpenBabel 2.3.2 bmse011656 Z30620520 InChI=1S/C14H17FN2O/c15-12-3-5-13(6-4-12)16-7-9-17(10-8-16)14(18)11-1-2-11/h3-6,11H,1-2,7-10H2 InChI ALATIS na bmse011656 Z30620520 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 cyclopropyl-[4-(4-fluorophenyl)piperazin-1-yl]methanone 'IUPAC NAME' http://cactus.nci.nih.gov/chemical/structure na bmse011656 Z30620520 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 bmse011656 Z30620520 C2 C N 0 no 2 bmse011656 Z30620520 C3 C N 0 yes 3 bmse011656 Z30620520 C4 C N 0 yes 4 bmse011656 Z30620520 C5 C N 0 yes 5 bmse011656 Z30620520 C6 C N 0 yes 6 bmse011656 Z30620520 C7 C N 0 no 7 bmse011656 Z30620520 C8 C N 0 no 8 bmse011656 Z30620520 C9 C N 0 no 9 bmse011656 Z30620520 C10 C N 0 no 10 bmse011656 Z30620520 C11 C N 0 no 11 bmse011656 Z30620520 C12 C N 0 yes 12 bmse011656 Z30620520 C13 C N 0 yes 13 bmse011656 Z30620520 C14 C N 0 no 14 bmse011656 Z30620520 F15 F N 0 no 15 bmse011656 Z30620520 N16 N N 0 no 16 bmse011656 Z30620520 N17 N N 0 no 17 bmse011656 Z30620520 O18 O N 0 no 18 bmse011656 Z30620520 H19 H N 0 no 19 bmse011656 Z30620520 H20 H N 0 no 20 bmse011656 Z30620520 H21 H N 0 no 21 bmse011656 Z30620520 H22 H N 0 no 22 bmse011656 Z30620520 H23 H N 0 no 23 bmse011656 Z30620520 H24 H N 0 no 24 bmse011656 Z30620520 H25 H N 0 no 25 bmse011656 Z30620520 H26 H N 0 no 26 bmse011656 Z30620520 H27 H N 0 no 27 bmse011656 Z30620520 H28 H N 0 no 28 bmse011656 Z30620520 H29 H N 0 no 29 bmse011656 Z30620520 H30 H N 0 no 30 bmse011656 Z30620520 H31 H N 0 no 31 bmse011656 Z30620520 H32 H N 0 no 32 bmse011656 Z30620520 H33 H N 0 no 33 bmse011656 Z30620520 H34 H N 0 no 34 bmse011656 Z30620520 H35 H N 0 no 35 bmse011656 Z30620520 stop_ loop_ _Atom_nomenclature.Naming_system _Atom_nomenclature.Atom_name _Atom_nomenclature.Atom_ID _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID author C5 C1 bmse011656 Z30620520 author C6 C2 bmse011656 Z30620520 author C16 C3 bmse011656 Z30620520 author C17 C4 bmse011656 Z30620520 author C13 C5 bmse011656 Z30620520 author C14 C6 bmse011656 Z30620520 author C10 C7 bmse011656 Z30620520 author C11 C8 bmse011656 Z30620520 author C8 C9 bmse011656 Z30620520 author C9 C10 bmse011656 Z30620520 author C4 C11 bmse011656 Z30620520 author C15 C12 bmse011656 Z30620520 author C7 C13 bmse011656 Z30620520 author C1 C14 bmse011656 Z30620520 author F18 F15 bmse011656 Z30620520 author N3 N16 bmse011656 Z30620520 author N2 N17 bmse011656 Z30620520 author O12 O18 bmse011656 Z30620520 author H20 H19 bmse011656 Z30620520 author H21 H20 bmse011656 Z30620520 author H22 H21 bmse011656 Z30620520 author H23 H22 bmse011656 Z30620520 author H34 H23 bmse011656 Z30620520 author H35 H24 bmse011656 Z30620520 author H32 H25 bmse011656 Z30620520 author H33 H26 bmse011656 Z30620520 author H28 H27 bmse011656 Z30620520 author H29 H28 bmse011656 Z30620520 author H30 H29 bmse011656 Z30620520 author H31 H30 bmse011656 Z30620520 author H24 H31 bmse011656 Z30620520 author H25 H32 bmse011656 Z30620520 author H26 H33 bmse011656 Z30620520 author H27 H34 bmse011656 Z30620520 author H19 H35 bmse011656 Z30620520 ALATIS C1 C1 bmse011656 Z30620520 ALATIS C2 C2 bmse011656 Z30620520 ALATIS C3 C3 bmse011656 Z30620520 ALATIS C4 C4 bmse011656 Z30620520 ALATIS C5 C5 bmse011656 Z30620520 ALATIS C6 C6 bmse011656 Z30620520 ALATIS C7 C7 bmse011656 Z30620520 ALATIS C8 C8 bmse011656 Z30620520 ALATIS C9 C9 bmse011656 Z30620520 ALATIS C10 C10 bmse011656 Z30620520 ALATIS C11 C11 bmse011656 Z30620520 ALATIS C12 C12 bmse011656 Z30620520 ALATIS C13 C13 bmse011656 Z30620520 ALATIS C14 C14 bmse011656 Z30620520 ALATIS F15 F15 bmse011656 Z30620520 ALATIS N16 N16 bmse011656 Z30620520 ALATIS N17 N17 bmse011656 Z30620520 ALATIS O18 O18 bmse011656 Z30620520 ALATIS H19 H19 bmse011656 Z30620520 ALATIS H20 H20 bmse011656 Z30620520 ALATIS H21 H21 bmse011656 Z30620520 ALATIS H22 H22 bmse011656 Z30620520 ALATIS H23 H23 bmse011656 Z30620520 ALATIS H24 H24 bmse011656 Z30620520 ALATIS H25 H25 bmse011656 Z30620520 ALATIS H26 H26 bmse011656 Z30620520 ALATIS H27 H27 bmse011656 Z30620520 ALATIS H28 H28 bmse011656 Z30620520 ALATIS H29 H29 bmse011656 Z30620520 ALATIS H30 H30 bmse011656 Z30620520 ALATIS H31 H31 bmse011656 Z30620520 ALATIS H32 H32 bmse011656 Z30620520 ALATIS H33 H33 bmse011656 Z30620520 ALATIS H34 H34 bmse011656 Z30620520 ALATIS H35 H35 bmse011656 Z30620520 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 bmse011656 Z30620520 2 covalent AROM C4 C6 yes N 2 bmse011656 Z30620520 3 covalent AROM C4 C12 yes N 3 bmse011656 Z30620520 4 covalent AROM C5 C13 yes N 4 bmse011656 Z30620520 5 covalent AROM C6 C13 yes N 5 bmse011656 Z30620520 6 covalent AROM C12 C3 yes N 6 bmse011656 Z30620520 7 carbonyl DOUB O18 C14 no N 7 bmse011656 Z30620520 8 covalent SING C1 C11 no N 8 bmse011656 Z30620520 9 covalent SING C1 H19 no N 9 bmse011656 Z30620520 10 covalent SING C1 H20 no N 10 bmse011656 Z30620520 11 covalent SING C2 C1 no N 11 bmse011656 Z30620520 12 covalent SING C2 C11 no N 12 bmse011656 Z30620520 13 covalent SING C2 H21 no N 13 bmse011656 Z30620520 14 covalent SING C2 H22 no N 14 bmse011656 Z30620520 15 covalent SING C3 H23 no N 15 bmse011656 Z30620520 16 covalent SING C4 H24 no N 16 bmse011656 Z30620520 17 covalent SING C5 H25 no N 17 bmse011656 Z30620520 18 covalent SING C6 H26 no N 18 bmse011656 Z30620520 19 covalent SING C7 C9 no N 19 bmse011656 Z30620520 20 covalent SING C7 N16 no N 20 bmse011656 Z30620520 21 covalent SING C7 H27 no N 21 bmse011656 Z30620520 22 covalent SING C7 H28 no N 22 bmse011656 Z30620520 23 covalent SING C8 C10 no N 23 bmse011656 Z30620520 24 covalent SING C8 H29 no N 24 bmse011656 Z30620520 25 covalent SING C8 H30 no N 25 bmse011656 Z30620520 26 covalent SING C9 N17 no N 26 bmse011656 Z30620520 27 covalent SING C9 H31 no N 27 bmse011656 Z30620520 28 covalent SING C9 H32 no N 28 bmse011656 Z30620520 29 covalent SING C10 N17 no N 29 bmse011656 Z30620520 30 covalent SING C10 H33 no N 30 bmse011656 Z30620520 31 covalent SING C10 H34 no N 31 bmse011656 Z30620520 32 covalent SING C11 C14 no N 32 bmse011656 Z30620520 33 covalent SING C11 H35 no N 33 bmse011656 Z30620520 34 covalent SING C13 N16 no N 34 bmse011656 Z30620520 35 covalent SING F15 C12 no N 35 bmse011656 Z30620520 36 covalent SING N16 C8 no N 36 bmse011656 Z30620520 37 amide SING N17 C14 no N 37 bmse011656 Z30620520 stop_ loop_ _Chem_comp_db_link.Author_supplied _Chem_comp_db_link.Database_code _Chem_comp_db_link.Accession_code _Chem_comp_db_link.Accession_code_type _Chem_comp_db_link.Entry_ID _Chem_comp_db_link.Comp_ID no 'wwPDB CCD' GX4 'comp ID' bmse011656 Z30620520 stop_ save_ ##################################### # Sample contents and methodology # ##################################### ######################## # Sample description # ######################## save_sample_1 _Sample.Sf_category sample _Sample.Sf_framecode sample_1 _Sample.Entry_ID bmse011656 _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 Z30620520 'natural abundance' 1 $assembly_1 1 $entity_1 solute 1 mM bmse011656 1 2 'Potassium phosphate' 'natural abundance' . . . . buffer 25 mM bmse011656 1 3 'Potassium chloride' 'natural abundance' . . . . salt 50 mM bmse011656 1 4 'Magnesium chloride' 'natural abundance' . . . . salt 5 mM bmse011656 1 5 D2O 'natural abundance' . . . . solvent 9 % bmse011656 1 6 H2O 'natural abundance' . . . . solvent 90 % bmse011656 1 7 DMSO '[2H U-100%]' . . . . solvent 1 % bmse011656 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 bmse011656 _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 bmse011656 1 pressure 1 . atm bmse011656 1 temperature 298 0.1 K bmse011656 1 stop_ save_ ############################ # Computer software used # ############################ save_software_topspin _Software.Sf_category software _Software.Sf_framecode software_topspin _Software.Entry_ID bmse011656 _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/ bmse011656 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID 'data analysis' bmse011656 1 'peak picking' bmse011656 1 processing bmse011656 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 bmse011656 _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 bmse011656 _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 bmse011656 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/ bmse011656 1 1 cmcproject.xml text/xml 'spectrum analysis' nmr/set01/1/pdata/1/ bmse011656 1 1 multiplet.txt text 'Peak list' nmr/set01/1/pdata/1/ bmse011656 1 1 spectrum_overview.pdf pdf 'Spectrum image' nmr/set01/1/pdata/1/ bmse011656 1 1 spectrum_overview.png image/png 'Spectral image' nmr/set01/1/pdata/1/ bmse011656 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 bmse011656 _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 bmse011656 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 bmse011656 _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 bmse011656 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 bmse011656 1 stop_ loop_ _Peak.ID _Peak.Entry_ID _Peak.Spectral_peak_list_ID 1 bmse011656 1 2 bmse011656 1 3 bmse011656 1 4 bmse011656 1 5 bmse011656 1 6 bmse011656 1 7 bmse011656 1 8 bmse011656 1 9 bmse011656 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 7.0565 d_4H bmse011656 1 2 1 4.6500 SUP bmse011656 1 3 1 3.6673 t_2H_Q1 bmse011656 1 4 1 0.8077 m_4H bmse011656 1 5 1 3.8862 t_2H bmse011656 1 6 1 2.6030 DMSO bmse011656 1 7 1 3.0328 t_2H bmse011656 1 8 1 3.1252 t_2H bmse011656 1 9 1 1.9355 t_1H bmse011656 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 6.2722 bmse011656 1 2 2 1 0.0000 bmse011656 1 3 3 1 5.0068 bmse011656 1 4 4 1 3.1573 bmse011656 1 5 5 1 5.0068 bmse011656 1 6 6 1 1.8982 bmse011656 1 7 7 1 5.0618 bmse011656 1 8 8 1 5.0068 bmse011656 1 9 9 1 8.0329 bmse011656 1 stop_ loop_ _Spectral_transition.ID _Spectral_transition.Entry_ID _Spectral_transition.Spectral_peak_list_ID 1 bmse011656 1 2 bmse011656 1 3 bmse011656 1 4 bmse011656 1 5 bmse011656 1 6 bmse011656 1 7 bmse011656 1 8 bmse011656 1 9 bmse011656 1 10 bmse011656 1 11 bmse011656 1 12 bmse011656 1 13 bmse011656 1 14 bmse011656 1 15 bmse011656 1 16 bmse011656 1 17 bmse011656 1 18 bmse011656 1 19 bmse011656 1 20 bmse011656 1 21 bmse011656 1 22 bmse011656 1 23 bmse011656 1 24 bmse011656 1 25 bmse011656 1 26 bmse011656 1 27 bmse011656 1 28 bmse011656 1 29 bmse011656 1 30 bmse011656 1 31 bmse011656 1 32 bmse011656 1 33 bmse011656 1 34 bmse011656 1 35 bmse011656 1 36 bmse011656 1 37 bmse011656 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 7.0513 bmse011656 1 2 1 7.0617 bmse011656 1 3 1 4.6500 bmse011656 1 4 1 3.6590 bmse011656 1 5 1 3.6674 bmse011656 1 6 1 3.6757 bmse011656 1 7 1 0.8418 bmse011656 1 8 1 0.8336 bmse011656 1 9 1 0.8292 bmse011656 1 10 1 0.8241 bmse011656 1 11 1 0.8204 bmse011656 1 12 1 0.8156 bmse011656 1 13 1 0.8109 bmse011656 1 14 1 0.8028 bmse011656 1 15 1 0.7995 bmse011656 1 16 1 0.7945 bmse011656 1 17 1 0.7912 bmse011656 1 18 1 0.7867 bmse011656 1 19 1 0.7821 bmse011656 1 20 1 0.7735 bmse011656 1 21 1 3.8779 bmse011656 1 22 1 3.8863 bmse011656 1 23 1 3.8946 bmse011656 1 24 1 2.5967 bmse011656 1 25 1 2.5998 bmse011656 1 26 1 2.6029 bmse011656 1 27 1 2.6060 bmse011656 1 28 1 2.6093 bmse011656 1 29 1 3.0244 bmse011656 1 30 1 3.0328 bmse011656 1 31 1 3.0413 bmse011656 1 32 1 3.1168 bmse011656 1 33 1 3.1251 bmse011656 1 34 1 3.1335 bmse011656 1 35 1 1.9221 bmse011656 1 36 1 1.9355 bmse011656 1 37 1 1.9489 bmse011656 1 stop_ save_