data_bmse011926

#######################
#  Entry information  #
#######################

save_entry_information_1
   _Entry.Sf_category                       entry_information
   _Entry.Sf_framecode                      entry_information_1
   _Entry.ID                                bmse011926
   _Entry.Title                             3-amino-N-cyclopropylbenzamide
   _Entry.Type                              'metabolite/natural product'
   _Entry.Version_type                      original
   _Entry.Submission_date                   2023-04-05
   _Entry.Accession_date                    2023-04-05
   _Entry.Last_release_date                 2023-08-11
   _Entry.Original_release_date             2023-08-11
   _Entry.Origination                       author
   _Entry.NMR_STAR_version                  3.2.10.4
   _Entry.Experimental_method               NMR
   _Entry.Experimental_method_subtype       solution
   _Entry.DOI                               10.12018/bmse011926

   loop_
      _Entry_experimental_methods.ID
      _Entry_experimental_methods.Method
      _Entry_experimental_methods.Subtype
      _Entry_experimental_methods.Entry_ID

     1   NMR   solution   bmse011926    

   stop_

   loop_
      _Entry_author.Ordinal
      _Entry_author.Given_name
      _Entry_author.Family_name
      _Entry_author.First_initial
      _Entry_author.Entry_ID

     1   Sridhar     Sreeramulu   S.   bmse011926    
     2   Christian   Richter      C.   bmse011926    
     3   Harald      Schwalbe     H.   bmse011926    
     4   Hannes      Berg         .    bmse011926    

   stop_

   loop_
      _Entry_src.ID
      _Entry_src.Project_name
      _Entry_src.Entry_ID

     1   EUOS   bmse011926    

   stop_

   loop_
      _Release.Release_number
      _Release.Format_type
      _Release.Format_version
      _Release.Date
      _Release.Type
      _Release.Author
      _Release.Entry_ID

     1   NMR-STAR   3.2.1.18   2023-11-09   original   author   bmse011926    

   stop_

   loop_
      _Auxiliary_files.ID
      _Auxiliary_files.Name
      _Auxiliary_files.Format
      _Auxiliary_files.URI
      _Auxiliary_files.Details
      _Auxiliary_files.Entry_ID

     1   bmse011926.mol   sdf   na   'Structure Definition File'   bmse011926    

   stop_

save_

###############
#  Citations  #
###############

save_citations_1
   _Citation.Sf_category                 citations
   _Citation.Sf_framecode                citations_1
   _Citation.Entry_ID                    bmse011926
   _Citation.ID                          1
   _Citation.PubMed_ID                   32533387
   _Citation.DOI                         10.1007/s10858-020-00327-9
   _Citation.Title                       'NMR quality control of fragment libraries for screening.'
   _Citation.Status                      published
   _Citation.Type                        journal
   _Citation.Journal_abbrev              'J Biomol NMR'
   _Citation.Journal_name_full           'Journal of biomolecular NMR'
   _Citation.Journal_volume              74
   _Citation.Journal_issue               10-11
   _Citation.Journal_ISSN                1573-5001
   _Citation.Page_first                  555
   _Citation.Page_last                   563
   _Citation.Year                        2020

   loop_
      _Citation_author.Ordinal
      _Citation_author.Given_name
      _Citation_author.Family_name
      _Citation_author.First_initial
      _Citation_author.Entry_ID
      _Citation_author.Citation_ID

     1    Sridhar               Sreeramulu    S.   bmse011926   1    
     2    Christian             Richter       C.   bmse011926   1    
     3    Till                  Kuehn         T.   bmse011926   1    
     4    Kamal                 Azzaoui       K.   bmse011926   1    
     5    'Marcel Jules Jose'   Blommers      .    bmse011926   1    
     6    Rebecca               'Del Conte'   R.   bmse011926   1    
     7    Marco                 Fragai        M.   bmse011926   1    
     8    Nils                  Trieloff      N.   bmse011926   1    
     9    Peter                 Schmieder     P.   bmse011926   1    
     10   Marc                  Nazare        M.   bmse011926   1    
     11   Edgar                 Specker       E.   bmse011926   1    
     12   Vladimir              Ivanov        V.   bmse011926   1    
     13   Hartmut               Oschkinat     H.   bmse011926   1    
     14   Lucia                 Banci         L.   bmse011926   1    
     15   Harald                Schwalbe      H.   bmse011926   1    

   stop_

save_

#############################################
#  Molecular system (assembly) description  #
#############################################

save_assembly_1
   _Assembly.Sf_category                      assembly
   _Assembly.Sf_framecode                     assembly_1
   _Assembly.Entry_ID                         bmse011926
   _Assembly.ID                               1
   _Assembly.Name                             3-amino-N-cyclopropylbenzamide
   _Assembly.Number_of_components             1
   _Assembly.Thiol_state                      'not present'

   loop_
      _Entity_assembly.ID
      _Entity_assembly.Entity_assembly_name
      _Entity_assembly.Entity_ID
      _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   chem_comp_1   1   yes   native   no   no   bmse011926   1    

   stop_

   loop_
      _Atom.Assembly_atom_ID
      _Atom.Entity_assembly_ID
      _Atom.Entity_ID
      _Atom.Comp_index_ID
      _Atom.Seq_ID
      _Atom.Atom_ID
      _Atom.Type_symbol
      _Atom.Entry_ID
      _Atom.Assembly_ID

     1    1   1   1   1   C1    C   bmse011926   1    
     2    1   1   1   1   C2    C   bmse011926   1    
     3    1   1   1   1   C3    C   bmse011926   1    
     4    1   1   1   1   C4    C   bmse011926   1    
     5    1   1   1   1   C5    C   bmse011926   1    
     6    1   1   1   1   C6    C   bmse011926   1    
     7    1   1   1   1   C7    C   bmse011926   1    
     8    1   1   1   1   C8    C   bmse011926   1    
     9    1   1   1   1   C9    C   bmse011926   1    
     10   1   1   1   1   C10   C   bmse011926   1    
     11   1   1   1   1   N11   N   bmse011926   1    
     12   1   1   1   1   N12   N   bmse011926   1    
     13   1   1   1   1   O13   O   bmse011926   1    

   stop_

save_

    ####################################
    #  Biological polymers and ligands #
    ####################################

save_entity_1
   _Entity.Sf_category                      entity
   _Entity.Sf_framecode                     entity_1
   _Entity.Entry_ID                         bmse011926
   _Entity.ID                               1
   _Entity.Name                             3-amino-N-cyclopropylbenzamide
   _Entity.Type                             non-polymer
   _Entity.Ambiguous_conformational_states  no
   _Entity.Ambiguous_chem_comp_sites        no
   _Entity.Nstd_linkage                     no
   _Entity.Nonpolymer_comp_label            chem_comp_1
   _Entity.Number_of_monomers               1
   _Entity.Number_of_nonpolymer_components  1
   _Entity.Thiol_state                      'not present'
   _Entity.Formula_weight                   176.21508

   loop_
      _Entity_comp_index.ID
      _Entity_comp_index.Auth_seq_ID
      _Entity_comp_index.Comp_label
      _Entity_comp_index.Entry_ID
      _Entity_comp_index.Entity_ID

     1   1   chem_comp_1   bmse011926   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                         bmse011926
   _Chem_comp.Name                             3-amino-N-cyclopropylbenzamide
   _Chem_comp.Number_atoms_all                 13
   _Chem_comp.InChI_code                       InChI=1S/C10H12N2O/c11-8-3-1-2-7(6-8)10(13)12-9-4-5-9/h1-3,6,9H,4-5,11H2,(H,12,13)
   _Chem_comp.Formal_charge                    0
   _Chem_comp.Aromatic                         yes
   _Chem_comp.Formula                          C10H12N2O
   _Chem_comp.Formula_weight                   176.21508
   _Chem_comp.Formula_mono_iso_wt_nat          176.094963014
   _Chem_comp.Formula_mono_iso_wt_13C          186.12851139400004
   _Chem_comp.Formula_mono_iso_wt_15N          178.0890328
   _Chem_comp.Formula_mono_iso_wt_13C_15N      188.12258118000005
   _Chem_comp.Image_file_name                  bmse011926.png
   _Chem_comp.Image_file_format                png
   _Chem_comp.Struct_file_name                 bmse011926.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

     Nc1cccc(C(=O)NC2CC2)c1                                                               SMILES_CANONICAL   RDKit       2022.03.5   bmse011926    
     Nc1cccc(C(=O)NC2CC2)c1                                                               SMILES_ISOMERIC    RDKit       2022.03.5   bmse011926    
     Nc1cccc(C(=O)NC2CC2)c1                                                               SMILES             RDKit       2022.03.5   bmse011926    
     Nc1cccc(c1)C(=O)NC1CC1                                                               SMILES_CANONICAL   OpenBabel   3.1.0       bmse011926    
     Nc1cccc(c1)C(=O)NC1CC1                                                               SMILES             OpenBabel   3.1.0       bmse011926    
     InChI=1S/C10H12N2O/c11-8-3-1-2-7(6-8)10(13)12-9-4-5-9/h1-3,6,9H,4-5,11H2,(H,12,13)   InChI              OpenBabel   3.1.0       bmse011926    
     XTQFXSVIFJUEAP-UHFFFAOYSA-N                                                          InChI_KEY          OpenBabel   3.1.0       bmse011926    
     InChI=1S/C10H12N2O/c11-8-3-1-2-7(6-8)10(13)12-9-4-5-9/h1-3,6,9H,4-5,11H2,(H,12,13)   InChI              ALATIS      na          bmse011926    

   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

     C1    C   N   0   yes   1    bmse011926    
     C2    C   N   0   yes   2    bmse011926    
     C3    C   N   0   yes   3    bmse011926    
     C4    C   N   0   no    4    bmse011926    
     C5    C   N   0   no    5    bmse011926    
     C6    C   N   0   yes   6    bmse011926    
     C7    C   N   0   yes   7    bmse011926    
     C8    C   N   0   yes   8    bmse011926    
     C9    C   N   0   no    9    bmse011926    
     C10   C   N   0   no    10   bmse011926    
     N11   N   N   0   no    11   bmse011926    
     N12   N   N   0   no    12   bmse011926    
     O13   O   N   0   no    13   bmse011926    

   stop_

   loop_
      _Atom_nomenclature.Atom_ID
      _Atom_nomenclature.Atom_name
      _Atom_nomenclature.Naming_system
      _Atom_nomenclature.Entry_ID

     C12   C1    ALATIS   bmse011926    
     C11   C2    ALATIS   bmse011926    
     C13   C3    ALATIS   bmse011926    
     C5    C4    ALATIS   bmse011926    
     C6    C5    ALATIS   bmse011926    
     C8    C6    ALATIS   bmse011926    
     C4    C7    ALATIS   bmse011926    
     C9    C8    ALATIS   bmse011926    
     C3    C9    ALATIS   bmse011926    
     C1    C10   ALATIS   bmse011926    
     N10   N11   ALATIS   bmse011926    
     N2    N12   ALATIS   bmse011926    
     O7    O13   ALATIS   bmse011926    

   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

     1    covalent   AROM   C1    C3    yes   N   1    bmse011926    
     2    covalent   AROM   C2    C1    yes   N   2    bmse011926    
     3    covalent   SING   C4    C5    no    N   3    bmse011926    
     4    covalent   AROM   C6    C8    yes   N   4    bmse011926    
     5    covalent   AROM   C7    C2    yes   N   5    bmse011926    
     6    covalent   AROM   C7    C6    yes   N   6    bmse011926    
     7    covalent   AROM   C8    C3    yes   N   7    bmse011926    
     8    covalent   SING   C8    N11   no    N   8    bmse011926    
     9    covalent   SING   C9    C4    no    N   9    bmse011926    
     10   covalent   SING   C9    C5    no    N   10   bmse011926    
     11   covalent   SING   C10   C7    no    N   11   bmse011926    
     12   amide      SING   C10   N12   no    N   12   bmse011926    
     13   carbonyl   DOUB   C10   O13   no    N   13   bmse011926    
     14   covalent   SING   N12   C9    no    N   14   bmse011926    

   stop_

   loop_
      _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

     EU-OPENSCREEN   EOS102636   'compound ID'   bmse011926    

   stop_

save_

#####################################
#  Sample contents and methodology  #
#####################################
	 
    ########################
    #  Sample description  #
    ########################

save_sample_1
   _Sample.Sf_category                     sample
   _Sample.Sf_framecode                    sample_1
   _Sample.Entry_ID                        bmse011926
   _Sample.ID                              1
   _Sample.Name                            'sample 1'
   _Sample.Type                            solution
   _Sample.Aggregate_sample_number         1

   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   3-amino-N-cyclopropylbenzamide   'natural abundance'   1   $assembly_1   1   $entity_1   solute      2     mM   bmse011926   1    
     2   'Sodium phosphate'               'natural abundance'   .   .             .   .           buffer      25    mM   bmse011926   1    
     3   'Sodium chloride'                'natural abundance'   .   .             .   .           salt        150   mM   bmse011926   1    
     4   DSS                              'natural abundance'   .   .             .   .           reference   10    uM   bmse011926   1    
     5   H2O                              'natural abundance'   .   .             .   .           solvent     95    %    bmse011926   1    
     6   DMSO                             '[2H U-100%]'         .   .             .   .           solvent     5     %    bmse011926   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      bmse011926
   _Sample_condition_list.ID            1
   _Sample_condition_list.Name          'sample conditions 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            7.5   .     pH    bmse011926   1    
     pressure      1     .     atm   bmse011926   1    
     temperature   298   0.1   K     bmse011926   1    

   stop_

save_

############################
#  Computer software used  #
############################

save_software_1
   _Software.Sf_category   software
   _Software.Sf_framecode  software_1
   _Software.Entry_ID      bmse011926
   _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/   bmse011926   1    

   stop_

   loop_
      _Task.Task
      _Task.Entry_ID
      _Task.Software_ID

     'data analysis'   bmse011926   1    
     'peak picking'    bmse011926   1    
     processing        bmse011926   1    

   stop_

save_

#########################
#  Experimental detail  #
#########################

    ##################################
    #  NMR Spectrometer definitions  #
    ##################################

save_NMR_spectrometer_1
   _NMR_spectrometer.Sf_category     NMR_spectrometer
   _NMR_spectrometer.Sf_framecode    NMR_spectrometer_1
   _NMR_spectrometer.Entry_ID        bmse011926
   _NMR_spectrometer.ID              1
   _NMR_spectrometer.Name            'spectrometer Bruker'
   _NMR_spectrometer.Manufacturer    Bruker
   _NMR_spectrometer.Model           Avance
   _NMR_spectrometer.Field_strength  600

save_

    #############################
    #  NMR applied experiments  #
    #############################

save_experiment_list_1
   _Experiment_list.Sf_category   experiment_list
   _Experiment_list.Sf_framecode  experiment_list_1
   _Experiment_list.Entry_ID      bmse011926
   _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   $NMR_spectrometer_1   bmse011926   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/             bmse011926   1    
     1   cmcproject.xml          text/xml         'spectrum analysis'          nmr/set01/1/pdata/1/   bmse011926   1    
     1   multiplet.txt           text             'Peak list'                  nmr/set01/1/pdata/1/   bmse011926   1    
     1   spectrum_overview.pdf   pdf              'Spectrum image'             nmr/set01/1/pdata/1/   bmse011926   1    
     1   spectrum_overview.png   image/png        'Spectral image'             nmr/set01/1/pdata/1/   bmse011926   1    

   stop_

save_

####################
#  NMR parameters  #
####################

    ##############################
    #  Assigned chemical shifts  #
    ##############################

	################################
	#  Chemical shift referencing  #
	################################

save_chem_shift_reference_1
   _Chem_shift_reference.Sf_category           chem_shift_reference
   _Chem_shift_reference.Sf_framecode          chem_shift_reference_1
   _Chem_shift_reference.Entry_ID              bmse011926
   _Chem_shift_reference.ID                    1
   _Chem_shift_reference.Name                  'chem shift ref set'

   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   DSS   'methyl protons'   ppm   0.0   internal   direct   1.0   bmse011926   1    

   stop_

save_

    #########################
    #  Spectral peak lists  #
    #########################

save_spectral_peak_list_1
   _Spectral_peak_list.Sf_category                     spectral_peak_list
   _Spectral_peak_list.Sf_framecode                    spectral_peak_list_1
   _Spectral_peak_list.Entry_ID                        bmse011926
   _Spectral_peak_list.ID                              1
   _Spectral_peak_list.Name                            'spectral peaks 1D 1H'
   _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.Chem_shift_reference_ID         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   bmse011926   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_1   bmse011926   1    

   stop_

   loop_
      _Peak.ID
      _Peak.Entry_ID
      _Peak.Spectral_peak_list_ID

     1   bmse011926   1    
     2   bmse011926   1    
     3   bmse011926   1    
     4   bmse011926   1    
     5   bmse011926   1    
     6   bmse011926   1    
     7   bmse011926   1    
     8   bmse011926   1    
     9   bmse011926   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   0.5291   8,9_m_Q1   bmse011926   1    
     2   1   6.8873   13_dd      bmse011926   1    
     3   1   4.6544   SUP        bmse011926   1    
     4   1   2.5702   DMSO       bmse011926   1    
     5   1   6.9846   6,7_m      bmse011926   1    
     6   1   0.0354   TMS        bmse011926   1    
     7   1   0.7326   8,9_m      bmse011926   1    
     8   1   7.1852   11_dd_Q2   bmse011926   1    
     9   1   2.6617   5,12_m     bmse011926   1    

   stop_

   loop_
      _Spectral_transition.ID
      _Spectral_transition.Entry_ID
      _Spectral_transition.Spectral_peak_list_ID

     1    bmse011926   1    
     2    bmse011926   1    
     3    bmse011926   1    
     4    bmse011926   1    
     5    bmse011926   1    
     6    bmse011926   1    
     7    bmse011926   1    
     8    bmse011926   1    
     9    bmse011926   1    
     10   bmse011926   1    
     11   bmse011926   1    
     12   bmse011926   1    
     13   bmse011926   1    
     14   bmse011926   1    
     15   bmse011926   1    
     16   bmse011926   1    
     17   bmse011926   1    
     18   bmse011926   1    
     19   bmse011926   1    
     20   bmse011926   1    
     21   bmse011926   1    
     22   bmse011926   1    
     23   bmse011926   1    
     24   bmse011926   1    
     25   bmse011926   1    
     26   bmse011926   1    
     27   bmse011926   1    
     28   bmse011926   1    
     29   bmse011926   1    
     30   bmse011926   1    
     31   bmse011926   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   0.5427   bmse011926   1    
     2    1   0.5349   bmse011926   1    
     3    1   0.5307   bmse011926   1    
     4    1   0.5280   bmse011926   1    
     5    1   0.5243   bmse011926   1    
     6    1   0.5155   bmse011926   1    
     7    1   6.8960   bmse011926   1    
     8    1   6.8925   bmse011926   1    
     9    1   6.8818   bmse011926   1    
     10   1   6.8786   bmse011926   1    
     11   1   4.6544   bmse011926   1    
     12   1   2.5702   bmse011926   1    
     13   1   7.0437   bmse011926   1    
     14   1   6.9255   bmse011926   1    
     15   1   0.0354   bmse011926   1    
     16   1   0.7584   bmse011926   1    
     17   1   0.7449   bmse011926   1    
     18   1   0.7445   bmse011926   1    
     19   1   0.7396   bmse011926   1    
     20   1   0.7305   bmse011926   1    
     21   1   0.7276   bmse011926   1    
     22   1   0.7185   bmse011926   1    
     23   1   0.7154   bmse011926   1    
     24   1   0.7105   bmse011926   1    
     25   1   0.7068   bmse011926   1    
     26   1   7.1985   bmse011926   1    
     27   1   7.1853   bmse011926   1    
     28   1   7.1853   bmse011926   1    
     29   1   7.1718   bmse011926   1    
     30   1   2.7280   bmse011926   1    
     31   1   2.5953   bmse011926   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   3.2572    bmse011926   1    
     2   2   1   1.9807    bmse011926   1    
     3   3   1   0.0000    bmse011926   1    
     4   4   1   0.0000    bmse011926   1    
     5   5   1   70.8859   bmse011926   1    
     6   6   1   0.0000    bmse011926   1    
     7   7   1   3.4397    bmse011926   1    
     8   8   1   7.9962    bmse011926   1    
     9   9   1   79.6505   bmse011926   1    

   stop_

save_
