data_bmse012438
#######################
# Entry information #
#######################
save_entry_information_1
_Entry.Sf_category entry_information
_Entry.Sf_framecode entry_information_1
_Entry.ID bmse012438
_Entry.Title (4R)-2-oxo-N-[[(3R)-oxolan-3-yl]methyl]-3,4-dihydro-1H-quinoline-4-carboxamide
_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/bmse012438
loop_
_Entry_experimental_methods.ID
_Entry_experimental_methods.Method
_Entry_experimental_methods.Subtype
_Entry_experimental_methods.Entry_ID
1 NMR solution bmse012438
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. bmse012438
2 Christian Richter C. bmse012438
3 Harald Schwalbe H. bmse012438
4 Hannes Berg . bmse012438
stop_
loop_
_Entry_src.ID
_Entry_src.Project_name
_Entry_src.Entry_ID
1 EUOS bmse012438
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 bmse012438
stop_
loop_
_Auxiliary_files.ID
_Auxiliary_files.Name
_Auxiliary_files.Format
_Auxiliary_files.URI
_Auxiliary_files.Details
_Auxiliary_files.Entry_ID
1 bmse012438.mol sdf na 'Structure Definition File' bmse012438
stop_
save_
###############
# Citations #
###############
save_citations_1
_Citation.Sf_category citations
_Citation.Sf_framecode citations_1
_Citation.Entry_ID bmse012438
_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. bmse012438 1
2 Christian Richter C. bmse012438 1
3 Till Kuehn T. bmse012438 1
4 Kamal Azzaoui K. bmse012438 1
5 'Marcel Jules Jose' Blommers . bmse012438 1
6 Rebecca 'Del Conte' R. bmse012438 1
7 Marco Fragai M. bmse012438 1
8 Nils Trieloff N. bmse012438 1
9 Peter Schmieder P. bmse012438 1
10 Marc Nazare M. bmse012438 1
11 Edgar Specker E. bmse012438 1
12 Vladimir Ivanov V. bmse012438 1
13 Hartmut Oschkinat H. bmse012438 1
14 Lucia Banci L. bmse012438 1
15 Harald Schwalbe H. bmse012438 1
stop_
save_
#############################################
# Molecular system (assembly) description #
#############################################
save_assembly_1
_Assembly.Sf_category assembly
_Assembly.Sf_framecode assembly_1
_Assembly.Entry_ID bmse012438
_Assembly.ID 1
_Assembly.Name (4R)-2-oxo-N-[[(3R)-oxolan-3-yl]methyl]-3,4-dihydro-1H-quinoline-4-carboxamide
_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 bmse012438 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 bmse012438 1
2 1 1 1 1 C2 C bmse012438 1
3 1 1 1 1 C3 C bmse012438 1
4 1 1 1 1 C4 C bmse012438 1
5 1 1 1 1 C5 C bmse012438 1
6 1 1 1 1 C6 C bmse012438 1
7 1 1 1 1 C7 C bmse012438 1
8 1 1 1 1 C8 C bmse012438 1
9 1 1 1 1 C9 C bmse012438 1
10 1 1 1 1 C10 C bmse012438 1
11 1 1 1 1 C11 C bmse012438 1
12 1 1 1 1 C12 C bmse012438 1
13 1 1 1 1 C13 C bmse012438 1
14 1 1 1 1 C14 C bmse012438 1
15 1 1 1 1 C15 C bmse012438 1
16 1 1 1 1 N16 N bmse012438 1
17 1 1 1 1 N17 N bmse012438 1
18 1 1 1 1 O18 O bmse012438 1
19 1 1 1 1 O19 O bmse012438 1
20 1 1 1 1 O20 O bmse012438 1
stop_
save_
####################################
# Biological polymers and ligands #
####################################
save_entity_1
_Entity.Sf_category entity
_Entity.Sf_framecode entity_1
_Entity.Entry_ID bmse012438
_Entity.ID 1
_Entity.Name (4R)-2-oxo-N-[[(3R)-oxolan-3-yl]methyl]-3,4-dihydro-1H-quinoline-4-carboxamide
_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 274.3150199999999
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 bmse012438 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 bmse012438
_Chem_comp.Name (4R)-2-oxo-N-[[(3R)-oxolan-3-yl]methyl]-3,4-dihydro-1H-quinoline-4-carboxamide
_Chem_comp.Number_atoms_all 20
_Chem_comp.InChI_code InChI=1S/C15H18N2O3/c18-14-7-12(11-3-1-2-4-13(11)17-14)15(19)16-8-10-5-6-20-9-10/h1-4,10,12H,5-9H2,(H,16,19)(H,17,18)/t10-,12-/m1/s1
_Chem_comp.Formal_charge 0
_Chem_comp.Aromatic yes
_Chem_comp.Formula C15H18N2O3
_Chem_comp.Formula_weight 274.3150199999999
_Chem_comp.Formula_mono_iso_wt_nat 274.131742446
_Chem_comp.Formula_mono_iso_wt_13C 289.182065016
_Chem_comp.Formula_mono_iso_wt_15N 276.125812232
_Chem_comp.Formula_mono_iso_wt_13C_15N 291.17613480200004
_Chem_comp.Image_file_name bmse012438.png
_Chem_comp.Image_file_format png
_Chem_comp.Struct_file_name bmse012438.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
O=C1C[C@@H](C(=O)NC[C@H]2CCOC2)c2ccccc2N1 SMILES_CANONICAL RDKit 2022.03.5 bmse012438
O=C1C[C@@H](C(=O)NC[C@H]2CCOC2)c2ccccc2N1 SMILES_ISOMERIC RDKit 2022.03.5 bmse012438
O=C1C[C@@H](C(=O)NC[C@H]2CCOC2)c2ccccc2N1 SMILES RDKit 2022.03.5 bmse012438
O=C1Nc2ccccc2[C@@H](C1)C(=O)NC[C@@H]1COCC1 SMILES_CANONICAL OpenBabel 3.1.0 bmse012438
O=C1Nc2ccccc2[C@@H](C1)C(=O)NC[C@@H]1COCC1 SMILES OpenBabel 3.1.0 bmse012438
InChI=1S/C15H18N2O3/c18-14-7-12(11-3-1-2-4-13(11)17-14)15(19)16-8-10-5-6-20-9-10/h1-4,10,12H,5-9H2,(H,16,19)(H,17,18)/t10-,12-/m1/s1 InChI OpenBabel 3.1.0 bmse012438
MDUWKGGVEPBIOE-ZYHUDNBSSA-N InChI_KEY OpenBabel 3.1.0 bmse012438
InChI=1S/C15H18N2O3/c18-14-7-12(11-3-1-2-4-13(11)17-14)15(19)16-8-10-5-6-20-9-10/h1-4,10,12H,5-9H2,(H,16,19)(H,17,18)/t10-,12-/m1/s1 InChI ALATIS na bmse012438
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 bmse012438
C2 C N 0 yes 2 bmse012438
C3 C N 0 yes 3 bmse012438
C4 C N 0 yes 4 bmse012438
C5 C N 0 no 5 bmse012438
C6 C N 0 no 6 bmse012438
C7 C N 0 no 7 bmse012438
C8 C N 0 no 8 bmse012438
C9 C N 0 no 9 bmse012438
C10 C R 0 no 10 bmse012438
C11 C N 0 yes 11 bmse012438
C12 C R 0 no 12 bmse012438
C13 C N 0 yes 13 bmse012438
C14 C N 0 no 14 bmse012438
C15 C N 0 no 15 bmse012438
N16 N N 0 no 16 bmse012438
N17 N N 0 no 17 bmse012438
O18 O N 0 no 18 bmse012438
O19 O N 0 no 19 bmse012438
O20 O N 0 no 20 bmse012438
stop_
loop_
_Atom_nomenclature.Atom_ID
_Atom_nomenclature.Atom_name
_Atom_nomenclature.Naming_system
_Atom_nomenclature.Entry_ID
C19 C1 ALATIS bmse012438
C20 C2 ALATIS bmse012438
C14 C3 ALATIS bmse012438
C15 C4 ALATIS bmse012438
C18 C5 ALATIS bmse012438
C17 C6 ALATIS bmse012438
C8 C7 ALATIS bmse012438
C12 C8 ALATIS bmse012438
C16 C9 ALATIS bmse012438
C13 C10 ALATIS bmse012438
C4 C11 ALATIS bmse012438
C2 C12 ALATIS bmse012438
C5 C13 ALATIS bmse012438
C3 C14 ALATIS bmse012438
C6 C15 ALATIS bmse012438
N7 N16 ALATIS bmse012438
N1 N17 ALATIS bmse012438
O9 O18 ALATIS bmse012438
O10 O19 ALATIS bmse012438
O11 O20 ALATIS bmse012438
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 C2 yes N 1 bmse012438
2 covalent AROM C3 C1 yes N 2 bmse012438
3 covalent AROM C4 C2 yes N 3 bmse012438
4 covalent SING C6 C5 no N 4 bmse012438
5 covalent SING C10 C5 no N 5 bmse012438
6 covalent SING C10 C8 no N 6 bmse012438
7 covalent SING C10 C9 no N 7 bmse012438
8 covalent AROM C11 C3 yes N 8 bmse012438
9 covalent AROM C11 C13 yes N 9 bmse012438
10 covalent SING C12 C7 no N 10 bmse012438
11 covalent SING C12 C11 no N 11 bmse012438
12 covalent SING C12 C15 no N 12 bmse012438
13 covalent AROM C13 C4 yes N 13 bmse012438
14 covalent SING C14 C7 no N 14 bmse012438
15 carbonyl DOUB C14 O18 no N 15 bmse012438
16 amide SING C15 N16 no N 16 bmse012438
17 carbonyl DOUB C15 O19 no N 17 bmse012438
18 covalent SING N16 C8 no N 18 bmse012438
19 covalent SING N17 C13 no N 19 bmse012438
20 amide SING N17 C14 no N 20 bmse012438
21 covalent SING O20 C6 no N 21 bmse012438
22 covalent SING O20 C9 no N 22 bmse012438
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 EOS103196 'compound ID' bmse012438
stop_
save_
#####################################
# Sample contents and methodology #
#####################################
########################
# Sample description #
########################
save_sample_1
_Sample.Sf_category sample
_Sample.Sf_framecode sample_1
_Sample.Entry_ID bmse012438
_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 (4R)-2-oxo-N-[[(3R)-oxolan-3-yl]methyl]-3,4-dihydro-1H-quinoline-4-carboxamide 'natural abundance' 1 $assembly_1 1 $entity_1 solute 2 mM bmse012438 1
2 'Sodium phosphate' 'natural abundance' . . . . buffer 25 mM bmse012438 1
3 'Sodium chloride' 'natural abundance' . . . . salt 150 mM bmse012438 1
4 DSS 'natural abundance' . . . . reference 10 uM bmse012438 1
5 H2O 'natural abundance' . . . . solvent 95 % bmse012438 1
6 DMSO '[2H U-100%]' . . . . solvent 5 % bmse012438 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 bmse012438
_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 bmse012438 1
pressure 1 . atm bmse012438 1
temperature 298 0.1 K bmse012438 1
stop_
save_
############################
# Computer software used #
############################
save_software_1
_Software.Sf_category software
_Software.Sf_framecode software_1
_Software.Entry_ID bmse012438
_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/ bmse012438 1
stop_
loop_
_Task.Task
_Task.Entry_ID
_Task.Software_ID
'data analysis' bmse012438 1
'peak picking' bmse012438 1
processing bmse012438 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 bmse012438
_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 bmse012438
_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 bmse012438 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/ bmse012438 1
1 cmcproject.xml text/xml 'spectrum analysis' nmr/set01/1/pdata/1/ bmse012438 1
1 multiplet.txt text 'Peak list' nmr/set01/1/pdata/1/ bmse012438 1
1 spectrum_overview.pdf pdf 'Spectrum image' nmr/set01/1/pdata/1/ bmse012438 1
1 spectrum_overview.png image/png 'Spectral image' nmr/set01/1/pdata/1/ bmse012438 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 bmse012438
_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 bmse012438 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 bmse012438
_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 bmse012438 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 bmse012438 1
stop_
loop_
_Peak.ID
_Peak.Entry_ID
_Peak.Spectral_peak_list_ID
1 bmse012438 1
2 bmse012438 1
3 bmse012438 1
4 bmse012438 1
5 bmse012438 1
6 bmse012438 1
7 bmse012438 1
8 bmse012438 1
9 bmse012438 1
10 bmse012438 1
11 bmse012438 1
12 bmse012438 1
13 bmse012438 1
14 bmse012438 1
15 bmse012438 1
stop_
loop_
_Peak_char.Peak_ID
_Peak_char.Spectral_dim_ID
_Peak_char.Chem_shift_val
_Peak_char.Details
_Peak_char.Entry_ID
_Peak_char.Spectral_peak_list_ID
1 1 2.5707 DMSO bmse012438 1
2 1 2.8082 m_1H bmse012438 1
3 1 7.0363 t_1H bmse012438 1
4 1 2.6754 m_1H bmse012438 1
5 1 4.6542 SUP bmse012438 1
6 1 3.2786 m_1H bmse012438 1
7 1 3.8539 dd_1H bmse012438 1
8 1 3.0040 m_1H bmse012438 1
9 1 3.6336 m_3H bmse012438 1
10 1 7.2276 m_2H bmse012438 1
11 1 1.8624 m_1H bmse012438 1
12 1 6.8741 d_1H_Q1 bmse012438 1
13 1 1.4196 m_1H bmse012438 1
14 1 3.1564 m_1H bmse012438 1
15 1 2.3314 quint_1H bmse012438 1
stop_
loop_
_Spectral_transition.ID
_Spectral_transition.Entry_ID
_Spectral_transition.Spectral_peak_list_ID
1 bmse012438 1
2 bmse012438 1
3 bmse012438 1
4 bmse012438 1
5 bmse012438 1
6 bmse012438 1
7 bmse012438 1
8 bmse012438 1
9 bmse012438 1
10 bmse012438 1
11 bmse012438 1
12 bmse012438 1
13 bmse012438 1
14 bmse012438 1
15 bmse012438 1
16 bmse012438 1
17 bmse012438 1
18 bmse012438 1
19 bmse012438 1
20 bmse012438 1
21 bmse012438 1
22 bmse012438 1
23 bmse012438 1
24 bmse012438 1
25 bmse012438 1
26 bmse012438 1
27 bmse012438 1
28 bmse012438 1
29 bmse012438 1
30 bmse012438 1
31 bmse012438 1
32 bmse012438 1
33 bmse012438 1
34 bmse012438 1
35 bmse012438 1
36 bmse012438 1
37 bmse012438 1
38 bmse012438 1
39 bmse012438 1
40 bmse012438 1
41 bmse012438 1
42 bmse012438 1
43 bmse012438 1
44 bmse012438 1
45 bmse012438 1
46 bmse012438 1
47 bmse012438 1
48 bmse012438 1
49 bmse012438 1
50 bmse012438 1
51 bmse012438 1
52 bmse012438 1
53 bmse012438 1
54 bmse012438 1
55 bmse012438 1
56 bmse012438 1
57 bmse012438 1
58 bmse012438 1
59 bmse012438 1
60 bmse012438 1
61 bmse012438 1
62 bmse012438 1
63 bmse012438 1
64 bmse012438 1
65 bmse012438 1
66 bmse012438 1
67 bmse012438 1
68 bmse012438 1
69 bmse012438 1
70 bmse012438 1
71 bmse012438 1
72 bmse012438 1
73 bmse012438 1
74 bmse012438 1
75 bmse012438 1
76 bmse012438 1
77 bmse012438 1
78 bmse012438 1
79 bmse012438 1
80 bmse012438 1
81 bmse012438 1
82 bmse012438 1
83 bmse012438 1
84 bmse012438 1
85 bmse012438 1
86 bmse012438 1
87 bmse012438 1
88 bmse012438 1
89 bmse012438 1
stop_
loop_
_Spectral_transition_char.Spectral_transition_ID
_Spectral_transition_char.Spectral_dim_ID
_Spectral_transition_char.Chem_shift_val
_Spectral_transition_char.Entry_ID
_Spectral_transition_char.Spectral_peak_list_ID
1 1 2.5707 bmse012438 1
2 1 2.8280 bmse012438 1
3 1 2.8163 bmse012438 1
4 1 2.8001 bmse012438 1
5 1 2.7884 bmse012438 1
6 1 7.0232 bmse012438 1
7 1 7.0361 bmse012438 1
8 1 7.0493 bmse012438 1
9 1 2.6925 bmse012438 1
10 1 2.6862 bmse012438 1
11 1 2.6644 bmse012438 1
12 1 2.6583 bmse012438 1
13 1 4.6542 bmse012438 1
14 1 3.2981 bmse012438 1
15 1 3.2844 bmse012438 1
16 1 3.2736 bmse012438 1
17 1 3.2700 bmse012438 1
18 1 3.2592 bmse012438 1
19 1 3.8631 bmse012438 1
20 1 3.8567 bmse012438 1
21 1 3.8513 bmse012438 1
22 1 3.8447 bmse012438 1
23 1 3.0256 bmse012438 1
24 1 3.0161 bmse012438 1
25 1 3.0044 bmse012438 1
26 1 2.9916 bmse012438 1
27 1 2.9823 bmse012438 1
28 1 3.6923 bmse012438 1
29 1 3.6887 bmse012438 1
30 1 3.6835 bmse012438 1
31 1 3.6786 bmse012438 1
32 1 3.6745 bmse012438 1
33 1 3.6696 bmse012438 1
34 1 3.6603 bmse012438 1
35 1 3.6522 bmse012438 1
36 1 3.6476 bmse012438 1
37 1 3.6451 bmse012438 1
38 1 3.6398 bmse012438 1
39 1 3.6373 bmse012438 1
40 1 3.6329 bmse012438 1
41 1 3.6248 bmse012438 1
42 1 3.6202 bmse012438 1
43 1 3.6146 bmse012438 1
44 1 3.6072 bmse012438 1
45 1 3.6016 bmse012438 1
46 1 3.5940 bmse012438 1
47 1 3.5882 bmse012438 1
48 1 3.5808 bmse012438 1
49 1 3.5749 bmse012438 1
50 1 7.2421 bmse012438 1
51 1 7.2271 bmse012438 1
52 1 7.2132 bmse012438 1
53 1 1.8916 bmse012438 1
54 1 1.8818 bmse012438 1
55 1 1.8779 bmse012438 1
56 1 1.8688 bmse012438 1
57 1 1.8646 bmse012438 1
58 1 1.8605 bmse012438 1
59 1 1.8558 bmse012438 1
60 1 1.8468 bmse012438 1
61 1 1.8429 bmse012438 1
62 1 1.8333 bmse012438 1
63 1 6.8811 bmse012438 1
64 1 6.8671 bmse012438 1
65 1 1.4565 bmse012438 1
66 1 1.4442 bmse012438 1
67 1 1.4308 bmse012438 1
68 1 1.4195 bmse012438 1
69 1 1.4085 bmse012438 1
70 1 1.3951 bmse012438 1
71 1 1.3828 bmse012438 1
72 1 3.1814 bmse012438 1
73 1 3.1765 bmse012438 1
74 1 3.1707 bmse012438 1
75 1 3.1692 bmse012438 1
76 1 3.1655 bmse012438 1
77 1 3.1584 bmse012438 1
78 1 3.1543 bmse012438 1
79 1 3.1533 bmse012438 1
80 1 3.1465 bmse012438 1
81 1 3.1435 bmse012438 1
82 1 3.1413 bmse012438 1
83 1 3.1357 bmse012438 1
84 1 3.1313 bmse012438 1
85 1 2.3063 bmse012438 1
86 1 2.3191 bmse012438 1
87 1 2.3313 bmse012438 1
88 1 2.3438 bmse012438 1
89 1 2.3565 bmse012438 1
stop_
loop_
_Peak_coupling.ID
_Peak_coupling.Peak_ID
_Peak_coupling.Spectral_dim_ID
_Peak_coupling.Coupling_val
_Peak_coupling.Entry_ID
_Peak_coupling.Spectral_peak_list_ID
1 1 1 0.0000 bmse012438 1
2 2 1 7.9228 bmse012438 1
3 3 1 7.8495 bmse012438 1
4 4 1 6.8469 bmse012438 1
5 5 1 0.0000 bmse012438 1
6 6 1 5.8321 bmse012438 1
7 7 1 3.8881 bmse012438 1
8 8 1 6.4923 bmse012438 1
9 9 1 3.3536 bmse012438 1
10 10 1 8.6564 bmse012438 1
11 11 1 3.8799 bmse012438 1
12 12 1 0.0000 bmse012438 1
13 13 1 7.3604 bmse012438 1
14 14 1 2.5065 bmse012438 1
15 15 1 7.5194 bmse012438 1
stop_
save_