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Wilson ID
Multiple hyphenation of liquid chromatography with nuclear magnetic resonance spectroscopy, mass spectrometry and beyond
Journal of Chromatography A 892(1-2) (2000)
315-327
b-D-Glcp1NA-(1-1)-Subst
Subst = 2-bromo-4-(trifluoromethyl)aniline = SMILES BrC1=CC(C(F)(F)F)=CC={1}C1N |
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Hypericum perforatum
(NCBI TaxID 65561,
species name lookup)
Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
NCBI PubMed ID: 11045496Publication DOI: 10.1016/s0378-4347(00)00071-2Journal NLM ID: 9318488Publisher: Amsterdam; New York: Elsevier
Correspondence: ian.wilson

astrazeneca.com
Institutions: Drug Metabolism and Pharmacokinetics Department, AstraZeneca Pharmaceuticals, Macclesfield, UK
The advent of sensitive and reliable HPLC-NMR and HPLC-MS systems has revolutionised the identification of compounds eluting from chromatographic systems. More recently systems have been described wherein both NMR and MS are used together to provide an immensely powerful means of characterising compounds in chromatographic eluents. Here the construction and application of combined HPLC-NMR-MS systems to the analysis of mixtures of pharmaceuticals, drug metabolites in biological fluids and natural products in plant extracts is reviewed. In addition preliminary work with alternative systems such as HPLC-UV-NMR-FTIR-MS is highlighted and the prospects for such complex systems considered.
multiple hyphenation; complex mixture analysis; reviews
Structure type: monomer
Location inside paper: p. 320, Fig. 2
Compound class: glycoside
Methods: 1H NMR, IR, MS, HPLC, extraction, 19F NMR, HPLC-NMR-MS, SEC-NMR-IR
Related record ID(s): 68620, 68621, 68622
NCBI Taxonomy refs (TaxIDs): 65561
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Wilson ID
Multiple hyphenation of liquid chromatography with nuclear magnetic resonance spectroscopy, mass spectrometry and beyond
Journal of Chromatography A 892(1-2) (2000)
315-327
b-D-GlcpA-(1-7)-Subst
Subst = N-(2-bromo-4-(trifluoromethyl)phenyl)hydroxylamine = SMILES BrC1=CC(C(F)(F)F)=CC={1}C1{7}NO |
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Hypericum perforatum
(NCBI TaxID 65561,
species name lookup)
Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
NCBI PubMed ID: 11045496Publication DOI: 10.1016/s0378-4347(00)00071-2Journal NLM ID: 9318488Publisher: Amsterdam; New York: Elsevier
Correspondence: ian.wilson

astrazeneca.com
Institutions: Drug Metabolism and Pharmacokinetics Department, AstraZeneca Pharmaceuticals, Macclesfield, UK
The advent of sensitive and reliable HPLC-NMR and HPLC-MS systems has revolutionised the identification of compounds eluting from chromatographic systems. More recently systems have been described wherein both NMR and MS are used together to provide an immensely powerful means of characterising compounds in chromatographic eluents. Here the construction and application of combined HPLC-NMR-MS systems to the analysis of mixtures of pharmaceuticals, drug metabolites in biological fluids and natural products in plant extracts is reviewed. In addition preliminary work with alternative systems such as HPLC-UV-NMR-FTIR-MS is highlighted and the prospects for such complex systems considered.
multiple hyphenation; complex mixture analysis; reviews
Structure type: monomer
Location inside paper: p. 320, Fig. 2
Compound class: glycoside
Contained glycoepitopes: IEDB_115136,IEDB_140630,IEDB_423153
Methods: 1H NMR, IR, MS, HPLC, extraction, 19F NMR, HPLC-NMR-MS, SEC-NMR-IR
Related record ID(s): 68619, 68621, 68622
NCBI Taxonomy refs (TaxIDs): 65561
Show glycosyltransferases
There is only one chemically distinct structure:
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Wilson ID
Multiple hyphenation of liquid chromatography with nuclear magnetic resonance spectroscopy, mass spectrometry and beyond
Journal of Chromatography A 892(1-2) (2000)
315-327
b-D-Glcp1NA-(1-1)-Subst
Subst = N-(2-bromo-4-(trifluoromethyl)phenyl)hydroxylamine = SMILES BrC1=CC(C(F)(F)F)=CC={1}C1{7}NO |
Show graphically |
Hypericum perforatum
(NCBI TaxID 65561,
species name lookup)
Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
NCBI PubMed ID: 11045496Publication DOI: 10.1016/s0378-4347(00)00071-2Journal NLM ID: 9318488Publisher: Amsterdam; New York: Elsevier
Correspondence: ian.wilson

astrazeneca.com
Institutions: Drug Metabolism and Pharmacokinetics Department, AstraZeneca Pharmaceuticals, Macclesfield, UK
The advent of sensitive and reliable HPLC-NMR and HPLC-MS systems has revolutionised the identification of compounds eluting from chromatographic systems. More recently systems have been described wherein both NMR and MS are used together to provide an immensely powerful means of characterising compounds in chromatographic eluents. Here the construction and application of combined HPLC-NMR-MS systems to the analysis of mixtures of pharmaceuticals, drug metabolites in biological fluids and natural products in plant extracts is reviewed. In addition preliminary work with alternative systems such as HPLC-UV-NMR-FTIR-MS is highlighted and the prospects for such complex systems considered.
multiple hyphenation; complex mixture analysis; reviews
Structure type: monomer
Location inside paper: p. 320, Fig. 2
Compound class: glycoside
Methods: 1H NMR, IR, MS, HPLC, extraction, 19F NMR, HPLC-NMR-MS, SEC-NMR-IR
Related record ID(s): 68619, 68620, 68622
NCBI Taxonomy refs (TaxIDs): 65561
Show glycosyltransferases
There is only one chemically distinct structure:
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Wilson ID
Multiple hyphenation of liquid chromatography with nuclear magnetic resonance spectroscopy, mass spectrometry and beyond
Journal of Chromatography A 892(1-2) (2000)
315-327
b-D-GlcpA-(1-1)-Subst
Subst = 2-amino-3-bromo-5-(trifluoromethyl)phenol = SMILES BrC1=CC(C(F)(F)F)=C{2}C(O)={1}C1N |
Show graphically |
Hypericum perforatum
(NCBI TaxID 65561,
species name lookup)
Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
NCBI PubMed ID: 11045496Publication DOI: 10.1016/s0378-4347(00)00071-2Journal NLM ID: 9318488Publisher: Amsterdam; New York: Elsevier
Correspondence: ian.wilson

astrazeneca.com
Institutions: Drug Metabolism and Pharmacokinetics Department, AstraZeneca Pharmaceuticals, Macclesfield, UK
The advent of sensitive and reliable HPLC-NMR and HPLC-MS systems has revolutionised the identification of compounds eluting from chromatographic systems. More recently systems have been described wherein both NMR and MS are used together to provide an immensely powerful means of characterising compounds in chromatographic eluents. Here the construction and application of combined HPLC-NMR-MS systems to the analysis of mixtures of pharmaceuticals, drug metabolites in biological fluids and natural products in plant extracts is reviewed. In addition preliminary work with alternative systems such as HPLC-UV-NMR-FTIR-MS is highlighted and the prospects for such complex systems considered.
multiple hyphenation; complex mixture analysis; reviews
Structure type: monomer
Location inside paper: p. 320, Fig. 2
Compound class: glycoside
Contained glycoepitopes: IEDB_115136,IEDB_140630,IEDB_423153
Methods: 1H NMR, IR, MS, HPLC, extraction, 19F NMR, HPLC-NMR-MS, SEC-NMR-IR
Related record ID(s): 68619, 68620, 68621
NCBI Taxonomy refs (TaxIDs): 65561
Show glycosyltransferases
There is only one chemically distinct structure:
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