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Kodama H, Fujimori T, Kato K
Non-volatile constituents in tobacco. Part IV. Three new sesquiterpenoid glycosides from tobacco
Agricultural and Biological Chemistry 49 (1985)
2537-2541
b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = 3β-hydroxy-solanascone = SMILES C[C@@H]1{3}[C@@H](O)C([C@H]2C[C@]3(C)[C@@]2(C)[C@]14CC[C@@H]3C4)=O |
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Nicotiana tabacum
(NCBI TaxID 4097,
species name lookup)
Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
The structure was elucidated in this paperPublication DOI: 10.1271/bbb1961.49.2537Journal NLM ID: 0370452Publisher: Tokyo: Agricultural Chemical Society Of Japan
Institutions: Central Research Institute, Japan Tobacco Inc., Yokohama, Japan
Three sesquiterpenoid glycosides, 3β-hydroxysolanascone-β-sophoroside la, 3β-hydroxysolavetivone-β-glucoside 2a and rishitin glycoside 3a, were isolated from tobacco.
Structure type: oligomer
Location inside paper: 1a
Compound class: glycoside
Contained glycoepitopes: IEDB_140628,IEDB_142488,IEDB_146664,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, enzymatic hydrolysis, acid hydrolysis, HPLC, methylation analysis, photocyclization
Comments, role: Pubchem shows stereo configurations other than published for 3β-hydroxy-solanascone. Aglycon was encoded according to the paper.
NCBI Taxonomy refs (TaxIDs): 4097Reference(s) to other database(s): CCSD:
47506, CBank-STR:4182
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Kodama H, Fujimori T, Kato K
Non-volatile constituents in tobacco. Part IV. Three new sesquiterpenoid glycosides from tobacco
Agricultural and Biological Chemistry 49 (1985)
2537-2541
b-D-Glcp-(1-3)-Subst
Subst = 3β-hydroxy-solavetivone = SMILES C[C@@H]1{3}[C@@H](O)C(C=C(C)[C@]12CC[C@@H](C(C)=C)C2)=O |
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Nicotiana tabacum
(NCBI TaxID 4097,
species name lookup)
Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
The structure was elucidated in this paperPublication DOI: 10.1271/bbb1961.49.2537Journal NLM ID: 0370452Publisher: Tokyo: Agricultural Chemical Society Of Japan
Institutions: Central Research Institute, Japan Tobacco Inc., Yokohama, Japan
Three sesquiterpenoid glycosides, 3β-hydroxysolanascone-β-sophoroside la, 3β-hydroxysolavetivone-β-glucoside 2a and rishitin glycoside 3a, were isolated from tobacco.
Structure type: oligomer
Location inside paper: 2a
Compound class: glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, enzymatic hydrolysis, acid hydrolysis, HPLC, methylation analysis, photocyclization
NCBI Taxonomy refs (TaxIDs): 4097Reference(s) to other database(s): CCSD:
48580, CBank-STR:1210
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There is only one chemically distinct structure:
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Kodama H, Fujimori T, Kato K
Non-volatile constituents in tobacco. Part IV. Three new sesquiterpenoid glycosides from tobacco
Agricultural and Biological Chemistry 49 (1985)
2537-2541
a-L-Rhap-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-3)-Subst
Subst = rishitin = SMILES C[C@@H]1{3}[C@@H](O){2}[C@H](O)CC2=C1C[C@H](C(C)=C)CC2 |
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Nicotiana tabacum
(NCBI TaxID 4097,
species name lookup)
Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
The structure was elucidated in this paperPublication DOI: 10.1271/bbb1961.49.2537Journal NLM ID: 0370452Publisher: Tokyo: Agricultural Chemical Society Of Japan
Institutions: Central Research Institute, Japan Tobacco Inc., Yokohama, Japan
Three sesquiterpenoid glycosides, 3β-hydroxysolanascone-β-sophoroside la, 3β-hydroxysolavetivone-β-glucoside 2a and rishitin glycoside 3a, were isolated from tobacco.
Structure type: oligomer
Location inside paper: 3a
Compound class: glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, enzymatic hydrolysis, acid hydrolysis, HPLC, methylation analysis, photocyclization
NCBI Taxonomy refs (TaxIDs): 4097Reference(s) to other database(s): CCSD:
13700, CBank-STR:7605
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There is only one chemically distinct structure:
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