Found 2 structures.
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1. Compound ID: 20697
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b-D-Manp-(1-23)-Subst
Subst = malsteroside A, B aglycon = SMILES C/C([C@H]1CCC2C3=C(C(C)=C4C{8}C(CCC4=C3)O)CC[C@]12C)=C\{23}C(O)C(C)C(C)C |
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Structure type: monomer
; 573.3762 [M+H]+
C34H52O7
Trivial name: malsteroside A
Compound class: glycoside
Contained glycoepitopes: IEDB_137485,IEDB_144983,IEDB_152206,IEDB_983930,SB_44,SB_72
The structure is contained in the following publication(s):
- Article ID: 8251
Wakana D, Itabashi T, Kawai K, Yaguchi T, Fukushima K, Goda Y, Hosoe T "Cytotoxic anthrasteroid glycosides, malsterosides A-C, from Malbranchea filamentosa" -
The Journal of Antibiotics 67(8) (2014) 585-588
cytotoxicity, glycoside
NCBI PubMed ID: 24802211Publication DOI: 10.1038/ja.2014.43Journal NLM ID: 0151115Publisher: London: Nature Publishing Group
Correspondence: Hosoe T
Institutions: Faculty of Pharmaceutical Science, Hoshi University, Tokyo, Japan, Division of pharmacognosy, phytochemistry and narcotics, National Institute of Health Sciences (NIHS), Tokyo, Japan, Medical Mycology Research Center (MMRC), Chiba University, Chiba, Japan
Methods: 13C NMR, 1H NMR, NMR-2D, IR, acid hydrolysis, HPLC, UV, ion-exchange chromatography, extraction, optical rotation measurement, ESI-TOF-MS, cytotoxicity assay
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2. Compound ID: 20698
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b-D-Manp-(1-23)-+
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a-D-GlcpNAc-(1-8)-Subst
Subst = malsteroside A, B aglycon = SMILES C/C([C@H]1CCC2C3=C(C(C)=C4C{8}C(CCC4=C3)O)CC[C@]12C)=C\{23}C(O)C(C)C(C)C |
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Structure type: monomer
; 776.4615 [M+H]+
C42H65NO12
Trivial name: malsteroside B
Compound class: glycoside
Contained glycoepitopes: IEDB_137485,IEDB_141807,IEDB_144983,IEDB_151531,IEDB_152206,IEDB_983930,SB_44,SB_72
The structure is contained in the following publication(s):
- Article ID: 8251
Wakana D, Itabashi T, Kawai K, Yaguchi T, Fukushima K, Goda Y, Hosoe T "Cytotoxic anthrasteroid glycosides, malsterosides A-C, from Malbranchea filamentosa" -
The Journal of Antibiotics 67(8) (2014) 585-588
cytotoxicity, glycoside
NCBI PubMed ID: 24802211Publication DOI: 10.1038/ja.2014.43Journal NLM ID: 0151115Publisher: London: Nature Publishing Group
Correspondence: Hosoe T
Institutions: Faculty of Pharmaceutical Science, Hoshi University, Tokyo, Japan, Division of pharmacognosy, phytochemistry and narcotics, National Institute of Health Sciences (NIHS), Tokyo, Japan, Medical Mycology Research Center (MMRC), Chiba University, Chiba, Japan
Methods: 13C NMR, 1H NMR, NMR-2D, IR, acid hydrolysis, HPLC, UV, ion-exchange chromatography, extraction, optical rotation measurement, ESI-TOF-MS, cytotoxicity assay
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