Found 4 publications.
Displayed publications from 1 to 4
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (Article ID: 7993)
Rezanka T, Guschina IA
Glycosidic compounds of murolic, protoconstipatic and allo-murolic acids from lichens of Central Asia
Phytochemistry 54(6) (2000)
635-645
Eleven compounds isolated from the extract of the Central Asian lichens comprised eight new glycosides having murolic, protoconstipatic and allo-murolic acids, as the aglycones and a saccharide moiety linked at C-18 made up of one or two sugars (glucose and apiose or rhamnose or xylose or arabinose). The structures were elucidated by using extensive spectroscopic analysis (1D and 2D NMR, MS, IR, UV and CD) and chemical methods.
glycosides, lichens, murolic acid, glucore, Central Asia, aglycones
NCBI PubMed ID: 10963458Publication DOI: 10.1016/S0031-9422(00)00147-3Journal NLM ID: 0151434Publisher: Elsevier
Correspondence: rezanka

biomed.cas.cz
Institutions: Institute of Microbiology, Academy of Sciences of Czech Republic, Prague, Czech Republic, Institute of Ecology of the Volga River Basin of the Russian Academy of Sciences, Togliatti, Russia
Methods: 13C NMR, 1H NMR, gel filtration, IR, FAB-MS, TLC, acid hydrolysis, GC, HPLC, UV, extraction, optical rotation measurement, CD, melting point determination, enzymatic assay, HR-FAB-MS, LR-FAB-MS
The publication contains the following compound(s):
- Compound ID: 20067
|
b-D-Xylp-(1-6)-b-D-Glcp-(1-18)-Subst
Subst = allo-murolic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 663.7800 [M+H]+, 662 [M-H]-
C32H54O14
Compound class: glycoside
- Compound ID: 20068
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-18)-Subst
Subst = murolic acid = SMILES C=C1{21}C(=O)O[C@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 677.8075 [M+H]+, 675[M-H]-
C33H56O14
Compound class: glycoside
- Compound ID: 20071
|
b-D-Apif-(1-6)-b-D-Glcp-(1-18)-Subst
Subst = allo-murolic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 663.7804 [M+H]+, 661 [M-H]-
C32H54O14
Compound class: glycoside
- Compound ID: 20065
|
b-D-Glcp-(1-18)-Subst
Subst = murolic acid = SMILES C=C1{21}C(=O)O[C@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: monomer
; 531.6645 [M+H]+, 529 [M-H]-
C27H46O10
Compound class: glycoside
- Compound ID: 20073
|
b-D-Apif-(1-6)-b-D-Glcp-(1-18)-Subst
Subst = murolic acid = SMILES C=C1{21}C(=O)O[C@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 663.7814 [M+H]+, 661 [M-H]-
C32H54O14
Compound class: glycoside
- Compound ID: 20066
|
b-D-Glcp-(1-18)-Subst
Subst = protoconstipatic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@H](C)O)[C@@H]1C(=O)O |
Show graphically |
Structure type: monomer
; 531.6648 [M+H]+, 529 [M-H]-
C27H46O10
Compound class: glycoside
- Compound ID: 20069
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-18)-Subst
Subst = protoconstipatic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@H](C)O)[C@@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 677.8079 [M+H]+, 675
C33H56O14
Compound class: glycoside
- Compound ID: 20070
|
a-D-Araf-(1-6)-b-D-Glcp-(1-18)-Subst
Subst = protoconstipatic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@H](C)O)[C@@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 663.7812 [M+H]+, 661 [M-H]-
C32H54O14
Compound class: glycoside
- Compound ID: 20072
|
b-D-Apif-(1-6)-b-D-Glcp-(1-18)-Subst
Subst = protoconstipatic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@H](C)O)[C@@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 663.7806 [M+H]+, 661 [M-H]-
C32H54O14
Compound class: glycoside
Expand this publication
Collapse this publication
2. (Article ID: 7995)
Rezanka T, Guschina IA
Glycoside esters from lichens of central Asia
Phytochemistry 58(3) (2001)
509-516
Ten compounds isolated from the extract of the central Asian lichens comprised new glycosides and glycoside esters having 18R-hydroxy-dihydroalloprotolichesterinic, 18S-hydroxy-dihydroprotolichesterinic and 18S-hydroxy-neodihydroprotolichesterinic acids, as the aglycones and a saccharide moiety linked at C-18 and also at C-21 made by glucose, xylose or rhamnose. The structures were elucidated using extensive spectroscopic analysis (1D and 2D NMR, MS, IR, UV and ORD) and by biochemical methods.
NMR, MS, glycoside esters, lichens of central Asia, IR, ORD, UV
NCBI PubMed ID: 11557085Publication DOI: 10.1016/S0031-9422(01)00261-8Journal NLM ID: 0151434Publisher: Elsevier
Correspondence: rezanka

biomed.cas.cz
Institutions: Institute of Ecology of the Volga River Basin of the Russian Academy of Sciences, Togliatti, Russia, Institute of Microbiology, Prague, Czech Republic
Methods: 13C NMR, 1H NMR, gel filtration, NMR-2D, IR, FAB-MS, GC-MS, TLC, acid hydrolysis, GC, HPLC, UV, extraction, optical rotation measurement, enzymatic assay, HR-FAB-MS, LR-FAB-MS
The publication contains the following compound(s):
- Compound ID: 20076
|
b-D-Glcp-(1-21)-Subst
Subst = 18S-hydroxyneodihydroprotolichesterinic acid = SMILES C{18}[C@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@H](C)[C@H]1{21}C(=O)O |
Show graphically |
Structure type: monomer
; 533.6797 [M+H]+, 531 [M-H]-
C27H48O10
Compound class: glycoside
- Compound ID: 20077
|
b-D-Glcp-(1-18)-+
|
a-L-Rhap-(1-21)-Subst
Subst = 18R-hydroxydihydroalloprotolichesterinic acid = SMILES C{18}[C@@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@H](C)[C@@H]1{21}C(=O)O |
Show graphically |
Structure type: oligomer
; 679.8234 [M+H]+, 677 [M-H]-
C33H58O14
Compound class: glycoside
- Compound ID: 20080
|
b-D-Glcp-(1-18)-+
|
b-D-Glcp-(1-21)-Subst
Subst = 18S-hydroxyneodihydroprotolichesterinic acid = SMILES C{18}[C@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@H](C)[C@H]1{21}C(=O)O |
Show graphically |
Structure type: oligomer
; 695.8224 [M+H]+, 693 [M-H]-
C33H58O15
Compound class: glycoside
- Compound ID: 20074
|
a-L-Rhap-(1-21)-Subst
Subst = 18R-hydroxydihydroalloprotolichesterinic acid = SMILES C{18}[C@@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@H](C)[C@@H]1{21}C(=O)O |
Show graphically |
Structure type: monomer
; 517.6801 [M+H]+, 515 [M-H]-
C27H48O9
Compound class: glycoside
- Compound ID: 20079
|
a-L-Rhap-(1-18)-+
|
b-D-Glcp-(1-21)-Subst
Subst = 18S-hydroxyneodihydroprotolichesterinic acid = SMILES C{18}[C@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@H](C)[C@H]1{21}C(=O)O |
Show graphically |
Structure type: oligomer
; 679.8233 [M+H]+, 677 [M-H]-
C33H58O14
Compound class: glycoside
- Compound ID: 20075
|
b-D-Glcp-(1-21)-Subst
Subst = 18S-hydroxydihydroprotolichesterinic acid = SMILES C{18}[C@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@@H](C)[C@H]1{21}C(=O)O |
Show graphically |
Structure type: monomer
; 533.6806 [M+H]+, 531 [M-H]-
C27H48O10
Compound class: glycoside
- Compound ID: 20078
|
b-D-Xylp-(1-18)-+
|
b-D-Glcp-(1-21)-Subst
Subst = 18S-hydroxydihydroprotolichesterinic acid = SMILES C{18}[C@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@@H](C)[C@H]1{21}C(=O)O |
Show graphically |
Structure type: oligomer
; 665.7961 [M+H]+, 663 [M-H]-
C32H56O14
Compound class: glycoside
Expand this publication
Collapse this publication
3. (Article ID: 7996)
Rezanka T, Guschina IA
Macrolactone glycosides of three lichen acids from Acarospora gobiensis, a lichen of Central Asia
Phytochemistry 58(8) (2001)
1281-1287
The compounds isolated from the extract of Central Asian lichen (Acarospora gobiensis H. Magn.) comprised three new glycosides having 18-hydroxy-dihydroalloprotolichesterinic, 18-hydroxy-neodihydroprotolichesterinic and 18-hydroxy-dihydroprotolichesterinic acids as aglycones and a di- or trisaccharide moiety linked at C-18 and at the carboxylic group. These compounds, called gobienines A-C, were found to be di- or trisacharides forming a macrolactone with the aglycone. The structures were elucidated by using extensive spectroscopic analysis (1D and 2D NMR, MS, IR and ORD) and chemical and enzymatic methods.
NMR, MS, IR spectra, lichens of central Asia, macrolactone glycoside esters, Acarospora gobiensis, Acarosporaceae
NCBI PubMed ID: 11738423Publication DOI: 10.1016/S0031-9422(01)00388-0Journal NLM ID: 0151434Publisher: Elsevier
Correspondence: rezanka

biomed.cas.cz
Institutions: Institute of Ecology of the Volga River Basin of the Russian Academy of Sciences, Togliatti, Russia, Institute of Microbiology, Prague, Czech Republic
Methods: 13C NMR, 1H NMR, gel filtration, NMR-2D, IR, FAB-MS, GC-MS, TLC, acid hydrolysis, GC, HPLC, UV, extraction, optical rotation measurement, enzymatic assay, HR-FAB-MS, LR-FAB-MS
The publication contains the following compound(s):
- Compound ID: 20081
| Cyclic
-2)-b-D-Glcp-(1-18)-Subst-(21-2)-b-D-Glcp-(1-
Subst = 18R-hydroxydihydroalloprotolichesterinic acid = SMILES C{18}[C@@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@H](C)[C@@H]1{21}C(=O)O |
Show graphically |
Structure type: cyclic polymer repeating unit
; n=1, 677.3751 [M+H]+, 675 [M-H]-
C33H55O14
Trivial name: gobienines A
Compound class: glycoside
- Compound ID: 20082
|
b-D-Glcp-(1-2)-b-D-Glcp-(1-18)-Subst
Subst = 18R-hydroxydihydroalloprotolichesterinic acid = SMILES C{18}[C@@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@H](C)[C@@H]1{21}C(=O)O |
Show graphically |
Structure type: oligomer
; 695 [M+H]+, 693 [M-H]-
C33H58O15
Compound class: glycoside
- Compound ID: 20083
| Cyclic
-2)-b-D-Glcp-(1-18)-Subst-(21-2)-a-L-Rhap-(1-
Subst = 18S-hydroxyneodihydroprotolichesterinic acid = SMILES C{18}[C@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@H](C)[C@H]1{21}C(=O)O |
Show graphically |
Structure type: cyclic polymer repeating unit
; n=1, 661.3801 [M+H]+, 659 [M-H]-
C33H55O13
Trivial name: gobienines B
Compound class: glycoside
- Compound ID: 20084
| Cyclic
a-L-Rhap-(1-3)-+
|
-2)-b-D-Glcp-(1-18)-Subst-(21-2)-b-D-Glcp-(1-
Subst = 18S-hydroxydihydroprotolichesterinic acid = SMILES C{18}[C@H](O)CCCCCCCCCCCCC[C@@H]1OC(=O)[C@@H](C)[C@H]1{21}C(=O)O |
Show graphically |
Structure type: cyclic polymer repeating unit
; n=1, 823.4331 [M+H]+, 821 [M-H]-
C39H65O18
Trivial name: gobienines C
Compound class: glycoside
Expand this publication
Collapse this publication
4. (Article ID: 8369)
Rezanka T, Guschina IA
Further glucosides of lichens' acids from Central Asian lichens
Phytochemistry 56(2) (2001)
181-188
Eight compounds isolated from an extract of Central Asian lichens comprised new glucosides having murolic, protoconstipatic and allo-murolic acids as the aglycones and a saccharide moiety linked at C-18 made up of four glucoses. The structures were elucidated using extensive spectroscopic analysis (1D and 2D NMR, MS, IR, UV and CD) and by chemical methods
lichens, glucosides, Central Asia, lichens' acids
NCBI PubMed ID: 11219812Publication DOI: 10.1016/s0031-9422(00)00372-1Journal NLM ID: 0151434Publisher: Elsevier
Correspondence: Rezanka T
biomed.cas.cz>
Institutions: Institute of Microbiology, Prague, Czech, Institute of Ecology of the Volga River Basin of the Russian Academy of Sciences, Togliatti, Russia
Methods: 13C NMR, 1H NMR, NMR-2D, IR, FAB-MS, acid hydrolysis, GC, methanolysis, UV, enzymatic digestion, extraction, optical rotation measurement, CC, RP-HPLC, derivatization, Gerwig method, DEPT, HOHAHA, HR-FAB-MS
The publication contains the following compound(s):
- Compound ID: 20946
|
b-D-Glcp-(1-2)-b-D-Glcp-(1-18)-Subst
Subst = allo-murolic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 693.8068 [M+H]+
C33H56O15
Compound class: glycoside
- Compound ID: 20949
|
b-D-Glcp-(1-3)-+
|
b-D-Glcp-(1-2)-b-D-Glcp-(1-18)-Subst
Subst = allo-murolic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 855.9503 [M+H]+
C39H66O20
Compound class: glycoside
- Compound ID: 20950
|
b-D-Glcp-(1-6)-+
|
b-D-Glcp-(1-2)-b-D-Glcp-(1-18)-Subst
Subst = allo-murolic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 855.9509 [M+H]+
C39H66O20
Compound class: glycoside
- Compound ID: 20952
|
b-D-Glcp-(1-6)-+
|
b-D-Glcp-(1-3)-b-D-Glcp-(1-18)-Subst
Subst = murolic acid = SMILES C=C1{21}C(=O)O[C@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 855.9508 [M+H]+
C39H66O20
Compound class: glycoside
- Compound ID: 20947
|
b-D-Glcp-(1-3)-b-D-Glcp-(1-18)-Subst
Subst = murolic acid = SMILES C=C1{21}C(=O)O[C@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 693.8064 [M+H]+
C33H56O15
Compound class: glycoside
- Compound ID: 20948
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-18)-Subst
Subst = protoconstipatic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@H](C)O)[C@@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 693.8066 [M+H]+
C33H56O15
Compound class: glycoside
- Compound ID: 20951
|
b-D-Glcp-(1-2)-b-D-Glcp-(1-2)-b-D-Glcp-(1-18)-Subst
Subst = protoconstipatic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@H](C)O)[C@@H]1C(=O)O |
Show graphically |
Structure type: oligomer
; 855.9503 [M+H]+
C39H66O20
Compound class: glycoside
- Compound ID: 20945
|
b-D-Glcp-(1-18)-Subst
Subst = protoconstipatic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@H](C)O)[C@@H]1C(=O)O |
Show graphically |
Structure type: monomer
Compound class: glycoside
- Compound ID: 20944
|
b-D-Glcp-(1-18)-Subst
Subst = murolic acid = SMILES C=C1{21}C(=O)O[C@H](CCCCCCCCCCCCC{18}[C@@H](C)O)[C@H]1C(=O)O |
Show graphically |
Structure type: monomer
Compound class: glycoside
- Compound ID: 20953
|
b-D-Glcp-(1-3)-+
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-2)-b-D-Glcp-(1-18)-Subst
Subst = protoconstipatic acid = SMILES C=C1{21}C(=O)O[C@@H](CCCCCCCCCCCCC{18}[C@H](C)O)[C@@H]1C(=O)O |
Show graphically |
Structure type: oligomer
C45H76O25
Compound class: glycoside
Expand this publication
Collapse this publication
Total list of publication IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
Execution: 1 sec