Found 9 structures.
Displayed structures from 1 to 9
Expand all compounds
Collapse all compounds
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. Compound ID: 20813
|
b-D-Glcp-(1-26)-+
|
b-D-Glcp-(1-4)-+ |
| |
a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = (20S,25R)-furosta-5,22-diene-3β,21α,26-triol = SMILES C[C@@H]({26}CO)C/C=C/5OC4CC3C2C/C=C\1C{3}[C@@H](O)CC[C@]1(C)C2CC[C@]3(C)C4{21}[C@]5(C)O |
Show graphically |
Structure type: oligomer
; 1061.5118 [M-H]-
C51H82O23
Compound class: saponin glycoside, glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 8311
Pang X, Wen D, Zhao Y, Xiong CQ, Wang XQ, Yu LY, Ma BP "Steroidal saponins obtained by biotransformation of total furostanol glycosides from Dioscorea zingiberensis with Absidia coerulea" -
Carbohydrate Research 402 (2015) 236-40
Five new steroidal saponins (1-5) were isolated from the fermentation broth of total furostanol glycosides from tubers of Dioscorea zingiberensis C.H. Wright incubated with a fungal, Absidia coerulea AS 3.3389, along with known saponins, zingiberensis new saponin (6), deltonin (7), prosapogenin A of dioscin (8), and protobioside (9), and their structures were established by NMR spectroscopy and mass spectrometry as well as by comparison with previously reported spectral data in the literatures. The induced effects in vitro on rat platelet aggregation of all compounds were evaluated
biotransformation, Absidia coerulea, Dioscorea zingiberensis, Dioscoreaceae, steroidal saponins, induced-platelet aggregation activity
NCBI PubMed ID: 25498025Publication DOI: 10.1016/j.carres.2014.11.011Journal NLM ID: 0043535Publisher: Elsevier
Correspondence: Ma BP
Institutions: Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China, Center for Culture Collection of Pharmaceutical Microorganisms, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, College of Pharmacy, Inner Mongolia Medical University, Hohhot, China
Methods: 13C NMR, 1H NMR, TLC, biological assays, HPLC, extraction, optical rotation measurement, CC, cell growth, HR-ESI-MS, centrifugation
Expand this compound
Collapse this compound
2. Compound ID: 20814
|
b-D-Glcp-(1-4)-+
|
a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = spirosta-5,20-diene-3β-ol = SMILES C=C5C4C(CC3C2C/C=C\1C{3}[C@@H](O)CC[C@]1(C)C2CC[C@@]34C)O[C@]56CC[C@@H](C)CO6 |
Show graphically |
Structure type: oligomer
; 881.4594 [M-H]-
C45H70O17
Compound class: saponin glycoside, glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 8311
Pang X, Wen D, Zhao Y, Xiong CQ, Wang XQ, Yu LY, Ma BP "Steroidal saponins obtained by biotransformation of total furostanol glycosides from Dioscorea zingiberensis with Absidia coerulea" -
Carbohydrate Research 402 (2015) 236-40
Five new steroidal saponins (1-5) were isolated from the fermentation broth of total furostanol glycosides from tubers of Dioscorea zingiberensis C.H. Wright incubated with a fungal, Absidia coerulea AS 3.3389, along with known saponins, zingiberensis new saponin (6), deltonin (7), prosapogenin A of dioscin (8), and protobioside (9), and their structures were established by NMR spectroscopy and mass spectrometry as well as by comparison with previously reported spectral data in the literatures. The induced effects in vitro on rat platelet aggregation of all compounds were evaluated
biotransformation, Absidia coerulea, Dioscorea zingiberensis, Dioscoreaceae, steroidal saponins, induced-platelet aggregation activity
NCBI PubMed ID: 25498025Publication DOI: 10.1016/j.carres.2014.11.011Journal NLM ID: 0043535Publisher: Elsevier
Correspondence: Ma BP
Institutions: Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China, Center for Culture Collection of Pharmaceutical Microorganisms, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, College of Pharmacy, Inner Mongolia Medical University, Hohhot, China
Methods: 13C NMR, 1H NMR, TLC, biological assays, HPLC, extraction, optical rotation measurement, CC, cell growth, HR-ESI-MS, centrifugation
Expand this compound
Collapse this compound
3. Compound ID: 20815
|
b-D-Glcp-(1-4)-+
|
a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = (20R,25R)-spirost-5-ene-3β-ol = SMILES C[C@@H]1CC[C@@]6(OC1)OC5CC4C3C/C=C\2C{3}[C@@H](O)CC[C@]2(C)C3CC[C@]4(C)C5[C@H]6C |
Show graphically |
Structure type: oligomer
; 883.4759 [M-H]-
C45H72O17
Compound class: saponin glycoside, glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 8311
Pang X, Wen D, Zhao Y, Xiong CQ, Wang XQ, Yu LY, Ma BP "Steroidal saponins obtained by biotransformation of total furostanol glycosides from Dioscorea zingiberensis with Absidia coerulea" -
Carbohydrate Research 402 (2015) 236-40
Five new steroidal saponins (1-5) were isolated from the fermentation broth of total furostanol glycosides from tubers of Dioscorea zingiberensis C.H. Wright incubated with a fungal, Absidia coerulea AS 3.3389, along with known saponins, zingiberensis new saponin (6), deltonin (7), prosapogenin A of dioscin (8), and protobioside (9), and their structures were established by NMR spectroscopy and mass spectrometry as well as by comparison with previously reported spectral data in the literatures. The induced effects in vitro on rat platelet aggregation of all compounds were evaluated
biotransformation, Absidia coerulea, Dioscorea zingiberensis, Dioscoreaceae, steroidal saponins, induced-platelet aggregation activity
NCBI PubMed ID: 25498025Publication DOI: 10.1016/j.carres.2014.11.011Journal NLM ID: 0043535Publisher: Elsevier
Correspondence: Ma BP
Institutions: Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China, Center for Culture Collection of Pharmaceutical Microorganisms, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, College of Pharmacy, Inner Mongolia Medical University, Hohhot, China
Methods: 13C NMR, 1H NMR, TLC, biological assays, HPLC, extraction, optical rotation measurement, CC, cell growth, HR-ESI-MS, centrifugation
Expand this compound
Collapse this compound
4. Compound ID: 20816
|
a-L-Rhap-(1-2)-+
|
b-D-Glcp-(1-3)-b-D-Glcp-(1-4)-b-D-Glcp-(1-3)-Subst
Subst = (20R,25R)-spirost-5-ene-3β-ol = SMILES C[C@@H]1CC[C@@]6(OC1)OC5CC4C3C/C=C\2C{3}[C@@H](O)CC[C@]2(C)C3CC[C@]4(C)C5[C@H]6C |
Show graphically |
Structure type: oligomer
; 1045.5256 [M-H]-
C51H82O22
Compound class: saponin glycoside, glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_153543,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 8311
Pang X, Wen D, Zhao Y, Xiong CQ, Wang XQ, Yu LY, Ma BP "Steroidal saponins obtained by biotransformation of total furostanol glycosides from Dioscorea zingiberensis with Absidia coerulea" -
Carbohydrate Research 402 (2015) 236-40
Five new steroidal saponins (1-5) were isolated from the fermentation broth of total furostanol glycosides from tubers of Dioscorea zingiberensis C.H. Wright incubated with a fungal, Absidia coerulea AS 3.3389, along with known saponins, zingiberensis new saponin (6), deltonin (7), prosapogenin A of dioscin (8), and protobioside (9), and their structures were established by NMR spectroscopy and mass spectrometry as well as by comparison with previously reported spectral data in the literatures. The induced effects in vitro on rat platelet aggregation of all compounds were evaluated
biotransformation, Absidia coerulea, Dioscorea zingiberensis, Dioscoreaceae, steroidal saponins, induced-platelet aggregation activity
NCBI PubMed ID: 25498025Publication DOI: 10.1016/j.carres.2014.11.011Journal NLM ID: 0043535Publisher: Elsevier
Correspondence: Ma BP
Institutions: Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China, Center for Culture Collection of Pharmaceutical Microorganisms, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, College of Pharmacy, Inner Mongolia Medical University, Hohhot, China
Methods: 13C NMR, 1H NMR, TLC, biological assays, HPLC, extraction, optical rotation measurement, CC, cell growth, HR-ESI-MS, centrifugation
Expand this compound
Collapse this compound
5. Compound ID: 20817
|
a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = (20R,25R)-spirost-5-ene-3β-ol = SMILES C[C@@H]1CC[C@@]6(OC1)OC5CC4C3C/C=C\2C{3}[C@@H](O)CC[C@]2(C)C3CC[C@]4(C)C5[C@H]6C |
Show graphically |
Structure type: oligomer
; 721.4117 [M-H]-
C39H62O12
Compound class: saponin glycoside, glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 8311
Pang X, Wen D, Zhao Y, Xiong CQ, Wang XQ, Yu LY, Ma BP "Steroidal saponins obtained by biotransformation of total furostanol glycosides from Dioscorea zingiberensis with Absidia coerulea" -
Carbohydrate Research 402 (2015) 236-40
Five new steroidal saponins (1-5) were isolated from the fermentation broth of total furostanol glycosides from tubers of Dioscorea zingiberensis C.H. Wright incubated with a fungal, Absidia coerulea AS 3.3389, along with known saponins, zingiberensis new saponin (6), deltonin (7), prosapogenin A of dioscin (8), and protobioside (9), and their structures were established by NMR spectroscopy and mass spectrometry as well as by comparison with previously reported spectral data in the literatures. The induced effects in vitro on rat platelet aggregation of all compounds were evaluated
biotransformation, Absidia coerulea, Dioscorea zingiberensis, Dioscoreaceae, steroidal saponins, induced-platelet aggregation activity
NCBI PubMed ID: 25498025Publication DOI: 10.1016/j.carres.2014.11.011Journal NLM ID: 0043535Publisher: Elsevier
Correspondence: Ma BP
Institutions: Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China, Center for Culture Collection of Pharmaceutical Microorganisms, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, College of Pharmacy, Inner Mongolia Medical University, Hohhot, China
Methods: 13C NMR, 1H NMR, TLC, biological assays, HPLC, extraction, optical rotation measurement, CC, cell growth, HR-ESI-MS, centrifugation
Expand this compound
Collapse this compound
6. Compound ID: 20818
|
a-L-Rhap-(1-2)-+
|
b-D-Glcp-(1-3)-b-D-Glcp-(1-4)-b-D-Glcp-(1-3)-Subst
Subst = (20L,25R)-spirost-5-ene-3β-ol = SMILES C[C@@H]1CC[C@@]6(OC1)OC5CC4C3C/C=C\2C{3}[C@@H](O)CC[C@]2(C)C3CC[C@]4(C)C5[C@@H]6C |
Show graphically |
Structure type: oligomer
Compound class: saponin glycoside, glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_153543,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 8311
Pang X, Wen D, Zhao Y, Xiong CQ, Wang XQ, Yu LY, Ma BP "Steroidal saponins obtained by biotransformation of total furostanol glycosides from Dioscorea zingiberensis with Absidia coerulea" -
Carbohydrate Research 402 (2015) 236-40
Five new steroidal saponins (1-5) were isolated from the fermentation broth of total furostanol glycosides from tubers of Dioscorea zingiberensis C.H. Wright incubated with a fungal, Absidia coerulea AS 3.3389, along with known saponins, zingiberensis new saponin (6), deltonin (7), prosapogenin A of dioscin (8), and protobioside (9), and their structures were established by NMR spectroscopy and mass spectrometry as well as by comparison with previously reported spectral data in the literatures. The induced effects in vitro on rat platelet aggregation of all compounds were evaluated
biotransformation, Absidia coerulea, Dioscorea zingiberensis, Dioscoreaceae, steroidal saponins, induced-platelet aggregation activity
NCBI PubMed ID: 25498025Publication DOI: 10.1016/j.carres.2014.11.011Journal NLM ID: 0043535Publisher: Elsevier
Correspondence: Ma BP
Institutions: Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China, Center for Culture Collection of Pharmaceutical Microorganisms, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, College of Pharmacy, Inner Mongolia Medical University, Hohhot, China
Methods: 13C NMR, 1H NMR, TLC, biological assays, HPLC, extraction, optical rotation measurement, CC, cell growth, HR-ESI-MS, centrifugation
Expand this compound
Collapse this compound
7. Compound ID: 20819
|
b-D-Glcp-(1-4)-+
|
a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = (20L,25R)-spirost-5-ene-3β-ol = SMILES C[C@@H]1CC[C@@]6(OC1)OC5CC4C3C/C=C\2C{3}[C@@H](O)CC[C@]2(C)C3CC[C@]4(C)C5[C@@H]6C |
Show graphically |
Structure type: oligomer
Trivial name: deltonin
Compound class: saponin glycoside, glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 8311
Pang X, Wen D, Zhao Y, Xiong CQ, Wang XQ, Yu LY, Ma BP "Steroidal saponins obtained by biotransformation of total furostanol glycosides from Dioscorea zingiberensis with Absidia coerulea" -
Carbohydrate Research 402 (2015) 236-40
Five new steroidal saponins (1-5) were isolated from the fermentation broth of total furostanol glycosides from tubers of Dioscorea zingiberensis C.H. Wright incubated with a fungal, Absidia coerulea AS 3.3389, along with known saponins, zingiberensis new saponin (6), deltonin (7), prosapogenin A of dioscin (8), and protobioside (9), and their structures were established by NMR spectroscopy and mass spectrometry as well as by comparison with previously reported spectral data in the literatures. The induced effects in vitro on rat platelet aggregation of all compounds were evaluated
biotransformation, Absidia coerulea, Dioscorea zingiberensis, Dioscoreaceae, steroidal saponins, induced-platelet aggregation activity
NCBI PubMed ID: 25498025Publication DOI: 10.1016/j.carres.2014.11.011Journal NLM ID: 0043535Publisher: Elsevier
Correspondence: Ma BP
Institutions: Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China, Center for Culture Collection of Pharmaceutical Microorganisms, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, College of Pharmacy, Inner Mongolia Medical University, Hohhot, China
Methods: 13C NMR, 1H NMR, TLC, biological assays, HPLC, extraction, optical rotation measurement, CC, cell growth, HR-ESI-MS, centrifugation
Expand this compound
Collapse this compound
8. Compound ID: 20820
|
a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = (20L,25R)-spirost-5-ene-3β-ol = SMILES C[C@@H]1CC[C@@]6(OC1)OC5CC4C3C/C=C\2C{3}[C@@H](O)CC[C@]2(C)C3CC[C@]4(C)C5[C@@H]6C |
Show graphically |
Structure type: oligomer
Trivial name: prosapogenin A, dioscin
Compound class: saponin glycoside, glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 8311
Pang X, Wen D, Zhao Y, Xiong CQ, Wang XQ, Yu LY, Ma BP "Steroidal saponins obtained by biotransformation of total furostanol glycosides from Dioscorea zingiberensis with Absidia coerulea" -
Carbohydrate Research 402 (2015) 236-40
Five new steroidal saponins (1-5) were isolated from the fermentation broth of total furostanol glycosides from tubers of Dioscorea zingiberensis C.H. Wright incubated with a fungal, Absidia coerulea AS 3.3389, along with known saponins, zingiberensis new saponin (6), deltonin (7), prosapogenin A of dioscin (8), and protobioside (9), and their structures were established by NMR spectroscopy and mass spectrometry as well as by comparison with previously reported spectral data in the literatures. The induced effects in vitro on rat platelet aggregation of all compounds were evaluated
biotransformation, Absidia coerulea, Dioscorea zingiberensis, Dioscoreaceae, steroidal saponins, induced-platelet aggregation activity
NCBI PubMed ID: 25498025Publication DOI: 10.1016/j.carres.2014.11.011Journal NLM ID: 0043535Publisher: Elsevier
Correspondence: Ma BP
Institutions: Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China, Center for Culture Collection of Pharmaceutical Microorganisms, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, College of Pharmacy, Inner Mongolia Medical University, Hohhot, China
Methods: 13C NMR, 1H NMR, TLC, biological assays, HPLC, extraction, optical rotation measurement, CC, cell growth, HR-ESI-MS, centrifugation
Expand this compound
Collapse this compound
9. Compound ID: 20821
|
a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = protobioside aglycon = SMILES C[C@@H]({26}CO)CC{22}[C@@]5(O)OC4CC3C2C/C=C\1C{3}[C@@H](O)CC[C@]1(C)C2CC[C@]3(C)C4[C@@H]5C |
Show graphically |
Structure type: oligomer
Trivial name: protobioside
Compound class: saponin glycoside, glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
The structure is contained in the following publication(s):
- Article ID: 8311
Pang X, Wen D, Zhao Y, Xiong CQ, Wang XQ, Yu LY, Ma BP "Steroidal saponins obtained by biotransformation of total furostanol glycosides from Dioscorea zingiberensis with Absidia coerulea" -
Carbohydrate Research 402 (2015) 236-40
Five new steroidal saponins (1-5) were isolated from the fermentation broth of total furostanol glycosides from tubers of Dioscorea zingiberensis C.H. Wright incubated with a fungal, Absidia coerulea AS 3.3389, along with known saponins, zingiberensis new saponin (6), deltonin (7), prosapogenin A of dioscin (8), and protobioside (9), and their structures were established by NMR spectroscopy and mass spectrometry as well as by comparison with previously reported spectral data in the literatures. The induced effects in vitro on rat platelet aggregation of all compounds were evaluated
biotransformation, Absidia coerulea, Dioscorea zingiberensis, Dioscoreaceae, steroidal saponins, induced-platelet aggregation activity
NCBI PubMed ID: 25498025Publication DOI: 10.1016/j.carres.2014.11.011Journal NLM ID: 0043535Publisher: Elsevier
Correspondence: Ma BP
Institutions: Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, China, Center for Culture Collection of Pharmaceutical Microorganisms, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China, College of Pharmacy, Inner Mongolia Medical University, Hohhot, China
Methods: 13C NMR, 1H NMR, TLC, biological assays, HPLC, extraction, optical rotation measurement, CC, cell growth, HR-ESI-MS, centrifugation
Expand this compound
Collapse this compound
Total list of structure IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
Execution: <1 sec