Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C19H32O7 |
| Molecular Weight | 372.4532 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](CC[C@H]1C(C)=CC(=O)CC1(C)C)O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O
InChI
InChIKey=NYLNHNDMNOPWAZ-ZLEFDVGRSA-N
InChI=1S/C19H32O7/c1-10-7-12(21)8-19(3,4)13(10)6-5-11(2)25-18-17(24)16(23)15(22)14(9-20)26-18/h7,11,13-18,20,22-24H,5-6,8-9H2,1-4H3/t11-,13+,14-,15-,16+,17-,18-/m1/s1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/20190461Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/24785825
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20190461
Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/24785825
Byzantionoside B was isolated from the aerial parts of Stachys byzantina as the C-9 epimer of blumenol C glucoside. Byzantionoside B showed osteogenic activity by increasing alkaline phosphatase activity and calcium contents to regulate differentiation and mineralization in human osteoblast cells.
Originator
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24785825
Byzantionoside B significantly increased alkaline phosphatase activity in human osteoblast cells when used at a concentration of 100 μM and also increased the calcium contents of the mineralized matrix. At the same concentration. Byzantionoside B upregulated the mRNA expression of osteopontin, bone morphogenetic protein-2, and runt-related transcription factor 2 in human osteoblast cells.
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14135395
Created by
admin on Mon Mar 31 23:39:44 GMT 2025 , Edited by admin on Mon Mar 31 23:39:44 GMT 2025
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135820-80-3
Created by
admin on Mon Mar 31 23:39:44 GMT 2025 , Edited by admin on Mon Mar 31 23:39:44 GMT 2025
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6C3V404S0G
Created by
admin on Mon Mar 31 23:39:44 GMT 2025 , Edited by admin on Mon Mar 31 23:39:44 GMT 2025
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SUBSTANCE RECORD