Chemical fact sheet: Strobilanthoside C

The BCDB-database is not an authoritative database. This sheet collates data stored for chemical entry strobilanthoside C and its related chemical compound entries (E)-methyl 3-O-β-D-glucopyranosyl-1H-indol-2-yl acrylate .

Strobilanthoside C

Basics

Category
Indolics & indole alkaloid derivatives
IUPAC-name
methyl (E)-3-(3-(((2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-yl)oxy)-1H-indol-2-yl)acrylate
Formula
No formula stored
Exact mass
379.12672 g/mol
Molecular weight
No weights stored
Structure
Chemical structure of strobilanthoside C
Figure 1.1: Chemical structure of strobilanthoside C

Sources

In summary, the chemical strobilanthoside C has been analyzed from following sources:

Note that an analysis result in the database may indicate either presence or lack thereof of a chemical in an analyzed sample.

References

  1. W. Gu, Y. Zhang, X. Hao, F. Yang, Q. Sun, S. Morris-Natschke, K. Lee, Y. Wang, and C. Long, "Indole alkaloid glycosides from the aerial parts of Strobilanthes cusia.," Journal of Natural Products , vol. 77 , no. 12 , pp. 2590–2594 , DOI: 10.1021/np5003274 .

Analysis results

Analysis result 1

Detection technique Values Units
UV/Vis 208
254
344
458
nm
M⁺ 378
379.12580
m/z
STD
False
TLC
True
UV/Vis detector description
UV
Mass spectrometer description
ESI-MS, HREI-MS, API hybrid quadrupole time-of-flight MS
Organism
Strobilanthes cusia
dried, powdered
Collection dates
2011-2
Sample note
The plant material was identified by one of the researchers, Chun-Lin, Long. A voucher specimen (BN0045) was deposited in the Key Laboratory of Economic Plants and Biotechnology, Kunming Insitute of Botany, Chinese Academy of Sciences.
Drying methods
air-dried
Extraction solvents
95 % EtOH
Extraction mass/volume-ratio
66.7 mg/mL
Extraction repeats
3
Extract drying method
evaporation under reduced pressure
Detection note
ESIMS m/z 378 [M - H]–; HREIMS m/z 379.1258 [M]+
References

W. Gu, Y. Zhang, X. Hao, F. Yang, Q. Sun, S. Morris-Natschke, K. Lee, Y. Wang, and C. Long, "Indole alkaloid glycosides from the aerial parts of Strobilanthes cusia.," Journal of Natural Products , vol. 77 , no. 12 , pp. 2590–2594 , DOI: 10.1021/np5003274 .

(E)-methyl 3-O-β-D-glucopyranosyl-1H-indol-2-yl acrylate

Basics

Category
None
IUPAC-name
methyl (E)-3-(3-((4,5,6-trihydroxy-3-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-1H-indol-2-yl)acrylate
Formula
No formula stored
Exact mass
379.12670 g/mol
Molecular weight
No weights stored
Structure
Chemical structure of (E)-methyl 3-O-β-D-glucopyranosyl-1H-indol-2-yl acrylate
Figure 2.1: Chemical structure of (E)-methyl 3-O-β-D-glucopyranosyl-1H-indol-2-yl acrylate

Sources

No links to any potential source for this chemical in the database.

References

  1. W. Gu, Y. Zhang, X. Hao, F. Yang, Q. Sun, S. Morris-Natschke, K. Lee, Y. Wang, and C. Long, "Indole alkaloid glycosides from the aerial parts of Strobilanthes cusia.," Journal of Natural Products , vol. 77 , no. 12 , pp. 2590–2594 , DOI: 10.1021/np5003274 .

Analysis results

No analysis results for this entry in the database.