Chemical fact sheet: Naringenin 7-O-glucoside

The BCDB-database is not an authoritative database. This sheet collates data stored for chemical entry naringenin 7-O-glucoside and its related chemical compound entries prunin .

Naringenin 7-O-glucoside

Basics

Category
Flavanone derivatives
IUPAC-name
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-(((3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)chroman-4-one
Formula
C21H22O10
Exact mass
434.12130 g/mol
Molecular weight
434.40000 g/mol
Structure
Chemical structure of naringenin 7-O-glucoside
Figure 1.1: Chemical structure of naringenin 7-O-glucoside

Sources

In summary, the chemical naringenin 7-O-glucoside 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. Ø. Andersen, and K. Markham, Flavonoids. Chemistry, biochemistry and applications.. CRC Press, 2006
  2. A. Lavola, M. Maukonen, and R. Julkunen-Tiitto, "Variability in the composition of phenolic compounds in winter-dormant Salix pyrolifolia in relation to plant part and age," Phytochemistry , vol. 153 , pp. 102–110 , DOI: 10.1016/j.phytochem.2018.05.021 .
  3. J. Kim, A. Assefa, J. Song, V. Mani, S. Park, S. Lee, K. Lee, D. Kim, and B. Hahn, "Assessment of metabolic profiles in florets of Carthamus species using ultra-performance liquid chromatography-mass spectrometry.," Metabolites , vol. 10 , no. 11 , pp. 440 , DOI: 10.3390/metabo10110440 .

Analysis results

Analysis result 1

STD
False
TLC
False
UV/Vis detector description
Mass spectrometer description
UHPLC-ESI-QTOF-MS, quadrupole time-of-flight
Organism
Carthamus tinctorius  L.
cultivated
dried, frozen
Sample note
The material (Accession Number 592391) were obtained from USDA National Plant Germplasm system. The seeds were planted and cultivated in a greenhouse at 18-25 °C located at the National Institute of Agricultural Sciences, Jeonju, Korea.These MIDDLE STAGE flower samples were collected when flowering was considered complete, i.e. more than 90 % of the florets were open. The florets were orange(-yellow).
Drying methods
freeze-dried
Dried material storage temperature
-80 °C
Extraction solvents
70 % methanol
Extraction mass/volume-ratio
25 mg/mL
Extraction repeats
5
Extraction time
35 min
Extraction temperature
4 °C
Analysis solvents
70 % methanol
Detection note
The exact mass obtained.
References

J. Kim, A. Assefa, J. Song, V. Mani, S. Park, S. Lee, K. Lee, D. Kim, and B. Hahn, "Assessment of metabolic profiles in florets of Carthamus species using ultra-performance liquid chromatography-mass spectrometry.," Metabolites , vol. 10 , no. 11 , pp. 440 , DOI: 10.3390/metabo10110440 .

Analysis result 2

STD
False
TLC
False
UV/Vis detector description
Mass spectrometer description
UHPLC-ESI-QTOF-MS, quadrupole time-of-flight
Organism
Carthamus tinctorius  L.
cultivated
dried, frozen
Sample note
The material (Accession Number 592391) were obtained from USDA National Plant Germplasm system. The seeds were planted and cultivated in a greenhouse at 18-25 °C located at the National Institute of Agricultural Sciences, Jeonju, Korea.These LATE STAGE flower samples were collected when the capitulum begins to expand and the seeds are about to start developing. The florets start to change color to orange/red.
Drying methods
freeze-dried
Dried material storage temperature
-80 °C
Extraction solvents
70 % methanol
Extraction mass/volume-ratio
25 mg/mL
Extraction repeats
5
Extraction time
35 min
Extraction temperature
4 °C
Analysis solvents
70 % methanol
Detection note
The exact mass obtained.
References

J. Kim, A. Assefa, J. Song, V. Mani, S. Park, S. Lee, K. Lee, D. Kim, and B. Hahn, "Assessment of metabolic profiles in florets of Carthamus species using ultra-performance liquid chromatography-mass spectrometry.," Metabolites , vol. 10 , no. 11 , pp. 440 , DOI: 10.3390/metabo10110440 .

Analysis result 3

STD
False
TLC
False
UV/Vis detector description
Mass spectrometer description
UHPLC-ESI-QTOF-MS, quadrupole time-of-flight
Organism
Carthamus palaestinus  L.
wild
dried, frozen
Sample note
The material (Accession Number 235663) were obtained from USDA National Plant Germplasm system. The seeds were planted and cultivated in a greenhouse at 18-25 °C located at the National Institute of Agricultural Sciences, Jeonju, Korea.These MIDDLE STAGE flower samples were collected when flowering was considered complete, i.e. more than 90 % of the florets were open. The florets were orange(-yellow).
Drying methods
freeze-dried
Dried material storage temperature
-80 °C
Extraction solvents
70 % methanol
Extraction mass/volume-ratio
25 mg/mL
Extraction repeats
5
Extraction time
35 min
Extraction temperature
4 °C
Analysis solvents
70 % methanol
Detection note
The exact mass obtained.
References

J. Kim, A. Assefa, J. Song, V. Mani, S. Park, S. Lee, K. Lee, D. Kim, and B. Hahn, "Assessment of metabolic profiles in florets of Carthamus species using ultra-performance liquid chromatography-mass spectrometry.," Metabolites , vol. 10 , no. 11 , pp. 440 , DOI: 10.3390/metabo10110440 .

Analysis result 4

STD
False
TLC
False
UV/Vis detector description
Mass spectrometer description
UHPLC-ESI-QTOF-MS, quadrupole time-of-flight
Organism
Carthamus palaestinus  L.
wild
dried, frozen
Sample note
The material (Accession Number 235663) were obtained from USDA National Plant Germplasm system. The seeds were planted and cultivated in a greenhouse at 18-25 °C located at the National Institute of Agricultural Sciences, Jeonju, Korea.These LATE STAGE flower samples were collected when the capitulum begins to expand and the seeds are about to start developing. The florets start to change color to orange/red.
Drying methods
freeze-dried
Dried material storage temperature
-80 °C
Extraction solvents
70 % methanol
Extraction mass/volume-ratio
25 mg/mL
Extraction repeats
5
Extraction time
35 min
Extraction temperature
4 °C
Analysis solvents
70 % methanol
Detection note
The exact mass obtained.
References

J. Kim, A. Assefa, J. Song, V. Mani, S. Park, S. Lee, K. Lee, D. Kim, and B. Hahn, "Assessment of metabolic profiles in florets of Carthamus species using ultra-performance liquid chromatography-mass spectrometry.," Metabolites , vol. 10 , no. 11 , pp. 440 , DOI: 10.3390/metabo10110440 .

Analysis result 5

Detection technique Values Units
UV/Vis 226
282
335
nm
[M⁻ H]⁻ 433.12193
457.11170
m/z
STD
True
TLC
False
UV/Vis detector description
HPLC-DAD
Mass spectrometer description
UHPLC-QTOF-MS
Organism
Salix pyrolifolia
dried buds, fresh, dried
Sample note
The researchers collected S. pyrolifolia samples from different -aged trees of the same clone grown in Kaavi, Finland.
Extraction solvents
cold methanol
Extraction repeats
5
Extract drying method
evaporation in vacuo
Analysis solvents
water:MeOH, 1:1
Detection note
Na+ -adduct = 23.98977; 457.1117-23.98977 = 433.12193; the compound was detected in the barks of all studied ages (1, 3 and 20 years)
References

A. Lavola, M. Maukonen, and R. Julkunen-Tiitto, "Variability in the composition of phenolic compounds in winter-dormant Salix pyrolifolia in relation to plant part and age," Phytochemistry , vol. 153 , pp. 102–110 , DOI: 10.1016/j.phytochem.2018.05.021 .

Prunin

Basics

Category
Flavanone
IUPAC-name
(S)-5-hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)chroman-4-one
Formula
C21H22O10
Exact mass
434.12130 g/mol
Molecular weight
No weights stored
Structure
Chemical structure of prunin
Figure 2.1: Chemical structure of prunin

Sources

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

References

  1. Ø. Andersen, and K. Markham, Flavonoids. Chemistry, biochemistry and applications.. CRC Press, 2006
  2. A. Lavola, M. Maukonen, and R. Julkunen-Tiitto, "Variability in the composition of phenolic compounds in winter-dormant Salix pyrolifolia in relation to plant part and age," Phytochemistry , vol. 153 , pp. 102–110 , DOI: 10.1016/j.phytochem.2018.05.021 .

Analysis results

No analysis results for this entry in the database.