Chemical fact sheet: Quercetin 4'-O-α-rhamnopyranosyl-(1→6)-β-glucopyranoside

The BCDB-database is not an authoritative database. This sheet collates data stored for chemical entry quercetin 4'-O-α-rhamnopyranosyl-(1→6)-β-glucopyranoside and its related chemical compound entries ulmarioside .

Quercetin 4'-O-α-rhamnopyranosyl-(1→6)-β-glucopyranoside

Basics

Category
Flavone and flavonol derivatives
IUPAC-name
3,5,7-trihydroxy-2-(3-hydroxy-4-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)phenyl)-4H-chromen-4-one
Formula
No formula stored
Exact mass
610.15338 g/mol
Molecular weight
No weights stored
Structure
Chemical structure of quercetin 4'-O-α-rhamnopyranosyl-(1→6)-β-glucopyranoside
Figure 1.1: Chemical structure of quercetin 4'-O-α-rhamnopyranosyl-(1→6)-β-glucopyranoside

Sources

In summary, the chemical quercetin 4'-O-α-rhamnopyranosyl-(1→6)-β-glucopyranoside has been analyzed from following sources:

Filipendula camtschatica  (Pall.) Maxim.
1st 2nd
Filipendula denudata  (J. Presl. & C. Presl.) Fritsch.
1st 2nd
Filipendula palmata  (Pall.) Maxim.
1st 2nd
Filipendula stepposa  Juz.
1st 2nd
Filipendula ulmaria  (L.) Maxim.
1st 2nd
Filipendula vulgaris  Moench
1st 2nd

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

References

  1. D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis results

Analysis result 1

Detection technique Values Units
UV/Vis 255
309 sh
366 		nm
[M⁺ H]⁺ 611
633.59400 		m/z
MS²⁺ 303
465 		m/z
STD
False
TLC
True
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula ulmaria  (L.) Maxim.
wild
ground, dried
Collection dates
2011-7
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
Detection note
HR-ESI-MS [M + Na]+ --> 633.594; ESI-MS [M + H]+ --> 611; [(M - rhamnose) + Na]+ --> 465; ,[(M - rhamnose - glucose) + H]+ --> 303
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 2

Detection technique Values Units
[M⁺ H]⁺ 611 : ND
633.59400 : ND 		m/z
STD
False
TLC
True
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula ulmaria  (L.) Maxim.
wild
ground, dried
Collection dates
2011-7
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 3

Detection technique Values Units
UV/Vis 255
309 sh
366 		nm
[M⁺ H]⁺ 611
633.59400 		m/z
MS²⁺ 303
465 		m/z
STD
False
TLC
False
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula stepposa  Juz.
wild
ground, dried
Collection dates
2012-7
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
Detection note
HR-ESI-MS [M + Na]+ --> 633.594; ESI-MS [M + H]+ --> 611; [(M - rhamnose) + Na]+ --> 465; ,[(M - rhamnose - glucose) + H]+ --> 303
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 4

Detection technique Values Units
[M⁺ H]⁺ 611 : ND
633.59400 : ND 		m/z
STD
False
TLC
False
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula stepposa  Juz.
wild
ground, dried
Collection dates
2012-7
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 5

Detection technique Values Units
[M⁺ H]⁺ 611 : ND
633.59400 : ND 		m/z
STD
False
TLC
False
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula camtschatica  (Pall.) Maxim.
wild
ground, dried
Collection dates
2012-7
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 ethanol
Extraction repeats
3
Extraction temperature
90 °C
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 6

Detection technique Values Units
[M⁺ H]⁺ 611 : ND
633.59400 : ND 		m/z
STD
False
TLC
False
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula camtschatica  (Pall.) Maxim.
wild
ground, dried
Collection dates
2012-7
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 7

Detection technique Values Units
[M⁺ H]⁺ 611 : ND
633.59400 : ND 		m/z
STD
False
TLC
False
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula palmata  (Pall.) Maxim.
wild
ground, dried
Collection dates
2012-7
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 8

Detection technique Values Units
[M⁺ H]⁺ 611 : ND
633.59400 : ND 		m/z
STD
False
TLC
False
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula palmata  (Pall.) Maxim.
wild
ground, dried
Collection dates
2012-7
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 9

Detection technique Values Units
[M⁺ H]⁺ 611 : ND
633.59400 : ND 		m/z
STD
False
TLC
False
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula vulgaris  Moench
wild
ground, dried
Collection dates
2012-6
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 10

Detection technique Values Units
[M⁺ H]⁺ 611 : ND
633.59400 : ND 		m/z
STD
False
TLC
False
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula vulgaris  Moench
wild
ground, dried
Collection dates
2012-6
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 11

Detection technique Values Units
UV/Vis 255
309 sh
366 		nm
[M⁺ H]⁺ 611
633.59400 		m/z
MS²⁺ 303
465 		m/z
STD
False
TLC
False
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula denudata  (J. Presl. & C. Presl.) Fritsch.
wild
ground, dried
Collection dates
2012-7
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
Detection note
HR-ESI-MS [M + Na]+ --> 633.594; ESI-MS [M + H]+ --> 611; [(M - rhamnose) + Na]+ --> 465; ,[(M - rhamnose - glucose) + H]+ --> 303
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis result 12

Detection technique Values Units
[M⁺ H]⁺ 611 : ND
633.59400 : ND 		m/z
STD
False
TLC
False
UV/Vis detector description
UV
Mass spectrometer description
HR-ESI-MS, HRMS
Organism
Filipendula denudata  (J. Presl. & C. Presl.) Fritsch.
wild
ground, dried
Collection dates
2012-7
Sample note
The species were defined by Cand. Pharm. Sci. G. V. Chekhirova (IGEB, SB, RAS). Specimens of raw material are preserved in the herbarium of the IGEB, SB, RAS .
Drying methods
air-dried
Extraction solvents
96 % ethanol, 70 % ethanol, 50 % ethanol
Extraction repeats
3
Extraction temperature
90 °C
References

D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Ulmarioside

Basics

Category
Flavonol
IUPAC-name
3,5,7-trihydroxy-2-(3-hydroxy-4-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)phenyl)-4H-chromen-4-one
Formula
No formula stored
Exact mass
610.15338 g/mol
Molecular weight
No weights stored
Structure
Chemical structure of ulmarioside
Figure 2.1: Chemical structure of ulmarioside

Sources

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

References

  1. D. Olennikov, and M. Kruglova, "A new quercetin glycoside and other phenolic compounds from the genus Filipendula.," Chemistry of Natural Compounds , vol. 49 , no. 4 , pp. 610–616 , DOI: 10.1007/s10600-013-0691-0 .

Analysis results

No analysis results for this entry in the database.