spiraeoside

Suppliers

Names

[ CAS No. ]:
20229-56-5

[ Name ]:
spiraeoside

[Synonym ]:
Spiraeosid
Quercetin 4'-b-D-glucopyranoside
Quercetin 4'-O-glucoside
Quercetin-4'-glucoside
EINECS 243-614-6
Spiraein
3,5,7-trihydroxy-2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one
quercetin 4'-O-beta-D-glucopyranoside
Spiraeoside

Chemical & Physical Properties

[ Density]:
1.809g/cm3

[ Boiling Point ]:
835.6ºC at 760mmHg

[ Melting Point ]:
209-211ºC

[ Molecular Formula ]:
C21H20O12

[ Molecular Weight ]:
464.37600

[ Flash Point ]:
294.6ºC

[ Exact Mass ]:
464.09500

[ PSA ]:
210.51000

[ Vapour Pressure ]:
1.28E-29mmHg at 25°C

[ Index of Refraction ]:
1.774

[ Storage condition ]:
?20°C

MSDS

Click to get detail MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
DJ3095000
CHEMICAL NAME :
4H-1-Benzopyran-4-one, 2-(4-(beta-D-glucopyranosyloxy)-3-hydroxyphenyl)-3,5, 7-trihydroxy-
CAS REGISTRY NUMBER :
20229-56-5
LAST UPDATED :
199503
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C21-H20-C12
MOLECULAR WEIGHT :
416.53

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Sex chromosome loss and nondisjunction
TEST SYSTEM :
Human Lymphocyte
DOSE/DURATION :
50 mg/L
REFERENCE :
MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 246,205,1991

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
22

[ RIDADR ]:
NONH for all modes of transport

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 2-(4-O-β-D-glucopyranosyloxy-3-benzyloxyphenyl)-3,5,7-tribenzyloxy-4H-chromen-4-one
  • Quercetin
  • 2,3,4,6-Tetra-O-acetyl-alpha-D-glucopyranosyl bromide
  • (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-(4-(3,7-bis(benzyloxy)-5-hydroxy-4-oxo-4H-chromen-2-yl)-2-hydroxyphenoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
  • 2-(2,2-diphenylbenzo[d][1,3]dioxol-5-yl)-3,5,7-trihydroxy-4H-chroMen-4-one
  • Uridine diphosphate glucose

DownStream

  • D-glucopyranose
  • Quercetin

Articles

The crystal structure of human cytosolic beta-glucosidase unravels the substrate aglycone specificity of a family 1 glycoside hydrolase.

J. Mol. Biol. 370(5) , 964-75, (2007)

Human cytosolic beta-glucosidase (hCBG) is a xenobiotic-metabolizing enzyme that hydrolyses certain flavonoid glucosides, with specificity depending on the aglycone moiety, the type of sugar and the l...

Flavonoid glycosides inhibit oral cancer cell proliferation--role of cellular uptake and hydrolysis to the aglycones.

J. Pharm. Pharmacol. 57(8) , 1037-42, (2005)

Epidemiologic evidence supports the view that dietary flavonoids exert protective effects in oral diseases, including cancer. However, the dietary forms of flavonoids, the flavonoid glycosides, are th...

Deglycosylation of flavonoid and isoflavonoid glycosides by human small intestine and liver beta-glucosidase activity.

FEBS Lett. 436(1) , 71-5, (1998)

Flavonoid and isoflavonoid glycosides are common dietary phenolics which may be absorbed from the small intestine of humans. The ability of cell-free extracts from human small intestine and liver to d...


More Articles

Related Compounds

  • N-(2,6-dimethylphenyl)-2-(5-(3-ethyl-1,2,4-oxadiazol-5-yl)-2-oxopyridin-1(2H)-yl)acetamide
  • 2-(5-(3-ethyl-1,2,4-oxadiazol-5-yl)-2-oxopyridin-1(2H)-yl)-N-(2-methoxyphenyl)acetamide
  • 2-(5-(3-ethyl-1,2,4-oxadiazol-5-yl)-2-oxopyridin-1(2H)-yl)-N-(3-methoxyphenyl)acetamide
  • 5-(4-bromophenyl)-2-(cyclopentylthio)-1-methyl-1H-imidazole
  • 2-(5-(3-ethyl-1,2,4-oxadiazol-5-yl)-2-oxopyridin-1(2H)-yl)-N-(4-methoxyphenyl)acetamide
  • 2-(isopropylthio)-1,5-diphenyl-1H-imidazole
  • 2-(isobutylthio)-1-phenyl-5-(p-tolyl)-1H-imidazole
  • 1-benzyl-2-(ethylthio)-5-phenyl-1H-imidazole
  • 1-benzyl-2-(cyclopentylthio)-5-(p-tolyl)-1H-imidazole
  • 5-methyl-N-(piperidin-4-yl)thiophene-2-carboxamide
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.