Spiraeoside structure, CAS 20229-56-5

Spiraeoside

CAS Number20229-56-5

SynonymsSpiraeosid; Quercetin 4'-b-D-glucopyranoside; Quercetin 4'-O-glucoside; Quercetin-4'-glucoside; EINECS 243-614-6; Spiraein; quercetin 4'-O-beta-D-glucopyranoside; Spiraeoside

Molecular FormulaC21H20O12

Molecular Weight464.38

Purity≥95.0 (HPLC)%

Density1.809g/cm3

Boiling Point835.6ºC at 760mmHg

Melting Point209-211ºC

Flash Point

AppearanceYellow powder with lumps

EINECS

MSDSChineseEnglish

Symboltransportation

Signal WordWarning

Cat. No.: 2A-9038340 Purity: ≥95.0 (HPLC)%
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Quality Control of [ 20229-56-5 ] Purity: ≥95.0 (HPLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number20229-56-5
Catalog No.2A-9038340
Chinese Name螺旋藻甙
SynonymsSpiraeosid; Quercetin 4'-b-D-glucopyranoside; Quercetin 4'-O-glucoside; Quercetin-4'-glucoside; EINECS 243-614-6; Spiraein; quercetin 4'-O-beta-D-glucopyranoside; Spiraeoside
Molecular FormulaC21H20O12
Molecular Weight464.38
Purity≥95.0 (HPLC)
Density1.809g/cm3
Boiling Point835.6ºC at 760mmHg
Melting Point209-211ºC
AppearanceYellow powder with lumps
Storage Condition?20°C
ApplicationSpirulina is an orally active natural compound that has antioxidant activity and inhibits the production of reactive oxygen species (ROS) and malondialdehyde. Spirulina has anti-allergic, anti-inflamm
MDL NumberMFCD00221723
SMILESOC[C@H]1O[C@@H](Oc2ccc(cc2O)C3=C(O)C(=O)c4c(O)cc(O)cc4O3)[C@H](O)[C@@H](O)[C@@H]1O
InChI1S/C21H20O12/c22-6-13-15(26)17(28)19(30)21(33-13)32-11-2-1-7(3-9(11)24)20-18(29)16(27)14-10(25)4-8(23)5-12(14)31-20/h1-5,13,15,17,19,21-26,28-30H,6H2/t13-,15-,17+,19-,21-/m1/s1
InChI KeyOIUBYZLTFSLSBY-HMGRVEAOSA-N
NACRES CodeNA.24
UNSPSC41116107
Hazard Symbolstransportation
MSDSmsds/38340_1_20229_56_5.pdf
BioactivitySpiraeoside, an orally active natural compound, exerts antioxidant activity, inhibits reactive oxygen species (ROS) and malondialdehyde production. Spiraeoside possesses antiallergic, anti-inflammatory and antitumor activities[1]. Related Catalog Research Areas >> Cancer Research Areas >> Inflammation/Immunology In Vitro Spiraeoside elevates HG stimulation-caused the decrease in the expression levels of p-Akt, nuclear Nrf2, and HO-1 in AC16 cells (the effects of Spiraeoside are reversedby LY294002)[1]. Spiraeoside protects AC16 cells against HG-induced oxidative stress, cell injury, and apoptosis[1]. Spiraeoside activates the PI3K/Akt/Nrf2 pathway in AC16 cells on exposure to HG[1]. Spiraeoside protects AC16 cells against HG-induced apoptosis through the PI3K/Akt/Nrf2 pathway[1]. Cell Viability Assay[1] Cell Line: AC16 cells. Concentration: 1, 5, 10, or 20 μM. Incubation Time: 0, 24, or 48 hours. Result: Inhibited AC16 cells viability (20 μM). In Vivo Spiraeoside (50 mg/kg, p.o.) shows ulcer preventive ability[2]. Animal Model: Male Wistar rats (6-8 weeks old)[2]. Dosage: 50 mg/kg. Administration: Oral gavage an hour before inducing the lesions. Result: Decreased severity of the formed lesions. References [1]. Hongyang Liu, et al. Spiraeoside protects human cardiomyocytes against high glucose-induced injury, oxidative stress, and apoptosis by activation of PI3K/Akt/Nrf2 pathway. J Biochem Mol Toxicol. 2020 Oct;34(10):e22548. [2]. Stevan Samardžić, et al. Antioxidant, anti-inflammatory and gastroprotective activity of Filipendula ulmaria (L.) Maxim. and Filipendula vulgaris Moench. J Ethnopharmacol. 2018 Mar 1;213:132-137. 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 InChIKey OIUBYZLTFSLSBY-HMGRVEAOSA-N SMILES O=c1c(O)c(-c2ccc(OC3OC(CO)C(O)C(O)C3O)c(O)c2)oc2cc(O)cc(O)c12 Storage condition ?20°C
Use ofSpiraeoside, an orally active natural compound, exerts antioxidant activity, inhibits reactive oxygen species (ROS) and malondialdehyde production. Spiraeoside possesses antiallergic, anti-inflammatory and antitumor activities[1]. Properties Articles25 Name quercetin 4ʼ-O-β-D-glucopyranoside Synonym More Synonyms spiraeoside Biological Activity Description Spiraeoside, an orally active natural compound, exerts antioxidant activity, inhibits reactive oxygen species (ROS) and malondialdehyde production. Spiraeoside possesses antiallergic, anti-inflammatory and antitumor activities[1]. Related Catalog Research Areas >> Cancer Research Areas >> Inflammation/Immunology References [1]. Hongyang Liu, et al. Spiraeoside protects human cardiomyocytes against high glucose-induced injury, oxidative stress, and apoptosis by activation of PI3K/Akt/Nrf2 pathway. J Biochem Mol Toxicol. 2020 Oct;34(10):e22548. [2]. Stevan Samardžić, et al. Antioxidant, anti-inflammatory and gastroprotective activity of Filipendula ulmaria (L.) Maxim. and Filipendula vulgaris Moench. J Ethnopharmacol. 2018 Mar 1;213:132-137. Chemical & Physical Properties Molecular Formula C21H20O12 Exact Mass 464.09500 PSA 210.51000 Index of Refraction 1.774 InChIKey OIUBYZLTFSLSBY-HMGRVEAOSA-N
Transport InfoShipping Name: UN
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available
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