
CAS Number522-12-3
Synonymsquercetin 3-O-α-L-rhamnopyranoside; quercetin-3-L-rhamnoside; 3-O-α-rhamnosylquercetine; Quercetin 3-O-L-rhamnoside; Quercitroside; QUERCETIN 3-L-RHAMNOSIDE; EINECS 208-322-5; Thujin; 3,3',4',5,7-Pentahydroxyflavone 3-(6-deoxy-a-L-mannopyranoside); Quercetin 3-O-α-L-rhamnoside; Quercetin-3-O-α-L-rhamnopyranoside; 3-[(6-Deoxy-α-L-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-benzopyran-4-one; Quercimelin; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl-6-deoxy-α-L-mannopyranoside; Quercetin-3-rhamnoside; Quercetrin; FLAVIN; Quercetin-3-O-rhamnoside; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl 6-deoxy-α-L-mannopyranoside; usafcf-2; quercetin 3-O-rhamnoside; MFCD00016932; 3-[(6-Deoxy-a-L-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-
Molecular FormulaC21H20O11
Molecular Weight448.38
Purity≥95.0 (HPLC)%
Density1.8±0.1 g/cm3
Boiling Point814.0±65.0 °C at 760 mmHg
Melting Point174-183ºC
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 522-12-3 |
| Catalog No. | 2A-0200674 |
| Chinese Name | 槲皮苷 |
| Synonyms | quercetin 3-O-α-L-rhamnopyranoside; quercetin-3-L-rhamnoside; 3-O-α-rhamnosylquercetine; Quercetin 3-O-L-rhamnoside; Quercitroside; QUERCETIN 3-L-RHAMNOSIDE; EINECS 208-322-5; Thujin; 3,3',4',5,7-Pentahydroxyflavone 3-(6-deoxy-a-L-mannopyranoside); Quercetin 3-O-α-L-rhamnoside; Quercetin-3-O-α-L-rhamnopyranoside; 3-[(6-Deoxy-α-L-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-benzopyran-4-one; Quercimelin; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl-6-deoxy-α-L-mannopyranoside; Quercetin-3-rhamnoside; Quercetrin; FLAVIN; Quercetin-3-O-rhamnoside; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl 6-deoxy-α-L-mannopyranoside; usafcf-2; quercetin 3-O-rhamnoside; MFCD00016932; 3-[(6-Deoxy-a-L-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1- |
| Molecular Formula | C21H20O11 |
| Molecular Weight | 448.38 |
| Purity | ≥95.0 (HPLC) |
| Density | 1.8±0.1 g/cm3 |
| Boiling Point | 814.0±65.0 °C at 760 mmHg |
| Melting Point | 174-183ºC |
| Storage Condition | 2-8°C |
| Application | Quercitrin is a natural compound in tartary buckwheat that has anti-inflammatory properties and is often used to treat cardiovascular disease. |
| MDL Number | MFCD00016932 |
| SMILES | C[C@@H]1O[C@@H](OC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)c(O)c4)[C@H](O)[C@H](O)[C@H]1O |
| InChI | 1S/C21H20O11/c1-7-15(26)17(28)18(29)21(30-7)32-20-16(27)14-12(25)5-9(22)6-13(14)31-19(20)8-2-3-10(23)11(24)4-8/h2-7,15,17-18,21-26,28-29H,1H3/t7-,15-,17+,18+,21-/m0/s1 |
| InChI Key | OXGUCUVFOIWWQJ-HQBVPOQASA-N |
| Beilstein/REAXYS | 68135 |
| NACRES Code | NA.24 |
| UNSPSC | 41116107 |
| Hazard Symbols | Transport |
| MSDS | msds/12224_1_522_12_3.pdf |
| Bioactivity | Quercitrin is a natural compound found in Tartary buckwheat with a potential anti-inflammation effect that is used to treat heart and vascular conditions.IC50 value:Target:In vitro: There were significant increases in caspase-3 activity, loss of MMP, and increases in the apoptotic cell population in response to quercitrin in DLD-1 colon cancer cells in a time- and dose-dependent manner. [1] In vivo: ICR mice received CCl4 intraperitoneally with or without quercitrin co-administration for 4 weeks. Data showed that quercitrin significantly suppressed the elevation of reactive oxygen species (ROS) production and malondialdehyde (MDA) content, reduced tissue plasminogen activator (t-PA) activity, enhanced the antioxidant enzyme activities and abrogated cytochrome P450 2E1 (CYP2E1) induction in mouse brains. [2] Related Catalog Signaling Pathways >> Autophagy >> Autophagy Signaling Pathways >> MAPK/ERK Pathway >> Ribosomal S6 Kinase (RSK) Natural Products >> Flavonoids Research Areas >> Inflammation/Immunology References [1]. Cincin ZB, et al. Apoptotic Effects of Quercitrin on DLD-1 Colon Cancer Cell Line. Pathol Oncol Res. 2015 Apr;21(2):333-8. [2]. Ma JQ, et al. Quercitrin offers protection against brain injury in mice by inhibiting oxidative stress and inflammation. Food Funct. 2016 Jan 20;7(1):549-56. [3]. Li W, et al. Quercitrin ameliorates the development of systemic lupus erythematosus-like disease in a chronic graft-versus-host murine model. Am J Physiol Renal Physiol. 2016 Feb 24:ajprenal.00249.2015. Chemical & Physical Properties Density 1.8±0.1 g/cm3 Boiling Point 814.0±65.0 °C at 760 mmHg Melting Point 174-183ºC Molecular Formula C21H20O11 Molecular Weight 448.377 Flash Point 288.3±27.8 °C Exact Mass 448.100555 PSA 190.28000 LogP 2.17 Vapour Pressure 0.0±3.1 mmHg at 25°C Index of Refraction 1.776 InChIKey OXGUCUVFOIWWQJ-HQBVPOQASA-N SMILES CC1OC(Oc2c(-c3ccc(O)c(O)c3)oc3cc(O)cc(O)c3c2=O)C(O)C(O)C1O Storage condition 2-8°C |
| Use of | Properties Articles58 Name quercitrin Synonym More Synonyms Quercitrin Biological Activity Related Catalog Signaling Pathways >> Autophagy >> Autophagy Signaling Pathways >> MAPK/ERK Pathway >> Ribosomal S6 Kinase (RSK) Natural Products >> Flavonoids Research Areas >> Inflammation/Immunology References [2]. Ma JQ, et al. Quercitrin offers protection against brain injury in mice by inhibiting oxidative stress and inflammation. Food Funct. 2016 Jan 20;7(1):549-56. [3]. Li W, et al. Quercitrin ameliorates the development of systemic lupus erythematosus-like disease in a chronic graft-versus-host murine model. Am J Physiol Renal Physiol. 2016 Feb 24:ajprenal.00249.2015. Chemical & Physical Properties Molecular Formula C21H20O11 Exact Mass 448.100555 PSA 190.28000 Index of Refraction 1.776 InChIKey OXGUCUVFOIWWQJ-HQBVPOQASA-N |
| Transport Info | Shipping Name: UN |
| MSDS Transport Info | Module 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 |
| Related Products in Botanical Reference Standards | ||
|---|---|---|
| Picroside II | 39012-20-9 | 2A-9012013 |
| Polisaponin | 8063-80-7 | 2A-9012073 |
| Propofol glucuronide | 114991-26-3 | 2A-9012169 |
| Psoralen | 66-97-7 | 2A-9012193 |
| Puerarin | 3681-99-0 | 2A-9012195 |
| Raspberry ketone glucoside | 38963-94-9 | 2A-9012272 |
| Rosmarinic acid | 20283-92-5 | 2A-9012345 |
| Ryanodine | 15662-33-6 | 2A-9012362 |
| Saikosaponin A | 20736-09-8 | 2A-9012369 |
| Saikosaponin B1 | 58558-08-0 | 2A-9012370 |
| Browse all Botanical Reference Standards products » | ||
Phone:
630-322-8886
630-322-8887
Email:
Office Locations:
Chicago, IL, USA
San Francisco, CA, USA