Introduction：Basic information about KAEMPFERITRIN CAS 482-38-2, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
KAEMPFERITRIN Basic information
| Product Name: | KAEMPFERITRIN |
| Synonyms: | KAEMPFEROL-3,7-DIRHAMNOSIDE,KaeMpferitrin;lespenefril;KAEMPFEROL-3,7-DIRHAMNOSIDE;3,7-Bis[(6-deoxy-α-L-mannopyranosyl)oxy]-4',5-dihydroxyflavone;3,7-Bis[(6-deoxy-α-L-mannopyranosyl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;Kaempherol 3,7-bismannoside;Lespedin;3,7-bis[(6-deoxy-beta-L-mannopyranosyl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one |
| CAS: | 482-38-2 |
| MF: | C27H30O14 |
| MW: | 578.52 |
| EINECS: | |
| Product Categories: | chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract |
| Mol File: | 482-38-2.mol |
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KAEMPFERITRIN Chemical Properties
| Melting point | 202～203℃ |
| Boiling point | 908.6±65.0 °C(Predicted) |
| density | 1.70 |
| storage temp. | -20°C |
| solubility | DMSO : 125 mg/mL (216.07 mM; Need ultrasonic) |
| pka | 5.81±0.40(Predicted) |
| form | powder |
| color | white to beige |
| biological source | (Cinnamomum sp.) |
| Stability: | Hygroscopic |
| Major Application | food and beverages |
| InChIKey | PUPKKEQDLNREIM-QNSQPKOQSA-N |
| SMILES | OC(C=C1)=CC=C1C2=C(O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)C(C4=C(O)C=C(O[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)C=C4O2)=O |
Safety Information
| Safety Statements | 24/25 |
| WGK Germany | WGK 3 |
| HS Code | 29389090 |
| Storage Class | 11 - Combustible Solids |
KAEMPFERITRIN Usage And Synthesis
| Description | Kaempferitrin is a flavonoid glycoside that has been found in B. pinnatum and has diverse biological activities. It scavenges DPPH radicals (IC50 = 8.73 μg/ml) and is active against the bacteria S. aureus, P. aeruginosa, and S. typhi, as well as the fungi C. albicans, C. parapsilosis, and C. neoformans (MICs = 16-32 μg/ml). Kaempferitrin inhibits LPS-and IFN-γ-induced nitric oxide (NO) production in isolated mouse macrophages (IC50 = 40 μM). It decreases blood glucose levels in a rat model of alloxan-induced diabetes when administered at a dose of 100 mg/kg. |
| Chemical Properties | Yellow crystals, soluble in organic solvents such as methanol, ethanol, DMSO, etc., derived from cockscomb, Umbelliferae plants Bupleurum, Marigold, and Kaempferia galanga. |
| Uses | Kaempferitirin is a glycoside of Kaempferol (K100000), a plant flavonoid that exhibits antioxidant properties and is known to reduce risks of various types cancer and cardiovascular diseases. Kaempferitirin have been isolated as natural products from plants such as Hedyotis Verticilata. |
| Definition | ChEBI: Kaempferol 3,7-di-O-alpha-L-rhamnoside is a glycosyloxyflavone that is kaempferol attached to alpha-L-rhamnopyranosyl residues at positions 3 and 7 respectively via glycosidic linkages. It has been isolated from the aerial parts of Vicia faba and Lotus edulis. It has a role as a bone density conservation agent, a hypoglycemic agent, an immunomodulator, an anti-inflammatory agent, an antineoplastic agent, a plant metabolite, an apoptosis inducer and an antidepressant. It is an alpha-L-rhamnoside, a monosaccharide derivative, a dihydroxyflavone, a glycosyloxyflavone and a polyphenol. It is functionally related to a kaempferol. |
| General Description | This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG |
| Biochem/physiol Actions | Kaempferitrin (Lespenefril) is a naturally-occurring kaempferol glycoside with antimicrobial, antioxidant, and anti-inflammatory activities. |
| References | [1] SIMPLICE JOEL NDENDOUNG TATSIMO. Antimicrobial and antioxidant activity of kaempferol rhamnoside derivatives from Bryophyllum pinnatum.[J]. BMC Research Notes, 2012, 5: 158. DOI: 10.1186/1756-0500-5-158
[2] SHIH-HUA FANG Yew M T Yerra Koteswara Rao. Inhibitory effects of flavonol glycosides from Cinnamomum osmophloeum on inflammatory mediators in LPS/IFN-γ-activated murine macrophages[J]. Bioorganic & Medicinal Chemistry, 2005, 13 7: Pages 2381-2388. DOI: 10.1016/j.bmc.2005.01.050
[3] ANA PAULA JORGE . Insulinomimetic effects of kaempferitrin on glycaemia and on 14C-glucose uptake in rat soleus muscle[J]. Chemico-Biological Interactions, 2004, 149 2: Pages 89-96. DOI: 10.1016/j.cbi.2004.07.001 |
KAEMPFERITRIN Preparation Products And Raw materials
