- Robinetin
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- $43.00 / 1mg
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2026-04-20
- CAS:490-31-3
- Min. Order:
- Purity: 98.95%
- Supply Ability: 10g
- ROBINETIN
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- $1.00 / 1kg
-
2019-07-06
- CAS:490-31-3
- Min. Order: 1 mg
- Purity: 99%
- Supply Ability: 100KG
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| | ROBINETIN Basic information |
| Product Name: | ROBINETIN | | Synonyms: | ROBINETIN;3,3’,4’,5’,7-pentahydroxy-flavon;3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4h-1-benzopyran-4-on;norkanugin;3,7,3',4',5'-PENTAHYDROXYFLAVONE;5-HYDROXYFISETIN;3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4-benzopyrone;3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl-4H-1-benzopyran-4-one) (Robinetin) | | CAS: | 490-31-3 | | MF: | C15H10O7 | | MW: | 302.24 | | EINECS: | 207-709-6 | | Product Categories: | Flavanols;Penta-substituted Flavones | | Mol File: | 490-31-3.mol |  |
| | ROBINETIN Chemical Properties |
| Melting point | 326-328°C | | Boiling point | 363.28°C (rough estimate) | | density | 1.3616 (rough estimate) | | refractive index | 1.4790 (estimate) | | storage temp. | 2-8°C | | solubility | DMSO (Sparingly), Methanol (Slightly, Heated) | | form | Solid | | pka | 6.82±0.40(Predicted) | | color | Yellow to Dark Yellow | | InChI | 1S/C15H10O7/c16-7-1-2-8-11(5-7)22-15(14(21)12(8)19)6-3-9(17)13(20)10(18)4-6/h1-5,16-18,20-21H | | InChIKey | SOEDEYVDCDYMMH-UHFFFAOYSA-N | | SMILES | [o]1c2c([c](c(c1c3cc(c(c(c3)O)O)O)O)=O)ccc(c2)O | | LogP | 2.550 (est) |
| Risk Statements | 22 | | Safety Statements | 22-45 | | RIDADR | 2811 | | WGK Germany | WGK 3 | | Storage Class | 11 - Combustible Solids |
| | ROBINETIN Usage And Synthesis |
| Uses | Robinetin (3,3',4',5',7-Pentahydroxyflavone), a naturally occurring flavonoid with remarkable ‘two color’ intrinsic fluorescence properties, has antifungal, antiviral, antibacterial, antimutagenesis, and antioxidant activity. Robinetin also can inhibit lipid peroxidation and protein glycosylation[1][2][3][4][5]. | | Definition | ChEBI: A pentahydroxyflavone that is flavone substituted by hydroxy groups at positions 3, 7, 3, 4' and 5'. | | References | [1] Fesen MR, et, al. Inhibition of HIV-1 integrase by flavones, caffeic acid phenethyl ester (CAPE) and related compounds. Biochem Pharmacol. 1994 Aug 3;48(3):595-608. DOI:10.1016/0006-2952(94)90291-7 [2] Cushnie TPT, et, al. Antimicrobial activity of flavonoids. Int J Antimicrob Agents. 2005 Nov;26(5):343-56. DOI:10.1016/j.ijantimicag.2005.09.002 [3] Chaudhuri S, et, al. Binding of the bioflavonoid robinetin with model membranes and hemoglobin: Inhibition of lipid peroxidation and protein glycosylation. J Photochem Photobiol B. 2010 Jan 21;98(1):12-9. DOI:10.1016/j.jphotobiol.2009.10.002 [4] Birt DF, et, al. Anti-mutagenesis and anti-promotion by apigenin, robinetin and indole-3-carbinol. Carcinogenesis. 1986 Jun;7(6):959-63. DOI:10.1093/carcin/7.6.959 [5] Manrique-de-la-Cuba MF, et, al. Theoretical study of the antioxidant capacity of the flavonoids present in the Annona muricata (Soursop) leaves. J Mol Model. 2019 Jun 25;25(7):200. DOI:10.1007/s00894-019-4083-7 |
| | ROBINETIN Preparation Products And Raw materials |
| Raw materials | 4H-1-Benzopyran-4-one, 7-hydroxy-3-methoxy-2-(3,4,5-trimethoxyphenyl)--->3,7-DIHYDROXY-3',4',5'-TRIMETHOXYFLAVONE-->3,4,5-TRIMETHOXYBENZOIC ANHYDRIDE-->1-(2,4-DIHYDROXYPHENYL)-2-METHOXYETHAN-1-ONE-->Paeonol-->2,3-DIHYDROROBINETIN-->4'-Benzyloxy-2'-hydroxyacetophenone-->2,4-Dihydroxyacetophenone-->3,4,5-Trimethoxybenzaldehyde |
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