IsorutarinCAS# 53846-51-8 |
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Cas No. | 53846-51-8 | SDF | Download SDF |
PubChem ID | 185756 | Appearance | Powder |
Formula | C20H24O10 | M.Wt | 424.4 |
Type of Compound | Coumarins | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | (2R)-9-hydroxy-2-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-7-one | ||
SMILES | CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)CO)O)O)O | ||
Standard InChIKey | QZUDEXAHKXCIDG-NUUDRHLNSA-N | ||
Standard InChI | InChI=1S/C20H24O10/c1-20(2,30-19-15(25)14(24)13(23)10(7-21)27-19)11-6-9-5-8-3-4-12(22)29-17(8)16(26)18(9)28-11/h3-5,10-11,13-15,19,21,23-26H,6-7H2,1-2H3/t10-,11-,13-,14+,15-,19+/m1/s1 | ||
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
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About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
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Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. |

Isorutarin Dilution Calculator

Isorutarin Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 2.3563 mL | 11.7813 mL | 23.5627 mL | 47.1254 mL | 58.9067 mL |
5 mM | 0.4713 mL | 2.3563 mL | 4.7125 mL | 9.4251 mL | 11.7813 mL |
10 mM | 0.2356 mL | 1.1781 mL | 2.3563 mL | 4.7125 mL | 5.8907 mL |
50 mM | 0.0471 mL | 0.2356 mL | 0.4713 mL | 0.9425 mL | 1.1781 mL |
100 mM | 0.0236 mL | 0.1178 mL | 0.2356 mL | 0.4713 mL | 0.5891 mL |
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. |

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A Candidate for Health Promotion, Disease Prevention and Treatment: Common Rue (Ruta graveolens L.), an Important Medicinal Plant in Traditional Medicine.[Pubmed:35538827]
Curr Rev Clin Exp Pharmacol. 2023;19(1):2-11.
BACKGROUND: Ruta graveolens L. belongs to Rutaceae; it is a semi-wood perennial or a small evergreen sub-shrub, which is native to Southern Europe, West Asia and Northern Africa. OBJECTIVE: The goal of this manuscript was to outline the most notable traditional and modern advantages and pharmaceutical benefits of common rue. METHODS: The manuscript covers review articles, randomized control experiments, analytical studies and observations, which have been gathered from different sources, such as Google Scholar, Scopus, Science Direct and PubMed. A review of the literature was carried out using the keywords rutin, Ruta graveolens L., rue, common rune, coumarin, natural products and pharmaceutical benefits. RESULTS: Rue contains quinoline alkaloids, such as graveoline and graveolinine, acridone alkaloids, such as furacridone and gravacridone, furanoquinoline dictamnine, coumarins, such as gravelliferone, Isorutarin, rutacultin, rutaretin, and suberenone, and the furanocoumarins 5-methoxypsoralen (bergapten) and 8-methoxypsoralen (xanthotoxine). Most of its aromatic and medicinal properties are due to the presence of rutin and its essential oil. It has been used in folk medicine as a stimulant, for its antiinflammatory and analgesic properties, anti-androgenic activity, anti-hyperglycemic effects, antihyperlipidemic effects, xanthine oxidase inhibition activity, and anticancer properties. CONCLUSION: According to pharmacological and phytochemical advantages, pennyroyal shows its importance as a medicinal plant in both modern medicinal science and traditional medicine.
[Chemical constituents from roots of Peucedanum praeruptorum (V)].[Pubmed:23477142]
Zhongguo Zhong Yao Za Zhi. 2012 Dec;37(23):3573-6.
OBJECTIVE: To study the chemical constituents in roots of Peucedanum praeruptorum from Henan. METHOD: The constituents were isolated by column chromatography on silica gel and ODS, and identified by NMR, MS spectroscopic methods. RESULT: Six compounds, Pd-I b(1), marmesinsin (2), rutarin (3), Isorutarin (4), 4H-1-benzopyran-4-one, 5-hydroxy-6-methoxy-2-phenyl-7-O-alpha-D-glucuronyl methyl ester (5), 4H-1-benzopyran-4-one, 5-hydroxy-6-methoxy-2-phenyl-7-O-alpha-D-glucuronyl acid (6) were isolated and identified. CONCLUSION: Compound 5 was a new compound, compounds 5 and 6 were isolated from Peucedanum plant for the first time.
Biological activities of Indian celery, Seseli diffusum (Roxb. ex Sm.) Sant. & Wagh.[Pubmed:22095902]
Phytother Res. 2012 May;26(5):783-6.
In continuation of our work on Indian celery (Seseli diffusum (Roxb. ex Sm.) Santapau & Wagh; Umbelliferae), the fractionation of the 80% MeOH-H(2) O extract of the seeds was performed to identify the principles responsible for its folk use as an antispasmodic and diuretic. Several compounds were isolated as active components: seselin (1) and anthriscinol methyl ether (4) showed a selective cytotoxicity to some yeast strains. Compound 1 also showed spasmolytic activity. On the other hand, isopimpinellin (3) and Isorutarin (5) exhibited a spasmogenic effect on the smooth muscle preparations. Compound 5 was also found to have antioxidant activity. Among them, compound 4 was isolated for the first time from this plant.
Structures of linear furano- and simple-coumarin glycosides of Bai-Hua Qian-Hu.[Pubmed:17262257]
Planta Med. 1989 Feb;55(1):64-7.
From the n-butanol extract of the crude drug "Bai-Hua Qian-Hu", the root of PEUCEDANUM PRAERUPTORUM Dunn. (Umbelliferae) praeroside I ( 1) and three known linear-type furanocoumarin glycosides, Isorutarin ( 2), rutarin ( 3), and marmesinin ( 4), along with two known simple coumarin glycosides, scopolin ( 5) and skimmin ( 6), were isolated. The structure of praeroside I was established as rutaretin-4'- O-(6-vanilloyl-beta- D-glucopyranoside) by spectroscopic and chemical methods.
A new biscoumarin glucoside ester from Ruta chalepensis cell cultures.[Pubmed:17265302]
Planta Med. 1988 Oct;54(5):398-400.
The investigation of a plant cell culture of RUTA CHALEPENSIS L. yielded three compounds: Isorutarin, rutacridone, and rutarensin, a so far unknown ester of daphnoretin glucoside ("daphnorin"), as well as 3-hydroxy-3-methylglutaric acid.