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Formula | C10H10O4 |
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Molecular Weight | 194.18 | CAS No. | 537-73-5 | |
Solubility (25°C)* | In vitro | DMSO | 38 mg/mL (195.69 mM) | |
* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | Isoferulic acid (Hesperetic acid, Hesperetate, Isoferulate), a major active ingredient of Cimicifuga heracleifolia, shows anti-inflammatory, antiviral, antioxidant, and antidiabetic properties. Isoferulic acid (3-Hydroxy-4-methoxycinnamic acid) is a cinnamic acid derivative that has antidiabetic activity. Isoferulic acid binds to and activates α1-adrenergic receptors (IC50=1.4 µM) to enhance secretion of β-endorphin (EC50=52.2 nM) and increase glucose use. |
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In vitro | Isoferulic acid can activate the α1A-AR to enhance glucose uptake into C2C12 cells[1]. Isoferulic acid is a potent inhibitors against intestinal maltase with an IC50 of 0.76±0.03 mM and it is also an intestinal sucrase inhibitor with IC50 of 0.45±0.01 mM. It activates α1-adrenoceptors to enhance the secretion of β-endorphin, which stimulates the opioid μ-receptors to increase glucose use and/or reduce hepatic gluconeogenesis, resulting in a reduction of the plasma glucose concentration[3]. |
In vivo | Isoferulic acid increases the glucose utilization in skeletal muscle and reduces the hepatic gluconeogenesis in insulin-deficient rat[1]. Isoferulic acid can inhibit hepatic gluconeogenesis and/or increase the glucose utilization in peripheral tissue to lower plasma glucose in diabetic rats lacking insulin[2]. |
Animal Study:[2] |
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