Name | Cimifugin |
Synonyms | CiMitin Cimifugin CIMIFUGIN(P) Cimifugin (Cimitin) (2S)-7-(Hydroxymethyl)-2-(2-hydroxypropan-2-yl)-4-methoxy-2,3-dihydrofuro[3,2-g]chromen-5-one 7-(hydroxymethyl)-2-(1-hydroxy-1-methylethyl)-4-methoxy-2,3-dihydro-5H-furo[3,2-g]chromen-5-one (2S)-7-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-4-methoxy-2,3-dihydro-5H-furo[3,2-g]chromen-5-one (S)-2,3-Dihydro-7-(hydroxymethyl)-2-(1-hydroxy-1-methylethyl)-4-methoxy-5H-furo[3,2-g][1]benzopyran-5-one |
CAS | 37921-38-3 |
InChI | InChI=1/C16H18O6/c1-16(2,19)13-5-9-11(22-13)6-12-14(15(9)20-3)10(18)4-8(7-17)21-12/h4,6,13,17,19H,5,7H2,1-3H3 |
Molecular Formula | C16H18O6 |
Molar Mass | 306.31 |
Density | 1.361±0.06 g/cm3(Predicted) |
Melting Point | 107~109℃ |
Boling Point | 546.4±50.0 °C(Predicted) |
Specific Rotation(α) | +79.2 (c, 0.8 in CHCl3) |
Flash Point | 204.9°C |
Solubility | Soluble in methanol, DMSO and other solvents, insoluble in petroleum ether. |
Vapor Presure | 8.98E-13mmHg at 25°C |
Appearance | White powder |
pKa | 14.25±0.29(Predicted) |
Storage Condition | -20°C |
Refractive Index | 1.599 |
MDL | MFCD23105630 |
Physical and Chemical Properties | Soluble in methanol, DMSO and other solvents, insoluble in petroleum ether. Rhizome derived from Cimicifnga foetida L. |
In vitro study | The effect of Cimifugin (Cimitin) on TSLP decreases significantly when expression of CLDN1 is interfered with siRNA and this implied Cimifugin inhibits initiative cytokines through restoring TJs. |
In vivo study | Cimifugin (Cimitin; 12.5 or 50 mg/kg/day; intragastrically; 2 days) significantly inhibits TSLP and IL-33 in the initial stage of Mice are sensitized and challenged with FITC to establish type 2 atopic dermatitis (AD) model. Simultaneously, Cimifugin reduces the separated gap among the epithelial cells and increased the expression of TJs. |
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