Molecular Formula | C21H19NO4 |
Molar Mass | 349.38 |
Density | 1.291±0.06 g/cm3(Predicted) |
Melting Point | 164-165 °C |
Boling Point | 565.9±50.0 °C(Predicted) |
pKa | 2.36±0.20(Predicted) |
Storage Condition | 2-8°C |
Physical and Chemical Properties | Free dihydrochelidine crystals are insoluble in water, slightly soluble in methanol, easily soluble in chloroform and dichloromethane. Dihydrochelidine will be slowly and directly converted into chelidine in polar deuterated reagents (such as DMSO-d6 and MeOD). In low-polar deuterated reagents (such as CD2Cl2), pseudoalkalis and dimeric intermediates will be produced, which will eventually be oxidized to oxychelidine. white-like powder, soluble in organic solvents such as methanol, ethanol, DMSO, etc., derived from the root of majus l., a Chelidonium of the poppy family. |
Reference Show more | 1. [IF=3.935] Qiyan Lin et al."Rapid identification and pharmacokinetic studies of multiple active alkaloids in rat plasma through UPLC-Q-TOF-MS and UPLC-MS/MS after the oral administration of Zanthoxylum nitidum extract."J Pharmaceut Biomed. 2020 Jul;186:113232 |
Chemical properties | Free dihydrochelidine crystals are insoluble in water, slightly soluble in methanol, and easily soluble in chloroform and dichloromethane. Dihydrochelidine will slowly and directly convert to chelidine in polar deuterated reagents (such as DMSO-d6 and MeOD); in low-polar deuterated reagents such as CD2Cl2, pseudobases and dimeric intermediates are produced, which are eventually oxidized to oxidized chelidine. white-like powder, soluble in organic solvents such as methanol, ethanol, DMSO, etc., derived from the root of majus l., a Chelidonium of the poppy family. |
biological activity | dihydrochelidine (Dihydrochelerythrine) is a natural compound isolated from banyan leaves and has antifungal activities. |
use | dihydrochelidine has the effects of clearing away heat and detoxification, antibacterial and anti-inflammatory. |