|
|
| | Linderaspirone A Basic information |
| Product Name: | Linderaspirone A | | Synonyms: | Linderaspirone A;(8R,16R)-rel-2,3,6,11,12,14-Hexamethoxy-8,16-diphenyldispiro[4.3.4.3]hexadeca-2,6,11,14-tetraene-1,4,10,13-tetrone;Dispiro[4.3.4.3]hexadeca-2,6,11,14-tetraene-1,4,10,13-tetrone, 2,3,6,11,12,14-hexamethoxy-8,16-diphenyl-, (8R,16R)-rel- | | CAS: | 1235126-46-1 | | MF: | C34H32O10 | | MW: | 600.61 | | EINECS: | | | Product Categories: | | | Mol File: | 1235126-46-1.mol |  |
| | Linderaspirone A Chemical Properties |
| Boiling point | 826.5±65.0 °C(Predicted) | | density | 1.33±0.1 g/cm3(Predicted) | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | form | powder | | color | Yellow |
| | Linderaspirone A Usage And Synthesis |
| Uses | Linderaspirone A is a natural compound that can be isolated from the roots of Lindera aggregate. Linderaspirone A shows significant inhibitory effects on the production of prostaglandin E2 (PGE2),TNF-α, and IL-6 [1][2]. | | References | [1] Lin Chen, et al. Lindera cyclopentenedione intermediates from the roots of Lindera aggregate. RSC Adv. 2018 May 16;8(32):17898-17904. DOI:10.1039/c8ra03094d
[2] Chi-Su Yoon, et al. Effects of Compounds Isolated from Lindera erythrocarpa on Anti-Inflammatory and Anti-Neuroinflammatory Action in BV2 Microglia and RAW264.7 Macrophage. Int J Mol Sci. 2022 Jun 27;23(13):7122. DOI:10.3390/ijms23137122 |
| | Linderaspirone A Preparation Products And Raw materials |
|