20787
1D-1-O-Butyryl-4,6-O-dibenzoyl-myo-inositol
≥98.0%
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Assay
≥98.0%
SMILES string
CCCC(=O)O[C@@H]1[C@H](O)[C@H](O)[C@@H](OC(=O)c2ccccc2)[C@H](O)[C@H]1OC(=O)c3ccccc3
InChI
1S/C24H26O9/c1-2-9-16(25)31-21-18(27)17(26)20(32-23(29)14-10-5-3-6-11-14)19(28)22(21)33-24(30)15-12-7-4-8-13-15/h3-8,10-13,17-22,26-28H,2,9H2,1H3/t17-,18+,19-,20+,21+,22+/m0/s1
InChI key
KTYAOQKEMRXFIY-NXOOKBFXSA-N
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Cell, 176(3), 581-596 (2019-01-22)
Genome-wide studies have identified genetic variants linked to neurologic diseases. Environmental factors also play important roles, but no methods are available for their comprehensive investigation. We developed an approach that combines genomic data, screens in a novel zebrafish model, computational
Cell, 179(7), 1483-1498 (2019-12-10)
Metabolism has been shown to control peripheral immunity, but little is known about its role in central nervous system (CNS) inflammation. Through a combination of proteomic, metabolomic, transcriptomic, and perturbation studies, we found that sphingolipid metabolism in astrocytes triggers the
Nature, 578(7796), 593-599 (2020-02-14)
Multiple sclerosis is a chronic inflammatory disease of the CNS1. Astrocytes contribute to the pathogenesis of multiple sclerosis2, but little is known about the heterogeneity of astrocytes and its regulation. Here we report the analysis of astrocytes in multiple sclerosis
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