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Solubility: DMSO: 33 mg/mL(66
Henderson G
Determination of the active stereoisomer of the MEP pathway-targeting antimalarial agent MMV008138
5-tetrahydropyrimidine-2
Smiles: OC[C@@H]1O[C@@H](OC2C(=O)C3=C(C=C(O)C=C3O)OC=2C2C=CC(O)=CC=2)[C@H](O)[C@H]1O
Cytochalasin J Size:Contact [email protected] for quotation Solubility: DMSO: 33 mg/mL(66Cytochalasin J can alter mitotic spindle microtubule organization and kinetochore structure. The cytochalasins are cell permeable fungal metabolites inhibiting actin polymerization, which can alter diverse processes including cell movement, growth, phagocytosis, degranulation, and secretion. In vitro: Cytochalasin J was identified as a deacetylated analog of cytochalasin H that weakly inhibited actin assembly but significantly altered mitotic spindle