Melting point	230 ºC**
Density	1.383±0.06 g/cm3 (20 º

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Source	SDS/MSDS Samples
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Synthetic Route

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Name	CAS

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Articles

Peer-Reviewed Papers

Molecular structure and QSAR study on antispasmodic activity of some xanthoxyline derivatives.Rodrigo dos Santos et al.Archiv der Pharmazie, 339(5), 227-237 (2006-03-31) In vitro antifungal evaluation and studies on the mode of action of xanthoxyline derivatives.T R Pinheiro et al.Arzneimittel-Forschung, 49(12), 1039-1043 (2000-01-15) Antifungal activity and studies on mode of action of novel xanthoxyline-derived chalcones.Paula Boeck et al.Archiv der Pharmazie, 338(2-3), 87-95 (2005-03-31) Fungicide and fungiostatic effects of xanthoxyline.V Cechinel Filho et al.Journal of ethnopharmacology, 53(3), 171-173 (1996-09-01) Antifeedant constituents from Fagara macrophylla.C Tringali et al.Fitoterapia, 72(5), 538-543 (2001-06-29) Antispasmodic activity of xanthoxyline derivatives: structure-activity relationships.V Cechinel Filho et al.Journal of pharmaceutical sciences, 84(4), 473-475 (1995-04-01) Antinociceptive effects of synthetic chalcones obtained from xanthoxyline.Fátima de Campos-Buzzi et al.Archiv der Pharmazie, 339(7), 361-365 (2006-07-14) Synthesis of chalcone analogues with increased antileishmanial activity.Paula Boeck et al.Bioorganic & medicinal chemistry, 14(5), 1538-1545 (2006-01-03) Antinociceptive action of 2-(4-bromobenzoyl)-3-methyl-4,6-dimethoxy benzofuran, a novel xanthoxyline derivative on chemical and thermal models of nociception in mice.Z R Vaz et al.The Journal of pharmacology and experimental therapeutics, 278(1), 304-312 (1996-07-01) Action of 2-hydroxy-4,6-dimethoxyacetophenone isolated from Sebastiania schottiana.J B Calixto et al.Planta medica, 56(1), 31-35 (1990-02-01) Collateral sensitivity of resistant MRP1-overexpressing cells to flavonoids and derivatives through GSH efflux.Doriane Lorendeau et al.Biochemical pharmacology, 90(3), 235-245 (2014-05-31)

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