Works matching DE "MEDICARPINS"
Results: 13
Heterologous biosynthesis of medicarpin using engineered Saccharomyces cerevisiae.
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- Synthetic & Systems Biotechnology, 2023, v. 8, n. 4, p. 749, doi. 10.1016/j.synbio.2023.11.003
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Identification of a core set of rhizobial infection genes using data from single cell-types.
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- Frontiers in Plant Science, 2015, p. 1, doi. 10.3389/fpls.2015.00575
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Medicago truncatula ABCG10 is a transporter of 4-coumarate and liquiritigenin in the medicarpin biosynthetic pathway.
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- Journal of Experimental Botany, 2017, v. 68, n. 12, p. 3231, doi. 10.1093/jxb/erx059
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Flavonoids from Twigs of Millettia leptobotrya Dunn.
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- Records of Natural Products, 2013, v. 7, n. 4, p. 307
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Identification of GRP78 as a molecular target of medicarpin in osteoblast cells by proteomics.
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- Molecular & Cellular Biochemistry, 2016, v. 418, n. 1/2, p. 71, doi. 10.1007/s11010-016-2734-x
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Medicarpin, a Natural Pterocarpan, Heals Cortical Bone Defect by Activation of Notch and Wnt Canonical Signaling Pathways.
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- PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0144541
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The Chemical Components of Sesbania grandiflora Root and Their Antituberculosis Activity.
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- Pharmaceuticals (14248247), 2012, v. 5, n. 8, p. 882, doi. 10.3390/ph5080882
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Extraction of biomedical compounds from the wood of Pterocarpus macarocarpus Kurz heartwood.
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- Pakistan Journal of Pharmaceutical Sciences, 2018, v. 31, n. 3, p. 913
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Unified Total Syntheses of (−)-Medicarpin, (−)-Sophoracarpan A, and (±)-Kushecarpin A with Some Structural Revisions.
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- Angewandte Chemie, 2015, v. 127, n. 6, p. 1884, doi. 10.1002/ange.201408910
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Isoflavonoids from Piptanthus concolor Harrow.
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- Natural Product Research & Development, 2012, v. 24, n. 5, p. 610
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Effect of lead treatment on medicarpin accumulation and on the gene expression of key enzymes involved in medicarpin biosynthesis in Medicago sativa L.
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- Environmental Science & Pollution Research, 2014, v. 21, n. 24, p. 14091, doi. 10.1007/s11356-014-3335-4
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A New Chalcone from the Heartwood of Dalbergia cochinchinensis.
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- Chemistry of Natural Compounds, 2016, v. 52, n. 3, p. 405, doi. 10.1007/s10600-016-1659-7
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Unified Total Syntheses of (−)-Medicarpin, (−)-Sophoracarpan A, and (±)-Kushecarpin A with Some Structural Revisions.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 6, p. 1864, doi. 10.1002/anie.201408910
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- Article