Results 161 to 170 of about 4,886 (206)
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Plant Science, 2020
Transcription factor (TF) gene clusters in plants, such as tomato, potato, petunia, tobacco, and almond, have been characterized for their roles in the biosynthesis of diverse array of specialized metabolites. In Catharanthus roseus, three AP2/ERF TFs, ORCA3, ORCA4, and ORCA5, have been shown to be present on the same genomic scaffold, forming a ...
Sanjay Kumar, Singh +5 more
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Transcription factor (TF) gene clusters in plants, such as tomato, potato, petunia, tobacco, and almond, have been characterized for their roles in the biosynthesis of diverse array of specialized metabolites. In Catharanthus roseus, three AP2/ERF TFs, ORCA3, ORCA4, and ORCA5, have been shown to be present on the same genomic scaffold, forming a ...
Sanjay Kumar, Singh +5 more
openaire +4 more sources
Semi-syntheses and interrogation of indole-substituted Aspidosperma terpenoid alkaloids
Organic & Biomolecular Chemistry, 2022Aspidosperma terpenoid alkaloids can be quickly prepared using semisynthesis from naturally sourced tabersonine, featuring multiple oxygen-based substituents on the indole ring such as hydroxy and methoxy groups for cancer-targeted SAR studies.
Jinfeng Kang +4 more
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Indole alkaloids and terpenoids fromTabernaemontana markgrafiana
Phytochemistry, 1994Abstract The bark of Tabernaemontana markgrafiana yielded five acetylated pentacyclic triterpenes and 24 monoterpene indole alkaloids.
Nielsen, Helene Bendstrup +4 more
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Biosynthesis of the teleocidin-type terpenoid indole alkaloids
Organic & Biomolecular Chemistry, 2018Teleocidin B is a terpenoid indole alkaloid with unique structures including indolactam and cyclic terpenoid, and is a strong protein kinase C activator. In this review, we describe the isolation and biosynthetic studies of teleocidins.
Takayoshi Awakawa, Ikuro Abe
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Biosynthetic pathway of terpenoid indole alkaloids in Catharanthus roseus
Frontiers of Medicine, 2014Catharanthus roseus is one of the most extensively investigated medicinal plants, which can produce more than 130 alkaloids, including the powerful antitumor drugs vinblastine and vincristine. Here we review the recent advances in the biosynthetic pathway of terpenoid indole alkaloids (TIAs) in C.
Xiaoxuan, Zhu +3 more
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Three New Terpenoid Indole Alkaloids fromCatharanthus roseus
Planta Medica, 2010Three new terpenoid indole alkaloids, vidolicine (1), normacusine B N-oxide (2), and lochnerine N-oxide (3), together with seven known ones (4-10), were isolated from whole plants of Catharanthus roseus. Their structures were elucidated by spectroscopic methods (NMR, MS, UV, and IR).
Lei, Wang +5 more
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Terpenoid Indole Alkaloids from Winchia calophylla
Journal of Natural Products, 2005Three new indole alkaloids, N(4)-demethyl-12-methoxyalstogustine (1), 17-carboxyl-N(4)-methylechitamidine chloride (2), and 17-carboxyl-12-methoxy-N(4)-methylechitamidine chloride (3), along with 15 known alkaloids, were isolated from the ethanolic extract of the stem bark of Winchia calophylla.
Li-She, Gan +4 more
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Terpenoid indole alkaloid profile changes in Catharanthus pusillus during development
Plant Science, 2001The terpenoid indole alkaloid content of Catharanthus pusillus was investigated during development from young to old plants. Different plant organs were assessed showing that the new leaves were the main repository site with vindoline ( approximately 4.8 mg/g DW) and catharanthine ( approximately 2.2 mg/g DW) being the major metabolites with the ...
R, Zárate +3 more
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Alkaloids Derived from Tryptophan: Terpenoid Indole Alkaloids
2013L-Tryptophan is an indole ring containing aromatic amino acid derived via the shikimate pathway. The tryptophan-derived alkaloids are found in eight families, of which, Apocynaceae, Loganiaceae, Rubiaceae, and Nyssaceae are the best sources. The alkaloids under discussion are theCatharanthus alkaloids, namely, ajmalicine, tabersonine, catharanthine ...
Shilpa Ramani +3 more
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Why are the terpenoid indole alkaloids of type I homochiral?
Chirality, 2001AbstractIn the presence of the enzyme strictosidine synthase, the coupling reaction of secologanin and tryptamine is completely stereoselective and affords strictosidine with 3S configuration, exclusively. The stereoselectivity is transferred and retained in most indole alkaloids of type I in which C‐3 is not involved in subsequent reactions.
G, Beke +3 more
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