Results 151 to 160 of about 134,369 (196)
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Terpenoid Indole Alkaloids from Winchia calophylla

Journal of Natural Products, 2005
Three 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 alkaloids from Mappianthus iodoides Hand.-Mazz.

Phytochemistry, 2014
Ten terpenoid indole alkaloids, mappiodines A-C and mappiodosides A-G, together with eight known compounds, were isolated from stems of Mappianthus iodoides Hand.-Mazz. Their structures were elucidated by spectroscopic analyses including 1D, 2D NMR, MS and CD methods. The ten compounds were evaluated for their cytotoxic activity, but were inactive.
Cong, Hai-Jian   +5 more
openaire   +3 more sources

Strictosidine synthase, an indispensable enzyme involved in the biosynthesis of terpenoid indole and β-carboline alkaloids

Chinese Journal of Natural Medicines, 2021
Terpenoid indole (TIAs) and β-carboline alkaloids (BCAs), such as suppressant reserpine, vasodilatory yohimbine, and antimalarial quinine, are natural compounds derived from strictosidine. These compounds can exert powerful pharmacological effects but be obtained from limited source in nature. the whole biosynthetic pathway of TIAs and BCAs, The Pictet-
Ning, Cao, Chang-Hong, Wang
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Identification and Characterization of Transcription Factors Regulating Terpenoid Indole Alkaloid Biosynthesis in Catharanthus roseus

2022
Biosynthesis of the therapeutically valuable terpenoid indole alkaloids (TIAs), in the medicinal plant Catharanthus roseus, is one of the most elaborate and complex metabolic processes. Although genomic and transcriptomic resources have significantly accelerated gene discovery in the TIA pathway, relatively few genes of transcription factors (TFs) have
Sanjay K, Singh   +8 more
openaire   +2 more sources

Alkaloids of Terpenoid Origin (excepting indole alkaloids and ergot alkaloids)

1998
A large number of alkaloids are based on terpenoid structures. In most instances, the source of the nitrogen is not established, but the remaining portions of the molecule typically arise via the pathways leading to the various groups of terpenes.
openaire   +1 more source

Microbial allies: exploring fungal endophytes for biosynthesis of terpenoid indole alkaloids

Archives of Microbiology
Terpenoid indole alkaloids (TIAs) are natural compounds found in medicinal plants that exhibit various therapeutic activities, such as antimicrobial, anti-inflammatory, antioxidant, anti-diabetic, anti-helminthic, and anti-tumor properties. However, the production of these alkaloids in plants is limited, and there is a high demand for them due to the ...
Jaya Prabha, Khalkho   +4 more
openaire   +2 more sources

Terpenoid indole alkaloid biotransformation capacity of suspension cultures of Tabernaemontana divaricata

Phytochemistry, 1994
Abstract Two cell lines of Tabernaemontana divaricata derived from the same suspension culture were compared with respect to their biotransformation capacity. One is a high indole alkaloid-producing culture which accumulated mainly O-acetylvallesamine. The other cell line biosynthesizes terpenoid indole alkaloids in much lower amounts.
Denise Dagnino   +2 more
openaire   +1 more source

Revisiting the ORCA gene cluster that regulates terpenoid indole alkaloid biosynthesis in Catharanthus roseus

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
openaire   +2 more sources

Metabolic engineering of terpenoid indole alkaloid pathway in Catharanthus roseus

Planta Medica, 2013
Eukaryotes such as higher plants have evolved to produce a diverse range of low-molecular-weight secondary compounds that can be used as food and feed additives, flavours, fragrances, cosmetics, agrochemicals and pharmaceuticals. The dominant role of secondary metabolites in the pharmaceutical industry is demonstrated by the fact that approximately 50%
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Establishment of transgenic Rhazya stricta hairy roots to modulate terpenoid indole alkaloid production

Plant Cell Reports, 2015
Transgenic hairy roots of R. stricta were developed for investigation of alkaloid accumulations. The contents of five identified alkaloids, including serpentine as a new compound, increased compared to non-transformed roots. Rhazya stricta Decne. is a rich source of pharmacologically active terpenoid indole alkaloids (TIAs).
Akhgari, Amir   +5 more
openaire   +3 more sources

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