Apocynaceae alkaloids

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Apocynaceae alkaloids are natural products found in the plant family of the dogbane family ( Apocynaceae ). [1]

Contents

Occurrence

Voacanga africana Voacanga africana.jpg
Voacanga africana

The alkaloid tabernanthin is found in Tabernaemontana laurifolia . [2] The alkaloids voacangin and voacristin were isolated from Voacanga africana . [3]

Representatives

Representatives include tabernanthine, voacangine and voacristine. [4] [5]

Uses

Plant parts of Voacanga africana are utilized by African natives for various purposes, including as hallucinogens, in cultic ceremonies, and as aphrodisiacs. [6]

Ethnomedicinal use

A decoction made from the stem or root bark is employed for the treatment of mental disorders and as an analgesic. The sap is applied to cavities in teeth. In southeastern Nigeria, Voacanga africana is an integral part of numerous healing rituals. [7]

Related Research Articles

<span class="mw-page-title-main">Apocynaceae</span> Dogbane and oleander family of flowering plants

Apocynaceae is a family of flowering plants that includes trees, shrubs, herbs, stem succulents, and vines, commonly known as the dogbane family, because some taxa were used as dog poison. Members of the family are native to the European, Asian, African, Australian, and American tropics or subtropics, with some temperate members. The former family Asclepiadaceae is considered a subfamily of Apocynaceae and contains 348 genera. A list of Apocynaceae genera may be found here.

<span class="mw-page-title-main">Voacangine</span> Chemical compound

Voacangine is an alkaloid found predominantly in the root bark of the Voacanga africana tree, as well as in other plants such as Tabernanthe iboga, Tabernaemontana africana, Trachelospermum jasminoides, Tabernaemontana divaricata and Ervatamia yunnanensis. It is an iboga alkaloid which commonly serves as a precursor for the semi-synthesis of ibogaine. It has been demonstrated in animals to have similar anti-addictive properties to ibogaine itself. It also potentiates the effects of barbiturates. Under UV-A and UV-B light its crystals fluoresce blue-green, and it is soluble in ethanol.

<i>Voacanga africana</i> Species of tree

Voacanga africana is a small tree native to tropical Africa belonging to the family Apocynaceae that grows to 6 m (20 ft) in height and bears leaves that are up to 30 cm (12 in) in length. The yellow or white flowers are succeeded by paired, follicular, dehiscent fruit with a mottled green exocarp and a pulpy, yellow mesocarp surrounding the seeds. The plant contains alkaloids acting as CNS depressants and hypotensives

<span class="mw-page-title-main">Toxiferine</span> Chemical compound

Toxiferine is a curare toxin. It is a bisindole alkaloid derived from Strychnos toxifera and a nicotinic acetylcholine receptor antagonist. This alkaloid is the main toxic component of Calabash curare, and one of the most toxic plant alkaloids known. The lethal dose (LD50) for mice has been determined as 10 - 60 µg/kg by intravenous administration. It is a muscle relaxant that causes paralysis of skeletal muscle, which takes approximately 2 hours to recovery for a moderate dose, and 8 hours of total paralysis with a 20-fold paralytic dose. The paralysis can be antagonized by neostigmine

<span class="mw-page-title-main">Voacamine</span> Chemical compound

Voacamine, also known under the older names voacanginine and vocamine, is a naturally occurring dimeric indole alkaloid of the secologanin type, found in a number of plants, including Voacanga africana and Tabernaemontana divaricata. It is approved for use as an antimalarial drug in several African countries. Voacamine exhibits cannabinoid CB1 receptor antagonistic activity.

<span class="mw-page-title-main">Steroidal alkaloid</span> Class of chemical compounds

Steroidal alkaloids have the basic steroidal skeleton with nitrogen-based functional groups attached to the skeleton. More specifically, they are distinguished by their tetracyclic cyclopentanoperhydrophenanthrene skeleton that marks their close relationship with sterols. They fall in two major categories: Solanum alkaloids and Veratrum alkaloids. A Steroidal alkaloid has also been found in Chonemorpha fragrans, 'chonemorphine' was used to treat intestinal infections in Wistar rats..

<span class="mw-page-title-main">Quinolizidine alkaloids</span>

Quinolizidine alkaloids are natural products that have a quinolizidine structure; this includes the lupine alkaloids.

<span class="mw-page-title-main">Tabernaemontanine</span> Chemical compound

Tabernaemontanine is a naturally occurring monoterpene indole alkaloid found in several species in the genus Tabernaemontana including Tabernaemontana divaricata.

<span class="mw-page-title-main">Dregamine</span> Chemical compound

Dregamine is a naturally occurring monoterpene indole alkaloid found in several species in the genus Tabernaemontana including Ervatamia hirta and Tabernaemontana divaricata.

<span class="mw-page-title-main">Vobasine</span> Chemical compound

Vobasine is a naturally occurring monoterpene indole alkaloid found in several species in the genus Tabernaemontana including Tabernaemontana divaricata.

<span class="mw-page-title-main">Voacristine</span> Chemical compound

Voacristine is a indole alkaloid occurring in Voacanga and Tabernaemontana genus. It is also an iboga type alkaloid.

<i>Voacanga grandifolia</i> Species of plant

Voacanga grandifolia is a plant native to Malesia and Queensland. It is an introduced species in India.

<span class="mw-page-title-main">Conopharyngine</span> Chemical compound

Conopharyngine is the major alkaloid present in the leaves and stem-bark of Tabernaemontana pachysiphon and Conopharyngia durissima. It is closely related voacangine and coronaridine. Conopharyngine pseudoindoxyl, a derivative of it, is also found in the same plant Tabernaemontana pachysiphon.

<span class="mw-page-title-main">Benzylisoquinoline alkaloids</span>

The benzylisoquinoline alkaloids are natural products that can be classified as isoquinoline alkaloids and are derived from benzylisoquinoline. They also include the benzyl(tetrahydro)isoquinoline alkaloids.

<span class="mw-page-title-main">Indolizidine alkaloids</span> Class of chemical compounds

Indolizidine alkaloids are natural products from various alkaloid groups whose structure can be derived from indolizidine.

<span class="mw-page-title-main">Imidazole alkaloids</span>

Imidazole alkaloids are a group of alkaloidss whose basic structure contains the imidazole ring system.

<span class="mw-page-title-main">Corydalis Alkaloids</span>

Corydalis Alkaloids are categorized as natural products of the isoquinoline alkaloid type.

<span class="mw-page-title-main">Diterpene alkaloids</span>

Diterpene alkaloids are natural products of the terpene alkaloid type.

<span class="mw-page-title-main">Dendrobium alkaloids</span>

Dendrobium alkaloids are natural products and so-called pseudoalkaloids.

<span class="mw-page-title-main">Pyrrolidine alkaloids</span>

The pyrrolidine alkaloids are natural products chemically derived from pyrrolidine.

References

  1. Entry on Apocynaceen-Alkaloide . at: Römpp Online . Georg Thieme Verlag, retrieved {{{Datum}}}.
  2. M.Hesse (1968), Indolalkaloide, Berlin Heidelberg: Springer-Verlag, p. 30, ISBN   978-3-540-04194-8
  3. U. Renner (1957), "Voacamidin und Voacristin, zwei neue Alkaloide aus Voacanga africana Stapf", Experientia, vol. 13, pp. 468–469, doi:10.1007/BF02159399
  4. Zetler, G., Lenschow, E. & Prenger-Berninghoff, W. (1968), "Die Wirkung von 11 Indol-Alkaloiden auf das Meerschweinchen-Herz in vivo und in vitro, verglichen mit 2 synthetischen Azepinoindolen, Chinidin und Quindonium.", Naunyn-Schmiedebergs Archiv für Pharmakologie und experimentelle Pathologie, vol. 260, pp. 26–49, doi:10.1007/BF00545005 {{citation}}: CS1 maint: multiple names: authors list (link)
  5. Robert F. Raffauf & M. B. Flagler (1960), "Alkaloids of the Apocynaceae", Economic Botany pages, vol. 14, pp. 37–55, doi:10.1007/BF02859365
  6. Lexicon of Medicinal Plants and Drugs, Spektrum Akademischer Verlag 1999.
  7. Maurice M. Iwu (2014), [ Voacanga africana auf S. 330 , p. 330, at Google Books Handbook of African Medicinal Plants] (2. ed.), CRC Press, ISBN   978-1-46657-198-3 {{citation}}: Check |url= value (help)