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New observations on the secondary chemistry of world Ephedra (Ephedraceae)
For several millennia, stem extracts of Ephedra (Ephedraceae, Gnetales) have been used as folk medicines in both the Old and New World. Some species were used in treatments of questionable efficacy for venereal disease in North America during the last century. Many Eurasian species produce phenyleth...
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Published in: | American journal of botany 2001-07, Vol.88 (7), p.1199-1208 |
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creator | Caveney, Stanley Charlet, David A Freitag, Helmut Maier-Stolte, Maria Starratt, Alvin N |
description | For several millennia, stem extracts of Ephedra (Ephedraceae, Gnetales) have been used as folk medicines in both the Old and New World. Some species were used in treatments of questionable efficacy for venereal disease in North America during the last century. Many Eurasian species produce phenylethylamine alkaloids, mostly ephedrine and pseudoephedrine, that interact with adrenergic receptors in the mammalian sympathetic nervous system. Asian Ephedra have been used recently in the clandestine manufacture of a street drug, methamphetamine. Although ephedrine alkaloids are not detectable in New World species of Ephedra, together with Asian species they contain other nitrogen-containing secondary metabolites with known neuropharmacological activity. Many mesic and particularly xeric species worldwide accumulate substantial amounts of quinoline-2-carboxylic acids, or kynurenates, in their aerial parts. Many species of Ephedra accumulate cyclopropyl amino acid analogues of glutamate and proline in their stems and roots, and particularly in the seed endosperm. Mesic species synthesize substantial amounts of three L-2-(carboxycyclopropyl)glycine stereomers rarely seen in nature. A cyclopropyl analogue of proline with known antimicrobial activity, cis-3,4-methanoproline, is found in large amounts in the stems and seeds of many Ephedra species. The ability to synthesize cyclopropyl amino acids may be an ancestral feature in the taxon. The natural function in the taxon of these three groups of secondary compounds remains to be established. |
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Some species were used in treatments of questionable efficacy for venereal disease in North America during the last century. Many Eurasian species produce phenylethylamine alkaloids, mostly ephedrine and pseudoephedrine, that interact with adrenergic receptors in the mammalian sympathetic nervous system. Asian Ephedra have been used recently in the clandestine manufacture of a street drug, methamphetamine. Although ephedrine alkaloids are not detectable in New World species of Ephedra, together with Asian species they contain other nitrogen-containing secondary metabolites with known neuropharmacological activity. Many mesic and particularly xeric species worldwide accumulate substantial amounts of quinoline-2-carboxylic acids, or kynurenates, in their aerial parts. Many species of Ephedra accumulate cyclopropyl amino acid analogues of glutamate and proline in their stems and roots, and particularly in the seed endosperm. Mesic species synthesize substantial amounts of three L-2-(carboxycyclopropyl)glycine stereomers rarely seen in nature. A cyclopropyl analogue of proline with known antimicrobial activity, cis-3,4-methanoproline, is found in large amounts in the stems and seeds of many Ephedra species. The ability to synthesize cyclopropyl amino acids may be an ancestral feature in the taxon. The natural function in the taxon of these three groups of secondary compounds remains to be established.</description><identifier>ISSN: 0002-9122</identifier><identifier>EISSN: 1537-2197</identifier><identifier>DOI: 10.2307/3558330</identifier><identifier>PMID: 11454619</identifier><identifier>CODEN: AJBOAA</identifier><language>eng</language><publisher>United States: Botanical Soc America</publisher><subject>6‐hydroxykynurenic acid ; 6‐methoxykynurenic acid ; Alkaloids ; Amino acids ; Biochemistry ; Chemistry ; cis‐3,4‐methanoproline ; Ephedra ; ephedrine alkaloids ; Flowers & plants ; Folk medicine ; Greenhouses ; kynurenic acid ; Leaves ; L‐2‐(carboxycyclopropyl)glycine ; Nitrogen ; Pharmacology ; Physiology and Biochemistry ; Plant biochemistry ; Plants ; Tannins ; Taxa</subject><ispartof>American journal of botany, 2001-07, Vol.88 (7), p.1199-1208</ispartof><rights>Copyright 2001 Botanical Society of America, Inc.</rights><rights>2001 Botanical Society of America</rights><rights>Copyright Botanical Society of America, Inc. 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Some species were used in treatments of questionable efficacy for venereal disease in North America during the last century. Many Eurasian species produce phenylethylamine alkaloids, mostly ephedrine and pseudoephedrine, that interact with adrenergic receptors in the mammalian sympathetic nervous system. Asian Ephedra have been used recently in the clandestine manufacture of a street drug, methamphetamine. Although ephedrine alkaloids are not detectable in New World species of Ephedra, together with Asian species they contain other nitrogen-containing secondary metabolites with known neuropharmacological activity. Many mesic and particularly xeric species worldwide accumulate substantial amounts of quinoline-2-carboxylic acids, or kynurenates, in their aerial parts. Many species of Ephedra accumulate cyclopropyl amino acid analogues of glutamate and proline in their stems and roots, and particularly in the seed endosperm. Mesic species synthesize substantial amounts of three L-2-(carboxycyclopropyl)glycine stereomers rarely seen in nature. A cyclopropyl analogue of proline with known antimicrobial activity, cis-3,4-methanoproline, is found in large amounts in the stems and seeds of many Ephedra species. The ability to synthesize cyclopropyl amino acids may be an ancestral feature in the taxon. The natural function in the taxon of these three groups of secondary compounds remains to be established.</description><subject>6‐hydroxykynurenic acid</subject><subject>6‐methoxykynurenic acid</subject><subject>Alkaloids</subject><subject>Amino acids</subject><subject>Biochemistry</subject><subject>Chemistry</subject><subject>cis‐3,4‐methanoproline</subject><subject>Ephedra</subject><subject>ephedrine alkaloids</subject><subject>Flowers & plants</subject><subject>Folk medicine</subject><subject>Greenhouses</subject><subject>kynurenic acid</subject><subject>Leaves</subject><subject>L‐2‐(carboxycyclopropyl)glycine</subject><subject>Nitrogen</subject><subject>Pharmacology</subject><subject>Physiology and Biochemistry</subject><subject>Plant biochemistry</subject><subject>Plants</subject><subject>Tannins</subject><subject>Taxa</subject><issn>0002-9122</issn><issn>1537-2197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp1kE1L7DAUhoMoOn7gH7hIuQs_FtWctGmSpYqfiG50HdL29LZDp5mbdCz-ezNOcUBwlRPy8LwnLyGHQM9ZQsVFwrlMErpBJsATETNQYpNMKKUsVsDYDtn1fhquKlVsm-wApDzNQE3I4zMOkc09unfTN7bzke2ivsbIY2G70riPqKhx1vg-TLaKBuvaMrqZ11g6E52OQ4EGz_bJVmVajwfjuUfebm9er-_jp5e7h-vLp7hIQ3xcJQVFSGlWcjAoDc9KmZqcq5zJouIsRypknpsK0kqgqtJSAFLkhgtFeZkle-Rk5Z07-3-BvtdhvQLb1nRoF15LASqTTCzJvz_IqV24LiynGXApQw10rSuc9d5hpeeumYWPa6B6Wa4eyw3k0ahb5DMs19zYZgDiFTA0LX785tGXj1cMQC35Pyt-6nvrvvl13vHquW7-1UPjUPuZaduQDnoYBim10F-eTx6NllM</recordid><startdate>200107</startdate><enddate>200107</enddate><creator>Caveney, Stanley</creator><creator>Charlet, David A</creator><creator>Freitag, Helmut</creator><creator>Maier-Stolte, Maria</creator><creator>Starratt, Alvin N</creator><general>Botanical Soc America</general><general>Botanical Society of America</general><general>Botanical Society of America, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>200107</creationdate><title>New observations on the secondary chemistry of world Ephedra (Ephedraceae)</title><author>Caveney, Stanley ; 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subjects | 6‐hydroxykynurenic acid 6‐methoxykynurenic acid Alkaloids Amino acids Biochemistry Chemistry cis‐3,4‐methanoproline Ephedra ephedrine alkaloids Flowers & plants Folk medicine Greenhouses kynurenic acid Leaves L‐2‐(carboxycyclopropyl)glycine Nitrogen Pharmacology Physiology and Biochemistry Plant biochemistry Plants Tannins Taxa |
title | New observations on the secondary chemistry of world Ephedra (Ephedraceae) |
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