Alkylation of manganese(II) tetraphenylporphyrin by a synthetic antimalarial trioxane
The synthesis and the antimalarial activity of a new kind of polycyclic 1,2,4-trioxanes are reported. The alkylation of the heme model MnIITPP by the biologically active (IC 50 = 320 nmol L-1) hemiperketal 2 is presented.
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Veröffentlicht in: | Organic & biomolecular chemistry 2003-08, Vol.1 (16), p.2859 |
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container_title | Organic & biomolecular chemistry |
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creator | Berrien, Jean-François Provot, Olivier Mayrargue, Joëlle Coquillay, Michel Cicéron, Liliane Gay, Frédérick Danis, Martin Robert, Anne Meunier, Bernard |
description | The synthesis and the antimalarial activity of a new kind of polycyclic 1,2,4-trioxanes are reported. The alkylation of the heme model MnIITPP by the biologically active (IC 50 = 320 nmol L-1) hemiperketal 2 is presented. |
doi_str_mv | 10.1039/b302835f |
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The alkylation of the heme model MnIITPP by the biologically active (IC 50 = 320 nmol L-1) hemiperketal 2 is presented.</description><subject>Alkylation</subject><subject>Animals</subject><subject>Antimalarials - chemical synthesis</subject><subject>Antimalarials - chemistry</subject><subject>Antimalarials - pharmacology</subject><subject>Chemical Sciences</subject><subject>Chloroquine - pharmacology</subject><subject>Crystallography, X-Ray</subject><subject>Heme - chemistry</subject><subject>Heterocyclic Compounds - chemical synthesis</subject><subject>Heterocyclic Compounds - chemistry</subject><subject>Heterocyclic Compounds - pharmacology</subject><subject>Inhibitory Concentration 50</subject><subject>Medicinal Chemistry</subject><subject>Metalloporphyrins - chemistry</subject><subject>Models, Chemical</subject><subject>Molecular Structure</subject><subject>Organic chemistry</subject><subject>Plasmodium falciparum - drug effects</subject><subject>Plasmodium falciparum - genetics</subject><issn>1477-0520</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkMFKw0AQhhdRrFbBJ5A9tofq7M5usjmWorZQ8GLPYbrZmGiahM0q5u1Naa2n-Rm-fxg-xu4EPAjA5HGLIA3q_IxdCRXHM9CYnJ-yhBG77roPAJHEkbpkIyGTyCBGV2wzrz77ikLZ1LzJ-Y7qd6pd5yar1ZQHFzy1hav7qm18W_S-rPm258S7vg6FC6XlVIdyRxX5kioefNn8DP0bdpFT1bnb4xyzzfPT22I5W7--rBbz9cxiFIdZHoPKYoMZKECNMsusIYlkrTIWRWIExVYmoDBRYHWUg0OrVaZJG6mNxjGbHu4WVKWtHx7xfdpQmS7n63S_AzlUI1TfYmAnB9b6puu8y08FAeneYvpncUDvD2j7td257B88asNf7fJr8g</recordid><startdate>20030821</startdate><enddate>20030821</enddate><creator>Berrien, Jean-François</creator><creator>Provot, Olivier</creator><creator>Mayrargue, Joëlle</creator><creator>Coquillay, Michel</creator><creator>Cicéron, Liliane</creator><creator>Gay, Frédérick</creator><creator>Danis, Martin</creator><creator>Robert, Anne</creator><creator>Meunier, Bernard</creator><general>Royal Society of Chemistry</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-9092-6776</orcidid></search><sort><creationdate>20030821</creationdate><title>Alkylation of manganese(II) tetraphenylporphyrin by a synthetic antimalarial trioxane</title><author>Berrien, Jean-François ; 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subjects | Alkylation Animals Antimalarials - chemical synthesis Antimalarials - chemistry Antimalarials - pharmacology Chemical Sciences Chloroquine - pharmacology Crystallography, X-Ray Heme - chemistry Heterocyclic Compounds - chemical synthesis Heterocyclic Compounds - chemistry Heterocyclic Compounds - pharmacology Inhibitory Concentration 50 Medicinal Chemistry Metalloporphyrins - chemistry Models, Chemical Molecular Structure Organic chemistry Plasmodium falciparum - drug effects Plasmodium falciparum - genetics |
title | Alkylation of manganese(II) tetraphenylporphyrin by a synthetic antimalarial trioxane |
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