Synthesis and antimalarial activity of some 9-substituted artemisinin derivatives. 1993

N Acton, and J M Karle, and R E Miller
Division of Experimental Therapeutics, Walter Reed Army Institute of Research, Washington, D.C. 20307-5100.

Several 9-substituted derivatives of the antimalarial drug artemisinin have been prepared by functionalizing the double bond of artemisitene and related compounds. Stereochemical assignments for these compounds were made using a combination of NMR experiments, an X-ray diffraction study of one compound, and chemical correlations of several other compounds with this one compound of unambiguous structure and with its epimer. The compounds synthesized show a wide variation in in vitro antimalarial activity.

UI MeSH Term Description Entries
D010963 Plasmodium falciparum A species of protozoa that is the causal agent of falciparum malaria (MALARIA, FALCIPARUM). It is most prevalent in the tropics and subtropics. Plasmodium falciparums,falciparums, Plasmodium
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D000962 Antimalarials Agents used in the treatment of malaria. They are usually classified on the basis of their action against plasmodia at different stages in their life cycle in the human. (From AMA, Drug Evaluations Annual, 1992, p1585) Anti-Malarial,Antimalarial,Antimalarial Agent,Antimalarial Drug,Anti-Malarials,Antimalarial Agents,Antimalarial Drugs,Agent, Antimalarial,Agents, Antimalarial,Anti Malarial,Anti Malarials,Drug, Antimalarial,Drugs, Antimalarial
D012717 Sesquiterpenes Fifteen-carbon compounds formed from three isoprenoid units with general formula C15H24. Farnesanes,Farnesene,Farnesenes,Sesquiterpene,Sesquiterpene Derivatives,Sesquiterpenoid,Sesquiterpenoids,Derivatives, Sesquiterpene
D013237 Stereoisomerism The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed) Molecular Stereochemistry,Stereoisomers,Stereochemistry, Molecular,Stereoisomer
D013329 Structure-Activity Relationship The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups. Relationship, Structure-Activity,Relationships, Structure-Activity,Structure Activity Relationship,Structure-Activity Relationships
D037621 Artemisinins A group of SESQUITERPENES and their analogs that contain a peroxide group (PEROXIDES) within an oxepin ring (OXEPINS).

Related Publications

N Acton, and J M Karle, and R E Miller
May 2011, Molecules (Basel, Switzerland),
N Acton, and J M Karle, and R E Miller
August 1982, Yao xue xue bao = Acta pharmaceutica Sinica,
N Acton, and J M Karle, and R E Miller
November 2017, Bioorganic & medicinal chemistry,
N Acton, and J M Karle, and R E Miller
January 2002, Arzneimittel-Forschung,
N Acton, and J M Karle, and R E Miller
October 2003, Bioorganic & medicinal chemistry,
N Acton, and J M Karle, and R E Miller
August 2012, Bioorganic & medicinal chemistry,
N Acton, and J M Karle, and R E Miller
April 2000, Journal of medicinal chemistry,
N Acton, and J M Karle, and R E Miller
December 2006, European journal of medicinal chemistry,
N Acton, and J M Karle, and R E Miller
December 2017, The Korean journal of parasitology,
N Acton, and J M Karle, and R E Miller
January 2003, Nucleosides, nucleotides & nucleic acids,
Copied contents to your clipboard!