Literature DB >> 2235891

Structure elucidation and thermospray high-performance liquid chromatography/mass spectroscopy (HPLC/MS) of the microbial and mammalian metabolites of the antimalarial arteether.

C D Hufford1, I S Lee, H N ElSohly, H T Chi, J K Baker.   

Abstract

Microbial metabolism studies of the antimalarial drug arteether (1) have shown that arteether is metabolized to six new metabolites in addition to those previously reported (3). Large-scale fermentations with Cunninghamella elegans (ATCC 9245) and Streptomyces lavendulae (L-105) have resulted in the characterization of these metabolites primarily by two-dimensional nuclear magnetic resonance (2D-NMR) methods as 9 beta-hydroxyarteether (2), a ring rearrangement metabolite (3), 3 alpha-hydroxy-11-epi-deoxydihydroartemisinin (4), 9 alpha-hydroxyarteether (5), 2 alpha-hydroxyarteether (6), and 14-hydroxyarteether (7). Thermospray mass spectroscopy/high-performance liquid chromatographic analyses have shown that four of these metabolites (2, 5, 6, 7) are also present in rat liver microsome preparations.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2235891     DOI: 10.1023/a:1015993722846

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  3 in total

1.  Microbial metabolism studies of the antimalarial drug arteether.

Authors:  I S Lee; H N ElSohly; C D Hufford
Journal:  Pharm Res       Date:  1990-02       Impact factor: 4.200

2.  Thermospray mass spectroscopy/high performance liquid chromatographic identification of the metabolites formed from arteether using a rat liver microsome preparation.

Authors:  J K Baker; R H Yarber; C D Hufford; I S Lee; H N ElSohly; J D McChesney
Journal:  Biomed Environ Mass Spectrom       Date:  1989-05

3.  Arteether, a new antimalarial drug: synthesis and antimalarial properties.

Authors:  A Brossi; B Venugopalan; L Dominguez Gerpe; H J Yeh; J L Flippen-Anderson; P Buchs; X D Luo; W Milhous; W Peters
Journal:  J Med Chem       Date:  1988-03       Impact factor: 7.446

  3 in total
  7 in total

1.  Microbial production of a crisnatol metabolite.

Authors:  C D Hufford; S H el-Sharkawy; T M Jurgens; J R Mikell
Journal:  Pharm Res       Date:  1992-05       Impact factor: 4.200

2.  Biomimetic metabolism of artelinic acid by chemical cytochrome P-450 model systems.

Authors:  O R Idowu; A J Lin; J M Grace; J O Peggins
Journal:  Pharm Res       Date:  1997-10       Impact factor: 4.200

3.  Clinical pharmacokinetics of the diastereomers of arteether in healthy volunteers.

Authors:  Sreedharan N Sabarinath; Omkar P Asthana; Sunil K Puri; Kumkum Srivastava; Kunnath P Madhusudanan; Ram C Gupta
Journal:  Clin Pharmacokinet       Date:  2005       Impact factor: 6.447

4.  Decomposition of arteether in simulated stomach acid yielding compounds retaining antimalarial activity.

Authors:  J K Baker; J D McChesney; H T Chi
Journal:  Pharm Res       Date:  1993-05       Impact factor: 4.200

5.  Microbial and mammalian metabolism studies on the semisynthetic antimalarial, deoxoartemisinin.

Authors:  S I Khalifa; J K Baker; M Jung; J D McChesney; C D Hufford
Journal:  Pharm Res       Date:  1995-10       Impact factor: 4.200

6.  Microbial and mammalian metabolism studies of the semisynthetic antimalarial, anhydrodihydroartemisinin.

Authors:  S I Khalifa; J K Baker; R D Rogers; F S el-Feraly; C D Hufford
Journal:  Pharm Res       Date:  1994-07       Impact factor: 4.200

Review 7.  Progress in the research of artemisinin-related antimalarials: an update.

Authors:  H J Woerdenbag; N Pras; W van Uden; T E Wallaart; A C Beekman; C B Lugt
Journal:  Pharm World Sci       Date:  1994-08-05
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.