Literature DB >> 9051911

Novel cytotoxic, alkylated hydroquinones from Lannea welwitschii.

A Groweiss1, J H Cardellina, L K Pannell, D Uyakul, Y Kashman, M R Boyd.   

Abstract

Two novel natural products, lanneaquinol (1) and 2'(R)-hydroxylanneaquinol (2), were isolated from the organic extract of the plant Lannea welwitschii (Hiern) Engl. Their structures were solved by spectroanalytical methods and confirmed by comparison to synthetic models. The absolute configuration of 2 was determined by the modified Mosher method. Both compounds exhibited modest cytotoxicity against the NCI panel of 60 human tumor cell lines. The structures of two isomeric 4,5-dihydroxy-5-alkyl-2-cyclohexenones (7 and 8), which appear to be biogenetic precursors of 1 and 2, were also elucidated.

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Year:  1997        PMID: 9051911     DOI: 10.1021/np960435t

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  3 in total

1.  General synthesis for chiral 4-alkyl-4-hydroxycyclohexenones.

Authors:  Christophe Hoarau; Thomas R R Pettus
Journal:  Org Lett       Date:  2006-06-22       Impact factor: 6.005

2.  Evaluation of Antimicrobial and Wound Healing Potential of Justicia flava and Lannea welwitschii.

Authors:  Christian Agyare; Solomon Boamah Bempah; Yaw Duah Boakye; Patrick George Ayande; Martin Adarkwa-Yiadom; Kwesi Boadu Mensah
Journal:  Evid Based Complement Alternat Med       Date:  2013-09-15       Impact factor: 2.629

3.  Choerosponins A and B, Two New Cytotoxic Bridged-Ring Ketones and the Determination of Their Absolute Configurations.

Authors:  Chang-Wei Li; Bing Han; Bing Cai; Cheng-Bin Cui
Journal:  Molecules       Date:  2017-03-27       Impact factor: 4.411

  3 in total

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