Literature DB >> 27389513

Preparation of 4-(4'-Hydroxyanilino)-5-anilinophthalimide and 4,5-Bis-(4'-hydroxyanilino)-phthalimide by Microbial Hydroxylation.

S Weidner1, K Goeke2, U Trinks2, P Traxler3, K Ucci-Stoll2, O Ghisalba2.   

Abstract

A microbial screening indicated that two fungal strains, Beauveria bassiana DSM 1344=ATCC 7159 and Cunninghamella elegans DSM 1908=ATCC 9245, as well as four bacterial strains belonging to the genus Streptomyces were able to hydroxylate 4,5-dianilinophthalimide (DAPH, CGP52411) to 4-(4'-hydroxyanilino)-5-anilinophthalimide. Cunninghamella elegans DSM 1908 turned out to be the most active biocatalyst and was also able to form the dihydroxy derivative, 4,5-bis(4'-hydroxyanilino)phthalimide. The reaction for the monohydroxylated biotransformation product was carried out on a preparative scale, and the culture conditions for the formation of 4-(4'-hydroxy- anilino)-5-anilinophthalimide with this strain were op-timized.

Entities:  

Keywords:  4,5-bis-(4′-hydroxyanilino)-phthalimide; 4-(4′-hydroxyanilino)-5-anilinophthalimide; PTK-inhibitors; microbial hydroxylation

Year:  1999        PMID: 27389513     DOI: 10.1271/bbb.63.1497

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  2 in total

1.  The CYPome of the model xenobiotic-biotransforming fungus Cunninghamella elegans.

Authors:  William Palmer-Brown; Raúl Miranda-CasoLuengo; Kenneth H Wolfe; Kevin P Byrne; Cormac D Murphy
Journal:  Sci Rep       Date:  2019-06-25       Impact factor: 4.379

2.  Evaluation of Microbial Transformation of 10-deoxoartemisinin by UPLC-ESI-Q-TOF-MSE.

Authors:  Yue Bai; Dong Zhang; Peng Sun; Yifan Zhao; Xiaoqiang Chang; Yue Ma; Lan Yang
Journal:  Molecules       Date:  2019-10-28       Impact factor: 4.411

  2 in total

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