Literature DB >> 12954062

5-benzylidene-1,2-dihydrochromeno[3,4-f]quinolines as selective progesterone receptor modulators.

Lin Zhi1, Christopher M Tegley, Barbara Pio, James P Edwards, Mehrnouch Motamedi, Todd K Jones, Keith B Marschke, Dale E Mais, Boris Risek, William T Schrader.   

Abstract

A series of 5-benylidene-1,2-dihydrochromeno[3,4-f]quinolines (4) were synthesized and tested in bioassays to evaluate their progestational activities, receptor- and tissue-selectivity profiles as selective progesterone receptor modulators (SPRMs). Most of the new analogues exhibited as highly potent progestins with more than 100-fold receptor selectivity over other steroid hormone receptors and LG120920 (7b) demonstrated tissue selectivity toward uterus and vagina versus breasts in a rodent model after oral administration.

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Year:  2003        PMID: 12954062     DOI: 10.1021/jm020477g

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  3 in total

1.  Molecular modeling on structure-function analysis of human progesterone receptor modulators.

Authors:  Ria Pal; Md Ataul Islam; Tabassum Hossain; Achintya Saha
Journal:  Sci Pharm       Date:  2011-06-30

2.  Synthesis of chromeno[3,4-B]quinoline derivatives by heterogeneous [Cu(II)BHPPDAH] catalyst without being immobilized on any support under mild conditions using PEG 300 as green solvent.

Authors:  Hashem Sharghi; Reza Khalifeh; Zahra Rashidi
Journal:  Mol Divers       Date:  2013-08-22       Impact factor: 2.943

3.  One-pot three-component tandem annulation of 4-hydroxycoumarine with aldehyde and aromatic amines using graphene oxide as an efficient catalyst.

Authors:  Rabindranath Singha; Aminul Islam; Pranab Ghosh
Journal:  Sci Rep       Date:  2021-10-06       Impact factor: 4.379

  3 in total

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