reference/30917052

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30917052

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	6743
issn	0022-2623 1520-4804
issueIdentifier	21
pageRange	6724-6743
publicationName	Journal of Medicinal Chemistry
startingPage	6724
bibliographicCitation	Bey E, Marchais-Oberwinkler S, Negri M, Kruchten P, Oster A, Klein T, Spadaro A, Werth R, Frotscher M, Birk B, Hartmann RW. New insights into the SAR and binding modes of bis(hydroxyphenyl)thiophenes and -benzenes: influence of additional substituents on 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) inhibitory activity and selectivity. J Med Chem. 2009 Nov 12;52(21):6724–43. doi: 10.1021/jm901195w. PMID: 19831396.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_74b515cf638ecfd502b3cb499ef84761 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_6823a1ffde20cdb51abf020995735749 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_257084ae97531dba5da570895fe62da9 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e6f1bd261430c679e10b7b5876a89794 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_34860cae47b24d696e50f40d83c69595 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_df6530657fc3aa4f3aeda8c7fa058d4e http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_2d762632ef31db9e79630bfc7211b382 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8db7a9eafb95772d791b1ebc52873e45 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_99e337f79d7361d24889290c7bdf46f5 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3aa251022f176d6e7a176a2473f063ec http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_1e069fe7fe7c0cc01a850846e1f0da40
date	2009-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1021/jm901195w https://pubmed.ncbi.nlm.nih.gov/19831396
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/4938 https://portal.issn.org/resource/ISSN/0022-2623 https://portal.issn.org/resource/ISSN/1520-4804
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	New insights into the SAR and binding modes of bis(hydroxyphenyl)thiophenes and -benzenes: influence of additional substituents on 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1) inhibitory activity and selectivity
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http://rdf.ncbi.nlm.nih.gov/pubchem/endpoint/SID103645302_AID441227_PMID19831396_VALUE4

http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1576
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1557
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129697511
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID2100
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID2099
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129369435
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID3294
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129506098
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID3292
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID246304963
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129957312
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1565

Total number of triples: 257.