Publications by authors named "Barry M Twenter"

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A 3-(4-nitronaphthen-1-yl) amino-benzoate analog as a bifunctional AKR1C3 inhibitor and AR antagonist: Head to head comparison with other advanced AKR1C3 targeted therapeutics.
Phumvadee Wangtrakuldee, Adegoke O Adeniji, Tianzhu Zang, Ling Duan, Buddha Khatri, Barry M Twenter

J Steroid Biochem Mol Biol· September 2019

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Total Synthesis of (±)-Phomoidride D.
Joyce C Leung, Aaron A Bedermann, Jón T Njardarson, David A Spiegel, Graham K Murphy, Barry M Twenter

Angew Chem Int Ed Engl· February 2018

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Toward the synthesis of phomoidride D.
Graham K Murphy, Tatsuya Shirahata, Naoto Hama, Aaron Bedermann, Ping Dong, Barry M Twenter

J Org Chem· January 2013

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Wharton-fragmentation-based approach to the carbocyclic core of the phomoidrides.
Graham K Murphy, Naoto Hama, Aaron Bedermann, Ping Dong, Chris M Schneider, Barry M Twenter

Org Lett· September 2012

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Crystal structures of AKR1C3 containing an N-(aryl)amino-benzoate inhibitor and a bifunctional AKR1C3 inhibitor and androgen receptor antagonist. Therapeutic leads for castrate resistant prostate cancer.
Mo Chen, Adegoke O Adeniji, Barry M Twenter, Jeffrey D Winkler, David W Christianson

Bioorg Med Chem Lett· May 2012

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Development of potent and selective inhibitors of aldo-keto reductase 1C3 (type 5 17β-hydroxysteroid dehydrogenase) based on N-phenyl-aminobenzoates and their structure-activity relationships.
Adegoke O Adeniji, Barry M Twenter, Michael C Byrns, Yi Jin, Mo Chen

J Med Chem· March 2012

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A NEW APPROACH TO THE SYNTHESIS OF SUBSTITUTED PHENAZINES VIA PALLADIUM-CATALYZED ARYL LIGATION.
Jeffrey D Winkler, Barry M Twenter, Thomas Gendrineau

Heterocycles· January 2012

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Discovery of substituted 3-(phenylamino)benzoic acids as potent and selective inhibitors of type 5 17β-hydroxysteroid dehydrogenase (AKR1C3).
Adegoke O Adeniji, Barry M Twenter, Michael C Byrns, Yi Jin, Jeffrey D Winkler

Bioorg Med Chem Lett· March 2011

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