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Bioorganic & Medicinal Chemistry Letters|June 17, 2006
Triazolo-tetrahydrofluorenones as selective estrogen receptor beta agonistsDann L Parker, Dongfang Meng, Ronald W Ratcliffe, et al.
Bioorganic & Medicinal Chemistry Letters|April 14, 1999
Synthesis and activity of 2-(sulfonamido)methyl-carbapenems: discovery of a novel, anti-MRSA 1,8-naphthosultam pharmacophoreR R Wilkening, R W Ratcliffe, K J Wildonger, et al.
Bioorganic & Medicinal Chemistry Letters|May 30, 2006
Estrogen receptor beta-subtype selective tetrahydrofluorenones: use of a fused pyrazole as a phenol bioisostereR R Wilkening, R W Ratcliffe, A K Fried, et al.
Bioorganic & Medicinal Chemistry Letters|June 8, 2012
Synthesis and biological evaluation of antifungal derivatives of enfumafungin as orally bioavailable inhibitors of β-1,3-glucan synthaseBrian H Heasley, Gregory J Pacofsky, Ahmed Mamai, et al.
Bioorganic & Medicinal Chemistry Letters|April 14, 1999
Synthesis and properties of 2-(naphthosultamyl)methyl-carbapenems with potent anti-MRSA activity: discovery of L-786,392R W Ratcliffe, R R Wilkening, K J Wildonger, et al.
Bioorganic & Medicinal Chemistry Letters|April 25, 2006
The discovery of tetrahydrofluorenones as a new class of estrogen receptor beta-subtype selective ligandsR R Wilkening, R W Ratcliffe, E C Tynebor, et al.
Bioorganic & Medicinal Chemistry Letters|November 7, 2015
Novel orally active inhibitors of β-1,3-glucan synthesis derived from enfumafunginJames M Apgar, Robert R Wilkening, Mark L Greenlee, et al.
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