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Bioorganic & Medicinal Chemistry Letters|May 5, 2005
Biaryl isoxazolinone antibacterial agentsClaude A Quesnelle, Patrice Gill, Stephan Roy, et al.
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|June 17, 2006
Arylpropionylpiperazines as antagonists of the human melanocortin-4 receptorWanlong Jiang, Fabio C Tucci, Caroline W Chen, et al.
Bioorganic & Medicinal Chemistry Letters|June 17, 2006
Amide-substituted farnesylcysteine analogs as inhibitors of human isoprenylcysteine carboxyl methyltransferaseJames L Donelson, Heather B Hodges, Daniel D Macdougall, et al.
Bioorganic & Medicinal Chemistry Letters|June 17, 2006
Opiate receptor binding properties of morphine-, dihydromorphine-, and codeine 6-O-sulfate ester congenersPeter A Crooks, Santosh G Kottayil, Abeer M Al-Ghananeem, et al.
Bioorganic & Medicinal Chemistry Letters|June 20, 2006
Synthesis of 2-C-hydroxymethylribofuranosylpurines as potent anti-hepatitis C virus (HCV) agentsByul Nae Yoo, Hea Ok Kim, Hyung Ryong Moon, et al.
Bioorganic & Medicinal Chemistry Letters|June 20, 2006
Synthesis of novel tricyclic oxazolidinones by a tandem SN2 and SNAr reaction: SAR studies on conformationally constrained analogues of LinezolidN Selvakumar, B Yadi Reddy, G Sunil Kumar, et al.
Bioorganic & Medicinal Chemistry Letters|June 20, 2006
Synthesis and anthelmintic activity of substituted (R)-phenyllactic acid containing cyclohexadepsipeptidesPeter Jeschke, Jordi Benet-Buchholz, Achim Harder, et al.
Bioorganic & Medicinal Chemistry Letters|August 5, 2006
Novel tricyclic azepine derivatives: Biological evaluation of pyrimido[4,5-b]-1,4-benzoxazepines, thiazepines, and diazepines as inhibitors of the epidermal growth factor receptor tyrosine kinaseLeon Smith, Wai C Wong, Alexander S Kiselyov, et al.
Bioorganic & Medicinal Chemistry Letters|July 28, 2006
Exploring alternative Zn-binding groups in the design of HDAC inhibitors: squaric acid, N-hydroxyurea, and oxazoline analogues of SAHAStephen Hanessian, Valerio Vinci, Luciana Auzzas, et al.
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