Bioorganic and Medicinal Chemistry Letters
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A small diversity library of α-methyl amide analogs of sulindac for probing anticancer structure-activity relationships
Diverse amide analogs of sulindac for cancer treatment and prevention
Examining the structure-activity relationship of benzopyran-based inhibitors of the hypoxia inducible factor-1 pathway
Repurposing of Proton Pump Inhibitors as first identified small molecule inhibitors of endo-β-N-acetylglucosaminidase (ENGase) for the treatment of NGLY1 deficiency, a rare genetic disease
Identification of initial leads directed at the calmodulin-binding region on the Src-SH2 domain that exhibit anti-proliferation activity against pancreatic cancer
Hydroxychalcone inhibitors of Streptococcus mutans glucosyl transferases and biofilms as potential anticaries agents
Synthesis and biological evaluation of ranitidine analogs as multiple-target-directed cognitive enhancers for the treatment of Alzheimer's disease
Evaluation of nicotine and cotinine analogs as potential neuroprotective agents for Alzheimer's disease.
Synthesis and SAR of geminal substitutions at the C5′ carbosugar position of pyrimidine-derived HCV inhibitors
Synthesis and SAR of pyridothiazole substituted pyrimidine derived HCV replication inhibitors
Pyridofuran substituted pyrimidine derivatives as HCV replication (replicase) inhibitors
5-Benzothiazole substituted pyrimidine derivatives as HCV replication (replicase) inhibitors
Novel substituted pyrimidines as HCV replication (replicase) inhibitors
Discovery of a new molecular probe ML228: An activator of the hypoxia inducible factor (HIF) pathway
Sulfonamides as a new scaffold for hypoxia inducible factor pathway inhibitors
Virtual screening to identify lead inhibitors for bacterial NAD synthetase (NADs)
Identification of novel inhibitors of bacterial surface enzyme Staphylococcus aureus Sortase A
Synthesis of symmetrical C- and pseudo-symmetrical O-linked disaccharide analogs for arabinosyltransferase inhibitory activity in Mycobacterium tuberculosis
Analogs of the marine alkaloid makaluvamines: Synthesis, topoisomerase II inhibition, and anticancer activity
Symmetrical and unsymmetrical analogues of isoxyl; active agents against Mycobacterium tuberculosis
Discover and SAR of 2-aminothiazole Inhibitors of Cyclin-dependent Kinase 5/p25 as a Potential Treatment for Alzheimer’s Disease
A new 2-carbamoyl pteridine that inhibits mycobacterial FtsZ
Activation and desensitization of heteromeric neuronal nicotinic receptors: Implications for non-synaptic transmission
Heterocyclic aminopyrrolidine derivatives as melatoninergic agents.
Synthesis and estrogen receptor binding affinities of 7-hydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-ones containing a basic side chain
Structure-activity relationships for a series of thiobenzamide influenza fusion inhibitors derived from 1,3,3-trimethyl-5-hydroxy-cyclohexylmethylamine.
Synthesis of an arabinofuranosyl disaccharide photoaffinity probe for arabinosyltransferase activity in Mycobacterium tuberculosis
An approach to the identification of potent inhibitors of influenza virus fusion using parallel synthesis methodology.
Atropisomeric Quinazolin-4-one Derivatives are Potent Noncompetitive Alpha-Amino-3-Hydroxy-5-Methyl-4-Isoxazolepropionic Acid (AMPA) Receptor Antagonists
Stereoselective binding of an enantiomeric pair of stromelysin-1 inhibitors caused by conformational entropy factors
Salicylamide inhibitors of influenza virus fusion.
Design of benzoic acid inhibitors of influenza neuraminidase containing a cyclic substitution for the N-acetyl grouping (vol 9, pg 1901, 1999)
Erratum: Design of benzoic acid inhibitors of influenza neuraminidase containing a cyclic substitution for the N-acetyl grouping (Bioorg. Med. Chem. Lett. (1999) 9 (1901) PII: S0960894X99003182)
Novel quinolizidine salicylamide influenza fusion inhibitors.
Design of benzoic acid inhibitors of influenza neuraminidase containing a cyclic substitution for the N-acetyl grouping
Uridine phosphorylase inhibitors: Chemical modification of benzyloxybenzyl-barbituric acid and its effects on UrdPase inhibition
Homologated aza analogs of arabinose as antimycobacterial agents
Conformationally constrained precursors to retinoic acid analogs which stabilize the 9Z-configuration
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