Quaternary indolylpyridinium salts. Oral hypoglycemic agents

A 90,000-dalton binding protein common to both steroid receptors and the Rous sarcoma virus transforming protein, pp60v-src.

The Journal of biological chemistry·1985

Immunological evidence that the nonhormone binding component of avian steroid receptors exists in a wide range of tissues and species.

Biochemistry·1985

Isolation of steroid receptor binding protein from chicken oviduct and production of monoclonal antibodies.

Biochemistry·1985

5-Aryl-3-azabicyclo[3.2.0]heptan-6-one ketals, compounds with morphine-like analgesic activity.

Journal of medicinal chemistry·1984

1-Aryl-3-azabicyclo[3.1.0]hexanes, a new series of nonnarcotic analgesic agents.

Journal of medicinal chemistry·1981

Thiophene systems. 5. Thieno[3,4-b][1,5]benzoxazepines, thieno[3,4-b][1,5]benzothiazepines, and thieno[3,4-b][1,4]benzodiazepines as potential central nervous system agents.

Journal of medicinal chemistry·1981

Neutral Backbone Modifications Enhance the Pharmacokinetics and Biodistribution of Antibody-Oligonucleotide Conjugates with High Drug-to-Antibody Ratios.

Journal of medicinal chemistry·2026

Discovery of TL10: A Soluble and Long-Acting MC4R Agonist with Tunable Lipidation for Sustained Pharmacological Activity.

Journal of medicinal chemistry·2026

Discovery, Synthesis, and Biological Evaluation of 1,3,4,5-Tetrahydro-6H-pyrano[4,3-c]isoquinolin-6-one Derivatives as Novel and Highly Selective PARP1 Inhibitors.

Journal of medicinal chemistry·2026

Discovery and Optimization of Novel Nonhydroxamate LpxC Inhibitors for the Treatment of Multidrug-Resistant Gram-Negative Infections.

Journal of medicinal chemistry·2026

Fragment-Based Discovery of Potent RNA-Competitive Inhibitors of the DEAH-Box RNA Helicase DHX8.

Journal of medicinal chemistry·2026

Discovery and Optimization of a WRN Helicase Inhibitor Series through Structure-Guided Drug Design from a Covalent Fragment Binding Insight.

Journal of medicinal chemistry·2026

Base-promoted dearomatization/1,6-addition of α-haloketones: synthesis of α-azido-α,α-diaryl ketones.

Chemical communications (Cambridge, England)·2026

Enantioselective Access to Trifluoromethylated Spirocyclopropyl Heterocycles.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Organocatalytic Enantioselective Electrophilic C-H Sulfenylation of Arenes.

Accounts of chemical research·2026

Palladium-Catalyzed Fluoroallylation of Aldimine Esters With gem-Difluorocyclopropanes: Synthesis of Fluorinated α-Amino Acid Derivatives.

Chemistry, an Asian journal·2026

Correction: Imine-anion-mediated alkoxy-group-elimination-type SNAr reaction: an efficient synthetic route to phenanthridines.

Chemical communications (Cambridge, England)·2026

Mechanochemical three-component radical sulfonamidation enabled by copper catalysis.

Chemical communications (Cambridge, England)·2026

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Quaternary indolylpyridinium salts. Oral hypoglycemic agents

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A 90,000-dalton binding protein common to both steroid receptors and the Rous sarcoma virus transforming protein, pp60v-src.

Immunological evidence that the nonhormone binding component of avian steroid receptors exists in a wide range of tissues and species.

Isolation of steroid receptor binding protein from chicken oviduct and production of monoclonal antibodies.

5-Aryl-3-azabicyclo[3.2.0]heptan-6-one ketals, compounds with morphine-like analgesic activity.

1-Aryl-3-azabicyclo[3.1.0]hexanes, a new series of nonnarcotic analgesic agents.

Thiophene systems. 5. Thieno[3,4-b][1,5]benzoxazepines, thieno[3,4-b][1,5]benzothiazepines, and thieno[3,4-b][1,4]benzodiazepines as potential central nervous system agents.

Neutral Backbone Modifications Enhance the Pharmacokinetics and Biodistribution of Antibody-Oligonucleotide Conjugates with High Drug-to-Antibody Ratios.

Discovery of TL10: A Soluble and Long-Acting MC4R Agonist with Tunable Lipidation for Sustained Pharmacological Activity.

Discovery, Synthesis, and Biological Evaluation of 1,3,4,5-Tetrahydro-6H-pyrano[4,3-c]isoquinolin-6-one Derivatives as Novel and Highly Selective PARP1 Inhibitors.

Discovery and Optimization of Novel Nonhydroxamate LpxC Inhibitors for the Treatment of Multidrug-Resistant Gram-Negative Infections.

Fragment-Based Discovery of Potent RNA-Competitive Inhibitors of the DEAH-Box RNA Helicase DHX8.

Discovery and Optimization of a WRN Helicase Inhibitor Series through Structure-Guided Drug Design from a Covalent Fragment Binding Insight.

Base-promoted dearomatization/1,6-addition of α-haloketones: synthesis of α-azido-α,α-diaryl ketones.

Enantioselective Access to Trifluoromethylated Spirocyclopropyl Heterocycles.

Organocatalytic Enantioselective Electrophilic C-H Sulfenylation of Arenes.

Palladium-Catalyzed Fluoroallylation of Aldimine Esters With gem-Difluorocyclopropanes: Synthesis of Fluorinated α-Amino Acid Derivatives.

Correction: Imine-anion-mediated alkoxy-group-elimination-type SNAr reaction: an efficient synthetic route to phenanthridines.

Mechanochemical three-component radical sulfonamidation enabled by copper catalysis.

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Quaternary indolylpyridinium salts. Oral hypoglycemic agents

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