Amanote Research

Amanote Research

  • Register
  • Sign In

Discovery of Conformationally Restricted Human Glutaminyl Cyclase Inhibitors as Potent Anti-Alzheimers Agents by Structure-Based Design

doi 10.1021/acs.jmedchem.9b00751.s001

Full Text

Abstract

Available in

Date

Unknown

Authors

Unknown

Publisher

American Chemical Society (ACS)


Related search

Conformationally Restricted Dipeptide Amides as Potent and Selective Neuronal Nitric Oxide Synthase Inhibitors

Journal of Medicinal Chemistry
Drug DiscoveryMolecular Medicine
2006English

Conformationally Restricted Dipeptide Amides as Potent and Selective Neuronal Nitric Oxide Synthase Inhibitors

English

Soluble Variants of Human Recombinant Glutaminyl Cyclase

PLoS ONE
Multidisciplinary
2013English

Structure-Based Design of Potent and Selective CK1γ Inhibitors

ACS Medicinal Chemistry Letters
Organic ChemistryBiochemistryDrug Discovery
2012English

Discovery of Potent and Orally Available Malonyl-CoA Decarboxylase Inhibitors as Cardioprotective Agents

English

Discovery of Potent 2Aryl-6,7-Dihydro5Hpyrrolo[1,2a]imidazoles as WDR5-WIN-Site Inhibitors Using Fragment-Based Methods and Structure-Based Design

English

Can Small Molecule Inhibitors of Glutaminyl Cyclase Be Used as a Therapeutic for Alzheimer's Disease?

Future Medicinal Chemistry
Drug DiscoveryMolecular MedicinePharmacology
2017English

Fluorinated Conformationally-Restricted G-Aminobutyric Acid Aminotransferase Inhibitors

English

Structure Based Design of Potent Selective Inhibitors of Protein Kinase D1 (PKD1)

English

Amanote Research

Note-taking for researchers

Follow Amanote


© 2026 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy