Results 11 to 20 of about 658,841 (317)

Atlas for drug discovery [PDF]

open access: yesProceedings of the National Academy of Sciences, 2014
Reports of increasing antibiotic resistance and sagging drug discovery rates are appearing with increasing frequency, and many warn that we are living on the wrong side of an antibiotic peak—a period in which ever-fewer new antibiotics are being discovered at ever-increasing costs (1).
Pierre, Stallforth, Jon, Clardy
openaire   +2 more sources

MicroED in drug discovery

open access: yesCurrent Opinion in Structural Biology, 2023
The cryo-electron microscopy (cryo-EM) method microcrystal electron diffraction (MicroED) was initially described in 2013 and has recently gained attention as an emerging technique for research in drug discovery. As compared to other methods in structural biology, MicroED provides many advantages deriving from the use of nanocrystalline material for ...
Emma Danelius   +3 more
openaire   +6 more sources

Computational drug discovery [PDF]

open access: yesActa Pharmacologica Sinica, 2012
Computational drug discovery is an effective strategy for accelerating and economizing drug discovery and development process. Because of the dramatic increase in the availability of biological macromolecule and small molecule information, the applicability of computational drug discovery has been extended and broadly applied to nearly every stage in ...
Si-Sheng, Ou-Yang   +5 more
openaire   +2 more sources

Mycobacterial drug discovery

open access: yesRSC Medicinal Chemistry, 2020
Innovations in mycobacterial drug discovery to accelerate the identification of new drug candidates with confirmed targets and whole cell activity.
Katherine A. Abrahams, Gurdyal S. Besra
openaire   +3 more sources

Discovery of Antiepileptic Drugs [PDF]

open access: yesNeurotherapeutics, 2007
Since 1993, the Anticonvulsant Drug Development Program has contributed to the successful development of nine clinically effective drugs for the symptomatic treatment of epilepsy. These include felbamate (1993), gabapentin (1994), lamotrigine (1994), fosphenytoin (1996), topiramate (1996), tiagabine (1997), levetiracetam (1999), zonisamide (2000), and ...
Misty, Smith   +2 more
openaire   +2 more sources

Screening a protein kinase inhibitor library against Plasmodium falciparum

open access: yesMalaria Journal, 2017
Background Protein kinases have been shown to be key drug targets, especially in the area of oncology. It is of interest to explore the possibilities of protein kinases as a potential target class in Plasmodium spp., the causative agents of malaria ...
Irene Hallyburton   +12 more
doaj   +1 more source

Toxins and drug discovery [PDF]

open access: yesToxicon, 2014
Components from venoms have stimulated many drug discovery projects, with some notable successes. These are briefly reviewed, from captopril to ziconotide. However, there have been many more disappointments on the road from toxin discovery to approval of a new medicine. Drug discovery and development is an inherently risky business, and the main causes
openaire   +4 more sources

Profitability and drug discovery

open access: yesIndustrial and Corporate Change, 2022
Abstract Pharmaceutical firms are highly profitable due to high markups enabled by high drug prices. This is justified by the argument that high profits provide incentives for innovation and help fund high research and development (R&D) costs.
Isik, Enes   +2 more
openaire   +1 more source

Development and validation of a high-throughput calcium mobilization assay for the orphan receptor GPR88

open access: yesJournal of Biomedical Science, 2017
Background GPR88 is an orphan G protein-coupled receptor highly expressed in the striatum and is implicated in basal ganglia-associated disorders. However, the receptor functions of GPR88 are still largely unknown due to the lack of potent and selective ...
Ann M. Decker   +6 more
doaj   +1 more source

Pharmacological inhibition of nSMase2 reduces brain exosome release and α-synuclein pathology in a Parkinson’s disease model

open access: yesMolecular Brain, 2021
Aim We have previously reported that cambinol (DDL-112), a known inhibitor of neutral sphingomyelinase-2 (nSMase2), suppressed extracellular vesicle (EV)/exosome production in vitro in a cell model and reduced tau seed propagation.
Chunni Zhu   +12 more
doaj   +1 more source

Home - About - Disclaimer - Privacy