Pesquisas alternativas:
od chem » food chem (Expandir a Pesquisa)
eus j » eus _ (Expandir a Pesquisa), eun j (Expandir a Pesquisa)
sun j » sun _ (Expandir a Pesquisa), sun x (Expandir a Pesquisa)
A mostrar 221 - 240 resultados de 355 para a pesquisa '((((((kur OR kuru) OR kurtz) j) OR (eus j))) OR (sun j)) ((med chem) OR (od chem))', tempo de pesquisa: 2.95seg Refinar resultados
Synthesis and evaluation of a bifunctional chelate for development of Bi(III)-labeled radioimmunoconjugates
2-Alkyl/alkenyl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists

The Structure-Activity Relationship of Peptide Conjugated Chloramphenicol for Inhibiting E. coli
Synthesis and Evaluation of Tripodal Peptide Analogues for Cellular Delivery of Phosphopeptides

Synthetic resveratrol aliphatic acid inhibits TLR2-mediated apoptosis and an involvement of Akt/GSK3β pathway
Degrasyn-like Symmetrical Compounds: Possible Therapeutic Agents for Multiple Myeloma (MM-I)

Design, Synthesis, and Evaluation of Prodrugs of Ertapenem
Discovery of 5-Phenyl-N-(pyridin-2-ylmethyl)-2-(pyrimidin-5-yl)quinazolin-4-amine as a Potent I(Kur) Inhibitor

Small molecule KDM4s inhibitors as anti-cancer agents
Identification of myricetin and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13

Sulfamoylbenzamide-based Capsid Assembly Modulators for Selective Inhibition of Hepatitis B Viral Replication
Structure–Activity Relationship in a Purine-Scaffold Compound Series with Selectivity for the Endoplasmic Reticulum Hsp90 Paralog Grp94

Development of 2,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one inhibitors of Aldehyde Dehydrogenase 1A (ALDH1A) as potential adjuncts to ovarian cancer chemotherapy
D-isoascorbyl palmitate: lipase-catalyzed synthesis, structural characterization and process optimization using response surface methodology

Fragment-based cocktail crystallography by the Medical Structural Genomics of Pathogenic Protozoa Consortium
Assessing the Perturbing Effects of Drugs on Lipid Bilayers Using Gramicidin Channel-Based In Silico and In Vitro Assays

Synthesis, modification and docking studies of 5-sulfonyl isatin derivatives as SARS-CoV 3C-like protease inhibitors
Site-Specific Photo-Crosslinking Proteomics Reveal Regulation of IFITM3 Trafficking and Turnover by VCP/p97 ATPase

Discovery of AM-1638: A Potent and Orally Bioavailable GPR40/FFA1 Full Agonist
Potent, Orally Bioavailable Diazabicyclic Small-Molecule Mimetics of Second Mitochondria-derived Activator of Caspases

Ferramentas de pesquisa: Obter Feed RSS — Enviar pesquisa por email — Guardar a pesquisa