Results 201 to 210 of about 330,401 (264)

Proteomic Profiling of Oxidative Stress Response Proteins with a Methionine Sulfoxide-Inspired Activity-Based Probe. [PDF]

JACS Au
Ahn S, Kee JM.
europepmc   +1 more source

Computational identification of epifriedelanol and derived analogs from Mikania cordata as potential HMG-CoA reductase inhibitors. [PDF]

PLoS One
Banu M, Ahmed SS, Begum M, Rahman MO.
europepmc   +1 more source

Identification and functional characterization of a novel thioredoxin MpTRX1 from Metschnikowia persimmonesis. [PDF]

Appl Microbiol Biotechnol
Kang CH, Lee JH, Lee YM, Lee YB, Kang Y, Ban Y, Haniffadli A, Rahmat E, Lim CO.   +8 more
europepmc   +1 more source

Natural products as HMG-CoA reductase inhibitors (statins) for the management of non-communicable diseases. [PDF]

Inflammopharmacology
Muhammad RN, Aborehab NM, Aly SH, Nasr NN, Hindam MO, Mustafa AM, Faheem SA, Fawzy MH, Abo-El Fetoh ME, El-Dessouki AM, Rabie MA, El-Shiekh RA, Youssef ME.   +12 more
europepmc   +1 more source

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Carbonyl reductase

Chemico-Biological Interactions, 2000
Carbonyl reductase (secondary-alcohol:NADP(+) oxidoreductase, EC 1.1. 1.184) belongs to the family of short chain dehydrogenases/reductases (SDR). Carbonyl reductases (CBRs) are NADPH-dependent, mostly monomeric, cytosolic enzymes with broad substrate specificity for many endogenous and xenobiotic carbonyl compounds.
G L, Forrest, B, Gonzalez
openaire   +2 more sources