Results 1 to 10 of about 27,164,775 (142)

Carboxylesterase 1 family knockout alters drug disposition and lipid metabolism. [PDF]

open access: yesActa Pharm Sin B, 2023
The mammalian carboxylesterase 1 (Ces1/CES1) family comprises several enzymes that hydrolyze many xenobiotic chemicals and endogenous lipids. To investigate the pharmacological and physiological roles of Ces1/CES1, we generated Ces1 cluster knockout ...
Gan C   +15 more
europepmc   +5 more sources

Enhanced triacylglycerol catabolism by carboxylesterase 1 promotes aggressive colorectal carcinoma. [PDF]

open access: yesJ Clin Invest, 2021
The ability to adapt to low-nutrient microenvironments is essential for tumor-cell survival and progression in solid cancers, such as colorectal carcinoma (CRC).
Capece D   +26 more
europepmc   +9 more sources

Carboxylesterase 1 and Precision Pharmacotherapy: Pharmacogenetics and Nongenetic Regulators. [PDF]

open access: yesDrug Metab Dispos, 2020
Carboxylesterase (CES) 1 is the most abundant drug-metabolizing enzyme in human livers, comprising approximately 1% of the entire liver proteome. CES1 is responsible for 80%–95% of total hydrolytic activity in the liver and plays a crucial role in the ...
Her L, Zhu HJ.
europepmc   +5 more sources

Functional Study of Carboxylesterase 1 Protein Isoforms. [PDF]

open access: yesProteomics, 2019
Carboxylesterase 1 (CES1) is a primary human hepatic hydrolase involved in hydrolytic biotransformation of numerous medications. Considerable interindividual variability in CES1 expression and activity has been consistently reported. Four isoforms of the
Wang X, Shi J, Zhu HJ.
europepmc   +5 more sources

A Comprehensive Functional Assessment of Carboxylesterase 1 Nonsynonymous Polymorphisms. [PDF]

open access: yesDrug Metab Dispos, 2017
Carboxylesterase 1 (CES1) is the predominant human hepatic hydrolase responsible for the metabolism of many clinically important medications. CES1 expression and activity vary markedly among individuals; and genetic variation is a major contributing factor to CES1 interindividual variability.
Wang X   +5 more
europepmc   +5 more sources

An in vitro evaluation of kratom (Mitragyna speciosa) on the catalytic activity of carboxylesterase 1 (CES1). [PDF]

open access: yesChem Biol Interact, 2023
Kratom, (Mitragyna Speciosa Korth.) is a plant indigenous to Southeast Asia whose leaves are cultivated for a variety of medicinal purposes and mostly consumed as powders or tea in the United States.
Melchert PW   +5 more
europepmc   +2 more sources

In silico analysis of selected nutrition rich fruit of Bunch berry (Lantana camara) constituents as human acetylcholinesterase (hAchE), carbonic anhydrase II (hCA-II) and carboxylesterase 1 (hCES-1) inhibitory agents. [PDF]

open access: yesSaudi J Biol Sci, 2023
Background Bunch berry (Lantana camara) is primarily composed of flavonoids and vitamin C; therefore, it has been shown to possess various medical characteristics, including the ability to relieve fever, inflammation, and urinary tract infections ...
Surya Prakash V   +6 more
europepmc   +2 more sources

Discovery of triterpenoids as potent dual inhibitors of pancreatic lipase and human carboxylesterase 1. [PDF]

open access: yesJ Enzyme Inhib Med Chem, 2022
Pancreatic lipase (PL) is a well-known key target for the prevention and treatment of obesity. Human carboxylesterase 1A (hCES1A) has become an important target for the treatment of hyperlipidaemia.
Zhang J   +12 more
europepmc   +2 more sources

Fluorine impairs carboxylesterase 1-mediated hydrolysis of T-2 toxin and increases its chondrocyte toxicity. [PDF]

open access: yesFront Nutr, 2022
Background T-2 toxin is recognized as one of the high-risk environmental factors for etiology and pathogenesis of Kashin-Beck disease (KBD). Previous evidence indicates decreased serum fluorine level in KBD patients.
Jia Y   +10 more
europepmc   +2 more sources

Carboxylesterase-1 Assisted Targeting of HDAC Inhibitors to Mononuclear Myeloid Cells in Inflammatory Bowel Disease. [PDF]

open access: yesJ Crohns Colitis, 2022
Background and Aims Histone deacetylase inhibitors [HDACi] exert potent anti-inflammatory effects. Because of the ubiquitous expression of HDACs, clinical utility of HDACi is limited by off-target effects.
Elfiky AMI   +21 more
europepmc   +2 more sources

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