Results 41 to 50 of about 512 (159)

Gut microbiome‐derived metabolites show promise in cancer research and therapy

open access: yesInterdisciplinary Medicine, Volume 4, Issue 2, March 2026.
The metabolites produced by the gut microbiome, which are subject to regulation by multiple factors, play a pivotal role in the progression of various types of cancer. These metabolites not only function as potential biomarkers for the early detection and monitoring of tumor development, but also actively participate in cancer therapeutic processes ...
Kangjie Yang   +4 more
wiley   +1 more source

Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine alpha-hydroxylating monooxygenase (PHM).

open access: yes, 2008
Peptidyl alpha-hydroxylating monooxygenase (PHM) functions in vivo towards the biosynthesis of alpha-amidated peptide hormones in mammals and insects. PHM is a potential target for the development of inhibitors as drugs for the treatment of human disease
Carpenter, Sarah E   +19 more
core   +1 more source

Fluorometric Microanalysis of Plasma Hippuric Acid and Comparison of Hippurate with P-Aminohippurate Clearances in Dogs.

open access: yesExperimental Biology and Medicine, 1964
Summary1. A method for analysis of microgram quantities of hippuric acid in plasma with good precision and accuracy is presented. 2. There is no significant difference in the clearance of hippuric acid and p-aminohippuric acid by the dog.
H C, ELLIOTT, A A, WALKER
openaire   +2 more sources

SYNTHESIS OF HIPPURIC ACID IN LIVER HOMOGENATE

open access: yesJournal of Biological Chemistry, 1947
The synthesis of hippuric acid from benaoic acid and glycine resembles in several respects the synthesis of a peptide bond. A CONH group is formed, it is a to a carboxyl group, and the free energy of its formation is of the same order of magnitude. The synthesis was demonstrated in liver and kidney slices of a number of animals; it is inhibited by 0 ...
H, BORSOOK, J W, DUBNOFF
openaire   +2 more sources

Induced pi-facial discrimination in the alkylation of chiral derivatives of glycine.

open access: yes, 1999
Part A. The alkylation trans 2-arylcyclohexyl hippurates with a series of electrophiles was examined. The reaction stereoselectivity varied from 46 to 81% depending on the steric and electronic nature of the electrophile when (Ar = phenyl).
Peters, Scott Owen.
core   +1 more source

Hippurate participates in the correction of metabolic acidosis

open access: yesKidney International, 2001
Hippurate (Hip), an endogenous conjugate, belongs to the group of uremic toxins. Hip stimulates P-independent glutaminase (PIG) localized at the proximal luminal membrane, desamidating glutamine with the formation of ammonia, a dominant and adaptive elimination product of H+.
Dzúrik, Rastislav   +3 more
openaire   +2 more sources

Protein-Bound Toxins-Update 2009

open access: yes, 2009
Protein-bound uremic retention solutes constitute a group whose common characteristic is their difficult removal by dialysis. In 2003, the EUTox group described 25 protein-bound solutes.
Jourde-Chiche, N   +10 more
core   +1 more source

Induced pi-facial discrimination in the alkylation of chiral derivatives of glycine.

open access: yes, 1998
Part A. The alkylation trans 2-arylcyclohexyl hippurates with a series of electrophiles was examined. The reaction stereoselectivity varied from 46 to 81% depending on the steric and electronic nature of the electrophile when (Ar = phenyl).
Peters, Scott Owen
core   +1 more source

Hippurate Hydrolysis in Klebsiella-Cloaca Classification [PDF]

open access: yesJournal of General Microbiology, 1957
SUMMARY: 169 strains of Klebsiella pneumoniae and 68 strains of Cloaca cloacae were used in an examination of Hajna & Damon's hippurate test and various modifications of it. The addition of a pH indicator (phenol red) to the medium enabled hydrolysis to be detected by a change of colour. Clear-cut distinction between K. pneumoniae and C.
openaire   +2 more sources

Substituted hippurates and hippurate analogs as substrates and inhibitors of peptidylglycine a-hydroxylating monooxygenase (PHM)

open access: yes, 2008
Peptidyl a-hydroxylating monooxygenase (PHM) functions in vivo towards the biosynthesis of a-amidated peptide hormones in mammals and insects. PHM is a potential target for the development of inhibitors as drugs for the treatment of human disease and as ...
M. Romero (11678484)   +19 more
core  

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