Results 71 to 80 of about 2,687,981 (207)
Homogentisic Acid: A Phenolic Acid as a Marker of Strawberry-Tree (Arbutus unedo L.) Honey
Analysis of organic acids in strawberry-tree (Arbutus unedo) honey showed the presence of an unknown acid as the main constituent. This compound was isolated and identified as homogentisic acid (2,5-dihydroxyphenylacetic acid) by MS and NMR techniques ...
Guillou C +6 more
core
Alkaptonuria (AKU) is a rare disease correlated with deficiency of the enzyme homogentisate 1,2 dioxygenase, which causes homogentisic acid (HGA) accumulation.
Millucci L. +13 more
core +1 more source
Ochronotic arthropathy: skeletal manifestations and orthopaedic treatment
Alkaptonuria is an extremely rare disorder of tyrosine metabolism caused by an autosomal recessive enzymatic deficiency of homogentisic acid (HGA) oxidase, causing its accumulation in collagenous structures, especially in hyaline cartilage.
Khaled Hamed Salem, Alyaa Diaa Elmoghazy
doaj +1 more source
Natural and bioactive products have been of great interest due to their benefit as health foods and drugs to prevent various diseases. The aim of this study is to efficiently reuse marine chitinous materials (CMs), abundant and low-cost fishery by ...
Van Bon Nguyen +6 more
doaj +1 more source
Ochronotic arthropathy of the hip with multiple joint involvement: a rare case report and literature review [PDF]
Ochronosis is a rare inherited genetic disorder that affects tyrosine and phenylalanine metabolism. It leads to the deposition of dark pigments in connective tissues and articular cartilage, which are rich in collagen.
Plaban N. Chowdhury +3 more
doaj +1 more source
The Dibromination of Homogentisic Acid Lactone
The recently described total synthetic pathway to clavatadine A, beneficial for its properties as an anticoagulant, is hindered by a step involving the dibromination of homogentisic acid lactone.
Bouchey, Sydney +3 more
core
Expanding the Interface: Overlooked Dermatologic Disorders With Ocular Involvement
JEADV Clinical Practice, Volume 4, Issue 5, Page 1239-1243, December 2025.
A George
wiley +1 more source
Ochronotic Arthropathy of the Knee: A Case Report
Alkaptonuria (AKU) is a low-prevalence genetic inherited disease expressed in an autosomal recessive and monogenic manner, characterized by a tissue accumulation of homogentisic acid (HGA).
MARZO NUNES SANTOS +2 more
doaj +1 more source
Alkaptonuria is a rare inborn error of metabolism with autosomal recessive inheritance with a mutation in homogentisate 1,2-dioxygenase. It results in accumulation of homogentisic acid in connective tissues (ochronosis). Most common ocular manifestations
Nirupama Damarla +5 more
doaj +1 more source
Antiplasmodial activities of homogentisic acid derivative protein kinase inhibitors isolated from a Vanuatu marine sponge Pseudoceratina sp. [PDF]
As part of our search for new antimalarial drugs in South Pacific marine sponges, we have looked for inhibitors of Pfnek-1, a specific protein kinase of Plasmodium falciparum.
Dominique Laurent +26 more
core +2 more sources

