guluronic acid

Guluronic acid (G2013) is an organic building block found in hyaluronic acid. It functions as a nonsteroidal anti-inflammatory agent and displays a beneficial anti-inflammatory effect.

L-Diguluronic acid, a linear polysaccharide copolymer consisting of two L-guluronic acid (G) units, serves as a precursor for Alginate[1], a categorically unbranched polyanionic polysaccharide. Alginate finds application in the development of antifungal agent delivery carriers[2].

L-Triguluronic acid, a linear polysaccharide copolymer consisting of three L-guluronic acid (G) units, serves as a precursor for Alginate[1]. Alginate, an unbranched polyanionic polysaccharide, has applications in the development of delivery carriers for anti-fungal agents[2].

L-Pentaguluronic acid, a linear polysaccharide copolymer, consists predominantly of four units of L-guluronic acid (G).

L-Hexaguluronic acid, a linear polysaccharide copolymer, consists of six units of L-guluronic acid (G).

L-Diguluronic acid disodium, a linear polysaccharide copolymer consisting of two L-guluronic acid units, serves as a precursor for Alginate production. Classified as an unbranched polyanionic polysaccharide, this compound is explored as a delivery carrier for antifungal agents [1].

L-Tetraguluronic acid is a straight-chain polysaccharide copolymer consisting of four repeating units involved in the formation of the alginate.L-Tetraguluronic acid interacts with Glu543 in the non-catalytic domain and can help AlyRm1 to bind the substrate more efficiently and to improve the catalytic efficiency.

L-heptaguluronic acid, derived from seaweed, is a constituent of alginates, which are natural biopolymers.

L-octaguluronic acid, derived from seaweed, is a constituent of alginates [natural biopolymers].