dl glutamic acid

DL-Glutamic acid, the conjugate acid of Glutamic acid, serves as a crucial metabolite. In comparison to the α and β polymorphs of L-Glutamic acid's second phase, DL-Glutamic acid exhibits enhanced stability[1].

DL-Glutamic acid monohydrate is a DL mixture of glutamic acid, widely used in biochemical experiments and drug synthesis research.

2-(Methylamino)pentanedioic acid (N-Methyl-DL-glutamic acid) is an endogenous metabolite that inhibits Glutaminase, adds freshness to edible products, and can be used in tuberculosis research.

DL-Glutamic acid-d3 is a deuterated compound of DL-Glutamic acid. DL-Glutamic acid has a CAS number of 617-65-2. DL-Glutamic acid is the conjugate acid of Glutamic acid, which acts as a fundamental metabolite. Comparing with the second phase of polymorphs α and β L-Glutamic acid, DL-Glutamic acid presents better stability[1].

DL-Glutamic acid (Standard) is the standard substance of DL-Glutamic acid, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. DL-Glutamic acid, the conjugate acid of Glutamic acid, serves as a crucial metabolite. In comparison to the α and β polymorphs of L-Glutamic acid's second phase, DL-Glutamic acid exhibits enhanced stability.

Dl-Glutamic Acid-D3 (Standard) is a reference standard of Dl-Glutamic Acid-D3 intended for quantitative analysis, quality control, and related biochemical research applications. DL-Glutamic acid-d3 is a deuterated compound of DL-Glutamic acid. DL-Glutamic acid has a CAS number of 617-65-2. DL-Glutamic acid is the conjugate acid of Glutamic acid, which acts as a fundamental metabolite. Comparing with the second phase of polymorphs α and β L-Glutamic acid, DL-Glutamic acid presents better stability[1].

DL-Theanine (DL-Glutamic acid γ-ethyl amide) is a natural compound known for its calming effects on the brain.

DL-Glutamine (2-amino-4-carbamoylbutanoic acid), a non-essential amino acid, exists abundantly throughout the body and is participated in many metabolic processes. It is synthesized from glutamic acid and ammonia, and is the main carrier of nitrogen in the body and is an important energy source for many cells.

Dimethyl DL-glutamate is a cell-permeant glutamic acid derivative that enhances insulin release in response to glucose in isolated islets and in animal models of diabetes.

DL-4-Hydroxy-2-ketoglutarate (DL-4KG) is a gamma-keto acid as well as a structural analogue of glutamic acid that functions as a biochemical substrate for enzymes such as 4-hydroxy-2-oxoglutarate aldolase (HOGA1) and glutamic-oxaloacetic transaminase (GOT),DL-4-Hydroxy-2-ketoglutarate also serves as a lysine analogue used in mechanistic studies of enzyme inhibition and metabolic pathways.