- Signaling Pathways
- Neuronal Signaling
- Amino Acid Decarboxylase
Amino Acid Decarboxylase
Amino Acid Decarboxylase
- [1]. Han SW, et al. Aromatic L-amino acid decarboxylases: mechanistic features and microbial applications. Appl Microbiol Biotechnol. 2022 Jun;106(12):4445-4458. [Content Brief]
- [2]. Aromatic L-Amino Acid Decarboxylase - an overview.
- [3]. Hirasawa N. Expression of histidine decarboxylase and its roles in inflammation[J]. International Journal of Molecular Sciences, 2019, 20(2): 376.
- [4]. Bale S, et al. Structural biology of S-adenosylmethionine decarboxylase. Amino Acids. 2010 Feb;38(2):451-60. [Content Brief]
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Amino Acid Decarboxylase Related Products (16)
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- (Z)-Aconitic acid
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DL-Allylglycine
0 ImagesSynonyms: 2-Aminopent-4-enoic acidDL-Allylglycine (2-Aminopent-4-enoic acid) is a glutamate decarboxylase (GAD) inhibitor. DL-Allylglycine significantly increases mouse brain ornithine decarboxylase (ODC) activity and decreases S-adenosyl-L-methionine decarboxylase (SAM-DC) activity. DL-Allylglycine causes a marked decrease in brain GABA concentration. DL-Allylglycine has convulsant activity that can be used in studies to induce epileptic seizures. -
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L-Allylglycine
0 ImagesSynonyms: L-2-AllylglycineL-Allylglycine (L-2-Allylglycine) is an amino acid derivative. L-Allylglycine is an inhibitor for glutamate decarboxylase (GAD) that reduces the GABA biosynthesis in the brain. L-Allylglycine exhibits convulsant activity. -
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Chelidamic acid
0 ImagesChelidamic acid is a heterocyclic organic acid with a pyran skeleton. Chelidamic acid has good coordination ability with noble metal ions. Chelidamic acid is also one of the most potent inhibitors of glutamate decarboxylase, with a Ki of 33 μM. -
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L-Allylglycine hydrochloride
0 ImagesSynonyms: L-2-Allylglycine hydrochlorideL-Allylglycine (L-2-Allylglycine) hydrochloride is an amino acid derivative. L-Allylglycine hydrochloride is an inhibitor for glutamate decarboxylase (GAD) that reduces the GABA biosynthesis in the brain. L-Allylglycine hydrochloride exhibits convulsant activity. -
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L-Phenylalanine decarboxylase, Streptococcus faecalis
0 ImagesCat. No.: HY-E70939L-Phenylalanine decarboxylase, Streptococcus faecalis (EC 4.1.1.53) belongs to the lyase family and is capable of cleaving carbon-carbon bonds. L-Phenylalanine decarboxylase, Streptococcus faecalis is involved in the metabolism of phenylalanine. This enzyme has one substrate, L-phenylalanine, and two products: phenylethylamine and CO2. -
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α-Fluoromethylhistidine dihydrochloride
0 Imagesα-Fluoromethylhistidine dihydrochloride is an orally active histidine decarboxylase inhibitor. α-Fluoromethylhistidine dihydrochloride depletes histamine in enterochromaffin-like (ECL) cells, reduces the number and volume density of secretory vesicles in ECL cells, and does not affect histamine storage in mast cells. α-Fluoromethylhistidine dihydrochloride abolishes Omeprazole (HY-B0113)-induced vacuolization of ECL cells and decreases gastrin-induced histamine efflux from ECL cells. α-Fluoromethylhistidine dihydrochloride does not alter the granular characteristics of ECL cells, omeprazole-induced hypertrophy of ECL cells, gastrin-induced pancreastatin-like immunoreactivity efflux, nor does it affect gastric acid secretion induced by histamine or vagal stimulation. α-Fluoromethylhistidine dihydrochloride inhibits basal and gastrin-stimulated gastric acid secretion, reduces acid output induced by gastrin+IBMX (HY-12318), but does not directly affect acid generation in isolated parietal cells. -
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Qc1
0 ImagesQc1 is a reversible and noncompetitive threonine dehydrogenase (TDH) inhibitor. Qc1 can be used for the research of Metabolic disease. -
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TES-991
0 ImagesTES-991 is a potent and selective human α Amino-β-carboxymuconate-ε-semialdehyde Decarboxylase (ACMSD) inhibitor, with an IC50 of 3 nM. -
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GAD65 (524-543) acetate
0 ImagesCat. No.: HY-P5396APurity: 98.08%GAD65 (524-543) acetate is a biological active peptide with amino acids 524 to 543 fragment of glutamic acid decarboxylase 65 (GAD65). GAD65 (524-543) acetate is one of the first fragments of the islet antigen to induce proliferative T cell responses in the non-obese diabetic (NOD) mouse model of spontaneous autoimmune diabetes. GAD65 (524-543) acetate is a specific, possibly low affinity, stimulus for the spontaneously arising diabetogenic T cell clone BDC2.5. Immunization with GAD65 (524-543) acetate increases the susceptibility of the NOD mice to type 1 diabetes induced by the adoptive transfer of BDC2.5 T cells. -
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α-FMH
0 ImagesCat. No.: HY-W1015419CAS No.: 73804-75-8Synonyms: α-Fluoromethylhistidineα-FMH (α-Fluoromethylhistidine) is an orally active histidine decarboxylase inhibitor. α-FMH depletes histamine in enterochromaffin-like (ECL) cells, reduces the number and volume density of secretory vesicles in ECL cells, and does not affect histamine storage in mast cells. α-FMH abolishes Omeprazole (HY-B0113)-induced vacuolization of ECL cells and decreases gastrin-induced histamine efflux from ECL cells. α-FMH does not alter the granular characteristics of ECL cells, omeprazole-induced hypertrophy of ECL cells, gastrin-induced pancreastatin-like immunoreactivity efflux, nor does it affect gastric acid secretion induced by histamine or vagal stimulation. α-FMH inhibits basal and gastrin-stimulated gastric acid secretion, reduces acid output induced by gastrin+IBMX (HY-12318), but does not directly affect acid generation in isolated parietal cells. -
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Flutroline
0 ImagesCat. No.: HY-123139CAS No.: 70801-02-4Synonyms: CP-36584Flutroline (CP-36584), a tetrahydro-7-carboline compound, is an orally active and potent anti-psychotic compound. -
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Tritoqualine
0 ImagesCat. No.: HY-U00065CAS No.: 14504-73-5Synonyms: Inhibostamin; HypostamineTritoqualine is a histidine decarboxylase inhibitor, that inhibits the release of histidine. -
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GAD65 (524-543)
0 ImagesCat. No.: HY-P5396CAS No.: 152468-44-5GAD65 (524-543) is a biological active peptide with amino acids 524 to 543 fragment of glutamic acid decarboxylase 65 (GAD65). GAD65 (524-543) is one of the first fragments of islet antigen to induce proliferative T cell responses in the non-obese diabetic (NOD) mouse model of spontaneous autoimmune diabetes. GAD65 (524-543) is a specific, possibly low affinity, stimulus for the spontaneously arising diabetogenic T cell clone BDC2.5. Immunization with GAD65 (524-543) increases the susceptibility of the NOD mice to type 1 diabetes induced by the adoptive transfer of BDC2.5 T cells. -
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Qc1 (Standard)
0 ImagesCat. No.: HY-103391RCAS No.: 403718-45-6 -
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Anti-GAD65 Antibody
0 ImagesCat. No.: HY-P990419Anti-GAD65 Antibody is a humanized antibody expressed in CHO cells that targets GAD65. The Anti-GAD65 Antibody has a huIgG1 heavy chain and a huλ light chain, with a predicted molecular weight (MW) of 146.48 kDa. The isotype control for Anti-GAD65 Antibody can refer to Human IgG1 kappa, Isotype Control (HY-P99001). -
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