1. Signaling Pathways
  2. Amino Acid Decarboxylase

Amino Acid Decarboxylase (氨基酸脱羧酶)

Amino Acid Decarboxylase

氨基酸脱羧酶 (Amino acid decarboxylase) 是一类催化特定氨基酸脱去羧基生成生物活性胺的酶,广泛参与多种生理过程,尤其是在神经递质和多胺的合成中。芳香族 L-氨基酸脱羧酶 (AADC)、组氨酸脱羧酶 (HDC) 和 S-腺苷甲硫氨酸脱羧酶 (SAMDC) 都属于氨基酸脱羧酶家族,各自在不同的代谢途径中发挥重要作用,调节细胞的功能。
AADC 主要负责将芳香族氨基酸前体 l-DOPA 和 5-羟色氨酸转化为神经递质多巴胺和血清素。这些神经递质对于大脑的正常功能至关重要,AADC 缺乏症会导致严重的神经系统疾病,包括运动障碍、自主神经功能障碍和行为异常。
HDC 则催化组氨酸转化为组胺。组胺是过敏反应和炎症反应中的重要介质,HDC 的缺乏与免疫功能紊乱和过敏症状密切相关。例如,在一些慢性炎症和过敏反应中,HDC 的上调在调节组胺水平和免疫细胞功能中发挥着重要作用。
SAMDC 是多胺合成途径中的关键酶,负责将 S-腺苷甲硫氨酸转化为脱羧后的 S-腺苷甲硫氨酸,这一产物是精胺和亚精胺合成的前体。这些多胺在细胞的生长、分化和增殖中起着重要作用。SAMDC 的活性与细胞的多胺浓度密切相关,SAMDC 抑制剂被广泛研究用于抗癌和抗寄生虫研究。
针对氨基酸脱羧酶的抑制剂在癌症和寄生虫疾病的研究领域具有应用潜力。例如,因为多胺合成途径在多种肿瘤中被上调,SAMDC 抑制剂可用于癌症研究中,而 SAMDC 抑制剂是抗寄生虫研究的重要工具[1][2][3][4]

Amino acid decarboxylases are a class of enzymes that catalyze the removal of the carboxyl group from specific amino acids to produce biologically active amines. These enzymes are widely involved in various physiological processes, particularly in the synthesis of neurotransmitters and polyamines. Aromatic L-amino acid decarboxylase (AADC), histidine decarboxylase (HDC), and S-adenosylmethionine decarboxylase (SAMDC) all belong to the amino acid decarboxylase family, each playing an important role in different metabolic pathways to regulate cellular functions.
AADC is primarily responsible for converting aromatic amino acid precursors l-DOPA and 5-hydroxytryptophan into the neurotransmitters dopamine and serotonin. These neurotransmitters are crucial for the normal functioning of the brain, and AADC deficiency leads to severe neurological disorders, including motor dysfunction, autonomic nervous system dysfunction, and behavioral abnormalities.
HDC catalyzes the conversion of histidine to histamine. Histamine is an important mediator in allergic and inflammatory reactions, and a deficiency in HDC is closely related to immune dysfunction and allergic symptoms. For example, in some chronic inflammation and allergic reactions, the upregulation of HDC plays a crucial role in regulating histamine levels and immune cell function.
SAMDC is a key enzyme in the polyamine biosynthetic pathway, responsible for converting S-adenosylmethionine into decarboxylated S-adenosylmethionine, a precursor for the synthesis of spermidine and spermine. These polyamines play vital roles in cell growth, differentiation, and proliferation. The activity of SAMDC is closely related to the cellular concentration of polyamines, and SAMDC inhibitors are widely studied for anticancer and antiparasitic treatments.
Inhibitors targeting amino acid decarboxylases have potential applications in cancer and parasitic disease research. For example, since the polyamine biosynthetic pathway is upregulated in many tumors, SAMDC inhibitors can be used in cancer research, and SAMDC inhibitors are also important tools in antiparasitic research[1][2][3][4].

Amino Acid Decarboxylase 相关产品 (7):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-W016349
    Chelidamic acid

    白屈氨酸

    Inhibitor 99.93%
    Chelidamic acid 是一种含有吡喃骨架的杂环有机酸,与金属离子有良好的配位能力。Chelidamic acid 也是最有效的谷氨酸脱羧酶 (glutamate decarboxylase) 抑制剂之一,其 Ki 值为 33 μM。
    Chelidamic acid
  • HY-103391
    Qc1 Inhibitor 98.42%
    Qc1 是一种苏氨酸脱氢酶 (TDH) 抑制剂,Qc1 可以用来研究代谢性疾病。
    Qc1
  • HY-P990419
    Anti-GAD65 Antibody
    Anti-GAD65 Antibody 是 CHO 表达的人源抗体,靶向 GAD65。Anti-GAD65 Antibody 带有 huIgG1 型重链和 huλ 型轻链,其预测的分子量 (MW) 为 146.48 kDa。Anti-GAD65 Antibody 的同型对照可参考 Human IgG1 kappa, Isotype Control (HY-P99001)。
    Anti-GAD65 Antibody
  • HY-P5396
    GAD65 (524-543)
    GAD65 (524-543) 是一种有生物活性的肽。(这是谷氨酸脱羧酶 65 (GAD65) 的氨基酸 524 至 543 片段。它是该胰岛抗原的首批片段之一,可在自发性自身免疫性糖尿病的非肥胖糖尿病 (NOD) 小鼠模型中诱导增殖性 T 细胞反应。该肽是对自发产生的糖尿病 T 细胞克隆 BDC2.5 的特异性刺激,可能亲和力较低。 p524-543 免疫增加了 NOD 小鼠对 BDC2.5 T 细胞过继转移诱导的 1 型糖尿病的易感性。)
    GAD65 (524-543)
  • HY-123139
    Flutroline
    Flutroline (CP-36584) 是一种四氢-7-咔啉化合物,是一种口服有效的抗精神病化合物。
    Flutroline
  • HY-115822
    α-Fluoromethylhistidine dihydrochloride Inhibitor
    α-Fluoromethylhistidine dihydrochloride 是组氨酸脱羧酶 (HDC) 和谷胱甘肽 S-转移酶的强效不可逆抑制剂,在研究组氨酸代谢和化合物代谢过程方面具有巨大潜力。α-Fluoromethylhistidine dihydrochloride 提供了一种抑制参与这些代谢途径的酶的有效方法。α-Fluoromethylhistidine dihydrochloride 通过揭示可能影响生理化合物代谢和消除机制的脱靶效应,对化合物开发具有重要意义。
    α-Fluoromethylhistidine dihydrochloride
  • HY-U00065
    Tritoqualine

    酞茂异喹

    Inhibitor
    Tritoqualine 是一种组氨酸脱羧酶抑制剂,抑制组氨酸释放。
    Tritoqualine