1. Signaling Pathways
  2. Metabolic Enzyme/Protease
  3. Glutaminase

Glutaminase (谷氨酰胺酶)

Glutaminase is the initial enzyme in glutamine metabolism, which catalyzes the hydrolysis of glutamine to glutamate in cells. Glutaminase plays a key role in cancer cell metabolism, growth, and proliferation. In mammalian cells, there are two paralogous GLS genes, GLS1 (or GLS) and GLS2. GLS1 encodes two alternatively spliced isozymes: kidney glutaminase (KGA) and glutaminase C (GAC). GLS2 also encodes two isozymes: liver glutaminase (LGA) and glutaminase B.

GLS1 is ubiquitously expressed in various tissues, and its expression can be induced by the oncogene MYC. GLS1 is frequently activated and/or overexpressed in various types of cancer, including hepatocellular carcinoma (HCC). GLS1 has been reported to promote tumorigenesis in different types of cancer, including HCC, which is mainly attributable to its glutaminase activity and role in promoting glutamine metabolism. GLS has emerged as a critical enzyme in a number of cancer types. Elevated GLS2 enzymatic activity has also been correlated with tumor cell growth in vitro and in vivo. N-Myc activates GLS2 to promote conversion of glutamine to glutamate in MYCN-amplified neuroblastoma cells. Abrogation of GLS2 function profoundly inhibits glutaminolysis and dramatically decreases cell proliferation and survival in vitro and in vivo. However, there is controversy over the role of GLS2 as a tumor suppressor. Enzymatic activity independent of GLS2 is up-regulated via p53 or p63 and plays a role of tumor suppressor.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-P99512
    Zampilimab Inhibitor 98.81%
    Zampilimab (UCB-7858) 是一种转谷氨酰胺酶 2 (TG2) 单克隆抗体。Zampilimab 在肾移植中有潜在的应用。
    Zampilimab
  • HY-119377
    UPGL00004 Inhibitor ≥98.0%
    UPGL00004 是一种有效的谷氨酰胺酶 C (GAC) 抑制剂 (IC50=29 nM; Kd=27 nM)。UPGL00004 强烈抑制高度侵袭性三阴性乳腺癌细胞系的增殖。
    UPGL00004
  • HY-103671A
    IPN60090 dihydrochloride Inhibitor 99.68%
    IPN-60090 dihydrochloride 是一种具有口服活性和高选择性的谷氨酰胺酶 1 GLS1 的抑制剂 (IC50=31 nM),对 GLS-2 无活性。IPN-60090 dihydrochloride 在体内表现出优良的物理化学和药代动力学特性。IPN-60090 dihydrochloride 可用于实体肿瘤的研究,如肺癌和卵巢癌。
    IPN60090 dihydrochloride
  • HY-145933
    BJJF078 Inhibitor 99.34%
    BJJF078 是一种氨基哌啶衍生物。BJJF078 是一种有效的重组人和小鼠谷氨酰胺转氨酶 (TG2) 活性的抑制剂,IC50 值分别为 41 和 54 nM。BJJF078 也抑制密切相关的 TG1 酶,其IC50 为 0.16 μM。 BJJF078 可用于多发性硬化症 (MS) 研究。
    BJJF078
  • HY-160132
    TG-2-IN-4 Inhibitor 99.62%
    TG-2-IN-4 (compound 8) 是一种转谷氨酰胺酶 2 (TG2) 的抑制剂,IC50 值 <0.5 mM。TG-2-IN-4 可用于炎症性疾病的研究。
    TG-2-IN-4
  • HY-155102
    PROTAC TG2 degrader-2 Degrader 99.15%
    PROTAC TG2 degrader-2 (compound 7) 是靶向 Transglutaminase 2 (TG2) 具有选择性的竞争性降解剂, Kd 值 > 100 μM。PROTAC TG2 degrader-2 抑制卵巢癌细胞迁移,降低细胞内的 TG2 水平。PROTAC TG2 degrader-2 可用于卵巢癌研究。
    PROTAC TG2 degrader-2
  • HY-144666
    GLS-1-IN-1 Inhibitor 99.64%
    GLS-1-IN-1 (compound 1d) 是一种 GLS-1 抑制剂。GLS-1-IN-1 对 Hep G2、MCF 7 和 MCF 10A 细胞有抑制作用。
    GLS-1-IN-1
  • HY-W006187
    2-Amino-2-(p-tolyl)acetic acid Inhibitor
    2-Amino-2-(p-tolyl)acetic acid 可用于优化叠氮骨架,是 1,3,4- 噻二唑类化合物的中间体。1,3,4- 噻二唑类化合物具有出潜在的抗癌活性,并对谷氨酰胺酶有抑制作用。
    2-Amino-2-(p-tolyl)acetic acid
  • HY-151434
    GLS1 Inhibitor-6 Inhibitor
    GLS1 Inhibitor-6 (Compound 24y) 是一种具有口服活性的、强效和选择性的谷氨酰胺酶 1 (GLS1) 抑制剂 (IC50=68 nM),对 GLS2 显示出 220 倍的选择性。GLS1 Inhibitor-6 可诱导凋亡,并表现出良好的抗肿瘤活性和抗癌细胞增殖活性。
    GLS1 Inhibitor-6
  • HY-12248A
    Telaglenastat hydrochloride Inhibitor
    Telaglenastat (CB-839) hydrochloride 是一种首创的,选择性的,可逆性的,口服活性的谷氨酰胺酶 1 (GLS1) 抑制剂。Telaglenastat hydrochloride 抑制 GLS1 剪接变异体 KGAGAC,比 GLS2 具有更高的选择性。Telaglenastat hydrochloride 对小鼠类肾和脑中的内源性谷氨酰胺酶的 IC50 值分别为 23 nM 和 28 nM。Telaglenastat hydrochloride 还可诱导细胞自噬 (autophagy),并具有强大的抗肿瘤活性。
    Telaglenastat hydrochloride
  • HY-146616
    GLS1 Inhibitor-3 Inhibitor
    GLS1 Inhibitor-3 (compound C147) 是一种有效的 GLS1 抑制剂,IC50 为 27.98 nM。GLS1 Inhibitor-3 具有抗增殖活性。
    GLS1 Inhibitor-3
  • HY-162141
    MD102 Inhibitor
    MD102 是一种有效的 TG2 抑制剂,IC50 值为 0.35 μM。MD102 通过抑制 TG2 稳定 p53,诱导 p-AKT 和 p-mTOR 下游信号传导减少,从而导致肿瘤细胞凋亡。
    MD102
  • HY-147718
    α-Glucosidase-IN-5 Inhibitor
    α-Glucosidase-IN-5 (compound 8) 是一种有效的 α-葡萄糖苷酶 抑制剂,IC50 为 57.9 µM。α-Glucosidase-IN-5 具有研究糖尿病的潜力[ 1]
    α-Glucosidase-IN-5
  • HY-100446
    NTU281 Inhibitor
    NTU281 是一种有效的转谷氨酰胺酶-2 (transglutaminase-2) 抑制剂。NTU281 能降低糖尿病大鼠血清肌酐和蛋白尿的升高。NTU281 还能降低肾小球 I 型胶原积累、Hic-5 和α-SMA 表达,以及减少细胞凋亡 (apoptosis)。NTU281 可用于研究糖尿病引起的肾小球硬化。
    NTU281
  • HY-157254
    AA10 Inhibitor
    AA10 是一种有效且不可逆的转谷氨酰胺酶 2 (TG2) 抑制剂,可用于癌症的研究。
    AA10
  • HY-N2916
    Barbinervic acid Inhibitor
    Barbinervic acid 是一种谷氨酰胺酶 (glutaminase) 抑制剂,IC50 为 14 μM。Barbinervic acid 可用于神经退行性疾病的研究。
    Barbinervic acid
  • HY-102073
    TG53 Inhibitor
    TG53 是组织转谷氨酰胺酶 (TG2) 和纤连蛋白 (FN) 蛋白质-蛋白质相互作用的有效抑制剂。 TG53 抑制与整合素 β1 形成复合物,并在 SKOV3 细胞附着到 FN 期间抑制 FAKc-Src 的激活。 TG53 可用于卵巢癌研究。
    TG53
  • HY-157975
    LM11 Inhibitor
    LM11 是一种转谷氨酰胺酶 2 (TG2) 抑制剂,具有通过维持 TG2 处于细胞毒性构象状态来杀死胶质母细胞瘤细胞的活性。
    LM11
  • HY-148241
    A-446 Inhibitor
    A-446 是一种有效的谷氨酰胺酶 (glutaminase) 抑制剂,IC50 为 31 nM。
    A-446
  • HY-155138
    GLS1 Inhibitor-7 Inhibitor
    GLS1 Inhibitor-7 (compound 4d) 是 GLS1 抑制剂 (IC50=46.7 μM),具有潜在抗癌、抗衰老、抗肥胖特性。
    GLS1 Inhibitor-7
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