GOT1 inhibitor-1 |
| カタログ番号GC60884 |
トリプタミンベースの誘導体である GOT1 インヒビター-1 (化合物 2c) は、グルタミン酸オキサロ酢酸トランスアミナーゼ 1 (GOT1) の新規で強力な非共有結合阻害剤として作用し、IC50 は 8.2 uM です。 GOT1 阻害剤-1 は、膵管腺癌 (PDAC) の研究に使用できます。
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 732973-87-4
Sample solution is provided at 25 µL, 10mM.
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GOT1 inhibitor-1 (compound 2c), a tryptamine-based derivative, acts as a novel, potent and non-covalent inhibitor of glutamate oxaloacetate transaminase 1 (GOT1) with IC50 of 8.2 uM. GOT1 inhibitor-1 can be used for the research of pancreatic ductal adenocarcinoma (PDAC)[1].
PDAC tumors are dependent upon a metabolic pathway involving aspartate aminotransferase 1 (glutamate-oxaloacetate transaminase 1 (GOT1)), for the maintenance of redox homeostasis and sustained proliferation. Small molecule inhibitors targeting this metabolic pathway may provide a novel way for cancer research.In the MDH coupled GOT1 enzymatic assay, GOT1 inhibitor-1 shows an inhibitory effect on GOT1 activity with an IC50 value of 8.2 uM[1].
[1]. Justin Anglin, et al. Discovery and optimization of aspartate aminotransferase 1 inhibitors to target redox balance in pancreatic ductal adenocarcinoma. Bioorg Med Chem Lett. 2018 Sep 1;28(16):2675-2678
Average Rating: 5 (Based on Reviews and 37 reference(s) in Google Scholar.)
GLPBIO products are for RESEARCH USE ONLY. Please make sure your review or question is research based.
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