异喹啉
生物碱
效力
石蒜科生物碱
石蒜科
石蒜碱
化学
酶
IC50型
立体化学
生物化学
重组DNA
药理学
抑制性突触后电位
生物
体外
植物
神经科学
基因
作者
Daniela Hulcová,Kateřina Breiterová,Lucie Zemanová,Tomáš Siatka,Marcela Šafratová,Nina Benešová,Anna Hošťálková,Vladimı́r Wsól,Lucie Cahlíková
标识
DOI:10.1177/1934578x1701200226
摘要
Aldo-keto reductase 103 (AKRIC3) is an important human enzyme that participates in the reduction of steroids and prostaglandins, which leads to proliferative signaling. AKRIC3 is frequently upregulated in various cancers, and this enzyme has been suggested as a therapeutic target for the treatment of these pathological conditions. The fact that the isoquinoline alkaloid stylopine has been identified as a potent AKRIC3 inhibitor has prompted us to screen a library of diverse types of Amaryllidaceae alkaloids, which biogenetically are isoquinoline alkaloids, on a recombinant form of AKRIC3. From the tested compounds, only tazettine showed moderate AKRIC3 inhibitory potency with an IC5o value of 15.8 ? 1.2 pM. Tazettine is a common Amaryllidaceac alkaloid, which could be used as a model substance for the further development of either analogues or related compounds with better inhibition potency.
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