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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T38684 |
AKR1C3-IN-4
AKR1C3-IN-4 |
NADPH | Metabolism |
AKR1C3-IN-4 是醛酮还原酶 1C3 (AKR1C3) 选择性抑制剂,IC50为 0.56 μM。它在去势抵抗性前列腺癌中有研究的价值。 | |||
T61790 | AKR1C3-IN-6 | ||
AKR1C3-IN-6 (Compound 1) is a powerful and specific inhibitor of AKR1C3, with IC50 values of 0.31 μM and 73.23 μM against AKR1C3 and AKR1C2, respectively. It demonstrates significant antitumor activity [1]. | |||
T61485 | S07-2010 | ||
S07-2010 is a potent pan-AKR1C inhibitor, effectively inhibiting AKR1C3, AKR1C4, AKR1C1, and AKR1C2 with IC50 values of 0.19, 0.36, 0.47, and 0.73 μM, respectively. This compound induces apoptosis in A549/DDP cells and enhances the cytotoxicity of chemotherapeutic agents in drug-resistant cells, making it a viable option for combating drug resistance. Furthermore, S07-2010 significantly inhibits the proliferation of drug-resistant cells [1]. | |||
T14151 |
AKR1C1-IN-1
|
NADPH | Metabolism |
AKR1C1-IN-1 是高选择性 AKR1C1抑制剂(Ki:4 nM)。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2899 |
Liquiritin
Liquiritigenin-4'-O-glucoside,Liquiritoside,甘草苷 |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
Liquiritin (Liquiritigenin-4'-O-glucoside) 是一种从甘草中分离出的类黄酮,是一种竞争性的 AKR1C1 抑制剂,对 AKR1C1,AKR1C2 和 AKR1C3 的 IC50分别为 0.62 μM,0.61 μM 和 3.72 μM,在体内有效抑制 AKR1C1 介导的孕酮代谢。它是一种抗氧化剂,具有神经保护、抗癌、抗炎的活性。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-03497 |
AKR1C2 Protein, Human, Recombinant (His)
AKR1C2,HBAB,SRXY8,AKR1C-pseudo,al... |
Human | E. coli |
AKR1C2 is a member of the aldo/keto reductase superfamily, which consists of more than 4 known enzymes and proteins. These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols using NADH and/or NADPH as cofactors. The enzymes display overlapping but distinct substrate specificity. This enzyme binds bile acid with high affinity, and shows minimal 3-alpha-hydroxysteroid dehydrogenase activity. AKR1C2 gene shares high sequence identity with three other gene ... | |||
TMPJ-00207 |
AKR1C2 Protein, Human, Recombinant
3-Alpha-HSD3,Chlordecone Reductase Homolog HAKRD,2-... |
Human | E. coli |
Aldo-Keto Reductase Family 1 Member C2 (AKR1C2) plays a role in concert with the 5-α/5-β-Steroid Reductases to convert Steroid hormones into the 3-α/5-α and 3-α/5-β-Tetrahydrosteroids. AKR1C2 catalyzes the inactivation of the most potent androgen 5-α-Dihydrotestosterone (5-α-DHT) to 5-α-Androstane-3-α, 17-β-diol (3-α-diol). |