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Targets Recommended: NADPH

4

抑制剂 & 化合物

1

天然产物

2

重组蛋白

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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)。

化合物

AKR1C3-IN-4
Cat.No: T38684
Synonym: AKR1C3-IN-4
Target: NADPH
AKR1C3-IN-6
Cat.No: T61790
Synonym:
Target:
S07-2010
Cat.No: T61485
Synonym:
Target:
AKR1C1-IN-1
Cat.No: T14151
Synonym:
Target: NADPH
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,AKR1C2AKR1C3 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。

天然产物

Liquiritin
Cat.No: T2899
Synonym: Liquiritigenin-4'-O-glucoside,Liquiritoside,甘草苷
Target: Reactive Oxygen Species
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).

重组蛋白

AKR1C2 Protein, Human, Recombinant (His)
Cat.No: TMPY-03497
Species: Human
Expression System: E. coli
AKR1C2 Protein, Human, Recombinant
Cat.No: TMPJ-00207
Species: Human
Expression System: E. coli
TargetMol Loading
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