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Cat. No. | Product Name | Target | Signaling Pathways |
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T34686 |
Sonoflora 1
SF 1,SF-1,Sonoflora1,Sonoflora-1,SF1 |
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Sonoflora 1, also known as SF1, a PDT photosensitivizer. Chemically, SF1 is an analog of chlorophyll in that its macrocycle backbone is porphyrin-based and the center of the porphyrin ring consists of a metal ion. Preclinical studies showed that SF1 had v | |||
T12075 |
ML-180
SR1848 |
Others | Others |
ML-180 (SR1848) 是孤儿核受体肝受体同源物 1 (LRH-1;NR5A2) 的反向激动剂(IC50:3.7 µM)。它不抑制类固醇生成因子 1 (SF-1;NR5A1; IC50>10 µM)。 它具有潜在的抗依赖 LRH-1 癌症作用。 | |||
T7687 |
AC 45594
4-庚氧基苯酚,4-Heptyloxyphenol |
Others | Others |
AC 45594 (4-Heptyloxyphenol) 是类固醇生成因子 1 (SF-1) 的激动剂 ( IC50 : 50-100 nM)。 | |||
T64363 |
(Iso)-RJW100
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Others | Others |
(Iso)-RJW100 是一种有效的肝受体同源物 1 (LRH-1,NR5A2) 和类固醇生成因子-1 (SF-1,NR5A1) 激动剂,pEC50 分别为 6.4 和 7.2。 | |||
T38680 |
RJW100
|
Others | Others |
RJW100是一种化合物,作为肝受体同源体1(LRH-1, NR5A2)和类固醇生成因子-1(SF-1, NR5A1)的强效激动剂,分别展现出6.6和7.5的pEC50值。此外,RJW100能强力激活miR-200c(miRNA-200c, microRNA-200c)启动子。 | |||
T23354 |
SID 7969543
|
Others | Others |
Selective steroidogenic factor-1 (SF-1, NR5A1) inhibitor | |||
T62757 |
SID7970631
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SID7970631 是一种异喹啉酮类似物,是一种选择性的、有效的亚微摩尔 SF-1 抑制剂,其 IC50 值为 260 nM。SID7970631 能够用于研究癌症。 | |||
T75865 |
Neuropeptide SF(mouse,rat) TFA
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Neuropeptide SF (mouse,rat) TFA 作为一种高效的 neuropeptide FF receptor 激动剂,对 NPFF1 和 NPFF2 的Ki值分别达到 48.4 nM 和 12.1 nM。该化合物还能够提升异表达的酸感离子通道 3 (ASIC3) 的持续电流幅值。 | |||
T79411 |
hCAXII-IN-7
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Carbonic Anhydrase | Metabolism |
hCAXII-IN-7 (compound 6e)为hCA XII抑制剂,且具备脑屏障通透性。此化合物能够诱导786-0、SF-539和HS 578 T细胞系的凋亡。 | |||
T73231 |
RR-RJW100
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RR-RJW100是RJW100的对映异构体之一,后者为核受体肝受体同源物1(LRH-1)和类固醇生成因子1(SF-1)的激动剂。相比于另一对映异构体SS-RJW100,RR-RJW100展现出更强的LRH-1激活能力。此化合物在调节代谢稳态方面具有潜力,因而在糖尿病、肝病以及炎症性肠病等疾病的研究中有所应用。 | |||
T61723 | SS-RJW100 | ||
SS-RJW100 is an enantiomer of RJW100, known as a racemic agonist that targets two nuclear receptors: liver receptor homolog 1 (LRH-1) and steroidogenic factor 1 (SF-1). In vitro experiments reveal that SS-RJW100 promotes the recruitment of coregulator protein fragments and enhances the interaction with the transcriptional intermediary factor 2 (Tif2) coactivator specifically for LRH-1. Additionally, SS-RJW100 disrupts the allosteric activation networks of LRH-1, displaying suboptimal thermal sta... | |||
T35438 |
(5E)-7-Oxozeaenol
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(5E)-7-Oxozeaenol is a resorcylic acid lactone that has been found in the fungus MSX 63935 and has enzyme inhibitory and anticancer activities.1,2 It inhibits TGF-β-activated kinase 1 (TAK-1; IC50 = 1.3 μM).1 (5E)-7-Oxozeaenol inhibits proliferation of MCF-7, H460, SF-268, HT-29, and MDA-MB-435 human cancer cells with IC50 values of 4.9, 1.2, 5.6, 4.4, and 5.5 μM, respectively.2 |1. Fakhouri, L., El-Elimat, T., Hurst, D.P., et al. Isolation, semisynthesis, covalent docking and transforming growt... | |||
T79706 |
TRK-IN-24
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Trk receptor | Tyrosine Kinase/Adaptors |
TRK-IN-24(compound 10g)是一种针对Trk Receptor的抑制剂,它对TRKA、TRKC、TRKAG595R、TRKAG667C和TRKAF589L的抑制作用的IC50值分别达到5.21、4.51、6.77、1.42和6.13 nM。该化合物在BaF3-CD74-NTRK1G595R和BaF3-CD74-NTRK1G667C异种移植模型中显示出明显的抗肿瘤活性。此外,TRK-IN-24 能有效抑制携带SF、GK、xDFG等单点突变的Ba/F3细胞增殖,其IC50范围为1.43至47.56 nM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T38069 |
Aquastatin A
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Aquastatin A is a fungal metabolite originally isolated fromF. aquaeductuumthat has diverse biological activities.1It is active againstS. aureus(MIC = 32 μg/ml) and inhibits enoyl-acyl carrier protein reductase (Fabl; IC50= 3.2 μM) andS. aureusfatty acid synthesis (IC50= 3.5 μM).2Aquastatin A also inhibits the Na+/K+-ATPase and H+/K+-ATPase (IC50s = 7.1 and 6.2 μM, respectively), as well as protein tyrosine phosphatase 1B (PTP1B; IC50= 0.19 μM).1,3 1.Hamano, K., Kinoshita-Okami, M., Minagawa, K.... |