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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1015 |
NFAT Inhibitor
VIVIT peptide |
Others | Others |
NFAT Inhibitor (VIVIT peptide) 是NFAT 的细胞渗透性肽抑制剂,能够选择性抑制钙调磷酸酶介导的NFAT 脱磷酸作用。 | |||
T50103 |
NFAT Inhibitor-2
|
Others | Others |
NFAT Inhibitor-2 是一种化学合成中的砌块。 | |||
T12218 |
NFAT Transcription Factor Regulator-1
|
IL Receptor | Immunology/Inflammation |
NFAT Transcription Factor Regulator-1 是 IL-2 合成 的抑制剂,IC50 值为182 nM。 | |||
TP1978L |
NFAT inhibitor, Cell Permeable aceate
|
Others | Others |
NFAT inhibitor, Cell Permeable aceate 是一种细胞可渗透的活化 T 细胞核因子 (NFAT) 抑制剂。 可用于足细胞和糖尿病肾病的研究。 | |||
TP1978 |
11R-VIVIT
NFAT inhibitor, Cell Permeable |
||
NFAT inhibitor. Inhibits LPS or LPS plus IFN-γ-induced IL-12 p40, IL-12 p70, IL-23 and TNF secretion from bone marrow-derived macrophages (BMDMs). Also attenuates NO production and Nos2 mRNA expression in LPS-stimulated BMDMs. Improves symptoms in a mouse | |||
T125647 |
Antibiotic NFAT 133
|
||
Antibiotic NFAT 133 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T125647,CAS号为 165133-85-7。 | |||
T27612 |
INI-43
INI 43,INI43 |
Others | Others |
INI-43 是Nuclear Import-43 的抑制剂,通过靶向 Kpnβ1 对各种宫颈和食管癌细胞系显示出显着的细胞毒性作用,并干扰 Kpnβ1 和已知的 Kpnβ1 cargo 蛋白、NFAT、NFκB、AP-1和NFY 的核定位。 | |||
T21807 |
INCA-6
Triptycene-1,4-quinone |
Others | Others |
INCA-6 (Triptycene-1,4-quinone) 是细胞渗透性的 NFAT 抑制剂。INCA-6 通过特异性阻断 NFAT 底物靶向钙调神经磷酸酶位点,有效抑制calcineurin (CN)-NFAT 信号传导。 | |||
T68594 | NFAT:AP-1 inhibitor-10 | ||
NFAT:AP-1 inhibitor-10 is a novel inhibitor of the NFAT:AP-1:DNA interaction on the ARRE-2 element, binding to DNA in a sequence-selective manner and inhibiting the transcription of the Il2 gene and several other cyclosporin A-sensitive cytokine genes important for the effector immune response. | |||
T61531 |
NFATc1-IN-1
|
RANKL/RANK | NF-κB |
NFATc1-IN-1 (also known as compound A04) is a highly effective inhibitor of osteoclast formation induced by RANKL, with an IC50 of 1.57 μM. It exerts its anti-osteoclastogenic effects by attenuating the RANKL-induced nuclear translocation of NFATc1. Due to its remarkable properties, NFATc1-IN-1 holds significant potential for advancing research related to osteoclastic diseases [1]. | |||
T23186 |
ProINDY
Pro-indy |
DYRK | Cell Cycle/Checkpoint; Tyrosine Kinase/Adaptors |
ProINDY(Pro-indy) 是一种有效的 DYRK 抑制剂,可激活激活 NFAT ,可用于研究唐氏综合征。 | |||
T35885 |
KRM-III
|
Others | Others |
KRM-III 是一种具有口服活性的 T 细胞抗原受体 (TCR) 抑制剂,具有抗炎活性,可有效抑制 TCR 和肉豆蔻酸乙酸酯/佛波霉素/离子霉素诱导的 NFAT 核因子活化和 T 细胞增殖,IC50 约为 5 μM。 | |||
T5339 |
YZ129
|
||
YZ129 是一种抗胶质母细胞瘤的HSP90-磷酸酶-NFAT 通路的抑制剂,直接与热休克蛋白 (HSP90)结合,对NFAT 核易位的IC50值为820 nM。YZ129 在 G2/M 期诱导GBM 细胞周期阻滞,促进细胞凋亡,抑制肿瘤细胞增值和迁移。 | |||
T69754 |
BTP1
|
||
BTP1 is an inhibitor of NFAT activation and T-cell cytokine production. BTP1 potently inhibits SOCE in many cells with considerable selectivity over voltage-gated Ca2+ entry. | |||
T35892 |
Q134R
Q134R |
||
Q134R, a neuroprotective hydroxyquinoline derivative that suppresses nuclear factor of activated T cell (NFAT) signaling. Q134R can across blood-brain barrier. Q134R has the potential for Alzheimer’s disease (AD) and aging-related disorders research[1]. Q134R (1-10 μM) suppresses NFAT signaling, without inhibiting calcineurin activity. Q134R partially inhibits NFAT activity in primary rat astrocytes, but does not prevent calcineurin-mediated dephosphorylation of a non-NFAT target, either in vivo... | |||
T71295 |
SOR-C13
|
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SOR-C13 is an inhibitor of transient receptor potential cation channel vanilloid family member 6 (TRPV6, CaT1 or CATL) with potential antineoplastic activity. TRPV6 calcium channel inhibitor SOR-C13 binds to TRPV6 and prevents the influx of calcium ions into TRPV6-expressing tumor cells. This inhibits the activation of nuclear factor of activated T-cell (NFAT) transcription complex which may result in an inhibition of calcium-dependent cancer cell proliferation and an induction of apoptosis in t... | |||
TP1978L1 |
11R-VIVIT TFA (592517-80-1 Free base)
|
||
11R-VIVIT TFA (592517-80-1 Free base) 是一种 NFAT 抑制剂。 11R-VIVIT TFA 抑制 LPS 或 LPS 加 IFN-γ 诱导的骨髓源性巨噬细胞 (BMDM) 分泌 IL-12 p40、IL-12 p70、IL-23 和 TNF。 11R-VIVIT TFA 减弱 LPS 刺激的 BMDM 中 NO 的产生和 Nos2 mRNA 的表达。 11R-VIVIT TFA 改善结肠炎小鼠模型的症状。 11R-VIVIT TFA 表现出免疫抑制作用并提高小鼠移植物的存活率。 11R-VIVIT TFA 具有细胞渗透性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TL0013 |
Heraclenin
独活内酯 |
Anti-infection; Immunology/Inflammation related | Immunology/Inflammation; Microbiology/Virology |
Heraclenin 是一种天然呋喃香豆素。它浓度依赖性的靶向激活的 T 细胞核因子 (NFAT) ,抑制人原代 T 细胞中 T 细胞受体介导的增殖。 | |||
T2S0843 |
Negletein
黄芩素-7-甲醚,7-O-Methylbaicalein,Baicalein-7-methylether |
IL Receptor; TNF; NOS; Interleukin | Apoptosis; Immunology/Inflammation |
Negletein (7-O-Methylbaicalein) 一种神经保护剂,可增强神经生长因子的作用并诱导 PC12 细胞中的神经突生长。它通过抑制TNF-α和IL-1β表现出抗炎活性,其 IC50值分别为 16.4 和 10.8 μM。它还具有抗菌、抗缺氧和抗阿尔茨海默病活性。 | |||
T38285 |
C24:1 3'-sulfo Galactosylceramide (d18:1/24:1(15Z))
C24:1 3'-sulfo Galactosylceramide (d18:1/24:1(15Z)) |
Others | Others |
C24:1 3'-sulfo Galactosylceramide (d18:1/24:1(15Z))是成熟髓鞘中主要的硫酸盐类化合物。C24:1 3'-sulfo Galactosylceramide (d18:1/24:1(15Z)) 在大鼠小脑中发现活跃的髓发生鞘化反应时积累率高于C24 3'-sulfo 半乳糖甘油酰胺。C24:1 3'-sulfo Galactosylceramide (d18:1/24:1(15Z))与C 型凝集素和免疫球蛋白样受体相互作用使对LMIR5的亲和力高。C24:1 3'-sulfo Galactosylceramide (d18:1/24:1(15Z))诱导嗜碱细胞产生MCP-1,可通过增加LMIR5激活NFAT,但不能诱导肥大细胞 。C24:1 3'-sulfo Galactosylceramide (d18:1/24:1(15Z))在体外与CD1d 结合,并增加游离小鼠脾细胞的增殖。 | |||
TN2249 | (+)-Syringaresinol | Sirtuin; Antifection | Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology |
(+)-Syringaresinol shows antioxidant potential, it exhibits cytoprotective activity in cultured MCF-7 cells stressed by H2O2. |