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Cat. No. | Product Name | Target | Signaling Pathways |
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T13336 |
VTP50469
|
Apoptosis; Epigenetic Reader Domain; Histone Methyltransferase | Apoptosis; Chromatin/Epigenetic |
VTP50469 是一种高选择性和口服活性的Menin-MLL 相互作用抑制剂,具有有效的抗白血病活性,Ki 为 104 pM。 | |||
T24584 |
P505-15 Acetate
PRT 062607 Acetate,P505 15 Acetate,PRT-062607 Acetate,PRT062607 Acetate,P50515 Acetate |
Tyrosinase | Proteases/Proteasome |
P505-15 Acetate 是脾脏酪氨酸激酶的选择性抑制剂,通过抑制白细胞免疫功能和炎症起作用,导致关节炎评分降低和组织学损伤减轻。 | |||
T80132 |
CBP501 Affinity Peptide
|
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CBP501 Affinity Peptide为Chk激酶抑制剂,具有消除DNA损伤剂诱导的G2停滞作用,主要应用于癌症研究领域。 | |||
TP2164 |
TP508 TFA (121341-81-9 free base)
TP508 TFA |
Others | Others |
TP508 TFA is a nonproteolytic thrombin peptide. TP508 TFA activates endothelial NO synthase (eNOS) and stimulates the production of NO in human endothelial cells. It activates endothelial cells and stem cells to revascularize and regenerates tissues. | |||
TP1853 |
TP508
|
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TP508 is a 23 amino acid synthetic peptide representing residues 508-530 of human prothrombin which is identified as a potential receptor-binding domain based on competition for high-affinity thrombin binding to fibroblasts.TP508 (Chrysalin) is an investi | |||
T62657 |
SHP504
|
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SHP504 是一种 SHP2 磷酸酶的抑制剂,能够作用于 SHP21–525 (IC50: 21 μM)。 | |||
T69846 |
VTP50469 mesylate
|
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VTP-50469 is a novel, potent, selective, orally-available MeninMLL1 inhibitor, being effectively against MLL-rearranged and NPM1c+ leukemia, selectively killing cell lines with MLLrearrangements and NPM1c+ mutations. | |||
T24736 |
RP5063 Hydrochloride
RP-5063 HCl,RP 5063 HCl,RP 5063 Hydrochloride,RP-5063 Hydrochloride,RP5063 HCl |
||
RP5063 Hydrochloride is a modulator of multimodal serotonin receptors. | |||
T13336L |
VTP50469 fumarate
|
Others | Others |
VTP50469 fumarate is a highly selective and orally active inhibitor of Menin-MLL interaction (Ki: 104 pM), and has potently anti-leukemia activity. | |||
T75763 |
TP508 TFA
|
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TP508 TFA为含23个氨基酸的非蛋白质水解凝血酶肽, 属凝血酶分子受体结合结构域部分。该化合物能激活内皮NO synthase(eNOS),促进人内皮细胞内NO生成,进而通过激活内皮细胞及干细胞,促进血管及组织再生。 | |||
T69091 |
CBP501
|
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CBP501 is a peptide with G2 checkpoint-abrogating activity. G2 checkpoint inhibitor CBP501 inhibits multiple serine/threonine kinases, including MAPKAP-K2, C-Tak1, and CHK1, that phosphorylate serine 216 of the dual-specific phosphatase Cdc25C (cell division checkpoint 25 C); disruption of Cdc25C activity results in the inhibition of Cdc25C dephosphorylation of the mitotic cyclin-dependent kinase complex Cdc2/cyclin B, preventing entry into the mitotic phase of the cell cycle. | |||
T72785 |
PRMT5:MEP50 PPI
|
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PRMT5:MEP50 PPI是一款新型的抑制剂,专门针对PRMT5:MEP50蛋白-蛋白相互作用,展现了抗肿瘤活性,并对肺癌及前列腺癌细胞具有显著的抗增殖效果。 | |||
T78846 | EP12 | Apoptosis | Apoptosis |
EP12是一种c-Myc抑制剂及c-MycG4稳定剂,能够诱导多发性骨髓瘤细胞的细胞凋亡(apoptosis)及DNA损伤,并通过干扰NF-κB信号通路破坏P65/P50的核转位,从而抑制多发性骨髓瘤的生长。 | |||
T38153 |
NF-κB Inhibitor (trifluoroacetate salt)
|
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NF-κB inhibitor is a synthetic peptide corresponding to the nuclear localization sequence of NF-κB p105 subunit (also known as p50) appended to a hydrophobic sequence to facilitate import into living cells.1It blocks the nuclear import of p105 in cells treated with activators of NF-κB signaling, including LPS and TNF-α.1In this way, NF-κB inhibitor blocks gene expression that is regulated by NF-κB.2,3This peptide is commonly used to evaluate the role of NF-κB signaling in cellular responses.4,5 | |||
T37559 |
NF-κB Control
|
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NF-κB inhibitor is a synthetic peptide corresponding to the nuclear localization sequence (NLS) of NF-κB p105 subunit (also known as p50) appended to a hydrophobic sequence to facilitate import into living cells. It blocks the nuclear import of p105 in cells treated with activators of NF-κB signaling, including LPS and TNF-α. NF-κB control is a peptide that is identical in sequence to NF-κB inhibitor, except two essential, basic residues of the p105 NLS are substituted with non-basic amino acids... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TWS1977 |
Kamebakaurin
尾叶香茶菜丙素,Kamebakaurine |
NF-κB | NF-κB |
Kamebakaurin (Kamebakaurine) 是一种提取自Isodon japonicus 中的天然产物,是一种NF-κB 的抑制剂,能够抑制 p50 的 DNA 结合活性。 | |||
T3012 |
Mangiferin
Alpizarin,Chinomin,芒果,Hedysarid |
Apoptosis; Others; NF-κB; Nrf2 | Apoptosis; Immunology/Inflammation; NF-κB; Others |
Mangiferin (Hedysarid) 是一种Nrf2激活剂。它抑制NF-κB 亚基p65和p50的核移位,具有抗氧化、抗糖尿病、抗高尿酸血症、抗病毒、抗癌和抗炎活性。 | |||
TN3922 |
Effusanin E
|
PARP; NF-κB; Caspase; COX; Antifection | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome |
Effusanin E shows antibacterial and anti-cancer activities, it significantly inhibits cell proliferation and induces apoptosis in NPC cells by suppressing p50/p65 proteins to down-regulate COX-2 expression . | |||
TN4635 | Neoechinulin A | NADPH-oxidase; Beta Amyloid; ASK; IκB/IKK; p38 MAPK; TNF; NOS; NF-κB; COX; Prostaglandin Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; MAPK; Neuroscience; NF-κB |
Neoechinulin A has anti-inflammatory effect against LPS-stimulated RAW264.7 macrophages through inhibition of the NF-κB and p38 MAPK pathways, it may block the phosphorylation of mitogen-activated protein kinase (MAPK) molecule p38, apoptosis signal-regu |