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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T41255 | Specific PXR antagonist 70 | Others | |
Specific PXR antagonist 70 is a selective pregnane X receptor (PXR) antagonist with an IC50 of 540 nM and Ki of 390 nM for human PCR and enhances the chemosensitivity of cancer cells. | |||
T36104 | Citrulline-specific Probe-Rhodamine | ||
Protein arginine deiminases (PADs) catalyze the posttranslational modification of arginine residues on proteins to form citrulline, which plays a large role in regulating gene expression. Abnormally high PAD activity has... | |||
T7347 | CU-CPT-8m | TLR8-specific antagonist | TLR |
CU-CPT-8m (TLR8-specific antagonist) is an toll-like receptor 8 (TLR8) antagonist (IC50 : 67 nM) | |||
T23486 | Ubiquitin specific protease 3 fragment | Others | |
The ubiquitin speci c protease 3 USP3 is a deubiquitinating enzyme for uH2A and uH2B. | |||
T36627 | Lysine-specific Demethylase Inhibitor (1C) (hydrochloride) | ||
Lysine-specific demethylase inhibitor (1C) (LSD inhibitor (1C)) is an inhibitor of LSD1, a repressive demethylase selective for histone H3 lysine 4 (H3K4).1,2LSD inhibitor (1C) inhibits LSD1 activity by 85.9% when used a... | |||
T7302 | CU-CPT9b | CU-CPT-9b,TLR8-specific antagonist 1 | TLR |
CU-CPT9b (TLR8-specific antagonist 1) is an antagonist of toll-like receptor 8 (TLR8; Kd = 21 nM). It inhibits activation of NF- B induced by the TLR8 agonist R-848 in TLR8-overexpressing HEK-Blue cells with an IC50 valu... | |||
T80552 | Prostate Specific Antigen Substrate | ||
Prostate Specific Antigen Substrate is a fluorescent substrate specific to prostate specific antigen (PSA) and facilitates the detection of PSA enzymatic activity [1]. | |||
T82387 | Fluorescent Substrate for Asp-Specific Proteases | ||
Fluorescent Substrate for Asp-Specific Proteases selectively cleaves the Asp-Val bond [1]. | |||
T82386 | Fluorescent Substrate for Glu-Specific Proteases | ||
Fluorescent Substrate for Glu-Specific Proteases is a chromogenic substrate specifically recognized by V8 protease [1]. | |||
T23351 | Shz 1 | Others | |
induces phenotypic differentiation | |||
T22795 | Gadolinium chloride | CaSR | |
Gadolinium chloride is a calcium-sensing receptor (CaSR) agonist | |||
T9202 | DDO-5936 | HSP | |
DDO-5936 is a potent and specific HSP90-Cdc37 PPI inhibitor. | |||
T24109 | GSK329 | GSK 329,GSK-329 | Others |
GSK329 is an effective and selective inhibitor of TNNI3 Interacting Kinase (TNNI3K). GSK329 exhibits positive cardioprotective outcomes in the model of ischemia/reperfusion cardiac injury. | |||
T26324 | VU0071063 | VU 0071063,VU-0071063 | Potassium Channel |
VU0071063 is a Kir6.2/SUR1 activator. | |||
T6052 | GW 441756 | Apoptosis , Raf , Trk receptor , CDK | |
GW 441756 is a specific Tropomyosin-related kinase A (TrkA) inhibitor with an IC50 value of 2 nM. | |||
T27719 | KD-026 | SLx 4090,SLx4090,KD026,SLx-4090 | CETP |
KD-026 (SLx 4090), a microsomal triglyceride transfer protein (MTP) inhibitor(IC50 = 8.0 nM), is used in type 2 diabetes studies. | |||
T15017 | CU-T12-9 | TLR | |
CU-T12-9 is a potent TLR1/2 agonist(EC50 of 52.9 nM in HEK-Blue hTLR2 SEAP assay). It acts by activating the NFkB pathway, upregulating proinflammatory cytokines, and enhancing TLR1 and TLR2 dimerization.CU-T12-9 activat... | |||
T41302 | Itaconate-alkyne | ITalk | Others |
Itaconate-alkyne (ITalk) is a bioorthogonal probe for quantitative and site-specific chemoproteomic profiling of itaconate in inflammatory macrophages and enables biochemical evaluation and proteomic analysis of its dire... | |||
T7008 | Vacquinol-1 | Vacquinol 1 | JNK |
Vacquinol-1 is an MKK4 activator, which rapidly and selectively induces glioma cell death. | |||
T7123 | AMG-47a | VEGFR , p38 MAPK , JAK , Src | |
AMG-47a is a potent inhibitor of Lck and T cell proliferation. AMG-47a could promote the degradation of the KRAS oncoprotein. AMG-47a selectively reduced the levels of EGFP-KRASG12V protein but did not affect EGFP protei... |