Free shipping on all orders over $ 500

 About 8 results found for searched term "OM-153" (0.136 seconds)

Cat.No.  Name Target
M15067 Recombinant Human FGF-4 (153AA, E.coli) Recombinant Proteins
Fibroblast growth factor 4; FGF-4; Heparin secretory-transforming protein 1
Recombinant human fibroblast growth factor 4 is produced by the escherichia coli expression system and expresses the target gene encoding SER54-LEU206. Accession # : P08620.
M21589 OM-153 PARP
OM-153 is a potent, orally active tankyrase inhibitor with IC50 of 13 nM for tankyrase 1 and 2 nM for tankyrase 2 (TNKS1/2). OM-153 inhibited luciferase based Wnt/β-catenin signal transduction reporter activity with IC50 of 0.63 nM. OM-153 inhibits Wnt/β-catenin signal transduction and proliferation in COLO 320DM.
M3229 PR-104A DNA/RNA Synthesis
PR-104A is a corresponding alcohol that is systemically converted from PR-104 and a hypoxia-targeted anticancer agent with IC50 of 153 and 60 μM for wild-type CHO AA8 under aerobic and anoxic conditions.
M3381 Nevirapine Reverse Transcriptase
BI-RG 587; NSC 641530; NVP
Nevirapine (NSC 641530) is a potent, specific non-nucleoside reverse transcriptase inhibitor (NNRTIs) that non-competitively inhibits human immunodeficiency virus type 1 (HIV-1) reverse transcriptase with a Ki of 220 nM. Nevirapine (NSC 641530) can be used in AIDS-related researchs.
M11386 Recombinant Human CD19 Protein (HEK293) Recombinant Proteins
Recombinant Human CD19 Protein (HEK293) Protein sequence: THE DNA sequence encoding human CD19 (UniProtKB/ Swiss-PROt: P15391.6) was expressed with His tag at the C-terminal. Bioactivity: Immobilized CD19 monoclonal antibody at 5μg/mL (100 μL/ well) can bind CD19 protein in a linear range of 5-100ng/mL
M21142 MK-8153 Potassium Channel
MK-8153 is a potent, selective and orally active extrarenal medullary potassium channel (ROMK) inhibitor with IC50 values of 5 nM and 34 μM for ROMK EP and hERG EP, respectively.MK-8153 can be used as a diuretic.
M42743 ALPK1-IN-3 NF-κB
ALPK1-IN-3 is an inhibitor of ALPK1 extracted from patent WO2022063153A1 compound T007.
M45317 (S)-BAY 2965501 DGK
(S)-BAY 2965501 is the left-handed isomer of BAY 2965501 (HY-153343).BAY 2965501 is a potent and selective diacylglycerol kinase zeta (DGKz) inhibitor and induces pERK activation. BAY 2965501 is a potent and selective inhibitor of diacylglycerol kinase zeta (DGKz) and induces pERK activation.



Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2023 AbMole BioScience. All Rights Reserved.