About 8 results found for searched term "OM-153" (0.136 seconds)
Cat.No. | Name | Target |
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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. |
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