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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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T129823-5mg | 5mg | In stock | $225.90 | |
T129823-10mg | 10mg | In stock | $375.90 | |
T129823-25mg | 25mg | Available within 1-2 weeks(?) Item is derived from our semi-finished stock and is processed in 1-2 weeks. | $846.90 | |
T129823-50mg | 50mg | Available within 1-2 weeks(?) Item is derived from our semi-finished stock and is processed in 1-2 weeks. | $969.90 |
Potent, reversible and selective ATP-binding site-targeting Tie2 kinase inhibitor. Cell-permeable.
Synonyms | 948557-43-5|Tie2 kinase inhibitor|Tie2 kinase inhibitor 1|Tie2 kinase-IN-1|Tie2-IN-5|4-(4-(6-methoxynaphthalen-2-yl)-2-(4-(methylsulfinyl)phenyl)-1H-imidazol-5-yl)pyridine|CHEMBL237352|4-[4-(6-Methoxy-2-naphthalenyl)-2-[4-(methylsulfinyl)phenyl]-1H-imidaz |
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Specifications & Purity | ≥97% |
Storage Temp | Store at -20°C |
Shipped In | Dry ice |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of TEK receptor tyrosine kinase |
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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Pubchem Sid | 488200358 |
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Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488200358 |
IUPAC Name | 4-[4-(6-methoxynaphthalen-2-yl)-2-(4-methylsulfinylphenyl)-1H-imidazol-5-yl]pyridine |
INCHI | InChI=1S/C26H21N3O2S/c1-31-22-8-5-19-15-21(4-3-20(19)16-22)25-24(17-11-13-27-14-12-17)28-26(29-25)18-6-9-23(10-7-18)32(2)30/h3-16H,1-2H3,(H,28,29) |
InChi Key | SINQIEAULQKUPD-UHFFFAOYSA-N |
Canonical SMILES | COC1=CC2=C(C=C1)C=C(C=C2)C3=C(NC(=N3)C4=CC=C(C=C4)S(=O)C)C5=CC=NC=C5 |
Isomeric SMILES | COC1=CC2=C(C=C1)C=C(C=C2)C3=C(NC(=N3)C4=CC=C(C=C4)S(=O)C)C5=CC=NC=C5 |
Alternate CAS | 948557-43-5 |
PubChem CID | 23625762 |
MeSH Entry Terms | 4-(6-methoxy-2-naphthyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)-1H-imidazole |
Molecular Weight | 439.53 |
PubChem SID | 488200358 |
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Enter Lot Number to search for COA:
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Lot Number | Certificate Type | Date | Item |
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D2313496 | Certificate of Analysis | Mar 03, 2023 | T129823 |
D2313497 | Certificate of Analysis | Mar 03, 2023 | T129823 |
D2313498 | Certificate of Analysis | Mar 03, 2023 | T129823 |
D2313499 | Certificate of Analysis | Mar 03, 2023 | T129823 |
D2313503 | Certificate of Analysis | Mar 03, 2023 | T129823 |
D2313504 | Certificate of Analysis | Mar 03, 2023 | T129823 |
D2313505 | Certificate of Analysis | Mar 03, 2023 | T129823 |
D2313506 | Certificate of Analysis | Mar 03, 2023 | T129823 |
Solubility | DMSO 35 mg/mL Water <1 mg/mL Ethanol <1 mg/mL |
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1. Semones M, Feng Y, Johnson N, Adams JL, Winkler J, Hansbury M. (2007) Pyridinylimidazole inhibitors of Tie2 kinase.. Bioorg Med Chem Lett, 17 (17): (4756-60). [PMID:17618114] |
2. Karabid NM et al.. (2022) Angpt2/Tie2 autostimulatory loop controls tumorigenesis.. EMBO Mol Med, 14 (5): (e14364). [PMID:35266635] |
3. Besnier M et al.. (2019) miR-15a/-16 Inhibit Angiogenesis by Targeting the Tie2 Coding Sequence: Therapeutic Potential of a miR-15a/16 Decoy System in Limb Ischemia.. Mol Ther Nucleic Acids, 17 (49-62). [PMID:31220779] |