Determine the necessary mass, volume, or concentration for preparing a solution.
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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T162506-100mg | 100mg | In stock | $238.90 | |
T162506-250mg | 250mg | In stock | $537.90 | |
T162506-1g | 1g | In stock | $1,935.90 |
Inactive tyrphostin
Synonyms | (p-Methoxybenzylidene)malononitrile | 2-Cyano-3-(p-methoxyphenyl)acrylonitrile | DTXSID10182508 | benzylidenemalononitrile (BMN) deriv. 1 | KBio3_000976 | p-methoxybenzylidenemalononitrile | p-methoxybenzylidene-malononitrile | T3074 | AKOS000357412 | Bio |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | Inactive tyrphostin. Negative control for tyrphostins such as AG 490 . Inhibits CD40 signaling pathway. Reduces IL-12 production in macrophages. Blocks CD40L-induced translocation of NFκB to the nucleus. Shows antiallergic effects in vivo. |
Storage Temp | Store at 2-8°C |
Shipped In | Wet ice |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of epidermal growth factor receptor |
Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description | Product description: Tyrphostin A1(AG9) inhibits CD40L-stimulated IL-12 production in macrophage cultures and antigen-induced generation of Th1 cells. IC50 value: Target: IL-12 production inhibitor Addition of increasing concentration of A1 resulted in a dose dependent decrease of IL-12 p40, with maximal inhibition (62.5%) occurring at a dose of 10 μM. tyrphostin A1 blocks CD40L-induced translocation of NF-κB to the nucleus, and reduces the activation of IL-12 p40 gene. In vivo therapy with A1 leads to decrease in generation of myelin basic protein (MBP) specific encephalitogenic T cells. In addition, treatment of SJL/J mice with A1 results in attenuation of experimental allergic encephalomyelitis (EAE) . Tyrphostin A1 is a much weaker inhibitor of TK than other tyrphostins (IC50>1250 μM for epidermal growth factor receptor (EGFR) kinase), and therefore often used to differentiate TK-mediated effects of tyrphostins from other non-specific effects. Application: Tyrphostin 1 has been used to study its effect on the increase of transgene expression in HeLa and NIH3T3 cells. |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | 2-[(4-methoxyphenyl)methylidene]propanedinitrile |
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INCHI | InChI=1S/C11H8N2O/c1-14-11-4-2-9(3-5-11)6-10(7-12)8-13/h2-6H,1H3 |
InChi Key | UOHFCPXBKJPCAD-UHFFFAOYSA-N |
Canonical SMILES | COC1=CC=C(C=C1)C=C(C#N)C#N |
Isomeric SMILES | COC1=CC=C(C=C1)C=C(C#N)C#N |
WGK Germany | 3 |
PubChem CID | 2063 |
Molecular Weight | 184.2 |
PubChem CID | 2063 |
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CAS Registry No. | 2826-26-8 |
ChEMBL Ligand | CHEMBL77456 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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G2308354 | Certificate of Analysis | Jun 14, 2023 | T162506 |
G2308360 | Certificate of Analysis | Jun 14, 2023 | T162506 |
G2308361 | Certificate of Analysis | Jun 14, 2023 | T162506 |
G2308366 | Certificate of Analysis | Jun 14, 2023 | T162506 |
G2308370 | Certificate of Analysis | Jun 14, 2023 | T162506 |
G2308377 | Certificate of Analysis | Jun 14, 2023 | T162506 |
Sensitivity | Heat Sensitive |
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Melt Point(°C) | 115 °C |
WGK Germany | 3 |
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1. Gazit A, Yaish P, Gilon C, Levitzki A. (1989) Tyrphostins I: synthesis and biological activity of protein tyrosine kinase inhibitors.. J Med Chem, 32 (10): (2344-52). [PMID:2552117] [10.1021/op500134e] |