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Cat. No.: HY-182596

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INHIB1X

INHIB1X is a tetracyclic MAPKAP-K2 (MK2) inhibitor with an IC₅₀ of 0.02 μM. INHIB1X inhibits LPS-induced TNFα release in human peripheral blood mononuclear cells (hPBMCs). INHIB1X suppresses the phosphorylation of hsp27 in Anisomycin-stimulated THP-1 cells. INHIB1X can be used for the research of inflammatory and tumor diseases.

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CAS No.: 1105659-16-2
화학식: C₂₃H₂₁FN₄O
분자량:388.44

보관:

Please store the product under the recommended conditions in the Certificate of Analysis.

INHIB1X Chemical Structure

CAS No.: 1105659-16-2

Amount: USD 0.00

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- 제품 설명
- Cellular Effect
- In Vitro
Chemical Information
순도&문서
References
Calculators
Help & FAQs
Classifications
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Biological Activity

제품 설명

Cellular Effect

Cell Line	Type	Value	Description	References
PBMC	IC₅₀	0.1 μM Compound: 16A	Inhibition of LPS-induced TNFalpha production in human PBMC preincubated for 30 mins measured after 3 hrs of LPS stimulation Inhibition of LPS-induced TNFalpha production in human PBMC preincubated for 30 mins measured after 3 hrs of LPS stimulation	[PMID: 20591669]

In Vitro

INHIB1X (Compound 29) potently inhibits recombinant MK2 enzyme, with an IC₅₀ of 0.02 μM^[1].
INHIB1X inhibits LPS (HY-D1056)-induced TNFα release from hPBMCs, with an IC₅₀ of 1.8 μM^[1].
INHIB1X inhibits the phosphorylation of hsp27 in THP-1 cells stimulated by Anisomycin (HY-18982), with an IC₅₀ of 1.3 μM^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Related Protocols :

Chemical Information

CAS No. 1105659-16-2
분자량 388.44
화학식 C₂₃H₂₁FN₄O
SMILES

O=C1NCC2(CN(C2)C)C3=C1C4=C(C5=CC(C6=C(F)C=CC=C6)=NC=C5CC4)N3
선적

Room temperature in continental US; may vary elsewhere.
보관

Please store the product under the recommended conditions in the Certificate of Analysis.

순도&문서

Handling Instructions (2659 KB)

References

[1]. Revesz L, et al. In vivo and in vitro SAR of tetracyclic MAPKAP-K2 (MK2) inhibitors. Part II. Bioorg Med Chem Lett. 2010;20(15):4719-4723. [Content Brief]

Calculators

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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MOQ

Minimum order quantity

100 mg

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