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Merck

J4455

JSH-23

≥98% (HPLC), NF-kB nuclear translocation inhibitor, solid

Sinónimos:

4-methyl-N1-(3-phenylpropyl)-1,2-benzenediamine

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Acerca de este artículo

Fórmula empírica (notación de Hill):
C16H20N2
Número CAS:
Peso molecular:
240.34
UNSPSC Code:
51111800
NACRES:
NA.77
Assay:
≥98% (HPLC)
Form:
solid
Quality level:
Storage condition:
protect from light
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Nombre del producto

JSH-23, ≥98% (HPLC), solid

SMILES string

N(CCCc2ccccc2)c1c(cc(cc1)C)N

InChI

1S/C16H20N2/c1-13-9-10-16(15(17)12-13)18-11-5-8-14-6-3-2-4-7-14/h2-4,6-7,9-10,12,18H,5,8,11,17H2,1H3

InChI key

YMFNPBSZFWXMAD-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

solid

storage condition

protect from light

color

off-white to gray-pink

solubility

DMSO: >10 mg/mL

shipped in

wet ice

storage temp.

−20°C

Quality Level

Application

JSH-23 has been used as a nuclear factor κB (NF-κB) p65 inhibitor.

Biochem/physiol Actions

JSH-23 is an inhibitor of NF-kB nuclear translocation.
JSH-23 is an inhibitor of NF-kB nuclear translocation. It inhibits LPS and cytokine-induced nuclear translocation of the p65 subunit of NF-kB as analyzed by EMSA and western blot. The compound displays modest potency (IC50 7.1 uM in RAW 264.7), but has the unique property that it does not affect IkB degradation or recovery. The compound dose dependently inhibits LPS induced expression of cytokines, COX2 and iNOS, and presumably binds to, or interferes with the NLS of p65.

Other Notes

Light and air sensitive.

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Skin Sens. 1B


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