A selective inhibitor of NF-κB activation
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CID-2858522

Item No. 14122

Technical Information
Formal Name
1-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-2-[2-[(3-hydroxypropyl)amino]-5,6-dimethyl-1H-benzimidazol-1-yl]-ethanone
CAS Number
758679-97-9
Synonyms
  • ML-029
Molecular Formula
C28H39N3O3
Formula Weight
Purity
≥98%
A crystalline solid
DMSO: 5 mg/mlEthanol: 5 mg/ml
λmax
215, 254, 292 nm
SMILES
CC1=C(C)C=C(N(CC(C2=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C2)=O)C(NCCCO)=N3)C3=C1
InChi Code
InChI=1S/C28H39N3O3/c1-17-12-22-23(13-18(17)2)31(26(30-22)29-10-9-11-32)16-24(33)19-14-20(27(3,4)5)25(34)21(15-19)28(6,7)8/h12-15,32,34H,9-11,16H2,1-8H3,(H,29,30)
InChi Key
CYCGGKILBWERDJ-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    CID-2858522 is an 2-amino benzimidazole that inhibits activation of the NF-κB pathway induced by the PKC activator PMA with an IC50 value of 0.07 μM.1 It has been shown to inhibit IL-8 production induced by PKC activators in HEK293 cells (IC50 ≤ 0.1 μM), attenuate CD3/CD28 and PMA/ionomycin-induced production of IL-2 by Jurkat T cells (IC50 ≤ 5 μM), and prevent anti-IgM-stimulated proliferation of mouse B-lymphocytes (IC50 = ∼2 μM).1 CID-2858522 does not, however, inhibit the NF-κB pathway activated by TNF-α.1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Peddibhotla, S., Shi, R., Khan, P., et alInhibition of protein kinase C-driven nuclear factor-κB activation: Synthesis, structure-activity relationship, and pharmacological profiling of pathway specific benzimidazole probe molecules. J. Med. Chem. 53(12), 4793-4797 (2010).