PS-1145
CAS No. 431898-65-6
PS-1145( PS1145 | PS 1145 )
Catalog No. M14463 CAS No. 431898-65-6
A specific IκB kinase (IKK) inhibitor with IC50 of 88 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 52 | In Stock |
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| 5MG | 76 | In Stock |
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| 10MG | 141 | In Stock |
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| 25MG | 267 | In Stock |
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| 50MG | 527 | In Stock |
|
| 100MG | 752 | In Stock |
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| 500MG | 1548 | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NamePS-1145
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NoteResearch use only, not for human use.
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Brief DescriptionA specific IκB kinase (IKK) inhibitor with IC50 of 88 nM.
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DescriptionA specific IκB kinase (IKK) inhibitor with IC50 of 88 nM; shows no activity for JNK2, c-Src, p38α, IRAK, Lck, etc.; blocks TNFα-induced NF-κB activation in MM cells through inhibition of IκBα phosphorylation and degradation of IκBα, respectively; blocks the protective effect of IL-6 against Dex-induced apotosis, inhibits both IL-6 secretion from BMSCs triggered by MM cell adhesion and proliferation of MM cells adherent to BMSCs.
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In VitroPS-1145 blocks TNFα-induced NF-κB activation in a dose- and time-dependent fashion in MM cells through inhibition of IκBα phosphorylation. Dexamethasone (Dex), which up-regulates IκBα protein, enhances blockade of NF-κB activation by PS-1145. PS-1145 blocks the protective effect of IL-6 against Dex-induced apotosis. TNFα-induced intracellular adhesion molecule (ICAM)-1 expression on both RPMI8226 and MM.1S cells is also inhibited by PS-1145. Moreover, PS-1145 inhibits both IL-6 secretion from bone marrow stromal cells (BMSCs)triggered by MM cell adhesion and proliferation of MM cells adherent to BMSCs.
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In VivoAdministration of either Bortezomib or PS-1145 (50 mg/kg) results in a significant decrease in serum levels of all 3 cytokines that is nonsignificantly different from those in mice that underwent transplantation with TCD BM alone. PS1145 is injectedintracerebroventricular (icv)as a pretreatment to block hypothalamic inflammation induced by IL-4 in adult male Wistar rats consuming a high-fat diet (HFD) over an 11-day period. The four groups of rats according to icv pretreatment/treatment condition are Veh/Veh, Veh/IL-4, PS1145/Veh, and PS1145/IL-4. Rats in the Veh/IL-4 group display increased weight gain on the HFD compared with the Veh/Veh group (P<0.05 on days 6-9).Importantly, the effect of icv IL-4 administration to increase body fat mass during high-fat (HF)feeding is completely blocked by icv PS1145 pretreatment at a dose that has no independent effect on body composition (on day 8: P<0.001, PS1145/Veh vs. PS1145/IL-4; P=not significant, PS1145/Veh vs. Veh/Veh).In PS1145/IL-4 injected rats, IL-1β mRNA content is decreased by ~75% compared with that of Veh/IL-4-injected rats.
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SynonymsPS1145 | PS 1145
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PathwayImmunology/Inflammation
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TargetIκB kinase (IKK)
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RecptorIKK
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Research AreaInflammation/Immunology
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Indication——
Chemical Information
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CAS Number431898-65-6
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Formula Weight322.7484
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Molecular FormulaC17H11ClN4O
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 43 mg/mL
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SMILESC1=CC(=CN=C1)C(=O)NC2=CC(=CC3=C2NC4=C3C=CN=C4)Cl
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Chemical Name3-Pyridinecarboxamide, N-(6-chloro-9H-pyrido[3,4-b]indol-8-yl)-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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BOT-64
BOT-64 is an IKK-2 inhibitor which targets the Ser177 and/or Ser181 residues in the kinase's activation loop domain.BOT-64 is a cell-permeable benzoxathiole compoundBOT-64 inhibits IKKbeta-mediated IkappaBalpha phosphorylation in LPS-activated macrophages, resulting in sequential prevention of downstream events, including proteolytic degradation of IkappaBalpha, DNA binding ability, and transcriptional activity of NF-kappaB.?
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GSK319347A
GSK319347A is a selective and potent dual inhibitor of TBK1 and IKKε with potential anti-tumor activity and inhibition of IKK2 activity, which can be used in the study of bladder cancer and lung adenocarcinoma.
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BI605906
BI605906 is a potent, specific IKKβ inhibitor with IC50 of 380 nM (0.1 mM ATP).
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