STAMBP-IN-1
CAS No. 896683-78-6
STAMBP-IN-1 ( —— )
Catalog No. M22992 CAS No. 896683-78-6
STAMBP-IN-1 is a small-molecule inhibitor of STAMBP deubiquitinase, and interrupts STAMBP-Ub-NALP7 interaction. STAMBP-IN-1 decreases protein level of its inflammasome substrate NALP7 and suppresses IL-1b release after Toll-like receptor (TLR) agonism. STAMBP-IN-1 inhibits the activity of STAMBP to cleave recombinant di-Ub with an IC50 value of 0.33 mM
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 147 | In Stock |
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10MG | 237 | In Stock |
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25MG | 507 | In Stock |
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50MG | 731 | In Stock |
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100MG | 1017 | In Stock |
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200MG | Get Quote | In Stock |
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Biological Information
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Product NameSTAMBP-IN-1
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NoteResearch use only, not for human use.
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Brief DescriptionSTAMBP-IN-1 is a small-molecule inhibitor of STAMBP deubiquitinase, and interrupts STAMBP-Ub-NALP7 interaction. STAMBP-IN-1 decreases protein level of its inflammasome substrate NALP7 and suppresses IL-1b release after Toll-like receptor (TLR) agonism. STAMBP-IN-1 inhibits the activity of STAMBP to cleave recombinant di-Ub with an IC50 value of 0.33 mM
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DescriptionSTAMBP-IN-1 is a small-molecule inhibitor of STAMBP deubiquitinase, and interrupts STAMBP-Ub-NALP7 interaction. STAMBP-IN-1 decreases protein level of its inflammasome substrate NALP7 and suppresses IL-1b release after Toll-like receptor (TLR) agonism. STAMBP-IN-1 inhibits the activity of STAMBP to cleave recombinant di-Ub with an IC50 value of 0.33 mM
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In VitroSTAMBP-IN-1 (0.1-10 μM; 6 h) exhibits the most potent ability to selectively decrease NALP7 abundance as well as endogenous NALP7 abundance in THP-1 cells, but not NALP6.STAMBP-IN-1 (0.01-100 μM; 37 ℃; 2 h) inhibits cleavage of K63-linked di-Ub (200 nM) to mono-Ub by purified recombinant STAMBP (25 nM) in a concentration dependent manner.STAMBP-IN-1 (0.01-10 μM; 37 ℃; 60 min) blocks STAMBP mediated deubi quitination of Ub-NALP7 in vitro in a concentration-dependent manner.STAMBP-IN-1 exhibits toxicity against THP-1 cells with an IC50 of 106 μg/mL. Western Blot Analysis Cell Line:THP-1 cells Concentration:0.01, 0.1, 1, 10, and 100 μM Incubation Time:6 hours Result:Inhibited the activity of STAMBP to cleave recombinant di-Ub in a concentrationdependent manner with an IC50 of 0.33 mM (0.09-1.21 mM).
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptordeubiquitinase STAM-binding protein (STAMBP)
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Research Area——
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Indication——
Chemical Information
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CAS Number896683-78-6
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Formula Weight504.6
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Molecular FormulaC27H28N4O4S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 3.29 mg/mL (6.52 mMw)
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SMILESO=C(NCC1=CC=CO1)CSC(N2CCC3=CC=CC=C3)=NC4=C(C=C(N5CCOCC5)C=C4)C2=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Joseph S Bednash, Nathaniel Weathington, James Londino.Targeting the deubiquitinase STAMBP inhibits NALP7 inflammasome activity.Nat Commun. 2017 May 11;8:15203.
molnova catalog
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