Chemical Structure : SHP1 agonist SCA1
Catalog No.: PC-26114Not For Human Use, Lab Use Only.
SHP1 agonist SCA1 is a highly selective covalent agonist of SHP1 (SHP-1) targeting Cys102, binds the N-SH2 domain to relieve autoinhibition and activate SHP1 with EC50 of 36.4 uM.
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SHP1 agonist SCA1 is a highly selective covalent agonist of SHP1 (SHP-1) targeting Cys102, binds the N-SH2 domain to relieve autoinhibition and activate SHP1 with EC50 of 36.4 uM.
SCA1 exhibits a very high degree of proteome-wide selectivity for SHP1 Cys102 at low micromolar concentrations.
SCA1 (5-40 uM) reproducibly and selectively labelled SHP1 Cys102 in THP-1 MDMs.
SCA1 could destabilize the auto-inhibited state of SHP1 and enhance SHP1 phosphatase activity.
SCA1 inhibits TLR4-driven cytokine production, inhibits LPS-induced phosphorylation at STAT3 Tyr705 and Ser727.
SCA1 inhibits production of NF-κB dependent pro-inflammatory cytokines including IL6 and TNF following LPS stimulation in a concentration-dependent manner.
SCA1 antagonizes IRAK signaling and LPS-induced pro-inflammatory cytokine production.
| M.Wt | 313.75 | |
| Formula | C15H12ClN5O | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Mei Ying Ng, et al. bioRxiv [Preprint]. 2026 Feb 22:2026.02.19.706790.

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