HG-9-91-01

Pricing Availability   Qty
Description: Potent pan-salt inducible kinases (SIK1, SIK2 and SIK3) inhibitor. Also inhibits Lat-B-induced EP differentiation via nuclear YAP1 accumulation.
Chemical Name: 1-(2,4-Dimethoxyphenyl)-3-(2,6-dimethylphenyl)-1-(6-((4-(4-methylpiperazin-1-yl)phenyl)amino)pyrimidin-4-yl)urea
Purity: ≥98% (HPLC)
Datasheet
Citations
Reviews

Biological Activity for HG-9-91-01

HG-9-91-01 is a potent pan-salt inducible kinases (pan-SIKs) inhibitor (IC50 values are 0.92, 6.6 and 9.6 nM for SIK1, SIK2 and SIK3 respectively). HG-9-91-01 inhibits latrunculin B (Lat-B)-induced endocrine progenitors (EP) differentiation via nuclear YAP1 accumulation in vitro. HG-9-91-01 increases LPS-stimulated IL-10 production and suppresses pro-inflammatory cytokine secretion in vitro. HG-9-91-01 increases β-cell proliferation in vitro and in vivo (mouse, zebrafish).

Technical Data for HG-9-91-01

M. Wt 567.68
Formula C32H37N7O3
Storage Store at -20°C
Purity ≥98% (HPLC)
CAS Number 1456858-58-4
PubChem ID 78357808
InChI Key UYUHRKLITDJEHB-UHFFFAOYSA-N
Smiles O=C(N(C1=CC=C(C=C1OC)OC)C2=CC(NC3=CC=C(N4CCN(CC4)C)C=C3)=NC=N2)NC5=C(C)C=CC=C5C

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

Tocris products are intended for laboratory research use only, unless stated otherwise.

Solubility Data for HG-9-91-01

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
ethanol 5.68 10
DMSO 56.77 100

Preparing Stock Solutions for HG-9-91-01

The following data is based on the product molecular weight 567.68. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Select a batch to recalculate based on the batch molecular weight:
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.76 mL 8.81 mL 17.62 mL
5 mM 0.35 mL 1.76 mL 3.52 mL
10 mM 0.18 mL 0.88 mL 1.76 mL
50 mM 0.04 mL 0.18 mL 0.35 mL

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References for HG-9-91-01

References are publications that support the biological activity of the product.

Clark et al (2012) Phosphorylation of CRTC3 by the salt-inducible kinases controls the interconversion of classically activated and regulatory macrophages. Proc.Natl.Acad.Sci.U.S.A. 109 16986 PMID: 23033494

Tian et al (2025) Salt-inducible kinases transduce mechanical forces into the specification of the pancreatic endocrine lineage. Stem Cell Rep. 20 102444 PMID: 40054471

Charbord et al (2021) In vivo screen identifies a SIK inhibitor that induces beta cell proliferation through a transient UPR. Nat.Metab. 3 682 PMID: 34031592


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Citations for HG-9-91-01

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