ERK1/2 inhibitor 9

SKU:BHB21901763
Overview
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ERK1/2 inhibitor 9 (CAS 2169302-75-2) is an inhibitor supplied as a solid. Reported to act on ERK1, ERK2. Relevant to MAPK/ERK Pathway and Stem Cell/Wnt research. Molecular formula C31H32ClN7O3, molecular weight 586.08 g/mol.
Purity 95.91%
CAS Number 2169302-75-2
Molecular Weight 586.08 g/mol
Form Solid
Target ERK1, ERK2
Storage -20°C as supplied; in solvent -80°C
Options selector
Catalog no. Size
HY-153738-1MG 1 mg
HY-153738-5MG 5 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 1 mg, 5 mg
  • Lead time: shown per option in the variant selector.
  • Storage: -20°C, protect from light. In solvent: -80°C, 6 months; -20°C, 1 month (protect from light).
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: transfer to -20°C as soon as possible.
Field Specification
Target ERK1, ERK2
CAS no. 2169302-75-2
Applications
  • Functional Assay (In Vitro)
Molecular weight 586.08
Molecular formula C31H32ClN7O3
Purity 95.91%
SMILES O=C(NCCC#CC1=NC=CC(NC2=NC=C(C(NC3=C(NC(C=C)=O)C=CC=C3)=N2)Cl)=C1)OC4CC/C=C\CCC4
Form Solid
Storage -20°C, protect from light. In solvent: -80°C, 6 months; -20°C, 1 month (protect from light).
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-153738
Main SKU BHB21901763
Inhibitors

Compound Overview

ERK1/2 inhibitor 9 (Probe 1) is a covalent inhibitor of ERK1/2, showing sub-micromolar activity in cells (A375 GI50 = 0.47 μM) and causing downregulation of phospho-ERK1/2. When tagged with trans-cyclo-octene (TCO), it can react with Tz-Thalidomide (tetrazine-tagged Thalidomide) to form the corresponding ERK-CLIPTAC, eliciting degradation of ERK1/2[1]. It is supplied as an off-white to light yellow solid (C31H32ClN7O3, MW 586.08) at 95.91% purity.

Physical & Chemical Properties

CAS Number 2169302-75-2
Molecular Formula C31H32ClN7O3
Molecular Weight 586.08 g/mol
Purity 95.91%
Appearance Solid
Color Off-white to light yellow
SMILES O=C(NCCC#CC1=NC=CC(NC2=NC=C(C(NC3=C(NC(C=C)=O)C=CC=C3)=N2)Cl)=C1)OC4CC/C=C\CCC4
Target ERK1, ERK2
Signaling Pathway MAPK/ERK Pathway; Stem Cell/Wnt
Solubility In Vitro: DMSO: 50 mg/mL (85.31 mM; Requires sonication; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Storage -20°C, protect from light. In solvent: -80°C, 6 months; -20°C, 1 month (protect from light).
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description. Peer-reviewed publications that used this product are listed under References.

[1]. Honorine Lebraud, et al. Protein Degradation by In-Cell Self-Assembly of Proteolysis Targeting Chimeras. ACS Cent Sci. 2016 Dec 28;2(12):927-934.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.

In Vitro

SolventSolubilityNotes
DMSO50 mg/mL (85.31 mM)requires sonication; use freshly opened DMSO (absorbed moisture lowers solubility)

Aliquot the stock solution and store it at -80°C (up to 6 months) or -20°C (up to 1 month); protect from light; avoid repeated freeze-thaw cycles.

Data provided by the manufacturer.

Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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