GLPBio

PFI-2

Catalog No.: GC17956Purity:>98%Synonyms: (R)-PFI-2
SETD7 methyltransferase inhibitor

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PFI-2
Cas No.: 1627676-59-8
10mM (in 1mL DMSO)In Stock
$97.00
1
5mgIn Stock
$54.00
1
25mgIn Stock
$182.00
1
50mgIn Stock
$320.00
1

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Description

PFI-2 is a potent and selective inhibitor of SETD7 methyltransferase with IC50 value of 2.0 nM [1].

SET domain containing (lysine methyltransferase) 7 (SETD7) is a protein lysine methyltransferase that acts as monomethyltransferase of lysine 4 on histone H3 (H3K4) and regulates DNA methyltransferase 1 (DNMT1) [1].

PFI-2 is a potent and selective SETD7 methyltransferase inhibitor. (R)-PFI-2 inhibited human SETD7 methyltransferase activity with IC50 value of 2.0 nM. However, (S)-PFI-2 was 500-fold less active with IC50 value of only 1.0 µM. (R)-PFI-2 potently inhibited SETD7 with Morrison Kiapp value of 0.33 nM. (R)-PFI-2 occupied the peptide binding groove and effectively inhibited the binding of SETD7 substrates. In the presence of 20 μM SAM, (R)-PFI-2 bound to SETD7 with KD value of 4.2 nM in a SAM-dependent way. In HEK293 cells, (R)-PFI-2 (10 µM) bound to and stabilized SETD7. In Setd7+/+ murine embryonic fibroblasts (MEFs), (R)-PFI-2 increased nuclear localization of Yes-associated protein (YAP) and the expression of YAP target genes Ctgf, Gli2 and Cdc20 [1].

Reference:
[1].  Barsyte-Lovejoy D, Li F, Oudhoff MJ, et al. (R)-PFI-2 is a potent and selective inhibitor of SETD7 methyltransferase activity in cells. Proc Natl Acad Sci U S A, 2014, 111(35): 12853-12858.

Protocol

Kinase experiment [1]:

Methyltransferase activity

Recombinant human SETD7 (residues 1–366) and SET domain only (residues109–366) were expressed in Escherichia coli and purified to homogeneity. Methyltransferase activity of SETD7(1-366) was assayed using a scintillation proximity assay monitoring the incorporation of the tritium-labeled methyl group of 3H-SAM into a peptide substrate corresponding to histone H3 residues 1-25 at 2 μM SAM and 2 μM H3(1–25) and 2 nM enzyme.

Cell experiment [1]:

Cell lines

MEFs and MCF7 cells

Preparation method

The solubility of this compound in DMSO is > 10 mM. General tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.

Reacting condition

0-10 μM, 2h

Applications

In Setd7+/+ murine embryonic fibroblasts (MEFs) in the presence of (R)-PFI-2 (10 μM), Setd7+/+ MEFs grown to confluence and displayed increased nuclear localization of YAP, as well as increased expression of YAP-dependent genes Ctgf, Gli2, and Cdc20. (R)-PFI-2 had no effect in Setd7-/- MEFs. In confluent MCF7 cells, (R)-PFI-2 (1 μM for 2h) dose-dependently increased nuclear YAP and increased expression of the YAP target genes AREG and CYR61.

References:

[1]. Barsyte-Lovejoy D, Li F, Oudhoff MJ, et al. (R)-PFI-2 is a potent and selective inhibitor of SETD7 methyltransferase activity in cells. Proc Natl Acad Sci U S A, 2014, 111(35): 12853-12858.

Chemical Properties

CAS No.
1627676-59-8
Synonyms
(R)-PFI-2
Chemical Name
8-fluoro-N-[(2R)-1-oxo-1-pyrrolidin-1-yl-3-[3-(trifluoromethyl)phenyl]propan-2-yl]-1,2,3,4-tetrahydroisoquinoline-6-sulfonamide
SMILES
C1CCN(C1)C(=O)C(CC2=CC(=CC=C2)C(F)(F)F)NS(=O)(=O)C3=CC(=C4CNCCC4=C3)F
Molecular Formula
C23H25F4N3O3S
Molecular Weight
499.52
Solubility
≥ 50mg/mL in DMSO
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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