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MilliporeSigma

SML0352

Sigma-Aldrich

PFI-1

≥98% (HPLC)

Sinónimos:

2-Methoxy-N-(3-methyl-2-oxo-1,2,3,4-tetrahydro-quinazolin-6-yl)-bezenesulfonamide, PF-06405761

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About This Item

Fórmula empírica (notación de Hill):
C16H17N3O4S
Número de CAS:
Peso molecular:
347.39
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.77

Quality Level

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: ≥10 mg/mL

storage temp.

2-8°C

SMILES string

COc1ccccc1S(=O)(=O)Nc2ccc3NC(=O)N(C)Cc3c2

InChI

1S/C16H17N3O4S/c1-19-10-11-9-12(7-8-13(11)17-16(19)20)18-24(21,22)15-6-4-3-5-14(15)23-2/h3-9,18H,10H2,1-2H3,(H,17,20)

InChI key

TXZPMHLMPKIUGK-UHFFFAOYSA-N

Application

PFI-1 has been used as a bromodomain inhibitor in breast cancer cell line MCF7 dechorionated zebrafish embryos. It has also been used in human peripheral blood mononuclear cells (PBMCs), to inhibit the release of interleukin-6 in lipopolysaccharide (LPS) challenge assay.

Biochem/physiol Actions

PFI-1 is a quinazolinone inhibits androgen receptor (AR) mediated signaling in prostate cancer cells. It elicits minimum toxicity and is effective for anti-HIV-latency therapy. In leukemia cells, PFI-1 inhibits Aurora B kinase and promotes caspase-dependent apoptosis.
The human BET family, which includes BRD2, BRD3, BRD4 and BRDT, play a role in regulation of gene transcription. PFI-1 is a selective BET bromodomain inhibitor with activity at BRD2 (IC50 = 98 nM) and BRD4 (IC50 = 220 nM). For full characterization details, please visit the PFI-1 probe summary on the Structural Genomics Consortium (SGC) website.

To learn about other SGC chemical probes for epigenetic targets, visit sigma.com/sgc

Features and Benefits

PFI-1 is an epigenetic chemical probe available through a partnership with the Structural Genomics Consortium (SGC). To learn more and view other SGC epigenetic probes, visit sigma.com/SGC.
This compound is a featured product for Gene Regulation research. Click here to discover more featured Gene Regulation products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

Other Notes

PFI-1 has been expertly reviewed and recommended by the Chemical Probes Portal. For more information, please visit the PFI-1 probe summary on the Chemical Probes Portal website.

Related product

Referencia del producto
Descripción
Precios

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Los clientes también vieron

PFI-1, a highly selective protein interaction inhibitor, targeting BET Bromodomains
Picaud S, et al.
Cancer Research, 73(11), 3336-3346 (2013)
Estrogen-dependent control and cell-to-cell variability of transcriptional bursting
Fritzsch C, et al.
Molecular Systems Biology, 14(2) (2018)
The BET-inhibitor PFI-1 diminishes AR/AR-V7 signaling in prostate cancer cells
Hupe MC, et al.
World Journal of Urology, 37(2), 343-349 (2019)
Marie C Hupe et al.
World journal of urology, 37(2), 343-349 (2018-06-24)
The bromodomain and extra-terminal (BET) family of proteins provides a scaffolding platform for the recruitment and tethering of transcription factors to acetylated chromatin, thereby modulating gene expression. In this study, we evaluated the efficacy of the BET-inhibitor PFI-1 to diminish
BET inhibitors RVX-208 and PFI-1 reactivate HIV-1 from latency
Lu P, et al.
Scientific reports, 7(1), 16646-16646 (2017)

Contenido relacionado

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