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PR-619

Catalog No. T1862   CAS 2645-32-1
Synonyms: PR 619, 2,6-Diamino-3,5-dithiocyanopyridine

PR-619 (2,6-Diamino-3,5-dithiocyanopyridine) is a non-selective, reversible inhibitor of the deubiquitinylating enzymes (DUBs).

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PR-619 Chemical Structure
PR-619, CAS 2645-32-1
Pack Size Availability Price/USD Quantity
5 mg In stock $ 45.00
10 mg In stock $ 55.00
25 mg In stock $ 83.00
50 mg In stock $ 113.00
100 mg In stock $ 158.00
200 mg In stock $ 238.00
500 mg In stock $ 393.00
1 mL * 10 mM (in DMSO) In stock $ 79.00
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Purity: 100%
Purity: 99.83%
Purity: 99.10%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description PR-619 (2,6-Diamino-3,5-dithiocyanopyridine) is a non-selective, reversible inhibitor of the deubiquitinylating enzymes (DUBs).
Targets&IC50 USP4:3.93 μM(EC50), JOSD2:1.17 μM(EC50), UCHL3:2.95 μM(EC50), SENP6 core:2.37 μM(EC50), USP8:4.90 μM(EC50)
Kinase Assay Ub-PLA2 assay: Recombinant enzymes in 20 mM Tris-HCl, pH 8.0, 2 mM CaCl2 and 2 mM β-mercaptoethanol (DUB assay buffer) are preincubated with single doses or dose ranges of PR-619 or P22077 for 30 minutes in a 96 well plate before the addition of Ub-PLA2 and NBD C6-HPC. The liberation of a fluorescent product within the linear range of the assay is monitored at room temperature using a fluorescence plate reader. Vehicle (2%(v/v) DMSO) and 10 mM N-ethylmaleimide are included as controls. Where ≥60% inhibition is observed, EC50 values are determined using a sigmoidal dose response equation.
Cell Research 72 h hours later, 0.2 mg/mL resazurin prepared in phosphate-buffered saline is added to each well and the cells are incubated for an additional 3-6 h. The fluorescence of the resazurin reduction product is measured using Ex=535 nm and Em=590 nm filters on a fluorimeter. The EC50 values are calculated in Prism.(Only for Reference)
Synonyms PR 619, 2,6-Diamino-3,5-dithiocyanopyridine
Molecular Weight 223.28
Formula C7H5N5S2
CAS No. 2645-32-1

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 201.5 mM

TargetMolReferences and Literature

1. Altun M, et al. Chem Biol, 2011, 18(11), 1401-1412. 2. Song P, Yang S, Hua H, et al. The regulatory protein GADD34 inhibits TRAIL-induced apoptosis via TRAF6/ERK-dependent stabilization of myeloid cell leukemia 1 in liver cancer cells[J]. Journal of Biological Chemistry, 2019: jbc. RA118. 006029.

TargetMolCitations

1. Song P, Yang S, Hua H, et al. The regulatory protein GADD34 inhibits TRAIL-induced apoptosis via TRAF6/ERK-dependent stabilization of myeloid cell leukemia 1 in liver cancer cells. Journal of Biological Chemistry. 2019: jbc. RA118. 006029

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library NO PAINS Compound Library Bioactive Compound Library Anti-Cancer Compound Library Cell Cycle Compound Library Bioactive Compounds Library Max HIF-1 Signaling Pathway Compound Library Apoptosis Compound Library Anti-Aging Compound Library Endoplasmic Reticulum Stress Compound Library

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.

Keywords

PR-619 2645-32-1 Apoptosis Autophagy Cell Cycle/Checkpoint DNA Damage/DNA Repair Ubiquitination DUB DUBs PR619 tau G0/G1 Deubiquitinase PR 619 ER-stress 2,6-Diamino-3,5-dithiocyanopyridine ubiquitination inhibit Inhibitor arrest inhibitor

 

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