PR-619
CAS No. 2645-32-1
PR-619( 2,6-Diamino-3,5-dithiocyanopyridine | DUB Inhibitor V )
Catalog No. M13810 CAS No. 2645-32-1
PR-619 is a non-selective, reversible inhibitor of the deubiquitinylating enzymes (DUBs) with EC50 of 1-20 μM in a cell-free assay.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 41 | In Stock |
|
| 10MG | 65 | In Stock |
|
| 25MG | 113 | In Stock |
|
| 50MG | 176 | In Stock |
|
| 100MG | 267 | In Stock |
|
| 200MG | 401 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NamePR-619
-
NoteResearch use only, not for human use.
-
Brief DescriptionPR-619 is a non-selective, reversible inhibitor of the deubiquitinylating enzymes (DUBs) with EC50 of 1-20 μM in a cell-free assay.
-
DescriptionPR-619 is a non-selective, reversible inhibitor of the deubiquitinylating enzymes (DUBs) with EC50 of 1-20 μM in a cell-free assay.
-
In VitroCell Cytotoxicity Assay Cell Line:OLN-t40 cells.Concentration:0-10 μM.Incubation Time:24 hours.Result:Exerted concentration-dependent cytotoxicity in a very narrow concentration range of 7-10 μM.
-
In VivoAnimal Model:Nude mice.Dosage:10 mg/kg/day (Cisplatin combined).Administration:Intraperitoneally.Result:Enhanced the antitumor effect of Cisplatin.
-
Synonyms2,6-Diamino-3,5-dithiocyanopyridine | DUB Inhibitor V
-
PathwayProteasome/Ubiquitin
-
TargetDUB
-
RecptorJOSD2| SENP6 core| UCH-L3| USP4| USP8
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number2645-32-1
-
Formula Weight223.33
-
Molecular FormulaC7H5N5S2
-
Purity>98% (HPLC)
-
SolubilityDMSO: 45 mg/mL (201.54 mM)
-
SMILESN#CSC1=C(N)N=C(N)C(SC#N)=C1
-
Chemical Name(2,6-diamino-5-thiocyanatopyridin-3-yl) thiocyanate
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Altun M, et al. Chem Biol, 2011, 18(11), 1401-1412.
molnova catalog
related products
-
USP10-IN-9
USP10-IN-9 is a HBX19818 analog, selective USP10 inhibitor with IC50 similar to HBX19818.
-
USP8-IN-2
USP8-IN-2 is a potent inhibitor of the deubiquitinating enzymes USP7 and USP8, with an IC50 of 4.0 μM against USP8D. USP8-IN-2 is a potential compound for the treatment of cancer and viral infections.
-
IMP-1710
IMP-1710 is a selective UCH-L1 inhibitor with an IC50 value of 38 nM in a fluorescence polarization assay.IMP-1710 has antifibrotic activity.
Cart
sales@molnova.com