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PR-619 is a non-selective reversible inhibitor of deubiquitinylating enzymes (DUBs) with EC50 of 1-20 μM in cell-free assays. PR-619 activates autophagy.
Brand: BCM
Target: USP4:3.93 μM(EC50), JOSD2:1.17 μM(EC50), UCH-L3:2.95 μM(EC50), SENP6 core:2.37 μM(EC50), USP8:4.90 μM(EC50)
Signaling Pathways: Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination
In Vivo: PR-619 increased global protein polyubiquitination in HEK293T cells in a dose - and time-dependent manner (20 to 150 μM,0.5 to 20 h). The PR619 treatment causes upregulation of the PolyB chain connecting K48 and K63. PR-619 induced HCT116 cell death with EC50 of 6.3 μM.
Melting Point: 210℃
Boiling Point: 406.0±45.0 °C(Predicted)
pKa: -0.19±0.50(Predicted)
Solubility: Soluble in DMSO. Insoluble in Water; insolluble in Ethanol.
GHS: GHS05,GHS07
Isomeric SMILES: C1=C(C(=NC(=C1SC#N)N)N)SC#N
InChIKey: ZXOBLNBVNROVLC-UHFFFAOYSA-N
InChI: InChI=1S/C7H5N5S2/c8-2-13-4-1-5(14-3-9)7(11)12-6(4)10/h1H,(H4,10,11,12)
Attribute [Chem Name] (2,6-diamino-5-thiocyanatopyridin-3-yl) thiocyanate [Synonym] PR-619; PR619 [CAS No.] 2645-32-1 [EINECS] 200-256-5 [MDL No.] MFCD00830384 [Formula] C7H5N5S2 [Molecular] 223.28 [Form] White to beige powder [Storage] Sealed in dry, 2-8°C
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