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Cat. No. Product Name Information
PC-62549

p32 inhibitor M36

p32 inhibitor

p32 inhibitor M36 is a novel small molecule inhibitor of p32 mitochondrial protein, binds directly to p32 and inhibits p32 association with LyP-1.
PC-62477

UCN-01

PKC inhibitor

UCN-01 (7-Hydroxystaurosporine, NSC 638850) is a synthetic derivative of staurosporine that has antiproliferative activity against several in vitro and in vivo cancer models.
PC-62415

PS432

PKC inhibitor

PS432 is an allosteric inhibitor of PKCι and PKCζ with IC50 of 16.9 and 18.5 uM, respectively.
PC-62375

BJE6-106

PKCδ inhibitor

BJE6-106 (B106) is a potent, selective PKCδ inhibitor with IC50 of 50 nM, displays excellent selectivity over classical PKC isozymes (a 1,000-fold PKCδ selectivity over PKCα).
PC-62078

LY379196

PKCβ inhibitor

LY379196 is a highly specific PKCβ inhibitor with IC50 of 30-50 nM for PKCβI and PKCβII, displays >10-fold selectivity of PKCα, δ, η, and γ (>600 nM).
PC-62077

CGP-53353

PKCβII inhibitor

CGP-53353 (DAPH-7) is a selective inhibitor of PKCβII with IC50 of 0.41 uM, shows weak activity on PKCβI with IC50 of 3.8 uM.
PC-61793

Rottlerin

PKCδ inhibitor

Rottlerin (Mallotoxin, NSC 94525) is a polyphenol natural product, cell-permeable and reversible PKC inhibitor that exhibits greater selectivity for PKCδ (IC50=3-6 uM) and PKCθ, with significantly reduced potency (IC50=30-42 uM) for PKCα, PKCβ, and PKCγ.
PC-70263

Calphostin C

PKC inhibitor

Calphostin C (UCN 1028C, PKF115-584) is a potent, selective and photo-dependent inhibitor of PKC with IC50 of 50 nM.
PC-60994

AS2521780

PKCθ inhibitor

AS2521780 is a potent, selective, orally bioavailable PKCθ inhibitor that inhibits combinant human PKCθ enzyme with IC50 of 0.48 nM, >30-fold higher than other PKC isoforms.
PC-60684

Go 6976

PKC inhibitor

Go 6976 is a potent, selective protein kinase C (PKC) inhibitor that selectively inhibits PKCα and PKCβ1 with IC50 of 2.3 and 6.2 nM, respectively.
PC-42543

Sotrastaurin

PKC inhibitor

Sotrastaurin (AEB071) is a potent, selective, orally available pan-PKC inhibitor with Ki of 0.22-3.2 nM for PKC isotypes.
PC-42441

Ruboxistaurin hydrochloride

PKCβ inhibitor

Ruboxistaurin hydrochloride (LY333531) is a potent, selective, ATP-competitive, orally available PKC beta (PKCβ) inhibitor with IC50 of 4.7 and 5.9 nM for PKCβ I and PKCβ II, respectively.

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