24 Results for "

PKCβ

" in MedChemExpress (MCE) Product Catalog:
Products (24)

24 Results for "PKCβ" in MCE Product Catalog:

  • Isoforms Recommended:
86
86 Publications Verification
Cat. No.: HY-13689
CAS No.: 133053-19-7
Purity:  99.32%
Synonyms: Gö 6983; Goe 6983
Target:  

PKC

Research Areas:  

Cancer

Go 6983 is a pan-PKC inhibitor against for PKCα, PKCβ, PKCγ, PKCδ and PKCζ with IC50 of 7 nM, 7 nM, 6 nM, 10 nM and 60 nM, respectively.
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23
23 Cited Publications
Cat. No.: HY-10343
CAS No.: 425637-18-9
Purity:  99.79%
Synonyms: AEB071
Target:  

MARCKS PKC

Research Areas:  

Inflammation/Immunology Cancer

Sotrastaurin (AEB071) is a potent and orally-active pan-PKC inhibitor, with Kis of 0.22 nM, 0.64 nM, 0.95 nM, 1.8 nM, 2.1 nM and 3.2 nM for PKCθ, PKCβ, PKCα, PKCη, PKCδ and PKCε, respectively .
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14
14 Cited Publications
Cat. No.: HY-10195
CAS No.: 169939-94-0
Purity:  99.48%
Synonyms: LY333531
Target:  

PKC

Research Areas:  

Metabolic Disease

Ruboxistaurin (LY333531) is an orally active, selective PKC beta inhibitor (Ki=2 nM). Ruboxistaurin exhibits ATP dependent competitive inhibition of PKC beta I with an IC50 of 4.7 nM. Ruboxistaurin inhibits PKC beta II with an IC50 of 5.9 nM .
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14
14 Cited Publications
Cat. No.: HY-10195B
CAS No.: 169939-93-9
Purity:  99.94%
Synonyms: LY333531 hydrochloride
Target:  

PKC

Research Areas:  

Metabolic Disease

Ruboxistaurin (LY333531) hydrochloride is an orally active, selective PKC beta inhibitor (Ki=2 nM). Ruboxistaurin hydrochloride exhibits ATP dependent competitive inhibition of PKC beta I with an IC50 of 4.7 nM. Ruboxistaurin hydrochloride inhibits PKC beta II with an IC50 of 5.9 nM .
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14
14 Cited Publications
Cat. No.: HY-10195A
CAS No.: 192050-59-2
Purity:  99.87%
Synonyms: LY333531 mesylate
Target:  

PKC

Ruboxistaurin (LY333531) mesylate is an orally active, selective and ATP competitive PKCβ inhibitor with IC50 values of 4.7 and 5.9 nM for PKCβI and PKCβII, respectively. Ruboxistaurin mesylate can be used for the research of eye disorders, heart failure and diabetes .
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12
12 Cited Publications
Cat. No.: HY-10342
CAS No.: 170364-57-5
Purity:  99.92%
Synonyms: LY317615
Enzastaurin (LY317615) is a potent, selective, and CNS-penetrant PKCβ inhibitor with an IC50 of 6 nM, showing 6- to 20-fold selectivity over PKCα, PKCγ and PKCε .
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5
5 Cited Publications
Cat. No.: HY-B0719
CAS No.: 75567-37-2
Synonyms: Ingenol 3-angelate; PEP005
Ingenol Mebutate is an active ingredient in Euphorbia peplus, acts as a potent PKC modulator, with Kis of 0.3, 0.105, 0.162, 0.376, and 0.171 nM for PKC-α, PKC-β, PKC-γ, PKC-δ, and PKC-ε, respectively, and has antiinflammatory and antitumor activity.
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1
1 Cited Publications
Cat. No.: HY-13335
CAS No.: 257879-35-9
Purity:  99.40%
Target:  

PKC Apoptosis

Research Areas:  

Cancer

PKCβ inhibitor 1 is a potent, ATP-competitive, and selective PKCβ inhibitor with IC50s of 21 and 5 nM for human PKCβ1 and PKCβ2, respectively. PKCβ inhibitor 1 exhibits selectivity of more than 60-fold in favor of PKCβ2 relative to other PKC isozymes (PKCα, PKCγ, and PKCε) .
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Cat. No.: HY-16903
CAS No.: 1046787-18-1
Target:  

PKC

Research Areas:  

Inflammation/Immunology

MS-553 is a potent, ATP-competitive and reversible inhibitor of conventional PKC enzymes with Kis of 5.3 and 10.4 nM for human PKCβ and PKCα, and IC50s of 2.3, 8.1, 7.6, 25.6, 57.5, 314, 808 nM for PKCα, PKCβI, PKCβII, PKCθ, PKCγ, PKC mu and PKCε, respectively.
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Cat. No.: HY-111083
CAS No.: 931695-79-3
Purity:  99.65%
Synonyms: CID23612552
Target:  

GPR55 PERK PKC ERK p38 MAPK

Research Areas:  

Metabolic Disease Cancer

ML191 (CID23612552) is a GPR55 antagonist. ML191 inhibits ERK phosphorylation and PKC β II translocation downstream of GPR55 signaling. ML191 suppresses LPI-induced activation of ERK1/2 and p38 MAPK signaling, blocks the transcription of RANKL-induced osteoclastogenesis markers, and reduces the bone resorption activity of mature osteoclasts promoted by RANKL. ML191 can be used to investigate diseases associated with bone degradation caused by excessive osteoclast activation, such as osteoporosis and bone damage during the formation stage of bone metastases .
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Cat. No.: HY-P1286
CAS No.: 172308-76-8
Target:  

PKC

Research Areas:  

Neurological Disease

PKC β pseudosubstrate is a selective cell-permeable inhibitor of PKC .
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Cat. No.: HY-P3818
CAS No.: 813416-46-5
Target:  

PKC

Research Areas:  

Others

PKCδ Peptide Substrate is a highly selective peptide substrate targeting PKCδ. PKCδ Peptide Substrate can only be efficiently catalyzed for phosphorylation modification by PKCδ, and Thr431 is the sole phosphorylation site. PKCδ Peptide Substrate binds to the catalytic pocket of PKC in a competitive manner, but exhibits no PKC agonistic or inhibitory activity. PKCδ Peptide Substrate is a dedicated biochemical probe for the quantitative detection of PKCδ in vitro, and can be used for studies on PKCδ-related pathways .
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Cat. No.: HY-10195BS
CAS No.: 1794767-04-6
Ruboxistaurin-d6 (hydrochloride) is the deuterium labeled Ruboxistaurin hydrochloride. Ruboxistaurin (LY333531) hydrochloride is an orally active, selective PKC beta inhibitor (Ki=2 nM). Ruboxistaurin hydrochloride exhibits ATP dependent competitive inhibition of PKC beta I with an IC50 of 4.7 nM. Ruboxistaurin hydrochloride inhibits PKC beta II with an IC50 of 5.9 nM .
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Cat. No.: HY-10539B
CAS No.: 359017-79-1
Synonyms: LY317615 hydrochloride
Target:  

PKC Autophagy Apoptosis

Research Areas:  

Cancer

Enzastaurin (LY317615) hydrochloride is a potent and selective PKCβ inhibitor with an IC50 of 6 nM, showing 6- to 20-fold selectivity over PKCα, PKCγ and PKCε .
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Cat. No.: HY-13689R
CAS No.: 133053-19-7
Synonyms: Gö 6983 (Standard); Goe 6983 (Standard)
Target:  

PKC Reference Standards

Research Areas:  

Cancer

Go 6983 (Standard) is the analytical standard of Go 6983. This product is intended for research and analytical applications. Go 6983 is a pan-PKC inhibitor against for PKCα, PKCβ, PKCγ, PKCδ and PKCζ with IC50 of 7 nM, 7 nM, 6 nM, 10 nM and 60 nM, respectively.
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Cat. No.: HY-119112A
Target:  

PKC

Research Areas:  

Neurological Disease

LY 379196 is a PKC-β inhibitor (IC50: 50 nM and 30 nM for PKC βI and βII respectively). LY 379196 inhibits the VEGF, IGF-1 and bFGF-induced proliferation of bovine retinal microvascular endothelial cells (BREC). LY 379196 is an antiproliferatory agentfor proliferative retinopathy .
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Cat. No.: HY-10195R
CAS No.: 169939-94-0
Synonyms: LY333531 (Standard)
Target:  

Reference Standards PKC

Research Areas:  

Metabolic Disease

Ruboxistaurin (Standard) is the analytical standard of Ruboxistaurin. This product is intended for research and analytical applications. Ruboxistaurin (LY333531) is an orally active, selective PKC beta inhibitor (Ki=2 nM). Ruboxistaurin exhibits ATP dependent competitive inhibition of PKC beta I with an IC50 of 4.7 nM. Ruboxistaurin inhibits PKC beta II with an IC50 of 5.9 nM .
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Cat. No.: HY-P1286A
Target:  

PKC

Research Areas:  

Neurological Disease

PKC β pseudosubstrate TFA is a selective cell-permeable inhibitor of PKC .
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Cat. No.: HY-10539
CAS No.: 365253-37-8
Synonyms: LY317615 dihydrochloride
Target:  

PKC Autophagy Apoptosis

Research Areas:  

Cancer

Enzastaurin (LY317615) dihydrochloride is a potent and selective PKCβ inhibitor with an IC50 of 6 nM, showing 6- to 20-fold selectivity over PKCα, PKCγ and PKCε .
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Cat. No.: HY-10342R
CAS No.: 170364-57-5
Synonyms: LY317615 (Standard)
Research Areas:  

Cancer

Enzastaurin (Standard) is the analytical standard of Enzastaurin. This product is intended for research and analytical applications. Enzastaurin (LY317615) is a potent and selective PKCβ inhibitor with an IC50 of 6 nM, showing 6- to 20-fold selectivity over PKCα, PKCγ and PKCε .
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