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PKC

PKC

Protein kinase C, commonly abbreviated to PKC, is a family of protein kinase enzymes that are involved in controlling the function of other proteins through the phosphorylation of hydroxyl groups of serine and threonine amino acid residues on these proteins, or a member of this family. PKC enzymes in turn are activated by signals such as increases in the concentration of diacylglycerol (DAG) or calcium ions (Ca2+). Hence PKC enzymes play important roles in several signal transduction cascades.
TargetMol
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Cat. No. Product Name CAS No. Purity Chemical Structure
TN2844 (2R,3S)-Dihydrodehydroconiferyl alcohol
化合物 TN2844
126253-41-6 98%
TargetMol Chemical Structure (2R,3S)-Dihydrodehydroconiferyl alcohol
(2R,3S)-Dihydrodehydroconiferyl alcohol can induce neurite outgrowth and enhance NGF-induced neurite outgrowth from PC12 cells by amplifying up-stream steps such...
TN2799 20-Deoxyingenol 3-angelate
化合物 TN2799
75567-38-3 98%
TargetMol Chemical Structure 20-Deoxyingenol 3-angelate
20-Deoxyingenol 3-angelate and ingenol 20-acetate 3-angelate are known as promoters of tumors of mouse skin. 20-Deoxyingenol 3-angelate can induce significant pl...
T14328 AS2521780
化合物 T14328
1214726-89-2 98%
TargetMol Chemical Structure AS2521780
AS2521780 is an inhibitor of PKCθ (IC50: 0.48 nM).
T17299 (-)-Indolactam V
化合物 T17299
90365-57-4 98%
TargetMol Chemical Structure (-)-Indolactam V
(-)-Indolactam V is a PKC activator (Kis: 3.36 nM, 1.03 μM for η-CRD2 , γ-CRD2). (-)-Indolactam V also has the Kds are 5.5 nM (η-C1B), 7.7 nM (ε-C1B), 8.3 nM (δ-...
T16526 Phorbol 12,13-dibutyrate
化合物 T16526
37558-16-0 98%
TargetMol Chemical Structure Phorbol 12,13-dibutyrate
Phorbol 12,13-dibutyrate is a PKC activator. It also is a potent skin tumor promoter.
T21260 Psychosine
鞘氨醇半乳糖苷
2238-90-6 98%
TargetMol Chemical Structure Psychosine
Psychosine (Galactosylsphingosine) 是一种 PKC 抑制剂,是半乳糖脑苷脂酶 (GALC) 酶的底物,是 Krabbe 病的潜在生物标志物。Psychosine 具有很强的细胞毒性,可诱导多种细胞死亡。
T15637 K-252b
化合物 T15637
99570-78-2 98%
TargetMol Chemical Structure K-252b
K-252b is an indolocarbazole isolated from the actinomycete Nocardiopsis and is a PKC inhibitor. K-252b can be used to inhibit extracellular kinases of cells in ...
T15638 K-252c
化合物 T15638
85753-43-1 98%
TargetMol Chemical Structure K-252c
K-252c is a staurosporine analog isolated from Nocardiopsis sp. and is a cell-permeable PKC inhibitor (IC50: 2.45 μM). K-252c also inhibits β-lactamase, chymotry...
T14831 Bryostatin 1
苔藓抑素1
83314-01-6 98%
TargetMol Chemical Structure Bryostatin 1
Bryostatin 1 is a natural macrolide isolated from the bryozoan Bugula neritina and is a CNS)permeable PKC modulator. Bryostatin 1 binds to the isolated C1 domain...
TN4300 Isojacareubin
化合物 TN4300
50597-93-8 98%
TargetMol Chemical Structure Isojacareubin
Isojacareubin displays potent activity against H. pylori HP40 clinical isolate with MIC 23.9 uM, which is approximately two times greater than that of the standa...
T40101 (±)-1,2-Diolein
甘油1,2-二油酸酯
2442-61-7 98%
TargetMol Chemical Structure (±)-1,2-Diolein
(±)-1,2-Diolein (1,2-Dioleoyl-rac-glycerol) 是一种PKC 激活剂,可以增加肌小管 Ca2+内流。
T13384 Y-33075
化合物 T13384
199433-58-4 98%
TargetMol Chemical Structure Y-33075
Y-33075 is a selective inhibitor of ROCK derived from Y-27632, and is more potent than Y-27632, with an IC50 of 3.6 nM.
T16848 SB-218078
化合物 T16848
135897-06-2 98%
TargetMol Chemical Structure SB-218078
SB-218078 is less potently inhibits Cdc2 (IC50: 250 nM) and PKC (IC50: 1000 nM). SB-218078 is a potent, ATP-competitive, and cell-permeable checkpoint kinase 1 i...
T10555 BJE6-106
化合物 T10555
1564249-38-2 98%
TargetMol Chemical Structure BJE6-106
BJE6-106 (B106) is a potent, selective PKCδ inhibitor (IC50: 0.05 μM) and targets selectivity over classical PKCα (IC50: 50 μM). BJE6-106 induces caspase-depende...
TN4431 Leucosceptoside A
米团花苷A
83529-62-8 98%
TargetMol Chemical Structure Leucosceptoside A
Leucosceptoside A shows inhibitory activity against PKCalpha with the IC50 value of 19.0 microM; it also exhibits strong inhibitory capacity against α-glucosidas...
TN3517 Bisacurone
化合物 TN3517
120681-81-4 98%
TargetMol Chemical Structure Bisacurone
Bisacurone has anti-oxidant, anti-inflammatory, and anti-metastatic activities, it may have a protective effect against ethanol-induced liver injury by suppressi...
T13605 Cercosporin
尾孢菌素
35082-49-6 98%
TargetMol Chemical Structure Cercosporin
Cercosporin is produced by a plant pathogen, Cercosporakikuchii, and the elsinochromes. Cercosporin is a potent photosensitizer with a short activation wavelengt...
TN4271 Isochamaejasmine
异狼毒素
93859-63-3 98%
TargetMol Chemical Structure Isochamaejasmine
Isochamaejasmine 分离自 S. chamaejasme L. 中分离出来,可抑制 NF-κB 活化。 Isochamaejasmine 通过抑制 Bcl-2 家族蛋白的活性诱导白血病细胞凋亡,可用于抗癌研究。
T16671 PS315
化合物 T16671
1221964-50-6 98%
TargetMol Chemical Structure PS315
PS315 inhibits the full-length and catalytic domain constructs of PKCζ (IC50=10 μM) and PKCη (IC50=30 μM). PS315 has anti-cancer activity. PS315 is a derivative ...
TN3655 Cimiside E
化合物 TN3655
154822-57-8 98%
TargetMol Chemical Structure Cimiside E
Cimiside E has anti-inflammatory activity, it selectively inhibits TNF-α-induced expression of VCAM-1 at least by upregulation of PPAR-γ, and signals for ERK1/2,...
(2R,3S)-Dihydrodehydroconiferyl alcohol
TN2844
(2R,3S)-Dihydrodehydroconiferyl alcohol can induce neurite outgrowth and enhance NGF-induced neurite outgrowth from PC12 cells by amplifying up-stream steps such...
20-Deoxyingenol 3-angelate
TN2799
20-Deoxyingenol 3-angelate and ingenol 20-acetate 3-angelate are known as promoters of tumors of mouse skin. 20-Deoxyingenol 3-angelate can induce significant pl...
AS2521780
T14328
AS2521780 is an inhibitor of PKCθ (IC50: 0.48 nM).
(-)-Indolactam V
T17299
(-)-Indolactam V is a PKC activator (Kis: 3.36 nM, 1.03 μM for η-CRD2 , γ-CRD2). (-)-Indolactam V also has the Kds are 5.5 nM (η-C1B), 7.7 nM (ε-C1B), 8.3 nM (δ-...
Phorbol 12,13-dibutyrate
T16526
Phorbol 12,13-dibutyrate is a PKC activator. It also is a potent skin tumor promoter.
Psychosine
T21260
Psychosine (Galactosylsphingosine) 是一种 PKC 抑制剂,是半乳糖脑苷脂酶 (GALC) 酶的底物,是 Krabbe 病的潜在生物标志物。Psychosine 具有很强的细胞毒性,可诱导多种细胞死亡。
K-252b
T15637
K-252b is an indolocarbazole isolated from the actinomycete Nocardiopsis and is a PKC inhibitor. K-252b can be used to inhibit extracellular kinases of cells in ...
K-252c
T15638
K-252c is a staurosporine analog isolated from Nocardiopsis sp. and is a cell-permeable PKC inhibitor (IC50: 2.45 μM). K-252c also inhibits β-lactamase, chymotry...
Bryostatin 1
T14831
Bryostatin 1 is a natural macrolide isolated from the bryozoan Bugula neritina and is a CNS)permeable PKC modulator. Bryostatin 1 binds to the isolated C1 domain...
Isojacareubin
TN4300
Isojacareubin displays potent activity against H. pylori HP40 clinical isolate with MIC 23.9 uM, which is approximately two times greater than that of the standa...
(±)-1,2-Diolein
T40101
(±)-1,2-Diolein (1,2-Dioleoyl-rac-glycerol) 是一种PKC 激活剂,可以增加肌小管 Ca2+内流。
Y-33075
T13384
Y-33075 is a selective inhibitor of ROCK derived from Y-27632, and is more potent than Y-27632, with an IC50 of 3.6 nM.
SB-218078
T16848
SB-218078 is less potently inhibits Cdc2 (IC50: 250 nM) and PKC (IC50: 1000 nM). SB-218078 is a potent, ATP-competitive, and cell-permeable checkpoint kinase 1 i...
BJE6-106
T10555
BJE6-106 (B106) is a potent, selective PKCδ inhibitor (IC50: 0.05 μM) and targets selectivity over classical PKCα (IC50: 50 μM). BJE6-106 induces caspase-depende...
Leucosceptoside A
TN4431
Leucosceptoside A shows inhibitory activity against PKCalpha with the IC50 value of 19.0 microM; it also exhibits strong inhibitory capacity against α-glucosidas...
Bisacurone
TN3517
Bisacurone has anti-oxidant, anti-inflammatory, and anti-metastatic activities, it may have a protective effect against ethanol-induced liver injury by suppressi...
Cercosporin
T13605
Cercosporin is produced by a plant pathogen, Cercosporakikuchii, and the elsinochromes. Cercosporin is a potent photosensitizer with a short activation wavelengt...
Isochamaejasmine
TN4271
Isochamaejasmine 分离自 S. chamaejasme L. 中分离出来,可抑制 NF-κB 活化。 Isochamaejasmine 通过抑制 Bcl-2 家族蛋白的活性诱导白血病细胞凋亡,可用于抗癌研究。
PS315
T16671
PS315 inhibits the full-length and catalytic domain constructs of PKCζ (IC50=10 μM) and PKCη (IC50=30 μM). PS315 has anti-cancer activity. PS315 is a derivative ...
Cimiside E
TN3655
Cimiside E has anti-inflammatory activity, it selectively inhibits TNF-α-induced expression of VCAM-1 at least by upregulation of PPAR-γ, and signals for ERK1/2,...
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