Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
TN2844 | (2R,3S)-Dihydrodehydroconiferyl alcohol
化合物 TN2844
|
126253-41-6 | 98% |
|
(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% |
|
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% |
|
AS2521780 is an inhibitor of PKCθ (IC50: 0.48 nM). | ||||
T17299 | (-)-Indolactam V
化合物 T17299
|
90365-57-4 | 98% |
|
(-)-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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
(±)-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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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% |
|
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,... |