PKC
PKC(蛋白激酶C)
PKC (protein kinase C) is a serine/threonine protein kinase that mediates insulin signaling, actin cytoskeleton, cell mobility, apoptosis and tumorigenesis etc.
PKC 相关产品(141)
- GC17591D-erythro-Sphingosine (synthetic)CAS: 123-78-4纯度: >98.00%
D-erythro-sphingosine (Erythrosphingosine) 是一种非常有效的 p32 激酶激活剂,EC50 值为 8μM。
- GC17727[Ala107]-MBP (104-118)CAS: 99026-77-4
[Ala107]-MBP (104-118) 是一种蛋白激酶 C (PKC) 的非竞争性肽抑制剂,IC50 范围为 46-145 μM。
- GC18354Bisindolylmaleimide X (hydrochloride)CAS: 145317-11-9纯度: >98.50% / >98.00%
Bisindolylmaleimide X (hydrochloride) 是一种新型的、具有细胞渗透性的蛋白激酶C(PKC)抑制剂。Bisindolylmaleimide X也可抑制细胞周期蛋白依赖性激酶2(CDK2)活性。
- GC25662N-DesmethyltamoxifenCAS: 31750-48-8
N-Desmethyltamoxifen, the major metabolite of Tamoxifen in humans and a ten-fold more potent protein kinase C (PKC) inhibitor than Tamoxifen, also is a potent regulator of ceramide metabolism in human AML cells, limiting ceramide glycosylation, hydrolysis, and sphingosine phosphorylation.
- GC26055WAY-301398CAS: 312607-68-4
WAY-301398 (6-methoxynaphthalene) can bind to protein kinase C (PKC).
- GC30200PKC-theta inhibitorCAS: 736048-65-0纯度: >99.50%
PKC-theta inhibitor (compound 20) inhibits PKC-θ with an IC50 of 18 nM.
- GC31656Ingenol Mebutate (Ingenol 3-angelate)CAS: 75567-37-2纯度: >99.00%
A natural cytotoxic diterpene ester
- GC31892Decursin ((+)-Decursin)CAS: 5928-25-6纯度: >98.00%
A phytochemical with diverse biological activities
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC17239 | Bisindolylmaleimide V | 113963-68-1 | - | |
A S6K inhibitor | ||||
| GC17242 | (-)-epigallocatechin | 970-74-1 | >98.00% | |
(-)-epigallocatechin是绿茶中的一种主要多酚类化合物,具有抗氧化特性。 | ||||
| GC17346 | KT 5823 | 126643-37-6 | >95.00% | |
Potent selective inhibitor of cGMP-dependent protein kinase (PKG) | ||||
| GC17352 | Phorbol 12,13-dibutyrate | 37558-16-0 | >99.50% | |
An activator of PKC | ||||
| GC17563 | LY 333531 hydrochloride | 169939-93-9 | >98.00% | |
A PKCβ inhibitor | ||||
| GC17591 | D-erythro-Sphingosine (synthetic) | 123-78-4 | >98.00% | |
D-erythro-sphingosine (Erythrosphingosine) 是一种非常有效的 p32 激酶激活剂,EC50 值为 8μM。 | ||||
| GC17670 | Bryostatin 1 | 83314-01-6 | >99.00% | |
A marine macrolide with diverse biological activities | ||||
| GC17727 | [Ala107]-MBP (104-118) | 99026-77-4 | - | |
[Ala107]-MBP (104-118) 是一种蛋白激酶 C (PKC) 的非竞争性肽抑制剂,IC50 范围为 46-145 μM。 | ||||
| GC17767 | Dihydrosphingosine | 3102-56-5 | - | |
A mixture of sphingolipid pathway intermediates | ||||
| GC17815 | L-threo-Sphingosine C-18 | 25695-95-8 | - | |
A D-erythro-sphingosine analog | ||||
| GC18055 | SC-9 | 102649-78-5 | - | |
An activator of PKC | ||||
| GC18062 | 1,2-Dilauroyl-sn-glycerol | 60562-15-4 | - | |
A long-chain DAG | ||||
| GC18246 | R-59-949 | 120166-69-0 | >98.00% | |
A DGK-α inhibitor | ||||
| GC18354 | Bisindolylmaleimide X (hydrochloride) | 145317-11-9 | >98.50% / >98.00% | |
Bisindolylmaleimide X (hydrochloride) 是一种新型的、具有细胞渗透性的蛋白激酶C(PKC)抑制剂。Bisindolylmaleimide X也可抑制细胞周期蛋白依赖性激酶2(CDK2)活性。 | ||||
| GC18521 | Cercosporin | 35082-49-6 | >95.00% | |
A cytotoxic phytotoxin | ||||
| GC25662 | N-Desmethyltamoxifen | 31750-48-8 | - | |
N-Desmethyltamoxifen, the major metabolite of Tamoxifen in humans and a ten-fold more potent protein kinase C (PKC) inhibitor than Tamoxifen, also is a potent regulator of ceramide metabolism in human AML cells, limiting ceramide glycosylation, hydrolysis, and sphingosine phosphorylation. | ||||
| GC26055 | WAY-301398 | 312607-68-4 | - | |
WAY-301398 (6-methoxynaphthalene) can bind to protein kinase C (PKC). | ||||
| GC26065 | WAY-354831 | 330572-32-2 | - | |
WAY-354831 exhibits antibacterial activity. | ||||
| GC30200 | PKC-theta inhibitor | 736048-65-0 | >99.50% | |
PKC-theta inhibitor (compound 20) inhibits PKC-θ with an IC50 of 18 nM. | ||||
| GC30545 | Malantide | 86555-35-3 | >98.50% | |
Malantide是一种十二肽,能够被PKA磷酸化,并且能够增强PKA的活性。 | ||||
| GC31656 | Ingenol Mebutate (Ingenol 3-angelate) | 75567-37-2 | >99.00% | |
A natural cytotoxic diterpene ester | ||||
| GC31711 | PKC-IN-1 | 1046787-18-1 | >98.00% / >98.50% | |
PKC-IN-1是一种有效的,ATP-竞争性的,可逆的PKC抑制剂,对人PKCβ和PKCα的Ki值分别为5.3和10.4nM,对人PKCα,PKCβI,PKCβII,PKCθ,PKCγ,PKCmu和PKCε的IC50值分别为2.3,8.1,7.6,25.6,57.5,314,808nM。 | ||||
| GC31892 | Decursin ((+)-Decursin) | 5928-25-6 | >98.00% | |
A phytochemical with diverse biological activities | ||||
| GC31912 | VTX-27 | 1321924-70-2 | >99.50% | |
A PKCθ inhibitor | ||||
