Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T20792 |
W-7 hydrochloride
N-(6-氨基己基)-5-氯-1-萘磺胺盐酸盐,W 7 HCl,W7 HCl,W-7 HCl |
CaMK; Apoptosis; Myosin; PDE | Apoptosis; Cytoskeletal Signaling; Metabolism; Neuroscience |
W-7 hydrochloride (W-7 HCl) 是一种选择性的钙调蛋白拮抗剂。它抑制Ca2+-钙调蛋白依赖性磷酸二酯酶和肌球蛋白轻链激酶,IC50值分别为 28 μM 和 51 μM。它可诱导细胞凋亡,具有抗癌活性。 | |||
T35095 |
W 7
BRN 2888957,W7,W-7 |
||
W 7 is a biochemical. | |||
T1800 |
GW788388
GW 788388 |
ALK; TGF-beta/Smad | Angiogenesis; Stem Cells; Tyrosine Kinase/Adaptors |
GW788388 是一种 ALK5抑制剂(IC50:18 nM)。它也抑制 TGF-β II 型受体和激活素 II 型受体的活性,但对 BMP II 型受体无影响。 | |||
T15633 |
JW74
|
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
JW74 能够拮抗 LiCl 诱导的经典 Wnt 信号激活 (IC50: 420 nM)。 | |||
T6079 |
NVP-ADW742
ADW742,ADW,GSK 552602A |
Apoptosis; IGF-1R | Apoptosis; Tyrosine Kinase/Adaptors |
NVP-ADW742 (ADW) 是一种具有口服活性,选择性的IGF-1R 酪氨酸激酶抑制剂,IC50为 0.17 μM。它抑制胰岛素受体,IC50为 2.8 μM,在肿瘤细胞中诱导多效性抗增殖/促凋亡。 | |||
T15453 |
GW7647
2-[[4-[2-[[环己基氨基)羰基](4-环己基丁基)氨基]乙基]苯基]硫基]-2-甲基丙酸 |
PPAR | DNA Damage/DNA Repair; Metabolism |
GW7647 是一种PPARα有效激动剂,对人 PPARα、PPARγ 和 PPARδ 的EC50值分别为 6、1.1 和 6.2 μM。 | |||
TP1474 |
LXW7
|
Integrin | Cytoskeletal Signaling |
LXW7 是一种整合素αvβ3抑制剂,是含 Arg-Gly-Asp (RGD) 的环状肽,对αvβ3整联蛋白具有很高的结合亲和力,IC50为 0.68 μM。它可增强 VEGFR-2 磷酸化和 ERK1/2 活化,具有抗炎活性。 | |||
T8866 |
GW779439X
|
Apoptosis; Antibacterial; CDK; Aurora Kinase | Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Microbiology/Virology |
GW779439X 属于吡唑并吡啶类,是一种金黄色葡萄球菌 PASTA 激酶 Stk1抑制剂。它是一种AURKA 抑制剂,可通过 caspases 3/7 诱导细胞凋亡。 | |||
T7805 |
GW791343 dihydrochloride
GW791343 (HCl) |
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
GW791343 dihydrochloride (GW791343 (HCl)) 是有种属特异性的 P2X7变构调节剂,对人 P2X7的 pIC50为6.9-7.2。 | |||
T24123 |
GW780056X
GW-780056-X,GW 780056 X |
||
GW780056X is a selective inhibitor of cyclin-dependent kinase. GW780056X is also an inhibitor of Yes1 kinase. It is an inhibitor of binding or entry into cells for the Lassa Virus. | |||
T11519 |
GW768505A free base
|
Others | Others |
GW768505A free base is a potent dual inhibitor of VEGFR2 (KDR) and Tie-2 (pIC50: 7.81 for VEGFR2) with anti-angiogenic activity. | |||
T15452 |
GW7604
|
Others | Others |
GW7604 is an antiestrogen and it also is the metabolite of GW5638. GW5638 is an antagonist of high-affinity estrogen receptor (ER). | |||
T6526 |
GW791343 trihydrochloride
GW791343 3HCl |
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
GW791343 trihydrochloride (GW791343 3HCl) 是 P2X7变构调节剂,有种属特异性,对人 P2X7的pIC50为6.9-7.2。 | |||
T35103 |
W7477
BRN 0626598,W 7477,W-7477,CP 14304 |
||
W7477 is a biochemical. | |||
TP2148 |
LXW7 TFA (1313004-77-1 free base)
LXW7 TFA |
Integrin | Cytoskeletal Signaling |
LXW7 TFA, a cyclic peptide containing Arg-Gly-Asp (RGD), is an integrin αvβ3 inhibitor with an anti-inflammatory effect. LXW7 has a high binding affinity to αvβ3 integrin (IC50: 0.68 μM). It increases the phosphorylation of VEGFR-2 and activation of ERK1/2. | |||
T27513 |
GW7845
GW 7845,GW-7845 |
||
GW7845, an L-tyrosine derivative, is a PPAR-γ agonist. | |||
T75724 |
LXW7 TFA
|
||
LXW7 TFA, 包含 Arg-Gly-Asp (RGD) 的环状肽,作为整合素αvβ3抑制剂,展示出对αvβ3整联蛋白高度的结合亲和力,其IC50值为0.68 μM。此外,LXW7 TFA 能够促进 VEGFR-2 磷酸化和 ERK1/2 激活,显示出抗炎活性。 |