Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11056 |
DLK-IN-1
|
DNA Alkylation | DNA Damage/DNA Repair |
DLK-IN-1 is a selective oral active inhibitor of bisleucine zipper kinase (DLK, MAP3K12) with Ki of 3 nM. DLK-IN-1 is active in the Alzheimer's disease model, retains excellent CNS permeability, and after multiple days of administration, its concentration | |||
T3707 |
GNE-3511
GNE3511 |
DNA Alkylation; MAPK | DNA Damage/DNA Repair; MAPK |
GNE-3511是双亮氨酸拉链激酶 (DLK)抑制剂(Ki:0.5 nM)。 | |||
T6057 |
URMC-099
|
ROCK; MLK; VEGFR; SGK; DNA Alkylation; Trk receptor; c-Met/HGFR; LRRK2; MEK; IGF-1R; Syk; Bcr-Abl; CDK; Src; Aurora Kinase; Autophagy | Angiogenesis; Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; MAPK; Metabolism; Stem Cells; Tyrosine Kinase/Adaptors |
URMC-099 是一种具有优异的血脑屏障穿透性的,可口服的混合谱系激酶 3 抑制剂,IC50为14 nM。 | |||
T73457 |
DN-1289
|
DNA Alkylation | DNA Damage/DNA Repair |
DN-1289 是一种可口服可通过血脑屏障且具有选择性高效性的抑制剂,对双亮氨酸拉链激酶 (DLK)的 IC50 值为17 nM,对 亮氨酸拉链轴承激酶 (LZK)的 IC50 值为 40 nM。DN-1289 对小鼠模型中视神经挤压 (ONC) 诱导的 p-c-Jun 有显著的抑制作用。 | |||
T11440 |
GNE-8505
|
DNA Alkylation | DNA Damage/DNA Repair |
GNE-8505 is an orally available inhibitor of Dual leucine zipper kinase (DLK). | |||
T79303 |
IACS-52825
|
||
IACS-52825是一种选择性DLK抑制剂,具有1.3 nM的Kd值,适用于研究化疗引起的周围神经病变。 |