ck

CK-636 (CK-0944636)是一种具有细胞渗透性的Arp2 3复合体抑制剂，能抑制肌动蛋白的聚合，对人，裂殖酵母和牛的IC50值分别为4、24 和 32 μM。

CK-666 是一种肌动蛋白相关蛋白 Arp2 3 复合物的细胞渗透性抑制剂。 它与 Arp2 3 复合物结合，稳定复合物的非活性状态，阻止 Arp2 和 Arp3 亚基进入活化的丝状短节距构象。

CK2 PIM1-IN-1 is an inhibitor of CK2 and PIM1 (IC50s: 3.787 μM and 4.327 μM). It is developed for the research of proliferative disorders such as cancer, as well as other kinase-associated conditions.

Vitamin CK3 is the combination of Vitamin C and vitamin K3 and has been shown to inhibit tumor growth and lung metastasis.

CK548 is a novel actin-related protein (Arp)2 3 complex inhibitor.

CK176 is a capsid targeted inhibitor of HIV-1 replication. CK176 shows an 11-fold improvement over I-XW-053 in blocking HIV-1 replication in primary human peripheral blood mononuclear cells (PBMCs).

CK-2-68 is a potent inhibitor of PfNDH2.

CK 102 is a bio-active chemical.

CK-17 is an interleukin-1 antagonist and an IL-1 blocker, which inhibits fibroblast proliferation in a concentration-dependent manner.

CK 2130 is a bio-active chemical.

CK 2289 is an inhibitor of type III cyclic 3'5' -adenosine monophosphate phosphodiesterase with potential use in the treatment of congestive heart failure.

CK 3197 is a selective positive inotropic agent for the treatment of congestive heart failure. It has hemodynamic and myocardial energetic effects.

CK 492B is a bio-active chemical.

CK-119 is an interleukin-1 blocker, which mainly inhibits the growth of fibroblast-like corneal and conjunctival cells by inhibiting the synthesis of DNA and RNA.

CK2 inhibitor 2 是一种有效的，选择性和口服CK2抑制剂，IC50值为 0.66 nM。CK2 inhibitor 2 对 Clk2 (IC50=32.69 nM) CK2 显示出高选择性。 CK2 inhibitor 2 表现出良好的抗增殖和抗肿瘤活性。

SGC-CK2-1 是一种具有高度特异性的 CK2 抑制剂，是胰腺 β 细胞中胰岛素产生和分泌的诱导剂，可用于研究神经退行性疾病。

CK1-IN-1 (PUN51207) 是一种酪蛋白激酶 1 抑制剂，对 CK1δ、CK1ε和p38σ MAPK 的IC50值为 15 nM、16 nM 和73 nM。

CK-869 是一种肌动蛋白相关蛋白 2 3 复合体抑制剂，其 IC50值为 7 μM。

CK0106023 was specific inhibitor of KSP. In tumor-bearing mice, CK0106023 exhibited antitumor activity comparable to or exceeding that of paclitaxel and caused the formation of monopolar mitotic figures identical to those produced in cultured cells. KSP was most abundant in proliferating human tissues and was absent from cultured postmitotic neurons.

CK37 controls the biological activity of Choline Kinase-α. This small molecule inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

Z-FK-ck (Z-Phe-Lys-2,4,6-Trimethylbenzoyloxy-methylketone) 作为一种选择性gingipain-K抑制剂，具有在剂量和时间依赖性的方式上延长血浆凝血酶时间 (TT) 的特性。

CK-963 是一种心肌肌钙蛋白(cTnC)的激活剂，Ki 为 11.5 μM，并能够增强 Sprague-Dawley 大鼠的心肌收缩力。

CK7是有效的Cdk2 9抑制剂。CK7可用于合成 Nek1 抑制剂 BSc5231 和BSc5367。

CK2 ERK8-IN-1 (TMCB) 是一种酪蛋白激酶 2 (CK2) (Ki 为 0.25 µM) 和 ERK8 (MAPK15, ERK7) 的双重抑制剂，IC50 均为 0.50 μM。CK2 ERK8-IN-1 也与 PIM1，HIPK2 和 DYRK1A 结合，Ki 值分别为 8.65 µM，15.25 µM 和 11.9 µM。