Nocodazole

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

Nocododium 是一种快速可逆的微管聚合抑制剂，还抑制 Abl、Abl(E255K) 和 Abl(T315I)，在无细胞测定中 IC50 分别为 0.21 μM、0.53 μM 和 0.64 μM。

Nocodazole is a rapidly-reversible inhibitor of microtubule polymerization, also inhibits Abl, Abl(E255K) and Abl(T315I) with IC50 of 0.21 μM, 0.53 μM and 0.64 μM in cell-free assays, respectively.(In Vitro):Nocodazole exhibits good affinity toward c-KIT, with a Kd value of 1.6?μM in highly malignant human cancer cells. Nocodazole displays good binding affinity toward the components of the mitogen-activated protein kinase (MAPK) pathway, such as BRAF (Kd=1.8?μM), BRAF(V600E) (Kd=1.1?μM), MEK1 (Kd=1.7?μM), and MEK2 (Kd=1.6?μM). Nocodazole has the highest affinity for αβIV and the lowest affinity for αβIII.Nocodazole (1 nM) induces apoptosis of COLO 205 cancer cells.Nocodazole (≥ 30 μg/mL) significantly increases the percentage of annexin-V-binding cells without significantly modifying average forward scatter of human erythrocytes.In CHO cells, the addition of 1 nM Nocodazole, a concentration that suppresses microtubule dynamics, slows migration and increases the frequency and duration of resting states, but the directionality of the cells is maintained. In contrast to the effects of the low drug concentration, the addition of 70 nM Nocodazole, a concentration that eliminates the microtubule network, causes cells to move much more randomly, i.e., the directionality of the cells toward the wound is lost.(In Vivo):Nocodazole (5 mg/kg/three times per week, i.p.) has antitumor effects in athymic mice bearing COLO 205 tumor xenografts. Nocodazole (1 nM) + R-41400 dramatically increase the levels of p21/CIP1 and p27/KIP1 protein in the tumor tissues.

Nocodazole exhibits good affinity toward c-KIT, with a Kd value of 1.6?μM in highly malignant human cancer cells. Nocodazole displays good binding affinity toward the components of the mitogen-activated protein kinase (MAPK) pathway, such as BRAF (Kd=1.8?μM), BRAF(V600E) (Kd=1.1?μM), MEK1 (Kd=1.7?μM), and MEK2 (Kd=1.6?μM). Nocodazole has the highest affinity for αβIV and the lowest affinity for αβIII. Nocodazole (1 nM) induces apoptosis of COLO 205 cancer cells.Nocodazole (≥ 30 μg/mL) significantly increases the percentage of annexin-V-binding cells without significantly modifying average forward scatter of human erythrocytes.In CHO cells, the addition of 1 nM Nocodazole, a concentration that suppresses microtubule dynamics, slows migration and increases the frequency and duration of resting states, but the directionality of the cells is maintained. In contrast to the effects of the low drug concentration, the addition of 70 nM Nocodazole, a concentration that eliminates the microtubule network, causes cells to move much more randomly, i.e., the directionality of the cells toward the wound is lost.

Nocodazole (5 mg/kg/three times per week, i.p.)?has antitumor effects in athymic mice bearing COLO 205 tumor xenografts. Nocodazole (1 nM) + R-41400 dramatically increase the levels of p21/CIP1 and p27/KIP1 protein in the tumor tissues.

NSC 238159 | Oncodazole | R 17934

Tyrosine Kinase

Bcr-Abl

Abl| Abl (E255K)| Abl (T315I)| microtubule

Cancer

——

31430-18-9

301.32

C14H11N3O3S

>98% (HPLC)

DMSO: 7mg/ml(23.23 mM); Water: <1mg/ml; Ethanol: <1mg/ml

O=C(OC)NC1=NC2=CC(C(C3=CC=CS3)=O)=CC=C2N1

methyl (5-(thiophene-2-carbonyl)-1H-benzo[d]imidazol-2-yl)carbamate

(-20℃)

With Ice Pack

≥ 2 years