
AZA1
CAS No. 1071098-42-4
AZA1 ( —— )
产品货号. M35559 CAS No. 1071098-42-4
AZA1 是 Rac1 和 Cdc42 的有效抑制剂。AZA1 诱导前列腺癌细胞凋亡并抑制增殖,迁移和侵袭。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥1253 | 有现货 |
![]() ![]() |
5MG | ¥1995 | 有现货 |
![]() ![]() |
10MG | ¥3206 | 有现货 |
![]() ![]() |
25MG | ¥5185 | 有现货 |
![]() ![]() |
50MG | ¥7390 | 有现货 |
![]() ![]() |
100MG | ¥9792 | 有现货 |
![]() ![]() |
500MG | ¥19661 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称AZA1
-
注意事项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
-
产品简述AZA1 是 Rac1 和 Cdc42 的有效抑制剂。AZA1 诱导前列腺癌细胞凋亡并抑制增殖,迁移和侵袭。
-
产品描述AZA1 is a potent dual inhibitor of Rac1 and Cdc42. AZA1 induces prostate cancer cells apoptosis and inhibits prostate cancer cells proliferation, migration and invasion.
-
体外实验AZA1 (Rac1/Cdc42-IN-1) (2-10 μM; 72 hours) blocks the proliferation of human prostate cancer cells 22Rv1 prostate cancer cells.AZA1 (2-10 μM; 24 hours) reduces phosphorylation of PAK1, AKT and BAD in EGF stimulated 22Rv1 prostate cancer cells.AZA1 (10 μM; 24 hours) blocks Rac1 and Cdc42-dependent cell cycle events in 22Rv1 prostate cancer cells.AZA1 blocks Rac1 and Cdc42-dependent migration of 22Rv1, DU 145 and PC-3 prostate cancer cells.AZA1 affects cell motility and actin rearrangement in prostate cancer cells by suppressing Rac1 and Cdc42 activity via PAK1/2 phosphorylation.Cell Proliferation Assay Cell Line:22Rv1 prostate cancer cells Concentration:2, 5, 10 μM Incubation Time:72 hours Result:Suppressed 22Rv1 prostate cancer cell proliferation in both unstimulated and EGF-stimulated cancer cells in a dose-dependent manner. Western Blot Analysis Cell Line:22Rv1 prostate cancer cells (EGF-stimulated)Concentration:2, 5, 10 μM Incubation Time:24 hours Result:Reduced phosphorylation of PAK1, AKT and BAD in EGF-stimulated 22Rv1 prostate cancer cells.
-
体内实验AZA1 (Rac1/Cdc42-IN-1) (100 μg; i.p.; daily for 2 weeks) is potent in suppressing human 22Rv1 xenograft growth in mice and improving survival.Animal Model:5 week-old athymic nu/nu (nude) mice (bearing 22Rv1 prostate cancer cell xenografts)Dosage:100 μg in 100 μl 30% DMSO Administration:I.p.; daily for 2 weeks Result:The suppressive effect of AZA1 on tumor growth was significant.
-
同义词——
-
通路Cell Cycle/DNA Damage
-
靶点Rho
-
受体Rho | Apoptosis | CDK
-
研究领域——
-
适应症——
化学信息
-
CAS Number1071098-42-4
-
分子量368.43
-
分子式C22H20N6
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO 中的溶解度 : 50 mg/mL (135.71 mM; 超声助溶 )
-
SMILESCc1cc2cc(Nc3ccnc(Nc4ccc5[nH]c(C)cc5c4)n3)ccc2[nH]1
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Zins K, et al. A Rac1/Cdc42 GTPase-specific small molecule inhibitor suppresses growth of primary human prostate cancer xenografts and prolongs survival in mice. PLoS One. 2013;8(9):e74924. Published 2013 Sep 11.?
产品手册




关联产品
-
Z62954982
Z62954982 (ZINC08010136) 是一种强效的、选择性的、细胞渗透性强的 Rac1 (IC50=12 μM) 抑制剂,比 NSC23766 (HY-15723A) (IC50=50 μM) 有效性强 4 倍。Z62954982 干扰 Rac1/Tiam1 复合物,降低活性 Rac1 (GTP 结合的 Rac1) 的细胞质水平,而不影响其他 Rho GTPases (如,Cdc42 或 RhoA) 的活性。
-
NS1643
NS1643 是一种有效的人 ether-a-go-go 相关基因 (hERG) KV11.1 通道激活剂,EC50 为 10.5 μM。
-
Digeranyl bisphospho...
Digeranyl bisphosphonate (DGBP) 是一种有效的香叶基焦磷酸香叶酯 (GGPP) 合酶抑制剂,抑制 Rac1 的香叶基焦磷酸化。