AZA1
CAS No. 1071098-42-4
AZA1( —— )
Catalog No. M35559 CAS No. 1071098-42-4
AZA1 (Rac1/Cdc42-IN-1) is a potent dual inhibitor of Rac1 and Cdc42. AZA1 induced apoptosis of prostate cancer cells and inhibited cell proliferation, migration and invasion.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 147 | Get Quote |
|
| 5MG | 235 | Get Quote |
|
| 10MG | 377 | Get Quote |
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| 25MG | 610 | Get Quote |
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| 50MG | 869 | Get Quote |
|
| 100MG | 1152 | Get Quote |
|
| 500MG | 2313 | Get Quote |
|
| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameAZA1
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NoteResearch use only, not for human use.
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Brief DescriptionAZA1 (Rac1/Cdc42-IN-1) is a potent dual inhibitor of Rac1 and Cdc42. AZA1 induced apoptosis of prostate cancer cells and inhibited cell proliferation, migration and invasion.
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DescriptionAZA1 is a potent dual inhibitor of Rac1 and Cdc42. AZA1 induces prostate cancer cells apoptosis and inhibits prostate cancer cells proliferation, migration and invasion.
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In VitroAZA1 (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.
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In VivoAZA1 (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.
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Synonyms——
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PathwayCell Cycle/DNA Damage
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TargetRho
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RecptorRho | Apoptosis | CDK
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Research Area——
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Indication——
Chemical Information
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CAS Number1071098-42-4
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Formula Weight368.43
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Molecular FormulaC22H20N6
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (135.71 mM; Ultrasonic )
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SMILESCc1cc2cc(Nc3ccnc(Nc4ccc5[nH]c(C)cc5c4)n3)ccc2[nH]1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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.?
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