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N2,N4-bis(2-methyl-1H-indol-5-yl)pyrimidine-2,4-diamine

Basic information Safety Supplier Related

N2,N4-bis(2-methyl-1H-indol-5-yl)pyrimidine-2,4-diamine Basic information

Product Name:
N2,N4-bis(2-methyl-1H-indol-5-yl)pyrimidine-2,4-diamine
Synonyms:
  • N2,N4-bis(2-methyl-1H-indol-5-yl)pyrimidine-2,4-diamine
  • N2,N?-bis(2-Methyl-1H-indol-5-yl)pyrimidine-2,4-diamine
  • 2,4-Pyrimidinediamine, N2,N4-bis(2-methyl-1H-indol-5-yl)-
  • 2-N,4-N-bis(2-methyl-1H-indol-5-yl)pyrimidine-2,4-diamine
  • AZA1, 10 mM in DMSO
  • Cdc42/Rac1 Dual Inhibitor, AZA1
  • AZA1 (Synonyms: Rac1/Cdc42-IN-1)
  • AZA1(Rac1/Cdc42-IN-1)
CAS:
1071098-42-4
MF:
C22H20N6
MW:
368.43
Mol File:
1071098-42-4.mol
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N2,N4-bis(2-methyl-1H-indol-5-yl)pyrimidine-2,4-diamine Chemical Properties

Boiling point:
711.0±70.0 °C(Predicted)
Density 
1.388±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO: 100mg/mL
form 
Solid
pka
17.48±0.30(Predicted)
color 
Light brown to brown
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N2,N4-bis(2-methyl-1H-indol-5-yl)pyrimidine-2,4-diamine Usage And Synthesis

Description

AZA1 is a Rac1/Cdc42 GTPase-specific inhibitor which suppresses prostate cancer.

Uses

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[1][2].

in vivo

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[1].

Animal Model:5 week-old athymic nu/nu (nude) mice (bearing 22Rv1 prostate cancer cell xenografts)[1]
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.

References

[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. DOI:10.1371/journal.pone.0074924
[2] Suzuki O, et al. Sialylation and glycosylation modulate cell adhesion and invasion to extracellular matrix in human malignant lymphoma: Dependency on integrin and the Rho GTPase family. Int J Oncol. 2015;47(6):2091‐2099. DOI:10.3892/ijo.2015.3211

N2,N4-bis(2-methyl-1H-indol-5-yl)pyrimidine-2,4-diamineSupplier

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N2,N4-bis(2-methyl-1H-indol-5-yl)pyrimidine-2,4-diamine(1071098-42-4)Related Product Information