ChemicalBook--->CAS DataBase List--->1071098-42-4

1071098-42-4

1071098-42-4 Structure

1071098-42-4 Structure
IdentificationBack Directory
[Name]

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

1071098-42-4
[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
[Molecular Formula]

C22H20N6
[MOL File]

1071098-42-4.mol
[Molecular Weight]

368.43
Chemical PropertiesBack Directory
[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
[InChI]

1S/C22H20N6/c1-13-9-15-11-17(3-5-19(15)24-13)26-21-7-8-23-22(28-21)27-18-4-6-20-16(12-18)10-14(2)25-20/h3-12,24-25H,1-2H3,(H2,23,26,27,28)
[InChIKey]

SYWHWWKOIJCMKF-UHFFFAOYSA-N
[SMILES]

CC1=CC2=C(N1)C=CC(=C2)NC3=NC(=NC=C3)NC4=CC5=C(C=C4)NC(=C5)C
Safety DataBack Directory
[WGK Germany ]

WGK 2
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[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
Spectrum DetailBack Directory
[Spectrum Detail]

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