ChemicalBook--->CAS DataBase List--->2097938-73-1

2097938-73-1

2097938-73-1 Structure

2097938-73-1 Structure
IdentificationBack Directory
[Name]

MBQ-167
[CAS]

2097938-73-1
[Synonyms]

MBQ-167
MBQ 167;MBQ167
9-Ethyl-3-(5-phenyl-1H-1,2,3-triazol-1-yl)-9H-carbazole
9H-Carbazole, 9-ethyl-3-(5-phenyl-1H-1,2,3-triazol-1-yl)-
Cyclin dependent kinase,MBQ-167,MBQ167,MBQ 167,Inhibitor,inhibit,CDK,Ras
[Molecular Formula]

C22H18N4
[MOL File]

2097938-73-1.mol
[Molecular Weight]

338.41
Chemical PropertiesBack Directory
[Boiling point ]

531.8±60.0 °C(Predicted)
[density ]

1.23±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[solubility ]

DMSO: Soluble
[form ]

A solid
[pka]

-0.06±0.70(Predicted)
[color ]

Light yellow to yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Uses]

MBQ-167 is a dual Rac/Cdc42 inhibitor, with IC50s of 103 nM for Rac 1/2/3 and 78 nM for Cdc42 in MDA-MB-231 cells, respectively.
[in vivo]

MBQ-167-treated mice demonstrate a statistically significant reduction in tumor growth. At sacrifice, 1.0 mg/kg BW of MBQ-167 results in a ~80% reduction in tumor growth, and the 10 mg/kg BW MBQ-167 treatment results in ~95% reduction in tumor growth. Since EHop-016 only exerts ~40% reduction of tumor growth at 10 mg/kg BW, MBQ-167 is 10X more effective than EHop-016. MBQ-167 treated mice demonstrate similar doubling times for both treatments (10 and 11 days)[1].

[IC 50]

Cdc42: 78 nM (IC50); Ras 1/2/3: 103 nM (IC50)
[References]

[1] Humphries-Bickley T, et al. Characterization of a Dual Rac/Cdc42 Inhibitor MBQ-167 in Metastatic Cancer. Mol Cancer Ther. 2017 May;16(5):805-818. DOI:10.1158/1535-7163.MCT-16-0442
Spectrum DetailBack Directory
[Spectrum Detail]

MBQ-167(2097938-73-1)1HNMR
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