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tri-tert-butyl 2,2’,2”-(10-(2-((4-aminobutyl)amino)-2-oxoethyl)-1,4,7,10-tetraazacyclododecan-1,4,7-triyl)triacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1402393-59-2

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1402393-59-2 Usage

Uses

4-Aminobutyl-DOTA-tris (t-butyl ester), is a bifunctional chelator.

Check Digit Verification of cas no

The CAS Registry Mumber 1402393-59-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,3,9 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1402393-59:
(9*1)+(8*4)+(7*0)+(6*2)+(5*3)+(4*9)+(3*3)+(2*5)+(1*9)=132
132 % 10 = 2
So 1402393-59-2 is a valid CAS Registry Number.

1402393-59-2Downstream Products

1402393-59-2Relevant academic research and scientific papers

Synthesis and characterization of a hypoxia-sensitive MRI probe

Rojas-Quijano, Federico A.,Tircs?, Gyula,Tircs?né Beny?, Enikó,Baranyai, Zsolt,Tran Hoang, Huan,Kálmán, Ferenc K.,Gulaka, Praveen K.,Kodibagkar, Vikram D.,Aime, Silvio,Kovács, Zoltán,Sherry, A. Dean

, p. 9669 - 9676 (2012)

Tissue hypoxia occurs in pathologic conditions, such as cancer, ischemic heart disease and stroke when oxygen demand is greater than oxygen supply. An imaging method that can differentiate hypoxic versus normoxic tissue could have an immediate impact on therapy choices. In this work, the gadolinium(III) complex of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) with a 2-nitroimidazole attached to one carboxyl group via an amide linkage was prepared, characterized and tested as a hypoxia-sensitive MRI agent. A control complex, Gd(DO3A-monobutylamide), was also prepared in order to test whether the nitroimidazole side-chain alters either the water proton T1 relaxivity or the thermodynamic stability of the complex. The stabilities of these complexes were lower than that of Gd(DOTA)- as expected for mono-amide derivatives. The water proton T1 relaxivity (r 1), bound water residence lifetime (τM) and rotational correlation time (τR) of both complexes was determined by relaxivity measurements, variable temperature 17O NMR spectroscopy and proton nuclear magnetic relaxation dispersion (NMRD) studies. The resulting parameters (r1=6.38 mM-1 s-1 at 20 MHz, τM=0.71 μs, τR=141 ps) determined for the nitroimidazole derivative closely parallel to those of other Gd(DO3A-monoamide) complexes of similar molecular size. In vitro MR imaging experiments with 9L rat glioma cells maintained under nitrogen (hypoxic) versus oxygen (normoxic) gas showed that both agents enter cells but only the nitroimidazole derivative was trapped in cells maintained under N2 as evidenced by an approximately twofold decrease in T1 measured for hypoxic cells versus normoxic cells exposed to this agent. These results suggest that the nitroimidazole derivative might serve as a molecular reporter for discriminating hypoxic versus normoxic tissues by MRI. Hunting hypoxic cells: The DO3A-monoamide ligand with a 2-nitroimidazole moiety was synthesized with an aim to complex the Gd III ion as well as to target and visualize hypoxic cells by using the MRI technique (see figure). In vitro MRI experiments revealed that the conjugate might be suitable for assessment of hypoxia in vivo as the agent was selectively trapped in hypoxic (9L rat glioma) cells. Copyright

RADIODRUG FOR DIAGNOSTIC/THERAPEUTIC USE IN NUCLEAR MEDICINE AND RADIO-GUIDED MEDICINE

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Page/Page column 24; 26, (2020/07/25)

Radio-drug suitable for performing radio-guided surgery, imaging diagnostics, radio-metabolic therapy.

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