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[ CAS No. 101-61-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 101-61-1
Chemical Structure| 101-61-1
Structure of 101-61-1 * Storage: {[proInfo.prStorage]}

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Product Citations

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Boyao Zhang ; George-Eugen Maftei ; Bartosz Bartmanski , et al. DOI:

Abstract: Organic carcinogens, in particular DNA-reactive compounds, contribute to the irreversible initiation step of tumorigenesis through introduction of genomic instability. Although carcinogen bioactivation and detoxification by human enzymes has been extensively studied, carcinogen biotransformation by human-associated bacteria, the microbiota, has not yet been systematically investigated. We tested the biotransformation of 68 mutagenic carcinogens by 34 bacterial species representative for the upper and lower human gastrointestinal tract and found that the majority (41) of the tested carcinogens undergo bacterial biotransformation. To assess the functional consequences of microbial carcinogen metabolism, we developed a pipeline to couple gut bacterial carcinogen biotransformation assays with Ames mutagenicity testing and liver biotransformation experiments. This revealed a bidirectional crosstalk between gut microbiota and host carcinogen metabolism, which we validated in gnotobiotic mouse models. Overall, the systematic assessment of gut microbiota carcinogen biotransformation and its interplay with host metabolism highlights the gut microbiome as an important modulator of exposome-induced tumorigenesis.

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Product Details of [ 101-61-1 ]

CAS No. :101-61-1 MDL No. :MFCD00008317
Formula : C17H22N2 Boiling Point : -
Linear Structure Formula :((CH3)2N)2C(C6H5)2 InChI Key :JNRLEMMIVRBKJE-UHFFFAOYSA-N
M.W : 254.37 Pubchem ID :7567
Synonyms :

Safety of [ 101-61-1 ]

Signal Word:Danger Class:9
Precautionary Statements:P201-P273-P308+P313 UN#:3077
Hazard Statements:H350-H410 Packing Group:Ⅲ
GHS Pictogram:

Application In Synthesis of [ 101-61-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 101-61-1 ]

[ 101-61-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 121-69-7 ]
  • [ 366-29-0 ]
  • [ 403-46-3 ]
  • [ 393-56-6 ]
  • [ 556-21-8 ]
  • [ 101-61-1 ]
  • [ 100-10-7 ]
YieldReaction ConditionsOperation in experiment
With N-fluorobis(benzenesulfon)imide; In chloroform; at 25℃; for 10.0h; General procedure: To a solution of amine (0.1mmol) in 3mL of CHCl3 the corresponding amount of NFSI in 2mL of the same solvent was added. The reaction mass was stirred at selected temperature during the time indicated in Table 1. The resulting solution was washed with water (2×15mL), dried over Na2SO4 and evaporated to dryness. The residue was analyzed either by GC/MS or separated by column chromatography.
  • 2
  • [ 121-69-7 ]
  • [ 366-29-0 ]
  • [ 403-46-3 ]
  • [ 393-56-6 ]
  • [ 698-01-1 ]
  • [ 556-21-8 ]
  • [ 101-61-1 ]
  • [ 100-10-7 ]
  • [ 98-09-9 ]
YieldReaction ConditionsOperation in experiment
6% With zirconium(IV) chloride; N-fluorobis(benzenesulfon)imide; In chloroform; for 5.0h;Reflux; General procedure: To a solution of amine (0.1mmol) in 3mL of CHCl3 the corresponding amount of NFSI in 2mL of the same solvent was added. The reaction mass was stirred at selected temperature during the time indicated in Table 1. The resulting solution was washed with water (2×15mL), dried over Na2SO4 and evaporated to dryness. The residue was analyzed either by GC/MS or separated by column chromatography.
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