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Chemical Structure| 3817-11-6 Chemical Structure| 3817-11-6
Chemical Structure| 3817-11-6

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BBN is a model compound that can induce high-level invasive tumors in the bladder.

Synonyms: N-Butyl-N-(4-hydroxybutyl)nitrosamine

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

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Product Citations

Product Citations

Boyao Zhang ; George-Eugen Maftei ; Bartosz Bartmanski ; Michael Zimmermann ;

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 BBN

CAS No. :3817-11-6
Formula : C8H18N2O2
M.W : 174.24
SMILES Code : O=NN(CCCCO)CCCC
Synonyms :
N-Butyl-N-(4-hydroxybutyl)nitrosamine
English Name :1-Butanol, 4-(butylnitrosoamino)-
MDL No. :MFCD00059008
InChI Key :DIKPQFXYECAYPC-UHFFFAOYSA-N
Pubchem ID :19665

Safety of BBN

Application In Synthesis of BBN

* 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 [ 3817-11-6 ]

[ 3817-11-6 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 4543-95-7 ]
  • [ 3817-11-6 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; sodium nitrite
  • 2
  • [ 3817-11-6 ]
  • [ 38252-74-3 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide; potassium permanganate
  • 3
  • [ 3817-11-6 ]
  • [ 70625-89-7 ]
YieldReaction ConditionsOperation in experiment
With Py*HClCrO3 In dichloromethane
With pyridine; dicyclohexyl-carbodiimide; trifluoroacetic acid In dimethyl sulfoxide; benzene
  • 4
  • [ 928-51-8 ]
  • [ 109-73-9 ]
  • [ 3817-11-6 ]
YieldReaction ConditionsOperation in experiment
(i), (ii) NaNO2, aq. HCl; Multistep reaction;
  • 5
  • [ 3817-11-6 ]
  • [ 70103-66-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: aq. KOH, KMnO4 2: (i) aq. NaOH, (ii) /BRN= 607604/, aq. HCl
  • 6
  • [ 3817-11-6 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With diisobutylaluminium hydride In tetrahydrofuran; hexane at 22℃; Sealed tube; Inert atmosphere;
  • 7
  • [ 3817-11-6 ]
  • [ 4543-95-7 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With sodium sulfate; sodium hydroxide In ethanol; water at 50℃; Sealed tube;
  • 8
  • [ 3817-11-6 ]
  • [ 4543-95-7 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride In ethanol at 50℃; Sealed tube;
 

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