(E)-3-Benzo[1,3]dioxol-5-yl-N,N-diphenyl-2-propenamide
(E)-3-Benzodioxol-5-yl-N,N-diphenyl-2-propenamide is a chemically synthesized flavoring substance and can be found in toothpaste products. (E)-3-Benzodioxol-5-yl-N,N-diphenyl-2-propenamide is non-genotoxic, shows no genotoxic activity in bacterial reverse mutation and in vitro mammalian cell micronucleus assays. (E)-3-Benzodioxol-5-yl-N,N-diphenyl-2-propenamide does not induce prenatal developmental toxicity in rats.
For research use only. We do not sell to patients.
- CAS No.: 1309389-73-8
- Formula: C22H17NO3
- Molecular Weight:343.38
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
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TRPM8 |
In Vitro
(E)-3-Benzo[1,3]dioxol-5-yl-N,N-diphenyl-2-propenamide (22-5500 μg/plate) does not exhibit mutagenic activity in the bacterial reverse mutation assay across Salmonella Typhimurium and Escherichia coli strains[1].
(E)-3-Benzo[1,3]dioxol-5-yl-N,N-diphenyl-2-propenamide (2-100 μg/mL, 3-24 h) does not induce clastogenicity or aneugenicity in human peripheral blood lymphocytes in the in vitro micronucleus test[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
In Vivo
(E)-3-Benzo[1,3]dioxol-5-yl-N,N-diphenyl-2-propenamide (10-1000 mg/kg bw per day; oral, dietary; daily; 14 days) is well tolerated by rats at doses up to 1000 mg/kg bw per day for 14 days[1].
(E)-3-Benzo[1,3]dioxol-5-yl-N,N-diphenyl-2-propenamide (125-1000 mg/kg bw per day; oral, gavage; daily; 15 days) does not induce prenatal developmental toxicity in rats at doses up to 1000 mg/kg bw per day[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:CRL Sprague-Dawley CD® IGS rats (pregnant females)[1]
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Dosage:125, 250, 500, 1000 mg/kg bw per day
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Administration:Oral, gavage; daily; 15 days (gestation days 5-19)
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Result:Reported no mortality, treatment-related effects on body weight, uterine/reproductive parameters, or fetal visceral/skeletal malformations/developmental variations.
Noted incidental clinical signs (alopecia, nose lesion) in some animals that were not treatment-related.
Chemical Information
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CAS No. 1309389-73-8
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Molecular Weight 343.38
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Formula C22H17NO3
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SMILES
O=C(N(C1=CC=CC=C1)C2=CC=CC=C2)/C=C/C3=CC=C(OCO4)C4=C3
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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Reproductive and Developmental Toxicity Study
Reproductive and developmental toxicity studies detect adverse effects of prenatal or peri/postnatal exposure on maternal condition, pregnancy maintenance, embryo-fetal survival, fetal growth, structural development, and offspring reproductive or developmental endpoints; classic rat protocols generate readouts by comparing treated groups with vehicle, pair-fed, or untreated controls for implantation, resorption, fetal weight, crown-rump length, external morphology, visceral morphology, skeletal ossification, anogenital distance, nipple/areola retention, and postnatal cohort outcomes.
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Genotoxicity/Mutagenicity Study
The bacterial reverse mutation assay detects point mutations that restore amino-acid prototrophy in auxotrophic Salmonella typhimurium or Escherichia coli tester strains; after exposure to a test article, mutagenic activity is read out as an increased number of revertant colonies on minimal agar compared with the vehicle control. The assay uses tester strains with different mutation targets so that base-substitution and frameshift mutagens can be detected, and testing is performed with and without exogenous mammalian metabolic activation because some chemicals require biotransformation to become mutagenic.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)