501-13-3
501-13-3
Chemical Structure
Feruloylputrescine
- CAS No.: 501-13-3
- Formula:C14H20N2O3
- Molecular Weight:264.32
IUPAC Name: (E)-N-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)acrylamide
InChIKey: SFUVCMKSYKHYLD-FNORWQNLSA-N
SMILES: COC1=C(O)C=CC(C=CC(NCCCCN)=O)=C1
Biological Activity: Feruloylputrescine is an oral active phenolamide found in citrus plants and formed through the decarboxylation of L-Arginine. Feruloylputrescine inhibits monooxygenase (cntA) and reductase (cntB) and trimethylamine production. Feruloylputrescine can be used for cardiovascular diseases research[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Feruloylputrescine | 99.68% | Feruloylputrescine is an oral active phenolamide found in citrus plants and formed through the decarboxylation of L-Arginine. Feruloylputrescine inhibits monooxygenase (cntA) and reductase (cntB) and trimethylamine production. Feruloylputrescine can be used for cardiovascular diseases research. | ||||||||||||||||||||
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Feruloylputrescine (Standard) | ≥98% | Feruloylputrescine is an oral active phenolamide found in citrus plants and formed through the decarboxylation of L-Arginine. Feruloylputrescine inhibits monooxygenase (cntA) and reductase (cntB) and trimethylamine production. Feruloylputrescine can be used for cardiovascular diseases research. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 1.00
HY-W707850N-trans-Feruloylputrescine -
Similarity Score 0.87
HY-N6085N-Caffeoylputrescine,(E)- -
Similarity Score 0.80
HY-180756p-Coumaroylputrescine -
Similarity Score 0.75
![(E)-[6]-Dehydroparadol Chemical Structure](//file.medchemexpress.com/product_pic/hy-77293.gif)
HY-77293(E)-[6]-Dehydroparadol -
Similarity Score 0.74
HY-N71526-Dehydrogingerdione -
Similarity Score 0.74
HY-N0061Ethyl ferulate -
Similarity Score 0.74
HY-W590845Ethyl (E)-ferulate -
Similarity Score 0.73
HY-N11021Feruloyl tyramine -
Similarity Score 0.73
HY-N2410N-trans-Feruloyltyramine -
Explore the MedChemAI to find more analogs
![(E)-[6]-Dehydroparadol Chemical Structure](http://file.medchemexpress.com/product_pic/hy-77293.gif)
References
- [1]. Hana Lee, et al. Discovery of a Novel Bioactive Compound in Orange Peel Polar Fraction on the Inhibition of Trimethylamine and Trimethylamine N-Oxide through Metabolomics Approaches and In Vitro and In Vivo Assays: Feruloylputrescine Inhibits Trimethylamine via Suppressing cntA/B Enzyme. J Agric Food Chem. 2024 Apr 10;72(14):7870-7881. [Content Brief]
