2494-12-4
2494-12-4
Chemical Structure
N-acetyldopamine
Synonym(s): NADA
- CAS No.: 2494-12-4
- Formula:C10H13NO3
- Molecular Weight:195.22
IUPAC Name: N-(3,4-dihydroxyphenethyl)acetamide
InChIKey: OFSAJYZMIPNPHE-UHFFFAOYSA-N
SMILES: CC(NCCC1=CC=C(O)C(O)=C1)=O
Biological Activity: N-acetyldopamine is a sepiapterin reductase inhibitor. N-acetyldopamine is a catecholamine that is used by insects as sclerotizing precursors to harden their cuticle. N-acetyldopamine can attenuate LPS-stimulated TNF-α production and superoxide production in THP-1 cells[1][2].
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N-acetyldopamine | 99.36% | N-acetyldopamine is a sepiapterin reductase inhibitor. N-acetyldopamine is a catecholamine that is used by insects as sclerotizing precursors to harden their cuticle. N-acetyldopamine can attenuate LPS-stimulated TNF-α production and superoxide production in THP-1 cells. | ||||||||||||||||||||
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N-acetyldopamine (Standard) | 99.80% | N-acetyldopamine is a sepiapterin reductase inhibitor. N-acetyldopamine is a catecholamine that is used by insects as sclerotizing precursors to harden their cuticle. N-acetyldopamine can attenuate LPS-stimulated TNF-α production and superoxide production in THP-1 cells. | ||||||||||||||||||||
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References
- [1]. Hanine Barek, et al. Unraveling Complex Molecular Transformations of N-β-alanyldopamine That Account for Brown Coloration of Insect Cuticle. Rapid Commun Mass Spectrom. 2017 Aug 30;31(16):1363-1373. [Content Brief]
- [2]. Perianayagam, M. C., et al., (2005). Immune-modulating effects of melatonin, N-acetylserotonin, and N-acetyldopamine. Annals of the New York Academy of Sciences, 1053, 386–393. [Content Brief]
