
CAS 105955-11-1: N-Oleoyldopamine
Formula:C26H43NO3
InChI:InChI=1S/C26H43NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-26(30)27-21-20-23-18-19-24(28)25(29)22-23/h9-10,18-19,22,28-29H,2-8,11-17,20-21H2,1H3,(H,27,30)/b10-9-
InChI key:InChIKey=QQBPLXNESPTPNU-KTKRTIGZSA-N
SMILES:C(CNC(CCCCCCC/C=C\CCCCCCCC)=O)C1=CC(O)=C(O)C=C1
Synonyms:- (9Z)-N-[2-(3,4-Dihydroxyphenyl)Ethyl]-9-Octadecenamide
- (9Z)-N-[2-(3,4-dihydroxyphenyl)ethyl]octadec-9-enamide
- 9-Octadecenamide, N-[2-(3,4-dihydroxyphenyl)ethyl]-, (9Z)-
- 9-Octadecenamide, N-[2-(3,4-dihydroxyphenyl)ethyl]-, (Z)-
- N-Oleoyldopamine
- N-[2-(3,4-Dihydroxyphenyl)Ethyl]9Z-Octadecenamide
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N-Oleoyldopamine
CAS:N-Oleoyldopamine is a lipid mediator that is known to affect the function of many cell types. N-Oleoyldopamine has been shown to have an anti-inflammatory effect by inhibiting the release of pro-inflammatory cytokines and chemokines, which are molecules involved in immune responses. It has also been found to have a protective effect on chronic arthritis and neuropathic pain. Studies have shown that N-oleoyldopamine can bind with dopamine receptors, resulting in increased locomotor activity, as well as binding with Trpv1 receptors, which are responsible for pain sensation. In vitro assays have shown that N-oleoyldopamine inhibits the production of inflammatory signals from cells such as wild type strains and neurokinin 1 receptor (NK1R). N-Oleoyldopamine also affects brain functions such as learning and memory by influencing neurotransmitters such as acetylcholine. It also influences metabolic disorders byFormula:C26H43NO3Purity:Min. 95%Molecular weight:417.62 g/molRef: 3D-FO137605
Discontinued product