1159908-42-5
1159908-42-5
Chemical Structure
N-Arachidonyldopamine-d8
- CAS No.: 1159908-42-5
- Formula:C28H33D8NO3
- Molecular Weight:447.68
IUPAC Name: (5E,8E,11E,14E)-N-(3,4-dihydroxyphenethyl)icosa-5,8,11,14-tetraenamide
InChIKey: MVVPIAAVGAWJNQ-VLPMGVFDSA-N
SMILES: CCCCC/C([2H])=C([2H])/C/C([2H])=C([2H])/C/C([2H])=C([2H])/C/C([2H])=C([2H])/CCCC(NCCC1=CC=C(O)C(O)=C1)=O
Biological Activity: N-Arachidonyldopamine-d8 is the deuterium labeled N-Arachidonyldopamine[1].
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N-Arachidonyldopamine-d8 | N-Arachidonyldopamine-d8 is the deuterium labeled N-Arachidonyldopamine. | |||||||||||||||||||||
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N-Arachidonyldopamine (Standard) | ≥98% | N-Arachidonyldopamine (Standard) is the analytical standard of N-Arachidonyldopamine (HY-110018). This product is intended for research and analytical applications. N-Arachidonyldopamine is a potent and selective endogenous CB1 receptor agonist with a Ki of 250 nM. N-Arachidonyldopamine is also a potent and selective TRPV1 agonist an with EC50 of ~ 50 nM. | ||||||||||||||||||||
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N-Arachidonyldopamine | 98.36% | N-Arachidonyldopamine acts as an Anandamide (HY-10863) membrane transport inhibitor, a selective CB1 cannabinoid receptor agonist, and a VR1 receptor activator. It exhibits an EC50 value of 48 nM for rat VR1 and a Ki value of 0.25 μM for CB1. N-Arachidonyldopamine exists in mammalian neural tissues. It stimulates intracellular Ca2+ mobilization, mediates cannabinoid-like effects, and induces hypothermia, hypomotility, catalepsy, analgesia, and hyperalgesia to heat. N-Arachidonyldopamine possesses anticancer activity against breast cancer. It can be used in research related to breast cancer and heat hyperalgesia. | ||||||||||||||||||||
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