Eticlopride

Eticlopride is a topic that has captured the attention of many people throughout history. Since its discovery, it has aroused the interest of researchers, scientists, and the general public. In this article, we will explore the different facets of Eticlopride, its impact on society, its relevance today, and its role in the future. From its influence on popular culture to its importance in science and technology, Eticlopride has left an indelible mark on the world around us. Through a comprehensive analysis, we will try to shed light on this fascinating topic and its implications in our daily lives.

Eticlopride
Clinical data
ATC code
  • none
Identifiers
  • 5-chloro-3-ethyl-N-methyl]-2-hydroxy-6-methoxybenzamide
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC17H25ClN2O3
Molar mass340.85 g·mol−1
3D model (JSmol)
  • CCC1=CC(=C(C(=C1O)C(=O)NCC2CCCN2CC)OC)Cl
 ☒NcheckY (what is this?)  (verify)

Eticlopride is a selective dopamine antagonist that acts on D2 dopamine receptor. It is primarily used in pharmacological research.[1][2][3][4]

References

  1. ^ "Eticlopride hydrochloride". Abcam.
  2. ^ Claytor R, Lile JA, Nader MA (March 2006). "The effects of eticlopride and the selective D3-antagonist PNU 99194-A on food- and cocaine-maintained responding in rhesus monkeys". Pharmacology, Biochemistry, and Behavior. 83 (3): 456–64. doi:10.1016/j.pbb.2006.03.007. PMID 16631246. S2CID 39482275.
  3. ^ Hemby SE, Smith JE, Dworkin SI (June 1996). "The effects of eticlopride and naltrexone on responding maintained by food, cocaine, heroin and cocaine/heroin combinations in rats". The Journal of Pharmacology and Experimental Therapeutics. 277 (3): 1247–58. doi:10.1016/S0022-3565(25)13070-X. PMID 8667185.
  4. ^ Haile CN, Kosten TA (November 2001). "Differential effects of D1- and D2-like compounds on cocaine self-administration in Lewis and Fischer 344 inbred rats". The Journal of Pharmacology and Experimental Therapeutics. 299 (2): 509–18. doi:10.1016/S0022-3565(24)29257-0. PMID 11602661.
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