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6-Br-APB

From Wikipedia, the free encyclopedia
Chemical compound
This article is about the dopamine D1 receptor agonist. For the amphetamine derivative, see6-APB.
Pharmaceutical compound
6-Br-APB
Clinical data
Drug classDopamineD1 receptoragonist;Stimulant
ATC code
  • None
Identifiers
  • 3-allyl-6-bromo-1-phenyl-1,2,4,5-tetrahydro-3-benzazepine-7,8-diol
CAS Number
PubChemCID
ChemSpider
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC19H20BrNO2
Molar mass374.278 g·mol−1
3D model (JSmol)
  • c3ccccc3C2CN(CC=C)CCc(c1Br)c2cc(O)c1O
  • InChI=1S/C19H20BrNO2/c1-2-9-21-10-8-14-15(11-17(22)19(23)18(14)20)16(12-21)13-6-4-3-5-7-13/h2-7,11,16,22-23H,1,8-10,12H2/t16-/m1/s1 checkY
  • Key:KKZGFVAZUKHFAC-MRXNPFEDSA-N checkY
 ☒NcheckY (what is this?)  (verify)

6-Br-APB is asynthetic andselectivedopamineD1 receptoragonist andstimulant-likedrug of the3-benzazepine family.[1] It is acyclized phenethylamine andmodifiedderivative of themonoamine neurotransmitterdopamine.[2] The (R)-enantiomer is apotent dopamine D1 receptorfull agonist, while the (S) enantiomer retains selectivity but is a weakpartial agonist of the receptor.[3] (R)-6-Br-APB and similar dopamine D1 receptor-selective full agonists likeSKF-81,297 andSKF-82,958 produce characteristicanorectic effects,stereotyped behaviour, andself-administration in animals, with a similar but not identical profile to that of dopaminergic stimulants such asamphetamine.[4][5][6]

See also

[edit]

References

[edit]
  1. ^Neumeyer JL, et al. (December 1991). "(+/-)-3-Allyl-6-bromo-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3- benzazepin, a new high-affinity D1 dopamine receptor ligand: synthesis and structure-activity relationship".Journal of Medicinal Chemistry.34 (12):3366–71.doi:10.1021/jm00116a004.PMID 1684995.
  2. ^Felsing DE, Jain MK, Allen JA (2019). "Advances in Dopamine D1 Receptor Ligands for Neurotherapeutics".Curr Top Med Chem.19 (16):1365–1380.doi:10.2174/1568026619666190712210903.PMID 31553283.
  3. ^Neumeyer JL, Kula NS, Baldessarini RJ, Baindur N (April 1992). "Stereoisomeric probes for the D1 dopamine receptor: synthesis and characterization of R-(+) and S-(-) enantiomers of 3-allyl-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine and its 6-bromo analogue".Journal of Medicinal Chemistry.35 (8):1466–71.doi:10.1021/jm00086a016.PMID 1533424.
  4. ^Rosenzweig-Lipson S, Hesterberg P, Bergman J (September 1994). "Observational studies of dopamine D1 and D2 agonists in squirrel monkeys".Psychopharmacology.116 (1):9–18.doi:10.1007/BF02244865.PMID 7862937.S2CID 24204026.
  5. ^Weed MR, Woolverton WL (December 1995). "The reinforcing effects of dopamine D1 receptor agonists in rhesus monkeys".The Journal of Pharmacology and Experimental Therapeutics.275 (3):1367–74.PMID 8531104.
  6. ^Barrett AC, Miller JR, Dohrmann JM, Caine SB (2004). "Effects of dopamine indirect agonists and selective D1-like and D2-like agonists and antagonists on cocaine self-administration and food maintained responding in rats".Neuropharmacology.47 (Suppl 1):256–73.doi:10.1016/j.neuropharm.2004.07.007.PMID 15464142.S2CID 2959198.

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