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Diphenpipenol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Diphenpipenol
Clinical data
ATC code
  • None
Identifiers
  • 3-[2-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylethyl]phenol
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC25H28N2O2
Molar mass388.511 g·mol−1
3D model (JSmol)
  • COc4ccccc4N1CCN(CC1)C(Cc2cccc(O)c2)c3ccccc3
  • InChI=1S/C25H28N2O2/c1-29-25-13-6-5-12-23(25)26-14-16-27(17-15-26)24(21-9-3-2-4-10-21)19-20-8-7-11-22(28)18-20/h2-13,18,24,28H,14-17,19H2,1H3
  • Key:ILCZMFSACNEMGK-UHFFFAOYSA-N

Diphenpipenol is anopioidanalgesic drug invented in the 1970s byDainippon Pharmaceutical Co.[1] It is chemically a 1-substituted-4-(1,2-diphenylethyl)piperazine derivative related to compounds such asMT-45 andAD-1211, but diphenpipenol is the most potent compound in the series, with the more active(S) enantiomer being around 105 times the potency ofmorphine in animal studies.[2] This makes it a similar strength tofentanyl and its analogues, and consequently diphenpipenol can be expected to pose a significant risk of producing life-threateningrespiratory depression, as well as other typical opioid side effects such assedation,itching,nausea andvomiting.

Diphenpipenol has been offered for sale online as adesigner drug, though analysis of a sample of supposed diphenpipenol found it to instead contain a structural isomer with much weaker opioid activity, and it is unclear if genuine diphenpipenol has actually been sold.[3]

Alternate isomer sold as diphenpipenol

See also

[edit]

References

[edit]
  1. ^US 4080453, Nishimura H, Uno H, Natsuka, Shimokawa N, Shimizu M, Nakamura H, "1-Substituted-4-(1,2-diphenylethyl)piperazine derivatives and compositions containing the same.", issued 21 March 1978, assigned to Dainippon Pharmaceutical Co Ltd 
  2. ^Natsuka K, Nakamura H, Nishikawa Y, Negoro T, Uno H, Nishimura H (October 1987). "Synthesis and structure-activity relationships of 1-substituted 4-(1,2-diphenylethyl)piperazine derivatives having narcotic agonist and antagonist activity".Journal of Medicinal Chemistry.30 (10):1779–87.doi:10.1021/jm00393a017.PMID 3656354.
  3. ^Cannaert A, Hulpia F, Risseeuw M, Van Uytfanghe K, Deconinck E, Van Calenbergh S, et al. (June 2020). "Report on a new opioid NPS: chemical and in vitro functional characterization of a structural isomer of the MT-45 derivative diphenpipenol".Journal of Analytical Toxicology.45 (2):134–140.doi:10.1093/jat/bkaa066.hdl:1854/LU-8664239.PMID 32514558.
μ-opioid
(MOR)
Agonists
(abridged;
full list)
Antagonists
δ-opioid
(DOR)
Agonists
Antagonists
κ-opioid
(KOR)
Agonists
Antagonists
Nociceptin
(NOP)
Agonists
Antagonists
Others
Phenylpiperazines
Benzylpiperazines
Naphthylpiperazines
Quinolinylpiperazines
Diphenylalkylpiperazines
Pyrimidinylpiperazines
Pyridinylpiperazines
Benzo(iso)thiazolylpiperazines
Tricyclic-linked piperazines
Others/uncategorized
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