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ADRIANA

From Wikipedia, the free encyclopedia

Pharmaceutical compound
ADRIANA
Clinical data
Routes of
administration
Oral[1]
Drug classSelectiveα2B-adrenergic receptorantagonist;Analgesic
ATC code
  • None
Identifiers
  • (1Z)-1-(3-ethyl-5-fluoro-1,3-benzothiazol-2-ylidene)propan-2-one
CAS Number
PubChemCID
ChemSpider
Chemical and physical data
FormulaC12H12FNOS
Molar mass237.29 g·mol−1
3D model (JSmol)
  • CCN\1C2=C(C=CC(=C2)F)S/C1=C\C(=O)C
  • InChI=1S/C12H12FNOS/c1-3-14-10-7-9(13)4-5-11(10)16-12(14)6-8(2)15/h4-7H,3H2,1-2H3/b12-6-
  • Key:KZNPXNKNIBBYSS-SDQBBNPISA-N

ADRIANA is aselectiveα2B-adrenergic receptorantagonist.[1] It is described as highly selective over theα2A- andα2C-adrenergic receptors.[1] The drug stimulatesnorepinephrine release in the spinaldorsal horn and haspotentanalgesic effects in rodents and non-human primates.[1] It isorally active.[1] ADRIANA was first described in thescientific literature by Masayasu Toyomoto and colleagues in 2025.[1] It is said to be the first selective α2B-adrenergic receptor antagonist to have been developed.[1]

See also

[edit]

References

[edit]
  1. ^abcdefgToyomoto M, Kurihara T, Nakagawa T, Inoue A, Kimura R, Kii I, et al. (August 2025). "Discovery and development of an oral analgesic targeting the α2B adrenoceptor".Proceedings of the National Academy of Sciences of the United States of America.122 (32) e2500006122.Bibcode:2025PNAS..12200006T.doi:10.1073/pnas.2500006122.PMC 12358833.PMID 40773228.
α1
Agonists
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Agonists
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Agonists
Antagonists
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