ADRIANA

Pharmaceutical compound From Wikipedia, the free encyclopedia

ADRIANA is a selective α2B-adrenergic receptor antagonist.[1] It is described as highly selective over the α2A- and α2C-adrenergic receptors.[1] The drug stimulates norepinephrine release in the spinal dorsal horn and has potent analgesic effects in rodents and non-human primates.[1] It is orally active.[1] ADRIANA was first described in the scientific 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]

ATC code
  • None
Quick facts Clinical data, Routes ofadministration ...
ADRIANA
Clinical data
Routes of
administration
Oral[1]
Drug classSelective α2B-adrenergic receptor antagonist; Analgesic
ATC code
  • None
Identifiers
  • (1Z)-1-(3-ethyl-5-fluoro-1,3-benzothiazol-2-ylidene)propan-2-one
CAS Number
PubChem CID
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
Close

See also

References

Related Articles

Wikiwand AI