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Nadoxolol

From Wikipedia, the free encyclopedia
Nadoxolol
Names
IUPAC name
N,3-Dihydroxy-4-naphthalen-1-yloxybutanimidamide
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 252-825-2
MeSHC006154
UNII
  • InChI=1S/C14H16N2O3/c15-14(16-18)8-11(17)9-19-13-7-3-5-10-4-1-2-6-12(10)13/h1-7,11,17-18H,8-9H2,(H2,15,16)
    Key: UPZVYDSBLFNMLK-UHFFFAOYSA-N
  • InChI=1/C14H16N2O3/c15-14(16-18)8-11(17)9-19-13-7-3-5-10-4-1-2-6-12(10)13/h1-7,11,17-18H,8-9H2,(H2,15,16)
    Key: UPZVYDSBLFNMLK-UHFFFAOYAW
  • C1=CC=C2C(=C1)C=CC=C2OCC(C/C(=N/O)/N)O
Properties
C14H16N2O3
Molar mass260.293 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Nadoxolol is anantiarrhythmic agent (i.e., a drug for the treatment of irregular heartbeat),[1] chemically related in structure tobeta-adrenergic receptor blocker drugs such aspropranolol.[2]

It does not appear to be marketed anywhere in the world.

References

[edit]
  1. ^Warembourg, H; Ducloux, G (1976). "Clinical study of a new anti-arrhythmia agent: nadoxolol".Lille Med.21 (4):386–8.PMID 957857.
  2. ^Kapoor, M; Anand, N; Koul, S; Chimni, SS; Manhas, KS; Raina, C; Parshad, R; Taneja, SC; Qazi, GN (2003). "Kinetic resolution of 1-chloro-3-(1-naphthyloxy)-2-propanol, an intermediate in the synthesis of beta-adrenergic receptor blockers".Bioorganic Chemistry.31 (3):259–69.doi:10.1016/s0045-2068(03)00050-6.PMID 12818235.
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
Channel blockers
class I
(Na+ channel blockers)
class Ia (Phase 0→ andPhase 3→)
class Ib (Phase 3←)
class Ic (Phase 0→)
class III
(Phase 3→,K+ channel blockers)
class IV
(Phase 4→,Ca2+ channel blockers)
Receptoragonists
andantagonists
class II
(Phase 4→,β blockers)
A1 agonist
M2
α receptors
Ion transporters
Na+/ K+-ATPase
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