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Ro48-8684

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Ro48-8684
Identifiers
  • 3-(5-dipropylaminomethyloxazol-2-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one
CAS Number
PubChemCID
ChemSpider
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC22H26FN5O2
Molar mass411.481 g·mol−1
3D model (JSmol)
  • CCCN(CC1=CN=C(C2=C(CN(C(C3=C4C=CC(F)=C3)=O)C)N4C=N2)O1)CCC
  • InChI=1S/C22H26FN5O2/c1-4-8-27(9-5-2)12-16-11-24-21(30-16)20-19-13-26(3)22(29)17-10-15(23)6-7-18(17)28(19)14-25-20/h6-7,10-11,14H,4-5,8-9,12-13H2,1-3H3
  • Key:YKKLHEHNUYCLQQ-UHFFFAOYSA-N
  (verify)

Ro48-8684 is a water-solublebenzodiazepine derivative developed byHoffman-LaRoche in the 1990s, which was designed along withRo48-6791 as an improved replacement formidazolam, but ultimately proved to have little advantages over the parent drug and has not been introduced into clinical practice.[1][2]

See also

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References

[edit]
  1. ^van Gerven JM, Roncari G, Schoemaker RC, Massarella J, Keesmaat P, Kooyman H, et al. (November 1997)."Integrated pharmacokinetics and pharmacodynamics of Ro 48-8684, a new benzodiazepine, in comparison with midazolam during first administration to healthy male subjects".British Journal of Clinical Pharmacology.44 (5):487–93.doi:10.1046/j.1365-2125.1997.t01-1-00613.x.PMC 2042863.PMID 9384466.
  2. ^Albrecht S, Hering W, Ihmsen H, Schwilden H, Schüttler J (October 1999). "[Pharmacokinetic-pharmacodynamic modeling in phase II of drug development. A comparative study with young and old volunteers with benzdiazepine as an example]".Anästhesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie.34 (10):634–7.doi:10.1055/s-1999-213.PMID 10548960.
1,4-Benzodiazepines
1,5-Benzodiazepines
2,3-Benzodiazepines*
Triazolobenzodiazepines
Imidazobenzodiazepines
Oxazolobenzodiazepines
Thienodiazepines
Thienotriazolodiazepines
Thienobenzodiazepines*
Pyridodiazepines
Pyridotriazolodiazepines
Pyrazolodiazepines
Pyrrolodiazepines
Tetrahydroisoquinobenzodiazepines
Pyrrolobenzodiazepines*
Benzodiazepine prodrugs
* atypical activity profile (notGABAA receptor ligands)
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Flavonoids
Imidazoles
Kava constituents
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted


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