Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ralph L. White"'
Publikováno v:
Journal of Pharmaceutical Sciences. 69:327-331
A series of quaternary ammonium salts of dantrolene and clodanolene was prepared and evaluated for skeletal muscle relaxant activity. The quaternary ammonium salts exhibit greater aqueous solubility and, therefore, facilitate intravenous administrati
Autor:
Schwe Fang Pong, Ralph L. White, Chau Ting Huang, Alan F. Moore, Robert R. Brooks, James R. Skuster
Publikováno v:
Drug Development Research. 7:141-151
EU-5476 is a new, orally active angiotensin I-converting enzyme (ACE) inhibitor. In vitro, EU-5476 produced a concentration-dependent inhibition of ACE purified from rabbit lung (IC50 = 0.084 μ). Inhibition showed complex kinetics and was reversible
Autor:
Ralph L. White, Thomas J. Schwan
Publikováno v:
Chemischer Informationsdienst. 7
The synthesis and structural elucidation of 5‐hydroxy‐1‐[[5‐( p ‐nitrophenyl)furfurylidene]amino]hydantoin, a compound proposed as a metabolite of dantrolene sodium, are reported. In addition, a chromatographic comparison of the biological
Publikováno v:
Journal of medicinal chemistry. 21(1)
A series of 5-hydroxy substitution products of 2,4-imidazolidinediones, including the 5-hydroxy metabolite of the skeletal muscle contraction antagonist, dantrolene sodium, has been synthesized and evaluated for skeletal muscle relaxant activity. Mos
Publikováno v:
Journal of medicinal chemistry. 30(2)
A series of 1-[[[5-(substituted phenyl)-2-oxazolyl]methylene]amino]- 2,4-imidazolidinediones (6a-t) was synthesized, and the compounds were evaluated for direct skeletal muscle inhibition in the pithed rat gastrocnemius muscle preparation. The correc
Publikováno v:
Chemischer Informationsdienst. 8
The synthesis of 5-hydroxy-1-[[(5-nitro-2-furanyl)methylenelamino]-2,4-imidazolidinedione is described, and its antibacterial activity is reported.
Publikováno v:
Journal of pharmaceutical sciences. 70(9)
A series of 3-(aminoacyl)-1-[[[5-(substituted phenyl)-2-furanyl]methylene]amino]-2, 4-imidazolidinediones was synthesized and evaluated for skeletal muscle relaxant activity. All compounds were active by the intravenous route, and nine of 11 were act
Publikováno v:
Chemischer Informationsdienst. 9
A series of 5-hydroxy substitution products of 2,4-imidazolidinediones, including the 5-hydroxy metabolite of the skeletal muscle contraction antagonist, dantrolene sodium, has been synthesized and evaluated for skeletal muscle relaxant activity. Mos
Publikováno v:
Journal of Pharmaceutical Sciences. 66:277-278
The synthesis of 5-hydroxy-1-[[(5-nitro-2-furanyl)methylenelamino]-2,4-imidazolidinedione is described, and its antibacterial activity is reported.
Publikováno v:
Journal of Heterocyclic Chemistry. 17:817-818
The conversion of 2-chloromethyl-5-methoxy-4H-pyran-4-one to 2-amino-5-hydroxy-6-methoxybenzothiazole hydrochloride under mild reaction conditions has been observed. The synthesis of the identical benzothiazole by an alternate unequivocal method is a