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Volumn 6, Issue 12, 1996, Pages 1297-1302

Synthesis and anticonvulsant evaluation of a series of (R)- and (S)-N-Cbz-α-aminoglutarimide and succinimide

Author keywords

[No Author keywords available]

Indexed keywords

ETHOSUXIMIDE; GLUTARIMIDE DERIVATIVE; MESUXIMIDE; PENTETRAZOLE; PHENOBARBITAL; PHENYTOIN; SUCCINIMIDE DERIVATIVE; TRIMETHADIONE; VALPROIC ACID;

EID: 0029937564     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0960-894X(96)00220-X     Document Type: Article
Times cited : (26)

References (31)
  • 5
    • 0003827997 scopus 로고
    • Foye, W. O., Ed; Lea & Febiger: Philadelphia, Chap. 11
    • Vida, J. A. Principle of Medicinal Chemistry, Foye, W. O., Ed; Lea & Febiger: Philadelphia, 1995, Chap. 11.
    • (1995) Principle of Medicinal Chemistry
    • Vida, J.A.1
  • 10
    • 0040281482 scopus 로고    scopus 로고
    • U.S. Patent. 3657341, April 8, 1972
    • (b) Thorne, D. E. U.S. Patent. 3657341, April 8, 1972.
    • Thorne, D.E.1
  • 27
    • 84984063678 scopus 로고
    • For the preparation of 4: Itoh, M. Chem. Pharm. Bull. 1969, 17, 1679. ; For the preparation of 1 and 2: Sandler, S. R.; Karo, W. Organic Functional Group Preparation; Academic Press: New York, 1972, Vol III, p. 253.
    • (1969) Chem. Pharm. Bull. , vol.17 , pp. 1679
    • Itoh, M.1
  • 28
    • 0039097530 scopus 로고
    • Academic Press: New York
    • For the preparation of 4: Itoh, M. Chem. Pharm. Bull. 1969, 17, 1679. ; For the preparation of 1 and 2: Sandler, S. R.; Karo, W. Organic Functional Group Preparation; Academic Press: New York, 1972, Vol III, p. 253.
    • (1972) Organic Functional Group Preparation , vol.3 , pp. 253
    • Sandler, S.R.1    Karo, W.2
  • 30
    • 0018129707 scopus 로고
    • (b) Krall, R. L.; Penry, J. K.; White, B. G.; Kupferberg, H. J; Swinyard, C. A. Epilepsia, 1978, 19, 409. The pharmacological tests were carried out as follows: All the tested compounds were dissolved in polyethylene glycol 400 and administered ip to male ICR mice and anticonvulsant tests were performed in groups of 4 mice and 30 min after administration. Seizure were then artificially induced by either electric shock or pentylenetetrazole. The maximal elelectric shock seizure(MES) test were elicited with a 60-cycle a.c. of 50 mA intensity delivered for 0.2 s via corneal electrod with ECT unit(UGO Basline, Itlay). A drop of 0.9% saline was istilled in the eye prior to application of electrods. Protection in this test was defined as the abolition of hind limb tonic extension component of seizure. The pentylenetetrazole seizure (PTZ) test entailed the administration of 80 mg/kg of pentylenetetrazole as a 0.5 % solution subcutaneously in the posterior midline of mice. And the animal was observed for 30 min. Protection was defined as the failure to observe even a threshold seizure(single episode of clonic spasms of at least 5 sec. duration). The effects of the compounds on forced and spontaneous motor activity were evaluated in mice by the rotorod test with Rotorod treadmill for mice(UGO Baseline, Itlay) as follows. The animal was placed on a rod an 1 inch diameter knurled plastic rod rotating at 6 rpm after the administration of the compounds. Normal mice can remain on a rod at this speed indifinitely. Neurological toxicity was defined as the failure of the animal to remain on the rod for 2 min.
    • (1978) Epilepsia , vol.19 , pp. 409
    • Krall, R.L.1    Penry, J.K.2    White, B.G.3    Kupferberg, H.J.4    Swinyard, C.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.