메뉴 건너뛰기




Volumn 9, Issue 16, 1999, Pages 2365-2370

Hydroxyoxazolidines as α-aminoacetaldehyde equivalents: Novel inhibitors of calpain

Author keywords

[No Author keywords available]

Indexed keywords

[1 [(1 FORMYL 2 PHENYLETHYL)CARBAMOYL] 2 METHYLPROPYL]CARBAMIC ACID BENZYL ESTER; [1 [5 HYDROXY 4 (PHENYLMETHYL) 3 OXAZOLIDINYL)CARBONYL] 2 ETHYLPROPYL]CARBAMIC ACID PHENYLMETHYL ESTER; CALPAIN; CALPASTATIN; OXAZOLIDINE DERIVATIVE; PRODRUG; UNCLASSIFIED DRUG; CARBAMIC ACID DERIVATIVE; MDL 104903; OXAZOLE DERIVATIVE; PROTEINASE INHIBITOR;

EID: 0033575512     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(99)00391-1     Document Type: Article
Times cited : (10)

References (36)
  • 18
    • 0009604870 scopus 로고    scopus 로고
    • 9 has been employed as the cyclizing agent
    • 9 has been employed as the cyclizing agent.
  • 24
    • 0009573348 scopus 로고    scopus 로고
    • 5: C, 66.98; H, 6.83; N, 6.79. Found: C, 66.88; H, 7.07; N, 6.81
    • 5: C, 66.98; H, 6.83; N, 6.79. Found: C, 66.88; H, 7.07; N, 6.81.
  • 25
    • 0009639473 scopus 로고    scopus 로고
    • note
    • 6: C, 66.07; H, 6.65; N, 6.16. Found: C, 65.76; H, 6.60; N, 6.16.
  • 28
    • 0009587462 scopus 로고    scopus 로고
    • 2)
    • 2).
  • 34
    • 0009642292 scopus 로고    scopus 로고
    • 13C NMR. The minor isomer was consistent with inverse stereochemistry for both the benzyl and hydroxyl groups. Resonance assignments for these two components were derived from a DFQ-COSY spectrum, and relative stereochemistry was assigned from observation of NOE signals in a NOESY spectrum
    • 13C NMR. The minor isomer was consistent with inverse stereochemistry for both the benzyl and hydroxyl groups. Resonance assignments for these two components were derived from a DFQ-COSY spectrum, and relative stereochemistry was assigned from observation of NOE signals in a NOESY spectrum.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.