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Volumn 10, Issue 2, 2000, Pages 101-103

Synthesis and biological activities of hapalosin derivatives with modification at the C12 position

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPEPTIDE; HAPALOSIN DERIVATIVE; SYNTHETIC PEPTIDE; UNCLASSIFIED DRUG; VERAPAMIL; VINCRISTINE;

EID: 0034677147     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(99)00647-2     Document Type: Article
Times cited : (16)

References (27)
  • 6
    • 85038070212 scopus 로고    scopus 로고
    • 50=5∼15 μg), see ref 1
    • 50=5∼15 μg), see ref 1.
  • 20
    • 85038064072 scopus 로고    scopus 로고
    • It was anticipated that alkyl groups such as ethyl or propyl, introduced at the N-position would conduct the cis-peptide geometry, according to computational calculations. However, coupling of the corresponding alkylated amino group, or insertion of alkyl groups to the peptide moiety were unsuccessful, owing to low reactivities
    • It was anticipated that alkyl groups such as ethyl or propyl, introduced at the N-position would conduct the cis-peptide geometry, according to computational calculations. However, coupling of the corresponding alkylated amino group, or insertion of alkyl groups to the peptide moiety were unsuccessful, owing to low reactivities.
  • 21
    • 85038057847 scopus 로고    scopus 로고
    • 22-24
    • 22-24
  • 24
    • 0017136359 scopus 로고
    • Mori K. Tetrahedron. 32:1976;1101-1106.
    • (1976) Tetrahedron , vol.32 , pp. 1101-1106
    • Mori, K.1
  • 25
    • 85038067852 scopus 로고    scopus 로고
    • 18,19
    • 18,19
  • 26
    • 85038056790 scopus 로고    scopus 로고
    • Low cytotoxicities of 5a-5e were determined
    • Low cytotoxicities of 5a-5e were determined.
  • 27
    • 85038064595 scopus 로고    scopus 로고
    • During preparation of this paper, this sample was reported: see ref 15
    • During preparation of this paper, this sample was reported: see ref 15.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.