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Volumn 55, Issue 3, 2007, Pages 435-441

Bioactive constituents from Chinese natural medicines. XXII. Absolute structures of new megastigmane glycosides, sedumosides E1, E 2, E3, F1, F2, and G, from Sedum sarmentosum (Crassulaceae)

Author keywords

Chinese natural medicine; Crassulaceae; Megastigmane; Sarmentol; Sedum sarmentosum; Sedumoside

Indexed keywords

CRASSULACEAE EXTRACT; GLYCOSIDE; MEGASTIGMANE; PLANT EXTRACT; SARMENTOIC ACID; SARMENTOL A; SEDUMOSIDE E1; SEDUMOSIDE E2; SEDUMOSIDE E3; SEDUMOSIDE F1; SEDUMOSIDE F2; SEDUMOSIDE G; UNCLASSIFIED DRUG;

EID: 34047143674     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.55.435     Document Type: Article
Times cited : (62)

References (47)
  • 1
    • 34249011468 scopus 로고    scopus 로고
    • Part XXI: Yoshikawa M., Morikawa T., Zhang Y., Nakamura S., Muraoka O., Matsuda H., J. Nat. Prod., 70 (4), (2007), in press.
    • Part XXI: Yoshikawa M., Morikawa T., Zhang Y., Nakamura S., Muraoka O., Matsuda H., J. Nat. Prod., 70 (4), (2007), in press.
  • 23
    • 34047123483 scopus 로고    scopus 로고
    • These known compounds were identified by comparison of their physical data with authentic samples
    • These known compounds were identified by comparison of their physical data with authentic samples.
  • 33
    • 34047184046 scopus 로고    scopus 로고
    • 3), 100.8 (1‴-C), 81.1 (2″-C), 70.2 (3″-C), 71.5 (4″-C), 70.1 (5″-C), 17.3 (6″-C), 105.8 (1‴-C), 73.8 (2‴-C), 76.1 (3‴-C), 69.2 (4‴-C), 76.6 (5‴-C), 60.4 (6‴-C), 98.3
    • 3), 100.8 (1‴-C), 81.1 (2″-C), 70.2 (3″-C), 71.5 (4″-C), 70.1 (5″-C), 17.3 (6″-C), 105.8 (1‴-C), 73.8 (2‴-C), 76.1 (3‴-C), 69.2 (4‴-C), 76.6 (5‴-C), 60.4 (6‴-C), 98.3 (1‴′-C), 69.7 (2‴′-C), 70.4 (3‴′-C), 71.5 (4‴′-C), 70.0 (5‴′-C), 17.8 (6‴′-C).
  • 43
    • 34047169096 scopus 로고    scopus 로고
    • 1H COSY), heteronuclear multiple quantum coherence (HMQC), and HMBC experiments.
    • 1H COSY), heteronuclear multiple quantum coherence (HMQC), and HMBC experiments.
  • 45
    • 34047107040 scopus 로고    scopus 로고
    • Authentic D-apiose was obtained by acid hydrolysis of 1,2, 3,5-di-O-isopropylidene-α-D-apiose (Funakoshi Co., Ltd., Tokyo, Japan).
    • Authentic D-apiose was obtained by acid hydrolysis of 1,2, 3,5-di-O-isopropylidene-α-D-apiose (Funakoshi Co., Ltd., Tokyo, Japan).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.