Curcapitoside, a novel glucosyl-fused phenanthropyran isolated from Curculigo capitulata

Tetrahedron Letters

Volumn 37, Issue 25, 1996, Pages 4405-4408

  Lee, Shoei Sheng ^a   Chang, Wen Liang ^a   Chen, Chung Hsiung ^a  

^a NATIONAL TAIWAN UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

CURCAPITOSIDE; PHENANTHRENE DERIVATIVE; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DRUG CONFORMATION; DRUG ISOLATION; DRUG STRUCTURE; DYSMENORRHEA; GLYCOSYLATION; HERB; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; NUCLEAR OVERHAUSER EFFECT; RHEUMATIC DISEASE; STEREOCHEMISTRY; TRADITIONAL MEDICINE; ULTRAVIOLET SPECTROSCOPY;

EID: 0029935977     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00862-3     Document Type: Article

References (7)

1. N.Y. Chiu, and K.H. Chang, The Illustrated Medicinal Plants of Taiwan (II); Southern Materials Center Inc.: Taipei, 1983; p 276.
2. K. Chifurdera, I. Messana, C. Galeffi, and Y. De Vicente, Tetrahedron, 1991, 47, 4369-4374.
3. K. Chifundera, G. Palazzino, I. Messana, L. Ping, C. Galeffi, and G. Cannarsa, Phytochem., 1994, 35, 1343-1348.
4. 18, 768.1901).
5. H. Guinaudeau, M. Leboeuf and A. Cave, J. Nat. Prod. 1988, 51, 389-474 and references therein.
6. C. Galeffi, G. Multan, J.D. Msonthi, M. Nicoletti, and G.B. Marini-Bettolo, Tetrahedron, 1987, 43, 3519-3522.
7. Molecular modeling was performed by Systematic Search of Sybyl using Tripos Force Fields (TRIPOS, Inc.) to obtain the favored conformation of 1a with minimum energy.