A new tricyclic-α,β-unsaturate ketone and a new δ-hexano lactone glycoside from Adenocaulon himalaicum

Natural Product Research

Volumn 21, Issue 2, 2007, Pages 161-166

  Wang, Xiaoxiong ^a   Zhang, Qi ^b   Jia, Zhongjian ^a  

^a LANZHOU UNIVERSITY   (China)

^b LANZHOU UNIVERSITY   (China)

Author keywords

hexanolactone glycoside; Adenocaulolide; Adenocaulon himalaicum; Adenocaulone; Antibacterial activity; Compositae; Tricyclic , unsaturate ketone

Indexed keywords

3 HYDROXY DEXTRO FRIEDOOLEANANE 3 EN 2 ONE; 3,5 O DICAFFEOYL QUINIC ACID; 3BETA HYDROXY 5BETA,6BETA EPOXY BETA IONONE; 3BETA HYDROXY BETA IONONE; ADENOCAULOLIDE; ADENOCAULON HIMALAICUM EXTRACT; ADENOCAULONE; CHLORAMPHENICOL; DAUCOSTEROL; FERULIC ACID ETHYLESTER; GLYCOSIDE; KETONE DERIVATIVE; LACTONE DERIVATIVE; LILIOLIDE; LUPENOL; NATURAL PRODUCT; OLEANOLIC ACID; PLANT EXTRACT; SITOSTEROL; UNCLASSIFIED DRUG; ANTIINFECTIVE AGENT; DRUG DERIVATIVE; GAMMA BUTYROLACTONE; KETONE; LACTONE; POLYCYCLIC HYDROCARBON;

ADENOCAULON HIMALAICUM; ANTIBACTERIAL ACTIVITY; ARTICLE; BACILLUS SUBTILIS; BACTERIAL STRAIN; CARBON NUCLEAR MAGNETIC RESONANCE; CONTROLLED STUDY; DRUG ISOLATION; DRUG STRUCTURE; ESCHERICHIA COLI; INFRARED SPECTROMETRY; MASS SPECTROMETRY; MEDICINAL PLANT; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; STAPHYLOCOCCUS AUREUS; ASTERACEAE; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECT; FAST ATOM BOMBARDMENT MASS SPECTROMETRY; ISOLATION AND PURIFICATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

ADENOCAULON; ASTERACEAE;

4-BUTYROLACTONE; ANTI-BACTERIAL AGENTS; ASTERACEAE; BACILLUS SUBTILIS; ESCHERICHIA COLI; GLYCOSIDES; KETONES; LACTONES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; PLANT EXTRACTS; POLYCYCLIC COMPOUNDS; SPECTROMETRY, MASS, FAST ATOM BOMBARDMENT; STAPHYLOCOCCUS AUREUS;

EID: 34250690378     PISSN: 14786419     EISSN: 14786427     Source Type: Journal    
DOI: 10.1080/14786410601130000     Document Type: Article

References (12)

1. Hak, CK and Kang, RL (2001) Planta Med., 67, p. 482.
2. Kulesh, NI, Krasovskaya, NP and Maksimov, OB (1986) Khim. Prir. Soedin., 22, p. 506.
3. Takashi, M., Yang, CX, Sasaki, H. and Qin, WZ (1995) Phytochemistry, 39, p. 1153.
4. Teng, RW and Zhou, ZH (2002) Chin. J. Magn. Reson., 19, p. 167.
5. Yi, JH and Chen, Y. (2003) Nat. Prod. Res. Dev., 15, p. 98.
6. Mori, K. (1974) Tetrahedron, 30, p. 1065.
7. Naomasa, OK (1994) Phytochemistry, 37, p. 281.
8. William, FR (1986) Tetrahedron, 42, p. 3419.
9. Zhang, ZF and Bian, BL (2004) Chin. J. Chin. Mater. Med., 29, p. 237.
10. Marina, DG and Pietro, M. (1990) J. Nat. Prod., 53, p. 1430.
11. Kuo, YH and Yeh, MH (1997) J. Chin. Chem. Soc., 44, p. 379.
12. Atsushi, N. and Kazuko, H. (1984) Chem. Pharm. Bull., 32, p. 2815.