Rearranged lanostane triterpenoids from Abies sachalinensis (III)

Chemical and Pharmaceutical Bulletin

Volumn 56, Issue 9, 2008, Pages 1352-1354

  Gao, Hui Yuan ^a   Wu, Li Jun ^a   Nakane, Takahisa ^b   Shirota, Osamu ^c   Kuroyanagi, Masanori ^d  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

^b Showa Parmaceutical University   (Japan)

^c TOKUSHIMA BUNRI UNIVERSITY   (Japan)

^d PREFECTURAL UNIVERSITY OF HIROSHIMA   (Japan)

Author keywords

Abies sachalinensis; Pinaceae; Rearranged lanostane type triterpene; Tautomerism

Indexed keywords

3,4 SECO 4(28),7,12,24 MARIESATETRAEN 26,23 OLIDE 23 HYDROXY 3 OIC ACID; ETHYL 3,4 SECO 8(14-31)ABEO 17,13 FRIEDO 4(28),7,14,24 LANOSTATETRAEN 26,23 OLIDE 23 HYDROXY 3 OATE; TRITERPENE DERIVATIVE; TRITERPENOID; UNCLASSIFIED DRUG;

ABIES; ABIES SACHALINENSIS; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG ISOLATION; DRUG STRUCTURE; MASS SPECTROMETRY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS;

ABIES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; SPECTROPHOTOMETRY, INFRARED; SPECTROPHOTOMETRY, ULTRAVIOLET; TRITERPENES;

EID: 51349125781     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.56.1352     Document Type: Article

References (5)

1. Barrero A. F., Sanchez J. F., Alvarez Manzaneda E. J., Dorado M. M., Phytochemistry, 32, 1261-1265 (1993).
2. Raldugin V. A., Shevtsov S. A., Shakirov M. M., Roschin V. I., Pentegova V. A., Khim. Prir. Soedin., 25, 207-212 (1989).
3. Hasegawa S., Miura T., Kaneko N., Hirose Y., Iitaka Y., Tetrahedron, 43, 1775-1784 (1987).
4. Kuroyanagi M., Sugiyama K., Kanazawa M., Kawahara N., Chem. Pharm. Bull., 48, 1917-1920 (2000).
5. Gao H. Y., Wu L. J., Nakane T., Shirota O., Kuroyanagi M., Chem. Pharm. Bull., 56, 554-558 (2008).