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ÇëÏ´ÎÓôÓСµ½´óµÄ˳ÐòÊäÈë¡£¡£ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½617¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . cadinane-4¦Â,5¦Á,10¦Â-triol C15H28O3 ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 2003 51(8) 986-989 Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 4¦Â,5¦Á, 10¦Â-trihydroxycadinane C15H26O2 ÏàËÆ¶È:73.3% Planta Medica 1997 63 250-254 Minor Components with Smooth Muscle Relaxing Properties from Scented Myrrh (Commiphora guidotti) Maria Andersson, Ola Bergendorff, Rudong Shan, Peter Zygmunt, and OIov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ( 1R*,4R*,5Z,9S*)-5-isopropyl-3,3,9-trimethylbicyclo[4. 3.0]nona-5-en-4-ol C15H26O ÏàËÆ¶È:73.3% Journal of Natural Products 1991 Vol 54 1025 New Sesquiterpenes and C15 Acetogenins from the Marine Red Alga Laurencia implicata Anthony D. Wright, Gabriele M. König, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4-hydroxy-5-brasilene C15H26O ÏàËÆ¶È:73.3% Phytochemistry 1991 30 1921-1927 Brasilane-type sesquiterpenoids from the mediterranean red alga Laurencia obtusa Vincenzo Amico, Salvatore Caccamese, Placido Neri, Giusy Russo, Mario Foti Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . triterpene 23, 24, 25-trihydroxycycloartan-3-one C30H50O4 ÏàËÆ¶È:66.6% Phytochemistry 2008 69 206-211 Flavaglines and triterpenoids from the leaves of Aglaia forbesii Nantiya Joycharat, Harald Greger, Otmar Hofer, Ekarin Saifah Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . nephthenol C15H26O ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1987 35 124-135 Marine Natural Products. XVII. Nephtheoxydiol, a New Cytotoxic Hydroperoxy-Germacrane Sesquiterpene, and Related Sesquiterpenoids from an Okinawan Soft Coral of Nephthea sp. (Nephtheidae) ISAO KITAGAWA,ZHENG CUI,BYENG WHA SON,MOTOMASA KOBAYASHI and YOSHIMASA KYOGOKU Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 2b ÏàËÆ¶È:66.6% Phytochemistry 1994 36 637-641 Cadinanes from Artemisia annua that may be intermediates in the biosynthesis of artemisinin Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (-)-1,6-germacradien-5-ol ÏàËÆ¶È:66.6% Acta Chemica Scandinavica 1999 53 124-132 Stereochemistry of 1,6-Germacradien-5-ol, a Constituent of the Needles of Scots Pine (Pinus sylvestris) and of the Defence Secretion from Larvae of the Pine Sawfly Neodiprion sertifer. Nordin, Ove; Hedenström, Erik; Högberg, Hans-Erik Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . isovalerenenol ÏàËÆ¶È:66.6% Tetrahedron 1996 52 9999-10010 Synthesis of isovalerenenol, a sesquiterpene alcohol isolated from a soft coral and the stability of related hydrindanone derivatives Motoo Tori, Masayo Ikawa, Tetsuya Sagawa, Hirosuke Furuta, Masakazu Sono, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1¦Á,3¦Á,4¦Á-trihydroxy-dihydro-¦Â-agarofuran ÏàËÆ¶È:66.6% Zeitschrift f¨¹r Naturforschung C 2004 59 215-217 Biotransformation of 3a,4a-Dihydroxy-dihydro-b-agarofuran by Rhizopus nigricans J. Alarc¨¢n and S. ¨¢guila Structure 13C NMR ̼Æ×Ä£Äâͼ |

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