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²éѯ½á¹û£º¹²²éµ½827¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . orientalol E 6-acetate C17H28O4 ÏàËÆ¶È:64.7% Phytochemistry 2003 63 877-881 Guaiane-type sesquiterpenoids from Alisma orientalis Guo-Ping Peng, Gang Tian, Xian-Feng Huang, Feng-Chang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . cyclokessyl acetate ÏàËÆ¶È:64.7% Phytochemistry 1992 31 3511-3514 Sesquiterpenoids and iridoid glycosides from Valeriana fauriei Koichi Nishiya, Takefumi Kimura, Koichi Takeya, Hideji Itokawa Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 7b ÏàËÆ¶È:64.7% Tetrahedron Letters 2003 44 579-582 A new diorganozinc-based enantioselective access to truncated d-ribo-phytosphingosine Tahar Ayad, Yves G¨¦nisson, Alexandre Verdu, Michel Baltas, Liliane Gorrichon Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-Acetylamino-4-hydroxy-1,1-dioxo-tetrahydro-1¦Ë6-thiophene-3-carboxylic acid C17H29NO6S ÏàËÆ¶È:64.7% Tetrahedron 2012 68 208-213 1,4-Dithiane-2,5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes Nikla Baricordi, Simonetta Benetti, Valerio Bertolasi, Carmela De Risi, Gian P. Pollini, Francesco Zamberlan, Vinicio Zanirato Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . orientalol E 6-acetate ÏàËÆ¶È:64.7% Natural Product Research and Development 2001 13(3) 1-3 CHEMICAL STUDIES ON ALISMA ORIENTALIS JUZEP. PENG Guo ping; LOU Feng chang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5(11)-epoxycadinane-4¦Â,5¦Â,10¦Â,11-tetraol C15H26O3 ÏàËÆ¶È:64.7% Planta Medica 2012 78 1010-1014 Sesquiterpenoids from the Rhizomes of Homalomena occulta Xie, Xiao-Yu; Wang, Rui; Shi, Yan-Ping: Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1-[N-[[(3R)-3-[[(2-Methylpropyl)amino]carbonyl]-(2R)-2-aziridinyl]carbonyl]-L-leucyl]-L-proline C19H32N4O5 ÏàËÆ¶È:64.7% Journal of Medicinal Chemistry 1995 38 3078-3085 Aziridine Analogs of [[trans-(Epoxysuccinyl)-L-leucyl]amino]-4-guanidinobutane (E-64) as Inhibitors of Cysteine Proteases Valeri Martichonok, Celine Plouffe, Andrew C. Storer, Robert Menard, J. Bryan Jones Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 5a ÏàËÆ¶È:64.7% Indian Journal of Chemistry 1995 34B 992-993 13C NMR assignments of ¦Á- and ¦Â-dihydroartemisinin Ashish Kumar Pathak, Dharam C Jain & Ram P Sharma Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . rumphellclovane E C15H24O3 ÏàËÆ¶È:64.7% Tetrahedron 2013 69 2740-2744 Rumphellclovanes C¨CE, new clovane-type sesquiterpenoids from the gorgonian coral Rumphella antipathies Hsu-Ming Chung, Jui-Hsin Su, Tsong-Long Hwang, Jan-Jung Li, Jih-Jung Chen, Yung-Husan Chen, Yu-Chia Chang, Yin-Di Su, Yu-Hsin Chen, Lee-Shing Fang, Jyh-Horng Sheu, Wei-Hsien Wang, Ping-Jyun Sung Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 8¦Â-acetoxy-10¦Á-oxyethyl-guaia-4¦Á,11diol C19H34O5 ÏàËÆ¶È:63.1% Chinese Chemical Letters 2004 15 791-793 A New Sesquiterpenoid from Magnolia delavayi Jian Xin CAO, Guo Fang LAI, Yi Feng WANG, Yuan Feng HUANG, Shi De LUO Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 17-epioxandrolone C19H32O3 ÏàËÆ¶È:63.1% Steroids 1992 57 306-312 Studies on anabolic steroids. 9. Tertiary sulfates of anabolic 17¦Á-methyl steroids: synthesis and rearrangement Honggang Bi, Robert Mass¨¦, George Just Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 17-Epioxandrolone ÏàËÆ¶È:63.1% Steroids 1992 57 537-550 17-Epimerization of 17¦Á-methyl anabolic steroids in humans: metabolism and synthesis of 17¦Á-hydroxy-17¦Â-methyl steroids Willi Schänzer, Georg Opfermann, Manfred Donike Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (1S)-1-C-[4-(adamant-1-ylmethoxy)butyl]-N-butyl-1-deoxynojirimycin C25H45NO5 ÏàËÆ¶È:63.1% European Journal of Organic Chemistry 2010 1258-1283 Synthesis and Evaluation of Lipophilic Aza-C-glycosides as Inhibitors of Glucosylceramide Metabolism Tom Wennekes, Richard J. B. H. N. van den Berg, Thomas J. Boltje, Wilma E. Donker-Koopman, Bastiaan Kuijper, Gijsbert A. van der Marel, Anneke Strijland, Carlo P. Verhagen, Johannes M. F. G. Aerts and Herman S. Overkleeft Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 4-acetoxy-3-acetylamino-1,1-dioxo-tetrahydro-1¦Ë6-thiophene-3-carboxylic acid C19H31NO7S ÏàËÆ¶È:61.1% Tetrahedron 2012 68 208-213 1,4-Dithiane-2,5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes Nikla Baricordi, Simonetta Benetti, Valerio Bertolasi, Carmela De Risi, Gian P. Pollini, Francesco Zamberlan, Vinicio Zanirato Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (2S,3S,4R)-2-Acetamido-1,3,4-triacetoxyhexadecane C24H43NO7 ÏàËÆ¶È:61.1% European Journal of Organic Chemistry 1988 1988 619-625 Biologically active glycosides from asteroidea, XV. Asymmetric synthesis of phytosphingosine and phytosphingosine anhydro base: Assignment of the absolute stereochemistry Shigeo Sugiyama, Masanori Honda and Tetsuya Komori Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 13,18-dihydroxystemodan-2-one ÏàËÆ¶È:60% Phytochemistry 2002 59 57-62 Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142 Avril R.M. Chen, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3-oxo-4¦Â-hydroxy-5¦Â,10¦Â-cis-17¦Á,20¦Á-cleroda-13(14)-en-15,16-olide C20H30O4 ÏàËÆ¶È:60% Phytochemistry 1988 27 3187-3196 Terpenoids from Ageratina saltillensis Nianbai Fang,Sanggong Yu,Tom J. Mabry,Khalil A. Abboud,Stanley H. Simonsen Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (1S)-N-[5-(adamant-1-ylmethoxy)pentyl]-1-C-butyl-1-deoxynojirimycin C26H48NO5 ÏàËÆ¶È:60% European Journal of Organic Chemistry 2010 1258-1283 Synthesis and Evaluation of Lipophilic Aza-C-glycosides as Inhibitors of Glucosylceramide Metabolism Tom Wennekes, Richard J. B. H. N. van den Berg, Thomas J. Boltje, Wilma E. Donker-Koopman, Bastiaan Kuijper, Gijsbert A. van der Marel, Anneke Strijland, Carlo P. Verhagen, Johannes M. F. G. Aerts and Herman S. Overkleeft Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (1S)-1-C-[5-(adamant-1-ylmethoxy)pentyl]-1-deoxy-N-hexylnojirimycin C28H51NO5 ÏàËÆ¶È:59.0% European Journal of Organic Chemistry 2010 1258-1283 Synthesis and Evaluation of Lipophilic Aza-C-glycosides as Inhibitors of Glucosylceramide Metabolism Tom Wennekes, Richard J. B. H. N. van den Berg, Thomas J. Boltje, Wilma E. Donker-Koopman, Bastiaan Kuijper, Gijsbert A. van der Marel, Anneke Strijland, Carlo P. Verhagen, Johannes M. F. G. Aerts and Herman S. Overkleeft Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Â,20R-bis(acetoxy)-5¦Â-12¦Á-hydroxy-pregn-14-ene C25H38O5 ÏàËÆ¶È:59.0% Steroids 2011 76 1166-1175 Norrish¨CPrins reaction as a key step in the synthesis of 14¦Â-hydroxy-5¦Á (or 5¦Â or ¦¤5,6)-pregnane derivatives Philippe Geoffroy, Blandine Ressault, Eric Marchioni, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (-)-Cumacrene, (4S)-4-[(1R,2S)-2-isopropenyl-1-methylcyclobutyl]-1-methylcyclohexene C15H24 ÏàËÆ¶È:58.8% Phytochemistry 2005 66 249-260 Sesquiterpenes from Cupressus macrocarpa foliage Laurence G. Cool Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (1R,4S,5R,7R,10S)-1,11-dihydroxyeudesman-14,4-olide C15H24O4 ÏàËÆ¶È:58.8% Phytochemistry 2003 1003-1011 Polar constituents of celery seed Junichi Kitajima, Toru Ishikawa, Mitsuru Satoh Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 5(9),6-tricyclohumulane-4¦Á,8¦Á,10¦Á-triol ÏàËÆ¶È:58.8% Phytochemistry 2002 59 39-44 Microbial metabolism of partheniol by Mucor circinelloides Galal T. Maatooq Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 10-bromo-9-hydroxy-chamigra-2,7(14)-diene C15H23BrO ÏàËÆ¶È:58.8% Phytochemistry 2001 58 517-523 Halogenated metabolites with antibacterial activity from the Okinawan Laurencia species Charles Santhanaraju Vairappan, Minoru Suzuki, Tsuyoshi Abe, Michio Masuda Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . (1S,4S,5S,6R,7S,8S,9R,10S)-1-acetoxy-9-benzoyloxy-8-cinnamoyloxy-4,6-dihydroxydihydro-¦Â-agarofuran C33H38O9 ÏàËÆ¶È:58.8% Journal of Natural Products 2008 71(8) 1331-1335 Sesquiterpenes from Celastrus vulcanicola as Photosynthetic Inhibitors David Torres-Romero, Beatriz King-D¨ªaz, Ignacio A.Jim¨¦nez, Blas Lotina-Hennsen, and Isabel L. Bazzocchi Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . lepadiformine C C16H29N ÏàËÆ¶È:58.8% Journal of Natural Products 2006 69(4) 558-562 Sensitivity of Cardiac Background Inward Rectifying K Outward Current (IK1) to the Alkaloids Lepadiformines A, B, and C Martin-Pierre Sauviat, Joseph Vercauteren, Nicole Grimaud, Marcel Jug, Mohamed Nabil, Jean-Yves Petit, and Jean-Franois Biard Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 1¦Á,6¦Â-dihydroxyambrox C16H28O3 ÏàËÆ¶È:58.8% Journal of Natural Products 2006 69(6) 957-959 Biotransformation of (− -Ambrox by Cell Suspension Cultures of Actinidia deliciosaAsma Nasib, Syed Ghulam Musharraf, Sajjad Hussain, Saifullah Khan,Shazia Anjum, Shamsher Ali, Atta-ur-Rahman, and M. Iqbal Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . dihydrobotrydialone ÏàËÆ¶È:58.8% Journal of Natural Products 2000 63 182-184 Secobotrytriendiol and Related Sesquiterpenoids: New Phytotoxic Metabolites from Botrytis cinerea Rosa Dur¨¢n-Patr¨®n, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . arnimollin acetate ÏàËÆ¶È:58.8% Planta Medica 1990 56 104-110 Germacranolides, Guaianolides, and Xanthanolides from the Flowers of Arnica moths and an X-Ray Structure Analysis of Baileyin Acetate Christoph Marcinek-Hupen-Bestendonk,G¨¹nter Willuhn,Alots Steigel,Detlef Wendisch,BirgitMiddelhauve, Michael Wiebcke and Dietrich Mootz Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 1(S*)-hydroxy-¦Á-bisabolo1oxide A acetate C17H28O4 ÏàËÆ¶È:58.8% Planta Medica 1988 54 463-464 ¦Á-Bisabololoxide Derivatives from Artemisia abrotanum A. H. Mericli, B. cubukcu, J. Jakupovict , and N. Ozhatay Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . ananosmin acetate ÏàËÆ¶È:58.8% Acta Botanica Yunnanica 1993 15(2) 196-200 SESQUITERPENOIDS FROM KADSURA ANANOSMA ZOU Cheng,PU Xiang-Yu,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . compound 1 C15H26O2 ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 1990 38 1405-1407 Studies on the Sesquiterpenoids of Panax ginseng C. A. MEYER. IV Hisakatsu IWABUCHI,Nobuo KATO and Masahiro YOSHIKURA Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . panasinsanol A C15H26O ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 1987 35 1975-1981 Studies on the Sesquiterpenoids of Panax ginseng C. A. MEYER. Isolation and Structure Determination of Sesquiterpene Alcohols, Panasinsanols A and B HISAKATSU IWABUCHI,MASAHIRO YOSHIKURA,YOSHITOMI IKAWA and WASUKE KAMISAKO Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . panasinsanol B C15H26O ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 1987 35 1975-1981 Studies on the Sesquiterpenoids of Panax ginseng C. A. MEYER. Isolation and Structure Determination of Sesquiterpene Alcohols, Panasinsanols A and B HISAKATSU IWABUCHI,MASAHIRO YOSHIKURA,YOSHITOMI IKAWA and WASUKE KAMISAKO Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 4¦Á,10¦Á-dihydroxy-5¦Â-H-guaj-6-en ÏàËÆ¶È:58.8% China Journal of Chinese Materia Medica 2009 34 994-998 Chemical constituents of A lisma orientalis and their immunosuppressive function ZHANG Chaofeng, ZHOU Aichun, ZHANG mian Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . (5S)-5-hydroxyacetylcaespitol C17H27Br2ClO4 ÏàËÆ¶È:58.8% Journal of Natural Products 2010 73 27-32 Cytotoxic Halogenated Metabolites from the Brazilian Red Alga Laurencia catarinensis Cintia Lhullier, Miriam Falkenberg, Efstathia Ioannou, Antonio Quesada, Panagiota Papazafiri, Paulo Antunes Horta, Eloir Paulo Schenkel, Constantinos Vagias and Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 3¦Â-acetoxyoplopanone C17H28O4 ÏàËÆ¶È:58.8% Phytochemistry 1997 46 1039-1043 Sesquiterpenoids from Pallenis spinosa Giovanni Appendino, Jasmin Jakupovic, Sven Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 1¦Â,15-diacetoxy-4¦Á,6¦Â-dihydroxyeudesmane ÏàËÆ¶È:58.8% Journal of Natural Products 1988 Vol 51 475 Epoxidation Reaction of 6¦Â-Acetoxyeudesmenes and Acid-catalyzed Transformations of the Epoxy Compounds E. Cabrera, A. Garcia-Granados, M. A. Quecuty Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . pyrazoline C17H26O2N2 ÏàËÆ¶È:58.8% Journal of Natural Products 1993 Vol 56 857 Preparation of a Cyclopropane-Containing Analogue of Artemisinin Soo-Un Kim, Jin-Hyuk Choi, Sang Soo Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . 10-epi-Dihydrobotrydial C17H28O5 ÏàËÆ¶È:58.8% Phytochemistry 1996 41 513-517 Biologically active sesquiterpenoid metabolites from the fungus Botrytis cinerea Isidro G. Collado, Rosario Hern¨¢ndez-Gal¨¢n, Victoria Prieto, James R. Hanson, Laureana G. Rebordinos Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . 1¦Â-Acetoxy-3-eudesmen-11-ol C17H28O3 ÏàËÆ¶È:58.8% Phytochemistry 1995 39 603-607 Sesquiterpenes from leaves of Cryptomeria japonica Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . compound(ref 2) ÏàËÆ¶È:58.8% Phytochemistry 1994 37 597-623(604) The daucane (carotane) class of sesquiterpenes Emilio L. Ghisalberti Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . 9-O-Acetylseiricardine B C17H28O3 ÏàËÆ¶È:58.8% Phytochemistry 1993 33 69-78 Seiricardines B and C, phytotoxic sesquiterpenes from three species of Seiridium pathogenic for cypress Antonio Evidente, Andrea Motta, Lorenzo Sparapano Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . intrlcatetraol diacetate C34H58Br2Cl2O8 ÏàËÆ¶È:58.8% Phytochemistry 1993 33 651-656 Intricatetraol, a halogenated triterpene alcohol from the red alga Laurencia intricata Minoru Suzuki, Yoshihide Matsuo, Satoshi Takeda, Teruaki Suzuki Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . isotrichodiol ÏàËÆ¶È:58.8% Phytochemistry 1991 30 2237-2243 Biosynthesis of trichothecene mycotoxins: Identification of isotrichodiol as a post-trichodiene intermediate Andrew R. Hesketh, Linden Gledhill, David C. Marsh, Barrie W. Bycroft, Paul M. Dewick, John Gilbert Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . 9-Epi-myrionine C15H26N2O ÏàËÆ¶È:58.8% Organic Letters 2007 Vol. 9, No. 18 3531-3534 Solution and Crystal Conformations of Myrionine, a New 8¦Â-Alkyl-cis-decahydroquinoline of Myrioneuron nutans Van Cuong Pham, Akino Jossang, Ang¨¨le Chiaroni, Thierry S¨¦venet,Van Hung Nguyen, and Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . (3S,5aR,6aS,7aS)-5,5a,6,6a,7,7a-Hexahydro-3-isobutyl-3,6,6,7a-tetramethylbicyclo[4.1.0]hept-1(6)-eno[3,4-b][1,4]oxazin-2(3H)-one C17H27NO2 ÏàËÆ¶È:58.8% The Journal of Organic Chemistry 2011 76 1621-1633 Asymmetric Synthesis of r-Methyl-r-Amino Acids via Diastereoselective Alkylation of (1S)-(+)-3-Carene Derived Tricyclic Iminolactone Ta-Jung Lu and Cheng-Kun Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . compound 3 C16H25NO5S ÏàËÆ¶È:58.8% Tetrahedron Letters 2000 41 7289-7292 Synthesis of the first enantiomerically pure 3-thiazolines via Asinger reaction Imre Schlemminger, Hans-Hermann Janknecht, Wolfgang Maison, Wolfgang Saak, J¨¹rgen Martens Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 7,15-dihydroxybisabol-10-ene acetate C17H28O2 ÏàËÆ¶È:58.8% Phytochemistry 1989 28 531-542 ent-clerodanes and other constituents from bolivian Baccharis species C. Zdero,F. Bohlmann,J.C. Solomon,R.M. King,H. Robinson Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 1-hydroxy-¦Á-bisabololoxide A acetaee ÏàËÆ¶È:58.8% Phytochemistry 1989 28 2163-2167 Sesquiterpene lactones from Artemisia hispanica Juan F. Sanz,Oscar Barbera,J.Alberto Marco Structure 13C NMR ̼Æ×Ä£Äâͼ |
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-Ambrox by Cell Suspension Cultures of Actinidia deliciosa