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»¯ºÏÎï1£º 1 . corchorifatty acid E C11H20O3 ÏàËÆ¶È:100% Chemical & Pharmaceutical Bulletin 1998 46 1008-1014 Medicinal Foodstuffs. XIV. On the Bioactive Constituents of Moroheiya. (2) : New Fatty Acids, Corchorifatty Acids A, B, C, D, E, and F, from the Leaves of Corchorus olitorius L. (Tiliaceae) : Structures and Inhibitory Effect on NO Production in Mouse Peri Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Hiromi SHIMADA,Satoshi YOSHIZUMI,Masami SAKA,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 8a C12H22O3 ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1998 46 1008-1014 Medicinal Foodstuffs. XIV. On the Bioactive Constituents of Moroheiya. (2) : New Fatty Acids, Corchorifatty Acids A, B, C, D, E, and F, from the Leaves of Corchorus olitorius L. (Tiliaceae) : Structures and Inhibitory Effect on NO Production in Mouse Peri Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Hiromi SHIMADA,Satoshi YOSHIZUMI,Masami SAKA,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 6-hydroxy-oct-7-enoic acid C8H14O3 ÏàËÆ¶È:72.7% Zeitschrift f¨¹r Naturforschung B 2009 64b 1199-1207 Three New Unsaturated Fatty Acids from the Marine Green Alga Ulva fasciata Delile Ghada S. E. Abou-ElWafa, Mohamed Shaaban, Khaled A. Shaaban,Mohamed E. E. El-Naggar, and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4-pentylcyclohex-3-ene-1¦Á,2¦Â-diol C11H20O2 ÏàËÆ¶È:63.6% Journal of Asian Natural Products Research 2009 11 805-810 Two new compounds from the roots of Ligusticum chuanxiong Xin-Liang Changa, Zhi-Yong Jianga, Yun-Bao Maa, Xue-Mei Zhanga,Karl W.K. Tsimb and Ji-Jun Chena Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 9-decenyl methanesulfonate ÏàËÆ¶È:63.6% Canadian Journal of Chemistry 2009 87 1180-1199 Design, chemical synthesis, and in vitro biological evaluation of simplified estradiol adenosine hybrids as inhibitors of 17¦Â-hydroxysteroid dehydrogenase type 1 Marie Be¨¦rub¨¦ and Donald Poirier Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 9-Hydroxynonanoic Acid ÏàËÆ¶È:63.6% Helvetica Chimica Acta 2012 95 428-447 Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 6m C14H23NO7SNa2 ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 1996 4 397-402 POLYANION INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS. Part IV. - POLYMERIZED ANIONIC SURFACTANTS : INFLUENCE OF THE DENSITY AND DISTRIBUTION OF ANIONIC GROUPS ON THE ANTIVIRAL ACTIVITY. Alain Leydet, Philippe Barth616my, Bernard Boyer, O6rard Lamaty and Jean-Pierre Roque*,Myriam Witvrouw, and Erik De C1er~, Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 7m C14H23NO6SNa2 ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 1996 4 397-402 POLYANION INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS. Part IV. - POLYMERIZED ANIONIC SURFACTANTS : INFLUENCE OF THE DENSITY AND DISTRIBUTION OF ANIONIC GROUPS ON THE ANTIVIRAL ACTIVITY. Alain Leydet, Philippe Barth616my, Bernard Boyer, O6rard Lamaty and Jean-Pierre Roque*,Myriam Witvrouw, and Erik De C1er~, Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . PtCl2(P((CH2)7CH=CH2)3)2 C54H102Cl2P2Pd ÏàËÆ¶È:63.6% Zeitschrift f¨¹r Naturforschung B 2010 65 414-424 Syntheses and Palladium, Platinum, and Borane Adducts of Symmetrical Trialkylphosphines with Three Terminal Vinyl Groups, P((CH2)mCH=CH2)3 A. J. Nawara-Hultzsch, K. Skopek, T. Shima, M. Barbasiewicz, G. D. Hess, D. Skaper, and J. A. Gladysz Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 11-hydroxyundecanoic acid C11H22O3 ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 2010 18 6429-6441 Synthesis and characterization of mitoQ and idebenone analogues as mediators of oxygen consumption in mitochondria Damien Y. Duveau, Pablo M. Arce, Robert A. Schoenfeld, Nidhi Raghav, Gino A. Cortopassi, Sidney M. Hecht Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . methoxymethyl (9R)-9-hydroxy-undec-10-ynoate C13H22O4 ÏàËÆ¶È:61.5% The Journal of Organic Chemistry 2007 72 4851-4855 Enantioselective Total Synthesis of Phomallenic Acid C Ya-Jun Jian, Chao-Jun Tang, and Yikang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 10-hydroxy-¦Ã-dodecalactone C12H22O3 ÏàËÆ¶È:58.3% Natural Product Research 2008 22 1151-1157 Chemical constituents of Antrodia camphorata submerged whole broth Yi-Yuan Shao; Chin-Chu Chen; Hsin-Yi Wang; Hsi-Lin Chiu; Tzong-Hsiung Hseu; Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Adamantane-2-spiro-3'-9'-carboxy-1',2',4',5'-tetraoxaspiro[5.5]undecane C17H24O6 ÏàËÆ¶È:58.3% Bioorganic & Medicinal Chemistry Letters 2011 21 5320-5323 The activity of dispiro peroxides against Fasciola hepatica Xiaofang Wang, Qingjie Zhao, Mireille Vargas, Yuxiang Dong, Kamaraj Sriraghavan, Jennifer Keiser, Jonathan L. Vennerstrom Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 9-acetoxycapric acid ÏàËÆ¶È:58.3% Phytochemistry 1988 27 2953-2959 Diterpenes and 5-methyl coumarin derivatives from Gypothamnium pinifolium and Plazia daphnoides C. Zdero,F. Bohlmann,H.M. Niemeyer Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . pentyl undecanoate C16H32O2 ÏàËÆ¶È:58.3% Indian Journal of Chemistry 2006 45B 314-317 Synthesis and antimicrobial screening of 5H,7H-N-(coumarin-6-yl)-2,8-diphenyl-5,7-dioxo-4,5,6,7-tetrahydrobenzimidazo[5,6-c]­furan and 5H,7H-N-(coumarin-6-yl)-2,8-diphenyl-5,7-dioxo-6-(7-methoxy-4-methylcoumarin-6-yl)-4,5,6,7-tetrahydro benzimidazo[5,6-c] Choudhari,B P; Mulwad,V V Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (R)-5-hydroxydodeca-1,11-diene C12H22O ÏàËÆ¶È:58.3% Heterocycles 2009 79 1043-1060 Catalytic Asymmetric Synthesis of Both Enantiomers of Pyrrolizidines 223H', 239K', 265H', and 267H' Found in Madagascan Frogs (Mantella) and Their Affinities for Nicotinic Acetylcholine Receptor Yukako Saito, Seiki Takahashi, Nehad Azer, Amira T. Eldefrawi, Mohyee E. Eldefrawi, and Hiroki Takahata Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 21 C16H24NO3F ÏàËÆ¶È:58.3% Tetrahedron 2011 67 10082-10088 Enantioenriched synthesis of Escitalopram using lithiation¨Cborylation methodology Benjamin M. Partridge, Stephen P. Thomas, Varinder K. Aggarwal Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 11-Dodecenoic acid C12H22O2 ÏàËÆ¶È:58.3% Zeitschrift f¨¹r Naturforschung B 2004 59 934-942 Synthesis and Biological Evaluation of a ''Natural'' Insect Repellent R. Csuk and A. Niesen Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . N,N-Dimethyldec-9-enamide C12H23NO ÏàËÆ¶È:58.3% Tetrahedron 2012 68 1177-1184 Cross-metathesis of allyl halides with olefins bearing amide and ester groups Jeong In Yun, Hyoung Rae Kim, Sang Kyum Kim, Deukjoon Kim, Jongkook Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 2-(Dec-9-enyloxy)acetic acid C12H22O3 ÏàËÆ¶È:58.3% Tetrahedron 2012 68 1177-1184 Cross-metathesis of allyl halides with olefins bearing amide and ester groups Jeong In Yun, Hyoung Rae Kim, Sang Kyum Kim, Deukjoon Kim, Jongkook Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (E)-1-iodo-1,11-dodecadiene ÏàËÆ¶È:58.3% Heterocycles 2000 52 1241-1249 Development of a Method for the Synthesis of ¦Á-Substituted ¦Á,¦Â-Unsaturated Lactones Based on Stille-Type Pd-catalyzed Carbonylation of (Z)-¦Ø-Iodoalkenols. An Efficient and Selective Synthesis of (+)-Hamabiwa-lactone B Baiqiao Liao and Ei-ichi Negishi* Structure 13C NMR ̼Æ×Ä£Äâͼ »¯ºÏÎï2£º 1 . ¦Á-tocopherol C29H52O2 ÏàËÆ¶È:100% Chemical & Pharmaceutical Bulletin 1998 46 1647-1649 Constituents of Ficus pumila Leaves Junichi KITAJIMA,Kaoru KIMIZUKA,Masanobu ARAI and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Á-tocopherol ÏàËÆ¶È:100% Korean Journal of Pharmacognosy 2008 39(1) 28-36 Phytochemical Studies on Paeoniae Radix (2);Phenolic and Related compounds Kim, Ju-Sun; Kim, Yoon-Jung; Lee, Joo-Young; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Á-tocopherol ÏàËÆ¶È:100% Journal of the Chinese Chemical Society 2000 47 555-560 The Chemical Constituents from the Heartwood of Eucalyptus citriodora Ching-Kuo Lee* and Ming-Huey Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Á-tocopherol ÏàËÆ¶È:93.1% Chinese Journal of Natural Medicines 2007 5 24-26 Chemical Constituents of the Seeds of Euryale ferox LI Mei-Hong; YANG Xue-Qiong; WAN Zhi-Jian; YANG Ya-Bin; LI Fan; DING Zhong-Tao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Á-Tocopherol ÏàËÆ¶È:93.1% Archives of Pharmacal Research 2002 25 628-635 Phytochemical constituens of Cirsium setidens Nakai and their cytotoxicity against human cancer cell lines Won Bin Lee, Hak Cheol Kwon, Ock Ryun Cho, Kang Choon Lee and Sang Un Choi, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Á-tocopherol ÏàËÆ¶È:93.1% Journal of the Brazilian Chemical Society 1996 7 115-118 Flavonol Glycosides from Davilla flexuosa. Jorge M. David, Frederico G. Cruz, Maria Lenise S. Guedes and Juceni P. Chavez Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyl-12-tridecenyl)-2H-1-benzopyran-6-ol ÏàËÆ¶È:89.6% Journal of Natural Products 1999 62 1685-1687 A New Vitamin E (¦Á-Tocomonoenol) from Eggs of the Pacific Salmon Oncorhynchus keta Yorihiro Yamamoto, Nobuo Maita, Akio Fujisawa, Junko Takashima, Youichi Ishii, and Walter C. Dunlap Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Á-tocopherol C29H50O2 ÏàËÆ¶È:89.6% Chinese Journal of Natural Medicines 2007 5 259-262 Non-alkaline Constituents From the Leaf of Alstonia scholaris DU Guo-Shun; CAI Xiang-Hai; SHANG Jian-Hua; LUO Xiao-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Á-ÉúÓý·Ó C29H50O2 ÏàËÆ¶È:89.6% Journal of Shenyang Pharmaceutical University 2003 20 425-427 Chemical constituents of Pyrrosia petiolosa(Christ) Ching WANG Nan, WANG Jin-hui, CHENG Jie, LI Xian Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Á-tocopherol C29H50O2 ÏàËÆ¶È:89.6% Chinese Traditional and Herbal Drugs 2012 43 653-657 Chemical constituents in twigs and leaves of Melodinus fusiformis WANG Ding-wei; LUO Xiao-dong; JIANG Bei Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3,4-dehydro-¦Á-tocopherol C29H48O2 ÏàËÆ¶È:86.2% Phytochemistry 2004 65 2719-2729 Antioxidant dehydrotocopherols as a new chemical character of Stemona species Brigitte Brem, Christoph Seger , Thomas Pacher, Markus Hartl, Franz Hadacek ,Otmar Hofer, Srunya Vajrodaya, Harald Greger Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Crassumtocopherol A C29H50O5 ÏàËÆ¶È:79.3% Bulletin of the Chemical Society of Japan 2011 84 783-787 ¦Á-Tocopherols from the Formosan Soft Coral Lobophytum crassum Shi-Yie Cheng, Shih-Tseng Lin, Shang-Kwei Wang, Chang-Yih Duh Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 5-nitro-¦Ã-tocopherol C28H47O4N ÏàËÆ¶È:79.3% Bioorganic & Medicinal Chemistry 2011 19 6483-6491 Tocotrienamines and tocopheramines: Reactions with radicals and metal ions Francesco Galli, Francesco Mazzini, Luca Bamonti, Lars Gille, Stefan Böhmdorfer, Marta Piroddi, Thomas Netscher, Frank J. Kelly, Thomas Rosenau Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 7a-methoxy-¦Á-tocopherol C30H52O3 ÏàËÆ¶È:79.3% Journal of the Chinese Chemical Society 2007 54 41-45 Tocopherols and Triterpenoids from Sida acuta Chiy-Rong Chen, Li-Hui Chao, Min-Hsiung Pan,Yun-Wen Liao and Chi-I Chang* Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Ã-tocopherol ÏàËÆ¶È:75.8% Agricultural and Biological Chemistry 1991 55 1727-1731 Prunusols A and B, Novel Antioxidative Tocopherol Derivatives Isolated from the Leaf Wax of Prunus grayana Maxim. Toshihiko OSAWA, Shigenori KUMAZAWA, Shunro KAWAKISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Á-tocoferol ÏàËÆ¶È:75.8% Qu¨ªmica Nova 1998 21 740-743 Triterpenes isolated from Eschweilera longipes miers (Lecythidaceae) Carvalho, Mario Geraldo de; Rinc¨®n Velandia, Javier; Oliveira, Lucilene Faustina de; Bezerra, Flavio Barbosa Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . isomeric 3,4-dehydro-¦Â-tocopherol C28H46O2 ÏàËÆ¶È:75% Phytochemistry 2004 65 2719-2729 Antioxidant dehydrotocopherols as a new chemical character of Stemona species Brigitte Brem, Christoph Seger , Thomas Pacher, Markus Hartl, Franz Hadacek ,Otmar Hofer, Srunya Vajrodaya, Harald Greger Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ¦Á-tocopherylquinone ÏàËÆ¶È:72.4% Phytochemistry 1990 29 2223-2228 Terpenoid compounds from Parentucellia latifolia J.G. Urones,I.S. Marcos,I. Cubillo,N.Martin Garrido,P. Basabe Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 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Fern¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,7,11,15-tetramethyl-hexadecan-1,3-diol ÏàËÆ¶È:84.2% Chinese Traditional and Herbal Drugs 2007 38 1779-1782 Acyclic diterpenoids and aliphatic compounds from green alga Chaetomorpha basiretorsa and their activities SHI Da-yong; HAN Li-jun; SUN Jie; YANG Yong-chun; SHI Jian-gong; FAN Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Isophytol ÏàËÆ¶È:84.2% Molecules 2013 18 2166-2182 Antibacterial/Antifungal Activity and Synergistic Interactions between Polyprenols and Other Lipids Isolated from Ginkgo Biloba L. 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(Asteraceae) Dirk Umlauf, Josef Zapp, Hans Becker, Klaus Peter Adam Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 7R,11R-phytol ÏàËÆ¶È:70% Phytochemistry 2003 64 303-323 Terpenoids from the seeds of Artemisia annua Geoffrey D. Brown, Guang-Yi Liang, Lai-King Sy Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . cassipourol C20H38O ÏàËÆ¶È:70% Journal of Natural Products 2006 69(2) 287-289 Cytotoxic Diterpenes from Cassipourea madagascariensis from the Madagascar Rainforest V. S. Prakash Chaturvedula, Andrew Norris, James S. Miller, Fidisoa Ratovoson,Rabodo Andriantsiferana, Vincent E. Rasamison, and David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 2-13C-D-Glucose ÏàËÆ¶È:70% Journal of Natural Products 1998 61 841-843 Biosynthesis of Phytol in the Cyanobacterium Synechocystis sp. UTEX 2470:Utilization of the Non-Mevalonate Pathway Philip J. Proteau Structure 13C NMR ̼Æ×Ä£Äâͼ |

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