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²éѯ½á¹û£º¹²²éµ½45¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . dankasterone A C28H40O3 ÏàËÆ¶È:76.6% Journal of Natural Products 2007 70 1731-1740 Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source Taro Amagata,Makoto Tanaka,Takeshi Yamada, Mitsunobu Doi, Katsuhiko Minoura, Hirofumi Ohishi,Takao Yamori, and Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . dankasterone A C28H40O3 ÏàËÆ¶È:76.6% China Journal of Chinese Materia Medica 2011 36 2515-2519 Studies on metabolites from marine microorganism Aspergillus terreus collected from nature reserve region of mangrove SHEN, Yi, ZOU, Jianhua, DAI, Jungui Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ursoxy acid C31H48O4 ÏàËÆ¶È:67.7% Helvetica Chimica Acta 2002 Vol. 85 2335 Three New Pentacyclic Triterpenoids from Lantana camara Sabira Begum, Aneela Wahab, and Bina S. Siddiqui Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . honu'enone C30H44O5 ÏàËÆ¶È:66.6% Journal of Natural Products 2000 63 1388-1392 Scalarane-Based Sesterterpenes from an Indonesian Sponge Strepsichordaia aliena Jorge I. Jim¨¦nez, Wesley Y. Yoshida, Paul J. Scheuer, and Michelle Kelly Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (R)-N-[1-(cyclohexylmethyl)-2,3-dioxohexyl]-N2-[N-(cyclopentylcarbonyl)-L-phenylalanyl]-L-leucinamide C34H51N3O5 ÏàËÆ¶È:66.6% Journal of Medicinal Chemistry 1993 36 2431-2447 Activated ketone based inhibitors of human renin Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, Sandra A. Smith, Edward W. Petrillo Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ilelatifol A methyl ester ÏàËÆ¶È:66.6% Natural Medicines 2000 54 297-305 Acyl-CoA : Cholesterol Acyltransferase(ACAT) Inhibitors from Ilex spp. Nishimura Keiichi,Miyase Toshio,Noguchi Hiroshi,Chen Xin-Min Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . methyl ursoxylate C32H50O4 ÏàËÆ¶È:65.6% Helvetica Chimica Acta 2002 Vol. 85 2335 Three New Pentacyclic Triterpenoids from Lantana camara Sabira Begum, Aneela Wahab, and Bina S. Siddiqui Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . methyl 2,3-dihydroxy urs-12-en-28-oates [ 2¦Â,3¦Á-(OH)2] ÏàËÆ¶È:64.5% Phytochemistry 1989 28 1703-1710 Configurational studies on hydroxy groups at C-2,3 and 23 or 24 of oleanene and ursene-type triterpenes by NMR spectroscopy Hisashi Kojima,Haruo Ogura Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . lantic acid ÏàËÆ¶È:63.3% Phytochemistry 1995 38 681-685 Pentacyclic triterpenoids from Lantana camara Bina Shaheen Siddiqui, Syed Mohammad Raza, Sabira Begum, Salimuzzaman Siddiqui, Sadiqa Firdous Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 215 ÏàËÆ¶È:63.3% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-oxo-ursolic acid ÏàËÆ¶È:63.3% Archives of Pharmacal Research 2000 23 155-158 Cytotoxic triterpenes from Crataegus pinnatifida Byung Sun Min, Young Ho Kim, Sang Myung Lee, Hyun Ju Jung and Jun Sung Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Trihydroxy ursolic acid C30H49O5 ÏàËÆ¶È:63.3% Journal of Pharmacognosy and Phytotherapy 2012 4 75-85 Anti-diabetic activity of Ocimum sanctum L. roots and isolation of new phytoconstituents using two-dimensional nuclear magnetic resonance spectroscopy M. Zaffer Ahmad, Mohd. Ali, Showkat R. Mir Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . methyl 3¦Â,23-dihydroxyurs-12-en-28-oate C31H50O4 ÏàËÆ¶È:61.2% Natural Product Research 2002 16 273-276 Partial Synthesis of 23-Hydroxyursolic Acid Isolated from Medicinal Plants of the Rubiaceae Family Lothar Bore; Tadashi Honda; Gordon Gribble Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Compound 4 ÏàËÆ¶È:61.2% Magnetic Resonance in Chemistry 2002 40 471-473 Reassignment of the 1H NMR spectrum of fusidic acid and total assignment of 1H and 13C NMR spectra of some selected fusidane derivatives Niels Rastrup-Andersen and Tore Duvold Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . methylcamaralate C33H50O6 ÏàËÆ¶È:60.6% Chemical & Pharmaceutical Bulletin 2003 51(2) 134-137 Pentacyclic Triterpenoids from the Aerial Parts of Lantana camara Sabira BEGUM, Aneela WAHAB, and Bina Shaheen SIDDIQU Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 9 C36H48N2O2 ÏàËÆ¶È:60.6% Journal of Medicinal Chemistry 2014 57 4692-4709 Tryptophan Hydroxylase 1 (Tph-1)-Targeted Bone Anabolic Agents for Osteoporosis Hai-Jian Fu, Yu-Ren Zhou, Bei-Hua Bao, Meng-Xuan Jia, Yang Zhao, Lei Zhang, Jian-Xin Li, Hai-Lang He, and Xian-Mei Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 22 C32H46N2O2 ÏàËÆ¶È:60.6% Journal of Medicinal Chemistry 2014 57 4692-4709 Tryptophan Hydroxylase 1 (Tph-1)-Targeted Bone Anabolic Agents for Osteoporosis Hai-Jian Fu, Yu-Ren Zhou, Bei-Hua Bao, Meng-Xuan Jia, Yang Zhao, Lei Zhang, Jian-Xin Li, Hai-Lang He, and Xian-Mei Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Benzyl 2¦Á-Hydroxyurs-12-en-28-oate C37H54O3 ÏàËÆ¶È:60% Journal of Natural Products 2009 72 1414-1418 Synthesis of 3-Deoxypentacyclic Triterpene Derivatives as Inhibitors of Glycogen Phosphorylase Pu Zhang,Jia Hao,Jun Liu,Qian Lu, Huaming Sheng, Luyong Zhang, and Hongbin Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . steroid C27H42O2 ÏàËÆ¶È:60% Journal of Natural Products 2004 67 1650-1653 Steroids and Sesquiterpenoids from the Soft Corals Dendronephthya gigantea and Lemnalia cervicorni Chang-Yih Duh, Ali A. H. El-Gamal, Pei-Ying Song, Shang-Kwei Wang, and Chang-Feng Dai Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Â-hydroxy-4¦Á,14¦Á-dimethyl-5¦Á-ergosta-8,24(28)-dien-11-one C30H48O2 ÏàËÆ¶È:60% Journal of Natural Products 2000 63 99-103 Bioactive Steroids from the Whole Herb of Euphorbia chamaesyce Reiko Tanaka,Kazuaki Kasubuchi, Shunji Kita, Harukuni Tokuda, Hoyoku Nishino, and Shunyo Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . compound 17 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1996 44 1540-1545 Studies on Nepalese Crude Drugs. XXXI. On the Diterpenoid Constituents of the Aerial Part of Scutellaria discolor COLEBR. Akiko OHNO,Haruhisa KIZU and Tsuyoshi TOMIMORI Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . adianenone C30H48O ÏàËÆ¶È:60% Chemistry of Natural Compounds 2007 43 563-566 CHEMICAL CONSTITUENTS FROM THE ROOTS OF Polygonum bistorta Xiao-Bai Sun, Pei-Hua Zhao, Yang-Jun Xu,Li-Mei Sun, Mei-Ai Cao, and Cheng-Shan Yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 18-Isopropyl-4,10-dimethyl-4,13-dimethoxycarbonyl-8,12-ethenocyclopentanoperhydrophenanthrene ÏàËÆ¶È:60% Chemistry of Natural Compounds 2002 38 246-248 SYNTHESIS OF DITERPENE INDOLES FROM CYCLOPENTENONEPIMARIC ACID E. V. Tret'yakova, O. B. Flekhter, F. Z. Galin,L. V. Spirikhin, and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3-oxo-urs-12-en-28-oic acid C30H46O3 ÏàËÆ¶È:60% Acta Botanica Boreali-Occidentalia Sinica 2007 27 1141-1146 The Triterpenes in Salvia umbratica LIU Qing, LIU Zhen-ling, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . Cholest-4-eno[3,2-c]-[1'H]-5'-methylthiopyrazole ÏàËÆ¶È:60% Steroids 2002 67 203-209 Synthesis of some A- and D-ring fused steroidal pyrazoles, isoxazoles and pyrimidines Warjeet S. Laitonjam, Tombisana S. Rajkumar, Brajakishor S. Chingakham Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . Cholest-4-eno[2,3-d]-3'-methylthioisoxazole ÏàËÆ¶È:60% Steroids 2002 67 203-209 Synthesis of some A- and D-ring fused steroidal pyrazoles, isoxazoles and pyrimidines Warjeet S. Laitonjam, Tombisana S. Rajkumar, Brajakishor S. Chingakham Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . methylursonate ÏàËÆ¶È:60% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound 352 ÏàËÆ¶È:60% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . ¦Á-spinasterone ÏàËÆ¶È:60% China Journal of Chinese Materia Medica 2010 35 327-330 Triterpenes from Kalimeris indica GONG Xiaojian; ZHOU Xin; ZHAO Chao; CHEN Huaguo; XU Wenqing; LONG Shangxiang Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . Methyl spongoate C28H44O3 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry Letters 2007 17 2661-2663 Methyl spongoate, a cytotoxic steroid from the Sanya soft coral Spongodes sp. Xiao-Hong Yan, Li-Ping Lin, Jian Ding, Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . Compound 12 ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 2002 40 471-473 Reassignment of the 1H NMR spectrum of fusidic acid and total assignment of 1H and 13C NMR spectra of some selected fusidane derivatives Niels Rastrup-Andersen and Tore Duvold Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . sanguisorbigenin V ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2010 41 1048-1052 Chemical constituents of charred Sanguisorbae Radix(¢ò) XIA Hong-min; ZHONG Ying; SUN Jing-yong; SUN Li-li; AN Kun; WANG Ju Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . Griffinisterone A C28H44O3 ÏàËÆ¶È:60% Tetrahedron 2008 64 3554-3560 Anti-inflammatory steroids from the octocoral Dendronephthya griffini Chih-Hua Chao, Zhi-Hong Wen, I.-Ming Chen, Jui-Hsin Su, Ho-Cheng Huang, Michael Y. Chiang, Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . compound 5 C27H42O2 ÏàËÆ¶È:60% Tetrahedron 1995 51 2497-2506 Isolation of novel bioactive steroids from the soft coral Alcyonium gracillimum Youngwan Seo, Jee H Jung, Jung-Rae Rho, Jongheon Shin, Jun-Im Song Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . (E)-3-oximeurs-12-en-28-oic acid ÏàËÆ¶È:60% European Journal of Medicinal Chemistry 2008 43 1865-1877 Evaluation of ursolic acid isolated from Ilex paraguariensis and derivatives on aromatase inhibition Simone C.B. Gnoatto, Alexandra Dassonville-Klimpt, Sophie Da Nascimento, Philippe Gal¨¦ra, Karim Boumediene, Grace Gosmann, Pascal Sonnet, Safa Moslemi Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . 2,3-dioxours-12-en-28-oic acid C30H44O4 ÏàËÆ¶È:60% Australian Journal of Chemistry 1993 46 1067-1071 Synthesis of 2¦Â-Hydroxyursolic Acid and Other Ursane Analogs From Ursonic Acid S Begum, Q Adil, BS Siddiqui and S Siddiqui Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . (S*,R*)-N-[1-(cyclohexylmethyl)-2-hydroxy-3-oxohexyl]-N-[N-(cyclopentylcarbonyl)-L-pnenylalanyl]-L-leucinamide C34H53N3O5 ÏàËÆ¶È:60% Journal of Medicinal Chemistry 1993 36 2431-2447 Activated ketone based inhibitors of human renin Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, Sandra A. Smith, Edward W. Petrillo Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . ursolic acid ÏàËÆ¶È:60% Academic Journal of Second Military Medical University 2004 25 1029-1030 Study on chemical constituents of Lycopus lucidus Turcz. ¢ñ ËïÁ¬ÄÈ, ³ÂÍòÉú, ÌÕ³¯Ñô, Ç®ÃùÈØ, ÕźºÃ÷ Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . cabralealactone 3-acetate-24-methyl ether C30H50O4 ÏàËÆ¶È:60% Zeitschrift f¨¹r Naturforschung C 2013 68C 29-38 Induction of Caspase-8 and Death Receptors by a New Dammarane Skeleton from the Dried Fruits of Forsythia koreana Usama W. Hawas, Amira M. Gamal-Eldeen, Samy K. El-Desouky, Young-Kyoon Kim, Antje Huefner, and Robert Saf Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . 3¦Â-hydroxy-stigmast-5,22-dien-7-one ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2011 42 251-254 Chemical constituents of Omphalia lapidescens XU Ming-feng, SHEN Lian-qing, WANG Kui-wu Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . acetyl-24,25-dihydroebelin lactone ÏàËÆ¶È:60% Australian Journal of Chemistry 1980 33 2071-2086 The triterpenes of Emmenospermum pancherianum GV Baddeley, JJH Simes and T Ai Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . methyl 3-oxours-12-en-28-oate ÏàËÆ¶È:60% Australian Journal of Chemistry 1983 36 2537-2547 Triterpenes of Lantana tiliaefolia. 24-Hydroxy-3-oxours-12-en-28-oic acid, a new triterpene SR Johns, JA Lamberton, TC Morton, H Suares and RI Willing Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . methyl 24-hydroxy-3-oxours-12-en-28-oate C36H46O3 ÏàËÆ¶È:60% Australian Journal of Chemistry 1983 36 2537-2547 Triterpenes of Lantana tiliaefolia. 24-Hydroxy-3-oxours-12-en-28-oic acid, a new triterpene SR Johns, JA Lamberton, TC Morton, H Suares and RI Willing Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . ferna-7,18-diene ÏàËÆ¶È:60% Natural Medicines 1998 52 409-413 Pharmacognostical Studies on "Ku-tui-po" III. : Constituents of the Rhizomes of Davallia solida Tanaka Yasuko,Kitajima Jun-ichi,Ageta Hiroyuki Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 3,25-epoxy-3¦Á,22¦Â-dihydroxyurs-12-en-28-oic acid C30H46O5 ÏàËÆ¶È:60% Chemistry & Biodiversity 2014 11 709-718 Leishmanicidal Triterpenes from Lantana camara Sabira Begum, Anjum Ayub, Syeda Qamar Zehra, Bina Shaheen Siddiqui, M. Iqbal Choudhary and Samreen Structure 13C NMR ̼Æ×Ä£Äâͼ |

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