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JINQH1982: ½ð±Ò+10, ¡ïÓаïÖú 2015-01-14 19:33:04
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²éѯ½á¹û£º¹²²éµ½2103¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 1a ÏàËÆ¶È:63.3% Journal of the Brazilian Chemical Society 1999 10 237-240 Complete Assignments of 1H and 13C-NMR Spectra of the 3,4-seco-Triterpene Canaric Acid isolated from Rudgea jasminoides. Marcia N. Lopes, Fabiano C. Mazza, Maria Claudia M. Young, and Vanderlan da S. Bolzani 237 Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 28-norlup-20(29)-en-3¦Â-hydroxy-17¦Á-hydroperoxide C29H48O3 ÏàËÆ¶È:60% Journal of Natural Products 2008 71(10) 1787-1790 Antiproliferative Triterpenes from Melaleuca ericifolia Fatma M. Abdel Bar, Ahmed M. Zaghloul, Sunitha V. Bachawal,Paul W. Sylvester, Kadria F. Ahmad, and Khalid A. El Sayed Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . ilekudinol A C29H42O4 ÏàËÆ¶È:60% Journal of Natural Products 1999 62 1061-1064 Activity-Guided Isolation of Triterpenoid Acyl CoA Cholesteryl Acyl Transferase (ACAT) Inhibitors from Ilex kudincha Keiichi Nishimura, Toshiyuki Fukuda, Toshio Miyase, Hiroshi Noguchi, and Xin-Min Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-methoxy-hop-22(29)-ene ÏàËÆ¶È:60% Journal of Natural Products 1997 60 909-911 24-Norhopene Derivatives from Diatenopteryx sorbifolia Juceni P. Ch¨¢vez, Jorge M. David, Shu-Wei Yang, and Geoffrey A. Cordell Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-Hydroxyimino-3-oxolup-20(29)-en-28-oic acid C30H47NO4 ÏàËÆ¶È:60% Chemistry of Natural Compounds 2009 45 673-676 SYNTHESIS AND ANTIVIRAL ACTIVITY OF2,3-seco-DERIVATIVES OF BETULONIC ACID I. A. Tolmacheva, V. V. Grishko, E. I. BorekoO. V. Savinova, and N. I. Pavlova Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 16¦Â-acetoxyolean-18-en-3-one C32H50O3 ÏàËÆ¶È:60% Journal of Natural Products 1989 Vol 52 567 ¦¤18 Oleane Triterpenes from Schaefferia cuneifolia Antonio G. Gonzalez, J. J. Mendoza, A. G. Ravelo, J. G. Luis, X. A. Dominguez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Ursa-1,12-dien-3-oxo-28-oic acid C30H44O3 ÏàËÆ¶È:60% Natural Products and Bioprospecting 2012 2 210-216 Exploring of drug leads from diversity-oriented Michael-acceptor library derived from natural products Xu DENG, Ling-Mei KONG,Yu ZHAO, Juan HE, Li-Yan PENG, Yan LI, and Qin-Shi ZHAO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 4-formyl lupenone C30H46O2 ÏàËÆ¶È:60% Journal of Wenzhou Medical College 2002 32 24-25 A study on chemical constituentes of humata tyermanni moore YE Xiao-qin; YANG Xiao-feng; HUANG Ke-xin; et al Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 2,3-seco-taraxer-14-ene-2,3,28-trioic acid 3-methyl ester C31H48O6 ÏàËÆ¶È:58.0% Journal of Natural Products 2008 71(2) 292-294 Seco-Terpenoids and Other Constituents from Elateriospermum tapos Duangpen Pattamadilok, and Rutt Suttisri Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . subprogenin D methyl ester ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 1991 39 1908-1910 FOUR NEW AND TWELVE KNOWN SAPOGENOLS FROM SOPHORAE SUBPROSTRATE RADIX Takashi TAKESHITA,Kei YOKOYAMA,Ding YI,Junei KINJO and Toshihiro NOHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . Methyl Ester of 2-Hydroxyimino-3-oxolup-20(29)-en-28-oic acid C31H47NO4 ÏàËÆ¶È:58.0% Chemistry of Natural Compounds 2008 44 606-611 SYNTHESIS OF LUPANE AND 19¦Â,28-EPOXY-18¦Á-OLEANANE 2,3-seco-DERIVATIVES BASED ON BETULIN I. A. Tolmacheva, A. V. Nazarov, O. A. Maiorova, and V. V. Grishko Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Â-methoxyhop-22(29)-ene C31H52O ÏàËÆ¶È:58.0% Phytochemistry 1992 31 702-703 3¦Â-methoxyhop-22(29)-ene from Chionochloa cheesemanii Daryl D. Rowan, Graeme B. Russell Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . Compound (2S,3R)-4 ÏàËÆ¶È:58.0% Bioorganic & Medicinal Chemistry Letters 2007 17 4140-4143 (2R,3S)-(+)- and (2S,3R)-(− -Halofuginone lactate: Synthesis, absolute configuration, and activity against Cryptosporidium parvum Michael R. Linder, Anja R. Heckeroth, Michael Najdrowski, Arwid Daugschies, Dieter Schollmeyer, Christian Miculka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 3,4-secolupa-4(23):20(29)-diene-3-dioic acid 28-methyl ester C31H48O4 ÏàËÆ¶È:58.0% Chemistry & Biodiversity 2011 8 2291-2298 Terpenoids from Maytenus Species and Assessment of Their Reversal Activity against a Multidrug-Resistant Leishmania tropica Line (pages 2291¨C2298) Mar¨ªa L. Kennedy, Gabriel G. Llanos, Santiago Castanys, Francisco Gamarro, Isabel L. Bazzocchi and Ignacio A. Jim¨¦nez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . Acanthosessiligenin I C31H48O5 ÏàËÆ¶È:58.0% Journal of Natural Products 2012 75 1138-1144 Bioactive 3,4-seco-Triterpenoids from the Fruits of Acanthopanax sessiliflorus Dae-Young Lee, Kyeong-Hwa Seo, Dong-Sung Lee, Youn-Chul Kim, In-Sik Chung, Gye-Won Kim, Dae-Sung Cheoi, and Nam-In Baek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . oleanderic acid C30H48O4 ÏàËÆ¶È:56.6% Journal of Natural Products 2005 68 198-206 Three New Triterpenes from Nerium oleander and Biological Activity of the Isolated Compounds Liwei Fu, Shujun Zhang, Na Li, Jinlan Wang, Ming Zhao, Junichi Sakai, Toshiaki Hasegawa,Tomokazu Mitsui, Takao Kataoka, Seiko Oka, Miwa Kiuchi, Katutoshi Hirose, and Masayoshi Ando Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 3¦Â-hydroxyurs-18,20(30)-dien-28-oic acid C30H46O3 ÏàËÆ¶È:56.6% Journal of Natural Products 1999 62 1624-1626 DNA Polymerase ¦Â Inhibitors from Baeckea gunniana Jing-Zhen Deng, Shelley R. Starck, and Sidney M. Hecht Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . (22E,24S)-7¦Á-hydroperoxystigmasta-5,22-dien-3¦Â-ol C29H48O3 ÏàËÆ¶È:56.6% Planta Medica 2003 69 757-764 Anti-Platelet Aggregation and Chemical Constituents from the Rhizome of Gynura japonica Wei-Yu Lin,Yueh-Hsiung Kuo,Ya-Ling Chang, Che-Ming Teng,Eng-Chi Wang, Tsutomu Ishikawa,Ih-Sheng Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . hancokinol C30H50O ÏàËÆ¶È:56.6% Chemical & Pharmaceutical Bulletin 1991 39 2271-2276 Stereochemistry of Novel Triterpenes from Cynanchum hancokianum Hongxiang LOU,Xian LI,Masayuki ONDA,Yaeko KONDA,Mieko URANO,Yoshihiro HARIGAYA,Hiroaki TAKAYANAGI and Haruo OGURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Â,22¦Â-dihydroxyolean-18-ene ÏàËÆ¶È:56.6% Chemical & Pharmaceutical Bulletin 1991 39 566-571 Incarnal. A New Antibacterial Sesquiterpene from Basidiomycetes Hideki TAKAZAWA and Setsuo KASHINO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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-Halofuginone lactate: Synthesis, absolute configuration, and activity against Cryptosporidium parvum