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1 . daedalol A C31H48O4 ÏàËÆ¶È:80.6% Bioorganic & Medicinal Chemistry 2011 19 6581-6586 Daedalols A¨CC, fungal-derived BACE1 inhibitors Analia Sorribas, Jorge I. Jim¨¦nez, Wesley Y. Yoshida, Philip G. Williams Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Á-hhydroxy-24-methylene-23-oxolanost-8-en-26-carboxylic acid C31H48O4 ÏàËÆ¶È:74.1% Fitoterapia 2009 80 263-266 Antibacterial triterpenes from the threatened wood-decay fungus Fomitopsis rosea Milena Popova, Boryana Trusheva, Melania Gyosheva, Iva Tsvetkova, Vassya Bankova Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . fomitopsin A C34H50O8 ÏàËÆ¶È:70.9% Phytochemistry 2005 66 1656-1661 Lanostane triterpenoids from the inedible mushroom Fomitopsis spraguei Dang Ngoc Quang, Yuuki Arakawa, Toshihiro Hashimoto, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 24-methylenecycloartanol ÏàËÆ¶È:68.9% Chinese Traditional and Herbal Drugs 2005 36 669-671 ÌÙ¿à²Î»¯Ñ§³É·ÖÑо¿(¢ò) ÕÅÁÕ,ÐìÀöÕä,ÑîÊÀÁÖ Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (3¦Á,18¦Â,20¦Â)-3-methoxyamino-11-oxo-olean-12-en-29-oicacid hydrochloride ÏàËÆ¶È:67.7% Bioorganic & Medicinal Chemistry 2010 18 7522-7541 Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11¦Â-hydroxysteroid dehydrogenase 2 inhibitors Christian Stanetty, Laszlo Czollner, Iris Koller, Priti Shah, Rawindra Gaware, Thierry Da Cunha, Alex Odermatt, Ulrich Jordis, Paul Kosma, Dirk Claßen-Houben Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (24S)-ergostane-6-acetate-3¦Â,5¦Á,6¦Â,25-tetraol C30H52O5 ÏàËÆ¶È:66.6% Marine Drugs 2012 10 1422-1432 Polyoxygenated Sterols from the South China Sea Soft Coral Sinularia sp. Rui Li, Chang-Lun Shao, Xin Qi, Xiu-Bao Li, Jing Li, Ling-Ling Sun and Chang-Yun Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Neoabiestrine H C30H52O4 ÏàËÆ¶È:66.6% Phytochemistry 2012 81 159-164 Cytotoxic triterpenoids from Abies recurvata Yong-Li Li, Yan-Xia Gao, Xian-Wen Yang, Hui-Zi Jin, Ji Ye, Luke Simmons, Ning Wang, Andre Steinmetz, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Neoabiestrine I C31H54O4 ÏàËÆ¶È:64.5% Phytochemistry 2012 81 159-164 Cytotoxic triterpenoids from Abies recurvata Yong-Li Li, Yan-Xia Gao, Xian-Wen Yang, Hui-Zi Jin, Ji Ye, Luke Simmons, Ning Wang, Andre Steinmetz, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Euphonerin A C31H52O3 ÏàËÆ¶È:64.5% Planta medica 2012 78 1370-1377 Cycloartane Triterpenes and Ingol Diterpenes Isolated from Euphorbia neriifolia in a Screening Program for Death-Receptor Expression-Enhancing Activity Toume, Kazufumi; Nakazawa, Takafumi; Hoque, Tahmina; Ohtsuki, Takashi; Arai, Midori A.; Koyano, Takashi; Kowithayakorn, Thaworn; Ishibashi, Masami: Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Euphonerin C C31H52O3 ÏàËÆ¶È:64.5% Planta medica 2012 78 1370-1377 Cycloartane Triterpenes and Ingol Diterpenes Isolated from Euphorbia neriifolia in a Screening Program for Death-Receptor Expression-Enhancing Activity Toume, Kazufumi; Nakazawa, Takafumi; Hoque, Tahmina; Ohtsuki, Takashi; Arai, Midori A.; Koyano, Takashi; Kowithayakorn, Thaworn; Ishibashi, Masami: Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . serrulatin E C30H50O6 ÏàËÆ¶È:63.3% Helvetica Chimica Acta 2008 Vol. 91 665 Triterpenoids from the Edible Leaves of Photinia serrulata Ya-Ling Song, Yue-Hu Wang, Qing Lu, Hui-Jun Qiao, and Yong-Xian Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . methyl 3¦Â,23(R)-dihydroxy-29-no¦Á-lanosta-8,24-dien-28-oate 3-sulfate C30H47O7S ÏàËÆ¶È:63.3% Journal of Natural Products 2000 63 210-216 New Triterpenoid Sulfates from the Red Alga Tricleocarpa fragilis1 F. David Horgen, Bryan Sakamoto, and Paul J. Scheuer Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . oleanolic acid ÏàËÆ¶È:63.3% Natural Product Sciences 2005 11 13-15 Phytochemical Investigation of the Leaves of Flaveria trinervia Umadevi, S.; Mohanta, G.P.; Balakrishna, K.; Manavalan, R. Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Caloncobic acid A C30H46O4 ÏàËÆ¶È:63.3% Journal of Natural Products 2012 75 599-604 Cycloartane and Friedelane Triterpenoids from the Leaves of Caloncoba glauca and Their Evaluation for Inhibition of 11¦Â-Hydroxysteroid Dehydrogenases James D. Simo Mpetga, Yu Shen, Pierre Tane, Shi-Fei Li, Hong-Ping He, Hippolyte K. Wabo, Mathieu Tene, Ying Leng, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Artabotryol D C30H50O4 ÏàËÆ¶È:63.3% Helvetica Chimica Acta 2010 93 1925-1932 Artabotryols A ¨C E, New Lanostane Triterpenes from the Seeds of Artabotrys odoratissimus Chitrasen Gupta, Subedar Prasad, Mahendra Sahai, Teigo Asai, Noriyuki Hara and Yoshinori Fujimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . sapinmusaponin B C42H72O14 ÏàËÆ¶È:63.3% Journal of Agricultural and Food Chemistry 2005 53 4722-4727 New Dammarane-Type Saponins from the Galls of Sapindus mukorossi Yao-Haur Kuo, Hui-Chi Huang, Li-Ming Yang Kuo, Ya-Wen Hsu, Kuo-Hsiung Lee, Fang-Rong Chang, and Yang-Chang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 20(R),24(S)-epoxy-6¦Á,16¦Â,25-trihydroxycycloartan-3-one C30H48O5 ÏàËÆ¶È:63.3% Phytochemistry 2013 88 99-104 Microbial transformation of cycloastragenol Melis Kuban, Gaye Öngen, Ikhlas A. Khan, Erdal Bedir Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (22R)-cycloart-23-ene-3¦Â,22¦Á,25-triol ÏàËÆ¶È:63.3% Bioorganic & Medicinal Chemistry 2006 14 938-943 Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure¨Cactivity relationship Mahmud Tareq Hassan Khan, Sher Bahadar Khan, Arjumand Ather Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . cycloart-20-ene-3¦Â,25-diol C30H48O ÏàËÆ¶È:63.3% Bioorganic & Medicinal Chemistry 2006 14 938-943 Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure¨Cactivity relationship Mahmud Tareq Hassan Khan, Sher Bahadar Khan, Arjumand Ather Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . cycloart-25-ene-3¦Â,(22R)22-diol C30H50O2 ÏàËÆ¶È:63.3% Bioorganic & Medicinal Chemistry 2006 14 938-943 Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure¨Cactivity relationship Mahmud Tareq Hassan Khan, Sher Bahadar Khan, Arjumand Ather Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 24¦Î,25-dimethyl-cholest-5-ene-2¦Â,3¦Á-diol disodium sulfate C29H48O8S2Na2 ÏàËÆ¶È:62.0% Natural Product Research 2007 21 953-958 A new cytotoxic cholesterol sulfate from marine sponge Halichondria rugosa Hong-Jun Zhang; Jing-Bo Sun; Hou-Wen Lin; Zeng-Lei Wang; Hua Tang; Ping Cheng; Wan-Sheng Chen; Yang-Hua Yi Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . olean-12-en-2¦Á,3¦Â-diol ÏàËÆ¶È:62.0% Fitoterapia 2001 72 585-587 Triterpenes from Licania licaniaeflora Alessandra Braca, Chandra Sortino, Jeannette Mendez, Ivano Morelli Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . crustulinol C30H50O6 ÏàËÆ¶È:62.0% Tetrahedron letters 1983 24 1635-1638 Fungal metabolites XIII: New cytotoxic triterpene from Hebeloma species (basidiomycetes) M. De Bernardi, G. Fronza, M.P. Gianotti, G. Mellerio, G. Vidari, P. Vita-Finzi Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . donellanic acid A C29H42O4 ÏàËÆ¶È:62.0% Tetrahedron 2012 68 4621-4627 Donellanic acids A¨CC: new cyclopropanic oleanane derivatives from Donella ubanguiensis (Sapotaceae) Aurelie V.B. Djoumessi, Louis P. Sandjo, Johannes C. Liermann, Dieter Schollmeyer, Victor Kuete, Vincent Rincheval, Abegaz M. Berhanu, Samuel O. Yeboah, Pascal Wafo, Bonaventure T. Ngadjui, Till Opatz Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Á-triol ÏàËÆ¶È:62.0% Chinese Journal of Applied & Environmental Biology 2009 15 615-620 Chemical Constituents from Polygonum perfoliatum LI Hongfang; MA Qingyun; LIU Yuqing; QIAN Jinfu; ZHOU Jun & ZHAO Youxing Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . fasciospongine A ÏàËÆ¶È:60% Journal of Natural Products 2009 72 319-323 Bioactive Sulfated Sesterterpene Alkaloids and Sesterterpene Sulfates from the Marine Sponge Fasciospongia sp. Guangmin Yao, Tamara P. Kondratyuk, Ghee T. Tan, John M. Pezzuto,and Leng Chee Chang Structure 13C NMR ̼Æ×Ä£Äâͼ |

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