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1 . daucosterol+stigmasterol-3-O-glucopyranoside ÏàËÆ¶È:56.8% Chinese Traditional and Herbal Drugs 2004 35 608-611 Studies on chemical constituents of Indigofera carlesii SU Yan-fang; ZHANG Xin-xin; YANG Jing; GUO Zeng-jun; L¨¹ Ju-xian; GUO De-an Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-sitosteryl glucoside-6'-palmitoleoate ÏàËÆ¶È:56.8% Chinese Journal of Applied & Environmental Biology 2000 6 194-196 CHEMICAL CONSTITUENTS FROM RUBUS SETCHUENENSIS HUANG Kexin; ZHANG Xiaorong; WANG Mingkui & DING Lisheng Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound A ÏàËÆ¶È:54.9% Yakugaku Zasshi 1983 103 43-48 The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A) EMI OKUYAMA, MIKIO YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Â-sitosteryl glucoside-3'-O-heptadecoicate ÏàËÆ¶È:52.9% Natural Product Research and Development 1997 9(2) 7-10 STUDIES ON THE CHEMICAL CONSTITUENTS OF THE CULTIVATED DESERTLIVING CISTANCHE (CISTANCHE DESERTICOLA) Tu Pengfei; He Yanping and Lou Zhicen Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 5-(4-Cholesteryloxybenzyl)-2,8,12,18-tetraethyl-3,7,13,17-tetramethyl-15-[4-¦Á/¦Â-D-galactopyranos-6-oxy)benzyl]-porphyrin C79H104N4O7 ÏàËÆ¶È:52.8% Bioorganic & Medicinal Chemistry 1999 7 1857-1865 Synthesis and investigation of glycosylated mono- and diarylporphyrins for photodynamic therapy Christian Schell, Hermann K. Hombrecher Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5-(4-Cholesteryloxybenzyl)-2,8,13,17-tetraethyl-3,7,12,18-tetramethyl-porphyrin C66H88N4O ÏàËÆ¶È:51.7% Bioorganic & Medicinal Chemistry 1999 7 1857-1865 Synthesis and investigation of glycosylated mono- and diarylporphyrins for photodynamic therapy Christian Schell, Hermann K. Hombrecher Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-[6'-O-n-acyl-¦Â-D-glucosyl]-22-dehydroclerosterol ÏàËÆ¶È:50.9% Phytochemistry 1994 36 167-170 Acylglucosylsterols from two Aegiphila species Suzana G. Leitão, Maria Auxiliadora C. Kaplan, Franco Delle Monache Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . pseudolaridimer A C50H78O5 ÏàËÆ¶È:50.9% Organic Letters 2012 14 5432-5435 Pseudolaridimers A and B, Hetero-Cycloartane¨CLabdane Diels¨CAlder Adducts from the Cone of Pseudolarix amabilis Bo Li, De-Yun Kong, Yun-Heng Shen, Hu Yuan, Rong-Cai Yue, Yi-Ren He, Lu Lu, Lei Shan, Hui-Liang Li, Ji Ye, Xian-Wen Yang, Juan Su, Run-Hui Liu, and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Â-sitosteryl-3'-glucopyranoside-6'-O-palmitate ÏàËÆ¶È:50.9% Chinese Herbal Medicines 2014 6 65-69 Chemical Constituents from Barks of Lannea coromandelica Xiao-juan Yun, Huo-ming Shu, Guang-ying Chen, Ming-hui Ji, Jin-yue Ding Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ritterazine T C54H76N2O8 ÏàËÆ¶È:50% The Journal of Organic Chemistry 1997 62 4484-4491 Isolation of 13 New Ritterazines from the Tunicate Ritterella tokioka and Chemical Transformation of Ritterazine B1 Seketsu Fukuzawa, Shigeki Matsunaga, and Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ritterazine U C54H76N2O9 ÏàËÆ¶È:50% The Journal of Organic Chemistry 1997 62 4484-4491 Isolation of 13 New Ritterazines from the Tunicate Ritterella tokioka and Chemical Transformation of Ritterazine B1 Seketsu Fukuzawa, Shigeki Matsunaga, and Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ritterazine W C54H76N2O8 ÏàËÆ¶È:50% The Journal of Organic Chemistry 1997 62 4484-4491 Isolation of 13 New Ritterazines from the Tunicate Ritterella tokioka and Chemical Transformation of Ritterazine B1 Seketsu Fukuzawa, Shigeki Matsunaga, and Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ |
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