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libinoookľ³æ (ÕýʽдÊÖ)
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[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý16
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| 13C NMR (126 MHz, Pyr) ¦Ä 15.65,16.31, 16.54, 18.67, 24.37, 27.80, 28.78, 31.00, 37.85, 39. 06, 39.36, 42.97, 43.53, 55.32, 59.16, 62.63, 5.92, 71.54, 71.69, 75.02,78.18, 78.32, 78.39, 103.66, 120.87, 122.85, 140.51. |
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libinoook: ½ð±Ò+10 2013-11-26 13:18:12
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libinoook: ½ð±Ò+10 2013-11-26 13:18:12
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²éѯ½á¹û£º¹²²éµ½1043¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Sylvestin C26H46O8 ÏàËÆ¶È:77.7% Natural Product Communications 2010 5 771-774 A New ent-Labdane Diterpene Glycoside from the Leaves ofCasearia sylvestris Wei Wang, Zulfiqar Ali, Xing-Cong Li and Ikhlas A. Khan Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . officinoside D C27H46O11 ÏàËÆ¶È:62.9% Chemical & Pharmaceutical Bulletin 2001 49(8) 974-978 Medicinal Flowers. IV.1) Marigold. (2): Structures of New Ionone and Sesquiterpene Glycosides from Egyptian Calendula officinalis Toshiyuki MARUKAMI, Akinobu KISHI, and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . goshonoside-F1 ÏàËÆ¶È:62.9% Phytochemistry 1984 23 615-621 Ent-labdane-type diterpene glucosides from leaves of Rubus chingii Takashi Tanaka, Keiko Kawamura, Takumi Kitahara, Hiroshi Kohda, Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Microtropioside A C26H44O9 ÏàËÆ¶È:62.9% Phytochemistry 2010 71 675-681 Microtropiosides A¨CF: ent-Labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae) Yuka Koyama, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . cholesteryl-¦Â-D-tetra-O-acetylgalactopyranoside ÏàËÆ¶È:62.9% Chemical Biology & Drug Design 2012 80 647-656 Novel Targeted Liposomes Deliver siRNA to Hepatocellular Carcinoma Cells in vitro Shantal Dorasamy, Nicolisha Narainpersad, Moganavelli Singh and Mario Ariatti Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 2 C30H48O4 ÏàËÆ¶È:62.0% Bioorganic & Medicinal Chemistry 2010 18 3934-3939 Dammaranes from Gynostemma pentaphyllum and synthesis of their derivatives as inhibitors of protein tyrosine phosphatase 1B Ji-Qing Xu, Qiang Shen, Jia Li, Li-Hong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . triterpenoid X C30H46O3 ÏàËÆ¶È:60.7% Phytochemistry 1992 31 2546-2547 A triterpenoid from the root-bark of Chiococca alba Jnanabrata Bhattacharyya, Emidio V.L. Cunha Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . isofouquierol ÏàËÆ¶È:60% Journal of Natural Products 2005 68 1787-1789 Dammarane Triterpenes from the Hypocotyls and Fruits of Ceriops tagal Charoen Pakhathirathien, Chatchanok Karalai, Chanita Ponglimanont, Sanan Subhadhirasakul, and Kan Chantrapromma Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 20S-dammarane-23-ene-3¦Â,20,25-triol ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2008 10 33-37 Dammarane triterpenes from Ligustrum lucidum XIAO-HUA XU, NIAN-YUN YANG, SHI-HUI QIAN, NING XIE and JING-AO DUAN Structure 13C NMR ̼Æ×Ä£Äâͼ |
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