| ²é¿´: 1002 | »Ø¸´: 1 | ||
ËμÒÁáÒø³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
666 ÒÑÓÐ1È˲ÎÓë
|
| 180.10, 143.17,123.50, 81.02, 77.80, 72.14, 56.34, 53.75, 48.27, 48.06, 47.94, 47.77, 46.57, 45.33, 43.81, 41.69, 39.17, 38.89, 37.57, 34.64, 32.74, 28.15, 28.13, 27.62, 25.88, 23.76, 19.99, 16.15, 15.19, 12.76 |
» ²ÂÄãϲ»¶
071000ÉúÎïѧµ÷¼ÁÇóÖú
ÒѾÓÐ14È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ9È˻ظ´
277Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
344Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
»¯¹¤µ÷¼ÁÇóµ¼Ê¦ÊÕÁô£¡Ò»Ö¾Ô¸Ê§Àû£¬Ì¤Êµ¿Ï¸É£¬ÓÐÖ²ÎïÌáÈ¡¿ÆÑоÀú
ÒѾÓÐ13È˻ظ´
Ò»Ö¾Ô¸Î÷½»»úеר˶Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
277 ÊýÒ»104£¬Ñ§Ë¶£¬Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
Çóµ÷¼Á ²ÄÁÏÓ빤³Ì 324·Ö ר˶
ÒѾÓÐ17È˻ظ´
342µç×ÓÐÅϢר˶Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
0835ѧ˶299Çóµ÷¼Á 08´óÀà¿É½ÓÊÜ
ÒѾÓÐ7È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48426.9
- ºì»¨: 52
- Ìû×Ó: 6748
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ËμÒÁá: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-02-02 12:39:59
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ËμÒÁá: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-02-02 12:39:59
|
1 . 3¦Â,22¦Á-dihydroxyolean-12-en-30-oic acid C30H48O4 ÏàËÆ¶È:70% Journal of Natural Products 2008 71(5) 789-792 Oleanane-Type Triterpenes from the Flowers and Roots of Saussurea muliensis Chun-Mei Liu, He-Xiang Wang, Shi-Lei Wei, and Kun Gao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . sumaresinolic acid ÏàËÆ¶È:70% Journal of Natural Products 2006 69(5) 807-810 Triterpenoids from the Resin of Styrax tonkinensis and Their Antiproliferative and Differentiation Effects in Human Leukemia HL-60 Cells Feng Wang, Huiming Hua, Yuehu Pei, Duo Chen, and Yongkui Jing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 19¦Á-hydroxyoleanonic acid C30H46O4 ÏàËÆ¶È:70% Journal of Natural Products 2006 69 1092-1094 Triterpenes from Natural and Transformed Roots of Plocama pendula Braulio M. Fraga, Carmen E. Daz, and Nayra Quintana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . wistariasapogenol A C30H48O4 ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 1989 37 1550-1553 Studies on the Constituents of Leguminous Plants. XI. : The Structures of New Triterpenoids from Wistaria brachybotrys SIEB. et ZUCC. Takao KONOSHIMA,Mutsuo KOZUKA,Mitsumasa HARUNA,Kazuo ITO and Takeatsu KIMURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . wistariasatmnenol A ÏàËÆ¶È:70% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . A1-barrigenol C30H50O5 ÏàËÆ¶È:70% Phytochemistry 1990 29 2539-2543 Caffeine and theanine from cultured cells of Camellia sinensis Tsutomu Furuya,Yutaka Orihara,Yumiko Tsuda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 2¦Á,3¦Â,19¦Á,23-tetrahydroxyolean-12-ene-24,28-dioic acid ÏàËÆ¶È:70% Phytochemical Analysis 2002 13 305-310 Identification of triterpene saponins in Quercus robur L. and Q. petraea Liebl. heartwood by LC-ESI/MS and NMR G. Arramon, C. Saucier, D. Colombani and Y. Glories Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ilexgenin A ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2007 38 995-997 붬Çà¸ùÖл¯Ñ§³É·ÖµÄÑо¿ ÒüÎÄÇå;ÖÜÖÐÁ÷;×Þ½ÚÃ÷;ÃϽÜ;¸µ´ºÑà Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . spinosic acid ÏàËÆ¶È:70% Magnetic Resonance in Chemistry 2011 49 184-189 Structure elucidation and NMR assignments of two new triterpenoids from the stems of Paragonia pyramidata (Bignoniaceae) Xiao-Ling Wang, Anne-Emmanuelle Hay, An Matheeussen, Mahabir P. Gupta and Kurt Hostettmann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 7¦Á,21¦Â-dihydroxyl oleanolic acid C30H48O5 ÏàËÆ¶È:70% Journal of Asian Natural Products Research 2011 13 160-167 Biotransformation of oleanolic acid by Alternaria longipes and Penicillium adametzi Dai-Lin Liu; Ying Liu; Feng Qiu; Ying Gao; Jing-Ze Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 19¦Á-hydroxy-3-oxo-olean-12-en-28-oic acid ÏàËÆ¶È:70% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 89-92 Chemical Constituents from Resin of Styrax tonkinensis WANG Feng, FANG Zhen-feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Coryternic acid C31H48O5 ÏàËÆ¶È:67.7% Planta Medica 2011 77 1555-1558 New Triterpenoids from the Tubers of Corydalis ternata:Structural Elucidation and Bioactivity Evaluation Ki Hyun Kim, Il Kyun Lee, Sang Un Choi, Jei Hyun Lee, Eunjung Moon, Sun Yeou Kim, Kang Ro Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . Pseudolarolide O C30H42O5 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2003 Vol. 86 787 Pseudolarolides O and P, Two Novel Triterpene Dilactones from Pseudolarix kaempferi Guo-Fu Chen, Chang-Heng Tan, Zhu-Lian Li, Shan-Hao Jiang, and Da-Yuan Zhu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . oleanolic acid derivative C30H48O4 ÏàËÆ¶È:66.6% Phytochemistry 2001 57 773-779 Triterpene glycosides from the roots of Sanguisorba officinalis Yoshihiro Mimaki, Masato Fukushima, Akihito Yokosuka, Yutaka Sashida,Shigenori Furuya, Hiroshi Sakagami Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 9 ÏàËÆ¶È:66.6% Journal of Natural Products 1996 59 304-307 Triterpenoids from Adina rubella Shi-yue Fang, Zhi-sheng He, and Gao-jun Fan, Hou-ming Wu and Jing-fei Xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 18-hydroxyursolic acid C30H48O4 ÏàËÆ¶È:66.6% Acta Botanica Yunnanica 1997 19(3) 327-330 CHEMICAL CONSTITUENTS OF SPIRAEA JAPONICAVAR. ACUM INA TA Nie Jinglei, Hao Xiao jiang, LiLi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . kudzusapogenol C ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1995 43 1176-1179 Oleanene-Type Triterpene Glycosides from Puerariae Radix. II. Isolation of Saponins and the Application of Tandem Mass Spectrometry to Their Structure Determination Tomonori ARAO,Junei KINJO,Toshihiro NOHARA and Ryuichi ISOBE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . abrisapogenol H ÏàËÆ¶È:66.6% 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 19 . kudzusapogenol C C50H50O5 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1985 33 1293-1296 OLEANENE-SAPOGENOLS FROM PUERARIAE RADIX Junei Kinjo,Izumi Miyamoto,Kotaro Murakami,Kiyoshi Kida,Toshiaki Tomimatsu,Masaki Yamasaki and Toshihiro Nohara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . longispinogenin ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1980 28 2367-2373 Isolation, Characterization, and Nuclear Magnetic Resonance Spectra of New Saponins from the Roots of Bupleurum falcatum L. HIROSHI ISHII,MIHARU NAKAMURA,SHUJIRO SEO,KAZUO TORI,TAKEHIKO TOZYO and YOHKO YOSHIMURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . olean-12-en-28-oic acid 3¦Â,24-diol ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1982 30 3340-3346 Studies on the Constituents of Clematis Species. V. On the Saponins of the Root of Clematis chinensis OSBECK. (5) HARUHISA KIZU and TSUYOSHI TOMIMORI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . 4-epihederagenin ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . Camelliagenin A ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . Kudzusapogenol C ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . 22¦Á-hydroxyoleanolic acid C30H48O4 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1997 45 1300-1305 Medicinal Foodstuffs. VII. On the Saponin Constituents with Glucose and Alcohol Absorption-Inhibitory Activity from a Food Garnish "Tonburi", the Fruit of Japanese Kochia scoparia (L.) SCHRAD. : Structures of Scoparianosides A, B, and C Masayuki YOSHIKAWA,Hiromi SHIMADA,Toshio MORIKAWA,Satoshi YOSHIZUMI,Narumi MATSUMURA,Toshiyuki MURAKAMI,Hisashi MATSUDA,Kazuyuki HORI and Johji YAMAHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-01-31 10:48:28













»Ø¸´´ËÂ¥