Znn3bq.jpeg
²é¿´: 472  |  »Ø¸´: 2

yaoxue1122

½ð³æ (СÓÐÃûÆø)

[ÇóÖú] ÇóÒ»»¯ºÏÎï ΢Æ×Êý¾Ý

16.7,16.9,17.6,17.6,18.7,20.6,21.3,23.7,27.4,27.7,28.2,29.0,31.0,33.0,34.1,37.0,38.2,39.0,39.4,41.1,43.8,45.3,55.1,59.1,61.6,130.5,165.2,171.2,199.9
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

kaola0916

Ìú¸Ëľ³æ (ÖøÃûдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yaoxue1122: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£¸Ðл~~~~~ 2012-04-19 09:16:07
´óÓÚ80%µÄ

²éѯ½á¹û£º¹²²éµ½9¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------

1 .     3¦Â-acetoxy-urs-12-ene-ll-one
    ÏàËÆ¶È:90.6%
Journal of Asian Natural Products Research          2000          2          81-86
A New Triterpenoid from Stelmatocrypton khasianum
QING-YING ZHANG, YU-YING ZHAO, TIE-MING CHENG,YU-XIN CUI and XUE-HUI LIU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     3¦Â-acetoxy-12-ursen-11-one
    ÏàËÆ¶È:90.6%
China Journal of Chinese Materia Medica          2008          33          905-908
Studies on chemical constituents from whole plants of Crossostephium chinense
YANG Xiuwei, ZOU Lei, WU Qi, FU Dexian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     3¦Â-ÒÒõ£»ù-12-Ï©-11-ͪ
C32H50O3     ÏàËÆ¶È:87.5%
Chinese Traditional and Herbal Drugs          2009          40          708-710
ºÚ¹ÇÌÙ»¯Ñ§³É·ÖµÄÑо¿
¸ÊÐ㺣;ÖÜÐÀ;ÕÔ³¬;¹¨Ð¡¼û;³Â»ª¹ú;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     3,11-dioxo-ursan-12-ene
C30H46O2     ÏàËÆ¶È:86.2%
Phytochemistry          1990          29          1691-1693
Terpenoids from Salvia mellifera
Antonio G. Gonz¨¢lez,Lucia S. Andres,Angel G. Ravelo,Javier G. Luis,Isabel L. Bazzocchi,Jan West
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     11-oxo-¦Á-amyrin acetate
    ÏàËÆ¶È:84.3%
China Journal of Chinese Materia Medica          2006          31          1166-1168
Studies on constituents from root and stem of Ervatamia hainanensis
HUANG Jianpeng, MA Yangmin, JIANG Jianshuang, ZHANG Peicheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     11-oxo-¦Á-amyrin acetate
C32H50O3     ÏàËÆ¶È:84.3%
Chinese Journal of Natural Medicines          2008          6          271-274
Chemical Constituents from the Roots and Stems of Ervatamia hainanensis
JIN Li; LU Jia; JIN Yong-Sheng; YANG Xiang-Nan; CHEN Hai-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     3¦Â-acetoxy-20-taraxasten-22-one
    ÏàËÆ¶È:81.2%
Natural Product Research          2009          23          1218-1230
Chemical composition of the stem bark and leaves of Ficus pandurata Hance
M. A. Ramadan; A. S. Ahmad; A. M. Nafady; A. I. Mansour
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     krukovine B
C30H46O3     ÏàËÆ¶È:80%
Journal of Natural Products          1997          60          1174-1177
Partial Synthesis of Krukovines A and B, Triterpene Ketones Isolated from the Brazilian Medicinal Plant Maytenus krukovii
Tadashi Honda, Heather J. Finlay, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     Glycyrrhetinic acid
    ÏàËÆ¶È:80%
Tetrahedron Letters          2005          46          2337-2340
Novel biotransformation of pentacyclic triterpenoid acids by Nocardia sp. NRRL 5646
Jian Zhang, Zhi-Hong Cheng, Bo-Yang Yu, Geoffrey A. Cordell, Samuel X. Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-04-19 09:04:44
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

СÂü1211

ľ³æ (³õÈëÎÄ̳)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
17.6Ó¦¸ÃûÊäÖØ°É ÎÒÊǰ´ÏÖÔÚÄãÊäµÄ²éµÄ



²éѯ½á¹û£º¹²²éµ½9136¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------





1 .     3¦Â-acetoxy-urs-12-ene-ll-one
    ÏàËÆ¶È:90.6%
Journal of Asian Natural Products Research          2000          2          81-86
A New Triterpenoid from Stelmatocrypton khasianum
QING-YING ZHANG, YU-YING ZHAO, TIE-MING CHENG,YU-XIN CUI and XUE-HUI LIU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




2 .     3¦Â-acetoxy-12-ursen-11-one
    ÏàËÆ¶È:90.6%
China Journal of Chinese Materia Medica          2008          33          905-908
Studies on chemical constituents from whole plants of Crossostephium chinense
YANG Xiuwei, ZOU Lei, WU Qi, FU Dexian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




3 .     3¦Â-ÒÒõ£»ù-12-Ï©-11-ͪ
C32H50O3     ÏàËÆ¶È:87.5%
Chinese Traditional and Herbal Drugs          2009          40          708-710
ºÚ¹ÇÌÙ»¯Ñ§³É·ÖµÄÑо¿
¸ÊÐ㺣;ÖÜÐÀ;ÕÔ³¬;¹¨Ð¡¼û;³Â»ª¹ú;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




4 .     3,11-dioxo-ursan-12-ene
C30H46O2     ÏàËÆ¶È:86.2%
Phytochemistry          1990          29          1691-1693
Terpenoids from Salvia mellifera
Antonio G. Gonz¨¢lez,Lucia S. Andres,Angel G. Ravelo,Javier G. Luis,Isabel L. Bazzocchi,Jan West
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




5 .     11-oxo-¦Á-amyrin acetate
    ÏàËÆ¶È:84.3%
China Journal of Chinese Materia Medica          2006          31          1166-1168
Studies on constituents from root and stem of Ervatamia hainanensis
HUANG Jianpeng, MA Yangmin, JIANG Jianshuang, ZHANG Peicheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




6 .     11-oxo-¦Á-amyrin acetate
C32H50O3     ÏàËÆ¶È:84.3%
Chinese Journal of Natural Medicines          2008          6          271-274
Chemical Constituents from the Roots and Stems of Ervatamia hainanensis
JIN Li; LU Jia; JIN Yong-Sheng; YANG Xiang-Nan; CHEN Hai-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     3¦Â-acetoxy-20-taraxasten-22-one
    ÏàËÆ¶È:81.2%
Natural Product Research          2009          23          1218-1230
Chemical composition of the stem bark and leaves of Ficus pandurata Hance
M. A. Ramadan; A. S. Ahmad; A. M. Nafady; A. I. Mansour
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     krukovine B
C30H46O3     ÏàËÆ¶È:80%
Journal of Natural Products          1997          60          1174-1177
Partial Synthesis of Krukovines A and B, Triterpene Ketones Isolated from the Brazilian Medicinal Plant Maytenus krukovii
Tadashi Honda, Heather J. Finlay, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




9 .     Glycyrrhetinic acid
    ÏàËÆ¶È:80%
Tetrahedron Letters          2005          46          2337-2340
Novel biotransformation of pentacyclic triterpenoid acids by Nocardia sp. NRRL 5646
Jian Zhang, Zhi-Hong Cheng, Bo-Yang Yu, Geoffrey A. Cordell, Samuel X. Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




10 .     18¦Á- Epimer
    ÏàËÆ¶È:78.1%
Chemistry of Natural Compounds          1991          27          313-317
1H AND 13C SPECTRA OF BIOLOGICALLY ACTIVE COMPOUNDS X.TWO-DIMENSIONAL HH COSY 45 ¡ã AND CH HET CORR SPECTRA OF THE 18¦Á- AND 18¦Â-ISOMERS OF GLYCYRRHETIC ACID 3-ACETATE
L. M. Khalilov, E. V. Vasil'eva, A. A. Fatykhov,and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




11 .     methyl glycyrrhetinate
    ÏàËÆ¶È:77.4%
Tetrahedron Letters          2005          46          2337-2340
Novel biotransformation of pentacyclic triterpenoid acids by Nocardia sp. NRRL 5646
Jian Zhang, Zhi-Hong Cheng, Bo-Yang Yu, Geoffrey A. Cordell, Samuel X. Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     11-oxoursolic acid
    ÏàËÆ¶È:76.6%
Magnetic Resonance in Chmesitry          2003          41          636-638
Complete assignments of 1H and 13C NMR resonances of oleanolic acid, 18-oleanolic acid, ursolic acid and their 11-oxo derivatives
Werner Seebacher, Nebojsa Simic, Robert Weis, Robert Saf and Olaf Kunert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




13 .     11-keto-¦Â-boswellic acid
C32H48O5     ÏàËÆ¶È:76.6%
Zeitschrift f¨¹r Naturforschung C          2003          58          505-516
Immunomodulatory Triterpenoids from the Oleogum Resin of Boswellia carterii Birdwood
F. A. Badria, B. R. Mikhaeil, G. T. Maatooq, and M. M. A. Amer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




14 .     3¦Â-acetoxy-11¦Á-hydroperoxy-12-ursene
C32H54O4     ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          2000          48(5)          593-596
Six New Ursane- and Oleanane-Type Triterpenes from the Aerial Roots of Ficus microcarpa
Yueh-Hsiung Kuo and Yi-Ming CHIANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




15 .     3¦Â-acetoxy-11¦Á-hydroxy-12-ursene
    ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          2000          48(5)          593-596
Six New Ursane- and Oleanane-Type Triterpenes from the Aerial Roots of Ficus microcarpa
Yueh-Hsiung Kuo and Yi-Ming CHIANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




16 .     3,11-dioxours-12-en-28-yl acetate
C32H48O4     ÏàËÆ¶È:75%
Journal of Natural Products          1997          60          1174-1177
Partial Synthesis of Krukovines A and B, Triterpene Ketones Isolated from the Brazilian Medicinal Plant Maytenus krukovii
Tadashi Honda, Heather J. Finlay, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




17 .     compound 1a
    ÏàËÆ¶È:74.1%
Chinese Chemical Letters          2005          16          867-870
Synthesis of Boswellic Acid Derivatives and Primary Research on their Activities
Yan Qiu MENG, Lin Xiang ZHAO, Zan WANG, Dan LIU, Yong Kui JING
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




18 .     BDGM-7(11-oxo-methyl ursolate)
C31H48O4     ÏàËÆ¶È:74.1%
Phytochemistry          1991          30          362-363
Triterpenoids of the resin of Bursera delpechiana
K.V. Syamasundar, Gopal R. Mallavarapu, E.Murali Krishna
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




19 .     ¦Á-amyrin acetate
    ÏàËÆ¶È:74.1%
Chinese Journal of Medicinal Chemistry          2010          20          520-523
Chemical constituents of radix Marsdeniae sinensis
HU Hu, i WU Yi-xuan, HE Xiang-jiu*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




20 .     (3¦Â,18¦Á,20¦Â)-3-hydroxy-11-oxo-olean-12-en-29-oic acidmethyl ester
    ÏàËÆ¶È:74.1%
Bioorganic & Medicinal Chemistry          2010          18          433-454
Synthesis of glycyrrhetinic acid derivatives for the treatment of metabolic diseases
Igor Beseda, Laszlo Czollner, Priti S. Shah, Rupesh Khunt, Rawindra Gaware, Paul Kosma, Christian Stanetty, Maria Carmen del Ruiz-Ruiz, Hassan Amer, Kurt Mereiter, Thierry Da Cunha, Alex Odermatt, Dirk Claßen-Houben, Ulrich Jordis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




21 .     (3¦Â,18¦Â,20¦Â)-3-acetoxy-N-hydroxy-11-oxo-olean-12-en-29-amide
    ÏàËÆ¶È:74.1%
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   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




22 .     3¦Â-acetoxy-11¦Á-ethoxy-12-ursene
C34H56O3     ÏàËÆ¶È:73.5%
Chemical & Pharmaceutical Bulletin          2000          48(5)          593-596
Six New Ursane- and Oleanane-Type Triterpenes from the Aerial Roots of Ficus microcarpa
Yueh-Hsiung Kuo and Yi-Ming CHIANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




23 .     ternstroemic acid
C30H46O5     ÏàËÆ¶È:73.3%
Journal of Natural Products          2003          66          1051-1054
Ursane- and Oleanane-Type Triterpenes from Ternstroemia gymnanthera Callus Tissues
Akira Ikuta,Hiroaki Tomiyasu,Yasumasa Morita,and Kouichi Yoshimura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




24 .     2R,3¦Â,11R-trihydroxy-urs-12-ene
C30H50O3     ÏàËÆ¶È:73.3%
Journal of Natural Products          1999          62          1605-1608
Terpenoids from Salvia kronenburgii
G¨¹ laçtı Topçu, and Ayhan Ulubelen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




25 .     11¦Â-hydroxy-3-oxo-urs-12-en-28-oic acid
C30H46O4     ÏàËÆ¶È:73.3%
Natural Product Research          1999          13          187-194
New Ursane Type Triterpenes From Salvia Mellifera Greene
Javier G. Luis; Luc¨ª S. Andr¨¦s
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




26 .     ¦Á-Amyrin acetate
C32H52O2     ÏàËÆ¶È:73.3%
Zeitschrift f¨¹r Naturforschung B          2010          65b          203-210
Phytochemical Studies on Alstonia scholaris
Nighat Sultanaa and Muhammad Saleem
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




27 .     18¦Â-glycyrrhetinic acid
    ÏàËÆ¶È:73.3%
Phytochemistry          1990          29          3123-3126
Biotransformation of 18¦Â-glycyrrhetinic acid by cultured cells ofEucalyptus perriniana andCoffea arabica
Yutaka Orihara,Tsutomu Furuya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




28 .     acetyl-11-keto-¦Â-boswellic acid
    ÏàËÆ¶È:73.3%
Chinese Journal of Natural Medicines          2010          8          25-27
Chemical Constituents of Boswellia carterii(Frankincense)
Li Fu-Shuang; YAN Dong-Lan; LIU Rang-Ru; XU Kang-Ping; TAN Gui-Shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




29 .     11-Oxo-olean-12-en-30-oic acid
    ÏàËÆ¶È:73.3%
Zeitschrift f¨¹r Naturforschung B          2011          66          521-532
Synthesis and Antitumor Activity of Ring A-modified Glycyrrhetinic Acid Derivatives
R. Csuk, S. Schwarz, B. Siewert, R. Kluge, and D. Ströhl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




30 .     11 Keto-¦Â-boswellic acid
C30H46O4     ÏàËÆ¶È:73.3%
Natural Product Communications          2008          3          21-26
Boswellic Acids with Acetylcholinesterase InhibitoryProperties from Frankincense
Masahiro Ota and Peter J. Houghton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




31 .     3¦Â-acetoxy-11¦Á-methoxy-12-ursene
C33H54O3     ÏàËÆ¶È:72.7%
Chemical & Pharmaceutical Bulletin          2000          48(5)          593-596
Six New Ursane- and Oleanane-Type Triterpenes from the Aerial Roots of Ficus microcarpa
Yueh-Hsiung Kuo and Yi-Ming CHIANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




32 .     3-O-Acetyl-18¦Á-liquiritic acid
    ÏàËÆ¶È:72.7%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




33 .     3¦Â-acetoxy-11-oxo-18¦Á-olean-12-en-29-oic acid methylester
    ÏàËÆ¶È:72.7%
Korean Journal of Pharmacognosy          1987          18(3)          151-167
13C NMR Spectroscopy of Amyrins
Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




34 .     1¦Â,2¦Á-dihydroxy-3¦Â-acetoxy-11-oxours-12-ene
C32H50O5     ÏàËÆ¶È:71.8%
Journal of Natural Products          2004          67          118-121
Highly Hydroxylated Triterpenes from Salvia kronenburgii
Glat Topu, Zeynep Trkmen, Ayhan Ulubelen, Jennifer K. Schilling, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




35 .     3¦Â-acetoxy-11¦Á-hydroperoxy-13¦ÁH-ursan-12-one
C32H52O5     ÏàËÆ¶È:71.8%
Journal of Natural Products          2001          64          436-439
New Peroxy Triterpenes from the Aerial Roots of Ficus microcarpa
Yi-Ming Chiang and Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




36 .     18¦Â- Epimer
    ÏàËÆ¶È:71.8%
Chemistry of Natural Compounds          1991          27          313-317
1H AND 13C SPECTRA OF BIOLOGICALLY ACTIVE COMPOUNDS X.TWO-DIMENSIONAL HH COSY 45 ¡ã AND CH HET CORR SPECTRA OF THE 18¦Á- AND 18¦Â-ISOMERS OF GLYCYRRHETIC ACID 3-ACETATE
L. M. Khalilov, E. V. Vasil'eva, A. A. Fatykhov,and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




37 .     ¦Á-amyrin acetate
C32H52O2     ÏàËÆ¶È:71.8%
Acta Botanica Sinica          2002          44          354-358
Triterpenoids from the Dai Medicinal Plant Winchia calophylla
ZHU Wei-Ming, SHEN Yue-Mao, HONG Xin, ZUO Guo-Ying, YANG Xiao-Sheng, HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




38 .     ¦Á-amyrin acetate
    ÏàËÆ¶È:71.8%
Chinese Pharmaceutical Sciences          1999          8          237-240
Chemical Constituents of Stelmatocrypton khasianum
Zhang Qingying; Zhao Yuying; Ma Libin; Cheng Tieming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




39 .     ¦Á-amyrin acetate
    ÏàËÆ¶È:71.8%
China Journal of Chinese Materia Medica          2008          33          905-908
Studies on chemical constituents from whole plants of Crossostephium chinense
YANG Xiuwei, ZOU Lei, WU Qi, FU Dexian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




40 .     ¦Á-amyrin acetate
    ÏàËÆ¶È:71.8%
China Journal of Chinese Materia Medica          2007          32          1296-1299
Study on chemical constituents in rhigome of Ervatamia hainanensis
LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




41 .     ¦Á-amyrin acetate
    ÏàËÆ¶È:71.8%
China Journal of Chinese Materia Medica          2006          31          1166-1168
Studies on constituents from root and stem of Ervatamia hainanensis
HUANG Jianpeng, MA Yangmin, JIANG Jianshuang, ZHANG Peicheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




42 .     ¦Á-amyrin acetate
    ÏàËÆ¶È:71.8%
China Journal of Chinese Materia Medica          2003          28          124-126
Studies on Chemical Constituents from the Bark of Morus macroura
WU Feng, SUN Shengguo, CHEN Ruoyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




43 .     3¦Â-hydroxy-11¦Á-ethoxyurs-12-ene (triptohypol D)
C32H54O2     ÏàËÆ¶È:71.8%
Phytochemistry          2000          53          715-722
Terpenoids from Tripterigyum hypoglaucum
Reiko Fujita, Hongquan Duan, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




44 .     germanicol acetate
    ÏàËÆ¶È:71.8%
Natural Product Sciences          2002          8          55-57
Terpenoid constituents from Youngia koidzumiana
Dat, Nguyen Tien; Cai, Xing Fu; Bae, Ki-Hwan; Kim, Young-Ho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




45 .     ¦Á-amyrin-3¦Â-acetate(¦Á-ÏãÊ÷ËØ-3¦Â-ÒÒËáõ¥)
    ÏàËÆ¶È:71.8%
Chemical Journal of Chinese Universities          2003          24          436-441
Chemical Constituents from the Roots of Biondia Hemsleyana
TAN Xing-Gen, ZHANG Xiao-Rong, PENG Shu-Lin, LIAO Xun, DING Li-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




46 .     (3¦Â,18¦Â,20¦Â)-[3-(1,2,4-Oxadiazole-5(2H)-one)]-11-oxoolean-12-en-29-oic acid
C32H46N2O6     ÏàËÆ¶È:71.8%
Bioorganic & Medicinal Chemistry          2011          19          1866-1880
Synthesis of new glycyrrhetinic acid derived ring A azepanone, 29-urea and 29-hydroxamic acid derivatives as selective 11b-hydroxysteroid dehydrogenase 2 inhibitors
Rawindra Gaware, Rupesh Khunt, Laszlo Czollner, Christian Stanetty, Thierry Da Cunha,Denise V. Kratschmar, Alex Odermatt, Paul Kosma, Ulrich Jordis, Dirk Claßen-Houben
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




47 .     3¦Á-acetyl-11-keto-¦Â-boswellic acid
C32H48O5     ÏàËÆ¶È:71.8%
Magnetic Resonance in Chmesitry          2003          41          115-122
Structural analysis of pentacyclic triterpenes from the gum resin of Boswellia serrata by NMR spectroscopy
Klaus Belsner, Berthold B¨¹chele, Udo Werz, Tatiana Syrovets and Thomas Simmet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




48 .     ¦Á-amyrinactetete
C32H52O2     ÏàËÆ¶È:71.8%
Chinese Traditional and Herbal Drugs          2006          37          519-520
Ïã¼ÓƤµÄ¿¹Ö×Áö»îÐԳɷÖÑо¿(¢ñ)
³ÂÊéºì;Ñî¾þɽ;ÈηçÖ¥;Áõ¸ÕÈþ;Õž²;µ¥±£¶÷;ÀîÄþ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




49 .     ¦Á-ÏãÊ÷Ö¬´¼ÒÒËáõ¥
    ÏàËÆ¶È:71.8%
Chinese Traditional and Herbal Drugs          2005          36          669-671
ÌÙ¿à²Î»¯Ñ§³É·ÖÑо¿(¢ò)
ÕÅÁÕ,ÐìÀöÕä,ÑîÊÀÁÖ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




50 .     ¦Á-amyrin acetate
    ÏàËÆ¶È:71.8%
Chinese Traditional and Herbal Drugs          2001          32          964-966
Studies on chemical constituents of Adenophora wawreana
ZHAO Kui jun; LIU Suo lan; YANG Jun; LI Xiu qing; YAN Xiao lin; ZHENG Cheng gui; TU Peng fei; CHEN Hu biao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2012-04-19 09:07:37
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ yaoxue1122 µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 352 Çóµ÷¼Á +4 yzion 2026-04-11 4/200 2026-04-11 08:38 by À´¿´Á÷ÐÇÓê10
[¿¼ÑÐ] 342µç×ÓÐÅϢר˶Çóµ÷¼Á +9 ÄãÈÃÎÒÔõôÀóÖ¦ 2026-04-10 10/500 2026-04-11 08:33 by zhq0425
[¿¼ÑÐ] »¹Óл¯¹¤¶þÂÖµ÷¼ÁµÄѧУÂð 5+13 »¯¹¤ÈË999 2026-04-09 47/2350 2026-04-11 00:20 by ÆïÅ£¶Éº®½­
[¿¼ÑÐ] µ÷¼Á +19 СÕÅZA 2026-04-10 20/1000 2026-04-10 22:08 by Öí»á·É
[¿¼ÑÐ] 0856ר˶Çóµ÷¼Á Ï£ÍûÊÇaÇøÔºÐ£ +21 ºÃºÃÐÝÏ¢ºÃ²»ºÃ 2026-04-09 24/1200 2026-04-10 16:58 by luoyongfeng
[¿¼²©] ²©Ê¿×Ô¼ö +7 ¿É¿ÉСÅÖ 2026-04-08 7/350 2026-04-10 08:28 by kimhero
[¿¼ÑÐ] ÉúÎïѧÇóµ÷¼Á Ò»Ö¾Ô¸»¦9£¬326·Ö +7 Áõīī 2026-04-06 7/350 2026-04-10 08:11 by kangsm
[¿¼ÑÐ] 284Çóµ÷¼Á +7 archer.. 2026-04-09 8/400 2026-04-09 21:30 by bljnqdcc
[¿¼ÑÐ] ¿¼Ñе÷¼Á-²ÄÁÏÀà-284 +28 Ïë»»ÊÖ»ú²»Ïë½âÊ 2026-04-08 28/1400 2026-04-09 20:08 by µ¹Êý321?
[¿¼ÑÐ] ²ÄÁÏר˶(0856) 339·ÖÇóµ÷¼Á +9 ¹þ¹þ¹þ¶ì¹þ¹þ¹þ 2026-04-09 10/500 2026-04-09 20:01 by Orcid
[¿¼ÑÐ] Çóµ÷¼Á²ÄÁÏ¿ÆÑ§Ó빤³ÌÒ»Ö¾Ô¸985³õÊÔ365·Ö +5 ²Ä»¯Àî¿É 2026-04-08 5/250 2026-04-09 17:00 by Lilly_Li
[¿¼ÑÐ] Ò»Ö¾Ô¸ÎäÀí³µÁ¾ 281 Çóµ÷¼Á +5 Éϰ¶Ñо¿Éú. 2026-04-07 5/250 2026-04-09 15:56 by onlyÖÜ
[¿¼ÑÐ] Çóµ÷¼Á +3 ÖíÈâ¶Õ·ÛÌõcc 2026-04-08 4/200 2026-04-09 10:05 by ÖíÈâ¶Õ·ÛÌõcc
[¿¼ÑÐ] Ò»Ö¾Ô¸985³õÊÔ354·ÖÉúÎïµ÷¼Á +3 031001 2026-04-06 3/150 2026-04-09 00:30 by Evan_Liu
[¿¼ÑÐ] ²ÄÁÏ¿¼ÑÐÇóµ÷¼Á×Ü·Ö280 +30 mkjlz1 2026-04-06 35/1750 2026-04-08 21:25 by cyh¡ª315
[¿¼ÑÐ] 338Çóµ÷¼Á +4 ÎÒÏëÉϰ¶ii 2026-04-05 4/200 2026-04-06 21:04 by ľ×Ó¾ý1218
[¿¼ÑÐ] 362Çóµ÷¼ÁÒ»Ö¾Ô¸ÖйúʯÓÍ´óѧ +4 ÎÒÒª¿¼´ó 2026-04-06 6/300 2026-04-06 14:11 by Î޼ʵIJÝÔ­
[¿¼ÑÐ] 328·Öµ÷¼Á +6 ÃÅmen 2026-04-04 6/300 2026-04-05 13:40 by imissbao
[¿¼ÑÐ] 298Çóµ÷¼Á +7 manman511 2026-04-05 7/350 2026-04-05 10:29 by ÌÆãå¶ù
[¿¼ÑÐ] 313Çóµ÷¼Á +3 º£ÈÕº£ÈÕ 2026-04-04 3/150 2026-04-05 07:48 by 544594351
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û