±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 1504  |  »Ø¸´: 7

Ò¹ò­¶ù

ľ³æ (СÓÐÃûÆø)


[ÇóÖú] ÇóÖú΢Æ×Êý¾Ý gf

GF-5 CDCL3
153.9,140.4,129.9,129.6,111.4,110.9,110.8,100.3,67.9,59.9,56,50.5,45.4,43.8,40.6,30.6,29.6,27.6,26,11.6

GF-8 MEOD
141.2,138.3,138.2,127.5,122.1,119.8,118.7,114.7,111.9,106.2,61.1,57,53.6,51.2,43.7,27.9,27.5,23.5,12.9

GF-9 MEOD
139.4,138.2,136.4,128.8,122,119.8,118.6,118,111.9,104.4,65.2,56.7,56.1,51.7
,45.5,34.5,28.7,27.8,13

GF-11 MEOD
166,164.4,157.1,151.8,131.7,129.5,113.3,113.3,104.8,103.6,95.2,78.9,78.5,74.5,71.3,62.5,58.6,56.1,40.9,38.9,32.6,29.4,28.6,27.2,11.7
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

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

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺
È磺21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
2Â¥2013-11-06 17:52:07
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

Ò¹ò­¶ù

ľ³æ (СÓÐÃûÆø)


Ò¹ò­¶ù: »ØÌûÖö¥ 2013-11-06 21:19:09
ÒýÓûØÌû:
2Â¥: Originally posted by lifeliuyan at 2013-11-06 17:52:07
°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺
È磺21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

GF-5 CDCL3
11.6,26,27.6,29.6,30.6,40.6,43.8,45.4,50.5,56,59.9,67.9,100.3,110.8,110.9,111.4,129.6,129.9,140.4,153.9

GF-8 MEOD
12.9,23.5,27.5,27.9,43.7,51.2,53.6,57,61.1,106.2,111.9,114.7,118.7,119.8,122.1,127.5,138.2,138.3,141.2

GF-9 MEOD
13,27.8,28.7,34.5,45.5,51.7,56.1,56.7,65.2,104.4,111.9,118,118.6,119.8,122,128.8
,136.4,138.2,139.4

GF-11 MEOD
11.7,27.2,28.6,29.4,32.6,38.9,40.9,56.1,58.6,62.5,71.3,74.5,78.5,78.9,95.2,103.6,104.8,113.3,113.3,129.5,131.7,151.8,157.1,164.4,166
3Â¥2013-11-06 21:18:22
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

²éѯ½á¹û£º¹²²éµ½108¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------



1 .     ibogaine
     ÏàËÆ¶È:60%
Phytochemistry          1991          30          3785-3792
Alkaloids from leaves and root bark ofErvatamia hirta
Pascale Clivio, Bernard Richard, Jean-Robert Deverre, Thierry Sevenet, Monique Zeches, Louisette Le Men-Oliver
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


2 .     ibogaine
     ÏàËÆ¶È:60%
Helvetica Chimica Acta          1976          59          2437-2442
13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids
Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


3 .     ibogaine
     ÏàËÆ¶È:60%
Phytochemistry          1984          23          175-178
13C NMR analysis of alkaloids from peschiera fuchsiaefolia
Raquel M. Braga, Hermogenes F. Leit¨¢o Filho, Francisco De A.M. Reist
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


4 .     2-Methoxy-3,17¦Â-O,O-bis(sulfamoyl)estradiol
C19H28N2O7S2     ÏàËÆ¶È:60%
Steroids          2012          77          864-870
Synthesis of 2-[11C]methoxy-3,17¦Â-O,O-bis(sulfamoyl)estradiol as a new potential PET agent for imaging of steroid sulfatase (STS) in cancers
Min Wang, Lu Xu, Mingzhang Gao, Kathy D. Miller, George W. Sledge, Qi-Huang Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


5 .     2-methoxy-5-methyl-5,6,7,8,9,10-hexahydrocyclohept-indole-10-carboxamide
C16H20N2O2     ÏàËÆ¶È:60%
Journal of Medicinal Chemistry          1998          41          451-467
Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles
David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


6 .     N-cyclobutanoyl-10-(aminomethyl)-2-methoxy-5-meth-yl-5,6,7,8,9,10-hexahydrocycloheptindole
C20H26N2O2     ÏàËÆ¶È:60%
Journal of Medicinal Chemistry          1998          41          451-467
Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles
David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


7 .     epiibogaine
C20H26N2O     ÏàËÆ¶È:60%
Tetrahedron          2012          68          7155-7165
Total synthesis of ibogaine, epiibogaine and their analogues
Goutam Kumar Jana, Surajit Sinha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


8 .     (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-methoxymethyl-17-acetylgona-1,3,5(10),13(17)-tetraene
C22H28O3     ÏàËÆ¶È:59.0%
Steroids          2006          71          459-468
Efficient synthesis of C-11 functionalized steroids
Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


9 .     (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-hydroxymethyl-17-acetylgona-1,3,5(10),13(17)-tetraene
C21H26O3     ÏàËÆ¶È:57.1%
Steroids          2006          71          459-468
Efficient synthesis of C-11 functionalized steroids
Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


10 .     (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-aminomethyl-17-acetylgona-1,3,5(10),13(17)-tetraene
C21H27NO2     ÏàËÆ¶È:57.1%
Steroids          2006          71          459-468
Efficient synthesis of C-11 functionalized steroids
Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


11 .     (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-aminomethyl-17-acetylgona-1,3,5(10),13(17)-tetraene ethylene ketal
C23H31NO3     ÏàËÆ¶È:56.5%
Steroids          2006          71          459-468
Efficient synthesis of C-11 functionalized steroids
Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


12 .     ibogaine
     ÏàËÆ¶È:55%
Helvetica Chimica Acta          1999          Vol. 82          170
A New Rearrangement in Iboga Alkaloids
Alberto Madinaveitia, Gabriel de la Fuente, and Antonio Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


13 .     Ibogaine
C20H26N2O     ÏàËÆ¶È:55%
Chemistry of Natural Compounds          2008          44          675-678
INDOLE ALKALOIDS FROM Ervatamia flabellformia
Shuang Liang, Haisheng Chen, Li Jin,Weidong Xuan, and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


14 .     (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-carboethoxy-17acetylgona-1,3,5(10),13(17)-tetraene
C23H28O4     ÏàËÆ¶È:55%
Steroids          2006          71          459-468
Efficient synthesis of C-11 functionalized steroids
Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


15 .     (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-amino-17-acetylgona-1,3,5(10),13(17)-tetraene
C20H25NO2     ÏàËÆ¶È:55%
Steroids          2006          71          459-468
Efficient synthesis of C-11 functionalized steroids
Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


16 .     ibogaine
     ÏàËÆ¶È:55%
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

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


17 .     7-methoxy-1,3,3-trimethyl-1-(phenylsulfanylmethyl)-1H-3,4-dihydro-2-benzopyran
C20H24O2S     ÏàËÆ¶È:55%
Heterocycles          2010          81          2361-2368
Synthesis of Isochromans by Hydriodic Acid or Iodine Mediated Cyclization Reactions of 1-(2-Vinylphenyl)propan-2-ols
Kazuhiro Kobayashi, Kazuaki Shikata, Hiroki Maegawa, Shuhei Fukamachi, Miyuki Tanmatsu, and Hisatoshi Konishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


18 .     Chrysoeriol-3'-O-¦Â-D-apifuranosidyl(1¡ú2)-glucopyranoside
     ÏàËÆ¶È:55%
Chemistry of Natural Compounds          2010          46          459-461
Chemical investigation of Ervatamia yunnanensis
Jing-Ling Du, Yong-Sheng Jin, Li-Ming Qiao, Li Jin and Hai-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


19 .     compound 1
     ÏàËÆ¶È:55%
Tetrahedron Letters          2003          44          583-586
Asymmetric synthesis and conformational analysis of the two enantiomers of the saturated analog of the potent thrombin inhibitor MOL-376
Jessy Mathew, Ken Farber, Hiroshi Nakanishi, Maher Qabar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


20 .     compound 2
     ÏàËÆ¶È:55%
Tetrahedron Letters          2003          44          583-586
Asymmetric synthesis and conformational analysis of the two enantiomers of the saturated analog of the potent thrombin inhibitor MOL-376
Jessy Mathew, Ken Farber, Hiroshi Nakanishi, Maher Qabar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4Â¥2013-11-06 21:43:58
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

²éѯ½á¹û£º¹²²éµ½167¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------



1 .     compound 1
C19H22N2O     ÏàËÆ¶È:78.9%
Tetrahedron Letters          2003          44          8013-8017
The first enantiospecific synthesis of (−-koumidine via the intramolecular palladium-catalyzed enolate driven cross coupling reaction. The stereospecific introduction of the 19-(Z) ethylidene side chain
Hui Cao, Jianming Yu, Xiangyu Z. Wearing, Chunchun Zhang, Xiaoxiang Liu, Jeffery Deschamps, James M. Cook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


2 .     Gardnerine
     ÏàËÆ¶È:75%
Tetrahedron Letters          2005          46          4219-4224
First regiospecific, enantiospecific total synthesis of gardnerine and gardnutine
Hao Zhou, Dongmei Han, Xuebin Liao, James M. Cook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


3 .     gardnerine
     ÏàËÆ¶È:73.6%
Chemical & Pharmaceutical Bulletin          1978          26          3444-3449
Gardneria Alkaloids. XII. Carbon Magnetic Resonance Spectra of Gardneria Alkaloids. A Study on the Configuration of the Side Chain Double Bonds of Indole Alkaloids
NORIO AIMI,KEIICHI YAMAGUCHI,SHINICHIRO SAKAI,JOJU HAGINIWA and AKINORI KUBO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


4 .     compound 18
     ÏàËÆ¶È:73.6%
Chemistry of Natural Compounds          1986          22          1-13
APPLICATIONS OF 1H AND 13C NMR SPECTROSCOPY IN STRUCTURAL INVESTIGATIONS OF Vinca INDOLE ALKALOIDS
M. R. Yagudaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


5 .     Gardnerine
     ÏàËÆ¶È:70%
Tetrahedron Letters          2005          46          4219-4224
First regiospecific, enantiospecific total synthesis of gardnerine and gardnutine
Hao Zhou, Dongmei Han, Xuebin Liao, James M. Cook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


6 .     N(4)-demethyltaberpsychine
C19H22N2O     ÏàËÆ¶È:68.4%
Phytochemistry          2009          70          1182-1186
Four tetracyclic oxindole alkaloids and a taberpsychine derivative from a Malayan Tabernaemontana
Kuan-Hon Lim, Kooi-Mow Sim, Guan-Huat Tan, Toh-Seok Kam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


7 .     18-hydroxygardnerine
     ÏàËÆ¶È:68.4%
Chemical & Pharmaceutical Bulletin          1978          26          3444-3449
Gardneria Alkaloids. XII. Carbon Magnetic Resonance Spectra of Gardneria Alkaloids. A Study on the Configuration of the Side Chain Double Bonds of Indole Alkaloids
NORIO AIMI,KEIICHI YAMAGUCHI,SHINICHIRO SAKAI,JOJU HAGINIWA and AKINORI KUBO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


8 .     compound 11
C19H20N2     ÏàËÆ¶È:68.4%
Tetrahedron Letters          2003          44          8013-8017
The first enantiospecific synthesis of (−-koumidine via the intramolecular palladium-catalyzed enolate driven cross coupling reaction. The stereospecific introduction of the 19-(Z) ethylidene side chain
Hui Cao, Jianming Yu, Xiangyu Z. Wearing, Chunchun Zhang, Xiaoxiang Liu, Jeffery Deschamps, James M. Cook
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


9 .     3-Hydroxykoumidine
C19H22N2O2     ÏàËÆ¶È:68.4%
Tetrahedron          2010          66          5987-5992
New oxindole and indole alkaloids from Gelsemium rankinii
Mariko Kitajima, Hiromi Kobayashi, Noriyuki Kogure, Hiromitsu Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


10 .     10-methoxypericyclivine
C21H24N2O3     ÏàËÆ¶È:66.6%
Phytochemistry          1990          29          3341-3344
Alkaloids from Alstonia undulata
The´rs`e-Marie Pinchon,Jean-Marc Nuzillard,Bernard Richard,Georges Massiot,Louisette Le Men-Olivier,Thierry Sevenet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


11 .     amsosinine
     ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2003          34          390-392
Studies on chemical constituents of Amsonia sinensis
WANG Ai-guo; FENG Xiao-zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


12 .     pericyclivine
     ÏàËÆ¶È:65%
Journal of Natural Products          1981          Vol 44          335-339
Catharanthus Alkaloids. XXXVI. Isolation of Vincaleukoblastine (VLB) and Periformyline From Catharanthus trichophyllus and Pericyclivine From Catharanthus roseus
Sibabrata Mukhopadhyay, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


13 .     isoretulinal
     ÏàËÆ¶È:65%
Phytochemistry          1988          27          3293-3304
Alkaloids from roots of Strychnos matopensis
Georges Massiot,Bernard Massoussa,Marie-Jos¨¦ Jacquier,Philippe Th¨¦p¨¦nier,Louisette Le Men-Olivier,Cl¨¦ment Delaude,Robert Verpoorte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


14 .     19(S),20(R)-dihydroperaksine
C18H22N2O     ÏàËÆ¶È:63.1%
Journal of Natural Products          2002          65          1006-1010
New Alkaloids of the Sarpagine Group from Rauvolfia serpentina Hairy Root Culture
Yuri Sheludko,Irina Gerasimenko, Heinz Kolshorn, and Joachim Stöckigt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


15 .     compound 19
     ÏàËÆ¶È:63.1%
Chemistry of Natural Compounds          1986          22          1-13
APPLICATIONS OF 1H AND 13C NMR SPECTROSCOPY IN STRUCTURAL INVESTIGATIONS OF Vinca INDOLE ALKALOIDS
M. R. Yagudaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


16 .     20-epiuleine
     ÏàËÆ¶È:63.1%
Journal of Natural Products          1983          Vol 46          200-205
Studies on the Uleine Alkaloids I. Carbon-13 Nmr Studies on Uleine, 20-Epiuleine and (4S)-Uleine-Nb-Oxide
Robert P. Borris, David C. Lankin, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


17 .     18-hydroxygardnerine
     ÏàËÆ¶È:63.1%
Journal of Natural Products          1986          Vol 49          829
Alcaloïdes Indoliques de Rauvolfia biauriculata
J. Abaul, E. Philog¨¨ne, P. Bourgeois, G. M¨¦rault, C. Poupat, A. Ahond, P. Potier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


18 .     18,19-dihydro-(20R)-antirhine
     ÏàËÆ¶È:63.1%
Phytochemistry          1992          31          2873-2876
Alkaloids from roots of Strychnos potatorum
Georges Massiot, Philippe Thepenier, Marie-Jos¨¦ Jacquier, Louisette Le Men-Olivier, Cl¨¦ment Delaude
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


19 .     normacusine B
     ÏàËÆ¶È:63.1%
Phytochemistry          1991          30          3785-3792
Alkaloids from leaves and root bark ofErvatamia hirta
Pascale Clivio, Bernard Richard, Jean-Robert Deverre, Thierry Sevenet, Monique Zeches, Louisette Le Men-Oliver
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


20 .     koumidine
     ÏàËÆ¶È:63.1%
Phytochemistry          1987          26          2875-2876
Revision of the stereochemistry of koumidine
Yeh Schun,Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5Â¥2013-11-06 21:44:15
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

²éѯ½á¹û£º¹²²éµ½172¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------



1 .     vellosiminol
C19H22N2O     ÏàËÆ¶È:89.4%
Journal of Ethnopharmacology          2012          139          471-477
In vitro antiplasmodial activity of indole alkaloids from the stem bark of Geissospermum vellosii
Flaubert Mbeunkui, Mary H. Grace, Carmen Lategan, Peter J. Smith, Ilya Raskin, Mary Ann Lila
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


2 .     compound 19
     ÏàËÆ¶È:84.2%
Chemistry of Natural Compounds          1986          22          1-13
APPLICATIONS OF 1H AND 13C NMR SPECTROSCOPY IN STRUCTURAL INVESTIGATIONS OF Vinca INDOLE ALKALOIDS
M. R. Yagudaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


3 .     affnisina
     ÏàËÆ¶È:75%
Qu¨ªmica Nova          2009          32          1834-1838
Iboga alkaloids from Peschiera affinis (Apocynaceae) - unequivocal 1H and 13C chemical shift assignments: antioxidant activity
Santos, Allana Kellen L.; Magalhães, Ticiane S.; Monte, Francisco Jose Q.; Mattos, Marcos Carlos de; Oliveira, Maria Conceição F. de; Almeida, Maria Mozarina B.; Lemos, Telma L. G.; Braz-Filho, Raimundo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


4 .     16-epigardnerine
     ÏàËÆ¶È:70%
Chemical & Pharmaceutical Bulletin          1978          26          3444-3449
Gardneria Alkaloids. XII. Carbon Magnetic Resonance Spectra of Gardneria Alkaloids. A Study on the Configuration of the Side Chain Double Bonds of Indole Alkaloids
NORIO AIMI,KEIICHI YAMAGUCHI,SHINICHIRO SAKAI,JOJU HAGINIWA and AKINORI KUBO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


5 .     gardnerine
     ÏàËÆ¶È:70%
Journal of Natural Products          1986          Vol 49          829
Alcaloïdes Indoliques de Rauvolfia biauriculata
J. Abaul, E. Philog¨¨ne, P. Bourgeois, G. M¨¦rault, C. Poupat, A. Ahond, P. Potier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


6 .     (16R)-16-hydroxy-16,17-dihydrouleine
     ÏàËÆ¶È:68.4%
Journal of Natural Products          1983          Vol 46          206-210
Studies on the Uleine Alkaloids. II. Some Chemical Transformations of Uleine
Robert P. Borris, David C. Lankin, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


7 .     19-(Z)-koumidine
C19H22N2O     ÏàËÆ¶È:68.4%
Chinese Traditional and Herbal Drugs          2011          42          222-225
Chemical constituents from Gelsemium elegans
ZHANG Zhen, LIU Guang-ming, XIAO Huai, ZHANG Zhen, HE Hong-ping, HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


8 .     alstoyunine A
C20H24N2O3     ÏàËÆ¶È:65%
Journal of Natural Products          2009          72          1836-1841
Monoterpenoid Indole Alkaloids from Alstonia yunnanensis
Tao Feng, Yan Li,Xiang-Hai Cai, Xun Gong, Ya-Ping Liu, Rong-Ting Zhang, Xiang-Yun Zhang, Qin-Gang Tan, and Xiao-Dong Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


9 .     19(S),20(R)-dihydroperaksine-17-al
C18H22N2O     ÏàËÆ¶È:63.1%
Journal of Natural Products          2002          65          1006-1010
New Alkaloids of the Sarpagine Group from Rauvolfia serpentina Hairy Root Culture
Yuri Sheludko,Irina Gerasimenko, Heinz Kolshorn, and Joachim Stöckigt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


10 .     (16R)-17- hydroxy-16,17-dihydrouleine
     ÏàËÆ¶È:63.1%
Journal of Natural Products          1983          Vol 46          206-210
Studies on the Uleine Alkaloids. II. Some Chemical Transformations of Uleine
Robert P. Borris, David C. Lankin, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


11 .     voachalotinal
C22H24N2O3     ÏàËÆ¶È:61.9%
Phytochemistry          1990          29          3341-3344
Alkaloids from Alstonia undulata
The´rs`e-Marie Pinchon,Jean-Marc Nuzillard,Bernard Richard,Georges Massiot,Louisette Le Men-Olivier,Thierry Sevenet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


12 .     pleiocarpamine
C20H22N2O2     ÏàËÆ¶È:60%
Phytochemistry          1990          29          3377-3379
17¦Á-O-Methylyohimbine and vallesiachotamine from roots ofAmsonia elliptica
Martina Sauerwein,Koichiro Shimomura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


13 .     vincamedine
C22H24NO     ÏàËÆ¶È:59.0%
Planta Medica          1986          52          66-67
A New Alkaloid Difforine and Normacusine B from Vinca difformis
J. Gamier and J. Mahuteau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


14 .     19(S),20(R)-dihydroperaksine
C18H22N2O     ÏàËÆ¶È:57.8%
Journal of Natural Products          2002          65          1006-1010
New Alkaloids of the Sarpagine Group from Rauvolfia serpentina Hairy Root Culture
Yuri Sheludko,Irina Gerasimenko, Heinz Kolshorn, and Joachim Stöckigt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


15 .     N(4)-demethyltaberpsychine
C19H22N2O     ÏàËÆ¶È:57.8%
Phytochemistry          2009          70          1182-1186
Four tetracyclic oxindole alkaloids and a taberpsychine derivative from a Malayan Tabernaemontana
Kuan-Hon Lim, Kooi-Mow Sim, Guan-Huat Tan, Toh-Seok Kam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


16 .     2,3,10,11-tetrasubstituted-5,6-dihydro-protoberberine
C19H17NO4     ÏàËÆ¶È:57.8%
Natural Product Research          2003          17          397-402
Two new alkaloids from Miliusa cuneata
Bin Chen; Chung Feng; Bio-Gang Li; Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


17 .     (16R)-16,17-dihydrouleine
     ÏàËÆ¶È:57.8%
Journal of Natural Products          1983          Vol 46          206-210
Studies on the Uleine Alkaloids. II. Some Chemical Transformations of Uleine
Robert P. Borris, David C. Lankin, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


18 .     normacusine B
     ÏàËÆ¶È:57.8%
Phytochemistry          1991          30          3785-3792
Alkaloids from leaves and root bark ofErvatamia hirta
Pascale Clivio, Bernard Richard, Jean-Robert Deverre, Thierry Sevenet, Monique Zeches, Louisette Le Men-Oliver
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


19 .     cleavamine
     ÏàËÆ¶È:57.8%
Helvetica Chimica Acta          1976          59          2711-2723
13C-NMR. Spectroscopy of Naturally Occuring Substances. XLII. Conformational analysis of quebrachamine-like indole alkaloids and related substances
Ernest Wenkert, Edward W. Hagaman, Nicole Kunesch, Nai-yi Wang and B¨¦la Zsadon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


20 .     dehydrokoumidine
C19H20N2O     ÏàËÆ¶È:57.8%
Chemistry ¨C An Asian Journal          2011          6          166-173
Seven New Monoterpenoid Indole Alkaloids from Gelsemium elegans
Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Sumphan Wongseripipatana, and Hiromitsu Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


21 .     koumidine
     ÏàËÆ¶È:57.8%
Phytochemistry          1987          26          2875-2876
Revision of the stereochemistry of koumidine
Yeh Schun,Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


22 .     2-[3-(1-methylpiperidin-4-yl)-1H-indol-5-yl]ethanesulfonic acid benzylmethylamide
C24H31N3O2S     ÏàËÆ¶È:57.8%
Heterocycles          2003          60          2441-2455
Synthesis of 5-Substituted Indole Derivatives. Part 4: Naratriptan from ¦Á-Anilinoacetaldehyde Dimethylacetal by TiCl4-Mediated Cyclisation
B¨¦la Pete,* Gyula Simig, L¨¢szl¨® Posz¨¢v¨¢cz, and L¨¢szl¨® Toke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


23 .     normacusine B
C19H22N2O     ÏàËÆ¶È:57.8%
Phytochemical Analysis          1997          8          115-119
Tertiary Alkaloid Fraction of Strychnos atlantica: Confirmation of the Identity and Structures of Indole Alkaloids by High Field Nuclear Magnetic Resonance Spectroscopy
Rabindranath Mukherjee, Tania M. S. da Silva, João B. L. Guimarães, Eduardo de J. Oliveira, Paul A. Keifer and James N. Shoolery
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6Â¥2013-11-06 21:46:24
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

²éѯ½á¹û£º¹²²éµ½50¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------



1 .     6-O-(p-methoxybenzoyl)-ajugol
     ÏàËÆ¶È:56%
Phytochemistry          1993          32          371-373
Iridoids from Tabebuia avellanedae
Kimiko Nakano, Kazuki Maruyama, Ktar Murakami, Yoshihisa Takaishi, Toshiaki Tomimatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


2 .     ligupurpuroside I
     ÏàËÆ¶È:56%
Chemistry & Biodiversity          2013          10          96-128
Chemical Constituents and Biological Activities of Plants from the Genus Ligustrum
Bei-Bei Gao, Gai-Mei She and Dong-Mei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


3 .     5'-¦Â-D-glucopyranosyloxyjasmonic butyl ester
C22H36O9     ÏàËÆ¶È:56%
Acta Chimica Sinica          2007          65          1649-1653
Chemical Constituents of Lavandula augustifolia
WU, Xia LIU, Jing YU, Zhi-Bing YE, Yun-Hua ZHOU, Ya-Wei*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


4 .     l0-hydroxystrictosam
C26H30N2O9     ÏàËÆ¶È:53.8%
Planta Medica          1991          57          149-152
New Indole Alkaloid Glycosides from Nauclea orientalis
C. A. J. Erdelmeier, A. D. Wright, .1. Orjala, B. Baumgartner, T. Rali, and O. Stiche
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


5 .     (8'R)(-)-¦Á-(E-3,4-Methylenedioxy-2-glucosyloxybenzylidene)-¦Â-(3',4'-dimethoxybenzyl)-¦Ã-butyrolactone
C27H30O12     ÏàËÆ¶È:53.8%
Phytochemistry          1994          37          1693-1698
Lignans and lignan glycosides fromHaplophyllum cappadocicum
Belkis Go¡§zler, Mustafa A. O¡§nu¡§r, Tekant Go¡§zler, Gu¡§lden Kadan, Manfred Hesse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


6 .     3-methoxy-D-dihomo-estra-17b¦Â-(¦Â-D-glucopyranosyloxy)-1,3,5(10),16-tetraene
C27H38O7     ÏàËÆ¶È:53.8%
European Journal of Organic Chemistry          2011                   1064-1077
Synthesis of a Small Library of Estradiol-Based Glycosteroid Mimics Containing a Modified D-Ring
Filip S. Ekholm, Gyula Schneider, J¨¢nos Wölfling and Reko Leino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


7 .     cauferoside
     ÏàËÆ¶È:53.3%
Journal of Natural Products          2010          73          1958-1962
Sesquiterpene Coumarins from Ferula gumosa
Mehrdad Iranshahi, Milena Masullo, Ali Asili, Ali Hamedzadeh, Bentolhoda Jahanbin, Michela Festa, Anna Capasso, and Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


8 .     2'-O-(4-methoxycinnamoyl)mussaenosidic acid
C26H32O12     ÏàËÆ¶È:52%
Chemistry & Biodiversity          2006          Vol. 3          799
Iridoid Glucosides and Flavones from the Aerial Parts of Avicennia marina
Yan Feng, Xiao-Ming Li, Xiao-Juan Duan, and Bin-Gui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


9 .     medicine
C25H22O12     ÏàËÆ¶È:52%
Helvetica Chimica Acta          2001          Vol. 84          656
Novel Coumarin Glycosides from Daphne oleoides
Muhammad Riaz and Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


10 .     spinonin dimethyl ether derivative
C25H28O10     ÏàËÆ¶È:52%
Journal of Natural Products          1997          60          378-381
Spinonin, a Novel Glycoside from Ononis spinosa subsp. Leiosperma
S¨¹heyla Kırmızıg¨¹l, Nezhun Gören, Shu-Wei Yang, Geoffrey A. Cordell, and Candan Bozok-Johansson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


11 .     alangiside
     ÏàËÆ¶È:52%
Chemical & Pharmaceutical Bulletin          1994          42          2208-2210
THREE TETRAHYDROISOQUINOLINE-MONOTERPENE GLUCOSIDES FROM ALANGIUM LAMARCKII : THE FIRST OCCURRENCE OF GLUCOSIDES WITH THE SAME ABSOLUTE CONFIGURATIONS AS DEACETYLISOIPECOSIDE, A KEY INTERMEDIATE IN THE BIOSYNTHESIS OF IPECAC ALKALOIDS
Atsuko ITOH,Takao TANAHASHI and Naotaka NAGAKURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


12 .     curculigoside
C22H26O11     ÏàËÆ¶È:52%
Acta Botanica Sinica          2004          46          621-624
Curculigoside C, a New Phenolic Glucoside from Rhizomes of Curculigo orchioides
FU Da-Xu, LEI Guang-Qing, CHENG Xiao-Wei, CHEN Jia-Kuan, ZHOU Tong-Shui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


13 .     compound 2
     ÏàËÆ¶È:52%
Natural Product Research          1998          11          119-126
Novel 11¦Á-O-¦Â-d-Glucopyranosylrotenoid Isolated from Clitoria fairchildiana
Leda Mathias; Ivo J. C. Vieira; Raimundo Braz-filho; Edson Rodrigues-filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


14 .     scuterivulactone D
C27H34O7     ÏàËÆ¶È:52%
Chemical & Pharmaceutical Bulletin          1997          45          152-160
Studies on the Constituents of Scutellaria Species. XVIII. Structures of Neoclerodane-Type Diterpenoids from the Whole Herb of Scutellaria rivularis WALL.
Haruhisa KIZU,Yoshitaka IMOTO,Tsuyoshi TOMIMORI,Tohru KIKUCHI,Shigetoshi KADOTA and Koji TSUBONO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


15 .     alangiside
     ÏàËÆ¶È:52%
Phytochemistry          1997          46          1225-1229
Five tetrahydroisoquinoline-monoterpene glycosides with a disaccharide moiety from Alangium lamarckii
Atsuko Itoh, Takao Tanahashi, Naotaka Nagakura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


16 .     macrophylloside D
     ÏàËÆ¶È:52%
Phytochemistry          1996          42          1305-1313
Acyl secoiridoids and antifungal constituents from Gentiana macrophylla
R. X. Tan, J. -L. Wolfender, L. X. Zhang, W. G. Ma, N. Fuzzati, A. Marston, K. Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


17 .     alangiside
     ÏàËÆ¶È:52%
Phytochemistry          1996          41          651-656
Acylated tetrahydroisoquinoline-monoterpene glucosides from Alangium lamarckii
Atsuko Itoh, Takao Tanahashi, Naotaka Nagakura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


18 .     (R)-peucedanol 7-O-¦Â-D-glucopyranoside
C20H26O10     ÏàËÆ¶È:52%
Phytochemistry          1994          35          1339-1341
Coumarin glycosides from Peucedanum japonicum
Yasumasa Ikeshiro, Izumi Mase, Yutaka Tomita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


19 .     Alanyiside
     ÏàËÆ¶È:52%
Phytochemistry          1994          36          383-387
Tetrahydroisoquinoline-monoterpene glucosides from Alangium lamarckii and Cephaelis ipecacuanha
Atsuko Itoh, Takao Tanahashi, Naotaka Nagakura, Hidekazu Nayeshiro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


20 .     10-ôÇ»ùÒ쳤´º»¨ÜÕÄÚõ£°·(10-hydroxy strictosamide)
     ÏàËÆ¶È:52%
China Journal of Chinese Materia Medica          2011          Vol 36,Issue 8          1037-1039
Study on chemical constituents from leaves of Naudea officinalis
XIE Dawen,LI Yonghui,ZHAO LI,DING Gang,YUAN Shao weI,XU Jia, ZHU Hua rong,XIAO Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


21 .     Macrophylloside D
C25H34O14     ÏàËÆ¶È:52%
Journal of Natural Medicines          2007          61          269-279
The chemical constituents of fresh Gentian Root
Hidehiro Ando, Yasuaki Hirai, Mikio Fujii, Yumiko Hori and Motonori Fukumura, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


22 .     2'-m-hydroxybenzoylsweroside
     ÏàËÆ¶È:52%
Chinese Traditional and Herbal Drugs          1995          26          7-10
Studies on the Glucoside Constituents of Shengengzhangyacai (Swertia elongata)
Kong Deyun; Jiang Yi; Yao Ying; et al(Address:Kong Deyun; shanghai Institute of Pharmaceutical Industry; Shanghai);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


23 .     8-O-¦Â-D-glucopyranosyl-1,5-dihydroxy-3-methoxyxanthone
     ÏàËÆ¶È:52%
Chinese Traditional and Herbal Drugs          1995          26          7-10
Studies on the Glucoside Constituents of Shengengzhangyacai (Swertia elongata)
Kong Deyun; Jiang Yi; Yao Ying; et al(Address:Kong Deyun; shanghai Institute of Pharmaceutical Industry; Shanghai);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


24 .     deacetylcentapicrin
     ÏàËÆ¶È:52%
Chinese Journal of Medicinal Chemistry          2010          20          125-128
Isolation and identification of the Chemical constituents from Swertia yunnanensis Burk.
YU Ying, WANG Shi-sheng*, DING Feng-uan, ZHU Jing-bo, ZHAO Wei-jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


25 .     drymariatin C
C27H30O13     ÏàËÆ¶È:52%
Journal of Integrative Plant Biology          2005          47          1140-1144
Three New Flavone Glycosides from Drymaria diandra Bl.
Zhong-Tao DING*, Xue-Qiong YANG, Qiu-E CAO and Fei LI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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


26 .     sclerochitonoside C
     ÏàËÆ¶È:52%
Journal of Chemical Ecology          2011          37          301-310
Leaf Chemistry and Foliage Avoidance by the Thrips Frankliniella occidentalis and Heliothrips haemorrhoidalis in Glasshouse Collections
Alison S. Scott Brown, Nigel C. Veitch, Monique S. J. Simmonds
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7Â¥2013-11-06 21:46:57
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
Ò¹ò­¶ù: ½ð±Ò+40, ¡ïÓаïÖú 2013-11-06 23:30:48
ÒÔÉϲéѯ °´Äã·¢µÄ˳ÐòÒÀ´Î¶ÔÓ¦
8Â¥2013-11-06 21:47:24
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ Ò¹ò­¶ù µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 2026Ä껪ÄÏʦ·¶´óѧ»¶Ó­»¯Ñ§£¬»¯¹¤£¬ÉúÎÉúÒ½¹¤µÈרҵÓÅÐãѧ×Ó¼ÓÈ룡 +3 llss0711 2026-03-28 6/300 2026-03-29 10:26 by llss0711
[¿¼ÑÐ] ¸÷λÀÏʦºÃ£¬ÎÒµÄһ־ԸΪ±±¾©¿Æ¼¼´óѧ085601²ÄÁÏר˶ +8 Koxui 2026-03-28 8/400 2026-03-29 09:50 by laoshidan
[¿¼ÑÐ] 0856Çóµ÷¼Á +7 —öèñ 2026-03-28 7/350 2026-03-29 08:28 by fmesaito
[¿¼ÑÐ] 356Çóµ÷¼Á +3 gysy?s?a 2026-03-28 3/150 2026-03-29 00:33 by 544594351
[¿¼ÑÐ] 0703»¯Ñ§µ÷¼Á£¬Çóµ¼Ê¦ÊÕ +9 ÌìÌìºÃÔËÀ´Éϰ¶° 2026-03-24 10/500 2026-03-28 22:17 by chemzp
[¿¼ÑÐ] 312£¬ÉúÎïѧÇóµ÷¼Á +3 СÒëͬѧabc 2026-03-28 3/150 2026-03-28 15:32 by ÂäÉ˼
[¿¼ÑÐ] ¸´ÊÔµ÷¼Á +3 raojunqi0129 2026-03-28 3/150 2026-03-28 15:27 by ÂäÉ˼
[¿¼ÑÐ] 304Çóµ÷¼Á +6 ÂüÊâ2266 2026-03-27 6/300 2026-03-28 14:10 by ÌÆãå¶ù
[¿¼ÑÐ] 283Çóµ÷¼Á +7 A child 2026-03-28 7/350 2026-03-28 12:05 by zllcz
[¿¼ÑÐ] ²ÄÁÏÓ뻯¹¤¿¼Ñе÷¼Á +17 ‹üÈA 2026-03-22 17/850 2026-03-28 08:35 by WYUMater
[¿¼ÑÐ] Çóµ÷¼ÁÍÆ¼ö ²ÄÁÏ 304 +15 ºÉ°üµ°hyj 2026-03-26 15/750 2026-03-28 04:13 by fmesaito
[¿¼ÑÐ] 331»·¾³¿ÆÑ§Ó빤³ÌÇóµ÷¼Á +3 ìÚÈ»ºÃÔËÆø 2026-03-27 3/150 2026-03-28 04:11 by fmesaito
[Óлú½»Á÷] ¸ßθßѹ·´Ó¦ÇóÖú 10+4 chibby 2026-03-25 4/200 2026-03-27 21:08 by BT20230424
[¿¼ÑÐ] 348Çóµ÷¼Á +4 СÀÁ³æ²»ÀÁÁË 2026-03-27 5/250 2026-03-27 12:47 by ¹û¹ûÂèßä
[¿¼ÑÐ] Ò»Ö¾Ô¸Ö£´ó085600£¬310·ÖÇóµ÷¼Á +5 Àîäì¿É 2026-03-26 5/250 2026-03-27 11:14 by ²»³Ôô~µÄ؈
[¿¼ÑÐ] 281Çóµ÷¼Á +3 ÑÇ¿ËÎ÷good 2026-03-26 5/250 2026-03-26 19:48 by ²»³Ôô~µÄ؈
[¿¼ÑÐ] 085602»¯Ñ§¹¤³ÌÇóµ÷¼Á¡£ +4 ƽÀÖÀÖÀÖ 2026-03-26 4/200 2026-03-26 17:57 by fmesaito
[¿¼ÑÐ] 334·Ö Ò»Ö¾Ô¸ÎäÀí ²ÄÁÏÇóµ÷¼Á +4 ÀîÀî²»·þÊä 2026-03-26 4/200 2026-03-26 16:00 by ²»³Ôô~µÄ؈
[¿¼ÑÐ] 341Çóµ÷¼Á(Ò»Ö¾Ô¸ºþÄÏ´óѧ070300) +5 ·¬ÇÑÍ·--- 2026-03-22 6/300 2026-03-23 23:45 by Txy@872106
[¿¼ÑÐ] 328Çóµ÷¼Á +4 LHHL66 2026-03-23 4/200 2026-03-23 14:55 by lbsjt
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û