| ²é¿´: 350 | »Ø¸´: 1 | ||
Ò¹ò¶ù
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö Íò·Ö¸Ðл£¡£¡£¡oa-10
|
|
OA-10 CDCL3 11.6,22.1,26.7,27.3,32,36.5,39.1,51.5,52.6,53.1,55,57.5,110.3,110.3,118.4,119.2,121.9,128.8,135.4,136.5,175.7 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
085600²ÄÁÏÓ뻯¹¤×¨Ë¶329 Çóµ÷¼Á
ÒѾÓÐ18È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
277¡¢Ñ§Ë¶£¬Çóµ÷¼Á ÊýÒ»104£¬
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤085600£¬Çóµ÷¼Á
ÒѾÓÐ32È˻ظ´
085602»¯Ñ§¹¤³Ì268·Ö¶×µ÷¼Á
ÒѾÓÐ13È˻ظ´
»·¾³×¨Ë¶µ÷¼Á
ÒѾÓÐ12È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ17È˻ظ´
²ÄÁÏÓ뻯¹¤×¨Ë¶306·ÖÕÒºÏÊʵ÷¼Á
ÒѾÓÐ15È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÓÐûÓÐÈËÖªµÀ 1,3-Ë«(¶þ±½»ù좱ûÍé)¶þÂÈ»¯Äø ÔõÃ´ÖÆ±¸Ñ½£¿ÇóÖúÏà¹ØÎÄÏ×£¿Íò·Ö¸Ðл£¡£¡
ÒѾÓÐ10È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬¸ø30J
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý YC-8
ÒѾÓÐ7È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ Èý¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
XPSÊý¾Ý·ÖÎöÇóÖú£¡£¡Íò·Ö¸Ðл£¡ÔõôÎÒµÄÇóÖúÌûûÈ˻ظ´ÄØ£¬ÓÐÖØ½ð°¡£¡
ÒѾÓÐ15È˻ظ´
XÉäÏß¹âµç×ÓÄÜÆ× XPSÊý¾Ý·ÖÎöÇóÖú£¡£¡¼±£¡Íò·Ö¸Ðл£¡
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
Çó´óϺ²é΢Æ×£¬Íò·Ö¸Ðл°¡£¡£¡£¡
ÒѾÓÐ3È˻ظ´
µç»¯Ñ§×迹Æ×µÄ·ÖÎö£¬Çë¸ßÊÖÖ¸½Ì£¬Íò·Ö¸Ðл£¡£¡
ÒѾÓÐ32È˻ظ´
Èý·½ÐÒéµÄÎÊÌ⣬Çë½Ì£¡Íò·Ö¸Ðл£¡
ÒѾÓÐ10È˻ظ´
ÊìϤexcelÊý¾Ý´¦ÀíµÄ½ø£¿Íò·Ö¸Ðл~~
ÒѾÓÐ7È˻ظ´
¸÷λ³æÓÑÃÇÇë°ï°ïæ°¡£¬Íò·Ö¸ÐлÁË£¡£¡£¡£¡£¡
ÒѾÓÐ13È˻ظ´
¡¾Çë½Ì¡¿ÓÐ×ö¹ýѹ¹¯ÒDzâÊÔµÄÂ𣿰ïæ·ÖÎö¸öÊý¾Ý£¬Íò·Ö¸Ðл
ÒѾÓÐ20È˻ظ´
¡¾ÇóÖú¡¿Çóѧ³¤ÃÇÍÆ¼öЩ¿¼ÑÐÓлú²»¿¼ÊýѧµÄԺУ¡£Íò·Ö¸Ðл
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú£ºÇó½Ì£ºµÂ¹ÌÈü Degussa P25 Íò·Ö¸Ðл~~£¡
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿¹ØÓÚMATLABÊýÁи³ÖµµÄÎÊÌâ¡¿ Íò·Ö¸Ðл
ÒѾÓÐ10È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ò¹ò¶ù: ½ð±Ò+10 2013-09-02 11:23:24
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ò¹ò¶ù: ½ð±Ò+10 2013-09-02 11:23:24
|
²éѯ½á¹û£º¹²²éµ½367¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound 1 C21H26N2O2 ÏàËÆ¶È:100% Chemical & Pharmaceutical Bulletin 1992 40 2041-2043 Indonesian Medicinal Plants. II. Chemical Structures of Pongapinones A and B, Two New Phenylpropanoids from the Bark of Pongamia pinnata (Papilionaceae) Isao KITAGAWA,Ru-song ZHANG,Kazuyuki HORI,Katsutoshi TSUCHIYA and Hirotaka SHIBUYA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . coronaridine ÏàËÆ¶È:100% Journal of Natural Products 1988 Vol 51 528 Heyneanine Hydroxyindolenine, A New Indole Alkaloid from Ervatamia coronaria var. plena Perveen Sharma, Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . coronaridine ÏàËÆ¶È:100% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . coronaridine ÏàËÆ¶È:100% Phytochemistry 1990 29 3007-3011 Alkaloids from leaves and stem bark of Ervatamia polyneura Pascale Clivio,Bernard Richard,Hamid A. Hadi,Bruno David,Thierry Sevenet,Monique Zeches,Louisette Le Men-Olivier Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . coronaridine ÏàËÆ¶È:100% Qu¨ªmica Nova 2008 31 20-24 Chemical constituents from Tabernaemontana catharinensis root bark: a brief NMR review of indole alkaloids and in vitro cytotoxicity Pereira, Paulo S¨¦rgio; França, Suzelei de Castro; Oliveira, Paulo Vinicius Anderson de; Breves, Camila Moniz de Souza; Pereira, Sarazete Izidia Vaz; Sampaio, Suely Vilela; Nomizo, Auro; Dias, Diones Aparecida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . coronaridine ÏàËÆ¶È:100% Acta Pharmaceutica Sinica 2010 45 471-474 Monomeric indole alkaloids from the aerial parts of Catharanthus roseus ZHONG Xiang-zhang, WANG Guo-cai, WANG Ying, ZHANG Xiao-qi, YE Wen-cai* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . coronaridine ÏàËÆ¶È:95.2% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . coronaridina ÏàËÆ¶È:95.2% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . coronaridine C21H26O2N2 ÏàËÆ¶È:95.2% Academic Journal of Second Military Medical University 2006 27 92-96 Antiaddictive indole alkaloids in Ervatamia yunnanensis and their bioactivity XUAN Wei-dong, CHEN Hai-sheng, YUAN Zhi-xian, ZHANG Xiao-dong, HUANG Mao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Coronaridine ÏàËÆ¶È:90.4% Phytochemistry 1980 19 1213-1218 Anticancer indole alkaloids of Ervatamia heyneana Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-08-23 11:52:17















»Ø¸´´ËÂ¥