| ²é¿´: 510 | »Ø¸´: 3 | ||
СССÌǶ¹Òø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
¼±£¡±ÏÒµÔÚ¼´£¬ÇóÖú¸÷λ¸ßÈ˰ïæ½âÎöһϻ¯ºÏÎ°ÝÍÐ ÒÑÓÐ1È˲ÎÓë
|
|
»¯ºÏÎï1£ºYB-1 ÈܼÁ£º¼×´¼ 13CNMRÊý¾Ý£º56.59,57.63,73.83,88.73,112.19,117.30,121.27,135.02,148.53,150.33 »¯ºÏÎï2£ºYB-2 ÈܼÁ£º¼×´¼ 13CNMRÊý¾Ý£º9.29,20.96,21.82,23.73,23.74,37.87,43.15,51.09,56.78,59.39,74.10,106.77,123.07,165.31,175.90 »¯ºÏÎï4£ºYB-4 ÈܼÁ£º¼×´¼ 13CNMRÊý¾Ý£º8.10,13.78,23.03,27.52,30.18,40.29,41.60,51.57,54.88,71.96,80.34,105.97,122.10,164.20,174.75 Âé·³¸÷λÓÐ΢Æ×Êý¾Ý¿â»òÕ߻ᲦÆ×½âÎöµÄÐֵܽãÃÃÃÇ£¬°ï°ï棬±ÏÒµÔÚ¼´£¬Ð¡Å®¸Ð¼¤²»¾¡£¡ |
» ²ÂÄãϲ»¶
085600²ÄÁÏÓ뻯¹¤329·ÖÇóµ÷¼Á
ÒѾÓÐ9È˻ظ´
283Çóµ÷¼Á 086004¿¼Ó¢¶þÊý¶þ
ÒѾÓÐ5È˻ظ´
ÉúÎïѧµ÷¼Á
ÒѾÓÐ5È˻ظ´
ũѧ0904 312Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ35È˻ظ´
µ÷¼ÁÇóÊÕÁô
ÒѾÓÐ10È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ18È˻ظ´
0831ÉúÒ½¹¤µÚÒ»ÂÖµ÷¼Áʧ°ÜÇóÖú
ÒѾÓÐ9È˻ظ´
ÉúÎïѧ308Çóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48433.9
- ºì»¨: 52
- Ìû×Ó: 6749
- 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 ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
СССÌǶ¹: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-26 09:31:28
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
СССÌǶ¹: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-26 09:31:28
|
YB-1 1 . (+)-securigtran I C20H22O6 ÏàËÆ¶È:90% Pharmazie 1998 53 710-715 Studies on Securigera securidacea(L.)Deg.et DORFL.(fabaceae)seeds,an antidiabetic Egyptian folk medicine A.A.ALI,M.H.MOHAMED,M.S.KAMEL,M.A.FOUAD and O.SPRING Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . èñÖ¬ËØ ÏàËÆ¶È:80% China Journal of Chinese Materia Medica 2012 37 2092-2099 Non-anthraquinones constituents from the roots of Knoxia valerianoides ZHAO Feng; WANG Sujuan; WU Xiuli; YU Yang; YUE Zhenggang; LIU Bo; LIN Sheng; ZHU Chenggen; YANG Yongchun; SHI Jiangong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 2,3-bis-(¦Á-hydroxy-4-hydroxy-3-methoxybenzyl)-butane-1,4-diol ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2015 46 178−186 Chemical constituents from roots of Kadsura longipedunculata CHEN Jia-bao, LIU Jia-bao, CUI Bao-song, LI Shuai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . guaiacylglycerol ÏàËÆ¶È:70% Chinese Pharmaceutical Journal 2010 45 101-103 Water-Soluble Chemical Constituents of Angelica Sinensis(Oliv.) Diels JIANG Wei, WANG Chang-hong, WANG Zheng-tao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (¡À)-1-(4-hydroxymethyl-2,5-dihydrofuran-2-yl)-5-methyl-1H-pyrimidine-2,4-dione C10H12N2O4 ÏàËÆ¶È:70% Journal of Medicinal Chemistry 2001 44 806-813 Syntheses and Structure−Activity Relationships of Novel Apio and Thioapio Dideoxydidehydronucleosides as Anti-HCMV Agents Lak Shin Jeong, Hea Ok Kim, Hyung Ryong Moon, Joon Hee Hong, Su Jeong Yoo, Won Jun Choi, Moon Woo Chun, and Chong-Kyo Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ YB-2 1 . Óú´´Ä¾-6(7)-Ï©-4,10-¶þ´¼ C15H26O2 ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2011 42 1477-1480 Chemical constituents of Patrinia scabiosaefolia GAO, Liang, ZHANG, Lin, LIU, Jiang-yun, CAI, Pei-lie, YANG, Shi-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . moreli-3,9-dien-7¦Â-ol-2-one ÏàËÆ¶È:53.3% Journal of Natural Products 1992 Vol 55 577 Molecular Rearrangements in the Longipinene Series Luisa U. Rom¨¢n, Juan D. Hern¨¢ndez, Carlos M. Cerda-Garc¨ªa-Rojas, Rosa Mar¨ªa Dom¨ªnguez-L¨®pez, Pedro Joseph-Nathan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 3 C15H20O3 ÏàËÆ¶È:53.3% Journal of Natural Products 1992 Vol 55 577 Molecular Rearrangements in the Longipinene Series Luisa U. Rom¨¢n, Juan D. Hern¨¢ndez, Carlos M. Cerda-Garc¨ªa-Rojas, Rosa Mar¨ªa Dom¨ªnguez-L¨®pez, Pedro Joseph-Nathan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 4a ÏàËÆ¶È:53.3% Phytochemistry 1993 32 57-60 Abscisic alcohol glucoside in quince Andrea Lutz, Peter Winterhalter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 9¦Â,10¦Â-Epoxytrichodiene ÏàËÆ¶È:53.3% Phytochemistry 1993 32 93-104 Potential inhibitors of trichothecene biosynthesis in Fusarium culmorum: Epoxidation of a trichodiene derivative Andrew R. Hesketh, Linden gledhill, Barrie W. Bycroft, Paul M. Dewick, John Gilbert Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (-)-10¦Á-Hydroxy-1¦ÁH-guaia-4,6-dien-3-one ÏàËÆ¶È:53.3% Organic Letters 2005 Vol. 7, No. 15 3291-3294 Total Syntheses of Four Stereoisomers of 4¦Á-Hydroxy-1¦Â,7¦Â-peroxy-10aH-guaia-5-ene Gonzalo Blay, Begoña Garcia, Eva Molina, and Jos¨¦ R. Pedro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ YB-3 1 . Serralactone C C15H22O5 ÏàËÆ¶È:100% Helvetica Chimica Acta 2009 92 1298-1303 Four New Eudesmane Sesquiterpenoid Lactones from Chloranthus serratus Fei Teng, Hui-Min Zhong, Chang-Xiang Chen, Hai-Yang Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Chloraeudolide C15H22O5 ÏàËÆ¶È:73.3% Journal of Natural Products 2011 74 16-20 Sesquiterpenes from Chloranthus japonicus Qiu-Hong Wang, Hai-Xue Kuang, Bing-You Yang, Yong-Gang Xia, Jun-Song Wang, and Ling-Yi Kong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 1¦Â,4¦Á 11¦Á-trihydroxyeudesmane C15H28O3 ÏàËÆ¶È:66.6% Chinese Chemical Letters 2000 11 1009-1012 New Sesquiterpenoids from Hedychium yunnanense gagnep Xiu Hua LIU, Dong Bao ZHAO, Chong Ren YANG, Han Qing WANG Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Disciferitriol C15H29O3 ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2007 9 277-283 Sesquiterpenoids from Hedychium yunnanense and Porana discifera, and the structural revision of two sesquiterpenoids from Laggera pterodonta W.-M. ZHU, Q. ZHAO, S.-L. LI and X.-J. HAO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . disciferitriol C15H28O3 ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 2014 50 732-734 Chemical Components of the Fibrous Root of Ophiopogon japonicus Tian Feng, Shen Lan, Wang ChenJie, Feng Yi, Zheng XiangWei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 1¦Â,4¦Á,13-trihydroxy-eudesm-11(12)-ene C15H26O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2006 54(5) 676-678 A New Eudesmane Derivative and a New Fatty Acid Ester from Sambucus williamsii Xujuan YANG,Mansau WONG,Naili WANG,Albert Sun-Chi CHAN,and Xinsheng YAO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . hedytriol C15H28O3 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2007 9 277-283 Sesquiterpenoids from Hedychium yunnanense and Porana discifera, and the structural revision of two sesquiterpenoids from Laggera pterodonta W.-M. ZHU, Q. ZHAO, S.-L. LI and X.-J. HAO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 1¦Â-hydroxyilicic acid C15H24O4 ÏàËÆ¶È:60% Natural Product Research 2003 17 99-102 A New Eudesmane Type Sesquiterpene from Inula Viscosa Musa H. Abu Zarga; Salim S. Sabri; Emad M. Hamed; Monther A. Khanfar; Klaus-Peter Zeller; Atta-Ur-Rahman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 1¦Â,4¦Â-dihydroxy-5¦Á,8¦Â-(H)-eudesm-7 ÏàËÆ¶È:60% Acta Botanica Yunnanica 2010 32 83-86 A New Phenolic Glycoside from Chloranthusmul tistachys (Chloranthaceae) RAN Xin-Hui, N I Wei, WEI Gang, CHEN Chang-Xiang, LIU Hai-Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . istanbulin B ÏàËÆ¶È:60% Journal of Chinese Medicinal Materials 2005 28 292-293 ²Ýɺº÷»¯Ñ§³É·ÖÑо¿ Ôø°®»ª, ÂÞÓÀÃ÷ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-25 22:27:39
СССÌǶ¹
Òø³æ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 542
- Ìû×Ó: 67
- ÔÚÏß: 19.7Сʱ
- ³æºÅ: 1851563
- ×¢²á: 2012-06-07
- ÐÔ±ð: MM
- רҵ: ÖÐÒ©ÖÆ¼Á
3Â¥2015-03-26 09:30:55
СССÌǶ¹
Òø³æ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 542
- Ìû×Ó: 67
- ÔÚÏß: 19.7Сʱ
- ³æºÅ: 1851563
- ×¢²á: 2012-06-07
- ÐÔ±ð: MM
- רҵ: ÖÐÒ©ÖÆ¼Á
4Â¥2015-03-26 10:15:55













»Ø¸´´ËÂ¥