| ²é¿´: 287 | »Ø¸´: 1 | |||||
·çÐÅ×Ó0208ľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»£¡ ÒÑÓÐ1È˲ÎÓë
|
| 13C NMR (101 MHz, Acetone) ¦Ä 13.24, 13.68, 14.47, 14.51, 16.41, 17.29, 17.57, 17.77, 19.44, 24.84, 27.40, 31.22, 34.48, 35.14, 35.34, 37.49, 38.54, 40.16, 40.42, 41.80, 43.26, 50.97, 51.79, 53.83, 55.90, 61.95, 63.00, 64.07, 64.78, 65.65, 66.36, 68.17, 68.90, 71.24, 82.00, 82.46, 83.04, 83.66, 91.03, 91.36, 97.37, 97.96, 98.70, 99.99, 126.45, 135.64, 141.98, 157.76, 205.14, 205.52. |
» ²ÂÄãϲ»¶
294Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
322Çóµ÷¼Á£ºÒ»Ö¾Ô¸ºþÄÏ´óѧ ²ÄÁÏÓ뻯¹¤£¨085600£©£¬ÒѹýÁù¼¶¡£
ÒѾÓÐ14È˻ظ´
282Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
µ÷¼Á
ÒѾÓÐ9È˻ظ´
315Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ8È˻ظ´
070300»¯Ñ§Ñ§Ë¶311·ÖÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
ÇóÖúһ΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú¡¢¡¢¡¢Ð»Ð»´óÉñ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¼±£¡Ð»Ð»£¡
ÒѾÓÐ5È˻ظ´
Asian J. Control Ò»ÉóÒâ¼ûÇóÖú
ÒѾÓÐ14È˻ظ´
΢Æ×ÇóÖú лл£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý gf
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ Èý¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
·çÐÅ×Ó0208: ½ð±Ò+8, ¡ïÓаïÖú 2014-10-15 13:11:02
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
·çÐÅ×Ó0208: ½ð±Ò+8, ¡ïÓаïÖú 2014-10-15 13:11:02
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½117¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Lobophorin F C54H78N2O17 ÏàËÆ¶È:61.1% The Journal of Antibiotics 2011 64 711-716 Lobophorins E and F, new spirotetronate antibiotics from a South China Sea-derived Streptomyces sp. SCSIO 01127 Siwen Niu, Sumei Li, Yuchan Chen, Xinpeng Tian, Haibo Zhang, Guangtao Zhang, Weimin Zhang, Xiaohong Yang, Si Zhang, Jianhua Ju and Changsheng Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 32-O-(4-iodobenzoyl)-O-¦Â-D-kijanosyl-(1¡ú17)-kijanolide C49H61IN2O13 ÏàËÆ¶È:58% Journal of the Chemical Society, Perkin Transactions 1 1983 1497-1534 Kijanimicin. Part 3. Structure and absolute stereochemistry of kijanimicin Alan K. Mallams, Mohindar S. Puar, Randall R. Rossman, Andrew T. McPhail, Ronald D. Macfarlane and Richard L. Stephens Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 32-O-(4-iodobenzoyl)-O-¦Â-D-kijanosyl-(1¡ú17)-methyl-kijanolide C50H63IN2O13 ÏàËÆ¶È:56% Journal of the Chemical Society, Perkin Transactions 1 1983 1497-1534 Kijanimicin. Part 3. Structure and absolute stereochemistry of kijanimicin Alan K. Mallams, Mohindar S. Puar, Randall R. Rossman, Andrew T. McPhail, Ronald D. Macfarlane and Richard L. Stephens Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5,6-epoxy-solasodine-3¦Â-acteate C29H45NO4 ÏàËÆ¶È:56% Steroids 2012 77 1069-1074 Application of hypoiodite-mediated aminyl radical cyclization to synthesis of solasodine acetate Yi Kou, Myong Chul Koag, Young Cheun, Aram Shin, Seongmin Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 12 C53H96N4O22 ÏàËÆ¶È:54.7% Journal of the American Chemical Society 1998 120 13301-13311 Saccharomicins, Novel Heptadecaglycoside Antibiotics Effective against Multidrug-Resistant Bacteria Fangming Kong, Ning Zhao, Marshall M. Siegel, Kasia Janota, Joseph S. Ashcroft, Frank E. Koehn, Donald B. Borders, and Guy T. Carter Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Tuberoside I5 C55H90O19 ÏàËÆ¶È:54% Phytochemistry 2009 70 1294-1304 8,14-Secopregnane glycosides from the aerial parts of Asclepias tuberosa Tsutomu Warashina , Tadataka Noro Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 9,32-Di-O-acetyl-O-¦Â-D-kijanosyl-(1¡ú17)-kijanolide C46H62N2O14 ÏàËÆ¶È:54% Journal of the Chemical Society, Perkin Transactions 1 1983 1497-1534 Kijanimicin. Part 3. Structure and absolute stereochemistry of kijanimicin Alan K. Mallams, Mohindar S. Puar, Randall R. Rossman, Andrew T. McPhail, Ronald D. Macfarlane and Richard L. Stephens Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . avermectin B2a C48H74O15 ÏàËÆ¶È:54% Chinese Journal of Pesticide Science 2007 9 25-28 Isolation and Identification of the Insecticidal Ingredients from the Fermentation Broth of Streptomyces qinlingnensis JI Zhi-qin; ZHANG Ji-wen; WEI Shao-peng; WU Wen-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 21¦Â-O-tigloyl-28-Oacetylprotoaescigenin-3¦Â-O-[¦Â-D-glucopyranosyl(1¡ú2)]-¦Â-D-glucopyranosiduronic acid ÏàËÆ¶È:54% Drugs & Clinic 2012 27 442-445 Chemical constituents in zymolyte of Aesculi Semen extract ZHAO Na-xia, XIA Guang-ping, HAN Ying-mei Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 6 ÏàËÆ¶È:53.8% Phytochemistry 1992 31 3177-3181 Saponins from Steganotaenia araliacea Catherine Lavaud, Georges Massiot, Louisette Le Men-Olivier, Alain Viari, Paul Vigny, Clement Delaude Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 7 ÏàËÆ¶È:52.9% Journal of Natural Products 2012 75 959-967 Bahamaolides A and B, Antifungal Polyene Polyol Macrolides from the Marine Actinomycete Streptomyces sp. Dong-Gyu Kim, Kyuho Moon, Seong-Hwan Kim, Seon-Hui Park, Sunghyouk Park, Sang Kook Lee, Ki-Bong Oh, Jongheon Shin, and Dong-Chan Oh Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-10-15 12:51:24














»Ø¸´´ËÂ¥
120