| ²é¿´: 287 | »Ø¸´: 1 | ||
ligk½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
άÆÕÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| 3-4CÆ×ÐÅÏ¢£º56.90,56.96,60.50,90.69,92.21,101.27,103.87,104.24,104.94,105.39,105.59,119.32,120.76,123.36,132.34,139.60,140.48,141.68,148.68,152.06,152.51,152.65,153.12,155.26,159.08,162.91,164.41,181.78,182.74. |
» ²ÂÄãϲ»¶
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
325Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸¹þ¶û±õ¹¤Òµ´óѧ085600Ó¢Ò»Êý¶þ337·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
22408Çóµ÷¼Á 354·Ö ¿É¿çרҵ
ÒѾÓÐ3È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á£¬326·Ö
ÒѾÓÐ3È˻ظ´

seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- 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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ligk: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-08 23:04:01
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ligk: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-08 23:04:01
|
1 . 4',4''',5,5''-Tetrahydroxy-6,6'',3'''-trimethoxy-[C7-O-C7'']-biflavone C33H24O12 ÏàËÆ¶È:58.0% Magnetic Resonance in Chemistry 2005 43 334-338 Total NMR assignments of new [C7-O-C7'']-biflavones from leaves of the limonene¨Ccarvone chemotype of Lippia alba (Mill) N. E. Brown Francisco Geraldo Barbosa, Mary Anne Sousa Lima and Edilberto Rocha Silveira Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . O-methylcervinomycin A2 C30H23NO9 ÏàËÆ¶È:56.6% The Journal of Antibiotics 1987 40 301-308 STRUCTURE OF CERVINOMYCIN, A NOVEL XANTONE ANTIBIOTIC ACTIVE AGAINST ANAEROBE AND MYCOPLASMA AKIRA NAKAGAWA, SATOSHI OMURA, KATSUHIKO KUSHIDA, HIDEKI SHIMIZU, GABOR LUKACS Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Heveaflavone C33H24O10 ÏàËÆ¶È:55.1% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 627-629 ANTHRAQUINONES AND BIFLAVONOIDS FROM Selaginella delicatula Fan Yang, Kang-ping Xu, Jian Shen, Fu-shuang Li, Hui Zou,Mei-chen Zhou, and Gui-shan Tan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-(3',4',5'-Trimethoxyphenyl)-4,5,6-trimethoxy,2-(2''-methoxybenzylidene)-indan-1-one ÏàËÆ¶È:55.1% Bioorganic & Medicinal Chemistry 2012 20 3049-3057 Synthesis and anticancer activity of 2-benzylidene indanones through inhibiting tubulin polymerization A.P. Prakasham, A.K. Saxena, Suaib Luqman, Debabrata Chanda, Tandeep Kaur, Atul Gupta, D.K. Yadav, C.S. Chanotiya, Karuna Shanker, F. Khan, Arvind S. Negi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (E)-N-(3,4,5-trimethoxybenzylidene)-2-(3,4,5-trimethoxyphenyl)-1H-benzo[d]imidazo[1,2-a]imidazol-3-amine C28H28N4O6 ÏàËÆ¶È:55.1% Tetrahedron 2013 69 2954-2960 Thiamine hydrochloride (VB1)-catalyzed one-pot synthesis of (E)-N-benzylidene-2-phenyl-1H-benzo[d]imidazo[1,2-a]imidazol-3-amine derivatives Fanglei Chen, Min Lei, Lihong Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . salcolin B ÏàËÆ¶È:51.7% Journal of Natural Products 2005 68 289-292 Flavonolignans from Avena sativa Eva Wenzig, Olaf Kunert, Daneel Ferreira, Martin Schmid,Wolfgang Schhly, Rudolf Bauer, and Alois Hiermann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . salcolin A ÏàËÆ¶È:51.7% Journal of Natural Products 2005 68 289-292 Flavonolignans from Avena sativa Eva Wenzig, Olaf Kunert, Daneel Ferreira, Martin Schmid,Wolfgang Schhly, Rudolf Bauer, and Alois Hiermann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-(3',4',5'-Trimethoxyphenyl)-4,5,6-trimethoxy,2-(2'',3''-methylenedioxybenzylidene)-indan-1-one ÏàËÆ¶È:51.7% Bioorganic & Medicinal Chemistry 2012 20 3049-3057 Synthesis and anticancer activity of 2-benzylidene indanones through inhibiting tubulin polymerization A.P. Prakasham, A.K. Saxena, Suaib Luqman, Debabrata Chanda, Tandeep Kaur, Atul Gupta, D.K. Yadav, C.S. Chanotiya, Karuna Shanker, F. Khan, Arvind S. Negi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . tricin 4'-O-(threo-¦Â-guaiacylglyceryl) ether ÏàËÆ¶È:51.7% Tetrahedron 2003 59 8011-8015 Six new flavonolignans from Sasa veitchii (Carr.) Rehder Yuki Nakajima, Young Sook Yun, Akira Kunugi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 167-B C29H21NO9 ÏàËÆ¶È:51.7% The Journal of Antibiotics 1994 47 342-348 167-A, A NEW ANTIBIOTIC PRODUCED BY A MUTANT OF AN INACTIVE WILD STRAIN OF Amycolata autotrophica NATALYA D. MALKINA, YURI V. DUDNIK, LYUDMILA N. LYSENKOVA, EDUARD I. LAZHKO, OL'GA A. GALATENKO, GUENRICH S. KATRUKHA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . cervinomycin A2 C29H21NO9 ÏàËÆ¶È:51.7% The Journal of Antibiotics 1987 40 301-308 STRUCTURE OF CERVINOMYCIN, A NOVEL XANTONE ANTIBIOTIC ACTIVE AGAINST ANAEROBE AND MYCOPLASMA AKIRA NAKAGAWA, SATOSHI OMURA, KATSUHIKO KUSHIDA, HIDEKI SHIMIZU, GABOR LUKACS Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . heveaflavone ÏàËÆ¶È:51.7% Central South Pharmacy 2011 9 565-566 Chemical constituents in Selaginella tamariscina LIU Rui, LIU Jian-feng, XU Kang-ping, ZOU Hui, SONG Li-ying, DANG Rui-Li, ZOU Zhen-xing, LI Guang, TAN Gui-shan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 7,4'-di-O-methylametoflavone ÏàËÆ¶È:51.7% Central South Pharmacy 2012 10 4-6 Biflavonoids from Selaginella moellendorfii Hieron ZOU Zhen-xing, XU Kang-ping, ZOU Hui, ZHANG Qiong, LIU Min-zhen, TAN Gui-shan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-12-08 20:57:48














»Ø¸´´ËÂ¥