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ר¼Ò¾Ñé: +726 - PhEPI: 3
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- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
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- ×¢²á: 2012-10-26
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1 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£º¹²²éµ½2273¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5,7,3',4'-tetrahydroxy-3-methoxyflavone ÏàËÆ¶È:100% Molecules 2010 15 2593-2599 A New Sulfated ¦Á-Ionone Glycoside from Sonchus erzincanicus Matthews Ufuk Ozgen, Handan Sevindik, Cavit Kazaz, Demet Yigit, Ali Kandemir, Hasan Secen and Ihsan Calis Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-O-methylquercetin ÏàËÆ¶È:100% Phytochemistry 1985 24 835-848 Chemistry of toxic range plants. Highly oxygenated flavonol methyl ethers from Gutierrezia microcephala James N. Roitman, Lynn F. James Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . quercetin-3-methyl ether ÏàËÆ¶È:100% Phytochemistry 1986 25 2357-2360 3-Methoxyflavones and coumarins from Artemisia incanescens Oscar Barber¨¢, J.Alberto Marco, Juan F. Sanz, Juan S¨¢nchez-Parareda Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-O-methylquercetin C16H12O7 ÏàËÆ¶È:100% Journal of Shenyang Pharmaceutical University 2009 26 701-703 Isolation, identification and activity determination on the anti-hypoxic components of Hypericum japonicum Thunb. WANG Xiao-wei, MAO Yu, FAN Ming, DING A i-shi, WANG Nai-li, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-O-Methylquercetin ÏàËÆ¶È:100% Archiv der Pharmazie 1997 330 313-316 An Improved Synthesis of the Anti-Picornavirus Flavone 3-O-Methylquercetin Frank Boers, Bo-Liang Deng, Guy Lemi¨¨re, Jozef Lepoivre, Alex De Groot, Roger Dommisse and Arnold J. Vlietinck Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-O-methylquercetin ÏàËÆ¶È:100% Chemistry & Biodiversity 2012 9 2096-2158 Flavonoids in Subtribe Centaureinae (Cass.) Dumort. (Tribe Cardueae, Asteraceae): Distribution and 13C-NMR Spectral Data Carmen Formisano, Daniela Rigano, Felice Senatore, Svetlana Bancheva, Antonella Maggio, Sergio Rosselli and Maurizio Bruno Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-methyl quercetin ÏàËÆ¶È:100% Journal of Chinese Pharmaceutical Sciences 2013 22 286-288 Flavanoids and xanthones isolated from Arenaria serpyllifolia L. Guanshen Zhou, Xiaojuan Yang, Yong Jiang , Pengfei Tu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-O-methyl-quercetin ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 2013 44 11-15 A new monoterpenoid isolated from flowers of Xanthoceras sorbifolia ZHAO Dan-dan, LI Dan-yi, HUA Hui-ming, LI Zhan-lin, Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-methoxyquercetin C16H12O7 ÏàËÆ¶È:100% Inflammopharmacology 2011 19 35-43 In vitro hepatoprotective and antioxidant activities of crude extract and isolated compounds from Ficus gnaphalocarpa Donfack J. Hubert, Amadou Dawe, Ngueguim T. Florence, Kapche D. W. F. Gilbert, Tchana N. Angele, D. Buonocore, P. Vita Finzi, G. Vidari, Ngadjui T. Bonaventure, Fulvio Marzatico, Moundipa F. Paul Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-O-methylquercetin ÏàËÆ¶È:100% International Journal of Molecular Sciences 2012 13 11349-11364 Phenolic Compounds from Halimodendron halodendron (Pall.) Voss and Their Antimicrobial and Antioxidant Activities Jihua Wang, Jingfeng Lou, Chao Luo, Ligang Zhou, Mingan Wang and Lan Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . quercetin-3-O-methyl ether ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2011 36 458-461 Chemical constituents in herb of Polygonum orientale ¢ò LI Yongjun, LI Cuibing, HE Xun, LIAO Shanggao, LAN Yanyu, WANG Aimin, WANG Yonglin Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-07-23 10:04:46
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
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ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
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2 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£º¹²²éµ½1646¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . kaemferide ÏàËÆ¶È:100% Natural Product Sciences 1998 4 215-220 Sulphated Flavonols of the Flowers of Tamarix amplexicaulis Souleman, Ahmed M.A. Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . kaempferide ÏàËÆ¶È:100% Natural Product Sciences 2000 6 91-95 Constitutive flavonoids of the flowers of Tamarix tetragyna El-Mousallamy, Amani M.D.; Ahmed, Sayed A. Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ɽÄÎËØ-4'-¼×ÃÑ ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 2006 37 663-664 Flavonoids of Alpinia officinarum AN Ning; YANG Shi-lin; ZOU Zhong-mei; XU Li-zhen Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . kaempferol ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 1996 27 707-711 A New Flavonol Glucoside from Aerial Parts of Manaplant Alhagi(Alhagi pseudoalhagi) Yang Xiuwei; Jiang Yumei; Li Junshan; et al(Address£º Yang Xiuwei; School of Pharmaceutical Sciences; Beijing Medical University; Beijing); Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 5a ÏàËÆ¶È:100% Archives of Pharmacal Research 1990 13 374-378 Phytochemical study on Prunus davidiana Jae Sue Choi, Won Sick Woo, Han Suk Young and Jong Hee Park Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . kaempferol-4'-methyl ether C16H12O6 ÏàËÆ¶È:100% Natural Product Research and Development 2001 13(5) 22-24 THE CHEMICAL CONSTITUENTS FROM EUPATORIUM ODORATUM DING Zhi hui; ZHANG Xue mei; LIU Ji kai; DING Jing kai; GU Kun Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2014-07-23 10:07:45
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
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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
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- ×¢²á: 2012-10-26
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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£º¹²²éµ½239¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4'-Demethylpodophyllotoxin C21H20O8 ÏàËÆ¶È:88.8% Journal of Separation Science 2013 36 1022-1028 Novel linear and step-gradient counter-current chromatography for bio-guided isolation and purification of cytotoxic podophyllotoxins from Dysosma versipellis (Hance) (pages 1022¨C1028) Zhi Yang, Xiaoman Liu, Kuiwu Wang, Xiaoji Cao and Shihua Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 4'-È¥¼×»ù¹í¾Ê¶¾ËØ C21H20O8 ÏàËÆ¶È:85% Lishizhen Medicine and Materia Medica Research 2011 22 871-873 Study on Chemical Constituents from Rootstalk of Dysosma versipellis Grown in Guizhou GAO Xiu-hong; LIU Ming-chuan; JIN Lin-hong; SONG Bao-an; HU De-yu; YANG Song Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4'-demethyl podophyllotoxin ÏàËÆ¶È:83.3% Phytochemical Analysis 2013 24 603-607 One-step Separation and Purification of Three Lignans and One Flavonol from Sinopodophyllum emodi by Medium-pressure Liquid Chromatography and High-speed Counter-current Chromatography Ping Wang, Yongling Liu, Tao Chen, Wenhua Xu, Jinmao You, Yongjun Liu and Yulin Li Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4'-demethylpodophyllotoxin ÏàËÆ¶È:75% Journal of the Indian Chemical Society 1997 74 692-694 Carbon-13NMR Chemical Shifts of some Podophyllum Lignans and Analogues JAYATI MITERA and ALOK KUMAR MITRA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¹í¾Ê¶¾ËØ ÏàËÆ¶È:73.6% Journal of Anhui Agricultural Sciences 2011 39 19781-19782 Chemical Components of CHINESE UMBRELLALEAF RHIZOME AND ROOT in Taibai Mountains MA Yang-min et al Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . podophyllotoxin ÏàËÆ¶È:73.6% Phytochemical Analysis 2013 24 603-607 One-step Separation and Purification of Three Lignans and One Flavonol from Sinopodophyllum emodi by Medium-pressure Liquid Chromatography and High-speed Counter-current Chromatography Ping Wang, Yongling Liu, Tao Chen, Wenhua Xu, Jinmao You, Yongjun Liu and Yulin Li Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Podophyllotoxin C22H22O8 ÏàËÆ¶È:73.6% Journal of Separation Science 2013 36 1022-1028 Novel linear and step-gradient counter-current chromatography for bio-guided isolation and purification of cytotoxic podophyllotoxins from Dysosma versipellis (Hance) (pages 1022¨C1028) Zhi Yang, Xiaoman Liu, Kuiwu Wang, Xiaoji Cao and Shihua Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . orthoquinone ÏàËÆ¶È:72.2% Journal of the Indian Chemical Society 1997 74 692-694 Carbon-13NMR Chemical Shifts of some Podophyllum Lignans and Analogues JAYATI MITERA and ALOK KUMAR MITRA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Podophyllotoxin C22H22O8 ÏàËÆ¶È:72.2% Helvetica Chimica Acta 1994 77 771-777 A Novel Rearrangement Product of Podophyllotoxone ¨C Ester Derivatives and in vitro cytotoxicity studies Peter H. Höfert and Rudolf Matusch Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . podophyllotoxin ÏàËÆ¶È:71.4% Journal of the Indian Chemical Society 1997 74 692-694 Carbon-13NMR Chemical Shifts of some Podophyllum Lignans and Analogues JAYATI MITERA and ALOK KUMAR MITRA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¹í¾Ê¶¾ËØ ÏàËÆ¶È:68.4% Chinese Traditional and Herbal Drugs 2010 41 1619-1622 ÌÒ¶ùÆß»¯Ñ§³É·ÖºÍϸ°û¶¾ÐÔÑо¿ ³ÂÓиù;ÕÅÀö·¼;ÁõÓý³½;Íõ±ÌËÉ;½ðöÎ;¸µÐÀÍ®;Öܽ¨Æ½;¹ùºé×£ Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2014-07-23 10:18:15
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
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ר¼Ò¾Ñé: +726 - PhEPI: 3
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- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
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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£º¹²²éµ½402¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¹í¾Ê¶¾ËØ ÏàËÆ¶È:84.2% Chinese Traditional and Herbal Drugs 2010 41 1619-1622 ÌÒ¶ùÆß»¯Ñ§³É·ÖºÍϸ°û¶¾ÐÔÑо¿ ³ÂÓиù;ÕÅÀö·¼;ÁõÓý³½;Íõ±ÌËÉ;½ðöÎ;¸µÐÀÍ®;Öܽ¨Æ½;¹ùºé×£ Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . podophyllotoxin ÏàËÆ¶È:83.3% Natural Product Research and Development 2005 17 588-591 Chemical Constituents of Sabina vulgaris Antoine WANG Wu-bao; BA Hang; HAJIA Aisa; LIAO Li-xin; DUO Li-kun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Podophyllotoxin C22H22O8 ÏàËÆ¶È:83.3% Helvetica Chimica Acta 1994 77 771-777 A Novel Rearrangement Product of Podophyllotoxone ¨C Ester Derivatives and in vitro cytotoxicity studies Peter H. Höfert and Rudolf Matusch Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Desoxypodophyllotoxin ÏàËÆ¶È:80% Molecules 2012 17 9506-9519 Cytotoxic Podophyllotoxin Type-Lignans from the Steam Bark of Bursera fagaroides var. fagaroides Andr¨¦s M. Rojas-Sep¨²lveda, Mario Mendieta-Serrano, Mayra Y. Ant¨²nez Mojica, Enrique Salas-Vidal, Silvia Marquina, Mar¨ªa Luisa Villarreal, Ana Mar¨ªa Puebla, Jorge I. Delgado and Laura Alvarez Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Podophyllotoxin ÏàËÆ¶È:78.9% Molecules 2012 17 9506-9519 Cytotoxic Podophyllotoxin Type-Lignans from the Steam Bark of Bursera fagaroides var. fagaroides Andr¨¦s M. Rojas-Sep¨²lveda, Mario Mendieta-Serrano, Mayra Y. Ant¨²nez Mojica, Enrique Salas-Vidal, Silvia Marquina, Mar¨ªa Luisa Villarreal, Ana Mar¨ªa Puebla, Jorge I. Delgado and Laura Alvarez Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound ÏàËÆ¶È:77.2% Phytochemistry 1998 49 491-496 Production of Podophyllotoxin in Juniperus Chinensis Callus Cultures Treated with Oligosaccharides and a Biogenetic Precursor in Honour of Professor G. H. Neil Towers 75th Birthday Toshio Muranak¦Á, Masaru Miyat¦Á, Kazutaka Ito, Sanro Tachibana Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . podophyllotoxin C22H22O8 ÏàËÆ¶È:77.2% Journal of Wood Science 1998 44 397-400 Extractives of Juniperus chinensis L. I: Isolation of podophyllotoxin and yatein from the leaves of J.chinensis Masaru Miyata, Kazutaka Itoh, Santo Tachibana Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . podophyllotoxin ÏàËÆ¶È:76.1% Phytochemistry 1980 19 1527-1530 13C NMR analysis of podophyllotoxin and some of its derivatives Sebasti¨¢o F. Fonseca, Edmundo A. R¨²veda, James D. McChesney Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¹í¾Ê¶¾ËØ ÏàËÆ¶È:73.6% Journal of Anhui Agricultural Sciences 2011 39 19781-19782 Chemical Components of CHINESE UMBRELLALEAF RHIZOME AND ROOT in Taibai Mountains MA Yang-min et al Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Podophyllotoxin C22H22O8 ÏàËÆ¶È:73.6% Journal of Separation Science 2013 36 1022-1028 Novel linear and step-gradient counter-current chromatography for bio-guided isolation and purification of cytotoxic podophyllotoxins from Dysosma versipellis (Hance) (pages 1022¨C1028) Zhi Yang, Xiaoman Liu, Kuiwu Wang, Xiaoji Cao and Shihua Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2'-Bromopodophyllotoxin ÏàËÆ¶È:71.4% Journal of Agricultural and Food Chemistry 2013 61 8148-8155 Synthesis of Novel 4¦Á-(Acyloxy)-2¡ä(2¡ä,6¡ä)-(di)halogenopodophyllotoxin Derivatives as Insecticidal Agents Zhiping Che, Xiang Yu, Xiaoyan Zhi, Lingling Fan, Xiaojun Yao, and Hui Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 4'-demethylpodophyllotoxin ÏàËÆ¶È:70% Journal of the Indian Chemical Society 1997 74 692-694 Carbon-13NMR Chemical Shifts of some Podophyllum Lignans and Analogues JAYATI MITERA and ALOK KUMAR MITRA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Compound 5 ÏàËÆ¶È:68.4% Bioorganic & Medicinal Chemistry Letters 1999 9 2131-2134 9-Deoxopodophyllotoxin derivatives as anti-cancer agents Duvvuri Subrahmanyam, B. Renuka, G. Sunil Kumar, V. Vandana, Danvanthri S. Deevi Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2¦Â-bromopicropodophyllotoxin ÏàËÆ¶È:68.4% Tetrahedron 2013 69 774-781 Stereoselective synthesis of 4¦Á-acyloxy-2¦Á/¦Â-bromopodophyllotoxin derivatives as insecticidal agents Yong Guo, Lingling Fan, Juanjuan Wang, Chun Yang, Huan Qu, Hui Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . podophyllotoxin acetate ÏàËÆ¶È:66.6% Journal of the Indian Chemical Society 1997 74 692-694 Carbon-13NMR Chemical Shifts of some Podophyllum Lignans and Analogues JAYATI MITERA and ALOK KUMAR MITRA Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Acetyl podophyllotoxin ÏàËÆ¶È:66.6% Molecules 2012 17 9506-9519 Cytotoxic Podophyllotoxin Type-Lignans from the Steam Bark of Bursera fagaroides var. fagaroides Andr¨¦s M. Rojas-Sep¨²lveda, Mario Mendieta-Serrano, Mayra Y. Ant¨²nez Mojica, Enrique Salas-Vidal, Silvia Marquina, Mar¨ªa Luisa Villarreal, Ana Mar¨ªa Puebla, Jorge I. Delgado and Laura Alvarez Structure 13C NMR ̼Æ×Ä£Äâͼ |

5Â¥2014-07-23 10:23:48
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
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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
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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£º¹²²éµ½402¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¹í¾Ê¶¾ËØ ÏàËÆ¶È:84.2% Chinese Traditional and Herbal Drugs 2010 41 1619-1622 ÌÒ¶ùÆß»¯Ñ§³É·ÖºÍϸ°û¶¾ÐÔÑо¿ ³ÂÓиù;ÕÅÀö·¼;ÁõÓý³½;Íõ±ÌËÉ;½ðöÎ;¸µÐÀÍ®;Öܽ¨Æ½;¹ùºé×£ Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . podophyllotoxin ÏàËÆ¶È:83.3% Natural Product Research and Development 2005 17 588-591 Chemical Constituents of Sabina vulgaris Antoine WANG Wu-bao; BA Hang; HAJIA Aisa; LIAO Li-xin; DUO Li-kun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Podophyllotoxin C22H22O8 ÏàËÆ¶È:83.3% Helvetica Chimica Acta 1994 77 771-777 A Novel Rearrangement Product of Podophyllotoxone ¨C Ester Derivatives and in vitro cytotoxicity studies Peter H. Höfert and Rudolf Matusch Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Desoxypodophyllotoxin ÏàËÆ¶È:80% Molecules 2012 17 9506-9519 Cytotoxic Podophyllotoxin Type-Lignans from the Steam Bark of Bursera fagaroides var. fagaroides Andr¨¦s M. Rojas-Sep¨²lveda, Mario Mendieta-Serrano, Mayra Y. Ant¨²nez Mojica, Enrique Salas-Vidal, Silvia Marquina, Mar¨ªa Luisa Villarreal, Ana Mar¨ªa Puebla, Jorge I. Delgado and Laura Alvarez Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Podophyllotoxin ÏàËÆ¶È:78.9% Molecules 2012 17 9506-9519 Cytotoxic Podophyllotoxin Type-Lignans from the Steam Bark of Bursera fagaroides var. fagaroides Andr¨¦s M. Rojas-Sep¨²lveda, Mario Mendieta-Serrano, Mayra Y. Ant¨²nez Mojica, Enrique Salas-Vidal, Silvia Marquina, Mar¨ªa Luisa Villarreal, Ana Mar¨ªa Puebla, Jorge I. Delgado and Laura Alvarez Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound ÏàËÆ¶È:77.2% Phytochemistry 1998 49 491-496 Production of Podophyllotoxin in Juniperus Chinensis Callus Cultures Treated with Oligosaccharides and a Biogenetic Precursor in Honour of Professor G. H. Neil Towers 75th Birthday Toshio Muranak¦Á, Masaru Miyat¦Á, Kazutaka Ito, Sanro Tachibana Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . podophyllotoxin C22H22O8 ÏàËÆ¶È:77.2% Journal of Wood Science 1998 44 397-400 Extractives of Juniperus chinensis L. I: Isolation of podophyllotoxin and yatein from the leaves of J.chinensis Masaru Miyata, Kazutaka Itoh, Santo Tachibana Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . podophyllotoxin ÏàËÆ¶È:76.1% Phytochemistry 1980 19 1527-1530 13C NMR analysis of podophyllotoxin and some of its derivatives Sebasti¨¢o F. Fonseca, Edmundo A. R¨²veda, James D. McChesney Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¹í¾Ê¶¾ËØ ÏàËÆ¶È:73.6% Journal of Anhui Agricultural Sciences 2011 39 19781-19782 Chemical Components of CHINESE UMBRELLALEAF RHIZOME AND ROOT in Taibai Mountains MA Yang-min et al Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Podophyllotoxin C22H22O8 ÏàËÆ¶È:73.6% Journal of Separation Science 2013 36 1022-1028 Novel linear and step-gradient counter-current chromatography for bio-guided isolation and purification of cytotoxic podophyllotoxins from Dysosma versipellis (Hance) (pages 1022¨C1028) Zhi Yang, Xiaoman Liu, Kuiwu Wang, Xiaoji Cao and Shihua Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2'-Bromopodophyllotoxin ÏàËÆ¶È:71.4% Journal of Agricultural and Food Chemistry 2013 61 8148-8155 Synthesis of Novel 4¦Á-(Acyloxy)-2¡ä(2¡ä,6¡ä)-(di)halogenopodophyllotoxin Derivatives as Insecticidal Agents Zhiping Che, Xiang Yu, Xiaoyan Zhi, Lingling Fan, Xiaojun Yao, and Hui Xu Structure 13C NMR ̼Æ×Ä£Äâͼ |

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