| ²é¿´: 270 | »Ø¸´: 1 | ||||
haijiaotangÒø³æ (ÕýʽдÊÖ)
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[ÇóÖú]
ÇóÖúÒÔÏ»¯ºÏÎï
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| 13C NMR (75 MHz, MeOD) ¦Ä 14.49, 17.63,18.50,20.26, 21.49,22.61,23.57, 24.45, 24.65,28.96, 29.47, 31.75, 32.17,32.87,35.15, 37.33, 38.73,39.22,42.22, 51.32, 51.78, 66.65, 68.42, 68.70, 71.10, 84.89, 85.24, 85.41,105.35, 122.14, 127.36, 129.00, 129.82, 131.10,132.31, 133.59, 167.63, 206.45 |
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haijiaotang: ½ð±Ò+10 2013-08-15 15:00:54
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haijiaotang: ½ð±Ò+10 2013-08-15 15:00:54
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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£º¹²²éµ½714¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ecdysterone 22,25-Di-O-benzoate ÏàËÆ¶È:63.1% Chemistry of Natural Compounds 1990 26 301-303 PHYTOECDYSTEROIDS OF PLANTS OF THE GENUS Silene.XVII. ECDYSTERONE 22,25-DI-O-BENZOATE FROM Silene scabrifolia A. Saatov, N. D. Abdullaev,M. B. Gorovits, and N. K. Abubakirov Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Momordicoside V C36H58O8 ÏàËÆ¶È:63.1% Magnetic Resonance in Chemistry 2010 48 392-396 Cucurbitane-type triterpene glycosides from the fruits of Momordica charantia (pages 392¨C396) Nguyen Xuan Nhiem, Phan Van Kiem, Chau Van Minh, Ninh Khac Ban, Nguyen Xuan Cuong, Le Minh Ha, Bui Huu Tai, Tran Hong Quang, Nguyen Huu Tung and Young Ho Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 7 ÏàËÆ¶È:63.1% Tetrahedron Letters 2003 44 6673-6677 Degradation of triterpenic compounds from olive-pressing residues. Synthesis of trans-decalin type chiral synthons Andr¨¦s Garcı́a-Granados, Pilar E L¨®pez, Enrique Melguizo, Andr¨¦s Parra, Yolanda Sime¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 8 C37H56O3 ÏàËÆ¶È:60.5% Journal of Natural Products 2007 70 147-153 Chemical Transformation and Biological Activities of Ambrein, a Major Product of Ambergris from Physeter macrocephalus (Sperm Whale) Ya-Ching Shen,Shi-Yie Cheng,Yao-Haur Kuo,Tsong-Long Hwang,Michael Y. Chiang,and Ashraf Taha Khalil Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3'-O-benzoyl-13do decanoylingenol ÏàËÆ¶È:60.5% Chinese Traditional and Herbal Drugs 2010 41 877-881 ¸ÊË컯ѧ³É·ÖµÄÑо¿ ÎâÏþÀÚ;ÅËÇÚ Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 5 C42H65BO7Si ÏàËÆ¶È:60.5% Journal of Asian Natural Products Research 2011 13 297-303 Synthesis of a novel phosphate analog of 20-hydroxylecdysone with potent hypoglycemic activity Dan Zhang; Min Zhang; Bao Ding; Xiao-Lin Wang; Zong-Yin Qiu; Yong Qin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â-(E)-cinnamoyleuphorbol ÏàËÆ¶È:60.5% Journal of the Brazilian Chemical Society 2011 22 1880-1887 Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br. Rosalina C. S. Mata, Dina I. M. D. de Mendonça, Liliana Vieira, Aldenir F. dos Santos, Luciana A. da Silva, Jorge F. Gaspar, C¨¦lia Martins, Jos¨¦ Rueff and Antônio E. G. Sant¡¯Ana Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 5,15-bis(4-dioxylborylphenyl)porphyrin with 20-hydroxyecdysone C86H104B2N4O14 ÏàËÆ¶È:60.5% Steroids 2012 77 1169-1175 Design and studies of novel polyoxysterol-based porphyrin conjugates Halina A. Zhylitskaya, Vladimir N. Zhabinskii, Raisa P. Litvinovskaya, Raffaella Lettieri, Donato Monti, Mariano Venanzi, Vladimir A. Khripach, Pavel Drašar Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 21-cis,cis,cis-9,12,15-Octadecatrienoyloxy-11¦Â,17¦Á-dihydroxypregn-4-en-3,20-dione C39H58O6 ÏàËÆ¶È:58.9% Steroids 2009 74 1007-1014 Lipase-catalyzed regioselective preparation of fatty acid esters of hydrocortisone Paula G. Quintana, Alicia Baldessari Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 28-(2'-Methyl-1H-imidazol-1-yl)-3,28-dioxours-12-en-2-(2'-methyl-1H-imidazol-1-yl)-methylene C39H54N4O2 ÏàËÆ¶È:58.9% Bioorganic & Medicinal Chemistry 2012 20 5774-5786 Synthesis of novel ursolic acid heterocyclic derivatives with improved abilities of antiproliferation and induction of p53, p21waf1 and NOXA in pancreatic cancer cells Ana S. Leal, Rui Wang, Jorge A.R. Salvador, Yongkui Jing Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Garcimultiflorone C C38H52O7 ÏàËÆ¶È:57.8% Journal of Natural Products 2009 72 253-258 Benzophenone Derivatives from the Fruits of Garcinia multiflora and Their Anti-inflammatory Activity Jih-Jung Chen, Chia-Wei Ting, Tsong-Long Hwang, and Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . carteriosulfonic acid B C38H69NO12S ÏàËÆ¶È:57.8% Journal of Natural Products 2009 72 1651-1656 Carteriosulfonic Acids A-C, GSK-3¦ÂInhibitors from a Carteriospongia sp. Malcolm W. B. McCulloch, Tim S. Bugni, Gisela P. Concepcion, Gary S. Coombs, Mary Kay Harper, Simran Kaur,Gina C. Mangalindan, Misha M. Mutizwa, Charles A. Veltri, David M. Virshup, and Chris M. Ireland Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-O-benzoyl-13-octanoyloxyingenol C35H46O8 ÏàËÆ¶È:57.8% Phytochemistry 2008 69 812-819 Ingenane diterpenoids from Euphorbia esula Zhi-Qiang Lu, Min Yang, Jin-Qiang Zhang, Guang-Tong Chen, Hui-Lian Huang,Shu-Hong Guan, Chao Ma, Xuan Liu, De-An Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3,20-O-diacetylingenol 5-O-(2' E,4' Z)-tetradecadienoate C38H54O8 ÏàËÆ¶È:57.8% Planta Medica 1996 62 260-262 Ingenane Diterpenes from Euphorbia petiolata Yan-Ping Shi, Zhong-Jian Jia, Bin Ma, Sadiq Saleh, and Jamil Lahham Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . makisterone C C35H56O7 ÏàËÆ¶È:57.8% Helvetica Chimica Acta 2009 92 753-761 Ecdysteroids from Silene viridiflora Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 15-Hydroxyponasterone A C27H44O7 ÏàËÆ¶È:57.8% Steroids 2008 73 502-514 Additional minor ecdysteroid components of Leuzea carthamoides Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . roylenine C37H58O12 ÏàËÆ¶È:57.8% Journal of Asian Natural Products Research 2008 10 1023-1028 A new pregnane glycoside from Marsdenia roylei as potential antioxidant and antidyslipidemic agents Arun Seth, Sudha Paswan, Sanjay Srivastav, Naveen Kumar Khare, Akriti Bhatia,Alok Kumar, Geetik Bhatia, Mohamm Mubin Khan, Ashok Kumar Khann and Jitendr Kumar Saxen Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 1a ÏàËÆ¶È:57.8% Journal of Natural Products 1995 Vol 58 1570-1574 Triterpenoids from the Aerial Parts of Lantana camara Sabira Begum, Syed Mohammad Raza, Bina Shaheen Siddiqui, Salimuzzaman Siddiqui Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . camarilic acid C36H54O6 ÏàËÆ¶È:57.8% Journal of Natural Products 1995 Vol 58 1570-1574 Triterpenoids from the Aerial Parts of Lantana camara Sabira Begum, Syed Mohammad Raza, Bina Shaheen Siddiqui, Salimuzzaman Siddiqui Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (25R)-26-acetyloxy-3¦Â-benzoyloxycholest-5-ene-16,22-dione C36H48O6 ÏàËÆ¶È:57.8% Steroids 2011 76 18-27 The synthesis of cholestane and furostan saponin analogues and the determination of sapogenin¡¯s absolute configuration at C-22 Haixing Wang, Yanshen Guo, Yuyao Guan, Liang Zhou, Pingsheng Lei Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Citrinadin A C35H52O6N4 ÏàËÆ¶È:57.8% Organic Letters 2004 Vol. 6, No. 18 3087-3089 Citrinadin A, a Novel Pentacyclic Alkaloid from Marine-Derived Fungus Penicillium citrinum Masashi Tsuda, Yuu Kasai, Kazusei Komatsu, Teruo Sone, Michiko Tanaka,Yuzuru Mikami, and Jun'ichi Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . niuxixinsterone A C34H50O9 ÏàËÆ¶È:57.8% Molecules 2011 16 5989-5997 Three New Phytoecdysteroids Containing a Furan Ring from the Roots of Achyranthes bidentata Bl. Qiu-Hong Wang, Liu Yang, Hai Jiang, Zhi-Bin Wang, Bing-You Yang and Hai-Xue Kuang Structure 13C NMR ̼Æ×Ä£Äâͼ |

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