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swaucq½ð³æ (ÕýʽдÊÖ)
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compound1: 12.9,21.1,22.3,24.9,28.9,29.1,29.3,30.0,31.5,32.9,44.3,65.8,65.9,76.3,108.0,171.0,173.4,197.9 compound2: 21.0,51.3,55.5,103.0,107.4,107.7,107.9,109.6,128.2,128.7,147.4,157.4,157.9,162.0,165.8,199.7 |
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»¯ºÏÎï1£º 1 . hexyl-6-(2,5-dioxopyrrolidin-1-yl)-2-(2-oxopyrrolidin-1-yl)hexanoate C20H32O5N2 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2010 18 73-79 Synthesis, physico-chemical properties and penetration activity of alkyl-6-(2, 5-dioxopyrrolidin-1-yl)-2-(2-oxopyrrolidin-1-yl)hexanoates as potential transdermal penetration enhancers Katerina Brychtova, Josef Jampilek, Radka Opatrilova, Ivan Raich, Oldrich Farsa, Jozef Csollei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . cinatrin C2 C18H30O8 ÏàËÆ¶È:66.6% The Journal of Antibiotics 1992 45 38-49 CINATRINS, A NOVEL FAMILY OF PHOSPHOLIPASE A2 INHIBITORS I. TAXONOMY AND FERMENTATION OF THE PRODUCING CULTURE; ISOLATION AND STRUCTURES OF CINATRINS HIROSHI ITAZAKI, KAZUO NAGASHIMA, YOSHIMI KAWAMURA, KOICHI MATSUMOTO, HIROSHI NAKAI, YOSHIHIRO TERUI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . diacetyl xestoaminol A ÏàËÆ¶È:61.1% Journal of Natural Products 1990 Vol 53 978 Novel Marine Sponge Amino Acids, 10. Xestoaminoh from Xestaspongia sp. Carlos Jim¨¦nez, Phillip Crews Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Exocarpic acid C18H26O2 ÏàËÆ¶È:61.1% Phytochemistry 1992 31 3929-3931 Viscumitol, a dimethyl-ether of muco-inositol from Viscum album Lovina A.C. Naidoo Siegfried E.^Drewes, J.Van Staden, Anne Hutchings Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (R)-N-Dodecanoyl-2-aminohexanol C18H38O2N ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 1995 3 1397-1403 New phospholipase A2 inhibitor: Synthesis and inhibition mechanism of oxazolidinone phospholipid analog Seiji Iwama, Takeshi Matsuda, Shigeo Katsumura, Takeshi Tani, Shinobu Fujii, Kiyoshi Ikeda, Hideki Takehara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (2R,3R)-2-Decanoylamino-1-morpholino-4-(E)-nonen-3-ol C23H44N2O3 ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 1998 6 1481-1489 Synthesis and evaluation of morpholino- and pyrrolidinosphingolipids as inhibitors of glucosylceramide synthase Tsuyoshi Miura, Tetsuya Kajimoto, Masayuki Jimbo, Kiwamu Yamagishi, Jin-Chi Inokuchi, Chi-Huey Wong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (E)-Hexadec-9-en-11-ynyl acetate ÏàËÆ¶È:61.1% Tetrahedron 2012 68 654-658 Synthesis of E-vinyl iodides via Pd-catalyzed hydrostannation of terminal alkynes Alla Darwish, J. Michael Chong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (9E,11Z)-Hexadeca-9,11-dien-1-yl acetate ÏàËÆ¶È:61.1% Tetrahedron 2012 68 654-658 Synthesis of E-vinyl iodides via Pd-catalyzed hydrostannation of terminal alkynes Alla Darwish, J. Michael Chong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (R)-1-Ethylicosyl acetate C24H48O2 ÏàËÆ¶È:61.1% Journal of the Chemical Society, Perkin Transactions 1 1999 513-518 Chemoenzymatic synthesis of (+)-docosa-4,15-dien-1-yn-3-ol, a component of the marine sponge Cribrochalina vasculum, and confirmation of the structure and absolute configuration of the acetylenic alcohol, by lipase-catalysed biotransformations Kiyoshi Morishita, Makoto Kamezawa, Takehiko Ohtani, Hojun Tachibana, Mayumi Kawase, Midori Kishimoto and Yoshinobu Naoshima Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound (2S,3R)-11 C18H35NO3 ÏàËÆ¶È:61.1% Bioscience, Biotechnology, and Biochemistry 2003 67 329-333 Determination of the Absolute Configuration of (+)-Xestoaminol C [(2S, 3R)-2-Amino-3-tetradecanol], a Metabolite of Fiji Sponge, Xestospongia sp., by the Synthesis of Its¡ Miwako ICHIHASHI and Kenji MORI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . methyl (5R,6S)-5,6-Isopropylideneoxyhexadecanoate C20H38O4 ÏàËÆ¶È:61.1% Heterocycles 2000 53 703-707 A New Synthesis of (-)-(5R,6S)-6-Acetoxy-5-hexadecanolide, the Mosquito Culex pipiens fatigans Oviposition Attractant Pheromone John K. Gallos,* Demetrios S. Mihelakis, Constantinos C. Dellios, and Minodora E. Pozarentzi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . heptyl-6-(2,5-dioxopyrrolidin-1-yl)-2-(2-oxopyrrolidin-1-yl)hexanoate C21H34O5N2 ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 2010 18 73-79 Synthesis, physico-chemical properties and penetration activity of alkyl-6-(2, 5-dioxopyrrolidin-1-yl)-2-(2-oxopyrrolidin-1-yl)hexanoates as potential transdermal penetration enhancers Katerina Brychtova, Josef Jampilek, Radka Opatrilova, Ivan Raich, Oldrich Farsa, Jozef Csollei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . clavaminol I C16H31NO3 ÏàËÆ¶È:61.1% Tetrahedron 2009 65 4384-4388 Clavaminols G¨CN, six new marine sphingoids from the Mediterranean ascidian Clavelina phlegraea Anna Aiello, Ernesto Fattorusso, Antonella Giordano, Marialuisa Menna, Carmen Navarrete, Eduardo Muñoz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . diacetyl xestoaminol C ÏàËÆ¶È:61.1% Tetrahedron 2001 57 4579-4588 Obscuraminols, new unsaturated amino alcohols from the tunicate Pseudodistoma obscurum: structure and absolute configuration Leda Garrido, Eva Zubı́a, Marı́a J Ortega, Santiago Naranjo, Javier Salv¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (S)-3-(cyclopentanecarbonyl)-4-[(R,E)-1-hydroxynon-2-enyl]oxazolidin-2-one C18H29NO4 ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 2011 19 6174-6181 3,4-Disubstituted oxazolidin-2-ones as constrained ceramide analogs with anticancer activities Alok Singh, Hyun-Joon Ha, Jungchan Park, Jun Hee Kim, Won Koo Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . compound 1b C18H31NO3S ÏàËÆ¶È:61.1% European Journal of Organic Chemistry 2011 2719-2729 Total Synthesis of the (+)-Antimycin A Family Makoto Inai, Takeshi Nishii, Ayako Tanaka, Hiroto Kaku, Mitsuyo Horikawa and Tetsuto Tsunoda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Amyl palmitate ÏàËÆ¶È:61.1% Natural Product Communications 2007 2 775-778 A Cytotoxic and Hepatoprotective Agent from Withaniasomnifera and Biological evaluation of its Ester Derivatives Mohit Saxena, Uzma faridi, S.K. Srivastava, M. P. Darokar, Rupal Mishra,Anirban Pal, Brijesh Shisodia and S. P. S. Khanuja Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . cis-(9S,10S,12R)-12-acetoxy-9,10-methyleneoctadecanoate ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2001 37 608-611 Catalytic Cyclopropanation of Ricinolic Acid Derivatives with Diazomethane A. M. Davletbakova, I. O. Maidanova, N. Z. Baibulatova, V. A. Dokichev and Yu. V. Tomilov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . cinatrin C2 dimethyl ester ÏàËÆ¶È:60% The Journal of Antibiotics 1992 45 38-49 CINATRINS, A NOVEL FAMILY OF PHOSPHOLIPASE A2 INHIBITORS I. TAXONOMY AND FERMENTATION OF THE PRODUCING CULTURE; ISOLATION AND STRUCTURES OF CINATRINS HIROSHI ITAZAKI, KAZUO NAGASHIMA, YOSHIMI KAWAMURA, KOICHI MATSUMOTO, HIROSHI NAKAI, YOSHIHIRO TERUI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 7b ÏàËÆ¶È:57.8% Journal of Natural Products 1989 Vol 52 153 Novel Acetylenic Acids from the Root Bark of Paramacrolobium caeruleum: Inhibitors of 3-Hydroxy-3-methyl-glutaryl Coenzyme A Reductase Ashok D. Patil, James A. Chan, Pearl Lois-Flamberg, Ruth J. Mayer, John W. Westley Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . Compound 2i ÏàËÆ¶È:57.8% Magnetic Resonance in Chemistry 2000 38 696-700 NMR spectral data for ester prodrugs of ganciclovir Hongwu Gao and Ashim K. Mitra Structure 13C NMR ̼Æ×Ä£Äâͼ »¯ºÏÎï2£º 1 . sulochrin C17H16O7 ÏàËÆ¶È:93.7% Journal of Natural Products 2002 65 7-10 New Chlorinated Diphenyl Ethers from an Aspergillus Species Jaih Hargreaves, Ja-on Park, Emilio L. Ghisalberti, Krishnapillai Sivasithamparam, Brian W. Skelton, and Allan H. White Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Sulochrin C17H16O7 ÏàËÆ¶È:87.5% Bioscience, Biotechnology, and Biochemistry 2003 67 442-444 Hydroxysulochrin, a Tea Pollen Growth Inhibitor from the Fungus Aureobasidium sp. Atsumi SHIMADA, Chisako SHIOKAWA, Miyako KUSANO, Shozo FUJIOKA and Yasuo KIMURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . sulochrin C17H16O7 ÏàËÆ¶È:87.5% The Journal of Antibiotics 2002 55 552-556 Fungal Metabolites, Asterric Acid Derivatives Inhibit Vascular Endothelial Growth Factor (VEGF)-induced Tube Formation of HUVECs HEE JUNG LEE,JEONG HYEONG LEE,BANG YEON HWANG,HANG SUB KIM and JUNG JOON LEE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . sulochrin ÏàËÆ¶È:87.5% The Journal of Antibiotics 1997 50 972-974 Sulochrin Inhibits Eosinophil Degranulation HIROSHI OHASHI, MASAHARU ISHIKAWA, JUNKO ITO, AKIHIRO UENO, GERALD J. GLEICH, HIROHITO KITA, HIROYUKI KAWAI, HIROMI FUKAMACHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . methyl 2-(2-formyl-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxybenzoate C17H16O7 ÏàËÆ¶È:82.3% Natural Product Research 2012 26 1224-1228 A new diphenyl ether from Phoma sp. strain, SHZK-2 M.J. Fang, H. Fang, W.J. Li, D.M. Huang, Z. Wu & Y.F. Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Hydroxysulochrin C17H16O8 ÏàËÆ¶È:68.7% Bioscience, Biotechnology, and Biochemistry 2003 67 442-444 Hydroxysulochrin, a Tea Pollen Growth Inhibitor from the Fungus Aureobasidium sp. Atsumi SHIMADA, Chisako SHIOKAWA, Miyako KUSANO, Shozo FUJIOKA and Yasuo KIMURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Sulochrin C17H16O7 ÏàËÆ¶È:62.5% Russian Chemical Bulletin 2011 60 760-763 4-Methoxy-3-methylgoniothalamin from marine-derived fungi of the genus Penicillium O. F. Smetanina, A. N. Yurchenko, A. I. Kalinovsky, M. A. Pushilin and N. N. Slinkina, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 1,2-seco-trypacidin ÏàËÆ¶È:61.1% Chinese Journal of Natural Medicines 2005 3 269-271 Secondary Metabolites of Aspergillus fumigatus var. fumigatus LU Chun-Hua; HUANG Yao-Jian; SHEN Yue-Mao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . monomethylsulochrin ÏàËÆ¶È:61.1% The Journal of Antibiotics 2006 59 362-365 A New Diphenyl Ether from Marine-derived Fungus Aspergillus sp. B-F-2 FREE Rui Liu, Weiming Zhu, Yapeng Zhang, Tianjiao Zhu, Hongbing Liu, Yuchun Fang and Qianqun Gu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . lespedezol A1 ÏàËÆ¶È:56.2% Phytochemistry 1999 52 303-310 Antioxidants from Lespedeza homoloba. (I) Toshio Miyase, Mitsuaki Sano, Haruko Nakai, Miyuki Muraoka, Miho Nakazawa, Masazumi Suzuki, Kyouji Yoshino, Yuichiro Nishihara, Junichi Tanai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 4 ÏàËÆ¶È:56.2% Tetrahedron Letters 2000 41 465-469 Studies toward the total synthesis of Sch 202596, an antagonist of the galanin receptor subtype GalR1: synthesis of geodin, the spirocoumaranone subunit of Sch 202596 Tadashi Katoh, Osamu Ohmori Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3-(2-benzyloxy-6-hydroxyphenyl)-1,5-dimethylpyrazole C18H18N2O2 ÏàËÆ¶È:56.2% Journal of Heterocyclic Chemistry 2000 37 1629-1634 Synthesis of 3-(2-benzyloxy-6-hydroxyphenyl)-1-methylpyrazoles by the reaction of chromones with methylhydrazine Diana C. G. A. Pinto, Artur M. S. Silva and Jos¨¦ A. S. Cavaleiro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 2-amino-5-[4-(2,4-dihydroxyphenyl)-5-(4-methoxyphenyl)-pyrimidin-2-ylamino]pentanoic acid C22H24N4O5 ÏàËÆ¶È:56.2% Journal of Heterocyclic Chemistry 2010 47 1209-1214 One-step synthesis of 2-amino-5-(4,5-diphenylpyrimidin-2-ylamino)pentanoic acid from isoflavones and arginine Zun-Ting Zhang, Wen-Yong Han and Li Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 5,4'-¶þôÇ»ù-7,8-¶þ¼×Ñõ»ù»ÆÍª ÏàËÆ¶È:56.2% Chinese Traditional and Herbal Drugs 2008 39 1463-1465 Ë®ÝÅÆÑµÄ»¯Ñ§³É·ÖÑо¿ Ф²ýÇ®;ÎÌÁÖ¼Ñ;ÕÅÏàÒË;ÕÔϼ;Öܳ¤Ð Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . Isosulochrin C17H16O7 ÏàËÆ¶È:56.2% Journal of the Brazilian Chemical Society 2011 22 993-996 Novel Anthraquinone Derivatives Produced by Pestalotiopsis guepinii, an Endophytic of the Medicinal Plant Virola michelii (Myristicaceae) Marilene N. Oliveira, Lourivaldo S. Santos, Giselle M. S. P. Guilhon, Alberdan S. Santos, Isabel C. S. Ferreira, Manoel L. Lopes-Junior, Mara Silvia P. Arruda, Andrey M. R. Marinho, Milton N. da Silva, Edson Rodrigues-Filho and Maria C. F. Oliveira Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . Chloroisosulochrin C17H15O6Cl ÏàËÆ¶È:56.2% Journal of the Brazilian Chemical Society 2011 22 993-996 Novel Anthraquinone Derivatives Produced by Pestalotiopsis guepinii, an Endophytic of the Medicinal Plant Virola michelii (Myristicaceae) Marilene N. Oliveira, Lourivaldo S. Santos, Giselle M. S. P. Guilhon, Alberdan S. Santos, Isabel C. S. Ferreira, Manoel L. Lopes-Junior, Mara Silvia P. Arruda, Andrey M. R. Marinho, Milton N. da Silva, Edson Rodrigues-Filho and Maria C. F. Oliveira Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . pestalotether D C18H18O8 ÏàËÆ¶È:55.5% Tetrahedron 2012 68 2299-2305 Chlorinated chromone and diphenyl ether derivatives from the mangrove-derived fungus Pestalotiopsis sp. PSU-MA69 Saranyoo Klaiklay, Vatcharin Rukachaisirikul, Kwanruthai Tadpetch, Yaowapa Sukpondma, Souwalak Phongpaichit, Jirayu Buatong, Jariya Sakayaroj Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . gliricidol C17H14O6 ÏàËÆ¶È:52.9% Journal of Natural Products 1999 62 188-190 New 12a-Hydroxyrotenoids from Gliricidia sepium Bark Luca Rastrelli, Ingeborg Berger, Wolfang Kubelka, Armando Caceres, Nunziatina De Tommasi, and Francesco De Simone Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . krametosan C17H14O5 ÏàËÆ¶È:52.9% Natural Product Research 2001 15 323-329 Kramentosan, a New Trinorlignan from the Roots of Krameria tomentosa Samia A. S. Silva; Janiza C. M. De Castro; Terezinha G. Da Silva; Emidio V. L. Da-cunha; Jos¨¦ Maria Barbosa-Filho; Marcelo S. Da Silva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . methyl 2-hydroxy-4-(2-hydroy-3-methoxy-5-methylphenoxy)-6-methylbenzoat C17H18O6 ÏàËÆ¶È:52.9% The Journal of Antibiotics 2011 64 465-467 Diphenyl etheric metabolites from Streptomyces sp. neau50 Dian-Liang Gong, Xiang-Jing Wang, Zhi-Dan Xiang, Ji-Dong Wang, Hui Zhang, Chong-Xi Liu, Ji Zhang and Wen-Sheng Xiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 2,8-dimethoxy-6-methyl-9-oxo-9Hxanthene-1-carboxylic acid methyl ester C18H16O6 ÏàËÆ¶È:50% Phytochemistry 2004 65 2373-2378 Xanthones from a microfungus of the genus Xylaria Peter C. Healy, Ailsa Hocking, Nai Tran-Dinh, John I. Pitt, Roger G. Shivas,Jennifer K. Mitchell, Mike Kotiw, Rohan A. Davis Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 2-methoxygliricidol C18H16O7 ÏàËÆ¶È:50% Journal of Natural Products 1999 62 188-190 New 12a-Hydroxyrotenoids from Gliricidia sepium Bark Luca Rastrelli, Ingeborg Berger, Wolfang Kubelka, Armando Caceres, Nunziatina De Tommasi, and Francesco De Simone Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . cercophorin A C20H16O9 ÏàËÆ¶È:50% Journal of Natural Products 1996 59 765-769 Cercophorins A-C: Novel Antifungal and Cytotoxic Metabolites from the Coprophilous Fungus Cercophora areolata Authrine C. Whyte and James B. Gloer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 4,9-dimethoxyphenanthrene-2,5-diol C16H14O4 ÏàËÆ¶È:50% Chemistry of Natural Compounds 2009 45 414-416 CHEMICAL CONSTITUENTS OF Dendrobium chrysotoxum Yu-Peng Li, Chen Qing, Tian-Tian Fang,Ying Liu,1 and Ye-Gao Chen1 Structure 13C NMR ̼Æ×Ä£Äâͼ |

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