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菲你莫属铁杆木虫 (正式写手)
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[求助]
求助微谱查询
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溶剂氘代氯仿，碳谱数据如下： 174.3, 170.2, 148.0, 138.8, 138.2, 137.5, 129.1, 129.1, 127.2, 127.2, 114.2, 74.4, 69.9, 53.9, 53.8, 51.9, 47.3, 45.7, 42.9, 33.0, 31.3, 28.6, 26.6, 21.0, 14.2 非常感谢  |
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wm0629
铁杆木虫 (著名写手)
- 应助: 341 (大学生)
- 金币: 6381.8
- 红花: 3
- 帖子: 1962
- 在线: 77.9小时
- 虫号: 2217415
- 注册: 2013-01-01
- 性别: GG
- 专业: 中药炮制
【答案】应助回帖
★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★ ★
感谢参与，应助指数 +1
菲你莫属: 金币+20, ★★★★★最佳答案, 谢谢~~ 2013-05-06 12:45:57
感谢参与，应助指数 +1
菲你莫属: 金币+20, ★★★★★最佳答案, 谢谢~~ 2013-05-06 12:45:57
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1 . cytochalasin H 相似度:82.1% The Journal of Antibiotics 1992 45 679-685 L-696, 474, A NOVEL CYTOCHALASIN AS AN INHIBITOR OF HIV-1 PROTEASE II. ISOLATION AND STRUCTURE J. ONDEYKA, O. D. HENSENS, D. ZINK, R. BALL, R. B. LINGHAM, G. BILLS, A. DOMBROWSKI, M. GOETZ Structure 13C NMR 碳谱模拟图 2 . compound 6 相似度:67.8% Journal of Natural Products 1993 Vol 56 755 Microbial Transformation of L-696, 474, a Novel Cytochalasin as an Inhibitor of HIV-1 Protease Tom S. Chen, George A. Doss, Annjia Hsu, Amy Hsu, Russell B. Lingham, Raymond F. White, Richard L. Monaghan Structure 13C NMR 碳谱模拟图 3 . 细胞松弛素 O 相似度:67.8% Chinese Traditional and Herbal Drugs 2006 37 343-345 黄花夹竹桃内生真菌产细胞松弛素的研究 彭小伟;杨丽源;李绍兰;周斌;李治滢;陈有为 Structure 13C NMR 碳谱模拟图 4 . 19,20-epoxycytochalasin D 相似度:64.2% Helvetica Chimica Acta 2002 Vol. 85 1439 Neoengleromycin, a Novel Compound from Engleromyces goetzii Liu Jikai, Tan Jianwen, Dong Zejun, Ding Zhihui, Wang Xianghua, and Liu Peigui Structure 13C NMR 碳谱模拟图 5 . (11)-cytochalasa-6(12),13,19-triene-1,21-dione-16,18-dimethyl-7-hydroxy-10-phenyl-(7S*,13E,16S*,18R*,19E) C28H35NO3 相似度:61.5% Phytochemistry 1996 41 821-828 Cytochalasins from a Daldinia sp. of fungus Malcolm S. Buchanan, Toshihiro Hashimoto, Yoshinori Asakawa Structure 13C NMR 碳谱模拟图 6 . 17-O-acetyl-Nb-demethylechitamine C23H28N2O5 相似度:60.8% Phytochemistry 1994 37 1745-1749 Indole alkaloids fromAlstonia glaucescens Niwat Keawpradub, Hiromitsu Takayama, Norio Aimi, Shin-Ichiro Sakai Structure 13C NMR 碳谱模拟图 7 . RKS-1778 C30H39NO4 相似度:60.7% Journal of Natural Products 1997 60 669-672 RKS-1778, a New Mammalian Cell-Cycle Inhibitor and a Key Intermediate of the [11]Cytochalasin Group Hideaki Kakeya, Masayuki Morishita, Chizuko Onozawa, Ron Usami, Koki Horikoshi, Ken-ichi Kimura, Makoto Yoshihama, and Hiroyuki Osada Structure 13C NMR 碳谱模拟图 8 . compound 1 相似度:60.7% Journal of Natural Products 1993 Vol 56 755 Microbial Transformation of L-696, 474, a Novel Cytochalasin as an Inhibitor of HIV-1 Protease Tom S. Chen, George A. Doss, Annjia Hsu, Amy Hsu, Russell B. Lingham, Raymond F. White, Richard L. Monaghan Structure 13C NMR 碳谱模拟图 9 . compound 2 相似度:60.7% Journal of Natural Products 1993 Vol 56 755 Microbial Transformation of L-696, 474, a Novel Cytochalasin as an Inhibitor of HIV-1 Protease Tom S. Chen, George A. Doss, Annjia Hsu, Amy Hsu, Russell B. Lingham, Raymond F. White, Richard L. Monaghan Structure 13C NMR 碳谱模拟图 10 . L-696,474 C30H39NO4 相似度:60.7% The Journal of Antibiotics 1992 45 679-685 L-696, 474, A NOVEL CYTOCHALASIN AS AN INHIBITOR OF HIV-1 PROTEASE II. ISOLATION AND STRUCTURE J. ONDEYKA, O. D. HENSENS, D. ZINK, R. BALL, R. B. LINGHAM, G. BILLS, A. DOMBROWSKI, M. GOETZ Structure 13C NMR 碳谱模拟图 11 . 16β-Acetoxymethyl-3-benzyloxy-17-methyl-18-nor-estra-1,3,5(10),13(17)-tetraene C28H32O3 相似度:60% Steroids 2006 71 141-153 Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols Ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, Árpád Márki, George Falkay, Gyula Schneider Structure 13C NMR 碳谱模拟图 12 . 3-benzyloxy-16β-iodomethyl-13α-estra-1,3,5(10)-trien-17α-ol C26H31IO2 相似度:58.3% Steroids 2003 68 277-288 Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers János Wölfling, Erzsébet Mernyák, Éva Frank, George Falkay, Árpád Márki, Renáta Minorics, Gyula Schneider Structure 13C NMR 碳谱模拟图 13 . 3-Benzyloxy-16α-bromomethylestra-1,3,5(10)-trien-17α-yl acetate C28H33O3Br 相似度:57.6% Steroids 2006 71 141-153 Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols Ágota Szájli, János Wölfling, Erzsébet Mernyák, Renáta Minorics, Árpád Márki, George Falkay, Gyula Schneider Structure 13C NMR 碳谱模拟图 14 . [11]-cytochalasa-6(12),13,19-triene-1,21-dione-7,18-dihydroxy-16,18-dimethyl-10-phenyl-(7S*,13E,16S*,18S*,19E) C28H35O4N 相似度:57.6% Phytochemistry 1995 40 135-140 Five 10-phenyl-[11]-cytochalasans from a Daldinia fungal species Malcolm Buchanan, Toshihiro Hashimoto, Yoshinori Asakawa Structure 13C NMR 碳谱模拟图 15 . cytochalasin D 相似度:57.1% Helvetica Chimica Acta 2002 Vol. 85 1439 Neoengleromycin, a Novel Compound from Engleromyces goetzii Liu Jikai, Tan Jianwen, Dong Zejun, Ding Zhihui, Wang Xianghua, and Liu Peigui Structure 13C NMR 碳谱模拟图 16 . cytochalasin D C30H37NO6 相似度:57.1% Journal of Asian Natural Products Research 2001 3 151-155 Cytochalasin D from Hypocrella Bambusae HONG XU, WEI-SHUO FANG, XIAO-GUANG CHEN,WEN-YI HE and KE-DI CHENG Structure 13C NMR 碳谱模拟图 17 . Cytochalasin D 相似度:57.1% Chinese Journal of Marine Drugs 2011 30(1) 15-17 Chemical constituents of mangrove plant Bruguiera gymnorrhiza CAI You-sheng, LIU Hai-li, GONG Jing-xu, GUO Yue-wei Structure 13C NMR 碳谱模拟图 18 . 19,20-epoxycytochalasin D 相似度:57.1% Tetrahedron 1997 53 6485-6492 New cytochalasins from the fungus Xylaria hypoxylon A. Espada, A. Rivera-Sagredo, J.M. de la Fuente, J.A. Hueso-Rodríguez, S.W. Elson Structure 13C NMR 碳谱模拟图 19 . Cytochalasin D 相似度:57.1% Archives of Pharmacal Research 2012 35 1127-1131 Metabolites from the mangrove-derived fungus Xylaria cubensis PSU-MA34 Saranyoo Klaiklay, Vatcharin Rukachaisirikul, Yaowapa Sukpondma, Souwalak Phongpaichit and Jirayu Buatong, et al. Structure 13C NMR 碳谱模拟图 20 . (1(10)E,4Z)-8β-(angeloylxy)-9α-ethoxy-6α,15-dihydroxy-13-methoxy-14-oxogermacra-1(10),4-dien-12-oic acid 12,6-lactone C23H32O8 相似度:56.5% Helvetica Chimica Acta 2005 Vol. 88 160 Novel Sesquiterpenoids from Siegesbeckia orientalis Ying Xiang, Cheng-Qi Fan, Jian-Min Yue Structure 13C NMR 碳谱模拟图 21 . phanginin F C21H26O5 相似度:56.5% Phytochemistry 2008 69 1242-1249 Phanginin A–K, diterpenoids from the seeds of Caesalpinia sappan Linn. Orapun Yodsaoue,Sarot Cheenpracha, Chatchanok Karalai, Chanita Ponglimanont,Suchada Chantrapromma, Hoong-Kun Fun,Akkharawit Kanjana-Opas Structure 13C NMR 碳谱模拟图 22 . 3-Benzyloxyestra-1,3,5(10)-trien-17-one C25H28O2 相似度:56.5% Steroids 2002 67 371-377 Synthesis and receptor-binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers Pál Tapolcsányi, János Wölfling, George Falkay, Árpád Márki, Renáta Minorics, Gyula Schneider Structure 13C NMR 碳谱模拟图 23 . 3-Benzyloxyestra-1,3,5(10)-trien-17-one C25H28O2 相似度:56.5% Steroids 2002 67 671-678 Synthesis and receptor-binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers Pál Tapolcsányi, János Wölfling, George Falkay, Árpád Márki, Renáta Minorics, Gyula Schneider Structure 13C NMR 碳谱模拟图 24 . 3-benzyloxy-1,3,5(10)-estratrien-17-one C25H28O2 相似度:56.5% Steroids 2006 71 911-921 Synthesis of unique 17β-estradiol homo-dimers, estrogen receptors binding affinity evaluation and cytocidal activity on breast, intestinal and skin cancer cell lines Gervais Bérubé, Daniel Rabouin, Valérie Perron, Blaise N’Zemba, René-C. Gaudreault, Sophie Parent, Éric Asselin Structure 13C NMR 碳谱模拟图 25 . (±)-(8β,9α,14α)-11α-Carbomethoxy-17-(propen-2-yl)-gona-1,3,5(10),13(17)-tetraene C22H26O2 相似度:56.5% Steroids 2007 72 297-304 Conjugate hydrocyanation of 17-acetyl-11-carbomethoxygona-1,3,5(10),13(17)-tetraenes Hélène Pellissier, Pierre-Yves Michellys, Maurice Santelli Structure 13C NMR 碳谱模拟图 26 . (±)-threo-N-(p-Azido-benzyl)-4-(tri-n-butylstannyl)methylphenidate C33H50N4O2Sn 相似度:56.5% Bioorganic & Medicinal Chemistry 2011 19 504-512 Azido-iodo-N-benzyl derivatives of threo-methylphenidate (Ritalin,Concerta): Rational design, synthesis, pharmacological evaluation,and dopamine transporter photoaffinity labeling David J. Lapinsky, Ranganadh Velagaleti, Nageswari Yarravarapu, Yi Liu, Yurong Huang,Christopher K. Surratt, John R. Lever, James D. Foster, Rejwi Acharya, Roxanne A. Vaughan,Howard M. Deutsch Structure 13C NMR 碳谱模拟图 |
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