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M201175065金虫 (正式写手)
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[求助]
维谱求助 已有1人参与
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| 13C-NMR(101MHz,MeOD)δ:10.21,19.96,47.44,54.80,79.46,100.75,102.51,105.75,107.76,143.49,156.55,160.57,161.26,165.01,202.07 |
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笑多会怀孕
铁杆木虫 (著名写手)
- 应助: 1216 (讲师)
- 金币: 9782.3
- 散金: 610
- 红花: 40
- 沙发: 3
- 帖子: 2721
- 在线: 1284.6小时
- 虫号: 2010893
- 注册: 2012-09-18
- 性别: GG
- 专业: 天然有机化学
【答案】应助回帖
★ ★ ★ ★ ★ ★ ★ ★ ★ ★
感谢参与,应助指数 +1
M201175065: 金币+10, ★★★很有帮助 2013-12-20 16:13:01
感谢参与,应助指数 +1
M201175065: 金币+10, ★★★很有帮助 2013-12-20 16:13:01
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查询结果:共查到19个化合物(查询结果仅供参考) 1 . ustilaginoidin D C30H26O10 相似度:60% Chemical & Pharmaceutical Bulletin 1988 36 146-152 Further Characterization of Seven Bis(naphtho-γ-pyrone) Congeners of Ustilaginoidins, Coloring Matters of Claviceps virens (Ustilaginoidea virens) KIYOTAKA KOYAMA and SHINSAKU NATORI Structure 13C NMR 碳谱模拟图 2 . fonsecin C16H14O6 相似度:60% Organic and Medicinal Chemistry Letters 2012 2 1-4 Seven naphtho-γ-pyrones from the marinederived fungus Alternaria alternata: structure elucidation and biological properties Mohamed Shaaban, Khaled A Shaaban and Mohamed S Abdel-Aziz Structure 13C NMR 碳谱模拟图 3 . (2S, 3R)-5-hydroxy-6,8-dimethoxy-2,3-dimethyl-2,3-dihydro-4H-naphtho[2,3-b]-pyran-4-one C17H18O5 相似度:58.8% Phytochemistry 2001 58 751-758 Phytotoxic naphthopyranone derivatives from the coprophilous fungus Guanomyces polythrix Martha Macías, Alicia Gamboa, Miguel Ulloa, Rubén A. Toscano, Rachel Mata Structure 13C NMR 碳谱模拟图 4 . (2S,3S)-5-hydroxy-6,8-dimethoxy-2,3-dimethyl-4H-2,3-dihydronaphtho[2,3-b]-pyran-4-one C17H18O5 相似度:58.8% Journal of Natural Products 2000 63 757-761 Phytotoxic Compounds from the New Coprophilous Fungus Guanomyces polythrix1 Martha Macías, Miguel Ulloa, Alicia Gamboa, and Rachel Mata Structure 13C NMR 碳谱模拟图 5 . chaetochromin A 相似度:53.3% Chemical & Pharmaceutical Bulletin 1988 36 146-152 Further Characterization of Seven Bis(naphtho-γ-pyrone) Congeners of Ustilaginoidins, Coloring Matters of Claviceps virens (Ustilaginoidea virens) KIYOTAKA KOYAMA and SHINSAKU NATORI Structure 13C NMR 碳谱模拟图 6 . ustilaginoidin F C28H22O10 相似度:53.3% Chemical & Pharmaceutical Bulletin 1988 36 146-152 Further Characterization of Seven Bis(naphtho-γ-pyrone) Congeners of Ustilaginoidins, Coloring Matters of Claviceps virens (Ustilaginoidea virens) KIYOTAKA KOYAMA and SHINSAKU NATORI Structure 13C NMR 碳谱模拟图 7 . cephalochromin 相似度:53.3% Chemical & Pharmaceutical Bulletin 1988 36 146-152 Further Characterization of Seven Bis(naphtho-γ-pyrone) Congeners of Ustilaginoidins, Coloring Matters of Claviceps virens (Ustilaginoidea virens) KIYOTAKA KOYAMA and SHINSAKU NATORI Structure 13C NMR 碳谱模拟图 8 . chaetochromin A C30H26O16 相似度:53.3% Chemical & Pharmaceutical Bulletin 1987 35 578-584 Chaetochromins B, C and D, Bis (naphtho-γ-pyrone) Derivatives from Chaetomium gracile KIYOTAKA KOYAMA and SHINSAKU NATORI Structure 13C NMR 碳谱模拟图 9 . 4' 5-dihydroxy,-7-methoxy-6-methylflavanone C17H16O5 相似度:53.3% Phytochemistry 1998 47 845-850 Terpenoids and flavonoids from Pseudotsuga wilsoniana Yaw-Lung Hsieh, Jim-Min Fang, Yu-Shia Cheng Structure 13C NMR 碳谱模拟图 10 . 1-(3-methoxyphenoxy)propan-2-amine 相似度:53.3% Bioorganic & Medicinal Chemistry 2010 18 6496-6511 Design, synthesis, and pharmacological effects of structurally simple ligands for MT1 and MT2 melatonin receptors Alessia Carocci, Alessia Catalano, Angelo Lovece, Giovanni Lentini, Andrea Duranti, Valeria Lucini, Marilou Pannacci, Francesco Scaglione, Carlo Franchini Structure 13C NMR 碳谱模拟图 11 . (-)-(R)-1-(3-methoxyphenoxy)propan-2-amine 相似度:53.3% Bioorganic & Medicinal Chemistry 2010 18 6496-6511 Design, synthesis, and pharmacological effects of structurally simple ligands for MT1 and MT2 melatonin receptors Alessia Carocci, Alessia Catalano, Angelo Lovece, Giovanni Lentini, Andrea Duranti, Valeria Lucini, Marilou Pannacci, Francesco Scaglione, Carlo Franchini Structure 13C NMR 碳谱模拟图 12 . cephalochromin 相似度:53.3% European Journal of Organic Chemistry 2009 2009 1427-1434 Pseudoanguillosporin A and B: Two New Isochromans Isolated from the Endophytic Fungus Pseudoanguillospora sp. Ines Kock, Siegfried Draeger, Barbara Schulz, Brigitta Elsässer, Tibor Kurtán, ágnes Kenéz, Sándor Antus, Gennaro Pescitelli, Piero Salvadori, John-Bryan Speakman, Joachim Rheinheimer and Karsten Krohn Structure 13C NMR 碳谱模拟图 13 . N-(Benzo[d][1,3]dioxol-5-yl)-3-(2,6-dimethoxyphenyl)-3-oxopropanamide C18H17NO6 相似度:53.3% Bioorganic & Medicinal Chemistry 2013 21 5064-5075 Design and synthesis of 6,7-methylenedioxy-4-substituted phenylquinolin-2(1H)-one derivatives as novel anticancer agents that induce apoptosis with cell cycle arrest at G2/M phase Yi-Fong Chen, Yi-Chien Lin, Po-Kai Huang, Hsu-Chin Chan, Sheng-Chu Kuo, Kuo-Hsiung Lee, Li-Jiau Huang Structure 13C NMR 碳谱模拟图 14 . 10,10'-bifonsecin B 相似度:50% Chemistry & Biodiversity 2008 Vol. 5 93-100 Isolation, Structure Elucidation, and Antimycobacterial Properties of Dimeric Naphtho-g-pyrones from the Marine-Derived Fungus Aspergillus carbonarius YapengZhang, Sun Ling, YuchunFang, Tianjiao Zhu, Qianqun Gu and Wei-Ming Zhu Structure 13C NMR 碳谱模拟图 15 . (2S)-5-hydroxy-6,8-dimethoxy-2-methyl-4H-2,3-dihydronaphtho[2,3-b]-pyran-4-one C16H16O5 相似度:50% Journal of Natural Products 2000 63 757-761 Phytotoxic Compounds from the New Coprophilous Fungus Guanomyces polythrix1 Martha Macías, Miguel Ulloa, Alicia Gamboa, and Rachel Mata Structure 13C NMR 碳谱模拟图 16 . sophoracarpan B C17H14O6 相似度:50% Chemical & Pharmaceutical Bulletin 1990 38 2756-2759 Chemical Studies on Sophora tomentosa : the Isolation of a New Class of Isoflavonoid Takeshi KINOSHITA,Koji ICHINOSE,Chiho TAKAHASHI,Feng-Chi HO,Jin-Bin WU and Ushio SANKAWA Structure 13C NMR 碳谱模拟图 17 . sophoracarpan B 相似度:50% Chemical & Pharmaceutical Bulletin 1986 34 3067-3070 THE ISOLATION OF A NEW CLASS OF ISOFLAVONOID METABOLITES FROM SOPHORA TOMENTOSA L. Takeshi Kinoshita,Koji Ichinose,Chiho Takahashi and Ushio Sankawa Structure 13C NMR 碳谱模拟图 18 . Agrimonolide 相似度:50% Phytochemistry 2010 71 1925-1929 Phenolic glycosides from Agrimonia pilosa Hiroyoshi Kato, Wei Li, Michihiko Koike, Yinghua Wang, Kazuo Koike Structure 13C NMR 碳谱模拟图 19 . TMC-256A2 C16H14O5 相似度:50% The Journal of Antibiotics 2002 55 685-692 |
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