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1 . N-[2-[3'-[2-(p-coumaramido)ethyl]-5,5'-dihydroxy-4,4'-bi-1H-indol-3-yl]ethyl]ferulamide
C39H36N4O7 ÏàËÆ¶È:65.5%
Chemical & Pharmaceutical Bulletin 1997 45 1910-1914
Antioxidative Compounds Isolated from Safflower (Carthamus tinctorius L.) Oil Cake
Hui Li ZHANG,Akito NAGATSU,Toshihiro WATANABE,SAKAKIBARA and Harumi OKUYAMA
Structure 13C NMR ̼Æ×Ä£Äâͼ
2 . N-Isoferuloyl serotonin-3'-O-¦Â-D-glucopyranoside
ÏàËÆ¶È:65.5%
Natural Product Research 2013 27 592-596
Biotransformation of serotonin derivatives by the larvae of common cutworm (Spodoptera litura)
Toshiyuki Takahashi & Mitsuo Miyazawa
Structure 13C NMR ̼Æ×Ä£Äâͼ
3 . 4-[N-(p-coumaroyl)serotonin-4''-yl]-N-feruloylserotonin
C39H36N4O7 ÏàËÆ¶È:62.0%
Chemical & Pharmaceutical Bulletin 1996 44 874-876
NOVEL ANTIOXIDANTS FROM SAFFLOWER (CARTHAMUS TINCTORIUS L.) OIL CAKE
Hui Li ZHANG,Akito NAGATSU and Jinsaku SAKAKIBARA
Structure 13C NMR ̼Æ×Ä£Äâͼ
4 . 9-O-[3-(ferulic acid)propyl] berberine bromide
C32H28NO8Br ÏàËÆ¶È:59.3%
Bioorganic & Medicinal Chemistry 2011 19 7228-7235
Benzenediol-berberine hybrids: Multifunctional agents for Alzheimer¡¯s disease
Huailei Jiang, Xu Wang, Ling Huang, Zonghua Luo, Tao Su, Ke Ding, Xingshu Li
Structure 13C NMR ̼Æ×Ä£Äâͼ
5 . (E)-N-benzyl-3-(3,4-dimethoxyphenyl)-2-(3,4-dimethoxyphenylacetylamino)-2-propenamide
C28H30N2O6 ÏàËÆ¶È:58.6%
Heterocycles 2006 68 993-1006
A Convenient Synthesis of Papaverine Analogs via Photocyclization of N-Acyl-¦Á-dehydroarylalaninamide Derivatives
Hideki Hoshina, Kei Maekawa, Kaori Kobayashi, Tetsutaro Igarashi, and Tadamitsu Sakurai*
Structure 13C NMR ̼Æ×Ä£Äâͼ
6 . 9-O-[3-(phenylol-2-yloxy) propyl] berberine bromide
C28H24NO6Br ÏàËÆ¶È:58.6%
Bioorganic & Medicinal Chemistry 2011 19 7228-7235
Benzenediol-berberine hybrids: Multifunctional agents for Alzheimer¡¯s disease
Huailei Jiang, Xu Wang, Ling Huang, Zonghua Luo, Tao Su, Ke Ding, Xingshu Li
Structure 13C NMR ̼Æ×Ä£Äâͼ
7 . (E)-N-(3,4-dimethoxybenzylidene)-2-(3,4-dimethoxyphenyl)-1H-benzo[d]imidazo[1,2-a]imidazol-3-amine
C26H24N4O4 ÏàËÆ¶È:58.6%
Tetrahedron 2013 69 2954-2960
Thiamine hydrochloride (VB1)-catalyzed one-pot synthesis of (E)-N-benzylidene-2-phenyl-1H-benzo[d]imidazo[1,2-a]imidazol-3-amine derivatives
Fanglei Chen, Min Lei, Lihong Hu
Structure 13C NMR ̼Æ×Ä£Äâͼ
8 . N-Feruloyl serotonin-4'-O-¦Â-D-glucopyranoside
ÏàËÆ¶È:58.6%
Natural Product Research 2013 27 592-596
Biotransformation of serotonin derivatives by the larvae of common cutworm (Spodoptera litura)
Toshiyuki Takahashi & Mitsuo Miyazawa
Structure 13C NMR ̼Æ×Ä£Äâͼ
9 . picrasidine-H
C28H24N4O4 ÏàËÆ¶È:55.1%
Chemical & Pharmaceutical Bulletin 1986 34 2090-2093
Studies on the Alkaloids from Picrasma quassioides BENNET.VII. : Structures of ¦Â-Carboline Dimer Alkaloids, Picrasidines-H and -R
KAZUO KOIKE and TAICHI OHMOTO
Structure 13C NMR ̼Æ×Ä£Äâͼ
10 . quassidine C
C26H22N4O2 ÏàËÆ¶È:55.1%
Journal of Natural Products 2010 73 167-171
Quassidines A−D, Bis-¦Â-carboline Alkaloids from the Stems of Picrasma quassioides
Wei-Hua Jiao, Hao Gao, Chen-Yang Li, Feng Zhao, Ren-Wang Jiang, Ying Wang, Guang-Xiong Zhou and Xin-Sheng Yao
Structure 13C NMR ̼Æ×Ä£Äâͼ
11 . (Z)-N-benzyl-3-(3,4-dimethoxyphenyl)-2-(3,4-dimethoxyphenylacetylamino)-2-propenamide
C28H30N2O6 ÏàËÆ¶È:55.1%
Heterocycles 2006 68 993-1006
A Convenient Synthesis of Papaverine Analogs via Photocyclization of N-Acyl-¦Á-dehydroarylalaninamide Derivatives
Hideki Hoshina, Kei Maekawa, Kaori Kobayashi, Tetsutaro Igarashi, and Tadamitsu Sakurai*
Structure 13C NMR ̼Æ×Ä£Äâͼ
12 . Compound 9
ÏàËÆ¶È:55.1%
Magnetic Resonance in Chemistry 2005 43 1077-1079
1H and 13C chemical shifts for acridines: part XIX. N, N'-diacylproflavine derivatives
K. Shimi, G. Boyer, R. Faure and J.-P. Galy
Structure 13C NMR ̼Æ×Ä£Äâͼ
13 . 1-(1,3-benzodioxol-5-yl)-8-({[2-(4-methylpiperazin-1-yl)pyridin-3-yl]carbonyl}-amino)-4,5-dihydro-1H-benzo[g]-indazole-3-carboxamide
30H29N7O4 ÏàËÆ¶È:55.1%
Bioorganic & Medicinal Chemistry 2010 18 403-414
Aminopyridinecarboxamide-based inhibitors: Structure¨Cactivity relationship
Dominique F. Bonafoux, Sheri L. Bonar, Michael Clare, Ann M. Donnelly, Jeanette L. Glaenzer, Julia A. Guzova, He Huang, Nandidni N. Kishore, Francis J. Koszyk, Patrick J. Lennon, Adam Libby, Sumathy Mathialagan, David S. Oburn, Sharon A Rouw, Cynthia D. S
Structure 13C NMR ̼Æ×Ä£Äâͼ
14 . 6-[2-(3,4-dimethoxyphenyl)ethylamino]-11H-indolo[3,2-c]quinoline hydrochloride
C25H23N3O2 ÏàËÆ¶È:55.1%
Bioorganic & Medicinal Chemistry 2010 18 1948-1957
Synthesis and antiproliferative evaluation of certain indolo[3, 2-c]quinoline derivatives
Chih-Ming Lu, Yeh-Long Chen, Hui-Ling Chen, Chyi-An Chen, Pei-Jung Lu, Chia-Ning Yang, Cherng-Chyi Tzeng
Structure 13C NMR ̼Æ×Ä£Äâͼ
15 . Sodium 3-[2-(3,4-dimethoxyphenyl)ethyl]-3,4-dihydro-1-(3-hydroxy-4-methoxyphenyl)-8-methoxy-4-oxo-[1]benzopyrano[3,4-b]pyrrol-7-yl sulfate
C29H26N2O11S ÏàËÆ¶È:55.1%
Bioorganic & Medicinal Chemistry 2011 19 7541-7550
Synthesis, structure¨Cactivity relationships, and mechanism of action of anti-HIV-1 lamellarin ¦Á 20-sulfate analogues
Haruka Kamiyama, Yoshinao Kubo, Hironori Sato, Naoki Yamamoto, Tsutomu Fukuda, Fumito Ishibashi, Masatomo Iwao
Structure 13C NMR ̼Æ×Ä£Äâͼ
16 . tert-butyl-3-(2,2-di(ethoxycarbonyl)vinyl)-2-(3,4-dimethoxybenzyl)-1H-indole-1-carboxylate
C30H35NO8 ÏàËÆ¶È:55.1%
Indian Journal of Chemistry Section B 2011 50B 843-857
Studies on Lewis-acid mediated domino reaction of N-protected bromomethylindoles with arenes/heteroarenes
Dhayalan, Vasudevan; Sureshbabu, Radhakrishnan; Mohanakrishnan, Arasambattu K
Structure 13C NMR ̼Æ×Ä£Äâͼ
17 . 1-(3-methoxybenzyl)-6-(3-methoxybenzyloxy)-1,2-dihydro-2,2,4-trimethylquinoline
C28H31NO3 ÏàËÆ¶È:55.1%
Journal of Medicinal Chemistry 2010 53 966-982
Antitrypanosomal Activity of 1,2-Dihydroquinolin-6-ols and Their Ester Derivatives
Jean Fotie, Marcel Kaiser, Dawn A. Delf¨ªn, Joshua Manley, Carolyn S. Reid, Jean-Marc Paris, Tanja Wenzler, Louis Maes, Kiran V. Mahasenan, Chenglong Li and Karl A. Werbovetz
Structure 13C NMR ̼Æ×Ä£Äâͼ
18 . 1-cyclohexyl-2-furan-3-yl-1H-benzimidazole-5-carboxylic acid [(S)-1-(2-aminothiazol-4-yl)-2-(5-hydroxy-1H-indol-3-yl)ethyl]amide
C31H30N6O3S ÏàËÆ¶È:55.1%
Journal of Medicinal Chemistry 2004 47 6884-6892
Non-Nucleoside Benzimidazole-Based Allosteric Inhibitors of the Hepatitis C Virus NS5B Polymerase: Inhibition of Subgenomic Hepatitis C Virus RNA Replicons in Huh-7 Cells
Pierre L. Beaulieu, Yves Bousquet, Jean Gauthier, James Gillard, Martin Marquis, Ginette McKercher, Charles Pellerin, Serge Valois, and George Kukolj
Structure 13C NMR ̼Æ×Ä£Äâͼ
19 . N-(3-(5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl)phenyl)-2-(3,4-dimethoxyphenyl)acetamide
C24H20ClN3O4 ÏàËÆ¶È:55.1%
Heterocycles 2012 85 2693-2712
Design, Synthesis and Biological Activity Evaluation of 2,5-Diphenyl-1,3,4-oxadiazole Derivatives as Novel Inhibitors of Fructose-1,6-bisphosphatase
Hai-Bing He, Li-Xin Gao, Yue-Yang Zhou, Ting Liu, Jie Tang, Xue-Ping Gong, Wen-Wei Qiu, Jing-Ya Li,* Jia Li,* and Fan Yang
Structure 13C NMR ̼Æ×Ä£Äâͼ
20 . (E)-ethyl 3-(2-((2-aminophenyl)thio)-1-cyano-9,10-dimethoxy-4-oxo-6,7-dihydro-4H-pyrido[2,1-a]isoquinolin-3-yl)acrylate
C27H25N3O5S ÏàËÆ¶È:55.1%
Heterocycles 2012 85 2933-2947
Synthesis and Reactivity of 2-Chloro-3-formylpyrido[2,1-a]isoquinoline Derivative. A Novel Routes to Pyrazolo[3',4':4,5]pyrido[2,1-a]isoquinoline and Isoquinolino[2,1-g][1,6]naphthyridines
Hamdi M. Hassaneen,* Wagnat W. Wardkhan, and Yasmin Sh. Mohammed
Structure 13C NMR ̼Æ×Ä£Äâͼ
21 . (E)-N-(3-methoxybenzylidene)-2-(3-methoxyphenyl)-1H-benzo[d]imidazo[1,2-a]imidazol-3-amine
C24H20N4O2 ÏàËÆ¶È:55.1%
Tetrahedron 2013 69 2954-2960
Thiamine hydrochloride (VB1)-catalyzed one-pot synthesis of (E)-N-benzylidene-2-phenyl-1H-benzo[d]imidazo[1,2-a]imidazol-3-amine derivatives
Fanglei Chen, Min Lei, Lihong Hu
Structure 13C NMR ̼Æ×Ä£Äâͼ
22 . 9-o-[2-(o-Methoxyl)thiophenyl]ethyl-berberine bromide
C28H26NO5SBr ÏàËÆ¶È:55.1%
Bioorganic & Medicinal Chemistry 2013 21 5830-5840
Synthesis and biological evaluation of berberine¨Cthiophenyl hybrids as multi-functional agents: Inhibition of acetylcholinesterase, butyrylcholinesterase, and A¦Â aggregation and antioxidant activity
Tao Su, Shishun Xie, Hui Wei, Jun Yan, Ling Huang, Xingshu Li
Structure 13C NMR ̼Æ×Ä£Äâͼ
23 . coptichine
C31H23NO8 ÏàËÆ¶È:54.8%
Fitoterapia 2014 93 74-80
Five new alkaloids from Coptidis Rhizoma¨CEuodiae Fructus couple and their cytotoxic activities against gastrointestinal cancer cells
Ping Qian, Xiu-Wei Yang
Structure 13C NMR ̼Æ×Ä£Äâͼ
24 . indicumine B
C30H24N2O9 ÏàËÆ¶È:53.3%
Fitoterapia 2013 84 360-365
Four new coumarinolignoids from seeds of Solanum indicum
Hai-Long Yin, Jie-Hui Li, Jian Li, Bin Li, Li Chen, Yin Tian, Shi-Jun Liu, Tao Zhang, Jun-Xing Dong
Structure 13C NMR ̼Æ×Ä£Äâͼ
25 . 8-O-4/8-O-4-ÍÑÇⰢκËáÈý¾ÛÌå
C30H26O12 ÏàËÆ¶È:53.3%
Chinese Traditional and Herbal Drugs 2011 42 1948-1951
Chemical constituents from roots of Pittosporum illicioides
XIAO, Bing-kun, HUANG, Rong-qing, YANG, Jian-yun, DONG, Jun-xing
Structure 13C NMR ̼Æ×Ä£Äâͼ
26 . Okaramine A
ÏàËÆ¶È:53.1%
Bioscience, Biotechnology, and Biochemistry 1995 59 246-250
New Okaramine Congeners, Okaramines D, E, and F, from Penicillium simplicissimum ATCC 90288
Hideo Hayashi, Yoshihide Asabu, Sawao Murao, Motoo Arai
Structure 13C NMR ̼Æ×Ä£Äâͼ
27 . okaramine A
C32H32N4O5 ÏàËÆ¶È:53.1%
Agricultural and Biological Chemistry 1989 53 461-469
Structure and Insecticidal Activity of New Indole Alkaloids, Okaramines A and B, from Penidllium simplidssimum AK-40
Hideo HAYASHI, Kunio TAKIUCHI, Sawao MURAO, Motoo ARAI
Structure 13C NMR ̼Æ×Ä£Äâͼ
28 . scutellaprostin F
C25H20O10 ÏàËÆ¶È:51.7%
Chemical & Pharmaceutical Bulletin 1991 39 1466-1472
Studies on Nepalese Crude Drugs. XIV. New Flavonoids from the Root of Scutellaria prostrata JACQ. ex BENTH.
Yuichi KIKUCHI,Yukinori MIYAICHI and Tsuyoshi TOMIMORI
Structure 13C NMR ̼Æ×Ä£Äâͼ
29 . Scutellaprostin F
C25H20O10 ÏàËÆ¶È:51.7%
Chemistry of Natural Compounds 2002 38 473-519
PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES
V. M. Malikov and M. P. Yuldashev
Structure 13C NMR ̼Æ×Ä£Äâͼ
30 . Quassidine F
C26H20N4O2 ÏàËÆ¶È:51.7%
Chemical & Pharmaceutical Bulletin 2011 59(3) 359-364
Anti-inflammatory Alkaloids from the Stems of Picrasma quassioides BENNET
Wei-Hua JIAO, Hao GAO, Feng ZHAO, Hou-Wen LIN, Yu-Min PAN, Guang-Xiong ZHOU, and Xin-Sheng YAO
Structure 13C NMR ̼Æ×Ä£Äâͼ
31 . impurity A
ÏàËÆ¶È:51.7%
Indian Journal of Chemistry Section B 2009 48B 741-745
Synthesis of impurity A in Carvedilol: a ¦Â-adrenergic receptor
Madhusudhan,G; Naidu,K Chinnam; Kumar,B Anand; Satyanarayana,R; Balraju,V
Structure 13C NMR ̼Æ×Ä£Äâͼ
32 . (Z)-N-butyl-3-(3,4-dimethoxyphenyl)-2-(3,4-dimethoxyphenylacetylamino)-2-propenamide
C25H32N2O6 ÏàËÆ¶È:51.7%
Heterocycles 2006 68 993-1006
A Convenient Synthesis of Papaverine Analogs via Photocyclization of N-Acyl-¦Á-dehydroarylalaninamide Derivatives
Hideki Hoshina, Kei Maekawa, Kaori Kobayashi, Tetsutaro Igarashi, and Tadamitsu Sakurai*
Structure 13C NMR ̼Æ×Ä£Äâͼ
33 . (E)-N-butyl-3-(3,4-dimethoxyphenyl)-2-(3,4-dimethoxyphenylacetylamino)-2-propenamide
C25H32N2O6 ÏàËÆ¶È:51.7%
Heterocycles 2006 68 993-1006
A Convenient Synthesis of Papaverine Analogs via Photocyclization of N-Acyl-¦Á-dehydroarylalaninamide Derivatives
Hideki Hoshina, Kei Maekawa, Kaori Kobayashi, Tetsutaro Igarashi, and Tadamitsu Sakurai*
Structure 13C NMR ̼Æ×Ä£Äâͼ
34 . (Z)-N-butyl-3-(3,4-dimethoxyphenyl)-2-(3,4-dimethoxyphenylacetylamino)-2-propenamide
C25H32N2O6 ÏàËÆ¶È:51.7%
Heterocycles 2003 60 1779-1786
A New Route to Papaverine Analogs via Photocyclization of Substituted N-Acyl-¦Á-dehydrophenylalaninamides
Hideki Hoshina, Kei Maekawa, Keisuke Taie, Tetsutaro Igarashi, and Tadamitsu Sakurai*
Structure 13C NMR ̼Æ×Ä£Äâͼ
35 . (E)-N-butyl-3-(3,4-dimethoxyphenyl)-2-(3,4-dimethoxyphenylacetylamino)-2-propenamide
C25H32N2O6 ÏàËÆ¶È:51.7%
Heterocycles 2003 60 1779-1786
A New Route to Papaverine Analogs via Photocyclization of Substituted N-Acyl-¦Á-dehydrophenylalaninamides
Hideki Hoshina, Kei Maekawa, Keisuke Taie, Tetsutaro Igarashi, and Tadamitsu Sakurai*
Structure 13C NMR ̼Æ×Ä£Äâͼ
36 . triFA3
C29H26O10 ÏàËÆ¶È:51.7%
Chinese Journal of Natural Medicines 2006 4 146-150
Isolation and Identification of Ferulic Acid Dehydrotrimers and Dehydrodimers Catalysed by Momordica Charantia Peroxidase
LIU Hai-Li; KONG Ling-Yi
Structure 13C NMR ̼Æ×Ä£Äâͼ
37 . 2-[1-(4-Chlorobenzyl)-1H-indol-3-yl]-2-(5-bromo-1H-indol-3-yl)-N-(pyridin-4-yl)acetamide
C30H23BrClN4O ÏàËÆ¶È:51.7%
Heterocycles 2011 83 1757-1769
A Facile Synthesis of Symmetrical and Unsymmetrical Bis(indolyl)acetamides Mediated by Protic Acid
Hai Shang, Fei-Yue Hao, Li Pan, Hong Chen,* and Mao-Sheng Cheng*
Structure 13C NMR ̼Æ×Ä£Äâͼ
38 . 5-(3,4-Dimethoxybenzoyl)-2-(3,4-dimethoxyphenyl)-Npyrid-2-ylpyridinium perchlorate
C27H25N2O9Cl ÏàËÆ¶È:51.7%
Zeitschrift f¨¹r Naturforschung B 2004 59 424-430
Reactions of 3-Chloropropeniminium Salts with Aminopyridines. Synthesis of N-Pyridylpyridinium and Pyrido[1,2-a]pyrimidinium Salts
U. Girreser, D. Heber, M. Rostaie-Gerylow, and M. Sch¨¹tt
Structure 13C NMR ̼Æ×Ä£Äâͼ
39 . 3-(4-methoxy-3-(3-methoxyphenyl)benzamido)-4-oxo-4H-chromen-7-yl acetate
C26H21NO7 ÏàËÆ¶È:51.7%
Bioorganic & Medicinal Chemistry 2010 18 249-266
The synthesis and evaluation of flavone and isoflavone chimeras of novobiocin and derrubone
Jared R. Mays, Stephanie A. Hill, Justin T. Moyers, Brian S.J. Blagg
Structure 13C NMR ̼Æ×Ä£Äâͼ
40 . 1-(1,3-benzodioxol-5-yl)-8-{[(2-morpholin-4-ylpyridin-3-yl)carbonyl]amino}-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide
C29H26N6O5 ÏàËÆ¶È:51.7%
Bioorganic & Medicinal Chemistry 2010 18 403-414
Aminopyridinecarboxamide-based inhibitors: Structure¨Cactivity relationship
Dominique F. Bonafoux, Sheri L. Bonar, Michael Clare, Ann M. Donnelly, Jeanette L. Glaenzer, Julia A. Guzova, He Huang, Nandidni N. Kishore, Francis J. Koszyk, Patrick J. Lennon, Adam Libby, Sumathy Mathialagan, David S. Oburn, Sharon A Rouw, Cynthia D. S
Structure 13C NMR ̼Æ×Ä£Äâͼ
41 . N'-cyclopentylidene-1-(3-hydroxy-4-methoxyphenyl)-¦Â-carboline-3-carbohydrazide
ÏàËÆ¶È:51.7%
Bioorganic & Medicinal Chemistry 2011 19 6400-6408
Synthesis and antitumor activity of ¦Â-carboline 3-(substituted-carbohydrazide) derivatives
Val¨¦ria Aquilino Barbosa, Anelise S. Nazari Formagio, Franciele Cristina Savariz, Mary Ann Foglio, Humberto Moreira Spindola, João Ernesto de Carvalho, Emerson Meyer, Maria Helena Sarragiotto
Structure 13C NMR ̼Æ×Ä£Äâͼ
42 . 10,10-dimethyl-7-(3,4-dimethoxyphenyl)-7,10,11,12-tetrahydro-9H-chromeno[4,3-b]quinoline-6,8-dione
C26H25NO5 ÏàËÆ¶È:51.7%
Heterocycles 2012 85 1629-1653
An Efficient One-Pot Three-Component Synthesis of Highly Functionalized Coumarin Fused Indenodihydropyridine and Chromeno[4,3-b]quinoline Derivatives
Naseem Ahmed,* B. Venkata Babu, Sandeep Singh, and Petar M. Mitrasinovic
Structure 13C NMR ̼Æ×Ä£Äâͼ
43 . (S,E)-N-((1-(2-amino-3-(1H-indol-3-yl)propyl)-1H-1,2,3-triazol-4-yl)methyl)-3-(4-hydroxy-3-methoxyphenyl)acrylamide
ÏàËÆ¶È:51.7%
Molecules 2012 17 8312-8333
From BACE1 Inhibitor to Multifunctionality of Tryptoline and Tryptamine Triazole Derivatives for Alzheimer¡¯s Disease
Jutamas Jiaranaikulwanitch, Piyarat Govitrapong, Valery V. Fokin and Opa Vajragupta
Structure 13C NMR ̼Æ×Ä£Äâͼ
44 . lamellarin¦Á 20-sulfate
C29H22NO11SNa ÏàËÆ¶È:51.7%
Journal of Medicinal Chemistry 1999 42 1901-1907
Lamellarin ¦Á 20-Sulfate, an Inhibitor of HIV-1 Integrase Active against HIV-1 Virus in Cell Culture
M. Venkata Rami Reddy, M. Rama Rao, Denise Rhodes, Mark S. T. Hansen, Kathleen Rubins, Frederic D. Bushman, Yenamandra Venkateswarlu, and D. John Faulkner
Structure 13C NMR ̼Æ×Ä£Äâͼ
45 . 2-(3,4-dimethoxyphenyl)-N-(3-(5-(2-methoxyphenyl)-1,3,4-oxadiazol-2-yl)phenyl)acetamide
C25H23N3O5 ÏàËÆ¶È:51.7%
Heterocycles 2012 85 2693-2712
Design, Synthesis and Biological Activity Evaluation of 2,5-Diphenyl-1,3,4-oxadiazole Derivatives as Novel Inhibitors of Fructose-1,6-bisphosphatase
Hai-Bing He, Li-Xin Gao, Yue-Yang Zhou, Ting Liu, Jie Tang, Xue-Ping Gong, Wen-Wei Qiu, Jing-Ya Li,* Jia Li,* and Fan Yang
Structure 13C NMR ̼Æ×Ä£Äâͼ
46 . N-(3-(4-benzyl-5-p-tolyl-4H-1,2,4-triazol-3-yl)phenyl)-2-(3,4-dimethoxyphenyl)acetamide
C32H30N4O3 ÏàËÆ¶È:51.7%
Heterocycles 2012 85 2693-2712
Design, Synthesis and Biological Activity Evaluation of 2,5-Diphenyl-1,3,4-oxadiazole Derivatives as Novel Inhibitors of Fructose-1,6-bisphosphatase
Hai-Bing He, Li-Xin Gao, Yue-Yang Zhou, Ting Liu, Jie Tang, Xue-Ping Gong, Wen-Wei Qiu, Jing-Ya Li,* Jia Li,* and Fan Yang
Structure 13C NMR ̼Æ×Ä£Äâͼ
47 . 1-(9H-carbazol-4-yloxy)-3-(2-(2-methoxy phenoxy)ethylamino)propan-2-ol
ÏàËÆ¶È:51.7%
Indian Journal of Chemistry Section B 2012 51B 1430-1435
Synthesis of racemic and chiral Carvedilol starting from corresponding 5-(chloromethyl)oxazolidin-2-one
Kumar, B Anand; Babu, K Veera; Rao, Rama Koteshwar; Srinivas, Kumbam; Madhusudhan, G; Mukkanti, K
Structure 13C NMR ̼Æ×Ä£Äâͼ
48 . N-(5-(8-aminoquinolin-4-ylamino)isoquinolin-1-yl)-4-chloro-3-(trifuoromethyl)benzamide
ÏàËÆ¶È:51.7%
Chemical & Pharmaceutical Bulletin 2013 61 747-756
Novel Quinolinylaminoisoquinoline Bioisosteres of Sorafenib as Selective RAF1 Kinase Inhibitors: Design, Synthesis, and Antiproliferative Activity against Melanoma Cell Line
Hye Jung Cho, Mohammed Ibrahim El-Gamal, Chang-Hyun Oh, So Ha Lee, Taebo Sim, Garam Kim, Hong Seok Choi, Jung Hoon Choi, Kyung Ho Yoo
Structure 13C NMR ̼Æ×Ä£Äâͼ
49 . ¦Â-D-mono-glucuronidecurcumin
C27H28O12 ÏàËÆ¶È:51.7%
Bioorganic & Medicinal Chemistry 2014 22 435-439
Curcumin glucuronides: Assessing the proliferative activity against human cell lines
Ashutosh Pal, Bokyung Sung, Basvoju A. Bhanu Prasad, Paul T. Schuber Jr., Sahdeo Prasad, Bharat B. Aggarwal, William G. Bornmann
Structure 13C NMR ̼Æ×Ä£Äâͼ
50 . 9-o-[2-(m-Methyl)thiophenyl]ethyl-berberine bromide
C28H26NO4SBr ÏàËÆ¶È:51.7%
Bioorganic & Medicinal Chemistry 2013 21 5830-5840
Synthesis and biological evaluation of berberine¨Cthiophenyl hybrids as multi-functional agents: Inhibition of acetylcholinesterase, butyrylcholinesterase, and A¦Â aggregation and antioxidant activity
Tao Su, Shishun Xie, Hui Wei, Jun Yan, Ling Huang, Xingshu Li
Structure 13C NMR ̼Æ×Ä£Äâͼ
51 . 9-o-[2-(o-Fluro)thiophenyl]ethyl-berberine bromide
C27H23NO4FSBr ÏàËÆ¶È:51.7%
Bioorganic & Medicinal Chemistry 2013 21 5830-5840
Synthesis and biological evaluation of berberine¨Cthiophenyl hybrids as multi-functional agents: Inhibition of acetylcholinesterase, butyrylcholinesterase, and A¦Â aggregation and antioxidant activity
Tao Su, Shishun Xie, Hui Wei, Jun Yan, Ling Huang, Xingshu Li
Structure 13C NMR ̼Æ×Ä£Äâͼ
52 . lamellarin ¦Á 20-sulfate
C29H22N2O11S ÏàËÆ¶È:51.6%
Heterocycles 2010 80 841-846
Divergent Synthesis of Lamellarin ¦Á 13-Sulfate, 20-Sulfate, and 13,20-Disulfate
Tsutomu Fukuda, Takeshi Ohta, Sho Saeki, and Masatomo Iwao
Structure 13C NMR ̼Æ×Ä£Äâͼ
53 . (E/Z)-3-(3,4-dimethoxyphenyl)-3-(3,4,5-trimethoxyphenyl)-acrylonitrile
C20H21NO5 ÏàËÆ¶È:51.6%
Bioorganic & Medicinal Chemistry 2011 19 6356-6374
1,1-Diarylalkenes as anticancer agents: Dual inhibitors of tubulin polymerization and phosphodiesterase 4
Alexander L. Ruchelman, Hon-Wah Man, Roger Chen, Wei Liu, Ling Lu, Dorota Cedzik, Ling Zhang, Jim Leisten, Alice Collette, Rama Krishna Narla, Heather K. Raymon, George W. Muller
Structure 13C NMR ̼Æ×Ä£Äâͼ
54 . (E/Z)-3-(3-ethoxy-4-methoxyphenyl)-3-(4-(methylamino)-phenyl)acrylonitrile
C19H20N2O2 ÏàËÆ¶È:51.6%
Bioorganic & Medicinal Chemistry 2011 19 6356-6374
1,1-Diarylalkenes as anticancer agents: Dual inhibitors of tubulin polymerization and phosphodiesterase 4
Alexander L. Ruchelman, Hon-Wah Man, Roger Chen, Wei Liu, Ling Lu, Dorota Cedzik, Ling Zhang, Jim Leisten, Alice Collette, Rama Krishna Narla, Heather K. Raymon, George W. Muller
Structure 13C NMR ̼Æ×Ä£Äâͼ
55 . (E/Z)-3-(4-(dimethylamino)phenyl)-3-(3-ethoxy-4-methoxyphenyl)acrylonitrile
C20H22N2O2 ÏàËÆ¶È:51.6%
Bioorganic & Medicinal Chemistry 2011 19 6356-6374
1,1-Diarylalkenes as anticancer agents: Dual inhibitors of tubulin polymerization and phosphodiesterase 4
Alexander L. Ruchelman, Hon-Wah Man, Roger Chen, Wei Liu, Ling Lu, Dorota Cedzik, Ling Zhang, Jim Leisten, Alice Collette, Rama Krishna Narla, Heather K. Raymon, George W. Muller
Structure 13C NMR ̼Æ×Ä£Äâͼ
56 . (E)-ethyl 3-(1-cyano-2-((3,4-dimethoxyphenethyl)amino)-9,10-dimethoxy-4-oxo-6,7-dihydro-4H-pyrido[2,1-a]isoquinolin-3-yl)acrylate
C31H33N3O7 ÏàËÆ¶È:51.6%
Heterocycles 2012 85 2933-2947
Synthesis and Reactivity of 2-Chloro-3-formylpyrido[2,1-a]isoquinoline Derivative. A Novel Routes to Pyrazolo[3',4':4,5]pyrido[2,1-a]isoquinoline and Isoquinolino[2,1-g][1,6]naphthyridines
Hamdi M. Hassaneen,* Wagnat W. Wardkhan, and Yasmin Sh. Mohammed
Structure 13C NMR ̼Æ×Ä£Äâͼ
57 . (2R)-3-(3,4-dimethoxyphenyl)-2-[[(2E)-3-[2-(3,4-dimethoxyphenyl)-7-methoxy-1-benzofuran-4-yl]prop-2-enoyl]oxy]propanoic acid
C31H30O10 ÏàËÆ¶È:51.6%
Organic & Biomolecular Chemistry 2013 11 2724-2727
Total synthesis of (+)-pentamethylsalvianolic acid C
Benjamin L. Alford and Helmut M. H¨¹gel
Structure 13C NMR ̼Æ×Ä£Äâͼ
58 . N-(1,2-Bis(4-isopropoxy-3-methoxyphenyl)-2-oxoethyl)-1-benzyl-5-(benzyloxy)-6-methoxy-1H-indole-2-carboxamide
C46H48N2O8 ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry 2011 19 4971-4984
Synthesis and topoisomerase I inhibitory activity of a novel diazaindeno[2, 1-b]phenanthrene analogue of Lamellarin D
Salvatore Cananzi, Lucio Merlini, Roberto Artali, Giovanni Luca Beretta, Nadia Zaffaroni, Sabrina Dallavalle
Structure 13C NMR ̼Æ×Ä£Äâͼ
59 . (2Z)-3-(3-Hydroxy-4-methoxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]-2-[4-((1E)-3-{[2-(4-hydroxyphenyl)ethyl]amino}-3-oxoprop-1-en-1-yl)-2-methoxyphenoxy]prop-2-enamide
C36H36N2O8 ÏàËÆ¶È:50%
Chemistry & Biodiversity 2012 9 769-776
Two New Norlignans and A New Lignanamide from Peperomia tetraphylla
Yun-Zhi Li,Ai-Ping Tong,and Jing Huang
Structure 13C NMR ̼Æ×Ä£Äâͼ
60 . 1-(1,3-benzodioxol-5-yl)-8-[({2-[(4-methoxybenzyl)amino]-pyridin-3-yl}carbonyl-)amino]-4,5-dihydro-1H-benzo[g]indazole-3-carboxamide
C33H28N6O5 ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry 2010 18 403-414
Aminopyridinecarboxamide-based inhibitors: Structure¨Cactivity relationship
Dominique F. Bonafoux, Sheri L. Bonar, Michael Clare, Ann M. Donnelly, Jeanette L. Glaenzer, Julia A. Guzova, He Huang, Nandidni N. Kishore, Francis J. Koszyk, Patrick J. Lennon, Adam Libby, Sumathy Mathialagan, David S. Oburn, Sharon A Rouw, Cynthia D. S
Structure 13C NMR ̼Æ×Ä£Äâͼ
61 . lamellarin I 20-sulfate
C30H25NO12SNa ÏàËÆ¶È:50%
Tetrahedron 1997 53 3457-3466
New lamellarin alkaloids from an unidentified ascidian from the Arabian Sea
M.Venkata Rami Reddy, D.John Faulkner, Y. Venkateswarlu, M.Rama Rao
Structure 13C NMR ̼Æ×Ä£Äâͼ
62 . Zanthocapensine
C30H27NO6 ÏàËÆ¶È:50%
Planta Medica 2012 78 148-153
Antibacterial Benzofuran Neolignans and Benzophenanthridine Alkaloids from the Roots of Zanthoxylum capense
Luo, Xuan; Pedro, Liliana; Milic, Vladimir; Mulhovo, Silva; Duarte, Aida; Duarte, No¨¦lia; Ferreira, Maria-Jos¨¦ U.:
Structure 13C NMR ̼Æ×Ä£Äâͼ |
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