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zhanghc521: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ÔÙ°ï°ïæ 2013-09-08 19:33:11
²éѯ½á¹û£º¹²²éµ½65¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     comopund 7b
    ÏàËÆ¶È:63.6%
Chemical & Pharmaceutical Bulletin          1989          37          1977-1983
Studies on the Constituents of Aster tataricus L.f. II. : Structures of Aster Saponins Isolated from the Root
Tsuneatsu NAGAO,Shizuko HACHIYAMA,Hikaru OKABE and Tatsuo YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Octyl6-O-[2-O-(4,6-di-O-acetyl-3-azido-2.3-dideoxy-2-phthalimido-¦Â-D-glucopyranosyl)-6-O-allyl-3,4-di-O-benzyl-¦Á-D-mannopyranosyll-2,3,4-tri-O-benzyl-¦Â-D-glucopyranoside
    ÏàËÆ¶È:63.6%
Bioorganic & Medicinal Chemistry          1994          2          1231-1241
Key involvement of all three GlcNAc hydroxyl groups in the recognition of ¦Â-D-GlcpNAc-(1¡ú2)-¦Á-D-Manp-(1¡ú6)-¦Â-D-Glcp-OR by N-acetylglucosaminyltransferase-V
Osamu Kanie, Suzanne C. Crawley, Monica M. Palcic, Ole Hindsgaul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Aurasperone F
    ÏàËÆ¶È:62.5%
Journal of Agricultural and Food Chemistry          2007          55          8920-8927
Occurrence of Naphtho-Gamma-Pyrones- and Ochratoxin A-Producing Fungi in French Grapes and Characterization of New Naphtho-Gamma-Pyrone Polyketide (Aurasperone G) Isolated from Aspergillus niger C-433
Noureddine Bouras, Florence Mathieu, Yannick Coppel, Stephen E. Strelkov and Ahmed Lebrihi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     nigerone
C32H26O10     ÏàËÆ¶È:56.2%
Journal of the Chemical Society, Perkin Transactions 1          1980                   2474-2479
Structural elucidation of the nigerones, four new naphthopyrones from cultures of Aspergillus niger
Dharles P. Gorst-Allman, Pieter S. Stern and Christiaan J. Rabie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     flavasperone
C16H14O3     ÏàËÆ¶È:56.2%
Journal of the Chemical Society, Perkin Transactions 1          1980                   2474-2479
Structural elucidation of the nigerones, four new naphthopyrones from cultures of Aspergillus niger
Dharles P. Gorst-Allman, Pieter S. Stern and Christiaan J. Rabie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     TMC-256C2
C16H14O5     ÏàËÆ¶È:56.2%
The Journal of Antibiotics          2002          55          685-692
TMC-256A1 and C1, New Inhibitors of IL-4 Signal Transduction Produced by Aspergillus niger var niger TC 1629
MASAAKI SAKURAI,JUN KOHNO,KOUZOU YAMAMOTO,TORU OKUDA,MAKI NISHIO,KIMIO KAWANO and TETSUO OHNUKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     rubrofusarin B
C16H14O5     ÏàËÆ¶È:56.2%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2007          46(4)          113-115
Pyrones in Metabolites of Marine Mangrove Endophytic Fungus(No.ZZF79) from the South China Sea
HUANG Zhong-jing, SHAO Chang-lun, CHEN Yi-guang, LIN Yong-cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     5,7-dimethoxy-3-methylpthalide
C11H12O4     ÏàËÆ¶È:54.5%
Journal of Natural Products          2008          71(8)          1393-1398
Characterization of Polyketide Metabolites from Foliar Endophytes of Picea glauca
Mark W. Sumarah, Eva Puniani, Barbara A. Blackwell, and J. David Miller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     6-hydroxymethyleugenin
    ÏàËÆ¶È:54.5%
Journal of Natural Products          2002          65          1681-1682
The Isolation of Two New Chromone Derivatives from the New Zealand Fungus Tolypocladium extinguens
Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     penta-O-methyleschweilenol B
C25H18O11     ÏàËÆ¶È:54.5%
Journal of Natural Products          1998          61          901-906
Three New Ellagic Acid Derivatives from the Bark of Eschweilera coriacea from the Suriname Rainforest1
Shu-Wei Yang, Bing-Nan Zhou, Jan H. Wisse, Randy Evans, Hendrik van der Werff, James S. Miller, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     methyl O-¦Â-D-xylopyranosyl-(1¡ú3)-O-¦Á-L-arabinopyranosyl-(1¡ú4)-[O-¦Â-D-apiofuranosyl-(1¡ú3)]-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-xylopyranoside
    ÏàËÆ¶È:54.5%
Chemical & Pharmaceutical Bulletin          1989          37          1977-1983
Studies on the Constituents of Aster tataricus L.f. II. : Structures of Aster Saponins Isolated from the Root
Tsuneatsu NAGAO,Shizuko HACHIYAMA,Hikaru OKABE and Tatsuo YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 11b
    ÏàËÆ¶È:54.5%
Chemical & Pharmaceutical Bulletin          1989          37          1977-1983
Studies on the Constituents of Aster tataricus L.f. II. : Structures of Aster Saponins Isolated from the Root
Tsuneatsu NAGAO,Shizuko HACHIYAMA,Hikaru OKABE and Tatsuo YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     5-hydroxy-6,7,3',4'-tetramethoxyflavone (3'-O-methyleupatorin)
C19H18O7     ÏàËÆ¶È:54.5%
Chemistry of Natural Compounds          2006          42          230-231
AGLYCONE FLAVONOIDS OF Centaurea tougourensis FROM ALGERIA
A. Nacer,A. Bernard, J. Boustie,R. Touzani, and Z. Kabouche
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Compound 3
    ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry Letters          1994          4          1501-1506
Synthesis of Gal-¦Â(1¡ú4)-6-O-SO3Na-GlcNAc-¦Â-(1¡ú6)-Man-¦Á-OR as a part of gp 120
Xiao-Gao Liu, Rakesh K. Jain, Raj Saha, Khushi L. Matta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Compound 4
    ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry Letters          1994          4          1501-1506
Synthesis of Gal-¦Â(1¡ú4)-6-O-SO3Na-GlcNAc-¦Â-(1¡ú6)-Man-¦Á-OR as a part of gp 120
Xiao-Gao Liu, Rakesh K. Jain, Raj Saha, Khushi L. Matta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Octyl6-O-[2-O-(3,4-di-O-acetyl-6-azido-2,6-dideoxy-2-phthalimido-¦Â-D-glucopyranosyl)-6-O-ally1-3,4-di-O-benzyl-¦Á-D-mannopyranosyl]-2,3,4-tri-O-benzyl-¦Â-D-glucopyranoside
    ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry          1994          2          1231-1241
Key involvement of all three GlcNAc hydroxyl groups in the recognition of ¦Â-D-GlcpNAc-(1¡ú2)-¦Á-D-Manp-(1¡ú6)-¦Â-D-Glcp-OR by N-acetylglucosaminyltransferase-V
Osamu Kanie, Suzanne C. Crawley, Monica M. Palcic, Ole Hindsgaul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     1,2,3,4-Di-O-isopropylidene-L-galactopyranoside
C12H20O6     ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry          2000          8          1937-1946
Chemo-enzymatic synthesis of fluorinated sugar nucleotide: useful mechanistic Probes for glycosyltransferases
Michael D Burkart, St¨¦phane P Vincent, Arno D¨¹ffels, Brion W Murray, Steven V Ley, Chi-Huey Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3-(1-Methylethyl)-1,2,4-trimethoxybenzene
    ÏàËÆ¶È:54.5%
Tetrahedron          2011          67          10129-10146
Synthesis of (¡À)- and (+)-perovskone
George Majetich, Yong Zhang, Xinrong Tian, Jonathan E. Britton, Yang Li, Ryan Phillips
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     maritimin
C11H10O4     ÏàËÆ¶È:54.5%
Journal of Chemical Research          2001          25          549-550
Synthesis of maritimin, a chromone from Pancratium maritimum
Asolkar, Ratnakar N.; Kamat, Vijayendra P.; Kirtany, Janardan K.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     N-(3-methoxyphenyl)-N'-(2,2-dimethoxyethyl)urea
C12H18N2O4     ÏàËÆ¶È:54.5%
Canadian Journal of Chemistry          2004          82          1649-1661
Lithiation of 1-arylimidazol-2(1H)-ones and 1-aryl-4,5-dihydroimidazol-2(1H)-ones
Carme Cantos Llopart, Conchita Ferrer, John A Joule
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     6-methoxymethyleugenin
C13H14O5     ÏàËÆ¶È:53.8%
Journal of Natural Products          2002          65          1681-1682
The Isolation of Two New Chromone Derivatives from the New Zealand Fungus Tolypocladium extinguens
Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     O-iso-baeckeol
    ÏàËÆ¶È:53.8%
Phytochemistry          1989          28          3543-3544
Phloroacylphenones in the essential oil of Thryptomene saxicola
Kim A. Dastlik,Emilio L. Ghisalberti,Phillip R. Jefferies
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     methyl 3-endo-(1,3-dioxoisoindolin-2-ylcarbamoyl)bicyclo[2.2.1]hept-5-ene-2-endo-carboxylate
C18H16N2O5     ÏàËÆ¶È:53.8%
Heterocycles          2008          75          1133-1149
Synthesis of Nitrogen Heterocycles by Intramolecular Cyclization of Alkenyl N-Acylaminophthalimides Using Phenyliodine(III) Bis(trifluoroacetate) (PIFA)
Masato Tsukamoto, Kousuke Murata, Takeshi Sakamoto, Setsuo Saito, and Yasuo Kikugawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Octyl6-O-[2-O-(2-acetamido-4,6-di-O-acetyl-3-azido-2,3-dideoxy-¦Â-D-glucopyranosyl)-6-O-allyl-3,4-di-O-benzyla-D-mannopyranosyl]-2,3,4-tri-O-benzyl-¦Â-D-glucopyranoside
    ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry          1994          2          1231-1241
Key involvement of all three GlcNAc hydroxyl groups in the recognition of ¦Â-D-GlcpNAc-(1¡ú2)-¦Á-D-Manp-(1¡ú6)-¦Â-D-Glcp-OR by N-acetylglucosaminyltransferase-V
Osamu Kanie, Suzanne C. Crawley, Monica M. Palcic, Ole Hindsgaul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     cassiarin Amethyl ether
C14H13O2N     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry          2009          17          8234-8240
Synthesis and structure¨Cactivity relationships of cassiarin A as potential antimalarials with vasorelaxant activity
Hiroshi Morita, Yuichiro Tomizawa, Jun Deguchi, Tokio Ishikawa, Hiroko Arai, Kazumasa Zaima, Takahiro Hosoya, Yusuke Hirasawa, Takayuki Matsumoto, Katsuo Kamata, Wiwied Ekasari, Aty Widyawaruyanti, Tutik Sri Wahyuni, Noor Cholies Zaini, Toshio Honda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     (+)-(1S,3S)-5,8-dimethoxy-1,3-dimethyl-3,4-dihydro-1H-benzo[c]pyran
C13H18O3     ÏàËÆ¶È:53.8%
European Journal of Organic Chemistry          2010                   4442-4449
Intra- and Intermolecular Oxa-Pictet¨CSpengler Cyclization Strategy for the Enantioselective Synthesis of Deoxy Analogues of (+)-Nanomycin A Methyl Ester, (+)-Eleutherin, (+)-Allo-Eleutherin, and (+)-Thysanone
Rajiv T. Sawant, Satish G. Jadhav and Suresh B. Waghmode
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     compound10
C13H14O3     ÏàËÆ¶È:53.8%
Tetrahedron          2013          69          1808-1814
Xanthouroleuconaphin: a yellowish pigment from the aphid Uroleucon nigrotuberculatum and its total synthesis
Taichi Nishimura, Mitsuyo Horikawa, Kouji Yamada, Ayaka Sogabe, Takeshi Nishii, Hiroto Kaku, Makoto Inai, Masami Tanaka, Shigeru Takahashi, Tetsuto Tsunoda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     1-(R/S)-5,6-Tri-O-acetyl-2S-azido-2,3,4-trideoxy-D /L-hexoseMethyl Hemiacetal
    ÏàËÆ¶È:53.8%
European Journal of Organic Chemistry          1998          1998          481-492
Enantiopure D-, L- (and 2-epi-) Purpurosamine C-Type Glycosyl Donors from Racemic Acrolein Dimer − Biocatalytic Resolution
Silke Erbeck, Xifu Liang, Richard Krieger and Horst Prinzbach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     6-Methoxymethyleugenin
    ÏàËÆ¶È:53.8%
European Journal of Plant Pathology          2012          134          239-247
Toxins from a symbiotic fungus, Leptographium qinlingensis associated with Dendroctonus armandi and their in vitro toxicities to Pinus armandi seedlings
Xiao-Jun Li, Jin-Ming Gao, Hui Chen, An-Ling Zhang, Ming Tang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     perforamone A
C16H18O5     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2006          54(1)          44-47
Chromones from the Branches of Harrisonia perforata
Pittaya TUNTIWACHWUTTIKUL,Photchana PHANSA,Yupa POOTAENG-ON,and Walter Charles TAYLOR
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (-)-sibiricin
    ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1996          44          1208-1211
Prenylcoumarins from Murraya paniculata var. omphalocarpa (Rutaceae) : The Absolute Configuration of Sibiricin, Mexoticin and Omphamurin
Takeshi KINOSHITA,Jin-Bin WU and Feng-Chi HO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     multiforisin C
C14H18O7K     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1995          43          547-552
Isolation of Some Immunosuppressive Components from an Ascomycete, Gelasinospora multiforis
Haruhiro FUJIMOTO,Yuji SATOH,Megumi NAKAYAMA,Tomoe TAKAYAMA and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     4,5-dimethoxyl-7-methyl-coumarin
C12H12O4     ÏàËÆ¶È:50%
Acta Botanica Sinica          1999          41          107-110
Chemical constituents of the Anemone tomentosa Root
Wang Jun-Ru, Peng Shu-Lin, Wang Ming-Kui, Feng Jun-Tao, Ding Li-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     montixanthone
C14H10O6     ÏàËÆ¶È:50%
Natural Product Research          2005          19          685-688
Xanthones and other constituents of 'Allanblackia monticola (Guttiferae)
Silvere Ngouela; Fabien Zelefack; Bruno N. Lenta; Erasmienne T. Ngouamegne; Diderot N. Tchamo; Etienne Tsamo; Joseph D. Connolly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-08 18:20:19
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zhanghc521

Ìú¸Ëľ³æ (ÕýʽдÊÖ)

ÒýÓûØÌû:
2Â¥: Originally posted by jasminelw at 2013-09-08 18:20:19
²éѯ½á¹û£º¹²²éµ½65¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     comopund 7b
    ÏàËÆ¶È:63.6%
Chemical & Pharmaceutical Bulletin          1989          37          1977-1983
Studies on the Constituent ...

²»ºÃÒâ˼ ÄÜÔÙ²éÒ»ÏÂÂ𣿸պ˴ÅÊý¾Ý ûÓÐÏÔʾÍêÈ« Ó¦¸ÃÊÇCNMR£º19.9,20.2,55.0,56.1,61.0,96.4,96.8,103.3,104.4,105.2,105.2,106.6,106.8,107.6,108.1,110.0,116.2,140.1,140.1,150.3,154.8,155.5,156.9,158.4,160.8,161.1,162.1,167.9,168.5,182.4,183.9
3Â¥2013-09-08 19:32:40
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jasminelw

Ìú¸Ëľ³æ (ÕýʽдÊÖ)

ÒýÓûØÌû:
3Â¥: Originally posted by zhanghc521 at 2013-09-08 19:32:40
²»ºÃÒâ˼ ÄÜÔÙ²éÒ»ÏÂÂ𣿸պ˴ÅÊý¾Ý ûÓÐÏÔʾÍêÈ« Ó¦¸ÃÊÇCNMR£º19.9,20.2,55.0,56.1,61.0,96.4,96.8,103.3,104.4,105.2,105.2,106.6,106.8,107.6,108.1,110.0,116.2,140.1,140.1,150.3,154.8,155.5,156.9,158.4,16 ...

²éѯ½á¹û£º¹²²éµ½337¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     asperpyrone A
C31H24O10     ÏàËÆ¶È:100%
Journal of Natural Products          2003          66          136-139
New Dimeric Naphthopyrones from Aspergillus niger
Kohki Akiyama, Seigo Teraguchi, Yukiko Hamasaki, Mika Mori, Kunihiko Tatsumi, Kenji Ohnishi, and Hideo Hayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     fonsecinone A
C32H26O10     ÏàËÆ¶È:96.8%
Magnetic Resonance in Chemistry          2005          43          962-965
Complete 1H and 13C NMR assignments of aurasperone A and fonsecinone A, two bis-naphthopyrones produced by Aspergillus aculeatus
Francinete Ramos Campos, Andersson Barison, Cristina Daolio, Antonio G. Ferreira and Edson Rodrigues-Fo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Asperpyrone E
C31H24O10     ÏàËÆ¶È:93.5%
Chemistry & Biodiversity          2013          10          1193-1201
Naphtho--pyrones from Endophyte Aspergillus niger Occurring in the Liverwort Heteroscyphus tener (Steph.) Schiffn.
Xiao-Bin Li, Fei Xie, Shan-Shan Liu, Ying Li, Jin-Chuan Zhou, Yong-Qing Liu, Hui-Qing Yuan and Hong-Xiang Lou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     asperpyrone B
C32H26O10     ÏàËÆ¶È:90.6%
Journal of Natural Products          2003          66          136-139
New Dimeric Naphthopyrones from Aspergillus niger
Kohki Akiyama, Seigo Teraguchi, Yukiko Hamasaki, Mika Mori, Kunihiko Tatsumi, Kenji Ohnishi, and Hideo Hayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     8'-O-demethylisonigerone
C31H24O10     ÏàËÆ¶È:87.5%
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   Ì¼Æ×Ä£Äâͼ
6 .     aurasperone A
C32H26O10     ÏàËÆ¶È:87.5%
Magnetic Resonance in Chemistry          2005          43          962-965
Complete 1H and 13C NMR assignments of aurasperone A and fonsecinone A, two bis-naphthopyrones produced by Aspergillus aculeatus
Francinete Ramos Campos, Andersson Barison, Cristina Daolio, Antonio G. Ferreira and Edson Rodrigues-Fo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     aurasperone A
C32H26O10     ÏàËÆ¶È:87.5%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2007          46(4)          113-115
Pyrones in Metabolites of Marine Mangrove Endophytic Fungus(No.ZZF79) from the South China Sea
HUANG Zhong-jing, SHAO Chang-lun, CHEN Yi-guang, LIN Yong-cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     asperpyrone D
C31H24O10     ÏàËÆ¶È:87.0%
Phytochemistry          2007          68          368-372
Asperpyrone D and other metabolites of the plant-associated fungal strain Aspergillus tubingensis
Jixun Zhan, G.M. Kamal B. Gunaherath, E.M. Kithsiri Wijeratne, A.A. Leslie Gunatilaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     rubasperone D
C31H24O10     ÏàËÆ¶È:87.0%
Helvetica Chimica Acta          2011          Vol. 94          1732-1740
Cytotoxic Naphtho-g-pyrones from the Mangrove Endophytic Fungus Aspergillus tubingensis (GX1-5E)
Hong-Bo Huang, Ze-En Xiao, Xiao-Jun Feng, Cai-Huan Huang, Xun Zhu, Jian-Hua Ju, Meng-Feng Li, Yong-Cheng Lin, Lan Liu, Zhi-Gang She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     asperpyrone C
C32H26O10     ÏàËÆ¶È:84.3%
Journal of Natural Products          2003          66          136-139
New Dimeric Naphthopyrones from Aspergillus niger
Kohki Akiyama, Seigo Teraguchi, Yukiko Hamasaki, Mika Mori, Kunihiko Tatsumi, Kenji Ohnishi, and Hideo Hayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     isonigerone
    ÏàËÆ¶È:83.8%
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   Ì¼Æ×Ä£Äâͼ
12 .     rubasperone A
C31H24O10     ÏàËÆ¶È:83.8%
Planta Medica          2010          76          1888-1891
Three Dimeric Naphtho-¦Ã-Pyrones from the Mangrove Endophytic Fungus Aspergillus tubingensis Isolated from Pongamia pinnata
Huang, Hong-Bo; Feng, Xiao-Jun; Liu, Lan; Chen, Bin; Lu, Yong-Jun; Ma, Lin; She, Zhi-Gang; Lin, Yong-Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     rubasperone B
C32H26O10     ÏàËÆ¶È:81.2%
Planta Medica          2010          76          1888-1891
Three Dimeric Naphtho-¦Ã-Pyrones from the Mangrove Endophytic Fungus Aspergillus tubingensis Isolated from Pongamia pinnata
Huang, Hong-Bo; Feng, Xiao-Jun; Liu, Lan; Chen, Bin; Lu, Yong-Jun; Ma, Lin; She, Zhi-Gang; Lin, Yong-Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     rubasperone C
C32H26O10     ÏàËÆ¶È:81.2%
Planta Medica          2010          76          1888-1891
Three Dimeric Naphtho-¦Ã-Pyrones from the Mangrove Endophytic Fungus Aspergillus tubingensis Isolated from Pongamia pinnata
Huang, Hong-Bo; Feng, Xiao-Jun; Liu, Lan; Chen, Bin; Lu, Yong-Jun; Ma, Lin; She, Zhi-Gang; Lin, Yong-Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     8'-O-demethylnigerone
C31H24O11     ÏàËÆ¶È:80.6%
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   Ì¼Æ×Ä£Äâͼ
16 .     aurasperone F
C31H26O11     ÏàËÆ¶È:77.4%
Natural Product Research          2005          19          653-659
Aurasperone F ¨C a new member of the naphtho-gamma-pyrone class isolated from a cultured microfungus, Aspergillus niger C-433
Noureddine Bouras; Florence Mathieu; Yannick Coppel; Ahmed Lebrihi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Aurasperone G
    ÏàËÆ¶È:77.4%
Journal of Agricultural and Food Chemistry          2007          55          8920-8927
Occurrence of Naphtho-Gamma-Pyrones- and Ochratoxin A-Producing Fungi in French Grapes and Characterization of New Naphtho-Gamma-Pyrone Polyketide (Aurasperone G) Isolated from Aspergillus niger C-433
Noureddine Bouras, Florence Mathieu, Yannick Coppel, Stephen E. Strelkov and Ahmed Lebrihi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     nigerasperone C
C31H26O11     ÏàËÆ¶È:74.1%
The Journal of Antibiotics          2007          60          204-210
Nigerasperones A~C, New Monomeric and Dimeric Naphtho--pyrones from a Marine Alga-derived Endophytic Fungus Aspergillus niger EN-13 FREE
Yi Zhang, Xiao-Ming Li and Bin-Gui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     ustilaginoidein B
C28H18O11     ÏàËÆ¶È:70.9%
Chemical & Pharmaceutical Bulletin          1988          36          146-152
Further Characterization of Seven Bis(naphtho-¦Ã-pyrone) Congeners of Ustilaginoidins, Coloring Matters of Claviceps virens (Ustilaginoidea virens)
KIYOTAKA KOYAMA and SHINSAKU NATORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     asperpyrone D
C31H24O10     ÏàËÆ¶È:70.9%
Natural Product Research and Development          2013          25          190-192
Chemical Constituents from the Endophytic Fungus Aspergillus sp.DCS31 of Daphniphyllum longeracemosum
MENG Xin-xin, GE Feng , ZENG Ying, ZHAO Pei-ji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     ustilaginoidin G
C28H20O10     ÏàËÆ¶È:67.7%
Chemical & Pharmaceutical Bulletin          1988          36          146-152
Further Characterization of Seven Bis(naphtho-¦Ã-pyrone) Congeners of Ustilaginoidins, Coloring Matters of Claviceps virens (Ustilaginoidea virens)
KIYOTAKA KOYAMA and SHINSAKU NATORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     ustilaginoidin I
C28H20O11     ÏàËÆ¶È:67.7%
Chemical & Pharmaceutical Bulletin          1988          36          146-152
Further Characterization of Seven Bis(naphtho-¦Ã-pyrone) Congeners of Ustilaginoidins, Coloring Matters of Claviceps virens (Ustilaginoidea virens)
KIYOTAKA KOYAMA and SHINSAKU NATORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     hypochromin B
C30H20O11     ÏàËÆ¶È:67.7%
Journal of Natural Products          2010          73          579-582
Antiangiogenic Metabolites from a Marine-Derived Fungus, Hypocrea vinosa
Yuu Ohkawa, Kazuhiko Miki, Toshihiro Suzuki, Kazuto Nishio, Takashi Sugita, Kaoru Kinoshita, Kunio Takahashi and Kiyotaka Koyama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     ustilaginoidin H
C28H20O11     ÏàËÆ¶È:64.5%
Chemical & Pharmaceutical Bulletin          1988          36          146-152
Further Characterization of Seven Bis(naphtho-¦Ã-pyrone) Congeners of Ustilaginoidins, Coloring Matters of Claviceps virens (Ustilaginoidea virens)
KIYOTAKA KOYAMA and SHINSAKU NATORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     rubasperone E
C32H28O11     ÏàËÆ¶È:62.5%
Helvetica Chimica Acta          2011          Vol. 94          1732-1740
Cytotoxic Naphtho-g-pyrones from the Mangrove Endophytic Fungus Aspergillus tubingensis (GX1-5E)
Hong-Bo Huang, Ze-En Xiao, Xiao-Jun Feng, Cai-Huan Huang, Xun Zhu, Jian-Hua Ju, Meng-Feng Li, Yong-Cheng Lin, Lan Liu, Zhi-Gang She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     nigerasperone B
C32H30O12     ÏàËÆ¶È:62.5%
The Journal of Antibiotics          2007          60          204-210
Nigerasperones A~C, New Monomeric and Dimeric Naphtho--pyrones from a Marine Alga-derived Endophytic Fungus Aspergillus niger EN-13 FREE
Yi Zhang, Xiao-Ming Li and Bin-Gui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     cathayanon C
C34H25O8     ÏàËÆ¶È:61.7%
Journal of Asian Natural Products Research          2009          11          267-273
Three new Diels¨CAlder type adducts from the stem bark of Morus cathayana
Qing-Jian Zhang, Gang Ni, Ying-Hong Wang, Ruo-Yun Chen and De-Quan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     rubasperone F/G
C32H28O11     ÏàËÆ¶È:61.7%
Helvetica Chimica Acta          2011          Vol. 94          1732-1740
Cytotoxic Naphtho-g-pyrones from the Mangrove Endophytic Fungus Aspergillus tubingensis (GX1-5E)
Hong-Bo Huang, Ze-En Xiao, Xiao-Jun Feng, Cai-Huan Huang, Xun Zhu, Jian-Hua Ju, Meng-Feng Li, Yong-Cheng Lin, Lan Liu, Zhi-Gang She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     Compound 3
    ÏàËÆ¶È:61.7%
Magnetic Resonance in Chemistry          2006          44          35-37
Carbon-13 and proton NMR assignments of a new agathisflavone derivative (pages 35¨C37)
Mario Geraldo de Carvalho, Mario Sergio do Rocha Gomes, Andr¨¦ Hil¨¢rio Fernandes Pereira, Juliana Feij¨® de Souza Daniel and Jan Schripsema
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     5,5''-dihydroxy-7,4',7'',4'''-tetramethoxybiflavone
C34H26O10     ÏàËÆ¶È:61.7%
Journal of Medicinal Plants Research          2012          6          2131-2135
Biological activity and a biflavonoid from Hypericum scabrum extracts
Farideh Abdollahi, Ali Shafaghat and Farshid Salimi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4Â¥2013-09-09 13:36:27
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zhanghc521

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4Â¥: Originally posted by jasminelw at 2013-09-09 13:36:27
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1 .     asperpyrone A
C31H24O10     ÏàËÆ¶È:100%
Journal of Natural Products          2003          66          136-139
New Dimeric Naphthopyrones ...

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