Heterocycles Database
Natural Products with
Heterocyclic Ring System
 
 1975-2010
 53,681 Compounds
 25 January, 2010
 
Search by:
Name
Group
Carbon:
Carbon
Molecular Weight
Name
Group
Molecular Fomula:
Molecular Weight:
Author:
Author
Group
Journal:
Journal
Year
 
 Nomenclature :
 
The natural products are listed under the name used in the original literature.
 
 The abbreviations :
 
The following abbreviations have been used :
 
act : biological activity
cd : circular dichroism
Cnmr : 13C-nuclear magnetic resonance spectrum
Hnmr : 1H-nuclear magnetic resonance spectrum
ir : infrared spectrum
mass : mass spectrum
syn : total synthesis
uv : ultraviolet spectrum
 
 Journals :
 
This database lists the natural products with heterocyclic ring system whose structure has been determined since 1975.
The journals which have been covered are as follows.
 
Angew. Chem. Int. Ed. Engl.
Angew. Chem. Int. Ed.
Bull. Chem. Soc. Japan
Chem. and Ind.
Chem. Ber.
J. Chem. Soc., Chem. Commun.
Chem. Commun.
Chem. Eur. J.
Chemistry Lett.
Chem. Pharm. Bull.
Coll. Czech. Chem. Commun.
Eur. J. Inorg. Chem.
Eur. J. Org. Chem.
Experientia
Helv. Chim. Acta
Heterocycles
J. Am. Chem. Soc.
J. Antibiot.
J. Chem. Soc., Perkin Trans. 1
J. Heterocycl. Chem.
J. Med. Chem.
J. Nat. Prod.
J. Org. Chem.
J. Pharm. Sci.
Liebigs Ann. Chem.
Monatsh. Chem.
Org. Lett.
Phytochemistry
Planta medica
Synlett
Synth. Commun.
Synthesis
Tetrahedron
Tetrahedron Asymmetry
Tetrahedron Lett.
Yakugaku Zasshi
 
 Editor :
 
Editor
Keiichiro Fukumoto

Associate Editor
Kunio Ogasawara
Yoshiharu Iwabuchi

Assistant Editors
Hayato Fukuda
Naoki Kanoh
Muneo Kawasumi
Yusuke Sasano
Masatoshi Sibuya
Hiroyuki Yamakoshi

Editorial Assistants
Kishiko Nakano
Sanae Ohura
Yuki Shima
Kazuko Todoroki
Michi Yamamoto
 New Heterocyclic Natural Products
This journal will list the new natural products with a heterocyclic ring system, collected from current chemical literature, whose structure has been established.
 
25 January, 2010
Search by Group:
Polyketides
Aromatics
Terpenes
Steroids
Alkaloids
Antibiotics
Miscellaneous
 
All
 
Search by Journal :
Vol.
No.
Angew. Chem. Int. Ed.
48
24
Chem. Pharm. Bull.
57
7
Eur. J. Org. Chem.
2009
19
Helv. Chim. Acta
92
7
Heterocycles
78
6,7
J. Antibiot.
62
7
J. Nat. Prod.
72
7
Org. Lett.
11
13,14
Phytochemistry
70
10
Tetrahedron
65
23
Tetrahedron Lett.
50
26,28-30
  196 data found. 1 - 30 listed Next Last   

Polyketides R85573
Fuligoic Acid
C15H15O5Cl = 310.5
Tetrahedron Lett.    2009, 50 , 3189
A. Shintani, T. Ohtsuki, Y. Yamamoto, T. Hakamatsuka, N. Kawahara, Y. Goda, M. Ishibashi
DOI: 10.1016/j.tetlet.2009.01.122
CrossRef 		 
[NS]  Fuligo septica f. flava
[mp]
[bp]
[α]D      - 31°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides R85471
Fusidilactone E
C17H28O6 = 312
Eur. J. Org. Chem.    2009, , 3279
S. Qin, K. Krohn, U. Flörke, B. Schulz, S. Draeger, G. Pescitelli, P. Salvadori, S. Antus, T. Kurtán 		 
[NS]  Fusidium species
[mp]
[bp]
[α]D      + 1.3°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]algicidal, antifungal, and antibacterial activities
Polyketides R85470
Fusidilactone D
C17H26O6 = 326
Eur. J. Org. Chem.    2009, , 3279
S. Qin, K. Krohn, U. Flörke, B. Schulz, S. Draeger, G. Pescitelli, P. Salvadori, S. Antus, T. Kurtán 		 
[NS]  Fusidium species
[mp]
[bp]
[α]D      + 37.3°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]algicidal, antifungal, and antibacterial activities
Polyketides R85795
Macarangioside F
C19H32O8 = 388
Phytochemistry    2009, 70 , 1277
K. Matsunami, H. Otsuka, K. Kondo, T. Shinzato, M. Kawahata, K. Yamaguchi, Y. Takeda
DOI: 10.1016/j.phytochem.2009.07.020
CrossRef 		 
[NS]  Macaranga tanarius
[mp]
[bp]
[α]D      - 6.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides R85610
Bistramide K, 39-Oxo-
C40H68N2O8 = 704
J. Nat. Prod.    2009, 72 , 1338
B. T. Murphy, S. Cao, P. Brodie, J. Maharavo, H. Andriamanantoanina, P. Ravelonandro, D. G. I. Kingston
DOI: 10.1021/np900072k
CrossRef 		 
[NS]  Trididemnum cyclops
[mp]
[bp]
[α]D      - 72°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antiproliferative activity
Aromatics R85620
Alcyopterosin P
C15H17O2Cl = 264.5
J. Nat. Prod.    2009, 72 , 1357
M. Carbone, L. Núñez-Pons, F. Castelluccio, C. Avila, M. Gavagnin
DOI: 10.1021/np900162t
CrossRef 		 
[NS]  Alcyonium grandis
[mp]
[bp]
[α]D      - 822.9°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85793
No Name
C15H17O4Cl = 296.5
Phytochemistry    2009, 70 , 1233
C. Kihampa, M. H. H. Nkunya, C. C. Joseph, S. M. Magesa, A. Hassanali, M. Heydenreich, E. Kleinpeter
DOI: 10.1016/j.phytochem.2009.07.024
CrossRef 		 
[NS]  Tessmannia densiflora
[mp]170 - 173 ℃
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85825
No Name
C18H14O5 = 310
Phytochemistry    2009, 70 , 1309
E. D. Coy-Barrera, L. E. Cuca-Suárez, M. Sefkow
DOI: 10.1016/j.phytochem.2009.07.010
CrossRef 		 
[NS]  Ocotea macrophylla
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85709
Xinjiastilbene B
C21H22O3 = 322
Heterocycles    2009, 78 , 1581
N. Iwasaki, M. Baba, H. Aishan, Y. Okada, T. Okuyama
DOI: 10.3987/COM-09-11673
CrossRef 		 
[NS]  Glycyrrhiza inflata
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85829
Albatrellutin
C22H32O2 = 328
Heterocycles    2009, 78 , 1807
A.-L. Zhang, T. Xu, J.-M. Gao, M.-S. Bai, G. Zhang, H.-W. Liu, S.-Q. Li, Y. Konishi
DOI: 10.3987/COM-09-11675
CrossRef 		 
[NS]  Albatrellus species
[mp]
[bp]
[α]D      - 2°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85607
Communin A
C23H18O3 = 342
J. Nat. Prod.    2009, 72 , 1335
P. Fu, S. Lin, L. Shan, M. Lu, Y.-H. Shen, J. Tang, R.-H. Liu, X. Zhang, R.-L. Zhu, W.-D. Zhang
DOI: 10.1021/np800830v
CrossRef 		 
[NS]  Polytrichum commune
[mp]212 - 213 ℃
[bp]
[α]D      - 52°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85608
Communin B
C23H18O3 = 342
J. Nat. Prod.    2009, 72 , 1335
P. Fu, S. Lin, L. Shan, M. Lu, Y.-H. Shen, J. Tang, R.-H. Liu, X. Zhang, R.-L. Zhu, W.-D. Zhang
DOI: 10.1021/np800830v
CrossRef 		 
[NS]  Polytrichum commune
[mp]247 - 250 ℃
[bp]
[α]D      - 47°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85827
No Name
C20H22O5 = 342
Phytochemistry    2009, 70 , 1309
E. D. Coy-Barrera, L. E. Cuca-Suárez, M. Sefkow
DOI: 10.1016/j.phytochem.2009.07.010
CrossRef 		 
[NS]  Ocotea macrophylla
[mp]
[bp]
[α]D      - 27.4°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]PAF-antagonistic activity
Aromatics R85537
Ugonin T
C20H18O6 = 354
J. Nat. Prod.    2009, 72 , 1273
Y.-C. Huang, T.-L. Hwang, C.-S. Chang, Y.-L. Yang, C.-N. Shen, W.-Y. Liao, S.-C. Chen, C.-C. Liaw
DOI: 10.1021/np900148a
CrossRef 		 
[NS]  Helminthostachys zeylanica
[mp]202 - 204 ℃
[bp]
[α]D      - 28.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory activity against superoxide anion
generation and elastase release
Aromatics R85826
No Name
C20H20O6 = 356
Phytochemistry    2009, 70 , 1309
E. D. Coy-Barrera, L. E. Cuca-Suárez, M. Sefkow
DOI: 10.1016/j.phytochem.2009.07.010
CrossRef 		 
[NS]  Ocotea macrophylla
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85708
Xinjiastilbene A
C24H28O3 = 364
Heterocycles    2009, 78 , 1581
N. Iwasaki, M. Baba, H. Aishan, Y. Okada, T. Okuyama
DOI: 10.3987/COM-09-11673
CrossRef 		 
[NS]  Glycyrrhiza inflata
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85611
No Name
C17H20O9 = 368
J. Nat. Prod.    2009, 72 , 1341
J. Kornsakulkarn, C. Thongpanchang, S. Lapanun, K. Srichomthong
DOI: 10.1021/np900082h
CrossRef 		 
[NS]  Torrubiella tenuis BCC 12732
[mp]191.7 - 193.0 ℃
[bp]
[α]D      - 63.41°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85523
Sophoronol A
C20H18O7 = 370
J. Nat. Prod.    2009, 72 , 1265
G.-P. Zhang, Z.-Y. Xiao, J. Rafique, M. Arfan, P. J. Smith, C. A. Lategan, L.-H. Hu
DOI: 10.1021/np900144c
CrossRef 		 
[NS]  Sophora mollis
[mp]
[bp]
[α]D      + 200°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85609
Ohioensin H
C23H16O5 = 372
J. Nat. Prod.    2009, 72 , 1335
P. Fu, S. Lin, L. Shan, M. Lu, Y.-H. Shen, J. Tang, R.-H. Liu, X. Zhang, R.-L. Zhu, W.-D. Zhang
DOI: 10.1021/np800830v
CrossRef 		 
[NS]  Polytrichum commune
[mp]270 - 272 ℃
[bp]
[α]D      - 22°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85612
No Name
C17H20O10 = 384
J. Nat. Prod.    2009, 72 , 1341
J. Kornsakulkarn, C. Thongpanchang, S. Lapanun, K. Srichomthong
DOI: 10.1021/np900082h
CrossRef 		 
[NS]  Torrubiella tenuis BCC 12732
[mp]243.4 - 244.7 ℃
[bp]
[α]D      - 32.37°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85613
No Name
C17H20O10 = 384
J. Nat. Prod.    2009, 72 , 1341
J. Kornsakulkarn, C. Thongpanchang, S. Lapanun, K. Srichomthong
DOI: 10.1021/np900082h
CrossRef 		 
[NS]  Torrubiella tenuis BCC 12732
[mp]242.3 - 242.8 ℃
[bp]
[α]D      - 11.05°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85469
Sch1385568
C21H20O7 = 384
J. Antibiot.    2009, 62 , 401
S.-W. Yang, T.-M. Chan, J. Terraciano, D. Loebenberg, M. Patel, V. Gullo, M. Chu
DOI: 10.1038/ja.2009.51
CrossRef 		 
[NS]  Aspergillus species SPRI-0814
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antifungal activity
Aromatics R85524
Sophoronol B
C21H20O8 = 400
J. Nat. Prod.    2009, 72 , 1265
G.-P. Zhang, Z.-Y. Xiao, J. Rafique, M. Arfan, P. J. Smith, C. A. Lategan, L.-H. Hu
DOI: 10.1021/np900144c
CrossRef 		 
[NS]  Sophora mollis
[mp]
[bp]
[α]D      + 159°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85526
Sophoronol D
C22H24O8 = 416
J. Nat. Prod.    2009, 72 , 1265
G.-P. Zhang, Z.-Y. Xiao, J. Rafique, M. Arfan, P. J. Smith, C. A. Lategan, L.-H. Hu
DOI: 10.1021/np900144c
CrossRef 		 
[NS]  Sophora mollis
[mp]
[bp]
[α]D      + 164°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85533
Ugonin P
C25H26O6 = 422
J. Nat. Prod.    2009, 72 , 1273
Y.-C. Huang, T.-L. Hwang, C.-S. Chang, Y.-L. Yang, C.-N. Shen, W.-Y. Liao, S.-C. Chen, C.-C. Liaw
DOI: 10.1021/np900148a
CrossRef 		 
[NS]  Helminthostachys zeylanica
[mp]214 - 216 ℃
[bp]
[α]D      + 55.3°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85536
Ugonin S
C25H26O6 = 422
J. Nat. Prod.    2009, 72 , 1273
Y.-C. Huang, T.-L. Hwang, C.-S. Chang, Y.-L. Yang, C.-N. Shen, W.-Y. Liao, S.-C. Chen, C.-C. Liaw
DOI: 10.1021/np900148a
CrossRef 		 
[NS]  Helminthostachys zeylanica
[mp]223 - 225 ℃
[bp]
[α]D      + 37.5°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory activity against superoxide anion
generation and elastase release
Aromatics R85532
Ugonin O
C25H22O7 = 434
J. Nat. Prod.    2009, 72 , 1273
Y.-C. Huang, T.-L. Hwang, C.-S. Chang, Y.-L. Yang, C.-N. Shen, W.-Y. Liao, S.-C. Chen, C.-C. Liaw
DOI: 10.1021/np900148a
CrossRef 		 
[NS]  Helminthostachys zeylanica
[mp]234 - 236 ℃
[bp]
[α]D      - 19.8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory activity against superoxide anion
generation and elastase release
Aromatics R85530
Ugonin M
C25H24O7 = 436
J. Nat. Prod.    2009, 72 , 1273
Y.-C. Huang, T.-L. Hwang, C.-S. Chang, Y.-L. Yang, C.-N. Shen, W.-Y. Liao, S.-C. Chen, C.-C. Liaw
DOI: 10.1021/np900148a
CrossRef 		 
[NS]  Helminthostachys zeylanica
[mp]248 - 250 ℃
[bp]
[α]D      + 79.6°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory activity against superoxide anion
generation and elastase release
Aromatics R85531
Ugonin N
C25H26O7 = 438
J. Nat. Prod.    2009, 72 , 1273
Y.-C. Huang, T.-L. Hwang, C.-S. Chang, Y.-L. Yang, C.-N. Shen, W.-Y. Liao, S.-C. Chen, C.-C. Liaw
DOI: 10.1021/np900148a
CrossRef 		 
[NS]  Helminthostachys zeylanica
[mp]222 - 224 ℃
[bp]
[α]D      + 14.9°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics R85534
Ugonin Q
C25H26O7 = 438
J. Nat. Prod.    2009, 72 , 1273
Y.-C. Huang, T.-L. Hwang, C.-S. Chang, Y.-L. Yang, C.-N. Shen, W.-Y. Liao, S.-C. Chen, C.-C. Liaw
DOI: 10.1021/np900148a
CrossRef 		 
[NS]  Helminthostachys zeylanica
[mp]236 - 238 ℃
[bp]
[α]D      - 38.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory activity against superoxide anion
generation and elastase release
  196 data found. 1 - 30 listed Next Last   
   
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