Heterocycles Database
Natural Products with
Heterocyclic Ring System
 
 1975-2012
 57,916 Compounds
 23 January, 2012
 
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
Naoki Kanoh
Muneo Kawasumi
Takashi Moriya
Keiichi Murakami
Kohei Sakanishi
Yusuke Sasano
Takuro Shibuta
Masatoshi Shibuya

Editorial Assistants
Sayaka Kametani
Kishiko Nakano
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.
 
23 January, 2012
Search by Group:
Polyketides
Aromatics
Terpenes
Steroids
Alkaloids
Antibiotics
Miscellaneous
 
All
 
Search by Journal :
Vol.
No.
Bull. Chem. Soc. Japan
84
6
Chem. Pharm. Bull.
59
6
Eur. J. Org. Chem.
2011
17
Helv. Chim. Acta.
94
5, 6
Heterocycles
83
6
J. Antibiot.
64
6
J. Nat. Prod.
74
6
Org. Biomol. Chem.
9
11
Org. Lett.
13
11, 12
Phytochemistry
72
7, 8, 9
Planta medica
77
9
Tetrahedron
67
23
Tetrahedron Lett.
52
23, 24, 25, 26
  212 data found. 1 - 30 listed Next Last   

Polyketides
Speciosin L
C10H10O3 = 178
Phytochemistry    2011, 72 , 923
M.-Y. Jiang, Y. Li, F. Wang, J.-K. Liu
DOI: 10.1016/j.phytochem.2011.03.011
CrossRef 		 
[NS]  Hexagonia speciosa
[mp]
[bp]
[α]D      + 56.5°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Speciosin N
C11H14O5 = 226
Phytochemistry    2011, 72 , 923
M.-Y. Jiang, Y. Li, F. Wang, J.-K. Liu
DOI: 10.1016/j.phytochem.2011.03.011
CrossRef 		 
[NS]  Hexagonia speciosa
[mp]
[bp]
[α]D      + 89.9°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Aporpinone A, 5’-O-Acetyl-
C13H14O5 = 250
Phytochemistry    2011, 72 , 923
M.-Y. Jiang, Y. Li, F. Wang, J.-K. Liu
DOI: 10.1016/j.phytochem.2011.03.011
CrossRef 		 
[NS]  Hexagonia speciosa
[mp]
[bp]
[α]D      - 8.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Speciosin M
C13H16O5 = 252
Phytochemistry    2011, 72 , 923
M.-Y. Jiang, Y. Li, F. Wang, J.-K. Liu
DOI: 10.1016/j.phytochem.2011.03.011
CrossRef 		 
[NS]  Hexagonia speciosa
[mp]
[bp]
[α]D      + 136.6°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Speciosin O
C13H16O6 = 268
Phytochemistry    2011, 72 , 923
M.-Y. Jiang, Y. Li, F. Wang, J.-K. Liu
DOI: 10.1016/j.phytochem.2011.03.011
CrossRef 		 
[NS]  Hexagonia speciosa
[mp]
[bp]
[α]D      + 161.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Inonotusin A
C15H14O6 = 290
Chem. Pharm. Bull.    2011, 59 , 770
L. Zan, J. Qin, Y. Zhang, Y. Yao, H. Bao, X. Li
DOI: 10.1248/cpb.59.770
CrossRef 		 
[NS]  Inonotus hispidus
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Simplextone B
C17H30O4 = 298
Org. Lett.    2011, 13 , 3154
X.-F. Liu, Y.-L. Song, H.-J. Zhang, F. Yang, H.-B. Yu, W.-H. Jiao, S.-J. Piao, W.-S. Chen, H.-W. Lin
DOI: 10.1021/ol201055w
CrossRef 		 
[NS]  Plakortis simplex
[mp]
[bp]
[α]D      + 21°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Simplextone A
C18H32O4 = 312
Org. Lett.    2011, 13 , 3154
X.-F. Liu, Y.-L. Song, H.-J. Zhang, F. Yang, H.-B. Yu, W.-H. Jiao, S.-J. Piao, W.-S. Chen, H.-W. Lin
DOI: 10.1021/ol201055w
CrossRef 		 
[NS]  Plakortis simplex
[mp]
[bp]
[α]D      + 28°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Annulohypoxylin
C19H26O6 = 350
Helv. Chim. Acta    2011, 94 , 1108
M.-J. Cheng, M.-D. Wu, S.-Y. Hsieh, M.-T. Hsieh, I.-S. Chen, G.-F. Yuan
DOI: 10.1002/hlca.201000368
CrossRef 		 
[NS]  Annulohypoxylon boveri var. microspora BCRC 34012
[mp]
[bp]
[α]D      0°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Arthrobotrisin A
C22H34O6 = 394
J. Nat. Prod.    2011, 74 , 1526
L.-X. Wei, H.-X. Zhang, J.-L. Tan, Y.-S. Chu, N. Li, H.-X. Xue, Y.-L. Wang, X.-M. Niu, Y. Zhang, K.-Q. Zhang
DOI: 10.1021/np200187z
CrossRef 		 
[NS]  Arthrobotrys oligospora
[mp]
[bp]
[α]D      - 3.56°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Arthrobotrisin B
C22H34O6 = 394
J. Nat. Prod.    2011, 74 , 1526
L.-X. Wei, H.-X. Zhang, J.-L. Tan, Y.-S. Chu, N. Li, H.-X. Xue, Y.-L. Wang, X.-M. Niu, Y. Zhang, K.-Q. Zhang
DOI: 10.1021/np200187z
CrossRef 		 
[NS]  Arthrobotrys oligospora
[mp]
[bp]
[α]D      - 12.29°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Arthrobotrisin C
C22H34O6 = 394
J. Nat. Prod.    2011, 74 , 1526
L.-X. Wei, H.-X. Zhang, J.-L. Tan, Y.-S. Chu, N. Li, H.-X. Xue, Y.-L. Wang, X.-M. Niu, Y. Zhang, K.-Q. Zhang
DOI: 10.1021/np200187z
CrossRef 		 
[NS]  Arthrobotrys oligospora
[mp]
[bp]
[α]D      + 19.36°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antibacterial activity
Polyketides
Komaroveside B
C19H30O9 = 402
Chem. Pharm. Bull.    2011, 59 , 773
I. K. Lee, K. H. Kim, S. Y. Lee, S. U. Choi, K. R. Lee
DOI: 10.1248/cpb.59.773
CrossRef 		 
[NS]  Cardamine komarovii
[mp]
[bp]
[α]D      - 65.4°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Komaroveside C
C19H32O9 = 404
Chem. Pharm. Bull.    2011, 59 , 773
I. K. Lee, K. H. Kim, S. Y. Lee, S. U. Choi, K. R. Lee
DOI: 10.1248/cpb.59.773
CrossRef 		 
[NS]  Cardamine komarovii
[mp]
[bp]
[α]D      - 61.4°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Rubrosinesiquione C
C14H8O6 = 272
Heterocycles    2011, 83 , 1377
A. Tanaka, K. Kinoshita, K. Ichinose, T. Togawa, K. Koyama, T. Narui, L.-s. Wang, K. Takahashi
DOI: 10.3987/COM-11-12179
CrossRef 		 
[NS]  Lethariella sinesis
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C18H16O5 = 312
Phytochemistry    2011, 72 , 662
K. Manning, E. Petrunak, M. Lebo, A. González-Sarrías, N. P. Seeram, G. E. Henry
DOI: 10.1016/j.phytochem.2011.01.032
CrossRef 		 
[NS]  Hypericum ellipticum
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Aromatics
No Name
C17H12O6 = 312
J. Nat. Prod.    2011, 74 , 1421
A. Bader, N. De Tommasi, R. Cotugno, A. Braca
DOI: 10.1021/np200143s
CrossRef 		 
[NS]  Scorzonera judaica
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C17H14O6 = 314
J. Nat. Prod.    2011, 74 , 1421
A. Bader, N. De Tommasi, R. Cotugno, A. Braca
DOI: 10.1021/np200143s
CrossRef 		 
[NS]  Scorzonera judaica
[mp]
[bp]
[α]D      + 18°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C18H14O6 = 326
Phytochemistry    2011, 72 , 662
K. Manning, E. Petrunak, M. Lebo, A. González-Sarrías, N. P. Seeram, G. E. Henry
DOI: 10.1016/j.phytochem.2011.01.032
CrossRef 		 
[NS]  Hypericum ellipticum
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C21H22O5 = 354
Phytochemistry    2011, 72 , 929
R. Heinke, K. Franke, A. Porzel, L. A. Wessjohann, N. A. A. Ali, J. Schmidt
DOI: 10.1016/j.phytochem.2011.03.008
CrossRef 		 
[NS]  Dorstenia foetida
[mp]
[bp]
[α]D      + 12.5°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]Nonpolar extracts of D. foetida exhibit antifungal, antibacterial and cytotoxic activites.
Aromatics
No Name
C22H32O4 = 360
Chem. Pharm. Bull.    2011, 59 , 757
J. I. Lee, Y. Seo
DOI: 10.1248/cpb.59.757
CrossRef 		 
[NS]  Sargassum siliquastrum
[mp]
[bp]
[α]D      + 12.00°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antioxidant activity
Aromatics
No Name
C21H24O6 = 372
Phytochemistry    2011, 72 , 929
R. Heinke, K. Franke, A. Porzel, L. A. Wessjohann, N. A. A. Ali, J. Schmidt
DOI: 10.1016/j.phytochem.2011.03.008
CrossRef 		 
[NS]  Dorstenia foetida
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]Nonpolar extracts of D. foetida exhibit antifungal, antibacterial and cytotoxic activities.
Aromatics
Rubrosinesiquione B
C18H15NO8 = 373
Heterocycles    2011, 83 , 1377
A. Tanaka, K. Kinoshita, K. Ichinose, T. Togawa, K. Koyama, T. Narui, L.-s. Wang, K. Takahashi
DOI: 10.3987/COM-11-12179
CrossRef 		 
[NS]  Lethariella sinesis
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C21H26O6 = 374
J. Nat. Prod.    2011, 74 , 1444
Y. Li, W. Cheng, C. Zhu, C. Yao, L. Xiong, Y. Tian, S. Wang, S. Lin, J. Hu, Y. Yang, Y. Guo, Y. Yang, Y. Li, Y. Yuan, N. Chen, J. Shi
DOI: 10.1021/np2001896
CrossRef 		 
[NS]  Machilus robusta
[mp]
[bp]
[α]D      - 2.2°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C21H26O6 = 374
J. Nat. Prod.    2011, 74 , 1444
Y. Li, W. Cheng, C. Zhu, C. Yao, L. Xiong, Y. Tian, S. Wang, S. Lin, J. Hu, Y. Yang, Y. Guo, Y. Yang, Y. Li, Y. Yuan, N. Chen, J. Shi
DOI: 10.1021/np2001896
CrossRef 		 
[NS]  Machilus robusta
[mp]
[bp]
[α]D      - 25.6°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C22H26O6 = 386
Phytochemistry    2011, 72 , 929
R. Heinke, K. Franke, A. Porzel, L. A. Wessjohann, N. A. A. Ali, J. Schmidt
DOI: 10.1016/j.phytochem.2011.03.008
CrossRef 		 
[NS]  Dorstenia foetida
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]Nonpolar extracts of D. foetida exhibit antifungal, antibacterial and cytotoxic activities.
Aromatics
No Name
C21H23ClO5 = 390.5
Phytochemistry    2011, 72 , 929
R. Heinke, K. Franke, A. Porzel, L. A. Wessjohann, N. A. A. Ali, J. Schmidt
DOI: 10.1016/j.phytochem.2011.03.008
CrossRef 		 
[NS]  Dorstenia foetida
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]Nonpolar extracts of D. foetida exhibit antifungal, antibacterial and cytotoxic activities.
Aromatics
Rubrosinesiquione A
C20H17NO8 = 399
Heterocycles    2011, 83 , 1377
A. Tanaka, K. Kinoshita, K. Ichinose, T. Togawa, K. Koyama, T. Narui, L.-s. Wang, K. Takahashi
DOI: 10.3987/COM-11-12179
CrossRef 		 
[NS]  Lethariella sinesis
[mp]
[bp]
[α]D      - 941.2°     [ DMSO ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Palatiferin A
C21H20O8 = 400
Planta medica    2011, 77 , 951
H. D. T. Mai, H. N. T. Minh, V. C. Pham, K. N. Bui, V. H. Nguyen, V. M. Chau
DOI: 10.1055/s-0030-1250683
CrossRef 		 
[NS]  Pseuderanthemum palatiferum
[mp]103 - 104 ℃
[bp]
[α]D      28.2°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Aromatics
No Name
C21H22O8 = 402
Phytochemistry    2011, 72 , 929
R. Heinke, K. Franke, A. Porzel, L. A. Wessjohann, N. A. A. Ali, J. Schmidt
DOI: 10.1016/j.phytochem.2011.03.008
CrossRef 		 
[NS]  Dorstenia foetida
[mp]
[bp]
[α]D      + 22.7°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]Nonpolar extracts of D. foetida exhibit antifungal, antibacterial and cytotoxic activities.
  212 data found. 1 - 30 listed Next Last   
   
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