Heterocycles Database
Natural Products with
Heterocyclic Ring System
 
 1975-2013
 58,387 Compounds
 25 April, 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.
 
25 April, 2012
Search by Group:
Polyketides
Aromatics
Terpenes
Steroids
Alkaloids
Antibiotics
Miscellaneous
 
All
 
Search by Journal :
Vol.
No.
Chem. Pharm. Bull.
59
9
Eur. J. Org. Chem.
26
Helv. Chim. Acta
94
9
Heterocycles
83
9
J. Med. Chem.
54
17
J. Nat. Prod.
74
9
Org. Lett.
13
17, 18
Planta medica
77
13, 14
Tetrahedron
67
35, 36, 37, 38, 39
Tetrahedron Lett.
52
36, 39
  176 data found. 1 - 30 listed Next Last   

Polyketides
Botryoxide, Cyclo-
C8H10O4 = 170
J. Nat. Prod.    2012, 75 , 1785
A. Andolfi, L. Maddau, A. Cimmino, B. T. Linaldeddu, A. Franceschini, S. Serra, S. Basso, D. Melck, A. Evidente
DOI: 10.1021/np300512m
CrossRef 		 
[NS]  Neofusicoccum australe
[mp]
[bp]
[α]D      - 73°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]phytotoxicity
Polyketides
JBIR-138
C19H24O7 = 364
J. Antibiot.    2012, 65 , 535
T. Kawahara, A. Nagai, M. Takagi, K. Shin-ya
DOI: 10.1038/ja.2012.64
CrossRef 		 
[NS]  Aspergillus species fA75
[mp]
[bp]
[α]D      - 31°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Chaetoviridin E, 7-epi-
C23H23O5Cl = 414.5
Planta medica    2012, 78 , 1683
G.-D. Chen, Y.-J. Li, H. Gao, Y. Chen, X.-X. Li, J. Li, L.-D, Guo, Y.-Z. Cen, X.-S. Yao
DOI: 10.1055/s-0032-1315211
CrossRef 		 
[NS]  Chaetomium elatum
[mp]
[bp]
[α]D      + 15.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory effect on caspase-3
Polyketides
Chaetomugilin S
C23H29O5Cl = 420.5
Planta medica    2012, 78 , 1683
G.-D. Chen, Y.-J. Li, H. Gao, Y. Chen, X.-X. Li, J. Li, L.-D, Guo, Y.-Z. Cen, X.-S. Yao
DOI: 10.1055/s-0032-1315211
CrossRef 		 
[NS]  Chaetomium elatum
[mp]
[bp]
[α]D      + 514.6°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory effect on caspase-3
Polyketides
Chaetoviridin A, 7,5’-Bis-epi-
C23H25O6Cl = 432.5
Planta medica    2012, 78 , 1683
G.-D. Chen, Y.-J. Li, H. Gao, Y. Chen, X.-X. Li, J. Li, L.-D, Guo, Y.-Z. Cen, X.-S. Yao
DOI: 10.1055/s-0032-1315211
CrossRef 		 
[NS]  Chaetomium elatum
[mp]
[bp]
[α]D      + 38.8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory effect on caspase-3
Polyketides
JBIR-129
C77H132O31 = 1552
J. Nat. Prod.    2012, 75 , 1814
T. Kawahara, J.-H. Hwang, M. Izumikawa, J. Hashimoto, M. Takagi, K. Shin-ya
DOI: 10.1021/np3004358
CrossRef 		 
[NS]  Streptomyces RK74
[mp]
[bp]
[α]D      + 11.2°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxicity
Polyketides
JBIR-139
C85H145NO36 = 1755
J. Nat. Prod.    2012, 75 , 1814
T. Kawahara, J.-H. Hwang, M. Izumikawa, J. Hashimoto, M. Takagi, K. Shin-ya
DOI: 10.1021/np3004358
CrossRef 		 
[NS]  Streptomyces RK74
[mp]
[bp]
[α]D      + 8.4°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxicity
Aromatics
Streblusol A, trans-
C18H18O3 = 282
Phytochemistry    2012, 82 , 100
J. Li, Y. Huang, X.-L. Guan, J. Li, S.-P. Deng, Q. Wu, Y.-J. Zhang, X.-J. Su, R.-Y. Yang
DOI: 10.1016/j.phytochem.2012.06.023
CrossRef 		 
[NS]  Strblus asper
[mp]
[bp]
[α]D      - 45.2°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Astropaquinone C, ent-
C16H16O6 = 304
J. Nat. Prod.    2012, 75 , 1828
W.-L. Geng, X.-Y. Wang, T. Kurtán, A. Mándi, H. Tang, B. Schulz, P. Sun, W. Zhang
DOI: 10.1021/np300642t
CrossRef 		 
[NS]  Torula herbarum
[mp]
[bp]
[α]D      - 27°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Astropaquinone B, ent-
C17H18O6 = 318
J. Nat. Prod.    2012, 75 , 1828
W.-L. Geng, X.-Y. Wang, T. Kurtán, A. Mándi, H. Tang, B. Schulz, P. Sun, W. Zhang
DOI: 10.1021/np300642t
CrossRef 		 
[NS]  Torula herbarum
[mp]
[bp]
[α]D      - 45°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C18H12O6 = 324
Tetrahedron    2012, 68 , 8480
J. Kornsakulkarn, S. Saepua, K. Srichomthong, S. Supothina, C. Thongpanchang
DOI: 10.1016/j.tet.2012.07.059
CrossRef 		 
[NS]  Aschersonia coffeae
[mp]
[bp]
[α]D      - 301.4°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic activity
Aromatics
No Name
C18H14O6 = 326
Tetrahedron    2012, 68 , 8480
J. Kornsakulkarn, S. Saepua, K. Srichomthong, S. Supothina, C. Thongpanchang
DOI: 10.1016/j.tet.2012.07.059
CrossRef 		 
[NS]  Aschersonia coffeae
[mp]
[bp]
[α]D      - 219.2°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Engelheptanoxide A
C20H24O4 = 328
Phytochemistry    2012, 82 , 118
H.-C. Wu, M.-J. Cheng, C.-F. Peng, S.-C. Yang, H.-S. Chang, C.-H. Lin, C.-J. Wang, I.-S. Chen
DOI: 10.1016/j.phytochem.2012.06.014
CrossRef 		 
[NS]  Engelhardia roxburghiana
[mp]
[bp]
[α]D      - 66.9°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Empetrifrazinan A
C20H26O4 = 330
J. Nat. Prod.    2012, 75 , 1697
S. Schmidt, G. Jürgenliemk, T. J. Schmidt, H. Skaltsa, J. Heilmann
DOI: 10.1021/np300237n
CrossRef 		 
[NS]  Hypericum empetrifolium
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Empetrifrazinan B
C20H26O4 = 330
J. Nat. Prod.    2012, 75 , 1697
S. Schmidt, G. Jürgenliemk, T. J. Schmidt, H. Skaltsa, J. Heilmann
DOI: 10.1021/np300237n
CrossRef 		 
[NS]  Hypericum empetrifolium
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Empetrikarinen A
C20H26O4 = 330
J. Nat. Prod.    2012, 75 , 1697
S. Schmidt, G. Jürgenliemk, T. J. Schmidt, H. Skaltsa, J. Heilmann
DOI: 10.1021/np300237n
CrossRef 		 
[NS]  Hypericum empetrifolium
[mp]
[bp]
[α]D      + 34°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Engelhardiol B
C19H22O5 = 330
Phytochemistry    2012, 82 , 118
H.-C. Wu, M.-J. Cheng, C.-F. Peng, S.-C. Yang, H.-S. Chang, C.-H. Lin, C.-J. Wang, I.-S. Chen
DOI: 10.1016/j.phytochem.2012.06.014
CrossRef 		 
[NS]  Engelhardia roxburghiana
[mp]122 - 124 ℃
[bp]
[α]D      + 186.9°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antitubercular activity
Aromatics
Empetriferdinan A
C20H28O4 = 332
J. Nat. Prod.    2012, 75 , 1697
S. Schmidt, G. Jürgenliemk, T. J. Schmidt, H. Skaltsa, J. Heilmann
DOI: 10.1021/np300237n
CrossRef 		 
[NS]  Hypericum empetrifolium
[mp]
[bp]
[α]D      + 40°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C18H12O7 = 340
Tetrahedron    2012, 68 , 8480
J. Kornsakulkarn, S. Saepua, K. Srichomthong, S. Supothina, C. Thongpanchang
DOI: 10.1016/j.tet.2012.07.059
CrossRef 		 
[NS]  Aschersonia coffeae
[mp]
[bp]
[α]D      - 360.5°     [ Acetone ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antimalarial activity and cytotoxic activity
Aromatics
No Name
C18H12O7 = 340
Tetrahedron    2012, 68 , 8480
J. Kornsakulkarn, S. Saepua, K. Srichomthong, S. Supothina, C. Thongpanchang
DOI: 10.1016/j.tet.2012.07.059
CrossRef 		 
[NS]  Aschersonia coffeae
[mp]
[bp]
[α]D      - 235.5°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C20H20O5 = 340
Phytochemistry    2012, 82 , 136
H. Sasaki, Y. Kashiwada, H. Shibata, Y. Takaishi
DOI: 10.1016/j.phytochem.2012.06.007
CrossRef 		 
[NS]  Desmodium caudatum
[mp]
[bp]
[α]D      - 71.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]anti-MRSA activity
Aromatics
Empetrifrazinan C
C21H28O4 = 344
J. Nat. Prod.    2012, 75 , 1697
S. Schmidt, G. Jürgenliemk, T. J. Schmidt, H. Skaltsa, J. Heilmann
DOI: 10.1021/np300237n
CrossRef 		 
[NS]  Hypericum empetrifolium
[mp]
[bp]
[α]D      - 48°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Empetrikarinen B
C21H28O4 = 344
J. Nat. Prod.    2012, 75 , 1697
S. Schmidt, G. Jürgenliemk, T. J. Schmidt, H. Skaltsa, J. Heilmann
DOI: 10.1021/np300237n
CrossRef 		 
[NS]  Hypericum empetrifolium
[mp]
[bp]
[α]D      - 8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Engelhardiol A
C20H24O5 = 344
Phytochemistry    2012, 82 , 118
H.-C. Wu, M.-J. Cheng, C.-F. Peng, S.-C. Yang, H.-S. Chang, C.-H. Lin, C.-J. Wang, I.-S. Chen
DOI: 10.1016/j.phytochem.2012.06.014
CrossRef 		 
[NS]  Engelhardia roxburghiana
[mp]
[bp]
[α]D      0°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antitubercular activity
Aromatics
Engelheptanoxide C
C20H24O5 = 344
Phytochemistry    2012, 82 , 118
H.-C. Wu, M.-J. Cheng, C.-F. Peng, S.-C. Yang, H.-S. Chang, C.-H. Lin, C.-J. Wang, I.-S. Chen
DOI: 10.1016/j.phytochem.2012.06.014
CrossRef 		 
[NS]  Engelhardia roxburghiana
[mp]
[bp]
[α]D      - 7.44°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Empetriferdinan B
C21H30O4 = 346
J. Nat. Prod.    2012, 75 , 1697
S. Schmidt, G. Jürgenliemk, T. J. Schmidt, H. Skaltsa, J. Heilmann
DOI: 10.1021/np300237n
CrossRef 		 
[NS]  Hypericum empetrifolium
[mp]
[bp]
[α]D      + 44°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C17H14O8 = 346
Tetrahedron    2012, 68 , 8480
J. Kornsakulkarn, S. Saepua, K. Srichomthong, S. Supothina, C. Thongpanchang
DOI: 10.1016/j.tet.2012.07.059
CrossRef 		 
[NS]  Aschersonia coffeae
[mp]
[bp]
[α]D      - 133.2°     [ acetone ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic activity
Aromatics
Empetrikarinol A
C20H28O5 = 348
J. Nat. Prod.    2012, 75 , 1697
S. Schmidt, G. Jürgenliemk, T. J. Schmidt, H. Skaltsa, J. Heilmann
DOI: 10.1021/np300237n
CrossRef 		 
[NS]  Hypericum empetrifolium
[mp]
[bp]
[α]D      - 24°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Engelheptanoxide B
C20H22O6 = 358
Phytochemistry    2012, 82 , 118
H.-C. Wu, M.-J. Cheng, C.-F. Peng, S.-C. Yang, H.-S. Chang, C.-H. Lin, C.-J. Wang, I.-S. Chen
DOI: 10.1016/j.phytochem.2012.06.014
CrossRef 		 
[NS]  Engelhardia roxburghiana
[mp]
[bp]
[α]D      + 82.7°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Rubrolide E, 3’-Bromo-
C17H11O4Br = 359
J. Nat. Prod.    2012, 75 , 1824
J. Sikorska, S. Parker-Nance, M. T. Davies-Coleman, O. B. Vining, A. E. Sikora, K. L. McPhail
DOI: 10.1021/np300580z
CrossRef 		 
[NS]  Synoicum globosum
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antibacterial activity
  176 data found. 1 - 30 listed Next Last   
   
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