Heterocycles Database
Natural Products with
Heterocyclic Ring System
 
 1975-2010
 54,726 Compounds
 26 July, 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
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.
 
26 July, 2010
Search by Group:
Polyketides
Aromatics
Terpenes
Steroids
Alkaloids
Antibiotics
Miscellaneous
 
All
 
Search by Journal :
Vol.
No.
Chem. Pharm. Bull.
58
1
Helv. Chim. Acta
93
1
Heterocycles
81
2
J. Nat. Prod.
73
1
J. Org. Chem.
75
1
Phytochemistry
71
1
Planta medica
76
1,2
Tetrahedron
66
1,3,4
Tetrahedron Lett.
51
2.4
  123 data found. 1 - 30 listed Next Last   

Polyketides
Vibralactone D
C12H18O3 = 210
Chem. Pharm. Bull.    2010, 58 , 113
M.-Y. Jiang, L. Zhang, Z.-J. Dong, Z.-L. Yang, Y. Leng, J.-K. Liu
DOI: 10.1248/cpb.58.113
CrossRef 		 
[NS]  Boreostereum vibrans
[mp]131 - 132 ℃
[bp]
[α]D      + 24.2°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibition against isozymes of HSD
Polyketides
Authdiol, 7-Epi-
C12H12O5 = 236
Planta medica    2010, 76 , 185
F. Liu, X.-L. Cai, H. Yang, X.-K. Xia, Z.-Y. Guo, J. Yuan, M.-F. Li, Z.-G. She, Y.-C. Lin
DOI: 10.1055/s-0029-1186047
CrossRef 		 
[NS]  Talaromyces species ZH-154
[mp]174 - 176 ℃
[bp]
[α]D      + 116.5°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Polyketides
Authdiol, 8-O-Methyl-7-epi-
C13H14O5 = 250
Planta medica    2010, 76 , 185
F. Liu, X.-L. Cai, H. Yang, X.-K. Xia, Z.-Y. Guo, J. Yuan, M.-F. Li, Z.-G. She, Y.-C. Lin
DOI: 10.1055/s-0029-1186047
CrossRef 		 
[NS]  Talaromyces sp. ZH-154
[mp]160 - 161 ℃
[bp]
[α]D      + 115.5°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Polyketides
Epoxydine B
C12H12O7 = 268
Helv. Chim. Acta    2010, 93 , 169
S. Qin, H. Hussain, B. Schulz, S. Draeger, K. Krohn
DOI: 10.1002/hlca.200900199
CrossRef 		 
[NS]  Phoma species
[mp]
[bp]
[α]D      - 72.7°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Furoaespitanelactol, (10S)-10-O-Methyl-
C13H18O3BrCl = 336.5
J. Nat. Prod.    2010, 73 , 27
C. Lhullier, M. Falkenberg, E. Ioannou, A. Quesada, P. Papazafiri, P. A. Horta, E. P. Schenkel, C. Vagias, V. Roussis
DOI: 10.1021/np900627r
CrossRef 		 
[NS]  Laurencia catarinensis
[mp]
[bp]
[α]D      + 61.3°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Polyketides
Furocaespitanelactol, (10R)-10-O-Methyl-
C13H18O3BrCl = 336.5
J. Nat. Prod.    2010, 73 , 27
C. Lhullier, M. Falkenberg, E. Ioannou, A. Quesada, P. Papazafiri, P. A. Horta, E. P. Schenkel, C. Vagias, V. Roussis
DOI: 10.1021/np900627r
CrossRef 		 
[NS]  Laurencia catarinensis
[mp]
[bp]
[α]D      + 14°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Polyketides
Stolonoxide E
C24H36O5 = 404
J. Nat. Prod.    2010, 73 , 83
F. Reyes, R. Rodríguez-Acebes, R. Fernández, S. Bueno, A. Francesch, C. Cuevas
DOI: 10.1021/np900700h
CrossRef 		 
[NS]  Stolonica socialis
[mp]
[bp]
[α]D      - 33.4°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Polyketides
Stolonoxide F
C24H36O5 = 404
J. Nat. Prod.    2010, 73 , 83
F. Reyes, R. Rodríguez-Acebes, R. Fernández, S. Bueno, A. Francesch, C. Cuevas
DOI: 10.1021/np900700h
CrossRef 		 
[NS]  Stolonica socialis
[mp]
[bp]
[α]D      + 18.5°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Polyketides
Peloruside B
C26H46O10 = 518
J. Org. Chem.    2010, 75 , 2
A. J. Singh, C.-X. Xu, X. Xu, L. M. West, A. Wilmes, A. Chan, E. Hamel, J. H. Miller, P. T. Northcote, A. K. Ghosh
DOI: 10.1021/jo9021265
CrossRef 		 
[NS]  Mycale hentscheli
[mp]
[bp]
[α]D      0°     [ CH2Cl2 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antitumor activity
Aromatics
No Name
C15H20O5 = 280
J. Nat. Prod.    2010, 73 , 75
R. Haritakun, M. Sappan, R. Suvannakad, K. Tasanathai, M. Isaka
DOI: 10.1021/np900520b
CrossRef 		 
[NS]  Ophiocordyceps communis
[mp]62 - 63 ℃
[bp]
[α]D      - 14°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
No Name
C16H22O5 = 294
J. Nat. Prod.    2010, 73 , 75
R. Haritakun, M. Sappan, R. Suvannakad, K. Tasanathai, M. Isaka
DOI: 10.1021/np900520b
CrossRef 		 
[NS]  Ophiocordyceps communis
[mp]
[bp]
[α]D      - 45°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Botryorhodine A
C16H12O6 = 300
Phytochemistry    2010, 71 , 110
R. Abdou, K. Scherlach, H.-M. Dahse, I. Sattler, C. Hertweck
DOI: 10.1016/j.phytochem.2009.09.024
CrossRef 		 
[NS]  Botryosphaeria rhodina
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Aromatics
Botryorhodine D
C16H14O6 = 302
Phytochemistry    2010, 71 , 110
R. Abdou, K. Scherlach, H.-M. Dahse, I. Sattler, C. Hertweck
DOI: 10.1016/j.phytochem.2009.09.024
CrossRef 		 
[NS]  Botryosphaeria rhodina
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Botryorhodine B
C17H14O6 = 314
Phytochemistry    2010, 71 , 110
R. Abdou, K. Scherlach, H.-M. Dahse, I. Sattler, C. Hertweck
DOI: 10.1016/j.phytochem.2009.09.024
CrossRef 		 
[NS]  Botryosphaeria rhodina
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Aromatics
Botryorhodine C
C17H16O6 = 316
Phytochemistry    2010, 71 , 110
R. Abdou, K. Scherlach, H.-M. Dahse, I. Sattler, C. Hertweck
DOI: 10.1016/j.phytochem.2009.09.024
CrossRef 		 
[NS]  Botryosphaeria rhodina
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Xestosaprol D
C20H18O4 = 322
Tetrahedron Lett.    2010, 51 , 751
N. Millán-Aguiñaga, I. E. Soria-Mercado, P. Williams
DOI: 10.1016/j.tetlet.2009.11.132
CrossRef 		 
[NS]  Xestospongia species
[mp]
[bp]
[α]D      + 18.8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Xestosaprol E
C20H18O4 = 322
Tetrahedron Lett.    2010, 51 , 751
N. Millán-Aguiñaga, I. E. Soria-Mercado, P. Williams
DOI: 10.1016/j.tetlet.2009.11.132
CrossRef 		 
[NS]  Xestospongia species
[mp]
[bp]
[α]D      - 2.4°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Hamigeromycin F
C20H26O7 = 378
Tetrahedron    2010, 66 , 955
M. Isaka, P. Chinthanom, S. Kongthong, S. Supothina, P. Ittiworapong
DOI: 10.1016/j.tet.2009.11.101
CrossRef 		 
[NS]  Hamigera avellanea BCC 17816
[mp]
[bp]
[α]D      + 41°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Hamigeromycin G
C20H26O7 = 378
Tetrahedron    2010, 66 , 955
M. Isaka, P. Chinthanom, S. Kongfhong, S. Supothina, P. Ittiworapong
DOI: 10.1016/j.tet.2009.11.101
CrossRef 		 
[NS]  Hamigera avellanea BCC 17816
[mp]
[bp]
[α]D      + 17°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Citrumedin B
C24H28O4 = 380
Chem. Pharm. Bull.    2010, 58 , 61
Y.-Y. Chan, C.-H. Li, Y.-C. Shen, T.-S. Wu
DOI: 10.1248/cpb.58.61
CrossRef 		 
[NS]  Citrus medica var. sarcodactylis SWINGLE
[mp]
[bp]
[α]D      + 14.4°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Hamigeromycin C
C20H26O8 = 394
Tetrahedron    2010, 66 , 955
M. Isaka, P. Chinthanom, S. Kongthong, S. Supothina, P. Ittiworapong
DOI: 10.1016/j.tet.2009.11.101
CrossRef 		 
[NS]  Hamigera avellanea BCC 17816
[mp]102 - 105 ℃
[bp]
[α]D      - 11°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Hamigeromycin D
C20H26O8 = 394
Tetrahedron    2010, 66 , 955
M. Isaka, P. Chinthanom, S. Kongthong, S. Supothina, P. Ittiworapong
DOI: 10.1016/j.tet.2009.11.101
CrossRef 		 
[NS]  Hamigera avellanea BCC 17816
[mp]115 - 117 ℃
[bp]
[α]D      + 24°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Hamigeromycin E
C20H26O8 = 394
Tetrahedron    2010, 66 , 955
M. Isaka, P. Chinthanom, S. Kongthong, S. Supothina, P. Ittiworapong
DOI: 10.1016/j.tet.2009.11.101
CrossRef 		 
[NS]  Hamigera avellanea BCC 17816
[mp]139 - 142 ℃
[bp]
[α]D      + 44°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Cleomiscosin A, 4’-O-Cinnamoyl-
C29H24O9 = 516
Phytochemistry    2010, 71 , 95
S. Cao, P. J. Brodie, M. Callmander, R. Randrianaivo, E. Rakotobe, V. E. Rasamison, D. G. I. Kingston
DOI: 10.1016/j.phytochem.2009.09.027
CrossRef 		 
[NS]  Terminalia tropophylla
[mp]
[bp]
[α]D      - 77°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Guttiferone I, Oxy-
C38H48O6 = 600
Tetrahedron    2010, 66 , 139
M. Masullo, C. Bassarello, G. Bifulco, S. Piacente
DOI: 10.1016/j.tet.2009.11.034
CrossRef 		 
[NS]  Garcinia cambogia
[mp]
[bp]
[α]D      + 23.8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Guttiferone K2, Oxy-
C38H48O6 = 600
Tetrahedron    2010, 66 , 139
M. Masullo, C. Bassarello, G. Bifulco, S. Piacente
DOI: 10.1016/j.tet.2009.11.034
CrossRef 		 
[NS]  Garcinia cambogia
[mp]
[bp]
[α]D      + 12.2°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Guttiferone M, Oxy-
C38H48O6 = 600
Tetrahedron    2010, 66 , 139
M. Masullo, C. Bassarello, G. Bifulco, S. Piacente
DOI: 10.1016/j.tet.2009.11.034
CrossRef 		 
[NS]  Garcinia cambogia
[mp]
[bp]
[α]D      - 96.2°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Aromatics
Sutherlandin D
C32H36O19 = 724
Planta medica    2010, 76 , 178
X. Fu, X.-C. Li, Y.-H. Wang, B. Avula, T. J. Smillie, W. Mabusela, J. Syce, Q. Johnson, W. Folk, L. A. Khan
DOI: 10.1055/s-0029-1186030
CrossRef 		 
[NS]  Sutherlandia frutescens
[mp]
[bp]
[α]D      - 77.1°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Terpenes
Platyphyllide, 9-Oxo-
C14H12O3 = 228
Planta medica    2010, 76 , 159
W.-J. Zhang, H.-Y. Qi, Y.-P. Shi
DOI: 10.1055/s-0029-1186036
CrossRef 		 
[NS]  Ligularia fischeri
[mp]118 - 120 ℃
[bp]
[α]D      - 60°     [ Acetone ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Terpenes
Daucoeudesmanolactone
C15H20O2 = 232
Helv. Chim. Acta    2010, 93 , 48
A. A. Sallam, Y. Hitotsuyanagi, E.-S. Mansour, A. F. Ahmed, S. Gedara, H. Fukuya, K. Takeya
DOI: 10.1002/hlca.200900126
CrossRef 		 
[NS]  Daucus glaber
[mp]137 - 138 ℃
[bp]
[α]D      + 60°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
  123 data found. 1 - 30 listed Next Last   
   
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