|
Heterocycles Database
Natural Products with Heterocyclic Ring System |
 |
| |
| 1975-2010 |
| 54,726 Compounds |
|
26 July, 2010 |
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Search by:
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Carbon:
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Molecular Fomula:
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Molecular Weight:
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Author:
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Journal:
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| |
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| Nomenclature : |
| |
| The natural products are listed under the name used in the original literature. |
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| The abbreviations : |
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| 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 Journal : | Vol. | No. | | 58 | 1 | | 93 | 1 | | 81 | 2 | | 73 | 1 | | 75 | 1 | | 71 | 1 | | 76 | 1,2 | | 66 | 1,3,4 | | 51 | 2.4 |  |  |  |
|  |  |  |
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| 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 | ] | |
|
|
|
|
|