|
Heterocycles Database
Natural Products with Heterocyclic Ring System |
 |
| |
| 1975-2013 |
| 58,387 Compounds |
|
25 April, 2012 |
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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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| 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
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
|
|
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| 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 Journal : | Vol. | No. | | 59 | 9 | | | 26 | | 94 | 9 | | 83 | 9 | | 54 | 17 | | 74 | 9 | | 13 | 17, 18 | | 77 | 13, 14 | | 67 | 35, 36, 37, 38, 39 | | 52 | 36, 39 |  |  |  |
|  |  |  |
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| 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 | ] | |
|
|
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| 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 |
|
|
|
|
|