HETEROCYCLES

An International Journal for Reviews and Communications in Heterocyclic Chemistry
Web Edition ISSN: 1881-0942
Published online by The Japan Institute of Heterocyclic Chemistry

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Search65,753 Compounds

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

Journal:

This database lists the natural products with heterocyclic ring system whose synthesis 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:
Kunio Ogasawara

Associate Editors:
Toshio Honda
Yoshiharu Iwabuchi

This journal will list the new natural products with a heterocyclic ring system, collected from current chemical literature, whose structure has been established.

• Search by Group: AllPolyketidesAromaticsTerpenesSteroidsAlkaloidsAntibioticsMiscellaneous
• Search by Journal: Chem. Pharm. Bull.Helv. Chim. ActaHeterocyclesJ. Antibiot.J. Nat. Prod.J. Org. Chem.Org. Biomol. Chem.Org. Lett.Phytochem. Lett.PhytochemistryPlanta medicaTetrahedronTetrahedron Lett.
• Year: 2014201420142014201420142014201420142014201420142014
• Vol: 6297896777791216107107807055
• No: 11111111112143, 4421, 22  1744-4745-48

Aromatics

Linderuca C

C32H36O10 = 580

Chem. Pharm. Bull. 2014, 62, 1136

K. H. Kim, E. Moon, S. K. Ha, W. S. Suh, H. K. Kim, S. Y. Kim, S. U. Choi, K. R. Lee

DOI: 10.1248/cpb.c14-00381

CrossRef

[	NS	]	Lindera glauca
[	mp	]
[	bp	]
[	α	] D	+ 23.4   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	antiproliferative activity and NO production inhibitory activity

Aromatics

Linderuca A

C33H38O11 = 610

Chem. Pharm. Bull. 2014, 62, 1136

K. H. Kim, E. Moon, S. K. Ha, W. S. Suh, H. K. Kim, S. Y. Kim, S. U. Choi, K. R. Lee

DOI: 10.1248/cpb.c14-00381

CrossRef

[	NS	]	Lindera glauca
[	mp	]
[	bp	]
[	α	] D	+ 37.2   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	antiproliferative activity and NO production inhibitory activity

Aromatics

Linderuca B

C33H38O11 = 610

Chem. Pharm. Bull. 2014, 62, 1136

K. H. Kim, E. Moon, S. K. Ha, W. S. Suh, H. K. Kim, S. Y. Kim, S. U. Choi, K. R. Lee

DOI: 10.1248/cpb.c14-00381

CrossRef

[	NS	]	Lindera glauca
[	mp	]
[	bp	]
[	α	] D	+ 42.3   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	antiproliferative activity and NO production inhibitory activity

Terpenes

Heterophyllin C, Hydroperoxy-

C17H22O7 = 338

Chem. Pharm. Bull. 2014, 62, 1092

Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori

DOI: 10.1248/cpb.c14-00426

CrossRef

[	NS	]	Eupatorium heterophyllum
[	mp	]
[	bp	]
[	α	] D	- 14.5   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Heterophyllin A, Keto-

C20H24O7 = 376

Chem. Pharm. Bull. 2014, 62, 1092

Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori

DOI: 10.1248/cpb.c14-00426

CrossRef

[	NS	]	Eupatorium heterophyllum
[	mp	]
[	bp	]
[	α	] D	+ 109.9   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Heterophyllin H, Hydroperoxy-

C22H28O8 = 420

Chem. Pharm. Bull. 2014, 62, 1092

Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori

DOI: 10.1248/cpb.c14-00426

CrossRef

[	NS	]	Eupatorium heterophyllum
[	mp	]
[	bp	]
[	α	] D	- 33.2   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Heterophyllin B, Hydroperoxy-

C22H28O9 = 436

Chem. Pharm. Bull. 2014, 62, 1092

Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori

DOI: 10.1248/cpb.c14-00426

CrossRef

[	NS	]	Eupatorium heterophyllum
[	mp	]
[	bp	]
[	α	] D	- 13.8   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Heterophyllin A, Hydroperoxy-

C22H28O10 = 452

Chem. Pharm. Bull. 2014, 62, 1092

Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori

DOI: 10.1248/cpb.c14-00426

CrossRef

[	NS	]	Eupatorium heterophyllum
[	mp	]
[	bp	]
[	α	] D	- 19.9   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Heterophyllin E, Hydroperoxy-

C24H30O10 = 478

Chem. Pharm. Bull. 2014, 62, 1092

Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori

DOI: 10.1248/cpb.c14-00426

CrossRef

[	NS	]	Eupatorium heterophyllum
[	mp	]
[	bp	]
[	α	] D	- 62.0   [ EtOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Heterophyllin G, Hydroperoxy-

C24H30O10 = 478

Chem. Pharm. Bull. 2014, 62, 1092

Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori

DOI: 10.1248/cpb.c14-00426

CrossRef

[	NS	]	Eupatorium heterophyllum
[	mp	]
[	bp	]
[	α	] D	+ 5.6   [ EtOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Heterophyllin D, Hydroperoxy-

C24H30O11 = 494

Chem. Pharm. Bull. 2014, 62, 1092

Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori

DOI: 10.1248/cpb.c14-00426

CrossRef

[	NS	]	Eupatorium heterophyllum
[	mp	]
[	bp	]
[	α	] D	- 6.9   [ EtOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Heterophyllin F, Hydroperoxy-

C24H30O11 = 494

Chem. Pharm. Bull. 2014, 62, 1092

Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori

DOI: 10.1248/cpb.c14-00426

CrossRef

[	NS	]	Eupatorium heterophyllum
[	mp	]
[	bp	]
[	α	] D	- 17.2   [ EtOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Miscellaneous

Onionin A2

C9H16O2S2 = 220

Chem. Pharm. Bull. 2014, 62, 1141

T. Nohara, Y. Fujiwara, R. Kudo, K. Yamaguchi, T. Ikeda, K. Murakami, M. Ono, T. Kajimoto, M. Takeya

DOI: 10.1248/cpb.c14-00461

CrossRef

[	NS	]	Allium cepa and Aliium fistulosum
[	mp	]
[	bp	]
[	α	] D	+ 16.0   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Miscellaneous

Onionin A3

C9H16O2S2 = 220

Chem. Pharm. Bull. 2014, 62, 1141

T. Nohara, Y. Fujiwara, R. Kudo, K. Yamaguchi, T. Ikeda, K. Murakami, M. Ono, T. Kajimoto, M. Takeya

DOI: 10.1248/cpb.c14-00461

CrossRef

[	NS	]	Allium cepa and Aliium fistulosum
[	mp	]
[	bp	]
[	α	] D	+ 12.5   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

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