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

Polyketides

Coriapentocin A

C35H64O8 = 612

Helv. Chim. Acta 2014, 97, 1469

T. da C. Alves, M. R. S. Gonçalves, F. C. S. Correia, V. C. da Silva, P. T. de Sousa Jr., M. G. de Carvalho, R. Braz-Filho, E. L. Dall’Oglio

DOI: 10.1002/hlca.201400034

CrossRef

[	NS	]	Annona coriacea
[	mp	]
[	bp	]
[	α	] D
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Polyketides

Coriapentocin B

C35H64O8 = 612

Helv. Chim. Acta 2014, 97, 1469

T. da C. Alves, M. R. S. Gonçalves, F. C. S. Correia, V. C. da Silva, P. T. de Sousa Jr., M. G. de Carvalho, R. Braz-Filho, E. L. Dall’Oglio

DOI: 10.1002/hlca.201400034

CrossRef

[	NS	]	Annona coriacea
[	mp	]
[	bp	]
[	α	] D
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Aromatics

No Name

C23H24O11 = 476

Helv. Chim. Acta 2014, 97, 1516

C. Zhang, Y.-M. Wang, F.-C. Zhao, L.-M. Chen, Q.-W. Zhang, H.-M. Gao, Z.-M. Wang

DOI: 10.1002/hlca.201400013

CrossRef

[	NS	]	Sophora flavescens
[	mp	]
[	bp	]
[	α	] D	– 12   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Aromatics

No Name

C27H30O14 = 578

Helv. Chim. Acta 2014, 97, 1516

C. Zhang, Y.-M. Wang, F.-C. Zhao, L.-M. Chen, Q.-W. Zhang, H.-M. Gao, Z.-M. Wang

DOI: 10.1002/hlca.201400013

CrossRef

[	NS	]	Sophora flavescens
[	mp	]
[	bp	]
[	α	] D	– 126   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Aromatics

Liacifloroside

C36H36O20 = 788

Helv. Chim. Acta 2014, 97, 1571

H. Kırmızıbekmez, H. Bardakcı, M. Masullo, Ö. Kamburoğlu, G. Eryılmaz, G. Akaydın, E. Yeşilada, S. Piacente

DOI: 10.1002/hlca.201400065

CrossRef

[	NS	]	Asperula lilaciflora
[	mp	]
[	bp	]
[	α	] D	+ 11.3   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Asperulogenin

C10H12O4 = 196

Helv. Chim. Acta 2014, 97, 1571

H. Kırmızıbekmez, H. Bardakcı, M. Masullo, Ö. Kamburoğlu, G. Eryılmaz, G. Akaydın, E. Yeşilada, S. Piacente

DOI: 10.1002/hlca.201400065

CrossRef

[	NS	]	Asperula lilaciflora
[	mp	]
[	bp	]
[	α	] D	+ 10.4   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Rhizomucronol A

C20H32O4 = 336

Helv. Chim. Acta 2014, 97, 1531

A. Madhu, A. S. C. V. A. Rao, S. Sushma, P. M. Gowri, T. V. Raju

DOI: 10.1002/hlca.201400022

CrossRef

[	NS	]	Rhizophora mucronata
[	mp	]
[	bp	]
[	α	] D	– 125   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Rhizomucronol B

C20H32O4 = 336

Helv. Chim. Acta 2014, 97, 1531

A. Madhu, A. S. C. V. A. Rao, S. Sushma, P. M. Gowri, T. V. Raju

DOI: 10.1002/hlca.201400022

CrossRef

[	NS	]	Rhizophora mucronata
[	mp	]
[	bp	]
[	α	] D	– 105   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Kuguacin U

C25H36O5 = 416

Helv. Chim. Acta 2014, 97, 1546

J.-C. Chen, X.-X. Yuan, L. Zhou, J.-Q. Liu, Y. Nian, Z.-R. Li, Y. Li, M.-J. Xie, M.-H. Qiu

DOI: 10.1002/hlca.201400051

CrossRef

[	NS	]	Momordica charantia
[	mp	]	295 - 296 ℃
[	bp	]
[	α	] D	+ 14.8   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Kuguacin V

C30H46O4 = 470

Helv. Chim. Acta 2014, 97, 1546

J.-C. Chen, X.-X. Yuan, L. Zhou, J.-Q. Liu, Y. Nian, Z.-R. Li, Y. Li, M.-J. Xie, M.-H. Qiu

DOI: 10.1002/hlca.201400051

CrossRef

[	NS	]	Momordica charantia
[	mp	]
[	bp	]
[	α	] D	– 26.6   [ Py. ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Kuguacin W

C30H46O4 = 470

Helv. Chim. Acta 2014, 97, 1546

J.-C. Chen, X.-X. Yuan, L. Zhou, J.-Q. Liu, Y. Nian, Z.-R. Li, Y. Li, M.-J. Xie, M.-H. Qiu

DOI: 10.1002/hlca.201400051

CrossRef

[	NS	]	Momordica charantia
[	mp	]	113 - 115 ℃
[	bp	]
[	α	] D	– 15.7   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Kuguacin T

C30H46O5 = 486

Helv. Chim. Acta 2014, 97, 1546

J.-C. Chen, X.-X. Yuan, L. Zhou, J.-Q. Liu, Y. Nian, Z.-R. Li, Y. Li, M.-J. Xie, M.-H. Qiu

DOI: 10.1002/hlca.201400051

CrossRef

[	NS	]	Momordica charantia
[	mp	]	193 - 195 ℃
[	bp	]
[	α	] D	+ 1.1   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Alkaloids

Evollionine C

C16H19NO3 = 273

Helv. Chim. Acta 2014, 97, 1481

Y.-H. Li, J. He, Y. Li, X.-D. Wu, L.-Y. Peng, R.-N. Du, X. Cheng, Q.-S. Zhao, R.-T. Li

DOI: 10.1002/hlca.201300449

CrossRef

[	NS	]	Evodia rutaecarpa
[	mp	]
[	bp	]
[	α	] D	– 5.26   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Alkaloids

Evollionine A

C19H15N3O2 = 317

Helv. Chim. Acta 2014, 97, 1481

Y.-H. Li, J. He, Y. Li, X.-D. Wu, L.-Y. Peng, R.-N. Du, X. Cheng, Q.-S. Zhao, R.-T. Li

DOI: 10.1002/hlca.201300449

CrossRef

[	NS	]	Evodia rutaecarpa
[	mp	]	167.9 - 169.2 ℃
[	bp	]
[	α	] D	– 6.4   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Alkaloids

Evollionine B

C20H19N3O5 = 381

Helv. Chim. Acta 2014, 97, 1481

Y.-H. Li, J. He, Y. Li, X.-D. Wu, L.-Y. Peng, R.-N. Du, X. Cheng, Q.-S. Zhao, R.-T. Li

DOI: 10.1002/hlca.201300449

CrossRef

[	NS	]	Evodia rutaecarpa
[	mp	]
[	bp	]
[	α	] D
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Miscellaneous

MKN-349A, 5,5’-Epoxy-

C22H34N4O5 = 434

Helv. Chim. Acta 2014, 97, 1564

Z.-F. Zhou, X.-H. Yang, H.-L. Liu, Y.-C. Gu, B.-P. Ye, Y.-W. Guo

DOI: 10.1002/hlca.201400062

CrossRef

[	NS	]	Penicillium species GD6
[	mp	]
[	bp	]
[	α	] D	– 62.8   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

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