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

Cart

Login / Registration

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

Pyrenocine N

C10H12O4 = 196

J. Antibiot. 2014, 67, 791

Z. Yang, L. Bao, Y. Yin, G. Ding, M. Ge, D. Chen, X. Qian

DOI: 10.1038/ja.2014.59

CrossRef

[	NS	]	Colletotrichum species HCCB03289
[	mp	]
[	bp	]
[	α	] D	+ 28.2   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Polyketides

Pyrenocine O

C10H12O4 = 196

J. Antibiot. 2014, 67, 791

Z. Yang, L. Bao, Y. Yin, G. Ding, M. Ge, D. Chen, X. Qian

DOI: 10.1038/ja.2014.59

CrossRef

[	NS	]	Colletotrichum species HCCB03289
[	mp	]
[	bp	]
[	α	] D	+ 63.0   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Polyketides

Aspergillusol A

C12H12O5 = 236

J. Nat. Prod. 2014, 77, 2375

V. Rukachaisirikul, N. Rungsaiwattana, S. Klaiklay, S. Phongpaichit, K. Borwornwiriyapan, J. Sakayaroj

DOI: 10.1021/np500324b

CrossRef

[	NS	]	Aspergillus species PSU-RSPG185
[	mp	]
[	bp	]
[	α	] D	- 4.6   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Polyketides

Aspergillusol B

C12H12O5 = 236

J. Nat. Prod. 2014, 77, 2375

V. Rukachaisirikul, N. Rungsaiwattana, S. Klaiklay, S. Phongpaichit, K. Borwornwiriyapan, J. Sakayaroj

DOI: 10.1021/np500324b

CrossRef

[	NS	]	Aspergillus species PSU-RSPG185
[	mp	]
[	bp	]
[	α	] D
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Polyketides

No Name

C12H14O5 = 238

Tetrahedron Lett. 2014, 55, 6530

D.-B. Hu, W.-X. Li, Z.-Z. Zhao, T. Feng, R.-H. Yin, Z.-H. Li, J.-K. Liu, H.-J. Zhu

DOI: 10.1016/j.tetlet.2014.09.132

CrossRef

[	NS	]	Junghuhnianitida
[	mp	]
[	bp	]
[	α	] D	– 8.3   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Polyketides

No Name

C13H16O5 = 252

Tetrahedron Lett. 2014, 55, 6530

D.-B. Hu, W.-X. Li, Z.-Z. Zhao, T. Feng, R.-H. Yin, Z.-H. Li, J.-K. Liu, H.-J. Zhu

DOI: 10.1016/j.tetlet.2014.09.132

CrossRef

[	NS	]	Junghuhnianitida
[	mp	]
[	bp	]
[	α	] D	– 7.6   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Polyketides

Cryptolactone A1

C18H30O4 = 310

J. Nat. Prod. 2014, 77, 2459

M. Horikawa, M. Inai, Y. Oguri, E. Kuroda, M. Tanaka, S. Suzuki, T. Ito, S Takahashi, H. Kaku, T. Tsunoda

DOI: 10.1021/np500542x

CrossRef

[	NS	]	Cryptomyzus species
[	mp	]
[	bp	]
[	α	] D	- 53.5   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity

Polyketides

Cryptolactone A2

C18H30O4 = 310

J. Nat. Prod. 2014, 77, 2459

M. Horikawa, M. Inai, Y. Oguri, E. Kuroda, M. Tanaka, S. Suzuki, T. Ito, S Takahashi, H. Kaku, T. Tsunoda

DOI: 10.1021/np500542x

CrossRef

[	NS	]	Cryptomyzus species
[	mp	]
[	bp	]
[	α	] D	- 44.1   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity

Polyketides

Cryptolactone B1

C20H34O4 = 338

J. Nat. Prod. 2014, 77, 2459

M. Horikawa, M. Inai, Y. Oguri, E. Kuroda, M. Tanaka, S. Suzuki, T. Ito, S Takahashi, H. Kaku, T. Tsunoda

DOI: 10.1021/np500542x

CrossRef

[	NS	]	Cryptomyzus species
[	mp	]
[	bp	]
[	α	] D	- 46.1   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity

Polyketides

Cryptolactone B2

C20H34O4 = 338

J. Nat. Prod. 2014, 77, 2459

M. Horikawa, M. Inai, Y. Oguri, E. Kuroda, M. Tanaka, S. Suzuki, T. Ito, S Takahashi, H. Kaku, T. Tsunoda

DOI: 10.1021/np500542x

CrossRef

[	NS	]	Cryptomyzus species
[	mp	]
[	bp	]
[	α	] D
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity

Polyketides

Borrelidin B

C28H47NO6 = 493

J. Nat. Prod. 2014, 77, 2570

C. J. Schulze, W. M. Bray, F. Loganzo, M.-H. Lam, T. Szal, A. Villalobos, F. E. Koehn, R. G. Linington

DOI: 10.1021/np500727g

CrossRef

[	NS	]	Streptomyces species
[	mp	]
[	bp	]
[	α	] D	+ 26.2   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	growth inhibit activity

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	]

Polyketides

Azaspiracid-33

C41H65NO9 = 715

J. Nat. Prod. 2014, 77, 2465

J. Kilcoyne, C. Nulty, T. Jauffrais, P. McCarron, F. Herve, B. Foley, F. Rise, S. Crain, A. L. Wilkins, M. J. Twiner, P. Hess, C. O. Miles

DOI: 10.1021/np500555k

CrossRef

[	NS	]	Azadinium spinosum
[	mp	]
[	bp	]
[	α	] D
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity

Polyketides

Azaspiracid-34

C45H69NO12 = 815

J. Nat. Prod. 2014, 77, 2465

J. Kilcoyne, C. Nulty, T. Jauffrais, P. McCarron, F. Herve, B. Foley, F. Rise, S. Crain, A. L. Wilkins, M. J. Twiner, P. Hess, C. O. Miles

DOI: 10.1021/np500555k

CrossRef

[	NS	]	Azadinium spinosum
[	mp	]
[	bp	]
[	α	] D
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity

Polyketides

Brevisulcatic Acid-4

C49H70O15 = 898

Org. Lett. 2014, 16, 5850

R. Suzuki, R. Irie, Y. Harntaweesup, K. Tachibana, P. T. Holland, D. T. Harwood, F. Shi, V. Beuzenberg, Y. Itoh, S. Pascal, P. J. B. Edwards, M. Satake

DOI: 10.1021/ol502700h

CrossRef

[	NS	]	Karenia brevisulcata
[	mp	]
[	bp	]
[	α	] D	+ 3.0   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Polyketides

Brevisulcatic Acid-1

C49H72O16 = 916

Org. Lett. 2014, 16, 5850

R. Suzuki, R. Irie, Y. Harntaweesup, K. Tachibana, P. T. Holland, D. T. Harwood, F. Shi, V. Beuzenberg, Y. Itoh, S. Pascal, P. J. B. Edwards, M. Satake

DOI: 10.1021/ol502700h

CrossRef

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

Polyketides

Amdigenol G

C60H101O25NaS = 1276

Tetrahedron Lett. 2014, 55, 6319

T. Inuzuka, K. Yamada, D. Uemura

DOI: 10.1016/j.tetlet.2014.09.094

CrossRef

[	NS	]	Amphidinium species
[	mp	]
[	bp	]
[	α	] D	– 5.3   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	inhibitory activity against N-type Ca2+ channel-opening

Polyketides

Amdigenol E

C82H137O37NaS = 1768

Tetrahedron Lett. 2014, 55, 6319

T. Inuzuka, K. Yamada, D. Uemura

DOI: 10.1016/j.tetlet.2014.09.094

CrossRef

[	NS	]	Amphidinium species
[	mp	]
[	bp	]
[	α	] D	– 6.4   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	inhibitory activity against N-type Ca2+ channel-opening

• Home / Prepress
  • Prepress / Regular & Special Issues
  • Prepress / Regular Issue
  • Prepress / Special Issue
• e-Journal
  • Current Regular Issue
  • Current Special Issue No.1
  • Most Cited Articles
  • Sample Issue
  • List of Special Issues
• Natural Products Database
  • Structure
  • Synthesis
• Authors & Referees
  • Info. for Authors
  • Info. for Referees
• about Heterocycles
  • Aims & Scope / Editors
  • Preface to Heterocycles
  • Kametani Award
  • Heterocycles Award
  • Privacy Statement
  • Sample Issue
  • Subscription Info.
• other Information
  • Privacy Statement
  • Announcement of Archives
• Contact us:
  • editorial@heterocycles.com

The Japan Institute of Heterocyclic Chemistry Publications is a partner of :   
Copyright ⓒ 2023 The Japan Institute of Heterocyclic Chemistry