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

Terpenes

Phyllaemblicin G3

C22H28O9 = 436

Org. Biomol. Chem. 2014, 12, 8764

J.-J. Lv, Y.-F. Wang, J.-M. Zhang, S. Yu, D. Wang, H.-T. Zhu, R.-R. Cheng, C.-R. Yang, M. Xu, Y.-J. Zhang

DOI: 10.1039/C4OB01196A

CrossRef

[	NS	]	Phyllanthus emblica
[	mp	]
[	bp	]
[	α	] D	+ 31.3   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Phyllaemblicin G4

C33H46O19 = 746

Org. Biomol. Chem. 2014, 12, 8764

J.-J. Lv, Y.-F. Wang, J.-M. Zhang, S. Yu, D. Wang, H.-T. Zhu, R.-R. Cheng, C.-R. Yang, M. Xu, Y.-J. Zhang

DOI: 10.1039/C4OB01196A

CrossRef

[	NS	]	Phyllanthus emblica
[	mp	]
[	bp	]
[	α	] D	+ 21.1   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Phyllaemblicin G5

C33H46O19 = 746

Org. Biomol. Chem. 2014, 12, 8764

J.-J. Lv, Y.-F. Wang, J.-M. Zhang, S. Yu, D. Wang, H.-T. Zhu, R.-R. Cheng, C.-R. Yang, M. Xu, Y.-J. Zhang

DOI: 10.1039/C4OB01196A

CrossRef

[	NS	]	Phyllanthus emblica
[	mp	]
[	bp	]
[	α	] D	+ 5.3   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Phyllaemblicin G1

C34H48O20 = 776

Org. Biomol. Chem. 2014, 12, 8764

J.-J. Lv, Y.-F. Wang, J.-M. Zhang, S. Yu, D. Wang, H.-T. Zhu, R.-R. Cheng, C.-R. Yang, M. Xu, Y.-J. Zhang

DOI: 10.1039/C4OB01196A

CrossRef

[	NS	]	Phyllanthus emblica
[	mp	]
[	bp	]
[	α	] D	+ 29.8   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Phyllaemblicin G2

C34H48O20 = 776

Org. Biomol. Chem. 2014, 12, 8764

J.-J. Lv, Y.-F. Wang, J.-M. Zhang, S. Yu, D. Wang, H.-T. Zhu, R.-R. Cheng, C.-R. Yang, M. Xu, Y.-J. Zhang

DOI: 10.1039/C4OB01196A

CrossRef

[	NS	]	Phyllanthus emblica
[	mp	]
[	bp	]
[	α	] D	- 24.9   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Terpenes

Phyllaemblicin G6

C54H68O27 = 1148

Org. Biomol. Chem. 2014, 12, 8764

J.-J. Lv, Y.-F. Wang, J.-M. Zhang, S. Yu, D. Wang, H.-T. Zhu, R.-R. Cheng, C.-R. Yang, M. Xu, Y.-J. Zhang

DOI: 10.1039/C4OB01196A

CrossRef

[	NS	]	Phyllanthus emblica
[	mp	]
[	bp	]
[	α	] D	+ 19.1   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	ant-HBV activity

Terpenes

Phyllaemblicin G7

C54H66O28 = 1162

Org. Biomol. Chem. 2014, 12, 8764

J.-J. Lv, Y.-F. Wang, J.-M. Zhang, S. Yu, D. Wang, H.-T. Zhu, R.-R. Cheng, C.-R. Yang, M. Xu, Y.-J. Zhang

DOI: 10.1039/C4OB01196A

CrossRef

[	NS	]	Phyllanthus emblica
[	mp	]
[	bp	]
[	α	] D	+ 5.7   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	ant-HBV activity

Terpenes

Phyllaemblicin G8

C54H66O28 = 1162

Org. Biomol. Chem. 2014, 12, 8764

J.-J. Lv, Y.-F. Wang, J.-M. Zhang, S. Yu, D. Wang, H.-T. Zhu, R.-R. Cheng, C.-R. Yang, M. Xu, Y.-J. Zhang

DOI: 10.1039/C4OB01196A

CrossRef

[	NS	]	Phyllanthus emblica
[	mp	]
[	bp	]
[	α	] D	+ 6.0   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	ant-HBV activity

Steroids

3-O-Urarigenin Lactate, (2’R)-

C26H38O6 = 446

Org. Biomol. Chem. 2014, 12, 8919

R.-R. Zhang, H.-Y. Tian, Y.-F. Tan, T.-Y. Chung, X.-H. Sun, X. Xia, W.-C. Ye, D. A. Middleton, N. Fedosova, M. Esmann, J. T. C. Tzen, R.-W. Jiang

DOI: 10.1039/C4OB01545B

CrossRef

[	NS	]	Asclepias curassavica
[	mp	]
[	bp	]
[	α	] D	- 67   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	inhibitory activity against DU145 prostate cancer cells

Steroids

3-O-Urarigenin Lactate, (2’S)-

C26H38O6 = 446

Org. Biomol. Chem. 2014, 12, 8919

R.-R. Zhang, H.-Y. Tian, Y.-F. Tan, T.-Y. Chung, X.-H. Sun, X. Xia, W.-C. Ye, D. A. Middleton, N. Fedosova, M. Esmann, J. T. C. Tzen, R.-W. Jiang

DOI: 10.1039/C4OB01545B

CrossRef

[	NS	]	Asclepias curassavica
[	mp	]
[	bp	]
[	α	] D	- 49   [ CHCl3 ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	inhibitory activity against DU145 prostate cancer cells

Steroids

19-O-Coroglaucigenin Lactate

C26H38O7 = 462

Org. Biomol. Chem. 2014, 12, 8919

R.-R. Zhang, H.-Y. Tian, Y.-F. Tan, T.-Y. Chung, X.-H. Sun, X. Xia, W.-C. Ye, D. A. Middleton, N. Fedosova, M. Esmann, J. T. C. Tzen, R.-W. Jiang

DOI: 10.1039/C4OB01545B

CrossRef

[	NS	]	Asclepias curassavica
[	mp	]
[	bp	]
[	α	] D	- 67   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	inhibitory activity against DU145 prostate cancer cells

Steroids

Calotropin, 19β-Oxhydryl-

C28H40O9 = 520

Org. Biomol. Chem. 2014, 12, 8919

R.-R. Zhang, H.-Y. Tian, Y.-F. Tan, T.-Y. Chung, X.-H. Sun, X. Xia, W.-C. Ye, D. A. Middleton, N. Fedosova, M. Esmann, J. T. C. Tzen, R.-W. Jiang

DOI: 10.1039/C4OB01545B

CrossRef

[	NS	]	Asclepias curassavica
[	mp	]
[	bp	]
[	α	] D	- 49   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	inhibitory activity against DU145 prostate cancer cells

Steroids

3,19-O-Coroglaucigenin Dilactate

C29H42O9 = 534

Org. Biomol. Chem. 2014, 12, 8919

R.-R. Zhang, H.-Y. Tian, Y.-F. Tan, T.-Y. Chung, X.-H. Sun, X. Xia, W.-C. Ye, D. A. Middleton, N. Fedosova, M. Esmann, J. T. C. Tzen, R.-W. Jiang

DOI: 10.1039/C4OB01545B

CrossRef

[	NS	]	Asclepias curassavica
[	mp	]
[	bp	]
[	α	] D	- 46   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	inhibitory activity against DU145 prostate cancer cells

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