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

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

Steroids

No Name

C32H50O8 = 562

Phytochemistry 2014, 107, 102

L. Tang, Z. Wang, H. Wu, A. Yokosuka, Y. Mimaki

DOI: 10.1016/j.phytochem.2014.07.021

CrossRef

[	NS	]	Dracaena thalioides
[	mp	]
[	bp	]
[	α	] D	- 75.6   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity against HL-60 cells

Steroids

No Name

C33H50O10 = 606

Phytochemistry 2014, 107, 182

L.-P. Kang, K.-L. Wu, H.-S. Yu, X. Pang, J. Liu, L.-F. Han, J. Zhang, Y. Zhao, C.-Q. Xiong, X.-B. Song, C. Liu, Y.-W. Cong, B.-P. Ma

DOI: 10.1016/j.phytochem.2014.08.003

CrossRef

[	NS	]	Tribulus Terrestris
[	mp	]
[	bp	]
[	α	] D	+ 48.0   [ pyridine ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Steroids

No Name

C33H52O10 = 608

Phytochemistry 2014, 107, 182

L.-P. Kang, K.-L. Wu, H.-S. Yu, X. Pang, J. Liu, L.-F. Han, J. Zhang, Y. Zhao, C.-Q. Xiong, X.-B. Song, C. Liu, Y.-W. Cong, B.-P. Ma

DOI: 10.1016/j.phytochem.2014.08.003

CrossRef

[	NS	]	Tribulus Terrestris
[	mp	]
[	bp	]
[	α	] D	+ 25.7   [ pyridine ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Steroids

No Name

C33H54O10 = 610

Phytochem. Lett. 2014, 107, 182

L.-P. Kang, K.-L. Wu, H.-S. Yu, X. Pang, J. Liu, L.-F. Han, J. Zhang, Y. Zhao, C.-Q. Xiong, X.-B. Song, C. Liu, Y.-W. Cong, B.-P. Ma

DOI: 10.1016/j.phytochem.2014.08.003

CrossRef

[	NS	]	Tribulus Terrestris
[	mp	]
[	bp	]
[	α	] D	+ 30.0   [ pyridine ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Steroids

No Name

C33H48O11 = 620

Phytochemistry 2014, 107, 182

L.-P. Kang, K.-L. Wu, H.-S. Yu, X. Pang, J. Liu, L.-F. Han, J. Zhang, Y. Zhao, C.-Q. Xiong, X.-B. Song, C. Liu, Y.-W. Cong, B.-P. Ma

DOI: 10.1016/j.phytochem.2014.08.003

CrossRef

[	NS	]	Tribulus Terrestris
[	mp	]
[	bp	]
[	α	] D	+ 40.5   [ pyridine ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Steroids

No Name

C33H52O11 = 624

Phytochemistry 2014, 107, 182

L.-P. Kang, K.-L. Wu, H.-S. Yu, X. Pang, J. Liu, L.-F. Han, J. Zhang, Y. Zhao, C.-Q. Xiong, X.-B. Song, C. Liu, Y.-W. Cong, B.-P. Ma

DOI: 10.1016/j.phytochem.2014.08.003

CrossRef

[	NS	]	Tribulus Terrestris
[	mp	]
[	bp	]
[	α	] D	+ 10.0   [ pyridine ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Steroids

No Name

C39H62O13 = 738

Phytochemistry 2014, 107, 102

L. Tang, Z. Wang, H. Wu, A. Yokosuka, Y. Mimaki

DOI: 10.1016/j.phytochem.2014.07.021

CrossRef

[	NS	]	Dracaena thalioides
[	mp	]
[	bp	]
[	α	] D	- 73.1   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity against HL-60 cells

Steroids

No Name

C39H60O15 = 768

Phytochemistry 2014, 107, 182

L.-P. Kang, K.-L. Wu, H.-S. Yu, X. Pang, J. Liu, L.-F. Han, J. Zhang, Y. Zhao, C.-Q. Xiong, X.-B. Song, C. Liu, Y.-W. Cong, B.-P. Ma

DOI: 10.1016/j.phytochem.2014.08.003

CrossRef

[	NS	]	Tribulus Terrestris
[	mp	]
[	bp	]
[	α	] D	+ 32.4   [ pyridine ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Steroids

No Name

C43H68O16 = 840

Phytochemistry 2014, 107, 102

L. Tang, Z. Wang, H. Wu, A. Yokosuka, Y. Mimaki

DOI: 10.1016/j.phytochem.2014.07.021

CrossRef

[	NS	]	Dracaena thalioides
[	mp	]
[	bp	]
[	α	] D	- 82.0   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity against HL-60 cells

Steroids

No Name

C47H74O18 = 926

Phytochemistry 2014, 107, 102

L. Tang, Z. Wang, H. Wu, A. Yokosuka, Y. Mimaki

DOI: 10.1016/j.phytochem.2014.07.021

CrossRef

[	NS	]	Dracaena thalioides
[	mp	]
[	bp	]
[	α	] D	- 81.8   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity against HL-60 cells

Steroids

No Name

C45H72O20 = 932

Phytochemistry 2014, 107, 182

L.-P. Kang, K.-L. Wu, H.-S. Yu, X. Pang, J. Liu, L.-F. Han, J. Zhang, Y. Zhao, C.-Q. Xiong, X.-B. Song, C. Liu, Y.-W. Cong, B.-P. Ma

DOI: 10.1016/j.phytochem.2014.08.003

CrossRef

[	NS	]	Tribulus Terrestris
[	mp	]
[	bp	]
[	α	] D	- 22.5   [ pyridine ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Steroids

No Name

C49H76O19 = 968

Phytochemistry 2014, 107, 102

L. Tang, Z. Wang, H. Wu, A. Yokosuka, Y. Mimaki

DOI: 10.1016/j.phytochem.2014.07.021

CrossRef

[	NS	]	Dracaena thalioides
[	mp	]
[	bp	]
[	α	] D	- 85.6   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]

Steroids

No Name

C57H84O27 = 1200

Phytochemistry 2014, 107, 102

L. Tang, Z. Wang, H. Wu, A. Yokosuka, Y. Mimaki

DOI: 10.1016/j.phytochem.2014.07.021

CrossRef

[	NS	]	Dracaena thalioides
[	mp	]
[	bp	]
[	α	] D	- 50.7   [ MeOH ]
[	Ph	]	uv Hnmr Cnmr ir Xray mass cd syn
[	act	]	cytotoxicity against HL-60 cells

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