Natural Products with Heterocyclic Ring System

Structure

New Heterocyclic Natural Products

Updated: 26 June, 2015

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

223 data found. 1 - 30 listed Next Last
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
Aromatics

Angularide A

C13H18O8 = 302
Phytochemistry 2014, 107, 111
Y. Jiang, K.-W. Zeng, B. David, G. Massiot
DOI: 10.1016/j.phytochem.2014.08.011
CrossRef
[ NS ] Vigna angularis
[ mp ]
[ bp ]
[ α ] D - 45   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Angularide B

C13H18O8 = 302
Phytochemistry 2014, 107, 111
Y. Jiang, K.-W. Zeng, B. David, G. Massiot
DOI: 10.1016/j.phytochem.2014.08.011
CrossRef
[ NS ] Vigna angularis
[ mp ]
[ bp ]
[ α ] D - 42   [ ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Angularide C

C13H18O8 = 302
Phytochemistry 2014, 107, 111
Y. Jiang, K.-W. Zeng, B. David, G. Massiot
DOI: 10.1016/j.phytochem.2014.08.011
CrossRef
[ NS ] Vigna angularis
[ mp ]
[ bp ]
[ α ] D - 44   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Bacillcoumacin A

C16H21NO5 = 307
Tetrahedron Lett. 2014, 55, 6286
J. Bai, D. Liu, S. Yu, P. Proksch, W. Lin
DOI: 10.1016/j.tetlet.2014.09.100
CrossRef
[ NS ] Bacillus species
[ mp ]
[ bp ]
[ α ] D – 95.6   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Cudracuspiphenone B

C18H16O5 = 312
J. Nat. Prod. 2014, 77, 2361
Y. H. Jo, B. Shin, Q. Liu, K. Y. Lee, D.-C. Oh, B. Y. Hwang, M. K. Lee
DOI: 10.1021/np5002797
CrossRef
[ NS ] Cudrania tricuspidata
[ mp ]
[ bp ]
[ α ] D
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antiproliferative activity
Aromatics

Angularide D

C15H20O8 = 328
Phytochemistry 2014, 107, 111
Y. Jiang, K.-W. Zeng, B. David, G. Massiot
DOI: 10.1016/j.phytochem.2014.08.011
CrossRef
[ NS ] Vigna angularis
[ mp ]
[ bp ]
[ α ] D - 56   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Eurotiumide C

C20H26O5 = 346
Tetrahedron 2014, 70, 9132
M. Chen, C.-L. Shao, K.-L. Wang, Y. Xu, Z.-G. She, C.-Y. Wang
DOI: 10.1016/j.tet.2014.08.055
CrossRef
[ NS ] Eurotium species XS-200900E6
[ mp ]
[ bp ]
[ α ] D *1   [ CH2Cl2 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antifouling activity
Notes:*1: (+): +28, (-): -25
Aromatics

Eurotiumide D

C20H26O5 = 346
Tetrahedron 2014, 70, 9132
M. Chen, C.-L. Shao, K.-L. Wang, Y. Xu, Z.-G. She, C.-Y. Wang
DOI: 10.1016/j.tet.2014.08.055
CrossRef
[ NS ] Eurotium species XS-200900E6
[ mp ]
[ bp ]
[ α ] D *1   [ CH2Cl2 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antifouling activity
Notes:*1: (+): +20, (-): -25
Aromatics

Eurotiumide E

C20H26O5 = 346
Tetrahedron 2014, 70, 9132
M. Chen, C.-L. Shao, K.-L. Wang, Y. Xu, Z.-G. She, C.-Y. Wang
DOI: 10.1016/j.tet.2014.08.055
CrossRef
[ NS ] Eurotium species XS-200900E6
[ mp ]
[ bp ]
[ α ] D *1   [ CH2Cl2 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Notes:*1: (+): +13, (-): -17
Aromatics

Eurotiumide A

C20H28O5 = 348
Tetrahedron 2014, 70, 9132
M. Chen, C.-L. Shao, K.-L. Wang, Y. Xu, Z.-G. She, C.-Y. Wang
DOI: 10.1016/j.tet.2014.08.055
CrossRef
[ NS ] Eurotium species XS-200900E6
[ mp ]
[ bp ]
[ α ] D *1   [ CH2Cl2 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antifouling activity
Notes:*1: (+): +38, (-): -40
Aromatics

Eurotiumide B

C20H28O5 = 348
Tetrahedron 2014, 70, 9132
M. Chen, C.-L. Shao, K.-L. Wang, Y. Xu, Z.-G. She, C.-Y. Wang
DOI: 10.1016/j.tet.2014.08.055
CrossRef
[ NS ] Eurotium species XS-200900E6
[ mp ]
[ bp ]
[ α ] D *1   [ CH2Cl2 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antifouling activity
Notes:*1: (+): +45, (-): -43
223 data found. 1 - 30 listed Next Last