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.

57 data found. 1 - 30 listed Next Last
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

Russulanobiline A

C15H20O3 = 248
Phytochemistry 2014, 107, 126
O. Malagòn, A. Porta, M. Clericuzio, G. Gilardoni, D. Gozzini, G. Vidari
DOI: 10.1016/j.phytochem.2014.08.018
CrossRef
[ NS ] Russula nobilis
[ mp ]
[ bp ]
[ α ] D + 181.2   [ CH2Cl2 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Russulanobiline B

C15H20O3 = 248
Phytochemistry 2014, 107, 126
O. Malagòn, A. Porta, M. Clericuzio, G. Gilardoni, D. Gozzini, G. Vidari
DOI: 10.1016/j.phytochem.2014.08.018
CrossRef
[ NS ] Russula nobilis
[ mp ]
[ bp ]
[ α ] D + 295.5   [ CH2Cl2 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Russulanobiline C

C15H18O4 = 262
Phytochemistry 2014, 107, 126
O. Malagòn, A. Porta, M. Clericuzio, G. Gilardoni, D. Gozzini, G. Vidari
DOI: 10.1016/j.phytochem.2014.08.018
CrossRef
[ NS ] Russula nobilis
[ mp ]
[ bp ]
[ α ] D + 154.5   [ CH2Cl2 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

No Name

C20H30O4 = 334
J. Nat. Prod. 2014, 77, 2342
Z.-Y. Wu, Y.-B. Zhang, K.-K. Zhu, C. Luo, J.-X. Zhang, C.-R. Cheng, R.-H. Feng, W.-Z. Yang, F. Zeng, Y. Wang, P.-P. Xu, J.-L. Guo, X. Liu, S.-H. Guan, D.-A. Guo
DOI: 10.1021/np500125x
CrossRef
[ NS ] Acanthopanax gracilistylus
[ mp ]
[ bp ]
[ α ] D - 24   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] inhibit effect of IL-8
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

Heterophyllin C, Hydroperoxy-

C17H22O7 = 338
Chem. Pharm. Bull. 2014, 62, 1092
Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori
DOI: 10.1248/cpb.c14-00426
CrossRef
[ NS ] Eupatorium heterophyllum
[ mp ]
[ bp ]
[ α ] D - 14.5   [ CHCl3 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Holophyllin A

C20H30O5 = 350
Tetrahedron Lett. 2014, 55, 6504
C. S. Kim, B. Shin, O. W. Kwon, S. Y. Kim, S. U. Choi, D.-C. Oh, K. H. Kim, K. R. Lee
DOI: 10.1016/j.tetlet.2014.10.030
CrossRef
[ NS ] Abies holophylla
[ mp ]
[ bp ]
[ α ] D – 12.3   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] inhibitory activity against NO production
Terpenes

Heterophyllin A, Keto-

C20H24O7 = 376
Chem. Pharm. Bull. 2014, 62, 1092
Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori
DOI: 10.1248/cpb.c14-00426
CrossRef
[ NS ] Eupatorium heterophyllum
[ mp ]
[ bp ]
[ α ] D + 109.9   [ 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

Heterophyllin H, Hydroperoxy-

C22H28O8 = 420
Chem. Pharm. Bull. 2014, 62, 1092
Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori
DOI: 10.1248/cpb.c14-00426
CrossRef
[ NS ] Eupatorium heterophyllum
[ mp ]
[ bp ]
[ α ] D - 33.2   [ CHCl3 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Heterophyllin B, Hydroperoxy-

C22H28O9 = 436
Chem. Pharm. Bull. 2014, 62, 1092
Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori
DOI: 10.1248/cpb.c14-00426
CrossRef
[ NS ] Eupatorium heterophyllum
[ mp ]
[ bp ]
[ α ] D - 13.8   [ CHCl3 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
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

Heterophyllin A, Hydroperoxy-

C22H28O10 = 452
Chem. Pharm. Bull. 2014, 62, 1092
Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori
DOI: 10.1248/cpb.c14-00426
CrossRef
[ NS ] Eupatorium heterophyllum
[ mp ]
[ bp ]
[ α ] D - 19.9   [ CHCl3 ]
[ 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

Heterophyllin E, Hydroperoxy-

C24H30O10 = 478
Chem. Pharm. Bull. 2014, 62, 1092
Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori
DOI: 10.1248/cpb.c14-00426
CrossRef
[ NS ] Eupatorium heterophyllum
[ mp ]
[ bp ]
[ α ] D - 62.0   [ EtOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Heterophyllin G, Hydroperoxy-

C24H30O10 = 478
Chem. Pharm. Bull. 2014, 62, 1092
Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori
DOI: 10.1248/cpb.c14-00426
CrossRef
[ NS ] Eupatorium heterophyllum
[ mp ]
[ bp ]
[ α ] D + 5.6   [ EtOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Hexatenuin B

C31H44O4 = 480
Tetrahedron 2014, 70, 8312
A. Umeyama, C. Ohta, Y. Shino, M. Okada, Y. Nakamura, T. Hamagaki, H. Imagawa, M. Tanaka, A. Ishiyama, M. Iwatsuki, K. Otoguro, S. Ōmura, T. Hashimoto
DOI: 10.1016/j.tet.2014.09.013
CrossRef
[ NS ] Hexagonia tenuis
[ mp ]
[ bp ]
[ α ] D - 189   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antitrypanosomal activity
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 ]
Terpenes

Heterophyllin D, Hydroperoxy-

C24H30O11 = 494
Chem. Pharm. Bull. 2014, 62, 1092
Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori
DOI: 10.1248/cpb.c14-00426
CrossRef
[ NS ] Eupatorium heterophyllum
[ mp ]
[ bp ]
[ α ] D - 6.9   [ EtOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Heterophyllin F, Hydroperoxy-

C24H30O11 = 494
Chem. Pharm. Bull. 2014, 62, 1092
Y. Saito, T. Mukai, Y. Iwamoto, M. Baba, K. Takiguchi, Y. Okamoto, X. Gong, T. Kawahara, C. Kuroda, M. Tori
DOI: 10.1248/cpb.c14-00426
CrossRef
[ NS ] Eupatorium heterophyllum
[ mp ]
[ bp ]
[ α ] D - 17.2   [ EtOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Nimbolinin C, 1-Decinnamoyl-

C29H40O8 = 516
Phytochemistry 2014, 107, 175
G.-Y. Zhu, L.-P. Bai, L. Liu, Z.-H. Jiang
DOI: 10.1016/j.phytochem.2014.08.009
CrossRef
[ NS ] Melia toosendan
[ mp ]
[ bp ]
[ α ] D - 73.0   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Havanensin 3,12-Diacetate, 14,15-Deoxy-11-oxo-

C30H40O8 = 528
Phytochemistry 2014, 107, 175
G.-Y. Zhu, L.-P. Bai, L. Liu, Z.-H. Jiang
DOI: 10.1016/j.phytochem.2014.08.009
CrossRef
[ NS ] Melia toosendan
[ mp ]
[ bp ]
[ α ] D - 28.1   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] TNFα-induced NF-κB luciferase activity
Terpenes

Volkensin, 3-Deacetyl-12-O-methyl-

C32H44O8 = 556
Phytochemistry 2014, 107, 175
G.-Y. Zhu, L.-P. Bai, L. Liu, Z.-H. Jiang
DOI: 10.1016/j.phytochem.2014.08.009
CrossRef
[ NS ] Melia toosendan
[ mp ]
[ bp ]
[ α ] D - 33.1   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Trichilinin, 11,15-Dioxo-

C30H38O10 = 558
Phytochemistry 2014, 107, 175
G.-Y. Zhu, L.-P. Bai, L. Liu, Z.-H. Jiang
DOI: 10.1016/j.phytochem.2014.08.009
CrossRef
[ NS ] Melia toosendan
[ mp ]
[ bp ]
[ α ] D + 12.9   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Swielimonoid A

C32H38O9 = 566
J. Nat. Prod. 2014, 77, 2367
Y.-B. Cheng, Y.-T. Chien, J.-C. Lee, C.-K. Tseng, H.-C. Wang, I-W. Lo, Y.-H. Wu, S.-Y. Wang, Y.-C. Wu, F.-R. Chang
DOI: 10.1021/np5002829
CrossRef
[ NS ] Swietenia macrophylla
[ mp ]
[ bp ]
[ α ] D + 23   [ CH2Cl2 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Hexatenuin A

C34H48O7 = 568
Tetrahedron 2014, 70, 8312
A. Umeyama, C. Ohta, Y. Shino, M. Okada, Y. Nakamura, T. Hamagaki, H. Imagawa, M. Tanaka, A. Ishiyama, M. Iwatsuki, K. Otoguro, S. Ōmura, T. Hashimoto
DOI: 10.1016/j.tet.2014.09.013
CrossRef
[ NS ] Hexagonia tenuis
[ mp ]
[ bp ]
[ α ] D - 208   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antitrypanosomal activity
Terpenes

Nimbolinin C, 1-Decinnamoyl-1-(2’-methylacryloyl)-

C33H44O9 = 584
Phytochemistry 2014, 107, 175
G.-Y. Zhu, L.-P. Bai, L. Liu, Z.-H. Jiang
DOI: 10.1016/j.phytochem.2014.08.009
CrossRef
[ NS ] Melia toosendan
[ mp ]
[ bp ]
[ α ] D - 5.8   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
57 data found. 1 - 30 listed Next Last