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. 31 - 60 listedFirst Previous Next Last
Aromatics

Eurotiumide F

C21H30O5 = 362
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
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Eurotiumide G

C21H30O5 = 362
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
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Claucoumarin B

C21H20O6 = 368
Phytochemistry 2014, 107, 141
H. Liu, F. Li, C.-J. Li, J.-Z. Yang, L. Li, N.-H. Chen, D.-M. Zhang
DOI: 10.1016/j.phytochem.2014.08.002
CrossRef
[ NS ] Clausena lansium
[ mp ]
[ bp ]
[ α ] D - 11.2   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Claucoumarin D

C22H24O5 = 368
Phytochemistry 2014, 107, 141
H. Liu, F. Li, C.-J. Li, J.-Z. Yang, L. Li, N.-H. Chen, D.-M. Zhang
DOI: 10.1016/j.phytochem.2014.08.002
CrossRef
[ NS ] Clausena lansium
[ mp ]
[ bp ]
[ α ] D
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] neuroprotective activity
Aromatics

Claucoumarin A

C21H22O6 = 370
Phytochemistry 2014, 107, 141
H. Liu, F. Li, C.-J. Li, J.-Z. Yang, L. Li, N.-H. Chen, D.-M. Zhang
DOI: 10.1016/j.phytochem.2014.08.002
CrossRef
[ NS ] Clausena lansium
[ mp ]
[ bp ]
[ α ] D + 2.1   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Pilobolusone B

C21H22O6 = 370
Planta medica 2014, 80, 1635
O. Rajachan, S. Kanokmedhakul, K. Kanokmedhakul, K. Soytong
DOI: 10.1055/s-0034-1383082
CrossRef
[ NS ] Pilobolus heterosporus
[ mp ] 168 - 170 ℃
[ bp ]
[ α ] D
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Pteroloterin A

C22H26O5 = 370
J. Nat. Prod. 2014, 77, 2432
J. Suthiwong, S. Pitchuanchom, W. Wattanawongdon, C. Hahnvajanawong, C. Yenjai
DOI: 10.1021/np500476h
CrossRef
[ NS ] Pterolobium macropterum
[ mp ] 148 - 150 ℃
[ bp ]
[ α ] D + 51   [ CHCl3 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] cytotoxicity
Aromatics

Bacillcoumacin G

C20H24N2O5 = 372
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 – 53.6   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] inhibitory activity against NO production
Aromatics

Pteroloterin B

C22H28O5 = 372
J. Nat. Prod. 2014, 77, 2432
J. Suthiwong, S. Pitchuanchom, W. Wattanawongdon, C. Hahnvajanawong, C. Yenjai
DOI: 10.1021/np500476h
CrossRef
[ NS ] Pterolobium macropterum
[ mp ]
[ bp ]
[ α ] D + 24   [ CHCl3 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] cytotoxicity
Aromatics

Halenaquinone, 1-Hydroxyethyl-

C22H16O6 = 376
Heterocycles 2014, 89, 2605
M. Yamakuma, H. Kato, K. Matsuo, A. H. El-Desoky, T. Kawabata, F. Losung, R. E. P. Mangindaan, N. J. de Voogd, H. Yokosawa, S. Tsukamoto
DOI: 10.3987/COM-14-13087
CrossRef
[ NS ] Xestospongia species
[ mp ]
[ bp ]
[ α ] D - 11.5   [ DMSO ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] chymotrypsin-like activity of the proteasome
Aromatics

Bacillcoumacin D

C20H25NO7 = 391
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 – 62.0   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Cudracuspixanthone B

C23H22O6 = 394
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 - 83   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antiproliferative activity
Aromatics

Taepeenin C, 1β-Acetoxy

C28H28O6 = 400
J. Nat. Prod. 2014, 77, 2432
J. Suthiwong, S. Pitchuanchom, W. Wattanawongdon, C. Hahnvajanawong, C. Yenjai
DOI: 10.1021/np500476h
CrossRef
[ NS ] Pterolobium macropterum
[ mp ] 179 - 183 ℃
[ bp ]
[ α ] D - 60   [ CHCl3 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Bacillcoumacin B

C20H28N2O7 = 408
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 – 82.0   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Cudracuspixanthone A

C24H26O6 = 410
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

Cudracuspixanthone C

C24H26O6 = 410
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 - 206   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antiproliferative activity
Aromatics

Cudracuspixanthone D

C24H26O6 = 410
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 + 96   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antiproliferative activity
Aromatics

No Name

C25H30O5 = 410
J. Nat. Prod. 2014, 77, 2418
M. C. de M. Burger, J. B. Fernandes, M. F. das G. F. da Silva, A. Escalante, J. Prudhomme, K. G. L. Roch, M. A. Izidoro, P. C. Vieira
DOI: 10.1021/np500453x
CrossRef
[ NS ] Metrodorea stipularis
[ mp ]
[ bp ]
[ α ] D
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] growth inhibit activity
Aromatics

No Name

C25H30O5 = 410
J. Nat. Prod. 2014, 77, 2418
M. C. de M. Burger, J. B. Fernandes, M. F. das G. F. da Silva, A. Escalante, J. Prudhomme, K. G. L. Roch, M. A. Izidoro, P. C. Vieira
DOI: 10.1021/np500453x
CrossRef
[ NS ] Metrodorea stipularis
[ mp ]
[ bp ]
[ α ] D
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Saffloflavoneside A

C21H18O9 = 414
Org. Lett. 2014, 16, 5714
J. He, Y.-N. Yang, J. Jiang, Z.-M. Feng, P.-C. Zhang
DOI: 10.1021/ol502789x
CrossRef
[ NS ] Carthamus tinctorius
[ mp ]
[ bp ]
[ α ] D - 54.2   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] inhibitory activity against PC12 cell damage induced by rotenone
Aromatics

Saffloflavoneside B

C21H18O9 = 414
Org. Lett. 2014, 16, 5714
J. He, Y.-N. Yang, J. Jiang, Z.-M. Feng, P.-C. Zhang
DOI: 10.1021/ol502789x
CrossRef
[ NS ] Carthamus tinctorius
[ mp ]
[ bp ]
[ α ] D - 76.6   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] inhibitory activity against PC12 cell damage induced by rotenone
Aromatics

Notoincisol B

C28H34O3 = 418
J. Nat. Prod. 2014, 77, 2513
X. Liu, O. Kunert, M. Blunder, N. Fakhrudin, S. M. Noha, C. Malainer, A. Schinkovitz, E. H. Heiss, A. G. Atanasov, M. Kollroser, D. Schuster, V. M. Dirsch, R. Bauer
DOI: 10.1021/np500605v
CrossRef
[ NS ] Notopterygium incisum
[ mp ]
[ bp ]
[ α ] D + 268.9   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] inhibition of NO production
Aromatics

Bacillcoumacin C

C21H28N2O7 = 420
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 – 86.8   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Notoincisol C

C27H32O4 = 420
J. Nat. Prod. 2014, 77, 2513
X. Liu, O. Kunert, M. Blunder, N. Fakhrudin, S. M. Noha, C. Malainer, A. Schinkovitz, E. H. Heiss, A. G. Atanasov, M. Kollroser, D. Schuster, V. M. Dirsch, R. Bauer
DOI: 10.1021/np500605v
CrossRef
[ NS ] Notopterygium incisum
[ mp ]
[ bp ]
[ α ] D + 25.8   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Pilobolusone A

C25H28O6 = 424
Planta medica 2014, 80, 1635
O. Rajachan, S. Kanokmedhakul, K. Kanokmedhakul, K. Soytong
DOI: 10.1055/s-0034-1383082
CrossRef
[ NS ] Pilobolus heterosporus
[ mp ] 172 - 173 ℃
[ bp ]
[ α ] D
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] cytotoxicity and antimalarial activity
Aromatics

Bacillcoumacin E

C21H27NO7S = 437
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 – 105.0   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Bacillcoumacin F

C21H27NO7S = 437
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 – 100.4   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Pilobolusone C

C25H26O8 = 454
Planta medica 2014, 80, 1635
O. Rajachan, S. Kanokmedhakul, K. Kanokmedhakul, K. Soytong
DOI: 10.1055/s-0034-1383082
CrossRef
[ NS ] Pilobolus heterosporus
[ mp ] 184 - 185 ℃
[ bp ]
[ α ] D
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] cytotoxicity
Aromatics

Rubialatin B

C27H20O7 = 456
Org. Lett. 2014, 16, 5576
S.-M. Zhao, Z. Wang, G.-Z. Zeng, W.-W. Song, X.-Q. Chen, X.-N. Li, N.-H. Tan
DOI: 10.1021/ol502603f
CrossRef
[ NS ] Rubia alata
[ mp ] 204 - 206 ℃
[ bp ]
[ α ] D
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] cytotoxic activity
Aromatics

Delitschiapyrone A

C24H26O9 = 458
Org. Lett. 2014, 16, 5944
J.-G. Luo, X.-B. Wang, Y.-M. Xu, J. M. U’Ren, A. E. Arnold, L.-Y. Kong, A. A. L. Gunatilaka
DOI: 10.1021/ol502973c
CrossRef
[ NS ] Delitschia species FL1581
[ mp ]
[ bp ]
[ α ] D + 121.0   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] cytotoxic activity
223 data found. 31 - 60 listedFirst Previous Next Last