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.

39 data found. 1 - 30 listed Next Last
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

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

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

Claucoumarin C

C22H26O11 = 466
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 - 31.2   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Aromatics

Quercetin-3-O-(3’’,4’’-di-O-galloyl)-α-L-rhamnopyranoside

C35H28O19 = 752
Phytochemistry 2014, 107, 148
E. W. L. Chan, A. Ⅰ. Gray, J. O. Igoli, S. M. Lee, J. K. Goh
DOI: 10.1016/j.phytochem.2014.07.028
CrossRef
[ NS ] Calliandra tergemina
[ mp ]
[ bp ]
[ α ] D + 27.7   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antibacterial activity against MRSA
Aromatics

Kaempferol-3-O-(2’’,3’’,4’’-tri-O-galloyl)-α-L-rhamnopyranoside

C42H32O22 = 888
Phytochemistry 2014, 107, 148
E. W. L. Chan, A. Ⅰ. Gray, J. O. Igoli, S. M. Lee, J. K. Goh
DOI: 10.1016/j.phytochem.2014.07.028
CrossRef
[ NS ] Calliandra tergemina
[ mp ]
[ bp ]
[ α ] D + 25.3   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antibacterial activity against MRSA
Aromatics

Quercetin-3-O-(2’’,3’’,4’’-tri-O-galloyl)-α-L-rhamnopyranoside

C42H32O23 = 904
Phytochemistry 2014, 107, 148
E. W. L. Chan, A. Ⅰ. Gray, J. O. Igoli, S. M. Lee, J. K. Goh
DOI: 10.1016/j.phytochem.2014.07.028
CrossRef
[ NS ] Calliandra tergemina
[ mp ]
[ bp ]
[ α ] D + 27.3   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antibacterial activity against MRSA
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

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

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 ]
Terpenes

MeliatooseninⅠ, 12α-Hydroxy-

C35H46O13 = 674
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 - 40.3   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Meliatoxin B1, 12α-Hydroxy-

C35H46O13 = 674
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 - 30.3   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] TNFα-induced NF-κB luciferase activity
Terpenes

Meliatoxin B2, 12α-Acetoxyl-

C36H46O14 = 702
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 - 11.8   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
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

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
39 data found. 1 - 30 listed Next Last