

HETEROCYCLES
An International Journal for Reviews and Communications in Heterocyclic ChemistryWeb Edition ISSN: 1881-0942
Published online by The Japan Institute of Heterocyclic Chemistry
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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.
- 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
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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | 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 | ] |
|
||||||||
[ | act | ] | cytotoxicity against HL-60 cells |