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
6 data found. 1 - 6 listed
Miscellaneous
Onionin A2
C9H16O2S2 = 220
Chem. Pharm. Bull. 2014, 62, 1141
T. Nohara, Y. Fujiwara, R. Kudo,
K. Yamaguchi, T. Ikeda,
K. Murakami, M. Ono, T. Kajimoto,
M. Takeya
DOI: 10.1248/cpb.c14-00461
CrossRef
| [ | NS | ] | Allium cepa and Aliium fistulosum | ||||||||
| [ | mp | ] | |||||||||
| [ | bp | ] | |||||||||
| [ | α | ] D | + 16.0 [ CHCl3 ] | ||||||||
| [ | Ph | ] |
|
||||||||
| [ | act | ] |
Miscellaneous
Onionin A3
C9H16O2S2 = 220
Chem. Pharm. Bull. 2014, 62, 1141
T. Nohara, Y. Fujiwara, R. Kudo,
K. Yamaguchi, T. Ikeda,
K. Murakami, M. Ono, T. Kajimoto,
M. Takeya
DOI: 10.1248/cpb.c14-00461
CrossRef
| [ | NS | ] | Allium cepa and Aliium fistulosum | ||||||||
| [ | mp | ] | |||||||||
| [ | bp | ] | |||||||||
| [ | α | ] D | + 12.5 [ CHCl3 ] | ||||||||
| [ | Ph | ] |
|
||||||||
| [ | act | ] |
Miscellaneous
MKN-349A, 5,5’-Epoxy-
C22H34N4O5 = 434
Helv. Chim. Acta 2014, 97, 1564
Z.-F. Zhou, X.-H. Yang, H.-L. Liu,
Y.-C. Gu, B.-P. Ye, Y.-W. Guo
DOI: 10.1002/hlca.201400062
CrossRef
| [ | NS | ] | Penicillium species GD6 | ||||||||
| [ | mp | ] | |||||||||
| [ | bp | ] | |||||||||
| [ | α | ] D | – 62.8 [ MeOH ] | ||||||||
| [ | Ph | ] |
|
||||||||
| [ | act | ] |
Miscellaneous
Pashinintide A
C28H35N7O6 = 565
Tetrahedron Lett. 2014, 55, 6231
L. Cai, M. Zhao, S. Liu, T. Yin,
H. Zhou, J. Dong, Y. Yang, Z. Ding
DOI: 10.1016/j.tetlet.2014.09.063
CrossRef
| [ | NS | ] | Pyrus pashia Buch.-Ham. ex D. Don | ||||||||
| [ | mp | ] | > 370 ℃ | ||||||||
| [ | bp | ] | |||||||||
| [ | α | ] D | – 10.9 [ MeOH ] | ||||||||
| [ | Ph | ] |
|
||||||||
| [ | act | ] |
Miscellaneous
Pashinintide B
C34H50N8O9 = 714
Tetrahedron Lett. 2014, 55, 6231
L. Cai, M. Zhao, S. Liu, T. Yin,
H. Zhou, J. Dong, Y. Yang, Z. Ding
DOI: 10.1016/j.tetlet.2014.09.063
CrossRef
| [ | NS | ] | Pyrus pashia Buch.-Ham. ex D. Don | ||||||||
| [ | mp | ] | 270.9 - 272.3 ℃ | ||||||||
| [ | bp | ] | |||||||||
| [ | α | ] D | – 12.0 [ Py. ] | ||||||||
| [ | Ph | ] |
|
||||||||
| [ | act | ] |
Miscellaneous
Jatrophidine Ⅰ
C42H62N10O9 = 850
Phytochemistry 2014, 107, 91
W. F. Altei, D. G. Picchi,
B. M. Abissi, G. M. Giesel,
O. Flausino Jr., M. Reboud-Ravaux,
H. Verli, E. Crusca Jr., E. R. Silveira,
E. M. Cilli, V. S. Bolzani
DOI: 10.1016/j.phytochem.2014.08.006
CrossRef
| [ | NS | ] | Jatropha curcas | ||||||||
| [ | mp | ] | |||||||||
| [ | bp | ] | |||||||||
| [ | α | ] D | - 68.0 [ MeOH ] | ||||||||
| [ | Ph | ] |
|
||||||||
| [ | act | ] | protease inhibition activity |
6 data found. 1 - 6 listed
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