Heterocycles Database
Natural Products with
Heterocyclic Ring System
 
 1975-2014
 58,387 Compounds
 25 April, 2012
 
Search by:
Name
Group

Carbon:
Carbon
Molecular Weight
Name
Group

Molecular Fomula:

Molecular Weight:

Author:
Author
Group

Journal:
Journal
Year
 
 Nomenclature :
 
The natural products are listed under the name used in the original literature.
 
 The abbreviations :
 
The following abbreviations have been used :
 
act : biological activity
cd : circular dichroism
Cnmr : 13C-nuclear magnetic resonance spectrum
Hnmr : 1H-nuclear magnetic resonance spectrum
ir : infrared spectrum
mass : mass spectrum
syn : total synthesis
uv : ultraviolet spectrum
 
 Journals :
 
This database lists the natural products with heterocyclic ring system whose structure has been determined since 1975.
The journals which have been covered are as follows.
 
Angew. Chem. Int. Ed. Engl.
Angew. Chem. Int. Ed.
Bull. Chem. Soc. Japan
Chem. and Ind.
Chem. Ber.
J. Chem. Soc., Chem. Commun.
Chem. Commun.
Chem. Eur. J.
Chemistry Lett.
Chem. Pharm. Bull.
Coll. Czech. Chem. Commun.
Eur. J. Inorg. Chem.
Eur. J. Org. Chem.
Experientia
Helv. Chim. Acta
Heterocycles
J. Am. Chem. Soc.
J. Antibiot.
J. Chem. Soc., Perkin Trans. 1
J. Heterocycl. Chem.
J. Med. Chem.
J. Nat. Prod.
J. Org. Chem.
J. Pharm. Sci.
Liebigs Ann. Chem.
Monatsh. Chem.
Org. Lett.
Phytochemistry
Planta medica
Synlett
Synth. Commun.
Synthesis
Tetrahedron
Tetrahedron Asymmetry
Tetrahedron Lett.
Yakugaku Zasshi
 
 Editor :
 
Editor
Keiichiro Fukumoto

Associate Editor
Kunio Ogasawara
Yoshiharu Iwabuchi

Assistant Editors
Naoki Kanoh
Muneo Kawasumi
Takashi Moriya
Keiichi Murakami
Kohei Sakanishi
Yusuke Sasano
Takuro Shibuta
Masatoshi Shibuya

Editorial Assistants
Sayaka Kametani
Kishiko Nakano
Yuki Shima
Kazuko Todoroki
Michi Yamamoto
 New Heterocyclic Natural Products
This journal will list the new natural products with a heterocyclic ring system, collected from current chemical literature, whose structure has been established.
 
25 April, 2012
Search by Group:
Polyketides
Aromatics
Terpenes
Steroids
Alkaloids
Antibiotics
Miscellaneous
 
All
 
Search by Journal :
Vol.
No.
Chem. Pharm. Bull.
59
9
Eur. J. Org. Chem.
26
Helv. Chim. Acta
94
9
Heterocycles
83
9
J. Med. Chem.
54
17
J. Nat. Prod.
74
9
Org. Lett.
13
17, 18
Planta medica
77
13, 14
Tetrahedron
67
35, 36, 37, 38, 39
Tetrahedron Lett.
52
36, 39
  238 data found. 1 - 30 listed Next Last   

Polyketides
Violapyrone A
C12H18O3 = 210
J. Nat. Prod.    2013, 76 , 2126
J. Zhang, Y. Jiang, Y. Cao, J. Liu, D. Zheng, X. Chen, L. Han, C. Jiang, X. Huang
DOI: 10.1021/np4003417
CrossRef
 
[NS]  Streptomyces violascens
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antibacterial activity

Polyketides
Violapyrone B
C13H20O3 = 224
J. Nat. Prod.    2013, 76 , 2126
J. Zhang, Y. Jiang, Y. Cao, J. Liu, D. Zheng, X. Chen, L. Han, C. Jiang, X. Huang
DOI: 10.1021/np4003417
CrossRef
 
[NS]  Streptomyces violascens
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antibacterial activity

Polyketides
Macrocarpon C
C13H12O4 = 232
J. Nat. Prod.    2013, 76 , 2094
A. R. B. Ola, D. Thomy, D. Lai, H. Brötz-Oesterhelt, P. Proksch
DOI: 10.1021/np400589h
CrossRef
 
[NS]  Bacillus subtilis
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Violapyrone C
C14H22O3 = 238
J. Nat. Prod.    2013, 76 , 2126
J. Zhang, Y. Jiang, Y. Cao, J. Liu, D. Zheng, X. Chen, L. Han, C. Jiang, X. Huang
DOI: 10.1021/np4003417
CrossRef
 
[NS]  Streptomyces violascens
[mp]
[bp]
[α]D      0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antibacterial activity

Polyketides
Violapyrone F
C13H20O4 = 240
J. Nat. Prod.    2013, 76 , 2126
J. Zhang, Y. Jiang, Y. Cao, J. Liu, D. Zheng, X. Chen, L. Han, C. Jiang, X. Huang
DOI: 10.1021/np4003417
CrossRef
 
[NS]  Streptomyces violascens
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
No Name
C13H22O4 = 242
Phytochemistry    2013, 93 , 170
E. Adelin, M.-T. Martin, S. Cortial, P. Retailleau, S. Lumyong, J. Ouazzani
DOI: 10.1016/j.phytochem.2013.02.012
CrossRef
 
[NS]  Phomopsis species CMU-LMA
[mp]
[bp]
[α]D      + 44.3°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Violapyrone D
C14H20O4 = 252
J. Nat. Prod.    2013, 76 , 2126
J. Zhang, Y. Jiang, Y. Cao, J. Liu, D. Zheng, X. Chen, L. Han, C. Jiang, X. Huang
DOI: 10.1021/np4003417
CrossRef
 
[NS]  Streptomyces violascens
[mp]
[bp]
[α]D      0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Violapyrone E
C14H22O4 = 254
J. Nat. Prod.    2013, 76 , 2126
J. Zhang, Y. Jiang, Y. Cao, J. Liu, D. Zheng, X. Chen, L. Han, C. Jiang, X. Huang
DOI: 10.1021/np4003417
CrossRef
 
[NS]  Streptomyces violascens
[mp]
[bp]
[α]D      + 17.2°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Violapyrone G
C14H22O4 = 254
J. Nat. Prod.    2013, 76 , 2126
J. Zhang, Y. Jiang, Y. Cao, J. Liu, D. Zheng, X. Chen, L. Han, C. Jiang, X. Huang
DOI: 10.1021/np4003417
CrossRef
 
[NS]  Streptomyces violascens
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
No Name
C15H24O5 = 284
Phytochemistry    2013, 93 , 170
E. Adelin, M.-T. Martin, S. Cortial, P. Retailleau, S. Lumyong, J. Ouazzani
DOI: 10.1016/j.phytochem.2013.02.012
CrossRef
 
[NS]  Phomopsis species CMU-LMA
[mp]
[bp]
[α]D      - 11.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Akaeolide
C22H32O6 = 392
Org. Lett.    2013, 15 , 5678
Y. Igarashi, T. Zhou, S. Sato, T. Matsumoto, L. Yu, N. Oku
DOI: 10.1021/ol402661r
CrossRef
 
[NS]  Streptomyces species NPS554
[mp]
[bp]
[α]D      + 33°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Linfuranone A
C22H34O6 = 394
J. Antibiot.    2013, 66 , 675
C. Indananda, Y. Igarashi, M. Ikeda, T. Oikawa, A. Thamchaipenet
DOI: 10.1038/ja.2013.67
CrossRef
 
[NS]  Microbispora species GMKU 363
[mp]
[bp]
[α]D      - 9.9°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Sorbicillamine B
C28H33NO8 = 511
J. Nat. Prod.    2013, 76 , 2106
W. Guo, J. Peng, T. Zhu, Q. Gu, R. A. Keyzers, D. Li
DOI: 10.1021/np4006647
CrossRef
 
[NS]  Penicillium species F23-2
[mp]
[bp]
[α]D      - 108°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Sorbicillamine C
C28H33NO8 = 511
J. Nat. Prod.    2013, 76 , 2106
W. Guo, J. Peng, T. Zhu, Q. Gu, R. A. Keyzers, D. Li
DOI: 10.1021/np4006647
CrossRef
 
[NS]  Penicillium species F23-2
[mp]
[bp]
[α]D      - 213°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Sorbicillamine D
C28H33NO8 = 511
J. Nat. Prod.    2013, 76 , 2106
W. Guo, J. Peng, T. Zhu, Q. Gu, R. A. Keyzers, D. Li
DOI: 10.1021/np4006647
CrossRef
 
[NS]  Penicillium species F23-2
[mp]
[bp]
[α]D      - 177°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Dankastatin C
C25H39NO6Cl2 = 518
Tetrahedron Lett.    2013, 54 , 5960
T. Amagata, M. Tanaka, T. Yamada, Y.-P. Chen, K. Minoura, A. Numata
DOI: 10.1016/j.tetlet.2013.08.044
CrossRef
 
[NS]  Gymnascella dankaliensis
[mp]72 - 74 ℃
[bp]
[α]D      - 137.9°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory activity against the murine P388 cell line

Polyketides
Onchidiol, 13-Propanoyl-
C35H50O9 = 614
J. Nat. Prod.    2013, 76 , 2065
M. Carbone, M. L. Ciavatta, J.-R. Wang, I. Cirillo, V. Mathieu, R. Kiss, E. Mollo, Y.-W. Guo, M. Gavagnin
DOI: 10.1021/np400483c
CrossRef
 
[NS]  Onchidium species
[mp]
[bp]
[α]D      + 14°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Ilikonapyrone, 11-(3-Methylbutanoyl)-
C37H56O8 = 628
J. Nat. Prod.    2013, 76 , 2065
M. Carbone, M. L. Ciavatta, J.-R. Wang, I. Cirillo, V. Mathieu, R. Kiss, E. Mollo, Y.-W. Guo, M. Gavagnin
DOI: 10.1021/np400483c
CrossRef
 
[NS]  Onchidium species
[mp]
[bp]
[α]D      - 1.9°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Onchidiol
C37H56O9 = 644
J. Nat. Prod.    2013, 76 , 2065
M. Carbone, M. L. Ciavatta, J.-R. Wang, I. Cirillo, V. Mathieu, R. Kiss, E. Mollo, Y.-W. Guo, M. Gavagnin
DOI: 10.1021/np400483c
CrossRef
 
[NS]  Onchidium species
[mp]
[bp]
[α]D      + 26°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Ilikonapyrone, 13-Acetyl-11-(3-methylbutanoyl)-
C39H58O9 = 670
J. Nat. Prod.    2013, 76 , 2065
M. Carbone, M. L. Ciavatta, J.-R. Wang, I. Cirillo, V. Mathieu, R. Kiss, E. Mollo, Y.-W. Guo, M. Gavagnin
DOI: 10.1021/np400483c
CrossRef
 
[NS]  Onchidium species
[mp]
[bp]
[α]D      - 1.7°     [ CH2Cl2 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antiproliferation activity

Polyketides
Ilikonapyrone, 11-(3-Methylbutanoyl)-13-propanoyl-
C40H60O9 = 684
J. Nat. Prod.    2013, 76 , 2065
M. Carbone, M. L. Ciavatta, J.-R. Wang, I. Cirillo, V. Mathieu, R. Kiss, E. Mollo, Y.-W. Guo, M. Gavagnin
DOI: 10.1021/np400483c
CrossRef
 
[NS]  Onchidium species
[mp]
[bp]
[α]D      - 1.9°     [ CH2Cl2 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antiproliferation activity

Polyketides
Onchidiol, 3-Acetyl-
C39H58O10 = 686
J. Nat. Prod.    2013, 76 , 2065
M. Carbone, M. L. Ciavatta, J.-R. Wang, I. Cirillo, V. Mathieu, R. Kiss, E. Mollo, Y.-W. Guo, M. Gavagnin
DOI: 10.1021/np400483c
CrossRef
 
[NS]  Onchidium species
[mp]
[bp]
[α]D      + 24°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Onchidiol, 3-Propanoyl-
C40H60O10 = 700
J. Nat. Prod.    2013, 76 , 2065
M. Carbone, M. L. Ciavatta, J.-R. Wang, I. Cirillo, V. Mathieu, R. Kiss, E. Mollo, Y.-W. Guo, M. Gavagnin
DOI: 10.1021/np400483c
CrossRef
 
[NS]  Onchidium species
[mp]
[bp]
[α]D      + 15°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Ilikonapyrone, 3,13-Diacetyl-11-(3-methylbutanoyl)-
C41H60O10 = 712
J. Nat. Prod.    2013, 76 , 2065
M. Carbone, M. L. Ciavatta, J.-R. Wang, I. Cirillo, V. Mathieu, R. Kiss, E. Mollo, Y.-W. Guo, M. Gavagnin
DOI: 10.1021/np400483c
CrossRef
 
[NS]  Onchidium species
[mp]
[bp]
[α]D      - 5.7°     [ CH2Cl2 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antiproliferation activity

Polyketides
Ilikonapyrone, 3-Acetyl-11-(3-methylbutanoyl)-13-propanoyl-
C42H62O10 = 726
J. Nat. Prod.    2013, 76 , 2065
M. Carbone, M. L. Ciavatta, J.-R. Wang, I. Cirillo, V. Mathieu, R. Kiss, E. Mollo, Y.-W. Guo, M. Gavagnin
DOI: 10.1021/np400483c
CrossRef
 
[NS]  Onchidium species
[mp]
[bp]
[α]D      - 1.4°     [ CH2Cl2 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antiproliferation activity

Polyketides
Ilikonapyrone, 11-(3-Methylbutanoyl)-3,13-dipropanoyl-
C43H64O10 = 740
J. Nat. Prod.    2013, 76 , 2065
M. Carbone, M. L. Ciavatta, J.-R. Wang, I. Cirillo, V. Mathieu, R. Kiss, E. Mollo, Y.-W. Guo, M. Gavagnin
DOI: 10.1021/np400483c
CrossRef
 
[NS]  Onchidium species
[mp]
[bp]
[α]D      - 2.3°     [ CH2Cl2 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Sorbicillamine E
C42H49NO12 = 759
J. Nat. Prod.    2013, 76 , 2106
W. Guo, J. Peng, T. Zhu, Q. Gu, R. A. Keyzers, D. Li
DOI: 10.1021/np4006647
CrossRef
 
[NS]  Penicillium species F23-2
[mp]
[bp]
[α]D      + 10.3°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Elaiophylin, 11’,12’-Dehydro-
C54H86O17 = 1006
J. Nat. Prod.    2013, 76 , 2153
C. Wu, Y. Tan, M. Gan, Y. Wang, Y. Guan, X. Hu, H. Zhou, X. Shang, X. You, Z. Yang, C. Xiao
DOI: 10.1021/np4006794
CrossRef
 
[NS]  Streptmyces species 7-145
[mp]
[bp]
[α]D      - 35.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antibacterial activity

Polyketides
Elaiophylin, 11,11’-O-Dimethyl-14’-deethyl-14’-methyl-
C55H90O18 = 1038
J. Nat. Prod.    2013, 76 , 2153
C. Wu, Y. Tan, M. Gan, Y. Wang, Y. Guan, X. Hu, H. Zhou, X. Shang, X. You, Z. Yang, C. Xiao
DOI: 10.1021/np4006794
CrossRef
 
[NS]  Streptmyces species 7-145
[mp]
[bp]
[α]D      + 21.6°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Gymnopalyne A
C12H7O2Cl = 218.5
J. Nat. Prod.    2013, 76 , 2141
B. Thongbai, F. Surup, K. Mohr, E. Kuhnert, K. D. Hyde, M. Stadler
DOI: 10.1021/np400609f
CrossRef
 
[NS]  Gymnopus species
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antimicrovial activity
cytotoxic activity

  238 data found. 1 - 30 listed Next Last   
   
Mail to us | Privacy Statement | Copyright © 2014 The Japan Institute of Heterocyclic Chemistry | Recommend to your Librarian