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
  205 data found. 1 - 30 listed Next Last   

Polyketides
No Name
C8H10O2 = 138
Eur. J. Org. Chem.    2013, , 2906
S. M. Wickel, C. A. Citron, J. S. Dickschat
DOI: 10.1002/ejoc.201300049
CrossRef
 
[NS]  Trichoderma viride, Trichoderma asperellum
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Fusarpyrone B
C8H8O4 = 168
Phytochem. Lett.    2013, 6 , 495
K. Trisuwan, V. Rukachaisirikul, K. Borwornwiriyapan, S. Phongpaichit, J. Sakayaroj
DOI: 10.1016/j.phytol.2013.06.008
CrossRef
 
[NS]  Fusarium solani PSU-RSPG37
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Fusarpyrone A
C10H12O3 = 180
Phytochem. Lett.    2013, 6 , 495
K. Trisuwan, V. Rukachaisirikul, K. Borwornwiriyapan, S. Phongpaichit, J. Sakayaroj
DOI: 10.1016/j.phytol.2013.06.008
CrossRef
 
[NS]  Fusarium solani PSU-RSPG37
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
No Name
C12H16O2 = 192
Eur. J. Org. Chem.    2013, , 2906
S. M. Wickel, C. A. Citron, J. S. Dickschat
DOI: 10.1002/ejoc.201300049
CrossRef
 
[NS]  Trichoderma viride, Trichoderma asperellum
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
No Name
C12H18O2 = 194
Eur. J. Org. Chem.    2013, , 2906
S. M. Wickel, C. A. Citron, J. S. Dickschat
DOI: 10.1002/ejoc.201300049
CrossRef
 
[NS]  Trichoderma viride
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Curvularone A
C11H12O4 = 208
J. Antibiot.    2013, 66 , 287
Y.-W. Pang, L.-J. Zhang, J.-S. Fang, Q.-F. Liu, H. Zhang, W.-S. Xiang, J.-D. Wang, X.-J. Wang
DOI: 10.1038/ja.2012.128
CrossRef
 
[NS]  Curvularia inaequalis HS-FG-257
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxicity

Polyketides
Radianthin, 4-Hydroxy-
C12H12O5 = 236
J. Antibiot.    2013, 66 , 287
Y.-W. Pang, L.-J. Zhang, J.-S. Fang, Q.-F. Liu, H. Zhang, W.-S. Xiang, J.-D. Wang, X.-J. Wang
DOI: 10.1038/ja.2012.128
CrossRef
 
[NS]  Curvularia inaequalis HS-FG-257
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Waol A, cis-Dihydro-
C13H18O4 = 238
Tetrahedron Lett.    2013, 54 , 4300
T. El-Elimat, M. Figueroa, H. A. Raja, A. F. Adcock, D. J. Kroll, S. M. Swanson, M. C. Wani, C. J. Pearce, N. H. Oberlies
DOI: 10.1016/j.tetlet.2013.06.008
CrossRef
 
[NS]  Volutella species
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Waol A, trans-Dihydro-
C13H18O4 = 238
Tetrahedron Lett.    2013, 54 , 4300
T. El-Elimat, M. Figueroa, H. A. Raja, A. F. Adcock, D. J. Kroll, S. M. Swanson, M. C. Wani, C. J. Pearce, N. H. Oberlies
DOI: 10.1016/j.tetlet.2013.06.008
CrossRef
 
[NS]  Volutella species
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Epicolactone
C17H16O8 = 348
Eur. J. Org. Chem.    2013, , 3174
F. M. Talontsi, B. Dittrich, A. Schüffler, H. Sun, H. Laatsch
DOI: 10.1002/ejoc.201300146
CrossRef
 
[NS]  Epicoccum species CAFTBO
[mp]298 ℃
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antimicrobial activity, antifungal activity

Polyketides
Testufuran A
C18H25O3Br = 369
Tetrahedron    2013, 69 , 6560
T. Akiyama, K. Takada, T. Oikawa, N. Matsuura, Y. Ise, S. Okada, S. Matsunaga
DOI: 10.1016/j.tet.2013.06.007
CrossRef
 
[NS]  Xestospongia testudinaria
[mp]
[bp]
[α]D      - 18°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]activity to enhance adiponectin

Polyketides
Phoslactomycin I
C23H35O8P = 470
J. Nat. Prod.    2013, 76 , 1509
S. Fotso, P. Graupner, Q. Xiong, D. Hahn, C. Avila-Adame, G. Davis
DOI: 10.1021/np400232j
CrossRef
 
[NS]  Streptomyces species MLA1839
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antifungal activity

Polyketides
Epothilone O
C27H41NO6S = 507
J. Antibiot.    2013, 66 , 285
Y.-J. Zhang, A.-W. Deng, H. Zhang, F.-Y. Xi, L.-P. Ying, J.-D. Wang, H. Bai
DOI: 10.1038/ja.2012.121
CrossRef
 
[NS]  Sorangium cellulosum So0157-2
[mp]
[bp]
[α]D      - 6.25°     [ EtOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxicity

Aromatics
Acremine R
C12H16O3 = 208
J. Nat. Prod.    2013, 76 , 1432
Suciati, J. A. Fraser, L. K. Lambert, G. K. Pierens, P. V. Bernhardt, M. J. Garson
DOI: 10.1021/np4002114
CrossRef
 
[NS]  Acremonium persicinum
[mp]
[bp]
[α]D      - 8°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Phialophoriol
C14H14O5 = 262
Tetrahedron Lett.    2013, 54 , 4551
F. Ye, G.-D. Chen, J.-W. He, X.-X. Li, X. Sun, L.-D. Guo, Y. Li, H. Gao
DOI: 10.1016/j.tetlet.2013.06.080
CrossRef
 
[NS]  Phialophora spp.
[mp]
[bp]
[α]D      + 101.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Corynether Lactone A
C15H12O6 = 288
Tetrahedron Lett.    2013, 54 , 4210
F. B. C. Okoye, S. Lu, C. S. Nworu, C. O. Esimone, P. Proksch, A. Chadli, A. Debbab
DOI: 10.1016/j.tetlet.2013.05.117
CrossRef
 
[NS]  Corynespora cassiicola
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Saiprzelactone
C18H16O4 = 296
Tetrahedron    2013, 69 , 6687
H.-L. Jiang, X.-Z. Wang, J. Xiao, X.-H. Luo, X.-J. Yao, Y.-Y. Zhao, Y.-J. Chen, P. Crews, Q.-X. Wu
DOI: 10.1016/j.tet.2013.05.115
CrossRef
 
[NS]  Salvia przewalskii
[mp]
[bp]
[α]D      + 2.86°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antibacterial activity

Aromatics
Boeravinone K
C17H12O6 = 312
J. Nat. Prod.    2013, 76 , 1393
K. Bairwa, I. N. Singh, S. K. Roy, J. Grover, A. Srivastava, S. M. Jachak
DOI: 10.1021/np300899w
CrossRef
 
[NS]  Boerhaavia diffusa
[mp]
[bp]
[α]D      0°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Boeravinone N
C16H10O7 = 314
J. Nat. Prod.    2013, 76 , 1393
K. Bairwa, I. N. Singh, S. K. Roy, J. Grover, A. Srivastava, S. M. Jachak
DOI: 10.1021/np300899w
CrossRef
 
[NS]  Boerhaavia diffusa
[mp]
[bp]
[α]D      0°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory effect of COX-1 and COX-2

Aromatics
Corynesidone D
C16H12O7 = 316
Tetrahedron Lett.    2013, 54 , 4210
F. B. C. Okoye, S. Lu, C. S. Nworu, C. O. Esimone, P. Proksch, A. Chadli, A. Debbab
DOI: 10.1016/j.tetlet.2013.05.117
CrossRef
 
[NS]  Corynespora cassiicola
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Butyraxanthone F
C19H18O5 = 326
Phytochem. Lett.    2013, 6 , 326
M. F. Tala, H. K. Wabo, G.-Z. Zeng, C.-J. Ji, P. Tane, N.-H. Tan
DOI: 10.1016/j.phytol.2013.03.016
CrossRef
 
[NS]  Pentadesma butyracea
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Boeravinone O
C17H12O7 = 328
J. Nat. Prod.    2013, 76 , 1393
K. Bairwa, I. N. Singh, S. K. Roy, J. Grover, A. Srivastava, S. M. Jachak
DOI: 10.1021/np300899w
CrossRef
 
[NS]  Boerhaavia diffusa
[mp]
[bp]
[α]D      0°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
No Name
C18H16O6 = 328
Phytochem. Lett.    2013, 6 , 407
S. Sutthivaiyakit, C. Seeka, N. Wetprasit, P. Sutthivaiyakit
DOI: 10.1016/j.phytol.2013.05.001
CrossRef
 
[NS]  Pisonia grandis
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antioxidant activity

Aromatics
No Name
C18H16O6 = 328
Phytochem. Lett.    2013, 6 , 407
S. Sutthivaiyakit, C. Seeka, N. Wetprasit, P. Sutthivaiyakit
DOI: 10.1016/j.phytol.2013.05.001
CrossRef
 
[NS]  Pisonia grandis
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antioxidant activity

Aromatics
Phaeolschidin E
C17H15NO6 = 329
J. Nat. Prod.    2013, 76 , 1448
J.-J. Han, L. Bao, L.-W. He, X.-Q. Zhang, X.-L. Yang, S.-J. Li, Y.-J. Yao, H.-w. Liu
DOI: 10.1021/np400234u
CrossRef
 
[NS]  Phaeolus schweinitzii
[mp]
[bp]
[α]D      0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antioxidant activity

Aromatics
No Name
C18H18O6 = 330
Phytochem. Lett.    2013, 6 , 407
S. Sutthivaiyakit, C. Seeka, N. Wetprasit, P. Sutthivaiyakit
DOI: 10.1016/j.phytol.2013.05.001
CrossRef
 
[NS]  Pisonia grandis
[mp]
[bp]
[α]D      - 81.17°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antioxidant activity

Aromatics
Danshenol A, Dehydro-
C21H18O4 = 334
Tetrahedron    2013, 69 , 6687
H.-L. Jiang, X.-Z. Wang, J. Xiao, X.-H. Luo, X.-J. Yao, Y.-Y. Zhao, Y.-J. Chen, P. Crews, Q.-X. Wu
DOI: 10.1016/j.tet.2013.05.115
CrossRef
 
[NS]  Salvia przewalskii
[mp]
[bp]
[α]D      + 6.25°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antibacterial activity

Aromatics
Derrisisoflavone G
C20H16O5 = 336
Phytochem. Lett.    2013, 6 , 498
S. Morel, J.-J. Helesbeux, D. Séraphin, S. Derbré, J. Gatto, M.-C. Aumond, Y. Abatuci, P. Grellier, M. A. Beniddir, P. L. Pape, F. Pagniez, M. Litaudon, A. Landreau, P. Richomme
DOI: 10.1016/j.phytol.2013.06.002
CrossRef
 
[NS]  Derris ferruginea
[mp]
[bp]
[α]D      - 50°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]anti-AGEs activity

Aromatics
Tephroapollin C, 2,3-Dihydro-
C21H22O4 = 338
J. Nat. Prod.    2013, 76 , 1498
L. B. Pérez, J. Li, D. D. Lantvit, L. Pan, T. N. Ninh, H.-B. Chai, D. D. Soejarto, S. M. Swanson, D. M. Lucas, A. D. Kinghorn
DOI: 10.1021/np400567c
CrossRef
 
[NS]  Indigofera spicata
[mp]
[bp]
[α]D      - 40.0°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]activation of the concentration required to double quinone reductase

Aromatics
Boeravinone M
C18H14O7 = 342
J. Nat. Prod.    2013, 76 , 1393
K. Bairwa, I. N. Singh, S. K. Roy, J. Grover, A. Srivastava, S. M. Jachak
DOI: 10.1021/np300899w
CrossRef
 
[NS]  Boerhaavia diffusa
[mp]
[bp]
[α]D      0°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory effect of COX-1 and COX-2

  205 data found. 1 - 30 listed Next Last   
   
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