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

Carbon:
Carbon
Molecular Weight
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Group

Molecular Fomula:

Molecular Weight:

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Author
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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
  212 data found. 1 - 30 listed Next Last   

Polyketides
Pyranonigrin E
C11H11NO4 = 221
J. Antibiot.    2014, 67 , 179
R. Riko, H. Nakamura, K. Shindo
DOI: 10.1038/ja.2013.91
CrossRef
 
[NS]  Aspergillus niger NBRC5374
[mp]
[bp]
[α]D      - 43.6°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]DPPH radical scavenging activity

Polyketides
Cleroindin D, 5-O-Butyl-
C12H20O4 = 228
Phytochem. Lett.    2014, 7 , 111
R.-L. Xu, R. Wang, W. Ha, Y.-P. Shi
DOI: 10.1016/j.phytol.2013.10.010
CrossRef
 
[NS]  Clerodendrum trichotomum
[mp]
[bp]
[α]D      - 1.32°     [ CH2Cl2 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
No Name
C14H24O4 = 256
Phytochem. Lett.    2014, 7 , 93
Ş. Akay, G. Ekiz, F. Kocabaş, E. E. Hameş-Kocabaş, K. S. Korkmaz, E. Bedir
DOI: 10.1016/j.phytol.2013.09.012
CrossRef
 
[NS]  Phomopsis amygdali
[mp]
[bp]
[α]D      - 42.1°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxicity against MDA-MB-231 cell line

Polyketides
No Name
C15H24O5 = 284
J. Nat. Prod.    2014, 77 , 206
D. R. McMullin, T. K. Nsiama, J. D. Miller
DOI: 10.1021/np4005486
CrossRef
 
[NS]  Penicillium corylophilum DAOM 242293
[mp]
[bp]
[α]D      - 44.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
No Name
C17H28O5 = 312
J. Nat. Prod.    2014, 77 , 206
D. R. McMullin, T. K. Nsiama, J. D. Miller
DOI: 10.1021/np4005486
CrossRef
 
[NS]  Penicillium corylophilum DAOM 242293
[mp]
[bp]
[α]D      + 8.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
No Name
C17H28O6 = 328
J. Nat. Prod.    2014, 77 , 206
D. R. McMullin, T. K. Nsiama, J. D. Miller
DOI: 10.1021/np4005486
CrossRef
 
[NS]  Penicillium corylophilum DAOM 242293
[mp]
[bp]
[α]D      + 20.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Geldanamycin, 6-Demethoxy-6-methyl-
C29H40N2O8 = 544
J. Antibiot.    2014, 67 , 183
S. Ni, B. Jiang, L. Wu, Y. Wang, H. Zhou, W. He, H. Wang, J. Zhu, S. Li, T. Li, K. Zhang
DOI: 10.1038/ja.2013.94
CrossRef
 
[NS]  Streptomyces hygroscopicus 17997
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxicity

Polyketides
No Name
C43H60O9 = 720
J. Antibiot.    2014, 67 , 187
J.-S. Li, J.-D. Wang, L.-Y. Yang, J. Zhang, H. Zhang, X.-J. Wang, W.-S. Xiang
DOI: 10.1038/ja.2013.97
CrossRef
 
[NS]  Streptomyces avermitilis NEAU1069-3
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
No Name
C44H66O12 = 786
J. Antibiot.    2014, 67 , 187
J.-S. Li, J.-D. Wang, L.-Y. Yang, J. Zhang, H. Zhang, X.-J. Wang, W.-S. Xiang
DOI: 10.1038/ja.2013.97
CrossRef
 
[NS]  Streptomyces avermitilis NEAU1069-3
[mp]
[bp]
[α]D      + 72.7°     [ EtOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Coniochaetone E
C14H14O4 = 246
Tetrahedron Lett.    2014, 55 , 1336
K. Trisuwan, V. Rukachaisirikul, K. Borwornwiriyapan, S. Phongpaichit, J. Sakayaroj
DOI: 10.1016/j.tetlet.2014.01.017
CrossRef
 
[NS]  Penicillium citrinum PSU-RSPG95
[mp]
[bp]
[α]D      + 44.8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Coniochaetone F
C15H16O4 = 260
Tetrahedron Lett.    2014, 55 , 1336
K. Trisuwan, V. Rukachaisirikul, K. Borwornwiriyapan, S. Phongpaichit, J. Sakayaroj
DOI: 10.1016/j.tetlet.2014.01.017
CrossRef
 
[NS]  Penicillium citrinum PSU-RSPG95
[mp]
[bp]
[α]D      + 38.8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Alternariol-10-methyl Ether
C15H12O5 = 272
Phytochemistry    2014, 98 , 183
S. Devari, S. Jaglan, M. Kumar, R. Deshidi, S. Guru, S. Bhushan, M. Kushwaha, A. P. Gupta, S. G. Gandhi, J. P. Sharma, S. C. Taneja, R. A. Vishwakarma, B. A. Shah
DOI: 10.1016/j.phytochem.2013.12.001
CrossRef
 
[NS]  Alternaria alternata
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxicity against a panel of human cancer cell lines and inducing apoptosis evidenced by Hoechst staining and loss of mitochondrial-membrane potential in HL-60 cells.

Aromatics
Sakenin G
C17H14O5 = 298
Planta medica    2014, 80 , 193
M. T. T. Nguyen, N. T. Nguyen, K. D. H. Nguyen, H. T. T. Dau, H. X. Nguyen, P. H. Dang, T. M. Le, T. H. N. Phan, A. H. Tran, B. D. Nguyen, J. Ueda, S. Awale
DOI: 10.1055/s-0033-1360181
CrossRef
 
[NS]  Artocarpus altilis
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Hydramicromelin D
C15H14O7 = 306
Phytochem. Lett.    2014, 7 , 165
W. Phakhodee, M. Pattarawarapan, P. Pongparn, S. Laphookhieo
DOI: 10.1016/j.phytol.2013.11.009
CrossRef
 
[NS]  Micromelum integerrimum
[mp]182 - 184 ℃
[bp]
[α]D      + 59.91°     [ Acetone ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Hindsiiquinoflavan B
C17H16O6 = 316
Phytochem. Lett.    2014, 7 , 169
X.-Q. Hu, W. Han, Z.-Z. Han, Q.-X. Liu, X.-K. Xu, P. Fu, H.-L. Li
DOI: 10.1016/j.phytol.2013.11.015
CrossRef
 
[NS]  Celastrus hindsii
[mp]
[bp]
[α]D      - 3.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxicity toward the NCI-H187 and
HCT116 cell lines

Aromatics
Penicillone C
C16H12O7 = 316
Tetrahedron Lett.    2014, 55 , 1336
K. Trisuwan, V. Rukachaisirikul, K. Borwornwiriyapan, S. Phongpaichit, J. Sakayaroj
DOI: 10.1016/j.tetlet.2014.01.017
CrossRef
 
[NS]  Penicillium citrinum PSU-RSPG95
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
Wentiquinone C
C16H12O7 = 316
Phytochem. Lett.    2014, 7 , 120
X. Li, X.-M. Li, G.-M. Xu, C.-S. Li, B.-G. Wang
DOI: 10.1016/j.phytol.2013.11.008
CrossRef
 
[NS]  Aspergillus wentii EN-48
[mp]287 - 289 ℃
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
No Name
C17H24O6 = 324
J. Nat. Prod.    2014, 77 , 206
D. R. McMullin, T. K. Nsiama, J. D. Miller
DOI: 10.1021/np4005486
CrossRef
 
[NS]  Penicillium corylophilum DAOM 242293
[mp]
[bp]
[α]D      - 40.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antifungal activity

Aromatics
No Name
C17H24O6 = 324
J. Nat. Prod.    2014, 77 , 206
D. R. McMullin, T. K. Nsiama, J. D. Miller
DOI: 10.1021/np4005486
CrossRef
 
[NS]  Penicillium corylophilum DAOM 242293
[mp]
[bp]
[α]D      - 58.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antifungal activity

Aromatics
Hindsiilactone A
C19H18O5 = 326
Phytochem. Lett.    2014, 7 , 169
X.-Q. Hu, W. Han, Z.-Z. Han, Q.-X. Liu, X.-K. Xu, P. Fu, H.-L. Li
DOI: 10.1016/j.phytol.2013.11.015
CrossRef
 
[NS]  Celastrus hindsii
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxicity toward the NCI-H187 and
HCT116 cell lines

Aromatics
Sakenin H
C18H18O6 = 330
Planta medica    2014, 80 , 193
M. T. T. Nguyen, N. T. Nguyen, K. D. H. Nguyen, H. T. T. Dau, H. X. Nguyen, P. H. Dang, T. M. Le, T. H. N. Phan, A. H. Tran, B. D. Nguyen, J. Ueda, S. Awale
DOI: 10.1055/s-0033-1360181
CrossRef
 
[NS]  Artocarpus altilis
[mp]
[bp]
[α]D      – 116°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic activity against PANC-1 cell line

Aromatics
No Name
C20H18O5 = 338
Tetrahedron Lett.    2014, 55 , 1285
M. Kaouadji
DOI: 10.1016/j.tetlet.2013.12.118
CrossRef
 
[NS]  Platanus acerifolia
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
No Name
C20H18O5 = 338
Tetrahedron Lett.    2014, 55 , 1285
M. Kaouadji
DOI: 10.1016/j.tetlet.2013.12.118
CrossRef
 
[NS]  Platanus acerifolia
[mp]
[bp]
[α]D      - 24.2°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
No Name
C17H24O7 = 340
J. Nat. Prod.    2014, 77 , 206
D. R. McMullin, T. K. Nsiama, J. D. Miller
DOI: 10.1021/np4005486
CrossRef
 
[NS]  Penicillium corylophilum DAOM 242293
[mp]
[bp]
[α]D      + 40.0°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antifungal activity

Aromatics
No Name
C17H24O7 = 340
J. Nat. Prod.    2014, 77 , 206
D. R. McMullin, T. K. Nsiama, J. D. Miller
DOI: 10.1021/np4005486
CrossRef
 
[NS]  Penicillium corylophilum DAOM 242293
[mp]
[bp]
[α]D      + 34.5°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antifungal activity

Aromatics
Hymenocardichromene A
C24H26O2 = 346
Phytochemistry    2014, 98 , 216
C. M. Starks, R. B. Williams, V. L. Norman, S. M. Rice, M. O’Neil-Johnson, J. A. Lawrence, G. R. Eldridge
DOI: 10.1016/j.phytochem.2013.11.012
CrossRef
 
[NS]  Hymenocardia acida
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Aromatics
No Name
C19H18O7 = 358
Phytochem. Lett.    2014, 7 , 194
Y.-H. Luo, Z.-Q. Zhou, S.-C. Ma, H.-Z. Fu
DOI: 10.1016/j.phytol.2013.12.001
CrossRef
 
[NS]  Callicarpa nudiflora
[mp]
[bp]
[α]D      + 72.0°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antioxidant activity

Aromatics
No Name
C19H18O7 = 358
Phytochem. Lett.    2014, 7 , 194
Y.-H. Luo, Z.-Q. Zhou, S.-C. Ma, H.-Z. Fu
DOI: 10.1016/j.phytol.2013.12.001
CrossRef
 
[NS]  Callicarpa nudiflora
[mp]
[bp]
[α]D      + 19.6°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antioxidant activity

Aromatics
No Name
C19H18O7 = 358
Phytochem. Lett.    2014, 7 , 194
Y.-H. Luo, Z.-Q. Zhou, S.-C. Ma, H.-Z. Fu
DOI: 10.1016/j.phytol.2013.12.001
CrossRef
 
[NS]  Callicarpa nudiflora
[mp]
[bp]
[α]D      + 20.4°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antioxidant activity

Aromatics
Biflorin, 7-Methoxy-iso-
C17H20O9 = 368
Phytochem. Lett.    2014, 7 , 150
H.-y. Gao, H.-y. Wang, G.-y. Li, X.-w. Du, X.-t. Zhang, Y. Han, J. Huang, X.-x. Li, J.-h. Wang
DOI: 10.1016/j.phytol.2013.11.011
CrossRef
 
[NS]  Zhuyeqing Liquor
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

  212 data found. 1 - 30 listed Next Last   
   
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