Heterocycles Database
Natural Products with
Heterocyclic Ring System
 
 1975-2010
 54,889 Compounds
 27 August, 2010
 
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
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.
 
27 August, 2010
Search by Group:
Polyketides
Aromatics
Terpenes
Steroids
Alkaloids
Antibiotics
Miscellaneous
 
All
 
Search by Journal :
Vol.
No.
Chem. Pharm. Bull.
58
2
Eur. J. Org. Chem.
2010
2,3
Helv. Chim. Acta
93
2
J. Antibiot.
63
2
J. Nat. Prod.
73
2
Org. Lett.
12
4
Phytochemistry
71
2-3
Planta medica
76
3
Tetrahedron
66
9
Tetrahedron Lett.
51
6
  163 data found. 121 - 150 listed First Previous Next Last   

Steroids
Tuberoside O1
C49H80O17 = 940
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 9.1°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Cambodianoside A
C48H72O20 = 968
Helv. Chim. Acta    2010, 93 , 302
M. Xu, C.-R. Yang, Y.-J. Zhang
DOI: 10.1002/hlca.200900157
CrossRef 		 
[NS]  Dracaena cambodiana
[mp]
[bp]
[α]D      - 21.74°     [ Pyridine ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside A3
C50H80O18 = 968
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 51°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside B3
C51H82O18 = 982
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 47°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside G6
C55H88O19 = 1052
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 62°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside I6
C55H88O19 = 1052
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 41°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside I5
C55H90O19 = 1054
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 27°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside S5
C55H90O19 = 1054
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 50°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside T5
C55H90O19 = 1054
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 40°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside R5
C56H92O19 = 1068
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 36°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside V5
C56H92O19 = 1068
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 38°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside W5
C56H92O19 = 1068
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 48°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside U1
C55H90O20 = 1070
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 38°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Steroids
Tuberoside I3
C57H92O21 = 1112
Chem. Pharm. Bull.    2010, 58 , 172
T. Warashina, T. Noro
DOI: 10.1248/cpb.58.172
CrossRef 		 
[NS]  Asclepias tuberosa
[mp]
[bp]
[α]D      - 33°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Alkaloids
Cespilactam A
C17H23NO2 = 273
Helv. Chim. Acta    2010, 93 , 281
Y.-C. Lin, M. H. A. EI-Razek, Y.-C. Shen
DOI: 10.1002/hlca.200900196
CrossRef 		 
[NS]  Cespitularia hypotentaculata
[mp]
[bp]
[α]D      + 35.2°     [ CH2Cl2 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Alkaloids
Bezerramycin A
C14H11N3O4 = 285
Eur. J. Org. Chem.    2010, 2010 , 231
P. B. Gomes, M. Nett, H.-M. Dahse, I. Sattler, K. Martin, C. Hertweck
DOI: 10.1002/ejoc.200901206
CrossRef 		 
[NS]  Streptmyces griseus
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antiproliferative activity and cytotoxic
Alkaloids
Annotine N-Oxide
C16H21NO4 = 291
Phytochemistry    2010, 71 , 149
E. S. Halldorsdottir, J. W. Jaroszewski, E. S. Olafsdottir
DOI: 10.1016/j.phytochem.2009.10.018
CrossRef 		 
[NS]  Lycopodium annotinum subspecies alpestre
[mp]
[bp]
[α]D      - 30°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]acetylcholinesterase inhibitory
Alkaloids
JBIR-46
C17H16N2O3 = 296
J. Nat. Prod.    2010, 73 , 208
M. Izumikawa, S. T. Khan, M. Takagi, K. Shin-ya
DOI: 10.1021/np900747t
CrossRef 		 
[NS]  Streptomyces species
SpC080624SC-11
[mp]
[bp]
[α]D      - 49.5°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Alkaloids
No Name
C17H15NO4 = 297
Phytochemistry    2010, 71 , 301
T. Řezanka, P. Řezanka, K. Sigler
DOI: 10.1016/j.phytochem.2009.10.016
CrossRef 		 
[NS]  Narcissus cultivar ‘Dutch Master’
[mp]
[bp]
[α]D      + 174°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Alkaloids
Bezerramycin C
C16H11N3O4 = 309
Eur. J. Org. Chem.    2010, 2010 , 231
P. B. Gomes, M. Nett, H.-M. Dahse, I. Sattler, K. Martin, C. Hertweck
DOI: 10.1002/ejoc.200901206
CrossRef 		 
[NS]  Streptmyces griseus
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antiproliferative activity and cytotoxic
Alkaloids
Hyrtiocarboline
C16H10N4O4 = 322
J. Nat. Prod.    2010, 73 , 255
W. D. Inman, W. M. Bray, N. C. Gassner, R. S. Lokey, K. Tenney, Y. Y. Shen, K. TenDyke, T. Suh, P. Crews
DOI: 10.1021/np9005426
CrossRef 		 
[NS]  Hyrtios reticulatus
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antiproliferative activity
Alkaloids
Bezerramycin B
C16H12N2O6 = 328
Eur. J. Org. Chem.    2010, 2010 , 231
P. B. Gomes, M. Nett, H.-M. Dahse, I. Sattler, K. Martin, C. Hertweck
DOI: 10.1002/ejoc.200901206
CrossRef 		 
[NS]  Streptmyces griseus
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antiproliferative activity and cytotoxic
Alkaloids
Discorhabdin D, 3-Dihydro-
C18H16N3O2S = 338
J. Nat. Prod.    2010, 73 , 258
J. Jeon, Z. Na, M. Jung, H.-S. Lee, C. J. Sim, K. Nahm, K.-B. Oh, J. Shin
DOI: 10.1021/np9005629
CrossRef 		 
[NS]  Sceptrella species
[mp]
[bp]
[α]D      - 188°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Alkaloids
JBIR-47
C22H24N2O2 = 348
J. Nat. Prod.    2010, 73 , 208
M. Izumikawa, S. T. Khan, M. Takagi, K. Shin-ya
DOI: 10.1021/np900747t
CrossRef 		 
[NS]  Streptomyces species
SpC080624SC-11
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Alkaloids
Discorhabdin Z
C18H18N3O5 = 356
J. Nat. Prod.    2010, 73 , 258
J. Jeon, Z. Na, M. Jung, H.-S. Lee, C. J. Sim, K. Nahm, K.-B. Oh, J. Shin
DOI: 10.1021/np9005629
CrossRef 		 
[NS]  Sceptrella species
[mp]
[bp]
[α]D      - 188°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Alkaloids
JBIR-48
C22H24N2O3 = 364
J. Nat. Prod.    2010, 73 , 208
M. Izumikawa, S. T. Khan, M. Takagi, K. Shin-ya
DOI: 10.1021/np900747t
CrossRef 		 
[NS]  Streptomyces species
SpC080624SC-11
[mp]
[bp]
[α]D      - 46.9°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Alkaloids
Quassidine C
C26H22N4O2 = 422
J. Nat. Prod.    2010, 73 , 167
W.-H. Jiao, H. Gao, C.-Y. Li, F. Zhao, R.-W. Jiang, Y. Wang, G.-X. Zhou, X.-S. Yao
DOI: 10.1021/np900538r
CrossRef 		 
[NS]  Picrasma quassioides
[mp]
[bp]
[α]D      0°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Alkaloids
Quassidine B
C27H24N4O3 = 452
J. Nat. Prod.    2010, 73 , 167
W.-H. Jiao, H. Gao, C.-Y. Li, F. Zhao, R.-W. Jiang, Y. Wang, G.-X. Zhou, X.-S. Yao
DOI: 10.1021/np900538r
CrossRef 		 
[NS]  Picrasma quassioides
[mp]246 ℃
[bp]
[α]D      0°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
Alkaloids
Teleocidin A1, 2-Oxo-
C27H39N3O3 = 453
J. Antibiot.    2010, 63 , 33
M. Izumikawa, S. T. Khan, H. Komaki, M. Takagi, K. Shin-ya
DOI: 10.1038/ja.2009.113
CrossRef 		 
[NS]  Streptomyces species NBRC 105896
[mp]58 - 62 ℃
[bp]
[α]D      - 226.3°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic
Alkaloids
No Name
C23H25NO9 = 459
Phytochemistry    2010, 71 , 301
T. Řezanka, P. Řezanka, K. Sigler
DOI: 10.1016/j.phytochem.2009.10.016
CrossRef 		 
[NS]  Narcissus cultivar ‘Dutch Master’
[mp]
[bp]
[α]D      + 178°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]
  163 data found. 121 - 150 listed First Previous Next Last   
   
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