Heterocycles Database
Natural Products with
Heterocyclic Ring System
 
 1975-2015
 58,387 Compounds
 25 April, 2012
 
Search by:
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Group

Carbon:
Carbon
Molecular Weight
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Group

Molecular Fomula:

Molecular Weight:

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Author
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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
C11H16O3 = 196
Tetrahedron Lett.    2014, 55 , 3478
A. M. Metwaly, F. R. Fronczek, G. Ma, H. A. Kadry, A. A. El-Hela, A.-E. I. Mohammad, S. J. Cutler, S. A. Ross
DOI: 10.1016/j.tetlet.2014.04.085
CrossRef
 
[NS]  Alternaria phragmospora
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
No Name
C11H14O4 = 210
Tetrahedron Lett.    2014, 55 , 3478
A. M. Metwaly, F. R. Fronczek, G. Ma, H. A. Kadry, A. A. El-Hela, A.-E. I. Mohammad, S. J. Cutler, S. A. Ross
DOI: 10.1016/j.tetlet.2014.04.085
CrossRef
 
[NS]  Alternaria phragmospora
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antileukemic activity

Polyketides
No Name
C11H16O4 = 212
Tetrahedron Lett.    2014, 55 , 3478
A. M. Metwaly, F. R. Fronczek, G. Ma, H. A. Kadry, A. A. El-Hela, A.-E. I. Mohammad, S. J. Cutler, S. A. Ross
DOI: 10.1016/j.tetlet.2014.04.085
CrossRef
 
[NS]  Alternaria phragmospora
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antileukemic activity

Polyketides
No Name
C11H16O4 = 212
Tetrahedron Lett.    2014, 55 , 3478
A. M. Metwaly, F. R. Fronczek, G. Ma, H. A. Kadry, A. A. El-Hela, A.-E. I. Mohammad, S. J. Cutler, S. A. Ross
DOI: 10.1016/j.tetlet.2014.04.085
CrossRef
 
[NS]  Alternaria phragmospora
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Thielavialide D
C14H18O5 = 266
J. Nat. Prod.    2014, 77 , 1467
E. M. K. Wijeratne, P. Espinosa-Artiles, R. Gruener, A. A. L. Gunatilaka
DOI: 10.1021/np500237h
CrossRef
 
[NS]  Thielavia species PA0001
[mp]
[bp]
[α]D      - 67.1°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Thielavialide A
C14H20O5 = 268
J. Nat. Prod.    2014, 77 , 1467
E. M. K. Wijeratne, P. Espinosa-Artiles, R. Gruener, A. A. L. Gunatilaka
DOI: 10.1021/np500237h
CrossRef
 
[NS]  Thielavia species PA0001
[mp]
[bp]
[α]D      - 109.4°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Thielavialide B
C14H20O5 = 268
J. Nat. Prod.    2014, 77 , 1467
E. M. K. Wijeratne, P. Espinosa-Artiles, R. Gruener, A. A. L. Gunatilaka
DOI: 10.1021/np500237h
CrossRef
 
[NS]  Thielavia species PA0001
[mp]
[bp]
[α]D      - 60.4°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Thielavialide C
C14H20O5 = 268
J. Nat. Prod.    2014, 77 , 1467
E. M. K. Wijeratne, P. Espinosa-Artiles, R. Gruener, A. A. L. Gunatilaka
DOI: 10.1021/np500237h
CrossRef
 
[NS]  Thielavia species PA0001
[mp]
[bp]
[α]D      - 46.2°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Oxirapentyn G
C16H22O6 = 310
J. Nat. Prod.    2014, 77 , 1321
A. N. Yurchenko, O. F. Smetanina, A. I. Kalinovsky, M. A. Pushilin, V. P. Glazunov, Y. V. Khudyakova, N. N. Kirichuk, S. P. Ermakova, S. A. Dyshlovoy, E. A. Yurchenko, S. S. Afiyatullov
DOI: 10.1021/np500014m
CrossRef
 
[NS]  Isaria felina KMM 4639
[mp]
[bp]
[α]D      - 21.6°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Isariketide
C14H16O8 = 312
J. Nat. Prod.    2014, 77 , 1321
A. N. Yurchenko, O. F. Smetanina, A. I. Kalinovsky, M. A. Pushilin, V. P. Glazunov, Y. V. Khudyakova, N. N. Kirichuk, S. P. Ermakova, S. A. Dyshlovoy, E. A. Yurchenko, S. S. Afiyatullov
DOI: 10.1021/np500014m
CrossRef
 
[NS]  Isaria felina KMM 4639
[mp]
[bp]
[α]D
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]cytotoxic activity

Polyketides
Neomacquarimicin
C19H24O4 = 316
J. Antibiot.    2014, 67 , 479
S. Sato, F. Iwata, T. Fukae, M. Katayama
DOI: 10.1038/ja.2014.17
CrossRef
 
[NS]  Micromonospora speceis NPS2077
[mp]
[bp]
[α]D      + 137.08°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Oxirapentyn F
C18H24O7 = 352
J. Nat. Prod.    2014, 77 , 1321
A. N. Yurchenko, O. F. Smetanina, A. I. Kalinovsky, M. A. Pushilin, V. P. Glazunov, Y. V. Khudyakova, N. N. Kirichuk, S. P. Ermakova, S. A. Dyshlovoy, E. A. Yurchenko, S. S. Afiyatullov
DOI: 10.1021/np500014m
CrossRef
 
[NS]  Isaria felina KMM 4639
[mp]
[bp]
[α]D      - 42.8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Oxirapentyn J
C18H24O7 = 352
J. Nat. Prod.    2014, 77 , 1321
A. N. Yurchenko, O. F. Smetanina, A. I. Kalinovsky, M. A. Pushilin, V. P. Glazunov, Y. V. Khudyakova, N. N. Kirichuk, S. P. Ermakova, S. A. Dyshlovoy, E. A. Yurchenko, S. S. Afiyatullov
DOI: 10.1021/np500014m
CrossRef
 
[NS]  Isaria felina KMM 4639
[mp]
[bp]
[α]D      - 119°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Oxirapentyn K
C18H24O7 = 352
J. Nat. Prod.    2014, 77 , 1321
A. N. Yurchenko, O. F. Smetanina, A. I. Kalinovsky, M. A. Pushilin, V. P. Glazunov, Y. V. Khudyakova, N. N. Kirichuk, S. P. Ermakova, S. A. Dyshlovoy, E. A. Yurchenko, S. S. Afiyatullov
DOI: 10.1021/np500014m
CrossRef
 
[NS]  Isaria felina KMM 4639
[mp]
[bp]
[α]D      - 98.3°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Oxirapentyn H
C18H26O8 = 370
J. Nat. Prod.    2014, 77 , 1321
A. N. Yurchenko, O. F. Smetanina, A. I. Kalinovsky, M. A. Pushilin, V. P. Glazunov, Y. V. Khudyakova, N. N. Kirichuk, S. P. Ermakova, S. A. Dyshlovoy, E. A. Yurchenko, S. S. Afiyatullov
DOI: 10.1021/np500014m
CrossRef
 
[NS]  Isaria felina KMM 4639
[mp]205 - 207 ℃
[bp]
[α]D      - 22.2°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Oxirapentyn I
C18H26O8 = 370
J. Nat. Prod.    2014, 77 , 1321
A. N. Yurchenko, O. F. Smetanina, A. I. Kalinovsky, M. A. Pushilin, V. P. Glazunov, Y. V. Khudyakova, N. N. Kirichuk, S. P. Ermakova, S. A. Dyshlovoy, E. A. Yurchenko, S. S. Afiyatullov
DOI: 10.1021/np500014m
CrossRef
 
[NS]  Isaria felina KMM 4639
[mp]
[bp]
[α]D      - 8.4°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Pyrenulic Acid A
C26H36O3 = 396
J. Nat. Prod.    2014, 77 , 1404
D. H. Le, Y. Takenaka, N. Hamada, Y. Mizushina, T. Tanahashi
DOI: 10.1021/np500143k
CrossRef
 
[NS]  Pyrenula species
[mp]
[bp]
[α]D      - 82°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory activity against mammalian DNA polymerases α and β and cytotoxic activity

Polyketides
Pyrenulic Acid G
C26H36O4 = 412
J. Nat. Prod.    2014, 77 , 1404
D. H. Le, Y. Takenaka, N. Hamada, Y. Mizushina, T. Tanahashi
DOI: 10.1021/np500143k
CrossRef
 
[NS]  Pyrenula species
[mp]
[bp]
[α]D      - 8.2°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]inhibitory activity against mammalian DNA polymerases α and β

Polyketides
Pyrenulic Acid D
C26H36O5 = 428
J. Nat. Prod.    2014, 77 , 1404
D. H. Le, Y. Takenaka, N. Hamada, Y. Mizushina, T. Tanahashi
DOI: 10.1021/np500143k
CrossRef
 
[NS]  Pyrenula species
[mp]
[bp]
[α]D      - 7.9°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Pyrenulic Acid H
C26H36O5 = 428
J. Nat. Prod.    2014, 77 , 1404
D. H. Le, Y. Takenaka, N. Hamada, Y. Mizushina, T. Tanahashi
DOI: 10.1021/np500143k
CrossRef
 
[NS]  Pyrenula species
[mp]146 - 147 ℃
[bp]
[α]D      + 86°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Pyrenulic Acid E
C26H38O5 = 430
J. Nat. Prod.    2014, 77 , 1404
D. H. Le, Y. Takenaka, N. Hamada, Y. Mizushina, T. Tanahashi
DOI: 10.1021/np500143k
CrossRef
 
[NS]  Pyrenula species
[mp]
[bp]
[α]D      + 5.2°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Pyrenulic Acid C
C26H36O6 = 444
J. Nat. Prod.    2014, 77 , 1404
D. H. Le, Y. Takenaka, N. Hamada, Y. Mizushina, T. Tanahashi
DOI: 10.1021/np500143k
CrossRef
 
[NS]  Pyrenula species
[mp]
[bp]
[α]D      - 10.7°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Pyrenulic Acid F
C26H38O6 = 446
J. Nat. Prod.    2014, 77 , 1404
D. H. Le, Y. Takenaka, N. Hamada, Y. Mizushina, T. Tanahashi
DOI: 10.1021/np500143k
CrossRef
 
[NS]  Pyrenula species
[mp]
[bp]
[α]D      - 11.2°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Hyapyrone B
C33H44O4 = 504
J. Nat. Prod.    2014, 77 , 1420
P. W. Okanya, K. I. Mohr, K. Gerth, W. Kessler, R. Jansen, M. Stadler, R. Müller
DOI: 10.1021/np500145f
CrossRef
 
[NS]  Hyalangium minutum
[mp]
[bp]
[α]D      + 10.8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antibacterial activity

Polyketides
Hyafurone B
C32H42O5 = 506
J. Nat. Prod.    2014, 77 , 1420
P. W. Okanya, K. I. Mohr, K. Gerth, W. Kessler, R. Jansen, M. Stadler, R. Müller
DOI: 10.1021/np500145f
CrossRef
 
[NS]  Hyalangium minutum
[mp]
[bp]
[α]D      - 31.8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]antibacterial activity

Polyketides
Hyapyrone A
C32H42O5 = 506
J. Nat. Prod.    2014, 77 , 1420
P. W. Okanya, K. I. Mohr, K. Gerth, W. Kessler, R. Jansen, M. Stadler, R. Müller
DOI: 10.1021/np500145f
CrossRef
 
[NS]  Hyalangium minutum
[mp]
[bp]
[α]D      - 69.1°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Hyafurone A1
C32H44O6 = 524
J. Nat. Prod.    2014, 77 , 1420
P. W. Okanya, K. I. Mohr, K. Gerth, W. Kessler, R. Jansen, M. Stadler, R. Müller
DOI: 10.1021/np500145f
CrossRef
 
[NS]  Hyalangium minutum
[mp]
[bp]
[α]D      - 49.6°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Hyafurone A2
C32H44O6 = 524
J. Nat. Prod.    2014, 77 , 1420
P. W. Okanya, K. I. Mohr, K. Gerth, W. Kessler, R. Jansen, M. Stadler, R. Müller
DOI: 10.1021/np500145f
CrossRef
 
[NS]  Hyalangium minutum
[mp]
[bp]
[α]D      - 11.8°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

Polyketides
Amphirionin-5
C32H54O7 = 550
Tetrahedron Lett.    2014, 55 , 3491
M. Akakabe, K. Kumagai, M. Tsuda, Y. Konishi, A. Tominaga, E. Fukushi, J. Kawabata
DOI: 10.1016/j.tetlet.2014.04.086
CrossRef
 
[NS]  Amphidinium species (strain KCA09053)
[mp]
[bp]
[α]D      - 15°     [ CHCl3 ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]proliferation-promoting activity

Polyketides
Hyapyrroline A
C34H49NO6 = 567
J. Nat. Prod.    2014, 77 , 1420
P. W. Okanya, K. I. Mohr, K. Gerth, W. Kessler, R. Jansen, M. Stadler, R. Müller
DOI: 10.1021/np500145f
CrossRef
 
[NS]  Hyalangium minutum
[mp]
[bp]
[α]D      - 54.2°     [ MeOH ]
[Ph]
uv Hnmr Cnmr ir
Xray mass cd syn
[act]

  205 data found. 1 - 30 listed Next Last   
   
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