Natural Products with Heterocyclic Ring System

Structure

New Heterocyclic Natural Products

Updated: 28 August, 2014

This journal will list the new natural products with a heterocyclic ring system, collected from current chemical literature, whose structure has been established.

6 data found. 1 - 6 listed
Polyketides

Calysolin V

C61H100O28 = 1281
Chem. Pharm. Bull. 2014, 62, 97
M. Ono, A. Takigawa, Y. Kanemaru, G. Kawakami, K. Kabata, M.. Okawa, J. Kinjo, K. Yokomizo, H. Yoshimitsu, T. Nohara
DOI: 10.1248/cpb.c13-00610
CrossRef
[ NS ] Calystegia soldanella
[ mp ]
[ bp ]
[ α ] D − 16.5   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antiviral activity
Polyketides

Calysolin VI

C61H102O28 = 1283
Chem. Pharm. Bull. 2014, 62, 97
M. Ono, A. Takigawa, Y. Kanemaru, G. Kawakami, K. Kabata, M.. Okawa, J. Kinjo, K. Yokomizo, H. Yoshimitsu, T. Nohara
DOI: 10.1248/cpb.c13-00610
CrossRef
[ NS ] Calystegia soldanella
[ mp ]
[ bp ]
[ α ] D − 24.2   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antiviral activity
Polyketides

Calysolin VII

C72H116O34 = 1525
Chem. Pharm. Bull. 2014, 62, 97
M. Ono, A. Takigawa, Y. Kanemaru, G. Kawakami, K. Kabata, M.. Okawa, J. Kinjo, K. Yokomizo, H. Yoshimitsu, T. Nohara
DOI: 10.1248/cpb.c13-00610
CrossRef
[ NS ] Calystegia soldanella
[ mp ]
[ bp ]
[ α ] D − 54.0   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antiviral activity
Polyketides

Calysolin IX

C72H120O34 = 1529
Chem. Pharm. Bull. 2014, 62, 97
M. Ono, A. Takigawa, Y. Kanemaru, G. Kawakami, K. Kabata, M.. Okawa, J. Kinjo, K. Yokomizo, H. Yoshimitsu, T. Nohara
DOI: 10.1248/cpb.c13-00610
CrossRef
[ NS ] Calystegia soldanella
[ mp ]
[ bp ]
[ α ] D − 25.6   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antiviral activity
Polyketides

Calysolin VIII

C72H120O34 = 1529
Chem. Pharm. Bull. 2014, 62, 97
M. Ono, A. Takigawa, Y. Kanemaru, G. Kawakami, K. Kabata, M.. Okawa, J. Kinjo, K. Yokomizo, H. Yoshimitsu, T. Nohara
DOI: 10.1248/cpb.c13-00610
CrossRef
[ NS ] Calystegia soldanella
[ mp ]
[ bp ]
[ α ] D − 20.4   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] antiviral activity
Aromatics

Phelliribsin A

C22H16O7 = 392
Chem. Pharm. Bull. 2014, 62, 122
M. Kubo, Y. Liu, M. Ishida, K. Harada, Y. Fukuyama
DOI: 10.1248/cpb.c13-00722
CrossRef
[ NS ] Phellinus ribis
[ mp ]
[ bp ]
[ α ] D
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] cytotoxic activity against PC12 cells
6 data found. 1 - 6 listed