Natural Products with Heterocyclic Ring System

Structure

New Heterocyclic Natural Products

Updated: 6 October, 2014

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

9 data found. 1 - 9 listed
Aromatics

Thotneoside A

C29H26O13 = 582
Chem. Pharm. Bull. 2014, 62, 191
H. R. Joshi, H. P. Devkota, T. Watanabe, S. Yahara
DOI: 10.1248/cpb.c13-00748
CrossRef
[ NS ] Aconogonon molle
[ mp ]
[ bp ]
[ α ] D - 11.6   [ Py. : H2O = 8 : 2 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] free radical scavenging activity
Aromatics

Thotneoside B

C29H26O13 = 582
Chem. Pharm. Bull. 2014, 62, 191
H. R. Joshi, H. P. Devkota, T. Watanabe, S. Yahara
DOI: 10.1248/cpb.c13-00748
CrossRef
[ NS ] Aconogonon molle
[ mp ]
[ bp ]
[ α ] D - 21.1   [ Py. ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] free radical scavenging activity
Aromatics

Zanthoxyloside A

C31H40O15 = 652
Chem. Pharm. Bull. 2014, 62, 196
W. Li, S. Y. Yang, X. T. Yan, Y. N. Sun, S. B. Song, H. K. Kang, Y. H. Kim
DOI: 10.1248/cpb.c13-00759
CrossRef
[ NS ] Zanthoxylum schinifolium
[ mp ]
[ bp ]
[ α ] D - 19.2   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] inhibition of NF-ĸB, inhibition of TNFα-induced expression o iNOS and ICAM-1, inhibition of iNOS promoter activity
Terpenes

Crassumol G

C20H28O4 = 332
Chem. Pharm. Bull. 2014, 62, 203
N. X. Cuong, N. P. Thao, B. T. T. Luyen, N. T. T. Ngan, D. T. T. Thuy, S. B. Song, N. H. Nam, P. V. Kiem, Y. H. Kim, C. V. Minh
DOI: 10.1248/cpb.c13-00805
CrossRef
[ NS ] Lobophytum crassum
[ mp ]
[ bp ]
[ α ] D + 7.9   [ CHCl3 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Crassumol D

C20H30O4 = 334
Chem. Pharm. Bull. 2014, 62, 203
N. X. Cuong, N. P. Thao, B. T. T. Luyen, N. T. T. Ngan, D. T. T. Thuy, S. B. Song, N. H. Nam, P. V. Kiem, Y. H. Kim, C. V. Minh
DOI: 10.1248/cpb.c13-00805
CrossRef
[ NS ] Lobophytum crassum
[ mp ]
[ bp ]
[ α ] D + 5.8   [ CHCl3 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Terpenes

Crassumol E

C20H30O4 = 334
Chem. Pharm. Bull. 2014, 62, 203
N. X. Cuong, N. P. Thao, B. T. T. Luyen, N. T. T. Ngan, D. T. T. Thuy, S. B. Song, N. H. Nam, P. V. Kiem, Y. H. Kim, C. V. Minh
DOI: 10.1248/cpb.c13-00805
CrossRef
[ NS ] Lobophytum crassum
[ mp ]
[ bp ]
[ α ] D - 4.6   [ CHCl3 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ] anti-inflammatory activity
Terpenes

Crassumol F

C20H30O4 = 334
Chem. Pharm. Bull. 2014, 62, 203
N. X. Cuong, N. P. Thao, B. T. T. Luyen, N. T. T. Ngan, D. T. T. Thuy, S. B. Song, N. H. Nam, P. V. Kiem, Y. H. Kim, C. V. Minh
DOI: 10.1248/cpb.c13-00805
CrossRef
[ NS ] Lobophytum crassum
[ mp ]
[ bp ]
[ α ] D + 10.4   [ CHCl3 ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Alkaloids

Nagelamide I

C22H22N10O2Br2 = 618
Chem. Pharm. Bull. 2014, 62, 213
T. Iwai, T. Kubota, J. Fromont, J. Kobayashi
DOI: 10.1248/cpb.c13-00821
CrossRef
[ NS ] Agelas species
[ mp ]
[ bp ]
[ α ] D
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
Alkaloids

Nagelamide B, 2,2’-Didebromo-

C22H24N10O3Br2 = 636
Chem. Pharm. Bull. 2014, 62, 213
T. Iwai, T. Kubota, J. Fromont, J. Kobayashi
DOI: 10.1248/cpb.c13-00821
CrossRef
[ NS ] Agelas species
[ mp ]
[ bp ]
[ α ] D - 2.5   [ MeOH ]
[ Ph ]
uv Hnmr Cnmr ir
Xray mass cd syn
[ act ]
9 data found. 1 - 9 listed