(Q34151970)

English

Interiotherins C and D, two new lignans from Kadsura interior and antitumor-promoting effects of related neolignans on Epstein-Barr virus activation

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Interiotherins C and D, two new lignans from Kadsura interior and antitumor-promoting effects of related neolignans on Epstein-Barr virus activation (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Epstein–Barr virus

0 references

interiotherin A

2 references

ChEBI release 2020-05-28

Kadsura interior

1 reference

1 reference

interiotherin B

1 reference

[(4S,5Z,7R,8R,9R)-4-(2-methoxy-2-oxoacetyl)-5-(2-methoxy-2-oxoethylidene)-7,8-dimethyl-2,13,15-trioxatetracyclo[8.6.1.04,17.012,16]heptadeca-1(17),10,12(16)-trien-9-yl] (Z)-2-methylbut-2-enoate

1 reference

(1S,12R,13R,14R)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-12-yl (2Z)-2-methylbut-2-enoate

1 reference

1 reference

schisantherin a

1 reference

[(11R,12R,13R)-12-hydroxy-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.02,10.04,8.017,21]docosa-1(22),2,4(8),9,15,17(21)-hexaen-11-yl] (E)-2-methylbut-2-enoate

1 reference

(9S,10S,11S)-3,4,5,19-tetramethoxy-9,10-dimethyl-11-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-10-ol

1 reference

1 reference

1 reference

1 reference

(18-Methoxy-13,14-dimethyl-19,20-dioxo-3,6,8-trioxapentacyclo[9.9.1.01,16.04,21.05,9]henicosa-4(21),5(9),10,15,17-pentaen-12-yl) 2-methylbut-2-enoate

1 reference

[(11S,12R,13R)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.02,10.04,8.017,21]docosa-1(22),2,4(8),9,15,17(21)-hexaen-11-yl] (E)-2-methylbut-2-enoate

1 reference

Rel-(5R,6R,7S,8S)-1,2,3,13-tetramethoxy-6,7-dimethyl-5,6,7,8-tetrahydro-5,8-epoxybenzo[3',4']cycloocta[1',2':4,5]benzo[1,2-d][1,3]dioxole

1 reference

(8S,9R,10S)-3,4,5,19-tetramethoxy-9,10-dimethyl-8-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-9-ol

1 reference

Interiotherin D

1 reference

1 reference

[(9R,10S,11S)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] acetate

1 reference

(1S,17R,18S,19R)-9,12,13,14-tetramethoxy-18,19-dimethyl-5,7,20-trioxapentacyclo[15.2.1.02,10.04,8.011,16]icosa-2,4(8),9,11,13,15-hexaene

1 reference

[(1S,12S,13R,14R)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.01,16.04,21.05,9]henicosa-4(21),5(9),10,16,19-pentaen-12-yl] (Z)-2-methylbut-2-enoate

1 reference

[(1S,12R,13S,14S)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.01,16.04,21.05,9]henicosa-4(21),5(9),10,16,19-pentaen-12-yl] (E)-2-methylbut-2-enoate

1 reference

Angeloylgomisin R

1 reference

(9S,10S)-besigomsin

1 reference

[(1S,12S,13R,14R)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.01,16.04,21.05,9]henicosa-4(21),5(9),10,16,18-pentaen-12-yl] (E)-2-methylbut-2-enoate

1 reference

[(1S,12R,13R,14R,15E)-18-methoxy-13,14-dimethyl-19,20-dioxo-3,6,8-trioxapentacyclo[9.9.1.01,16.04,21.05,9]henicosa-4(21),5(9),10,15,17-pentaen-12-yl] (Z)-2-methylbut-2-enoate

1 reference

[(8S,9S,10R,11S)-8-acetyloxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] (Z)-2-methylbut-2-enoate

1 reference

interiotherin C

1 reference

1 reference

(7S)-6,7beta-Dimethyl-1,10,11,12-tetramethoxy-2,3-methylenedioxy-5,6,7,8-tetrahydrodibenzo[a,c]cyclooctene-5beta,6beta-diol 5-benzoate

1 reference

[(1S,12R,13R,14R)-18-methoxy-13,14-dimethyl-19,20-dioxo-3,6,8-trioxapentacyclo[9.9.1.01,16.04,21.05,9]henicosa-4(21),5(9),10,15,17-pentaen-12-yl] (Z)-2-methylbut-2-enoate

1 reference

[4-(2-Methoxy-2-oxoacetyl)-5-(2-methoxy-2-oxoethylidene)-7,8-dimethyl-2,13,15-trioxatetracyclo[8.6.1.04,17.012,16]heptadeca-1(17),10,12(16)-trien-9-yl] 2-methylbut-2-enoate

1 reference

Kadsura heteroclita

1 reference

10

object named as

Hoyoku Nishino

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Harukuni Tokuda

9

object named as

Harukuni Tokuda

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Susan L Morris-Natschke

12

object named as

Susan L Morris-Natschke

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

13

object named as

Kuo-Hsiung Lee

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

Dao-Feng Chen

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Shun-Xiang Zhang

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Mutsuo Kozuka

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Quan-Zhong Sun

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Ju Feng

5

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Qiang Wang

6

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Teruo Mukainaka

7

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Yoshitaka Nobukuni

8

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Hui-Kang Wang

11

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

publication date

1 September 2002

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Journal of Natural Products

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

65

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1242-1245

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Isolation of novel lignans, heteroclitins F and G, from the stems of Kadsura heteroclita, and anti-lipid peroxidative actions of heteroclitins A-G and related compounds in the in vitro rat liver homogenate system

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.40.1510

Anti-lipid Peroxidative Effect of an Extract of the Stems of Kadsura heteroclita and Its Major Constituent, Kadsurin, in Mice

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.40.406

Identifiers

10.1021/NP0105127

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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