Carboline alkaloids from trigonostemon lii

Planta Medica

Volumn 75, Issue 10, 2009, Pages 1157-1161

  Hu, Xu Jia ^a,b,c   Di, Ying Tong ^a   Wang, Yue Hu ^a   Kong, Ling Yi ^c   Gao, Suo ^a   Li, Chun Shun ^a   Liu, Hai Yang ^a   He, Hong Ping ^a   Ding, Jian ^d   Xie, Hua ^d   Hao, Xiao Jiang ^a  

^a KUNMING INSTITUTE OF BOTANY   (China)

^b Yunnan Institute for Drug Control   (China)

^c CHINA PHARMACEUTICAL UNIVERSITY   (China)

^d SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

Carboline alkaloids; Cytotoxic activity; Euphorbiaceae; Trigonostemon lii

Indexed keywords

BETA CARBOLINE DERIVATIVE; TRIGONOSTEMONINE A; TRIGONOSTEMONINE B; TRIGONOSTEMONINE C; TRIGONOSTEMONINE D; TRIGONOSTEMONINE E; TRIGONOSTEMONINE F; UNCLASSIFIED DRUG; ALKALOID; CARBOLINE DERIVATIVE;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CELL STRAIN HL 60; CONTROLLED STUDY; CYTOTOXICITY; DRUG ISOLATION; DRUG STRUCTURE; HUMAN; HUMAN CELL; MEDICINAL PLANT; PLANT ROOT; PLANT STEM; STRUCTURE ANALYSIS; TRIGONOSTEMON LII; CHEMISTRY; DRUG SCREENING; EUPHORBIA; ISOLATION AND PURIFICATION; METHODOLOGY; SPECTROSCOPY;

EUPHORBIACEAE; TRIGONOSTEMON;

ALKALOIDS; CARBOLINES; DRUG SCREENING ASSAYS, ANTITUMOR; EUPHORBIACEAE; HL-60 CELLS; HUMANS; SPECTRUM ANALYSIS;

EID: 70350774265     PISSN: 00320943     EISSN: 14390221     Source Type: Journal    
DOI: 10.1055/s-0029-1185505     Document Type: Article

References (15)

1. Kiu HS, Huang SM, Chang YT. Euphorbiaceae. In: Wu ZY, editor. Flora reipublicae popularis sinicae, Vol.44 (2). Beijing: Science Press; 1996: 162-169
2. Jayasuriya H, Zink DL, Singh SB, Borris RP, Nanakorn W, Beck HT, Balick MJ, Goetz MA, Slayton L, Gregory L, Zakson-Aiken M, Shoop W, Singh SB. Structure and stereochemistry of rediocide A, a highly modified daphnane from Trigonostemon reidioides exhibiting potent insecticidal activity. J Am Chem Soc 2000; 122: 4998-4999
3. Jayasuriya H, Zink DL, Borris RP, NanakornW, Beck, HT, Balick MJ, Goetz MA, Gregory L, Shoop WL, Singh SB. Rediocides B-E, potent insecticides from Trigonostemon reidioides. J Nat Prod 2004; 67: 228-231
4. Soonthornchareonnon N, Sakayarojkul M, Isaka M, Mahakittikun V, Chuakul W, Wongsinkongman P. Acaricidal daphnane diterpenoids from Trigonostemon reidioides (Kurz) Craib roots. Chem Pharm Bull 2005; 53: 241-243
5. Tempeam A, Thasana N, Chitkavee P, Chuakul W, Siripong P, Ruchirawat S. A new cytotoxic daphnane diterpenoid, rediocide G, from Trigonostemon reidioides. Chem Pharm Bull 2005; 53: 1321-1323
6. Kokpol U, Thebpatiphat S, Boonyaratavej S, Chedchuskulcai V, Ni CZ, Clardy J, Chaichantipyuth C, Chittawong V, Miles DH. Structure of trigonostemone, a new phenanthrenone from the Thai plant Trigonostemon reidioides. J Nat Prod 1990; 53: 1148-1151
7. Kanchanapoom T, Kasai R, Chumsri P, Kraisintu K, Yamasaki K. Lotthanongine, an unprecedented flavonoidal indole alkaloid from the roots of Thai medicinal plant, Trigonostemon reidioides. Tetrahedron Lett 2002; 43: 2941-2943
8. Alley MC, Scudiero DA, Monks A, Hursey ML, Czerwinski MJ, Fine DL, Abbott BJ, Mayo JG, Shoemaker RH, Boyd MR. Feasibility of drug screening with panels of human tumor cell lines using a microculture tetrazolium assay. Cancer Res 1988; 48: 589-601
9. Choia SJ, Parka HJ, Leea SK, Kimb SW, Hanc G, Park Chooa HY. Solid phase combinatorial synthesis of benzothiazoles and evaluation of topoisomerase II inhibitory activity. Bioorg Med Chem 2006; 14: 1229-1235
10. Skehan P, Storeng R, Scudiero D, Monks A, McMahon J, Vistica D, Warren JT, Bokesch H, Kenney S, Boyd MR. New colorimetric cytotoxicity assay for anticancer-drug screening. J Natl Cancer Inst 1990; 82: 1107-1112
11. Wu FE, Koike K, Nikaido T, Sakamoto Y, Ohmoto T, Ikeda K. New β-carboline alkaloids from a Chinese medicinal plant, Arenaria kansuensis. Structures of arenarines A, B, C, and D. Chem Pharm Bull 1989; 37: 1808-1809
12. Herdeis C, Dimmerling A. Synthesis with hydroxylactames. III. A facile entry to the 1-oxo-carboline skeleton. Synthesis of strychnocarpine. Heterocycles 1984; 22: 2277-2283
13. Chung F, Tisne C, Lecourt T, Dardel F, Micowin L. NMR-guided fragmentbased approach for the design of tRNALys3 ligands. Angew Chem Int Ed 2007; 46: 4489-4491
14. Tulyaganov TS. Alkaloids from Nitraria komarovii. Structures of nitraridine, dihydronitraridine, and tetrahydronitraridine. Chem Nat Compounds 2006; 42: 459-461
15. Lehmann J, Nieger M, Witt T. Indoles. XI. Syntheses and stereochemistry of 5,6,7,8,13,13b-hexahydrobenz[a]indolo[2,3-h]quinolizines and of 5,6,7,8,13,13b-hexahydro-14H-bis-indolo[3,2-a][2,3-h]quinolizine. Heterocycles 1994; 38: 511-528