138 related articles for article (PubMed ID: 23373959)
1. Total synthesis, structural elucidation, and structure-cytotoxic activity relationship of (-)-gummiferol.
Takamura H; Wada H; Lu N; Ohno O; Suenaga K; Kadota I
J Org Chem; 2013 Mar; 78(6):2443-54. PubMed ID: 23373959
[TBL] [Abstract][Full Text] [Related]
2. Total synthesis and absolute configuration of (-)-gummiferol.
Takamura H; Wada H; Lu N; Kadota I
Org Lett; 2011 Jul; 13(14):3644-7. PubMed ID: 21688861
[TBL] [Abstract][Full Text] [Related]
3. Gummiferol, a cytotoxic polyacetylene from the leaves of Adenia gummifera.
Fullas F; Brown DM; Wani MC; Wall ME; Chagwedera TE; Farnsworth NR; Pezzuto JM; Kinghorn AD
J Nat Prod; 1995 Oct; 58(10):1625-8. PubMed ID: 8676132
[TBL] [Abstract][Full Text] [Related]
4. Synthesis and in vitro evaluation of analogues of avocado-produced toxin (+)-(R)-persin in human breast cancer cells.
Brooke DG; Shelley EJ; Roberts CG; Denny WA; Sutherland RL; Butt AJ
Bioorg Med Chem; 2011 Dec; 19(23):7033-43. PubMed ID: 22044656
[TBL] [Abstract][Full Text] [Related]
5. New cytotoxic analogues of annonaceous acetogenins.
Rodier S; Le Huerou Y; Renoux B; Doyon J; Renard P; Pierré A; Gesson JP; Grée R
Anticancer Drug Des; 2001; 16(2-3):109-17. PubMed ID: 11962508
[TBL] [Abstract][Full Text] [Related]
6. A bidirectional approach to the synthesis of a complete library of adjacent-bis-THF annonaceous acetogenins.
Das S; Li LS; Abraham S; Chen Z; Sinha SC
J Org Chem; 2005 Jul; 70(15):5922-31. PubMed ID: 16018687
[TBL] [Abstract][Full Text] [Related]
7. Validation of lanthanide chiral shift reagents for determination of absolute configuration: total synthesis of glisoprenin A.
Adams CM; Ghosh I; Kishi Y
Org Lett; 2004 Dec; 6(25):4723-6. PubMed ID: 15575670
[TBL] [Abstract][Full Text] [Related]
8. Stereoselective synthesis of alpinoid-C and its analogues and study of their cytotoxic activity against cancer cell lines.
Purushotham Reddy S; Chinnababu B; Shekhar V; Kumar Reddy D; Bhanuprakash GV; Velatoor LR; Venkateswara Rao J; Venkateswarlu Y
Bioorg Med Chem Lett; 2012 Jun; 22(12):4182-4. PubMed ID: 22578452
[TBL] [Abstract][Full Text] [Related]
9. Molecular simplification in bioactive molecules: formal synthesis of (+)-muconin.
Pinacho Crisóstomo FR; Carrillo R; León LG; Martín T; Padrón JM; Martín VS
J Org Chem; 2006 Mar; 71(6):2339-45. PubMed ID: 16526782
[TBL] [Abstract][Full Text] [Related]
10. Chemoenzymatic asymmetric total syntheses of antitumor agents (3R,9R,10R)- and (3S,9R,10R)-Panaxytriol and (R)- and (S)-Falcarinol from Panax ginseng using an enantioconvergent enzyme-triggered cascade reaction.
Mayer SF; Steinreiber A; Orru RV; Faber K
J Org Chem; 2002 Dec; 67(26):9115-21. PubMed ID: 12492310
[TBL] [Abstract][Full Text] [Related]
11. Synthesis and evaluation of derrubone and select analogues.
Hastings JM; Hadden MK; Blagg BS
J Org Chem; 2008 Jan; 73(2):369-73. PubMed ID: 18154304
[TBL] [Abstract][Full Text] [Related]
12. Biogenetic relationships between Annonaceous acetogenins: squamocin is not a precursor of chamuvarinin based on a semisynthetic study.
Derbré S; Poupon E; Gleye C; Hocquemiller R
J Nat Prod; 2007 Feb; 70(2):300-3. PubMed ID: 17279796
[TBL] [Abstract][Full Text] [Related]
13. Stereoselective synthesis of C18-guggultetrol and C18-phytosphingosine analogues from D-fructose.
Ramu Sridhar P; Suresh M; Venu Kumar P; Seshadri K; Venkata Rao C
Carbohydr Res; 2012 Oct; 360():40-6. PubMed ID: 22975277
[TBL] [Abstract][Full Text] [Related]
14. Induction of cell death of gastric cancer cells by a modified compound of the annonaceous acetogenin family.
Huang GR; Jiang S; Wu YL; Jin Y; Yao ZJ; Wu JR
Chembiochem; 2003 Nov; 4(11):1216-21. PubMed ID: 14613114
[TBL] [Abstract][Full Text] [Related]
15. Acetogenins from Annonaceae: recent progress in isolation, synthesis and mechanisms of action.
Bermejo A; Figadere B; Zafra-Polo MC; Barrachina I; Estornell E; Cortes D
Nat Prod Rep; 2005 Apr; 22(2):269-303. PubMed ID: 15806200
[TBL] [Abstract][Full Text] [Related]
16. Structural development of benzhydrol-type 1'-acetoxychavicol acetate (ACA) analogs as human leukemia cell-growth inhibitors based on quantitative structure-activity relationship (QSAR) analysis.
Misawa T; Aoyama H; Furuyama T; Dodo K; Sagawa M; Miyachi H; Kizaki M; Hashimoto Y
Chem Pharm Bull (Tokyo); 2008 Oct; 56(10):1490-5. PubMed ID: 18827399
[TBL] [Abstract][Full Text] [Related]
17. Cytotoxic labdane alkaloids from an ascidian Lissoclinum sp.: isolation, structure elucidation, and structure-activity relationship.
Uddin J; Ueda K; Siwu ER; Kita M; Uemura D
Bioorg Med Chem; 2006 Oct; 14(20):6954-61. PubMed ID: 16854586
[TBL] [Abstract][Full Text] [Related]
18. A cytotoxic diacetylene from Dendropanax arboreus.
Setzer WN; Green TJ; Whitaker KW; Moriarity DM; Yancey CA; Lawton RO; Bates RB
Planta Med; 1995 Oct; 61(5):470-1. PubMed ID: 7480210
[TBL] [Abstract][Full Text] [Related]
19. Unexpected stereochemical tolerance for the biological activity of tyroscherin.
Tae HS; Hines J; Schneekloth AR; Crews CM
Bioorg Med Chem; 2011 Mar; 19(5):1708-13. PubMed ID: 21315614
[TBL] [Abstract][Full Text] [Related]
20. Total synthesis of the antitumor acetogenin mosin B: desymmetrization approach to the stereodivergent synthesis of threo/trans/erythro-type acetogenins.
Maezaki N; Kojima N; Sakamoto A; Tominaga H; Iwata C; Tanaka T; Monden M; Damdinsuren B; Nakamori S
Chemistry; 2003 Jan; 9(2):389-99. PubMed ID: 12532287
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]