151 related articles for article (PubMed ID: 19994845)
41. Chaetoglobosin U, a cytochalasan alkaloid from endophytic Chaetomium globosum IFB-E019.
Ding G; Song YC; Chen JR; Xu C; Ge HM; Wang XT; Tan RX
J Nat Prod; 2006 Feb; 69(2):302-4. PubMed ID: 16499339
[TBL] [Abstract][Full Text] [Related]
42. 1-Methyl-3H-pyrazolo[1,2-a]benzo[1,2,3,4]tetrazin-3-ones. Design, synthesis, and biological activity of new antitumor agents.
Almerico AM; Mingoia F; Diana P; Barraja P; Lauria A; Montalbano A; Cirrincione G; Dattolo G
J Med Chem; 2005 Apr; 48(8):2859-66. PubMed ID: 15828824
[TBL] [Abstract][Full Text] [Related]
43. Synthesis and evaluation of functionalized isoindigos as antiproliferative agents.
Wee XK; Yeo WK; Zhang B; Tan VB; Lim KM; Tay TE; Go ML
Bioorg Med Chem; 2009 Nov; 17(21):7562-71. PubMed ID: 19783149
[TBL] [Abstract][Full Text] [Related]
44. Synthesis and in-vitro cytotoxicity evaluation of novel naphtindolizinedione derivatives, part II: improved activity for aza-analogues.
Defant A; Guella G; Mancini I
Arch Pharm (Weinheim); 2009 Feb; 342(2):80-6. PubMed ID: 19173337
[TBL] [Abstract][Full Text] [Related]
45. Design, synthesis and antiproliferative activity of some new azapyranoxanthenone aminoderivatives.
Kolokythas G; Pouli N; Marakos P; Pratsinis H; Kletsas D
Eur J Med Chem; 2006 Jan; 41(1):71-9. PubMed ID: 16300857
[TBL] [Abstract][Full Text] [Related]
46. Synthesis of (±)-actinophyllic acid and analogs: applications of cascade reactions and diverted total synthesis.
Granger BA; Jewett IT; Butler JD; Hua B; Knezevic CE; Parkinson EI; Hergenrother PJ; Martin SF
J Am Chem Soc; 2013 Sep; 135(35):12984-6. PubMed ID: 23972114
[TBL] [Abstract][Full Text] [Related]
47. Synthesis and differential antiproliferative activity of Biginelli compounds against cancer cell lines: Monastrol, oxo-monastrol and oxygenated analogues.
Russowsky D; Canto RF; Sanches SA; D'Oca MG; de Fátima A; Pilli RA; Kohn LK; Antônio MA; de Carvalho JE
Bioorg Chem; 2006 Aug; 34(4):173-82. PubMed ID: 16765411
[TBL] [Abstract][Full Text] [Related]
48. Synthesis and evaluation of curcumin analogues as potential thioredoxin reductase inhibitors.
Qiu X; Liu Z; Shao WY; Liu X; Jing DP; Yu YJ; An LK; Huang SL; Bu XZ; Huang ZS; Gu LQ
Bioorg Med Chem; 2008 Sep; 16(17):8035-41. PubMed ID: 18678491
[TBL] [Abstract][Full Text] [Related]
49. Indolobenzazepin-7-ones and 6-, 8-, and 9-membered ring derivatives as tubulin polymerization inhibitors: synthesis and structure--activity relationship studies.
Putey A; Popowycz F; Do QT; Bernard P; Talapatra SK; Kozielski F; Galmarini CM; Joseph B
J Med Chem; 2009 Oct; 52(19):5916-25. PubMed ID: 19743863
[TBL] [Abstract][Full Text] [Related]
50. Development of novobiocin analogues that manifest anti-proliferative activity against several cancer cell lines.
Burlison JA; Avila C; Vielhauer G; Lubbers DJ; Holzbeierlein J; Blagg BS
J Org Chem; 2008 Mar; 73(6):2130-7. PubMed ID: 18293999
[TBL] [Abstract][Full Text] [Related]
51. 2-triazenoindoles: synthesis and biological activity.
Barraja P; Diana P; Lauria A; Montalbano A; Almerico AM; Dattolo G; Cirrincione G
Anticancer Res; 2002; 22(2A):837-40. PubMed ID: 12014660
[TBL] [Abstract][Full Text] [Related]
52. Studies on quinones. Part 42: Synthesis of furylquinone and hydroquinones with antiproliferative activity against human tumor cell lines.
Benites J; Valderrama JA; Rivera F; Rojo L; Campos N; Pedro M; José Nascimento MS
Bioorg Med Chem; 2008 Jan; 16(2):862-8. PubMed ID: 17964791
[TBL] [Abstract][Full Text] [Related]
53. Cytotoxic bisindole alkaloids from a marine sponge Spongosorites sp.
Bao B; Sun Q; Yao X; Hong J; Lee CO; Sim CJ; Im KS; Jung JH
J Nat Prod; 2005 May; 68(5):711-5. PubMed ID: 15921415
[TBL] [Abstract][Full Text] [Related]
54. In-vitro antiproliferative activities and kinase inhibitory potencies of glycosyl-isoindigo derivatives.
Sassatelli M; Bouchikhi F; Aboab B; Anizon F; Fabbro D; Prudhomme M; Moreau P
Anticancer Drugs; 2007 Oct; 18(9):1069-74. PubMed ID: 17704657
[TBL] [Abstract][Full Text] [Related]
55. Design, synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors.
Lee S; Shinji C; Ogura K; Shimizu M; Maeda S; Sato M; Yoshida M; Hashimoto Y; Miyachi H
Bioorg Med Chem Lett; 2007 Sep; 17(17):4895-900. PubMed ID: 17588744
[TBL] [Abstract][Full Text] [Related]
56. Synthesis of 1,7-annulated indoles and their applications in the studies of cyclin dependent kinase inhibitors.
Zhu G; Conner SE; Zhou X; Chan HK; Shih C; Engler TA; Al-Awar RS; Brooks HB; Watkins SA; Spencer CD; Schultz RM; Dempsey JA; Considine EL; Patel BR; Ogg CA; Vasudevan V; Lytle ML
Bioorg Med Chem Lett; 2004 Jun; 14(12):3057-61. PubMed ID: 15149644
[TBL] [Abstract][Full Text] [Related]
57. Synthesis of paullones with aminoalkyl side chains.
Wieking K; Knockaert M; Leost M; Zaharevitz DW; Meijer L; Kunick C
Arch Pharm (Weinheim); 2002 Jul; 335(7):311-7. PubMed ID: 12207280
[TBL] [Abstract][Full Text] [Related]
58. Concise synthesis and structure-activity relationships of combretastatin A-4 analogues, 1-aroylindoles and 3-aroylindoles, as novel classes of potent antitubulin agents.
Liou JP; Chang YL; Kuo FM; Chang CW; Tseng HY; Wang CC; Yang YN; Chang JY; Lee SJ; Hsieh HP
J Med Chem; 2004 Aug; 47(17):4247-57. PubMed ID: 15293996
[TBL] [Abstract][Full Text] [Related]
59. Omega-alkoxy analogues of SAHA (vorinostat) as inhibitors of HDAC: a study of chain-length and stereochemical dependence.
Hanessian S; Auzzas L; Giannini G; Marzi M; Cabri W; Barbarino M; Vesci L; Pisano C
Bioorg Med Chem Lett; 2007 Nov; 17(22):6261-5. PubMed ID: 17892933
[TBL] [Abstract][Full Text] [Related]
60. Novel diarylsulfonylurea derivatives as potent antimitotic agents.
Kim S; Park JH; Koo SY; Kim JI; Kim MH; Kim JE; Jo K; Choi HG; Lee SB; Jung SH
Bioorg Med Chem Lett; 2004 Dec; 14(24):6075-8. PubMed ID: 15546733
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
