227 related articles for article (PubMed ID: 18314944)
21. Synthesis and structure-activity correlation of natural-product inspired cyclodepsipeptides stabilizing F-actin.
Tannert R; Milroy LG; Ellinger B; Hu TS; Arndt HD; Waldmann H
J Am Chem Soc; 2010 Mar; 132(9):3063-77. PubMed ID: 20148556
[TBL] [Abstract][Full Text] [Related]
22. Progress toward the total synthesis of lucentamycin A: total synthesis and biological evaluation of 8-epi-lucentamycin A.
Daniels RN; Melancon BJ; Wang EA; Crews BC; Marnett LJ; Sulikowski GA; Lindsley CW
J Org Chem; 2009 Nov; 74(22):8852-5. PubMed ID: 19908916
[TBL] [Abstract][Full Text] [Related]
23. Design, synthesis, and biological properties of highly potent tubulysin D analogues.
Patterson AW; Peltier HM; Sasse F; Ellman JA
Chemistry; 2007; 13(34):9534-41. PubMed ID: 17828721
[TBL] [Abstract][Full Text] [Related]
24. First total synthesis of tubulysin B.
Pando O; Dörner S; Preusentanz R; Denkert A; Porzel A; Richter W; Wessjohann L
Org Lett; 2009 Dec; 11(24):5567-9. PubMed ID: 19919080
[TBL] [Abstract][Full Text] [Related]
25. D-ring modified novel isosteviol derivatives: design, synthesis and cytotoxic activity evaluation.
Zhang T; Lu LH; Liu H; Wang JW; Wang RX; Zhang YX; Tao JC
Bioorg Med Chem Lett; 2012 Sep; 22(18):5827-32. PubMed ID: 22901386
[TBL] [Abstract][Full Text] [Related]
26. Versatile synthesis of new cytotoxic agents structurally related to hemiasterlins.
Simoni D; Lee RM; Durrant DE; Chi NW; Baruchello R; Rondanin R; Rullo C; Marchetti P
Bioorg Med Chem Lett; 2010 Jun; 20(11):3431-5. PubMed ID: 20430617
[TBL] [Abstract][Full Text] [Related]
27. Synthesis and antiproliferative activity of culicinin D analogues containing simplified AHMOD-based residues.
Stubbing LA; Kavianinia I; Abbattista MR; Harris PWR; Smaill JB; Patterson AV; Brimble MA
Eur J Med Chem; 2019 Sep; 177():235-246. PubMed ID: 31152989
[TBL] [Abstract][Full Text] [Related]
28. β-Glucuronidase triggers extracellular MMAE release from an integrin-targeted conjugate.
López Rivas P; Müller C; Breunig C; Hechler T; Pahl A; Arosio D; Belvisi L; Pignataro L; Dal Corso A; Gennari C
Org Biomol Chem; 2019 May; 17(19):4705-4710. PubMed ID: 31020985
[TBL] [Abstract][Full Text] [Related]
29. Expeditious Total Synthesis of Hemiasterlin through a Convergent Multicomponent Strategy and Its Use in Targeted Cancer Therapeutics.
Charoenpattarapreeda J; Walsh SJ; Carroll JS; Spring DR
Angew Chem Int Ed Engl; 2020 Dec; 59(51):23045-23050. PubMed ID: 32894646
[TBL] [Abstract][Full Text] [Related]
30. Synthesis and antitumour activity of new muricatacin and goniofufurone analogues.
Popsavin V; Srećo B; Krstić I; Popsavin M; Kojić V; Bogdanović G
Eur J Med Chem; 2006 Oct; 41(10):1217-22. PubMed ID: 16891043
[TBL] [Abstract][Full Text] [Related]
31. Synthesis and anticancer activity of novel C6-piperazine substituted purine steroid-nucleosides analogues.
Huang LH; Xu HD; Yang ZY; Zheng YF; Liu HM
Steroids; 2014 Apr; 82():1-6. PubMed ID: 24378780
[TBL] [Abstract][Full Text] [Related]
32. Toward Angiogenesis Inhibitors Based on the Conjugation of Organometallic Platinum(II) Complexes to RGD Peptides.
Zamora A; Gandioso A; Massaguer A; Buenestado S; Calvis C; Hernández JL; Mitjans F; Rodríguez V; Ruiz J; Marchán V
ChemMedChem; 2018 Sep; 13(17):1755-1762. PubMed ID: 29932312
[TBL] [Abstract][Full Text] [Related]
33. New analogues of laminin active fragment YIGSR: synthesis and biological activity in vitro and in vivo.
Witkowska E; Oriowska A; Izdebski J; Salwa J; Wietrzyk J; Opolski A
J Pept Sci; 2004 May; 10(5):285-90. PubMed ID: 15160840
[TBL] [Abstract][Full Text] [Related]
34. Preliminary studies of new proteasome inhibitors in the tumor targeting approach: synthesis and in vitro cytotoxicity.
Vivier M; Jarrousse AS; Bouchon B; Galmier MJ; Auzeloux P; Sauzieres J; Madelmont JC
J Med Chem; 2005 Oct; 48(21):6731-40. PubMed ID: 16220988
[TBL] [Abstract][Full Text] [Related]
35. A new strategy for the synthesis of crucigasterin A, and cytotoxic activity of this compound and its related analogues.
Kumar JN; Reddy PR; Das B; Kumar CG; Sujitha P
Bioorg Med Chem Lett; 2013 Sep; 23(18):5192-4. PubMed ID: 23932340
[TBL] [Abstract][Full Text] [Related]
36. Tumor-cell-targeted methionine-enkephalin analogues containing unnatural amino acids: design, synthesis, and in vitro antitumor activity.
Horvat S; Mlinarić-Majerski K; Glavas-Obrovac L; Jakas A; Veljković J; Marczi S; Kragol G; Roscić M; Matković M; Milostić-Srb A
J Med Chem; 2006 Jun; 49(11):3136-42. PubMed ID: 16722632
[TBL] [Abstract][Full Text] [Related]
37. N-methylsansalvamide a peptide analogues. Potent new antitumor agents.
Liu S; Gu W; Lo D; Ding XZ; Ujiki M; Adrian TE; Soff GA; Silverman RB
J Med Chem; 2005 May; 48(10):3630-8. PubMed ID: 15887970
[TBL] [Abstract][Full Text] [Related]
38. Syntheses and biological evaluation of C-3'-N-acyl modified taxane analogues from 1-deoxybaccatin-VI.
Li QF; Lin HX; Cui YM; Xu PP
Eur J Med Chem; 2015 Nov; 104():97-105. PubMed ID: 26448037
[TBL] [Abstract][Full Text] [Related]
39. Synthesis and structure-activity relationship studies of novel tubulysin U analogues--effect on cytotoxicity of structural variations in the tubuvaline fragment.
Shankar SP; Jagodzinska M; Malpezzi L; Lazzari P; Manca I; Greig IR; Sani M; Zanda M
Org Biomol Chem; 2013 Apr; 11(14):2273-87. PubMed ID: 23411563
[TBL] [Abstract][Full Text] [Related]
40. Synthesis and cytotoxicity of 3-aryl acrylic amide derivatives of the simplified saframycin-ecteinascidin skeleton prepared from L-dopa.
Guo J; Dong W; Liu W; Yan Z; Wang N; Liu Z
Eur J Med Chem; 2013 Apr; 62():670-6. PubMed ID: 23434640
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]