Supplemental material
Journal of Enzyme Inhibition and Medicinal Chemistry
Volume 33, 2018 - Issue 1
Related Research Data
Novel Combretastatin Analogues Effective against Murine Solid Tumors: Design and Structure−Activity Relationships
Source:
American Chemical Society (ACS)
Synthesis and biological evaluation of novel 4,5-disubstituted 2H-1,2,3-triazoles as cis-constrained analogues of combretastatin A-4
Source:
Elsevier BV
Design, Synthesis, and Biological Evaluation of Novel Pyridine-Bridged Analogues of Combretastatin-A4 as Anticancer Agents
Source:
American Chemical Society (ACS)
(Z)-2-(2-bromophenyl)-3-{[4-(1-methyl-piperazine)amino]phenyl}acrylonitrile (DG172): an orally bioavailable PPARβ/δ-selective ligand with inverse agonistic properties.
Source:
American Chemical Society (ACS)
Anticancer sulfonamide hybrids that inhibit bladder cancer cells growth and migration as tubulin polymerisation inhibitors.
Source:
Informa UK Limited
Lead identification of conformationally restricted β-lactam type combretastatin analogues: Synthesis, antiproliferative activity and tubulin targeting effects
Source:
France : Elsevier Masson
Synthesis and characterisation of celastrol derivatives as potential anticancer agents.
Source:
Taylor & Francis Group
Preparation of 4,5 disubstituted-2H-1,2,3-triazoles from (Z)-2,3-diaryl substituted acrylonitriles
Source:
Elsevier BV
Rho-associated kinase (ROCK) inhibition reverses low cell activity on hydrophobic surfaces
Source:
Elsevier BV
Syntheses and biological evaluation of 1,2,3-triazole and 1,3,4-oxadiazole derivatives of imatinib
Source:
Elsevier BV
Synthesis and bioactivity evaluation of 2,3-diaryl acrylonitrile derivatives as potential anticancer agents.
Source:
Elsevier BV
Synthesis and biological evaluation of novel 7-hydroxy-4-phenylchromen-2-one-linked to triazole moieties as potent cytotoxic agents.
Source:
Informa UK Limited
Nature: a vital source of leads for anticancer drug development
Source:
Springer Science and Business Media LLC
Substituted quinazolines, part 3. Synthesis, in vitro antitumor activity and molecular modeling study of certain 2-thieno-4(3H)-quinazolinone analogs.
Source:
Elsevier BV
Linking provided by
