Potenial antitumor agents. 28. Deoxyribonucleic acid polyintercalating agents.
about
Selective toxicity of nitracrine to hypoxic mammalian cellsA novel small molecular weight compound with a carbazole structure that demonstrates potent human immunodeficiency virus type-1 integrase inhibitory activity.Dichamanetin inhibits cancer cell growth by affecting ROS-related signaling components through mitochondrial-mediated apoptosis.Radiosensitization of E. coli B/r by 9-anilinoacridines.Stimuli responsive charge-switchable lipids: Capture and release of nucleic acidsSynthesis, characterization, and in vitro transfection activity of charge-reversal amphiphiles for DNA delivery.Acridine derivatives: a patent review (2009 - 2010).DNA Interaction Studies of Selected Polyamine Conjugates.Merbarone inhibits the catalytic activity of human topoisomerase IIalpha by blocking DNA cleavage.Synthesis, Biological Activity and Preliminary in Silico ADMET Screening of Polyamine Conjugates with Bicyclic Systems.Functionalized polyglycerol amine nanogels as nanocarriers for DNA.Design, synthesis and biological evaluation of ezrin inhibitors targeting metastatic osteosarcoma.pH luminescence switch, DNA binding and photocleavage, and cytotoxicity of a dinuclear ruthenium complex.Cationic nucleoside lipids based on a 3-nitropyrrole universal base for siRNA delivery.Surface charge density determines the efficiency of cationic gemini surfactant based lipofection.1H NMR study of an ethidium dimer poly(dA-dT) complex: evidence of a transition between bis and monointercalation.DNA-binding characterization of a novel anti-tumour benzo[a]phenazine derivative NC-182: spectroscopic and viscometric studiesDifferential effects of spermine and its analogues on the structures of polynucleotides complexed with ethidium bromide.Effects of variation in the structure of spermine on the association with DNA and the induction of DNA conformational changesIntracellular DNA damage produced by a series of diacridinesUtilizing combinatorial chemistry and rational design: peptidic tweezers with nanomolar affinity to DNA can be transformed into efficient vectors for gene delivery by addition of a lipophilic tail.Equilibrium constants for the binding of an homologous series of monofunctional and bifunctional intercalating diacridines to calf thymus DNA.The regiochemical distribution of positive charges along cholesterol polyamine carbamates plays significant roles in modulating DNA binding affinity and lipofection.The effects of structural variations of thiophene-containing Ru(II) complexes on the acid-base and DNA binding properties.Double-degradable responsive self-assembled multivalent arrays--temporary nanoscale recognition between dendrons and DNA.An exploration of the structure-activity relationships of 4-aminoquinolines: novel antimalarials with activity in-vivo.Self-Assembled Multivalent (SAMul) Polyanion Binding-Impact of Hydrophobic Modifications in the Micellar Core on DNA and Heparin Binding at the Peripheral Cationic Ligands.Chiral recognition at self-assembled multivalent (SAMul) nanoscale interfaces - enantioselectivity in polyanion binding.Electrostatic binding of polyanions using self-assembled multivalent (SAMul) ligand displays - structure-activity effects on DNA/heparin bindingPolyglycerol-based amphiphilic dendrons as potential siRNA carriers for in vivo applicationsEffects of a PEG additive on the biomolecular interactions of self-assembled dendron nanostructuresControlled Release of DNA From Photoresponsive Hyperbranched Polyglycerols with Oligoamine Shells
P2860
Q28367034-CC4E6693-4E85-46AA-A2D9-337EEF5B076DQ33228536-9F164984-F375-4E8A-B3F2-8C6426FB97D5Q34802941-A318C5BC-A71A-45F4-9BF1-95AE2186BB27Q36043432-B6F788E1-F677-48F8-89B4-455DA18A07A3Q36986774-18A9D56D-1841-48FC-A616-7AA3285579D1Q37427328-CF051EBB-D892-4C76-B88C-D49DBF5D882CQ37842441-ECDF24B8-3049-44E9-A913-FD2DB189B693Q38290849-5923661A-0FC2-41CD-94E5-0ACE62C4D50CQ38335859-6B643DC1-D9F5-45D1-AE61-87FF849ABA9BQ38703748-49535C5E-F6E7-47C7-B268-518C02C48989Q38991303-4164275D-B2A9-4032-BF74-8DA3C54836F2Q39044688-CBC190B9-8981-4546-A500-A45D8B2CB830Q39187037-789E3CC9-82E8-4D09-9FEA-6DB5C68DED1CQ39892536-6ED0703F-236F-43B8-9921-45FCEA4EDF94Q40227616-D6455851-9E8A-47D1-BA8F-93192A663F87Q40491952-804FB87A-9068-4224-9176-AE90C8811990Q41932022-25B64D39-FF34-49EB-B0EA-AE38C34358AEQ42161306-DE339561-A183-435F-BF57-BCE32AA1A7D0Q42162314-58D6473A-D47D-4F33-86C7-4E353F3EBA5BQ42849073-5DCBA282-A130-48AA-A532-81702713FFECQ44308999-81E47FA9-9B62-4802-8841-485813A43954Q44534851-D971A991-A1BB-4B17-A118-BA1EAE90C2ADQ44986644-5FE117B5-883B-4420-B5BB-DF2EB062BF31Q45873320-A2FD6D20-AB2C-44B2-9CEF-3E81428E3781Q46365854-F8D5F4A1-3B31-4624-B410-4B3DF877F001Q48033243-E033248A-283F-4B52-8C0F-6DB51BE7F8B0Q48106027-91BA12C1-6D46-496B-AAD6-229789C14391Q51216425-FC06AB8A-CC90-4EBB-8375-EBF378842C94Q58324562-CE74F2CD-FC12-4DE6-8382-5ABBB1C0D0A8Q58324580-B9821C26-E36A-4A66-A854-69C7ED217034Q58324586-B29D0F68-9350-4742-977D-1D38B27942B0Q58324590-C06CCB6D-87C3-438A-BD5D-2D2283EB6C6B
P2860
Potenial antitumor agents. 28. Deoxyribonucleic acid polyintercalating agents.
description
1978 nî lūn-bûn
@nan
1978年の論文
@ja
1978年学术文章
@wuu
1978年学术文章
@zh
1978年学术文章
@zh-cn
1978年学术文章
@zh-hans
1978年学术文章
@zh-my
1978年学术文章
@zh-sg
1978年學術文章
@yue
1978年學術文章
@zh-hant
name
Potenial antitumor agents. 28. Deoxyribonucleic acid polyintercalating agents.
@en
Potenial antitumor agents. 28. Deoxyribonucleic acid polyintercalating agents.
@nl
type
label
Potenial antitumor agents. 28. Deoxyribonucleic acid polyintercalating agents.
@en
Potenial antitumor agents. 28. Deoxyribonucleic acid polyintercalating agents.
@nl
prefLabel
Potenial antitumor agents. 28. Deoxyribonucleic acid polyintercalating agents.
@en
Potenial antitumor agents. 28. Deoxyribonucleic acid polyintercalating agents.
@nl
P2093
P356
P1476
Potenial antitumor agents. 28. Deoxyribonucleic acid polyintercalating agents.
@en
P2093
P304
P356
10.1021/JM00205A013
P407
P577
1978-07-01T00:00:00Z