Pages that link to "Q69804725"
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The following pages link to Antimitotic natural products combretastatin A-4 and combretastatin A-2: studies on the mechanism of their inhibition of the binding of colchicine to tubulin (Q69804725):
Displaying 50 items.
- Antivascular and antitumor properties of the tubulin-binding chalcone TUB091 (Q27705273) (← links)
- KPU-300, a Novel Benzophenone-Diketopiperazine-Type Anti-Microtubule Agent with a 2-Pyridyl Structure, Is a Potent Radiosensitizer That Synchronizes the Cell Cycle in Early M Phase (Q28551906) (← links)
- Comparative molecular field analysis of colchicine inhibition and tubulin polymerization for combretastatins binding to the colchicine binding site on beta-tubulin (Q30305847) (← links)
- Antiproliferative 4-(1,2,4-oxadiazol-5-yl)piperidine-1-carboxamides, a new tubulin inhibitor chemotype. (Q30370844) (← links)
- New arylthioindoles and related bioisosteres at the sulfur bridging group. 4. Synthesis, tubulin polymerization, cell growth inhibition, and molecular modeling studies. (Q33555754) (← links)
- Synthesis and Biological Evaluation of 2-Methyl-4,5-Disubstituted Oxazoles as a Novel Class of Highly Potent Antitubulin Agents (Q33560133) (← links)
- A-ring dihalogenation increases the cellular activity of combretastatin-templated tetrazoles (Q33630470) (← links)
- A boronic acid chalcone analog of combretastatin A-4 as a potent anti-proliferation agent (Q33641044) (← links)
- Synthesis and antitumor activity of 1,5-disubstituted 1,2,4-triazoles as cis-restricted combretastatin analogues (Q33921024) (← links)
- Synthesis, anti-tubulin and antiproliferative SAR of steroidomimetic dihydroisoquinolinones (Q33967160) (← links)
- Substituted 2-(3',4',5'-trimethoxybenzoyl)-benzo[b]thiophene derivatives as potent tubulin polymerization inhibitors. (Q34070809) (← links)
- Optimisation of tetrahydroisoquinoline-based chimeric microtubule disruptors (Q34094248) (← links)
- Application of the McMurry coupling reaction in the synthesis of tri- and tetra-arylethylene analogues as potential cancer chemotherapeutic agents (Q34109712) (← links)
- New pyrrole derivatives with potent tubulin polymerization inhibiting activity as anticancer agents including hedgehog-dependent cancer (Q34133912) (← links)
- Synthesis, antimitotic and antivascular activity of 1-(3',4',5'-trimethoxybenzoyl)-3-arylamino-5-amino-1,2,4-triazoles (Q34155028) (← links)
- New agents in cancer clinical trials (Q34293629) (← links)
- Targeting tumour vasculature: the development of combretastatin A4. (Q34572069) (← links)
- The biology of the combretastatins as tumour vascular targeting agents (Q34680614) (← links)
- Synthesis and biological evaluation of 2-(3',4',5'-trimethoxybenzoyl)-3-aryl/arylaminobenzo[b]thiophene derivatives as a novel class of antiproliferative agents. (Q34783706) (← links)
- Design and synthesis of 3,5-disubstituted boron-containing 1,2,4-oxadiazoles as potential combretastatin A-4 (CA-4) analogs (Q34987894) (← links)
- Synthesis of novel antimitotic agents based on 2-amino-3-aroyl-5-(hetero)arylethynyl thiophene derivatives (Q35008501) (← links)
- Convergent synthesis and biological evaluation of 2-amino-4-(3',4',5'-trimethoxyphenyl)-5-aryl thiazoles as microtubule targeting agents (Q35148206) (← links)
- Drugs that target dynamic microtubules: a new molecular perspective (Q35163252) (← links)
- 2-Methoxyestradiol, an endogenous mammalian metabolite, inhibits tubulin polymerization by interacting at the colchicine site (Q35207843) (← links)
- Synthesis and antitumor molecular mechanism of agents based on amino 2-(3',4',5'-trimethoxybenzoyl)benzo[b]furan: inhibition of tubulin and induction of apoptosis (Q35309200) (← links)
- Design and synthesis of imidazo[2,1-b]thiazole-chalcone conjugates: microtubule-destabilizing agents (Q35330786) (← links)
- Fragment based group QSAR and molecular dynamics mechanistic studies on arylthioindole derivatives targeting the α-β interfacial site of human tubulin (Q35529563) (← links)
- Design, synthesis, in vitro, and in vivo anticancer and antiangiogenic activity of novel 3-arylaminobenzofuran derivatives targeting the colchicine site on tubulin. (Q35532093) (← links)
- One-pot synthesis and biological evaluation of 2-pyrrolidinyl-4-amino-5-(3',4',5'-trimethoxybenzoyl)thiazole: a unique, highly active antimicrotubule agent (Q35591338) (← links)
- Secondary metabolites as DNA topoisomerase inhibitors: A new era towards designing of anticancer drugs. (Q35646690) (← links)
- Design and synthesis of 2-heterocyclyl-3-arylthio-1H-indoles as potent tubulin polymerization and cell growth inhibitors with improved metabolic stability. (Q35682298) (← links)
- Synthesis and evaluation of 1,5-disubstituted tetrazoles as rigid analogues of combretastatin A-4 with potent antiproliferative and antitumor activity (Q35694476) (← links)
- Regioselective synthesis of water-soluble monophosphate derivatives of combretastatin A-1. (Q35743971) (← links)
- Substituted 3-(5-imidazo[2,1-b]thiazolylmethylene)-2-indolinones and analogues: synthesis, cytotoxic activity, and study of the mechanism of action (Q35815432) (← links)
- Antineoplastic agents. 515. Synthesis of human cancer cell growth inhibitors derived from 3,4-methylenedioxy-5,4'-dimethoxy-3'-amino-Z-stilbene (Q35909593) (← links)
- New Indole Tubulin Assembly Inhibitors Cause Stable Arrest of Mitotic Progression, Enhanced Stimulation of Natural Killer Cell Cytotoxic Activity, and Repression of Hedgehog-Dependent Cancer (Q36004162) (← links)
- Discovery and optimization of a series of 2-aryl-4-amino-5-(3',4',5'-trimethoxybenzoyl)thiazoles as novel anticancer agents. (Q36079759) (← links)
- Interaction of pseudolaric acid B with the colchicine site of tubulin (Q36110135) (← links)
- Disrupting tumour blood vessels (Q36146900) (← links)
- Novel 3-Substituted 7-Phenylpyrrolo[3,2-f]quinolin-9(6H)-ones as Single Entities with Multitarget Antiproliferative Activity (Q36239589) (← links)
- SYNTHESIS AND BIOLOGICAL EVALUATION OF BIARYL ANALOGS OF ANTITUBULIN COMPOUNDS (Q36320567) (← links)
- Novel water-soluble substituted pyrrolo[3,2-d]pyrimidines: design, synthesis, and biological evaluation as antitubulin antitumor agents (Q36328577) (← links)
- Synthesis and biological evaluation of 2-substituted-4-(3',4',5'-trimethoxyphenyl)-5-aryl thiazoles as anticancer agents (Q36503104) (← links)
- Synthesis and biological evaluation of N-alkyl-N-(4-methoxyphenyl)pyridin-2-amines as a new class of tubulin polymerization inhibitors (Q36536517) (← links)
- Toward highly potent cancer agents by modulating the C-2 group of the arylthioindole class of tubulin polymerization inhibitors (Q36584618) (← links)
- Synthesis and biological evaluation of 2-(alkoxycarbonyl)-3-anilinobenzo[b]thiophenes and thieno[2,3-b]pyridines as new potent anticancer agents (Q36822993) (← links)
- Design and Synthesis of Potent in Vitro and in Vivo Anticancer Agents Based on 1-(3',4',5'-Trimethoxyphenyl)-2-Aryl-1H-Imidazole (Q36928505) (← links)
- An Amino-Benzosuberene Analogue That Inhibits Tubulin Assembly and Demonstrates Remarkable Cytotoxicity (Q36929601) (← links)
- Synthesis and biological evaluation of 2-(3',4',5'-trimethoxybenzoyl)-3-N,N-dimethylamino benzo[b]furan derivatives as inhibitors of tubulin polymerization. (Q36952871) (← links)
- Synthesis and biological evaluation of 2-amino-3-(3',4',5'-trimethoxybenzoyl)-6-substituted-4,5,6,7-tetrahydrothieno[2,3-c]pyridine derivatives as antimitotic agents and inhibitors of tubulin polymerization (Q37021662) (← links)