Erscheinungsjahr
Medientyp
Format
Lizenz
Sprache
Synonyme wurden verwendet für: Chemistry
Suche ohne Synonyme: journal:(Journal of Medicinal Chemistry)
Verwendete Synonyme:
- allgemeine chemie
- chemie
-
1,3,4-Oxadiazole-naphthalene hybrids as potential VEGFR-2 inhibitors: design, synthesis, antiproliferative activity, apoptotic effect, and in silico studies
Freier ZugriffTaylor & Francis Verlag | 2022| -
First-in-Class Cyclic Temporin L Analogue: Design, Synthesis, and Antimicrobial Assessment
Freier ZugriffAmerican Chemical Society | 2021| -
Rational design of small molecules able to inhibit α-synuclein amyloid aggregation for the treatment of Parkinson’s disease
Freier ZugriffTaylor & Francis Verlag | 2020| -
Inhibition studies of bacterial α-carbonic anhydrases with phenols
Freier ZugriffTaylor & Francis Verlag | 2022| -
Synthesis and characterisation of thiobarbituric acid enamine derivatives, and evaluation of their α-glucosidase inhibitory and anti-glycation activity
Freier ZugriffTaylor & Francis Verlag | 2020| -
In vitro anticancer potentiality and molecular modelling study of novel amino acid derivatives based on N1,N3-bis-(1-hydrazinyl-1-oxopropan-2-yl) isophthalamide
Freier ZugriffTaylor & Francis Verlag | 2019| -
In vitro investigating of anticancer activity of new 7-MEOTA-tacrine heterodimers
Freier ZugriffTaylor & Francis Verlag | 2019| -
Cyanobacteria and microalgae bioactive compounds in skin-ageing: potential to restore extracellular matrix filling and overcome hyperpigmentation
Freier ZugriffTaylor & Francis Verlag | 2021| -
Antibiotic Conjugates with an Artificial MECAM-Based Siderophore Are Potent Agents against Gram-Positive and Gram-Negative Bacterial Pathogens
Freier ZugriffAmerican Chemical Society | 2021| -
Echinocandins – structure, mechanism of action and use in antifungal therapy
Freier ZugriffTaylor & Francis Verlag | 2022| -
Activation studies of the β-carbonic anhydrases from Escherichia coli with amino acids and amines
Freier ZugriffTaylor & Francis Verlag | 2020| -
Unveiling the interaction profile of rosmarinic acid and its bioactive substructures with serum albumin
Freier ZugriffTaylor & Francis Verlag | 2020| -
Recent progress in the development of steroid sulphatase inhibitors – examples of the novel and most promising compounds from the last decade
Freier ZugriffTaylor & Francis Verlag | 2020| -
C-2 phenyl replacements to obtain potent quinoline-based Staphylococcus aureus NorA inhibitors
Freier ZugriffTaylor & Francis Verlag | 2020| -
In vitro inhibition of Mycobacterium tuberculosis β-carbonic anhydrase 3 with Mono- and dithiocarbamates and evaluation of their toxicity using zebrafish developing embryos
Freier ZugriffTaylor & Francis Verlag | 2020| -
Pharmacological Targeting of Executioner Proteins: Controlling Life and Death
Freier ZugriffAmerican Chemical Society | 2021| -
7-Acylamino-3H-1,2-benzoxathiepine 2,2-dioxides as new isoform-selective carbonic anhydrase IX and XII inhibitors
Freier ZugriffTaylor & Francis Verlag | 2020| -
Anticancer sulfonamide hybrids that inhibit bladder cancer cells growth and migration as tubulin polymerisation inhibitors
Freier ZugriffTaylor & Francis Verlag | 2019| -
Synthesis and biological evaluation of novel 8-substituted quinoline-2-carboxamides as carbonic anhydrase inhibitors
Freier ZugriffTaylor & Francis Verlag | 2019| -
Identification of 1H-pyrazolo[3,4-b]pyridine derivatives as potent ALK-L1196M inhibitors
Freier ZugriffTaylor & Francis Verlag | 2019| -
Discovery of novel dual-active 3-(4-(dimethylamino)phenyl)-7-aminoalcoxy-coumarin as potent and selective acetylcholinesterase inhibitor and antioxidant
Freier ZugriffTaylor & Francis Verlag | 2019| -
Design and application of oral colon administration system
Freier ZugriffTaylor & Francis Verlag | 2019| -
Phaeodactylum tricornutum as a model organism for testing the membrane penetrability of sulphonamide carbonic anhydrase inhibitors
Freier ZugriffTaylor & Francis Verlag | 2019| -
Small molecule inhibitors of cyclin-dependent kinase 9 for cancer therapy
Freier ZugriffTaylor & Francis Verlag | 2021| -
Activation of carbonic anhydrases from human brain by amino alcohol oxime ethers: towards human carbonic anhydrase VII selective activators
Freier ZugriffTaylor & Francis Verlag | 2021| -
Novel 2-indolinones containing a sulfonamide moiety as selective inhibitors of candida β-carbonic anhydrase enzyme
Freier ZugriffTaylor & Francis Verlag | 2019| -
Organoruthenium(II) complexes of acetazolamide potently inhibit human carbonic anhydrase isoforms I, II, IX and XII
Freier ZugriffTaylor & Francis Verlag | 2019| -
Discovery of BPR1R024, an Orally Active and Selective CSF1R Inhibitor that Exhibits Antitumor and Immunomodulatory Activity in a Murine Colon Tumor Model
Freier ZugriffAmerican Chemical Society | 2021| -
Design, Synthesis, and Biological Evaluation of Boron-Containing Macrocyclic Polyamines and Their Zinc(II) Complexes for Boron Neutron Capture Therapy
Freier ZugriffAmerican Chemical Society | 2021| -
Soyasaponins from Zolfino bean as aldose reductase differential inhibitors
Freier ZugriffTaylor & Francis Verlag | 2019| -
New peptide derived antimalaria and antimicrobial agents bearing sulphonamide moiety
Freier ZugriffTaylor & Francis Verlag | 2019| -
Dual and selective inhibitors of pteridine reductase 1 (PTR1) and dihydrofolate reductase-thymidylate synthase (DHFR-TS) from Leishmania chagasi
Freier ZugriffTaylor & Francis Verlag | 2019| -
Hydroxypropyl-β-cyclodextrin as an effective carrier of curcumin – piperine nutraceutical system with improved enzyme inhibition properties
Freier ZugriffTaylor & Francis Verlag | 2020| -
From cycloheptathiophene-3-carboxamide to oxazinone-based derivatives as allosteric HIV-1 ribonuclease H inhibitors
Freier ZugriffTaylor & Francis Verlag | 2019| -
Carboxylesterase Notum Is a Druggable Target to Modulate Wnt Signaling
Freier ZugriffAmerican Chemical Society | 2021| -
Synthesis and Pharmacological Evaluation of Novel Non-nucleotide Purine Derivatives as P2X7 Antagonists for the Treatment of Neuroinflammation
Freier ZugriffAmerican Chemical Society | 2021| -
Towards discovery of new leishmanicidal scaffolds able to inhibit Leishmania GSK-3
Freier ZugriffTaylor & Francis Verlag | 2020| -
Novel 4-arylaminoquinazolines bearing N,N-diethyl(aminoethyl)amino moiety with antitumour activity as EGFRwt-TK inhibitor
Freier ZugriffTaylor & Francis Verlag | 2019| -
Exploration of TRPM8 Binding Sites by β‑Carboline-Based Antagonists and Their In Vitro Characterization and In Vivo Analgesic Activities
Freier ZugriffAmerican Chemical Society | 2020| -
Solubility enhancement of mefenamic acid by inclusion complex with β-cyclodextrin: in silico modelling, formulation, characterisation, and in vitro studies
Freier ZugriffTaylor & Francis Verlag | 2021| -
Design, synthesis and biological evaluation of 1-Aryl-5-(4-arylpiperazine-1-carbonyl)-1H-tetrazols as novel microtubule destabilizers
Freier ZugriffTaylor & Francis Verlag | 2021| -
Synthesis of thiazolidin-4-ones and thiazinan-4-ones from 1-(2-aminoethyl)pyrrolidine as acetylcholinesterase inhibitors
Freier ZugriffTaylor & Francis Verlag | 2020| -
Inhibition of African swine fever virus protease by myricetin and myricitrin
Freier ZugriffTaylor & Francis Verlag | 2020| -
A structure-based approach towards the identification of novel antichagasic compounds: Trypanosoma cruzi carbonic anhydrase inhibitors
Freier ZugriffTaylor & Francis Verlag | 2020| -
Exosomes in head and neck cancer. Updating and revisiting
Freier ZugriffTaylor & Francis Verlag | 2019| -
Cinnamic acid derivatives: inhibitory activity against Escherichia coli β-glucuronidase and structure–activity relationships
Freier ZugriffTaylor & Francis Verlag | 2020| -
Discovery of novel quinoline-based analogues of combretastatin A-4 as tubulin polymerisation inhibitors with apoptosis inducing activity and potent anticancer effect
Freier ZugriffTaylor & Francis Verlag | 2021| -
DNDI-6148: A Novel Benzoxaborole Preclinical Candidate for the Treatment of Visceral Leishmaniasis
Freier ZugriffAmerican Chemical Society | 2021| -
Design, Synthesis, and Characterization of TNP-2198, a Dual-Targeted Rifamycin-Nitroimidazole Conjugate with Potent Activity against Microaerophilic and Anaerobic Bacterial Pathogens
Freier ZugriffAmerican Chemical Society | 2022|
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