about
Bacterial Sliding Clamp Inhibitors that Mimic the Sequential Binding Mechanism of Endogenous Linear MotifsRNA polymerase-induced remodelling of NusA produces a pause enhancement complex.Identification of inhibitors of bacterial RNA polymerase.From indole to pyrrole, furan, thiophene and pyridine: Search for novel small molecule inhibitors of bacterial transcription initiation complex formation.Bacterial Transcription Inhibitor of RNA Polymerase Holoenzyme Formation by Structure-Based Drug Design: From in Silico Screening to Validation.Identification and validation of small molecule modulators of the NusB-NusE interaction.Bacterial Transcription as a Target for Antibacterial Drug Development.Catalytic asymmetric C-N bond formation: phosphine-catalyzed intra- and intermolecular γ-addition of nitrogen nucleophiles to allenoates and alkynoatesSynthesis and Antibacterial Evaluation of Novel 3-Substituted Ocotillol-Type Derivatives as Leads.Design, synthesis, nitric oxide release and antibacterial evaluation of novel nitrated ocotillol-type derivatives.First-In-Class Inhibitor of Ribosomal RNA Synthesis with Antimicrobial Activity against Staphylococcus aureus.Synthesis and biological activity of novel mono-indole and mono-benzofuran inhibitors of bacterial transcription initiation complex formation.Cascade Metathesis Reactions for the Synthesis of Taxane and Isotaxane Derivatives.Inhibitors of bacterial transcription initiation complex formation.Ring-closing metathesis in the synthesis of BC ring-systems of taxol.Small molecule inhibitors of bacterial transcription complex formation.In Vitro Transcription Assays and Their Application in Drug Discovery.Synthesis and biological activity of novel bis-indole inhibitors of bacterial transcription initiation complex formation.Synthesis and biological evaluation of 2,5-di(7-indolyl)-1,3,4-oxadiazoles, and 2- and 7-indolyl 2-(1,3,4-thiadiazolyl)ketones as antimicrobials.A vector system that allows simple generation of mutant Escherichia coli RNA polymerase.Small-Molecule Inhibitors of the NusB-NusE Protein-Protein Interaction with Antibiotic ActivityDesign, Synthesis and Antibacterial Evaluation of 3-Substituted Ocotillol-Type DerivativesSynthesis and biological evaluation of novel ocotillol-type triterpenoid derivatives as antibacterial agentsNovel 3-substituted ocotillol-type triterpenoid derivatives as antibacterial candidatesHighly efficient synthesis of the tricyclic core of Taxol by cascade metathesisDiscovery of Novel Inhibitors Targeting Multi-UDP-hexose Pyrophosphorylases as Anticancer AgentsHPLC, quantitative NMR and HRMS spectroscopic data of nusbiarylins as a new class of antimicrobial agentsDiscovery of Novel Quinoline-Chalcone Derivatives as Potent Antitumor Agents with Microtubule Polymerization Inhibitory ActivityDesign, synthesis and biological evaluation of quinoline-indole derivatives as anti-tubulin agents targeting the colchicine binding siteSynthesis, molecular properties prediction and biological evaluation of indole-vinyl sulfone derivatives as novel tubulin polymerization inhibitors targeting the colchicine binding siteDesign, synthesis, and biological evaluation of truncated deguelin derivatives as Hsp90 inhibitorsSimple Method for Studying in Vitro Protein-Protein Interactions Based on Protein Complementation and Its Application in Drug Screening Targeting Bacterial TranscriptionFirst-In-Class Inhibitors Targeting the Interaction between Bacterial RNA Polymerase and Sigma Initiation Factor Affect the Viability and Toxin Release of Streptococcus pneumoniaeDesign, synthesis and biological evaluation of antimicrobial diarylimine and -amine compounds targeting the interaction between the bacterial NusB and NusE proteinsNusbiarylins, a new class of antimicrobial agents: Rational design of bacterial transcription inhibitors targeting the interaction between the NusB and NusE proteinsDesign, synthesis and biological evaluation of pyridine-chalcone derivatives as novel microtubule-destabilizing agentsNovel N-Substituted oseltamivir derivatives as potent influenza neuraminidase inhibitors: Design, synthesis, biological evaluation, ADME prediction and molecular docking studiesMetal-Free Synthesis of N-(Pyridine-2-yl)amides from Ketones via Selective Oxidative Cleavage of C(O)-C(Alkyl) Bond in Water
P50
Q27700835-7FC0F6E9-735A-47F3-A054-826FA640D2E7Q35171597-8A1101A7-7AA9-4E13-B510-E530866511D3Q35632405-D723E005-91E4-4C72-9651-E0754CA11EF2Q35918795-A71387AF-BF99-4145-8361-AA4C3B3C918FQ36131412-9E676B6F-5D8B-45B7-A973-E7BA757EC948Q36222699-85104ECD-567D-4780-ACE3-2A1541CA0543Q36631410-B2BFC210-5BE8-44BC-A4C6-A96460784986Q37284527-F6C32566-7BC8-494D-A453-603C57FC4D17Q38848194-E2CEB4D2-54AD-4DDB-8379-2B41A656F97CQ38859783-2BADEB2B-D944-47EC-8ECE-DD89A1C9AB4CQ40104200-3151A8CD-84E6-4BC9-9505-F4BEC50E1EE7Q41426310-0B938E4B-ED0B-4476-B912-8D83A4304ED5Q42362195-41F79032-5F3E-4418-9ECF-333CE17EA7BBQ44129023-975DB619-E2F6-44ED-9FCD-3E0732E339DFQ46502083-35AAED66-1FF2-481E-B573-6F53490AD509Q47864764-DB2E5977-85CA-4F3B-B60B-F9BFA2E4E54FQ51449885-DA77AE65-B4A0-4DF5-AD97-677D01CAC219Q54292330-A00D15CE-C6CA-4883-9052-6207F16F28D2Q54295153-E5D2496C-875D-4EC3-80A9-6330C4E3BB71Q54340263-F07E3481-B7A3-4919-AAEE-38AA7EA6BB80Q58200362-494689FB-D61C-462E-8CE6-531832017019Q60955658-3A8A64E4-A83B-4E9B-8F3B-E05A289B519DQ87342016-0FE8FB48-69A3-45E1-8117-7A9F6D0CB036Q87840611-8C0F47AA-9D5D-4811-8397-A687A5EAF9AEQ88025021-8F66F347-DFFD-4634-9E1C-D3F043FEEAABQ89578223-9B24A7E1-F8A5-434E-8AEB-E8090FB18188Q90182377-8E1A6426-689A-4887-B5B0-EDFEC1AA4E5FQ90331159-E243D324-474E-4C06-99B5-2394C71FCC0CQ90362107-CE5E0D6B-B6AA-4B50-8E7E-4F347B65AB24Q90837762-059629F4-68D4-4EF5-8F07-758967E3D5F4Q91740221-8F59B125-CB45-4023-B7F9-38D189BB2027Q92134745-D8C3F53A-8E9F-4DFA-BBF8-2DD9026F2041Q92570432-936BE3DA-8C6C-4D4E-94D3-39A8DA5E706DQ92660380-524FEC8F-3F25-406D-B595-ABEFCA3466A1Q92847098-1CDD9273-F772-40F0-8EEC-82B6A9CAE4BBQ93072431-CFFB535C-6919-4759-A51E-2F45D2D12FEAQ93167522-21C9F82E-D61F-4F0C-9394-FB68B835C5F9Q93205300-05A5836C-BBEB-472D-ADCF-0C6340A90A04
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Cong Ma
@ast
Cong Ma
@en
Cong Ma
@es
Cong Ma
@nl
Cong Ma
@sl
type
label
Cong Ma
@ast
Cong Ma
@en
Cong Ma
@es
Cong Ma
@nl
Cong Ma
@sl
prefLabel
Cong Ma
@ast
Cong Ma
@en
Cong Ma
@es
Cong Ma
@nl
Cong Ma
@sl
P106
P1153
15071243800
P31
P496
0000-0001-9245-0356