نتائج البحث - "Alkynes/chemistry"

1

Does a Conjugation Site Affect Transport of Vitamin B12–Peptide Nucleic Acid Conjugates into Bacterial Cells?

المؤلفون: Aleksandra Wincenciuk, Dorota Gryko, Joanna Trylska, Ksenia Maximova, Aleksandra J. Wierzba, Monika Wojciechowska, Marcin Równicki, Ebba Nexo

المصدر: Wierzba, A J, Maximova, K, Wincenciuk, A, Równicki, M, Wojciechowska, M, Nexø, E, Trylska, J & Gryko, D 2018, ' Does a Conjugation Site Affect Transport of Vitamin B12-Peptide Nucleic Acid Conjugates into Bacterial Cells? ', Chemistry: A European Journal, vol. 24, no. 70, pp. 18772-18778 . https://doi.org/10.1002/chem.201804304

مصطلحات موضوعية: Drug Carriers/chemistry, 010402 general chemistry, medicine.disease_cause, 01 natural sciences, Oligomer, Catalysis, chemistry.chemical_compound, Corrinoid, medicine, Escherichia coli, Peptide Nucleic Acids/chemistry, Natural products, Bioconjugation, Cycloaddition Reaction, biology, Peptide nucleic acid, 010405 organic chemistry, Oligonucleotide, structure-activity relationships, Organic Chemistry, Corrin, Salmonella typhimurium/metabolism, Azides/chemistry, Biological Transport, Vitamin B 12/chemistry, General Chemistry, Alkynes/chemistry, biology.organism_classification, 0104 chemical sciences, chemistry, Biochemistry, Escherichia coli/metabolism, Drug delivery, Copper/chemistry, Peptide nucleic acids, Bacteria

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b58aab6bd1e3d453f586bdc398e81dd8
https://doi.org/10.1002/chem.201804304

View record at Wiley

2

Methylation of geometrically constrained lysine analogues by histone lysine methyltransferases

المؤلفون: Anita Wegert, Jasmin Mecinović, Richard H. Blaauw, Abbas H. K. Al Temimi, Paul B. White, Floris P. J. T. Rutjes, Nicole G. A. van der Linden, Marcus J M Mulders

المصدر: Chemical Communications
Al Temimi, A H K, White, P B, Mulders, M J M, van der Linden, N G A, Blaauw, R H, Wegert, A, Rutjes, F P J T & Mecinović, J 2020, ' Methylation of geometrically constrained lysine analogues by histone lysine methyltransferases ', Chemical Communications, vol. 56, no. 20, pp. 3039-3042 . https://doi.org/10.1039/c9cc09098c
Chemical Communications, 56, 20, pp. 3039-3042
Chemical Communications, 56, 3039-3042

مصطلحات موضوعية: Methyltransferase, Stereochemistry, Lysine, Molecular Conformation, Alkyne, Synthetic Organic Chemistry, Alkenes, 010402 general chemistry, 01 natural sciences, Methylation, Catalysis, 03 medical and health sciences, Histone-lysine methyltransferase, Histone methylation, Materials Chemistry, Humans, 030304 developmental biology, chemistry.chemical_classification, Histone-Lysine N-Methyltransferase/metabolism, 0303 health sciences, Lysine/analogs & derivatives, biology, Metals and Alloys, Histone-Lysine N-Methyltransferase, General Chemistry, Alkenes/chemistry, Alkynes/chemistry, 3. Good health, 0104 chemical sciences, Surfaces, Coatings and Films, Electronic, Optical and Magnetic Materials, Histone, chemistry, Biocatalysis, Alkynes, Ceramics and Composites, biology.protein

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cbc722f82559522af27d7984fcce2eb

3

Biologically Active Acetylenic Amino Alcohol and N -Hydroxylated 1,2,3,4-Tetrahydro-β-carboline Constituents of the New Zealand Ascidian Pseudodistoma opacum

المؤلفون: Jiayi Wang, Michael J. Page, Siouxsie Wiles, Susanna T. S. Chan, A. Norrie Pearce, James P. Dalton, Alexis Valentin, Richard B. Taylor, Brent R. Copp, Marie-Lise Bourguet-Kondracki

المساهمون: University of Auckland [Auckland], National Institute of Water and Atmospheric Research [Auckland] (NIWA), Pharmacochimie et Biologie pour le Développement (PHARMA-DEV), Institut de Recherche pour le Développement (IRD)-Institut de Chimie de Toulouse (ICT-FR 2599), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC), Molécules de Communication et Adaptation des Micro-organismes (MCAM), Muséum national d'Histoire naturelle (MNHN)-Centre National de la Recherche Scientifique (CNRS), University of Auckland, Institut de Recherche pour le Développement (IRD)-Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)

المصدر: Journal of Natural Products
Journal of Natural Products, American Chemical Society, 2015, 79 (3), pp.607-610. ⟨10.1021/acs.jnatprod.5b00770⟩
Journal of Natural Products, 2015, 79 (3), pp.607-610. ⟨10.1021/acs.jnatprod.5b00770⟩

مصطلحات موضوعية: 0301 basic medicine, Circular dichroism, Metabolite, [SDV]Life Sciences [q-bio], Bacterial / drug effects, Drug Resistance, Pharmaceutical Science, medicine.disease_cause, 01 natural sciences, Staphylococcus aureus / drug effects, Analytical Chemistry, chemistry.chemical_compound, Drug Discovery, Antimalarials / chemistry, biology, Molecular Structure, Escherichia coli / drug effects, Absolute configuration, Biological activity, Chloroquine, Chloroquine / pharmacology, Mycobacterium tuberculosis / drug effects, 3. Good health, Staphylococcus aureus, Alkynes, Molecular Medicine, Urochordata / chemistry, Carbolines / isolation & purification, Carbolines / pharmacology, Stereochemistry, Plasmodium falciparum, Alkynes / chemistry, Microbial Sensitivity Tests, 03 medical and health sciences, Antimalarials, Inhibitory Concentration 50, Drug Resistance, Bacterial, Plasmodium falciparum / drug effects, medicine, Escherichia coli, Antimalarials / isolation & purification, Animals, Urochordata, Antimalarials / pharmacology, IC50, Alkynes / isolation & purification, Pharmacology, 010405 organic chemistry, Organic Chemistry, Carbolines / chemistry, Mycobacterium tuberculosis, biology.organism_classification, 0104 chemical sciences, 030104 developmental biology, Complementary and alternative medicine, chemistry, Alkynes / pharmacology, Carbolines, New Zealand

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c56d014e49dd6ceaddc72db8f700a0d
https://hal-univ-tlse3.archives-ouvertes.fr/hal-03184421

Find this issue from the American Chemical Society

4

Charge dependent substrate activity of C3' and N3 functionalized, organometallic Technetium and Rhenium-labeled thymidine derivatives toward human thymidine kinase 1

المؤلفون: Marek Kosinski, David Viertl, Franz Buchegger, Harriet Struthers, Roger Schibli, Bernhard Spingler

المساهمون: University of Zurich, Schibli, R

المصدر: Bioconjugate Chemistry, Vol. 21, No 4 (2010) pp. 622-634

مصطلحات موضوعية: Models, Molecular, 10120 Department of Chemistry, Rhenium/*chemistry, 3003 Pharmaceutical Science, Pharmaceutical Science, Crystallography, X-Ray, chemistry.chemical_compound, 540 Chemistry, Technetium/*chemistry, Thymidine/*chemistry/*metabolism, Molecular Structure, Chemistry, Technetium, Azides/chemistry, Stereoisomerism, Cycloaddition, Rhenium, 3004 Pharmacology, Alkynes, Click chemistry, 1305 Biotechnology, Copper/chemistry, Biotechnology, Azides, Stereochemistry, Biomedical Engineering, 2204 Biomedical Engineering, Bioengineering, ddc:616.0757, Thymidine Kinase, Catalysis, Organometallic Compounds, Humans, Chelation, Thymidine kinase 1, Pharmacology, Staining and Labeling, 1502 Bioengineering, Ligand, Organometallic Compounds/chemical synthesis/*chemistry, Organic Chemistry, Cationic polymerization, Thymidine Kinase/*chemistry/*metabolism, Substrate (chemistry), Alkynes/chemistry, Cyclization, Thymidine, Copper, 1605 Organic Chemistry

وصف الملف: accepted_manuscript_BioconjChem_2010.pdf - application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67a7e897061129d4f54cc8eb6805c449
https://www.zora.uzh.ch/id/eprint/44991/

Find this issue from the American Chemical Society

5

مورد إلكتروني

Formation of high-quality self-assembled monolayers of conjugated dithiols on gold: base matters.

المؤلفون: Valkenier, Hennie, Huisman, Everardus, van Hal, Paul, de Leeuw, Dago, Chiechi, Ryan, Hummelen, Jan

المصدر: Journal of the American Chemical Society, 133 (13

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Alkynes -- chemistry, Ethers -- chemistry, Ethylamines -- chemical synthesis -- chemistry, Gold -- chemistry, Membranes, Artificial, Molecular Structure, Solutions, Toluene -- analogs & derivatives -- chemistry, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/227340
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL

6

مورد إلكتروني

Aggregation-Induced Emission: Phenomenon, Mechanism and Applications

المؤلفون: Hong, Yuning, Lam, Jacky Wing Yip, Tang, Ben Zhong

مصطلحات الفهرس: Alkynes: chemistry, Fluorescent Dyes: chemistry, Molecular Structure, Organic Chemicals: chemistry, Silicon Compounds: chemistry, Solutions: chemistry, Article

URL: http://repository.ust.hk/ir/Record/1783.1-30532
http://lbdiscover.ust.hk/uresolver?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rfr_id=info:sid/HKUST:SPI&rft.genre=article&rft.issn=1359-7345&rft.volume=&rft.issue=29&rft.date=2009&rft.spage=4332&rft.epage=4353&rft.aulast=Hong&rft.aufirst=Yuning&rft.atitle=Aggregation-induced+emission:+phenomenon,+mechanism+and+applications
http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=LinksAMR&SrcApp=PARTNER_APP&DestLinkType=FullRecord&DestApp=WOS&KeyUT=000268081300002
http://www.scopus.com/record/display.url?eid=2-s2.0-68749120723&origin=inward

7

مورد إلكتروني

A versatile approach to beta-amyloid fibril-binding compounds exploiting the Shirakawa/Hayashi protocol for trans-alkene synthesis

المؤلفون: Huynh, Tri H V, Mantel, Mette Louise H, Mikkelsen, Katrine, Lindhardt, Anders T, Nielsen, Niels Chr, Otzen, Daniel, Skrydstrup, Troels

المصدر: Huynh , T H V , Mantel , M L H , Mikkelsen , K , Lindhardt , A T , Nielsen , N C , Otzen , D & Skrydstrup , T 2009 , ' A versatile approach to beta-amyloid fibril-binding compounds exploiting the Shirakawa/Hayashi protocol for trans-alkene synthesis ' , Organic Letters , vol. 11 , no. 4 , pp. 999-1002 .

مصطلحات الفهرس: Alkenes/chemical synthesis, Alkynes/chemistry, Amyloid beta-Peptides/metabolism, Aniline Compounds/chemical synthesis, Molecular Structure, Protein Binding, Stereoisomerism, Stilbenes/chemical synthesis, Styrenes/chemical synthesis, article