Tips on using this search form
- All search terms are case-insensitive
- If you specify more than one search option (e.g. you search for both "Authors" and "Paper title") then the publications returned will be those that match all of your search terms
- To reset the search form, click here
- Currently displaying 221 - 240 of 252 publications
Generation of carbon monoxide releasing molecules (CO-RMs) as drug candidates for the treatment of acute liver injury: Targeting of CO-RMs to the liver
– Organometallics
(2012)
31,
5810
(doi: 10.1021/om300360c)
Fucose-specific conjugation of hydrazide derivatives to a vascular-targeting monoclonal antibody in IgG format
– Chemical Communications
(2012)
48,
7100
(doi: 10.1039/c2cc32412a)
A novel carbon monoxide-releasing molecule fully protects mice from severe malaria.
– Antimicrob Agents Chemother
(2012)
56,
1281
(doi: 10.1128/aac.05571-11)
Developing drug molecules for therapy with carbon monoxide.
– Chemical Society reviews
(2012)
41,
3571
(doi: 10.1039/c2cs15317c)
Chemical site-selective radiolabelling of proteins using fluorosugars
– ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2012)
243,
Building well-defined glycoproteins
– ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2012)
243,
Chemical site-selective protein modification: Development of a traceless vascular targeting ADC for cancer therapy
– ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2012)
243,
Selenenylsulfide-linked homogeneous glycopeptides and glycoproteins: Synthesis of human "hepatic Se MetaboliteA"
– Angewandte Chemie - International Edition
(2011)
51,
1432
(doi: 10.1002/anie.201106658)
A Traceless Vascular-Targeting Antibody-Drug Conjugate for Cancer Therapy
– Angewandte Chemie - International Edition
(2011)
51,
941
(doi: 10.1002/anie.201106527)
Direct radiolabelling of proteins at cysteine using [ 18 F]-fluorosugars
– Chemical communications (Cambridge, England)
(2011)
47,
10010
(doi: 10.1039/c1cc13524d)
Methods for converting cysteine to dehydroalanine on peptides and proteins
– Chemical Science
(2011)
2,
1666
(doi: 10.1039/c1sc00185j)
Towards improved therapeutic CORMs: understanding the reactivity of CORM-3 with proteins.
– Current Medicinal Chemistry
(2011)
18,
3361
(doi: 10.2174/092986711796504583)
Site‐Selective Traceless Staudinger Ligation for Glycoprotein Synthesis Reveals Scope and Limitations
– Chembiochem : a European journal of chemical biology
(2011)
12,
1383
(doi: 10.1002/cbic.201100125)
A "Tag-and-Modify" Approach to Site-Selective Protein Modification
– Acc Chem Res
(2011)
44,
730
(doi: 10.1021/ar200056q)
A coordinated synthesis and conjugation strategy for the preparation of homogeneous glycoconjugate vaccine candidates.
– Angewandte Chemie International Edition
(2011)
50,
4127
(doi: 10.1002/anie.201006327)
CORM-3 Reactivity toward Proteins: The Crystal Structure of a Ru(II) Dicarbonyl−Lysozyme Complex
– J Am Chem Soc
(2011)
133,
1192
(doi: 10.1021/ja108820s)
Chemical Site-selective Modification of Proteins: Tools for Synthetic Biology
– FASEB JOURNAL
(2011)
25,
Site-selective chemoenzymatic construction of synthetic glycoproteins using endoglycosidases
– Chemical Science
(2010)
1,
709
(doi: 10.1039/c0sc00265h)
Design, synthesis and biological evaluation of carbohydrate-functionalized cyclodextrins and liposomes for hepatocyte-specific targeting.
– Organic & Biomolecular Chemistry
(2010)
8,
4987
(doi: 10.1039/c0ob00372g)
Fluoroglycoproteins: Ready chemical site-selective incorporation of fluorosugars into proteins
– Chemical Communications
(2010)
46,
8142
(doi: 10.1039/c0cc01576h)