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
Spacer length shapes drug release and therapeutic efficacy of traceless disulfide-linked ADCs targeting the tumor neovasculature
Chemical Science
(2013)
4
297
(doi: 10.1039/C2SC21107F)
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
Chem Commun (Camb)
(2012)
48
7100
(doi: 10.1039/c2cc32412a)
A novel carbon monoxide-releasing molecule fully protects mice from severe malaria.
Antimicrobial agents and chemotherapy
(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)
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
Chemical site-selective radiolabelling of proteins using fluorosugars
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
(2012)
243
Selenenylsulfide‐Linked Homogeneous Glycopeptides and Glycoproteins: Synthesis of Human “Hepatic Se Metabolite A”
Angewandte Chemie (International ed. in English)
(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 [18F]-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.
Curr Med Chem
(2011)
18
3361
(doi: 10.2174/092986711796504583)
Site-selective traceless Staudinger ligation for glycoprotein synthesis reveals scope and limitations.
Chembiochem
(2011)
12
1383
(doi: 10.1002/cbic.201100125)
A "tag-and-modify" approach to site-selective protein modification.
Accounts of chemical research
(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
Journal of the American Chemical Society
(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)
