About: Stephen Caddick

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

British chemist

Attributes	Values
rdf:type	Item
description	ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) British chemist (en) Suurbritannia keemik (et) brittisk kemist (sv) ব্রিটিশ রসায়নবিদ (bn) chimist britanic (ro) britisk kemiker (da) britisk kjemikar (nn) químico británico (es) כימאי בריטי (he) chimiste britannique (fr) químic britànic (ca) químico británico (gl) كيميائي بريطاني (ar) químicu británicu (ast) شیمیدان بریتانیایی (fa) հետազոտող (hy) hulumtues (sq)
rdfs:label	Stephen Caddick (en) Stephen Caddick (es) Stephen Caddick (nl) Stephen Caddick (sl) Stephen Caddick (sq) Stephen Caddick (ast)
skos:prefLabel	Stephen Caddick (en) Stephen Caddick (es) Stephen Caddick (nl) Stephen Caddick (sl) Stephen Caddick (sq) Stephen Caddick (ast)
name	Stephen Caddick (en) Stephen Caddick (es) Stephen Caddick (nl) Stephen Caddick (sl) Stephen Caddick (sq) Stephen Caddick (ast)
affiliation	wds:Q42699411-E4BD4350-5FC2-48FE-8255-2F736234680C
affiliation string	wds:Q42699411-BA0F9F98-1F1C-4D39-B7F0-D53A1A73BF57
affiliation	Wellcome Trust
affiliation string	The Wellcome Trust
given name	wds:Q42699411-417597BC-FE60-4722-985B-AE1858016907
given name	Stephen
instance of	wds:Q42699411-8AD23147-FCD0-4421-B411-86D682AB01CD
instance of	Homo sapiens
occupation	wds:Q42699411-A3588257-BA7A-46FA-854E-D3B90376DB9B
employer	wds:Q42699411-1ED6DAB9-3EAB-412D-80B2-72F21261EE79
participant in	wds:Q42699411-97399DA0-EC35-42BB-B294-150D5E1C37FC wds:Q42699411-FA57B5F1-0049-4D00-9FEB-11F9C4D55793
sex or gender	wds:Q42699411-A4AF45DE-11CA-410E-A9F7-83A905F2280E
Who's Who UK ID	wds:Q42699411-439bc9dd-4a2f-a835-ef37-0d130403867d
date of birth	wds:Q42699411-71EE1D0E-2373-4EAD-825F-F229691F3B9E
family name	wds:Q42699411-6A74C747-72D1-4BE3-B20B-56B91E50AB1B
official website	wds:Q42699411-4B5DB145-CB0A-493E-8D9C-9F5636132738
occupation	chemist
employer	University College London
participant in	World Economic Forum Annual Meeting 2016 World Economic Forum Annual Meeting 2017
sex or gender	male
Who's Who UK ID	U288878
date of birth	1963-01-01 00:00:00Z (xsd:dateTime)
family name	Caddick
official website	http://iris.ucl.ac.uk/iris/browse/profile?upi=SCADD46
ORCID iD	wds:Q42699411-6E14037E-1589-44B7-9792-C52EB3B10A21
ORCID iD	https://orcid.org/0000-0002-3267-7302
ORCID iD	0000-0002-3267-7302
ResearcherID	wds:Q42699411-7DF1B3F4-9524-495E-9910-CA0E97F8BE4E
Publons author ID	wds:Q42699411-4d6ecc42-b786-44e6-a636-18a7d50a253e
ResearcherID	B-8550-2009
Publons author ID	2864802
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42699411
is author of	Inhibition of dimethylarginine dimethylaminohydrolase (DDAH) and arginine deiminase (ADI) by pentafluorophenyl (PFP) sulfonates. Optical control of trimeric P2X receptors and acid-sensing ion channels Characterization of an Arabidopsis inositol 1,3,4,5,6-pentakisphosphate 2-kinase (AtIPK1). Inhibition of tRNA-dependent ligase MurM from Streptococcus pneumoniae by phosphonate and sulfonamide inhibitors Protein-small molecule interactions in neocarzinostatin, the prototypical enediyne chromoprotein antibiotic. Synthetic, structural, and mechanistic studies on the oxidative addition of aromatic chlorides to a palladium (N-heterocyclic carbene) complex: relevance to catalytic amination Tuning the Reactivity of Dirhodium(II) Complexes with Axial N-Heterocyclic Carbene Ligands: The Arylation of Aldehydes Microwave enhanced palladium catalysed coupling reactions: a diversity-oriented synthesis approach to functionalised flavones A plug-and-play approach to antibody-based therapeutics via a chemoselective dual click strategy. Next generation maleimides enable the controlled assembly of antibody-drug conjugates via native disulfide bond bridging Functional native disulfide bridging enables delivery of a potent, stable and targeted antibody-drug conjugate (ADC) Targeting cancer cells with folic acid-iminoboronate fluorescent conjugates. Solid-phase intermolecular radical reactions 2: synthesis of C-glycopeptide mimetics via a novel acrylate acceptor The design, synthesis and pharmacological characterization of novel β₂-adrenoceptor antagonists. Inhibition of HIV-1 replication by isoxazolidine and isoxazole sulfonamides Unusual reactivity of a nickel N-heterocyclic carbene complex: tert-butyl group cleavage and silicone grease activation Synthesis of inositol phosphate ligands of plant hormone-receptor complexes: pathways of inositol hexakisphosphate turnover. NHC/Iron cooperative catalysis: aerobic oxidative esterification of aldehydes with phenols Triflic acid-mediated phenylation of N-acylaminoalkyl diethylacetals and N-acyl-2-phenyl cyclic amides Recent advances in the construction of antibody-drug conjugates Regioselective and stoichiometrically controlled conjugation of photodynamic sensitizers to a HER2 targeting antibody fragment Bromomaleimide-linked bioconjugates are cleavable in mammalian cells A platform for efficient, thiol-stable conjugation to albumin's native single accessible cysteine. A mild TCEP-based para-azidobenzyl cleavage strategy to transform reversible cysteine thiol labelling reagents into irreversible conjugates. Axial coordination of NHC ligands on dirhodium(II) complexes: generation of a new family of catalysts. NMR spectroscopic studies on the metabolism and futile deacetylation of phenacetin in the rat Hydroacylation of alpha,beta-unsaturated esters via aerobic C-H activation

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