About: Peter C Tyler

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organic chemist in New Zealand

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) organic chemist in New Zealand (en)
rdfs:label	Peter C Tyler (en) Peter C Tyler (es) Peter C Tyler (nl) Peter C Tyler (sl) Peter C Tyler (ast) بيتر كلارك تايلر (ar) পিটার সি টাইলার (bn)
skos:prefLabel	Peter C Tyler (en) Peter C Tyler (es) Peter C Tyler (nl) Peter C Tyler (sl) Peter C Tyler (ast) بيتر كلارك تايلر (ar) পিটার সি টাইলার (bn)
name	Peter C Tyler (en) Peter C Tyler (es) Peter C Tyler (nl) Peter C Tyler (sl) Peter C Tyler (ast) بيتر كلارك تايلر (ar) পিটার সি টাইলার (bn)
given name	wds:Q47855321-17FDF30A-57C2-4072-831A-C6F078A1B1B4 wds:Q47855321-AF3C72F8-06AE-4401-8F76-C865E1883997
given name	Peter Charles
instance of	wds:Q47855321-949C634D-AE36-44D5-A6E9-852EC3F0048B
instance of	Homo sapiens
award received	wds:Q47855321-A83A0A4A-FDBA-458F-A05F-F5D825F11664
award received	Fellow of the Royal Society Te Apārangi
skos:altLabel	Peter Tyler (en) Peter Charles Tyler (en)
occupation	wds:Q47855321-0B58F204-F80B-4DF1-9096-C82AF5338E40
employer	wds:Q47855321-1A7B4D4C-D3DF-4060-97C1-3BD9E50FEF51
sex or gender	wds:Q47855321-FEE66873-4272-4B7A-BE9B-FA74596EF274
on focus list of Wikimedia project	wds:Q47855321-E2894897-9246-48FE-8A66-2E50652FCB2F
academic degree	wds:Q47855321-4C1B74AC-9FAE-4838-AB52-3E49AEAF66E3
date of birth	wds:Q47855321-73E233CC-4293-4EC4-AA44-57496A8F4116
educated at	wds:Q47855321-7C363446-BD31-415C-BB62-B8F298EAEAEC
family name	wds:Q47855321-32C144AA-FA0B-462D-B02A-7540515DB5D8
occupation	researcher
employer	Victoria University of Wellington
sex or gender	male
on focus list of Wikimedia project	NZThesisProject
academic degree	Doctor of Philosophy
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
educated at	Victoria University of Wellington
family name	Tyler
ORCID iD	wds:Q47855321-80A261FE-5467-4ED5-B36C-06B2F1A34E5F
ORCID iD	https://orcid.org/0000-0002-3151-6208
ORCID iD	0000-0002-3151-6208
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q47855321
is author of	8-Aza-immucillins as transition-state analogue inhibitors of purine nucleoside phosphorylase and nucleoside hydrolases Exploring structure-activity relationships of transition state analogues of human purine nucleoside phosphorylase. Synthesis of second-generation transition state analogues of human purine nucleoside phosphorylase Plasmodium falciparum purine nucleoside phosphorylase: crystal structures, immucillin inhibitors, and dual catalytic function Targeting the polyamine pathway with transition-state analogue inhibitors of 5'-methylthioadenosine phosphorylase Synthesis of a Transition State Analogue Inhibitor of Purine Nucleoside Phosphorylase via the Mannich Reaction Ionic states of substrates and transition state analogues at the catalytic sites of N-ribosyltransferases Picomolar inhibitors as transition-state probes of 5'-methylthioadenosine nucleosidases Transition state analogue discrimination by related purine nucleoside phosphorylases Atomic dissection of the hydrogen bond network for transition-state analogue binding to purine nucleoside phosphorylase Targeting a novel Plasmodium falciparum purine recycling pathway with specific immucillins Energetic mapping of transition state analogue interactions with human and Plasmodium falciparum purine nucleoside phosphorylases. Femtomolar transition state analogue inhibitors of 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase from Escherichia coli Transition state analogue inhibitors of purine nucleoside phosphorylase from Plasmodium falciparum Purine-less death in Plasmodium falciparum induced by immucillin-H, a transition state analogue of purine nucleoside phosphorylase Transition state analogues rescue ribosomes from saporin-L1 ribosome inactivating protein Inhibition of ricin A-chain with pyrrolidine mimics of the oxacarbenium ion transition state. Inhibitors of ADP-ribosylating bacterial toxins based on oxacarbenium ion character at their transition states Achieving the ultimate physiological goal in transition state analogue inhibitors for purine nucleoside phosphorylase Azetidine based transition state analogue inhibitors of N-ribosyl hydrolases and phosphorylases Transition state analogues in quorum sensing and SAM recycling Second generation transition state analogue inhibitors of human 5'-methylthioadenosine phosphorylase Syntheses and bio-activities of the L-enantiomers of two potent transition state analogue inhibitors of purine nucleoside phosphorylases. A practical synthesis of (3R,4R)-N-tert-butoxycarbonyl-4-hydroxymethylpyrrolidin-3-ol Four generations of transition-state analogues for human purine nucleoside phosphorylase. Acyclic Ribooxacarbenium Ion Mimics as Transition State Analogues of Human and Malarial Purine Nucleoside Phosphorylases Structure and inhibition of a quorum sensing target from Streptococcus pneumoniae Synthesis of Transition State Analogue Inhibitors for Purine Nucleoside Phosphorylase and N-Riboside Hydrolases Over-the-barrier transition state analogues and crystal structure with Mycobacterium tuberculosis purine nucleoside phosphorylase Imino-C-nucleoside synthesis: heteroaryl lithium carbanion additions to a carbohydrate cyclic imine and nitrone Acyclic phosph(on)ate inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase Immucillins ImmA and ImmH Are Effective and Non-toxic in the Treatment of Experimental Visceral Leishmaniasis Synthesis and utility of sulfated chromogenic carbohydrate model substrates for measuring activities of mucin-desulfating enzymes New Antibiotic Candidates against Helicobacter pylori Transition-State Analogues of Campylobacter jejuni 5'-Methylthioadenosine Nucleosidase Immucillins in Infectious Diseases

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