PMID

Data

Article Title

Organization

Quantitative structure-activity relationships of N2-phenylguanines as inhibitors of herpes simplex virus thymidine kinases.

University of Massachusetts Medical School

Non-charged thiamine analogs as inhibitors of enzyme transketolase.

Array Biopharma

Synthesis, in vitro and in vivo activity of thiamine antagonist transketolase inhibitors.

Array Biopharma

Understanding the binding of 5-substituted 2'-deoxyuridine substrates to thymidine kinase of herpes simplex virus type-1.

Katholieke Universiteit Leuven

N2-phenyldeoxyguanosine: a novel selective inhibitor of herpes simplex thymidine kinase.

Istituto Di Genetica Biochimica Ed Evoluzionistica

Design, synthesis and enzymatic activity of highly selective human mitochondrial thymidine kinase inhibitors.

Universit£

Structure-activity relationships of compounds targeting mycobacterium tuberculosis 1-deoxy-D-xylulose 5-phosphate synthase.

University of Illinois At Chicago

Prodrug thiamine analogs as inhibitors of the enzyme transketolase.

Array Biopharma

Nucleoside analogues as highly potent and selective inhibitors of herpes simplex virus thymidine kinase.

Roche Discovery Welwyn

Structure-antiviral activity relationship in the series of pyrimidine and purine N-[2-(2-phosphonomethoxy)ethyl] nucleotide analogues. 1. Derivatives substituted at the carbon atoms of the base.

Academy of Sciences of The Czech Republic

Structure-activity relationships of N2-substituted guanines as inhibitors of HSV1 and HSV2 thymidine kinases.

University of Massachusetts Medical School

Inhibition of herpes simplex virus thymidine kinases by 2-phenylamino-6-oxopurines and related compounds: structure-activity relationships and antiherpetic activity in vivo.

Glsynthesis