26 articles for VL Schramm
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Cmpds
Data
Article Title
Organization
4
Tight binding enantiomers of pre-clinical drug candidates.
Victoria University of Wellington
22
Acyclic phosph(on)ate inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase.
Industrial Research
17
Transition state analogue inhibitors of human methylthioadenosine phosphorylase and bacterial methylthioadenosine/S-adenosylhomocysteine nucleosidase incorporating acyclic ribooxacarbenium ion mimics.
Industrial Research
37
Third-generation immucillins: syntheses and bioactivities of acyclic immucillin inhibitors of human purine nucleoside phosphorylase.
Industrial Research
10
Immucillins in custom catalytic-site cavities.
Albert Einstein College of Medicine of Yeshiva University
18
Second generation transition state analogue inhibitors of human 5'-methylthioadenosine phosphorylase.
Industrial Research
17
Targeting the polyamine pathway with transition-state analogue inhibitors of 5'-methylthioadenosine phosphorylase.
Industrial Research
6
Synthesis of second-generation transition state analogues of human purine nucleoside phosphorylase.
Industrial Research
21
Exploring structure-activity relationships of transition state analogues of human purine nucleoside phosphorylase.
Industrial Research
14
Design and synthesis of potent"sulfur-free" transition state analogue inhibitors of 5'-methylthioadenosine nucleosidase and 5'-methylthioadenosine phosphorylase.
Industrial Research
2
Enzymatic transition states and dynamic motion in barrier crossing.
Albert Einstein College of Medicine
22
Transition State Analogs of Human DNPH1 Reveal Two Electrophile Migration Mechanisms.
Albert Einstein College of Medicine
4
8-Aza-immucillins as transition-state analogue inhibitors of purine nucleoside phosphorylase and nucleoside hydrolases.
Industrial Research
13
Selective Inhibitors of Helicobacter pylori Methylthioadenosine Nucleosidase and Human Methylthioadenosine Phosphorylase.
Albert Einstein College of Medicine
6
Substituted 1,4-benzodiazepine-2,5-diones as alpha-helix mimetic antagonists of the HDM2-p53 protein-protein interaction.
Johnson & Johnson Pharmaceutical Research & Development
107
Structural requirements for factor Xa inhibition by 3-oxybenzamides with neutral P1 substituents: combining X-ray crystallography, 3D-QSAR, and tailored scoring functions.
Aventis Pharma Deutschland