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WILLIAM GREENLEE, MD
Neuroradiology Physician
NPI: 1649257510Individual
Specialties, Licenses & Credentials
Neuroradiology PhysicianPrimary
Radiology — Neuroradiology
Code: 2085N0700X
36072848(IL)
Research & Publications (20)
Muscarinic agonists and antagonists in the treatment of Alzheimer's disease.
PMID 11421251·Farmaco·2001
6-review
Identification of 3-substituted N-benzhydryl-nortropane analogs as nociceptin receptor ligands for the management of cough and anxiety.
PMID 19332374·Bioorg Med Chem Lett·2009
7-preclinical
Tricyclic thienopyridine-pyrimidones/thienopyrimidine-pyrimidones as orally efficacious mGluR1 antagonists for neuropathic pain.
PMID 19433355·Bioorg Med Chem Lett·2009
7-preclinical
The discovery of azepane sulfonamides as potent 11beta-HSD1 inhibitors.
PMID 19625185·Bioorg Med Chem Lett·2009
7-preclinical
The discovery of tropane derivatives as nociceptin receptor ligands for the management of cough and anxiety.
PMID 19339177·Bioorg Med Chem Lett·2009
7-preclinical
Potent and selective adenosine A2A receptor antagonists: 1,2,4-Triazolo[1,5-c]pyrimidines.
PMID 19109019·Bioorg Med Chem Lett·2009
7-preclinical
Design and discovery of 1,3-benzodiazepines as novel dopamine antagonists.
PMID 19643610·Bioorg Med Chem Lett·2009
8-other
Discovery of orally active 3-pyridinyl-tropane as a potent nociceptin receptor agonist for the management of cough.
PMID 19678644·J Med Chem·2009
7-preclinical
Structure-activity relationships of 3-substituted N-benzhydryl-nortropane analogs as nociceptin receptor ligands for the treatment of cough.
PMID 18990569·Bioorg Med Chem Lett·2008
7-preclinical
Discovery of a novel, orally active himbacine-based thrombin receptor antagonist (SCH 530348) with potent antiplatelet activity.
PMID 18447380·J Med Chem·2008
7-preclinical
Design, synthesis, and evaluation of fused heterocyclic analogs of SCH 58261 as adenosine A2A receptor antagonists.
PMID 18558486·Bioorg Med Chem Lett·2008
7-preclinical
Biaryl and heteroaryl derivatives of SCH 58261 as potent and selective adenosine A2A receptor antagonists.
PMID 18562199·Bioorg Med Chem Lett·2008
7-preclinical
Discovery of novel orally active ureido NPY Y5 receptor antagonists.
PMID 18160282·Bioorg Med Chem Lett·2008
7-preclinical
Discovery of amide and heteroaryl isosteres as carbamate replacements in a series of orally active gamma-secretase inhibitors.
PMID 17988864·Bioorg Med Chem Lett·2008
7-preclinical
Synthesis and structure-activity relationships of 4-hydroxy-4-phenylpiperidines as nociceptin receptor ligands: Part 2.
PMID 17420123·Bioorg Med Chem Lett·2007
7-preclinical
3H-[1,2,4]-Triazolo[5,1-i]purin-5-amine derivatives as adenosine A2A antagonists.
PMID 17234414·Bioorg Med Chem Lett·2007
8-other
Potent, selective, and orally active adenosine A2A receptor antagonists: arylpiperazine derivatives of pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines.
PMID 17236762·Bioorg Med Chem Lett·2007
7-preclinical
Synthesis and structure-activity relationships of 4-hydroxy-4-phenylpiperidines as nociceptin receptor ligands: Part 1.
PMID 17428659·Bioorg Med Chem Lett·2007
7-preclinical
2,6-Disubstituted N-arylsulfonyl piperidines as gamma-secretase inhibitors.
PMID 17055268·Bioorg Med Chem Lett·2007
8-other
Discovery of gamma-secretase inhibitors efficacious in a transgenic animal model of Alzheimer's disease.
PMID 17079141·Bioorg Med Chem Lett·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2160 S 1ST AVE, MCGAW ENT., RM. 47
MAYWOOD, IL 60153 - Phone
- (708) 216-5221
Quick Facts
- NPI
- 1649257510
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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