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PAUL GRIECO, DMD
DMD
General Practice Dentistry
NPI: 1801089396Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
DS028352L(PA)
Research & Publications (20)
New insight into the binding mode of peptide ligands at Urotensin-II receptor: structure-activity relationships study on P5U and urantide.
PMID 19432421·J Med Chem·2009
8-other
Design and microwave-assisted synthesis of novel macrocyclic peptides active at melanocortin receptors: discovery of potent and selective hMC5R receptor antagonists.
PMID 18412316·J Med Chem·2008
8-other
Further structure-activity studies of lactam derivatives of MT-II and SHU-9119: their activity and selectivity at human melanocortin receptors 3, 4, and 5.
PMID 17482720·Peptides·2007
8-other
Structure-activity studies of new melanocortin peptides containing an aromatic amino acid at the N-terminal position.
PMID 16303211·Peptides·2006
8-other
Morphiceptin analogues containing a dipeptide mimetic structure: an investigation on the bioactive topology at the mu-receptor.
PMID 15857121·J Med Chem·2005
7-preclinical
Design and synthesis of melanocortin peptides with candidacidal and anti-TNF-alpha properties.
PMID 15743181·J Med Chem·2005
8-other
Urotensin-II receptor ligands. From agonist to antagonist activity.
PMID 16279788·J Med Chem·2005
7-preclinical
Recent structure-activity studies of the peptide hormone urotensin-II, a potent vasoconstrictor.
PMID 15078159·Curr Med Chem·2004
6-review
Extensive structure-activity studies of lactam derivatives of MT-II and SHU-9119: their activity and selectivity at human melanocortin receptors 3, 4, and 5.
PMID 14531843·J Pept Res·2003
4-observational
Novel alpha-melanocyte stimulating hormone peptide analogues with high candidacidal activity.
PMID 12593664·J Med Chem·2003
8-other
A structure-activity relationship study on position-2 of the Galpha(s) C-terminal peptide able to inhibit G(s) activation by A2A adenosine receptor.
PMID 12593912·Eur J Med Chem·2003
8-other
A new, potent urotensin II receptor peptide agonist containing a Pen residue at the disulfide bridge.
PMID 12238917·J Med Chem·2002
7-preclinical
Design, synthesis, conformational analysis, and biological studies of urotensin-II lactam analogues.
PMID 12413830·Bioorg Med Chem·2002
7-preclinical
Synthesis and biological evaluation on hMC3, hMC4 and hMC5 receptors of gamma-MSH analogs substituted with L-alanine.
PMID 11966977·J Pept Res·2002
7-preclinical
Structure-activity studies of the melanocortin peptides: discovery of potent and selective affinity antagonists for the hMC3 and hMC4 receptors.
PMID 12431055·J Med Chem·2002
7-preclinical
Design and synthesis of highly potent and selective melanotropin analogues of SHU9119 modified at position 6.
PMID 11944925·Biochem Biophys Res Commun·2002
8-other
Preparation of 'side-chain-to-side-chain' cyclic peptides by Allyl and Alloc strategy: potential for library synthesis.
PMID 11298927·J Pept Res·2001
8-other
D-Amino acid scan of gamma-melanocyte-stimulating hormone: importance of Trp(8) on human MC3 receptor selectivity.
PMID 11150170·J Med Chem·2000
7-preclinical
Substitution of arginine with proline and proline derivatives in melanocyte-stimulating hormones leads to selectivity for human melanocortin 4 receptor.
PMID 19473029·J Med Chem·2009
8-other
Imaging of alpha(v)beta(3) expression by a bifunctional chimeric RGD peptide not cross-reacting with alpha(v)beta(5).
PMID 19671851·Clin Cancer Res·2009
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
- 3894 OLD WILLIAM PENN HWY
MURRYSVILLE, PA 15668 - Phone
- (724) 327-4130
Quick Facts
- NPI
- 1801089396
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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