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SCOTT MOSSER, MD
MD
Plastic and Reconstructive Surgery Physician
NPI: 1669552212Individual
Specialties, Licenses & Credentials
Plastic and Reconstructive Surgery PhysicianPrimary
Surgery — Plastic and Reconstructive Surgery
Code: 2086S0122X
A82437(CA)
Research & Publications (20)
The anatomy of the greater occipital nerve: implications for the etiology of migraine headaches.
PMID 14758238·Plast Reconstr Surg·2004
8-other
Synthesis and evaluation of novel tricyclic benzo[4.5]cyclohepta[1.2]pyridine derivatives as NMDA/NR2B antagonists.
PMID 19648007·Bioorg Med Chem Lett·2009
8-other
The identification of potent, orally bioavailable tricyclic CGRP receptor antagonists.
PMID 19577468·Bioorg Med Chem Lett·2009
7-preclinical
The discovery of highly potent CGRP receptor antagonists.
PMID 19010673·Bioorg Med Chem Lett·2009
7-preclinical
Potent benzimidazolone-based CGRP receptor antagonists.
PMID 18947992·Bioorg Med Chem Lett·2008
7-preclinical
Alpha-hydroxy amides as a novel class of bradykinin B1 selective antagonists.
PMID 18061443·Bioorg Med Chem Lett·2008
7-preclinical
Pharmacological characterization of MK-0974 [N-[(3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1-(2,2,2-trifluoroethyl)azepan-3-yl]-4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carboxamide], a potent and orally active calcitonin gene-related peptide receptor antagonist for the treatment of migraine.
PMID 18039958·J Pharmacol Exp Ther·2008
4-observational
Calcitonin gene-related peptide (CGRP) receptor antagonists: investigations of a pyridinone template.
PMID 18039571·Bioorg Med Chem Lett·2008
7-preclinical
Potent, orally bioavailable calcitonin gene-related peptide receptor antagonists for the treatment of migraine: discovery of N-[(3R,6S)-6-(2,3-difluorophenyl)-2-oxo-1- (2,2,2-trifluoroethyl)azepan-3-yl]-4- (2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin- 1-yl)piperidine-1-carboxamide (MK-0974).
PMID 17929795·J Med Chem·2007
7-preclinical
Caprolactams as potent CGRP receptor antagonists for the treatment of migraine.
PMID 17616394·Bioorg Med Chem Lett·2007
7-preclinical
Cyclic benzamidines as orally efficacious NR2B-selective NMDA receptor antagonists.
PMID 17498948·Bioorg Med Chem Lett·2007
7-preclinical
Identification and characterization of 4-methylbenzyl 4-[(pyrimidin-2-ylamino)methyl]piperidine-1-carboxylate, an orally bioavailable, brain penetrant NR2B selective N-methyl-D-aspartate receptor antagonist.
PMID 17249648·J Med Chem·2007
7-preclinical
Identification of novel, orally bioavailable spirohydantoin CGRP receptor antagonists.
PMID 17027263·Bioorg Med Chem Lett·2006
8-other
Benzodiazepine calcitonin gene-related peptide (CGRP) receptor antagonists: optimization of the 4-substituted piperidine.
PMID 16889959·Bioorg Med Chem Lett·2006
8-other
Non-peptide calcitonin gene-related peptide receptor antagonists from a benzodiazepinone lead.
PMID 16527483·Bioorg Med Chem Lett·2006
7-preclinical
Investigation of the species selectivity of a nonpeptide CGRP receptor antagonist using a novel pharmacodynamic assay.
PMID 15680472·Regul Pept·2005
7-preclinical
NR2B-selective N-methyl-D-aspartate antagonists: synthesis and evaluation of 5-substituted benzimidazoles.
PMID 15056006·J Med Chem·2004
7-preclinical
Macrocyclic piperazinones as potent dual inhibitors of farnesyltransferase and geranylgeranyltransferase-I.
PMID 14741259·Bioorg Med Chem Lett·2004
8-other
Orally efficacious NR2B-selective NMDA receptor antagonists.
PMID 12639561·Bioorg Med Chem Lett·2003
7-preclinical
Preclinical and clinical pharmacodynamic assessment of L-778,123, a dual inhibitor of farnesyl:protein transferase and geranylgeranyl:protein transferase type-I.
PMID 12479371·Mol Cancer Ther·2002
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
- 450 SUTTER ST RM 1010
SAN FRANCISCO, CA 94108 - Phone
- (415) 780-1515
Quick Facts
- NPI
- 1669552212
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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