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MONICA COWART, PHD
PHD
Mental Health Counselor
NPI: 1841491867Individual
Specialties, Licenses & Credentials
Mental Health CounselorPrimary
Counselor — Mental Health
Code: 101YM0800X
Research & Publications (20)
Rotationally constrained 2,4-diamino-5,6-disubstituted pyrimidines: a new class of histamine H4 receptor antagonists with improved druglikeness and in vivo efficacy in pain and inflammation models.
PMID 18817367·J Med Chem·2008
7-preclinical
Novel heterocyclic-substituted benzofuran histamine H3 receptor antagonists: in vitro properties, drug-likeness, and behavioral activity.
PMID 17371699·Biochem Pharmacol·2007
7-preclinical
A new family of histamine H3 receptor antagonists based on a natural product: discovery, SAR, and properties of the series.
PMID 17806176·Inflamm Res·2007
7-preclinical
Fluorescent benzofuran histamine H(3) receptor antagonists with sub-nanomolar potency.
PMID 16705379·Inflamm Res·2006
8-other
Achievement of behavioral efficacy and improved potency in new heterocyclic analogs of benzofuran H3 antagonists.
PMID 15928820·Inflamm Res·2005
7-preclinical
4-(2-[2-(2(R)-methylpyrrolidin-1-yl)ethyl]benzofuran-5-yl)benzonitrile and related 2-aminoethylbenzofuran H3 receptor antagonists potently enhance cognition and attention.
PMID 15634000·J Med Chem·2005
7-preclinical
Discovery of 2-(4-pyridin-2-ylpiperazin-1-ylmethyl)-1H-benzimidazole (ABT-724), a dopaminergic agent with a novel mode of action for the potential treatment of erectile dysfunction.
PMID 15239663·J Med Chem·2004
7-preclinical
Medicinal chemistry and biological properties of non-imidazole histamine H3 antagonists.
PMID 15544558·Mini Rev Med Chem·2004
6-review
A new class of potent non-imidazole H(3) antagonists: 2-aminoethylbenzofurans.
PMID 14741270·Bioorg Med Chem Lett·2004
4-observational
Structure-activity studies of 5-substituted pyridopyrimidines as adenosine kinase inhibitors.
PMID 11140740·Bioorg Med Chem Lett·2001
7-preclinical
Use of the H3 receptor antagonist radioligand [3H]-A-349821 to reveal in vivo receptor occupancy of cognition enhancing H3 receptor antagonists.
PMID 19413577·Br J Pharmacol·2009
4-observational
Design of a new histamine H3 receptor antagonist chemotype: (3aR,6aR)-5-alkyl-1-aryl-octahydropyrrolo[3,4-b]pyrroles, synthesis, and structure-activity relationships.
PMID 19588934·J Med Chem·2009
7-preclinical
In vitro and in vivo characterization of A-940894: a potent histamine H4 receptor antagonist with anti-inflammatory properties.
PMID 19413570·Br J Pharmacol·2009
7-preclinical
Minimization of potential hERG liability in histamine H3 receptor antagonists.
PMID 18345496·Inflamm Res·2008
7-preclinical
The histamine H3 receptor: an attractive target for the treatment of cognitive disorders.
PMID 18469850·Br J Pharmacol·2008
6-review
A robust and high-capacity [(35)S]GTPgammaS binding assay for determining antagonist and inverse agonist pharmacological parameters of histamine H(3) receptor ligands.
PMID 18593375·Assay Drug Dev Technol·2008
8-other
The alkaloid conessine and analogues as potent histamine H3 receptor antagonists.
PMID 18683917·J Med Chem·2008
7-preclinical
Structure-activity studies on a series of a 2-aminopyrimidine-containing histamine H4 receptor ligands.
PMID 18811133·J Med Chem·2008
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
- 142 HAGGETTS POND RD
ANDOVER, MA 01810 - Phone
- (978) 475-7168
Quick Facts
- NPI
- 1841491867
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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