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CANDICE DERSCH, MD

MD

Obstetrics & Gynecology Physician

NPI: 1437358157IndividualAccepts Medicare

Specialties, Licenses & Credentials

Obstetrics & Gynecology PhysicianPrimary

Obstetrics & Gynecology

Code: 207V00000X

MD18808(ME)

CMS Specialties

PrimaryOBSTETRICS/GYNECOLOGY

Education

MEDICAL COLLEGE OF WISCONSIN

Class of 2007

Research & Publications (20)

Opioid ligands with mixed properties from substituted enantiomeric N-phenethyl-5-phenylmorphans. Synthesis of a micro-agonist delta-antagonist and delta-inverse agonists.
PMID 17406716·Org Biomol Chem·2007
7-preclinical
Probes for narcotic receptor mediated phenomena. 39. Enantiomeric N-substituted benzofuro[2,3-c]pyridin-6-ols: synthesis and topological relationship to oxide-bridged phenylmorphans.
PMID 19627147·J Med Chem·2009
7-preclinical
Design, synthesis, and characterization of 6beta-naltrexol analogs, and their selectivity for in vitro opioid receptor subtypes.
PMID 19364645·Bioorg Med Chem Lett·2009
7-preclinical
Studies of the biogenic amine transporters. 13. Identification of "agonist" and "antagonist" allosteric modulators of amphetamine-induced dopamine release.
PMID 19244097·J Pharmacol Exp Ther·2009
7-preclinical
Probes for narcotic receptor mediated phenomena. 37. Synthesis and opioid binding affinity of the final pair of oxide-bridged phenylmorphans, the ortho- and para-b-isomers and their N-phenethyl analogues, and the synthesis of the N-phenethyl analogues of the ortho- and para-d-isomers.
PMID 19053757·J Med Chem·2008
8-other
Differential effects of opioid agonists on G protein expression in CHO cells expressing cloned human opioid receptors.
PMID 18639745·Brain Res Bull·2008
7-preclinical
Synthesis and pharmacological effects of the enantiomers of the N-phenethyl analogues of the ortho and para e- and f-oxide-bridged phenylmorphans.
PMID 18688479·Org Biomol Chem·2008
7-preclinical
Design and synthesis of 2- and 3-substituted-3-phenylpropyl analogs of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine and 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenylpropyl)piperazine: role of amino, fluoro, hydroxyl, methoxyl, methyl, methylene, and oxo substituents on affinity for the dopamine and serotonin transporters.
PMID 18393401·J Med Chem·2008
8-other
Evidence for a mu-delta opioid receptor complex in CHO cells co-expressing mu and delta opioid peptide receptors.
PMID 18472184·Peptides·2008
7-preclinical
Herkinorin analogues with differential beta-arrestin-2 interactions.
PMID 18380425·J Med Chem·2008
8-other
Studies of the biogenic amine transporters. 12. Identification of novel partial inhibitors of amphetamine-induced dopamine release.
PMID 18441249·J Pharmacol Exp Ther·2008
4-observational
Synthetic studies of neoclerodane diterpenes from Salvia divinorum: preparation and opioid receptor activity of salvinicin analogues.
PMID 17580847·J Med Chem·2007
7-preclinical
Probes for narcotic receptor mediated phenomena. 34. Synthesis and structure-activity relationships of a potent mu-agonist delta-antagonist and an exceedingly potent antinociceptive in the enantiomeric C9-substituted 5-(3-hydroxyphenyl)-N-phenylethylmorphan series.
PMID 17625813·J Med Chem·2007
7-preclinical
DAT/SERT selectivity of flexible GBR 12909 analogs modeled using 3D-QSAR methods.
PMID 17127069·Bioorg Med Chem·2007
8-other
Salvinorin A: allosteric interactions at the mu-opioid receptor.
PMID 17060492·J Pharmacol Exp Ther·2007
7-preclinical
Restoration of 3,4-methylenedioxymethamphetamine-induced 5-HT depletion by the administration of L-5-hydroxytryptophan.
PMID 17629409·Neuroscience·2007
7-preclinical
Structure-activity relationships of substituted N-benzyl piperidines in the GBR series: Synthesis of 4-(2-(bis(4-fluorophenyl)methoxy)ethyl)-1-(2-trifluoromethylbenzyl)piperidine, an allosteric modulator of the serotonin transporter.
PMID 16563775·Bioorg Med Chem·2006
8-other
Synthetic studies of neoclerodane diterpenes from Salvia divinorum: selective modification of the furan ring.
PMID 16621556·Bioorg Med Chem Lett·2006
7-preclinical
Design and synthesis of noncompetitive metabotropic glutamate receptor subtype 5 antagonists.
PMID 16678408·Bioorg Med Chem Lett·2006
7-preclinical
Synthesis of salvinorin A analogues as opioid receptor probes.
PMID 16792410·J Nat Prod·2006
8-other

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
887 CONGRESS ST, SUITE 200
PORTLAND, ME 04102

Location

Practice Location

887 CONGRESS ST, PORTLAND, ME
(207) 771-5549

Quick Facts

NPI
1437358157
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
19
Publications
20

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