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-Jeffrey R Deschamps Researcher Activity Profile

Research Author Detailed Information 

profile photo of Jeffrey R DeschampsJeffrey R deschamps researcher

Jeffrey R Deschamps Publication Rate By Year

Jeffrey R Deschamps has published 2 paper(s) in 2005, 2 paper(s) in 2006, 7 paper(s) in 2007, for a total of 11 research publications in total.

Jeffrey R Jr Deschamps Author Information

LAST NAME: deschamps

FIRST NAME: Jeffrey R

INITIALS: jr

AFFILIATION:

Papers

Jeffrey R Deschamps's Publication Record

  1. Synthesis of 8-thiabicyclo[3.2.1]octanes and their binding affinity for the dopamine and serotonin transporters. Year Published: 2006
  2. Organix Inc., 240 Salem Street, Woburn, MA 01801, USA.
  3. Slow-onset, long-duration, alkyl analogues of methylphenidate with enhanced selectivity for the dopamine transporter. Year Published: 2007
  4. Massachusetts College of Pharmacy and Health Sciences, Boston, Massachusetts 02115, USA. mfroimowitz@mcphs.edu
  5. Conformational analysis of the cis- and trans-adducts of the Pictet - Spengler reaction. Evidence for the structural basis for the C(1) - N(2) scission process in the cis- to trans-isomerization. Year Published: 2007
  6. Department of Chemistry, University of Wisconsin-Milwaukee, Milwaukee, Wisconsin 53211, USA.
  7. Sculpting the bicyclo[3.1.0]hexane template of carbocyclic nucleosides to improve recognition by herpes thymidine kinase. Year Published: 2007
  8. Laboratory of Medicinal Chemistry, Center for Cancer Research, National Cancer Institute at Frederick, 376 Boyles Street, Frederick, Maryland 21702, USA.
  9. Synthetic studies of neoclerodane diterpenes from Salvia divinorum: preparation and opioid receptor activity of salvinicin analogues. Year Published: 2007
  10. Division of Medicinal & Natural Products Chemistry, College of Pharmacy, The University of Iowa, Iowa City, Iowa 52242, USA.
  11. 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. Year Published: 2007
  12. Drug Design and Synthesis Section, Chemical Biology Research Branch, National Institute on Drug Abuse, National Institutes of Health, DHHS, Bethesda, MD 20892, USA.
  13. Functionalization of the 6,14-bridge of the orvinols. Part 3: preparation and pharmacological evaluation of 18- and 19-hydroxyl substituted orvinols. Year Published: 2007
  14. Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, MD 21201, USA.
  15. Ru2(ap)4(sigma-oligo(phenyleneethynyl)) molecular wires: synthesis and electronic characterization. Year Published: 2005
  16. Naval Research Laboratory, Washington, D.C. 20375, USA. amyblum@cbmse.nrl.navy.mil
  17. Structure-based design of potent non-peptide MDM2 inhibitors. Year Published: 2005
  18. Departments of Internal Medicine and Medicinal Chemistry and Comprehensive Cancer Center, and Life Sciences Institute, University of Michigan, 1500 East Medical Center Drive, Ann Arbor, Michigan 48109, USA.
  19. Synthesis of salvinorin A analogues as opioid receptor probes. Year Published: 2006
  20. Division of Medicinal & Natural Products Chemistry, College of Pharmacy, The University of Iowa, Iowa City, Iowa 52242, USA.
  21. Synthetic studies of neoclerodane diterpenes from Salvia divinorum: preparation and opioid receptor activity of salvinicin analogues. Year Published: 2007
  22. Division of Medicinal & Natural Products Chemistry, College of Pharmacy, The University of Iowa, Iowa City, Iowa 52242, USA.
 

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