M. Eissenstat

发表

3-benzyl-quinolones: Novel, potent inhibitors of mammalian topoisomerase II☆

T. Corbett, M. Eissenstat, G. Kuo, 1995 .

Potent mammalian topoisomerase II inhibitors: 1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-(2,6-dimethyl-4-pyridinyl)-4-substituted-quinolines

M. Eissenstat, G. Kuo, M. Wentland, 1995 .

Acidity of Organic Molecules in the Gas Phase and in Aqueous Solvent

Gregory J. Tawa, Stanley K. Burt, Igor A. Topol, 2000 .

Antirhinoviral activity of heterocyclic analogs of Win 54954.

J. Mallamo, M. Eissenstat, P M Carabateas, 1992, Journal of medicinal chemistry.

Conformationally restrained analogues of pravadoline: nanomolar potent, enantioselective, (aminoalkyl)indole agonists of the cannabinoid receptor.

M. Eissenstat, D. Haycock, E. Baizman, 1992, Journal of medicinal chemistry.

Aminoalkylindoles: structure-activity relationships of novel cannabinoid mimetics.

M. Eissenstat, E. J. Alexander, M. Bell, 1995, Journal of medicinal chemistry.

Morpholinoalkylindenes as antinociceptive agents: Novel cannabinoid receptor agonists

M. Eissenstat, D. Haycock, J. Kuster, 1995 .

Antinociceptive (aminoalkyl)indoles.

J. R. Wetzel, D. Rosi, D. Hlasta, 1991, Journal of medicinal chemistry.

Unsymmetric nonpeptidic HIV protease inhibitors containing anthranilamide as a P2' ligand.

T. Bhat, S. Gulnik, B. Yu, 1998, Bioorganic & medicinal chemistry letters.

High-resolution NMR and computer modeling studies of the cannabimimetic aminoalkylindole prototype WIN-55212-2.

A. Makriyannis, M. Eissenstat, J. Chen, 1999, Journal of medicinal chemistry.

Common cannabimimetic pharmacophoric requirements between aminoalkyl indoles and classical cannabinoids.

A. Makriyannis, M. Eissenstat, X. Xie, 1995, Life sciences.

C-Attached aminoalkylindoles: potent cannabinoid mimetics

W. A. Hill, J. Abt, A. Makriyannis, 1996 .

Aminoalkylindoles (AAIs): a new route to the cannabinoid receptor?

S. Childers, A. Howlett, M. Eissenstat, 1990, NIDA research monograph.

Facile Stereoselective Synthesis of γ‐Substituted γ‐Amino Acids from the Corresponding α‐Amino Acids.

E. Majerová, M. Eissenstat, P. Majer, 1998 .

Facile stereoselective synthesis of ?-substituted ?-amino acids from the corresponding ?-amino acids

E. Majerová, M. Eissenstat, P. Majer, 1997 .

Enamino-oxindole HIV protease inhibitors.

S. Gulnik, J. Erickson, H. Yokoe, 2012, Bioorganic & medicinal chemistry letters.

Novel cAMP PDE III inhibitors: imidazo[4,5-b]pyridin-2(3H)-ones and thiazolo[4,5-b]pyridin-2(3H)-ones and their analogs.

G. Y. Lesher, E. Bacon, M. Reuman, 1994, Journal of medicinal chemistry.

HIV Protease as a Target for the Design of Antiviral Agents for AIDS

J. Erickson, M. Eissenstat, 1999 .

A general methodology for pseudoguaiane synthesis: total synthesis of (.+-.)-damsinic acid and (.+-.)-confertin

P. Wender, M. Eissenstat, Michael P. Filosa, 1979 .

A general methodology for pseudoguaiane synthesis: total synthesis of (.+-.)-damsinic acid and (.+-.)-confertin

P. Wender, M. Eissenstat, Michael P. Filosa, 1979 .

Three-dimensional quantitative structure-activity relationship study of the cannabimimetic (aminoalkyl)indoles using comparative molecular field analysis.

W. Welsh, A. Howlett, E. Collantes, 1998, Journal of medicinal chemistry.

Facile stereoselective synthesis of γ-amino acids from the corresponding α-amino acids

E. Majerová, M. Eissenstat, P. Majer, 2002 .

Experimental determination and calculations of redox potential descriptors of compounds directed against retroviral zinc fingers: Implications for rational drug design

J. Casas-Finet, E. Chertova, I. Topol, 2001, Protein science : a publication of the Protein Society.

Regiospecific generation of lithioenamines from .alpha.,.beta.-unsaturated imines. An alternative method for reduction-alkylation of enones

P. Wender, M. Eissenstat, 1978 .

Nitriles from Ketones: Cyclohexanecarbonitrile

P. Wender, M. Eissenstat, F. Ziegler, 2003 .

A short and general synthesis of 1,3‐dihydro‐6‐heteroaryl‐5‐perfluoroalkyl‐2H‐imidazo[4,5‐b]pyridin‐2‐ones

Baldev Singh, G. Y. Lesher, E. Bacon, 1993 .

A Short and General Synthesis of 1,3‐Dihydro‐6‐heteroaryl‐5‐ perfluoroalkyl‐2H‐imidazo(4,5‐b)pyridin‐2‐ones.

Baldev Singh, G. Y. Lesher, E. Bacon, 1993 .

Approaches to the design of HIV protease inhibitors with improved resistance profiles

S. Gulnik, M. Eissenstat, 2008, Current opinion in HIV and AIDS.

A retro-Diels-Alder approach to oxazoles and imidazoles

M. Eissenstat, J. Weaver, 1993 .

Unsymmetric Nonpeptidic HIV Protease Inhibitors Containing Anthranilamide as a P2′ Ligand.

T. Bhat, S. Gulnik, J. Erickson, 1999 .

Approaches to the design of HIV protease inhibitors with improved resistance profiles

S. Gulnik, M. Eissenstat, 2008, Current opinion in HIV and AIDS.