-
1
-
-
0036721054
-
Probes for the dopamine transporter: New leads toward a cocaine-abuse therapeutic - A focus on analogues of benztropine and rimcazole
-
Newman, A. H.; Kulkarni, S. Probes for the Dopamine Transporter: New Leads toward a Cocaine-Abuse Therapeutic - A Focus on Analogues of Benztropine and Rimcazole. Med. Res. Rev. 2002, 22(5), 429-464.
-
(2002)
Med. Res. Rev.
, vol.22
, Issue.5
, pp. 429-464
-
-
Newman, A.H.1
Kulkarni, S.2
-
2
-
-
0038416872
-
2002 Medicinal chemistry Division Award Address: Monoamine transporters and opioid receptors. Targets for addiction therapy
-
Carroll, F. I. 2002 Medicinal Chemistry Division Award Address: Monoamine Transporters and Opioid Receptors. Targets for Addiction Therapy. J. Med. Chem. 2003, 46(10), 1175-1194.
-
(2003)
J. Med. Chem.
, vol.46
, Issue.10
, pp. 1175-1194
-
-
Carroll, F.I.1
-
3
-
-
0242408732
-
Dopamine transporter as target for drug development of cocaine dependence medications
-
Dutta, A. K.; Zhang, S.; Kolhatkar, R.; Reith, M. E. A. Dopamine Transporter as Target for Drug Development of Cocaine Dependence Medications. Eur. J. Pharmacol. 2003, 479, 93-106.
-
(2003)
Eur. J. Pharmacol.
, vol.479
, pp. 93-106
-
-
Dutta, A.K.1
Zhang, S.2
Kolhatkar, R.3
Reith, M.E.A.4
-
4
-
-
0026566383
-
Cocaine receptor: Biochemical characterization and structure-activity relationships of cocaine analogues at the dopamine transporter
-
Carroll, F. I.; Lewin, A. H.; Boja, J. W.; Kuhar, M. J. Cocaine Receptor: Biochemical Characterization and Structure-Activity Relationships of Cocaine Analogues at the Dopamine Transporter. J. Med. Chem. 1992, 35, 969-981.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 969-981
-
-
Carroll, F.I.1
Lewin, A.H.2
Boja, J.W.3
Kuhar, M.J.4
-
5
-
-
0026542607
-
2β-substitued analogues of cocaine. Synthesis and inhibition of binding to the cocaine receptor
-
Lewin, A. H.; Gao, Y.; Abraham, P.; Boja, J. W.; Kukar, M. J.; Carroll, F. I. 2β-Substitued Analogues of Cocaine. Synthesis and Inhibition of Binding to the Cocaine Receptor. J. Med. Chem. 1992, 35, 135-140.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 135-140
-
-
Lewin, A.H.1
Gao, Y.2
Abraham, P.3
Boja, J.W.4
Kukar, M.J.5
Carroll, F.I.6
-
6
-
-
0027064877
-
Structure-activity relationship studies of cocaine: Replacement of the C-2 ester group by vinyl argues against H;-bonding and provides an esterase-resistant high-affinity cocaine analogue
-
Kozikowski, A. P.; Roberti, M.; Xiang, L.; Bergmann, J. S.; Callahan, P. M.; Cunningham, K. A.; Johnson, K. M. Structure-Activity Relationship Studies of Cocaine: Replacement of the C-2 Ester Group by Vinyl Argues Against H;-Bonding and Provides an Esterase-Resistant High-Affinity Cocaine Analogue. J. Med. Chem. 1992, 35, 4764-4766.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 4764-4766
-
-
Kozikowski, A.P.1
Roberti, M.2
Xiang, L.3
Bergmann, J.S.4
Callahan, P.M.5
Cunningham, K.A.6
Johnson, K.M.7
-
7
-
-
0027446171
-
Novel 2-substituted cocaine analogs: Binding properties at dopamine transporter sites in rat striatum
-
Davies, H. M. L.; Saikali, E.; Sexton, T. Childers, S. R. Novel 2-substituted Cocaine Analogs: Binding Properties at Dopamine Transporter Sites in Rat Striatum. Eur. J. Pharmacol.-Mol. Pharmcol. Sect. 1993, 244, 93-97.
-
(1993)
Eur. J. Pharmacol.-Mol. Pharmcol. Sect.
, vol.244
, pp. 93-97
-
-
Davies, H.M.L.1
Saikali, E.2
Sexton, T.3
Childers, S.R.4
-
8
-
-
0027363641
-
3-Aryl-2-(3′-substituted-1′,2′,4-oxadiazol-5′-yl) tropane analogues of cocaine: Affinities at the cocaine binding Site at the dopamine, serotonin and norepinephrine Transporter
-
Carroll, F. I.; Gray, J. L.; Abraham, P.; Kuzemko, M. A.; Lewin, A. H.; Boja, J. W.; Kuhar, M. J. 3-Aryl-2-(3′-substituted-1′,2′,4- oxadiazol-5′-yl)tropane analogues of Cocaine: Affinities at the Cocaine binding Site at the Dopamine, Serotonin and Norepinephrine Transporter. J. Med. Chem. 1993, 36, 2886-2890.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2886-2890
-
-
Carroll, F.I.1
Gray, J.L.2
Abraham, P.3
Kuzemko, M.A.4
Lewin, A.H.5
Boja, J.W.6
Kuhar, M.J.7
-
9
-
-
0029063953
-
Cocaine and 3β-(4′-substituted phenyl)tropane-2/9-carboxylic acid ester and amide analogues. New high affinity and selective compounds for the dopamine transporter
-
Carroll, F. I.; Kotian, P.; Dehghani, A.; Gray, J. L.; Kuzemko, M. A.; Parham, K. A.; Abraham, P.; Lewin, A. H.; Boja, J. W.; Kuhar, M. J. Cocaine and 3β-(4′-substituted phenyl)tropane-2/9-carboxylic Acid Ester and Amide Analogues. New High Affinity and Selective Compounds for the Dopamine Transporter. J. Med. Chem. 1995, 38, 379-388.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 379-388
-
-
Carroll, F.I.1
Kotian, P.2
Dehghani, A.3
Gray, J.L.4
Kuzemko, M.A.5
Parham, K.A.6
Abraham, P.7
Lewin, A.H.8
Boja, J.W.9
Kuhar, M.J.10
-
10
-
-
0029122828
-
Chemistry an biology of the 2β-alkyl-3β-phenyl analogues of cocaine: Subnanomolar affinity ligands that suggest new pharmacophore model at the C-2 position
-
Kozikowski, A. P.; Saiah, M. K. E.; Johnson, K. M.; Bergmann, J. S. Chemistry an Biology of the 2β-alkyl-3β-phenyl Analogues of Cocaine: Subnanomolar Affinity Ligands That Suggest New Pharmacophore Model at the C-2 Position. J. Med. Chem. 1995, 38, 3086-3093.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3086-3093
-
-
Kozikowski, A.P.1
Saiah, M.K.E.2
Johnson, K.M.3
Bergmann, J.S.4
-
11
-
-
0029899173
-
Synthesis, ligand binding and quantitative structure-activity relationship study of 3β-(4′-substituted phenyl)-2β-heterocyclic tropanes: Evidance for an electrostatic interaction at the 2-position
-
Kotian, P.; Muscarella, S. W.; Abraham, P.; Lewin, A. H.; Boja, J. W.; Kuhar, M. J.; Carroll, F. I. Synthesis, Ligand Binding and Quantitative Structure-Activity Relationship Study of 3β-(4′-substituted phenyl)-2β-heterocyclic Tropanes: Evidance for an Electrostatic Interaction at the 2-Position. J. Med. Chem. 1996, 39, 2753-2763.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2753-2763
-
-
Kotian, P.1
Muscarella, S.W.2
Abraham, P.3
Lewin, A.H.4
Boja, J.W.5
Kuhar, M.J.6
Carroll, F.I.7
-
12
-
-
0030896771
-
Synthesis, dopamine transporter affinity, dopamine uptake inhibition, and locomotor stimulant activity of 2-substituted 3β-phenyltropane derivatives
-
Xu, L.; Kelkar, S. V.; Lomenzo, S. A.; Izenwasser, S.; Katz, J. L.; Kline, R. H.; Trudell, M. L. Synthesis, Dopamine Transporter Affinity, Dopamine Uptake Inhibition, and Locomotor Stimulant Activity of 2-Substituted 3β-phenyltropane Derivatives. J. Med. Chem. 1997, 40, 858-863.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 858-863
-
-
Xu, L.1
Kelkar, S.V.2
Lomenzo, S.A.3
Izenwasser, S.4
Katz, J.L.5
Kline, R.H.6
Trudell, M.L.7
-
13
-
-
0035800785
-
The uptake inhibitors cocaine and benztropine differentially alter the conformation of the human dopamine transporter
-
Reith, M. E. A.; Berfield, J. L.; Wang, L. C.; Ferrer, J. V.; Javitch, J. A. The Uptake Inhibitors Cocaine and Benztropine Differentially Alter the Conformation of the Human Dopamine Transporter. J. Biol. Chem. 2001, 276, 29012-29018.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 29012-29018
-
-
Reith, M.E.A.1
Berfield, J.L.2
Wang, L.C.3
Ferrer, J.V.4
Javitch, J.A.5
-
14
-
-
22944448022
-
Recognition of benztropine by the dopamine transporter (DAT) differs from that of the classical dopamine uptake inhibitors cocaine, methylphenidate and mazindol as a function of a DAT transmembrane 1 aspartic acid residue
-
Ukairo, O. T.; Bondi, C. D.; Newman, A. H.; Kulkarni, S. S.; Kozikowski, A. P., Pan, S.; Surratt, C. K. Recognition of benztropine by the dopamine transporter (DAT) differs from that of the classical dopamine uptake inhibitors cocaine, methylphenidate and mazindol as a function of a DAT transmembrane 1 aspartic acid residue. J. Pharmacol. Exp. Ther. 2005, 314, 575-583.
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.314
, pp. 575-583
-
-
Ukairo, O.T.1
Bondi, C.D.2
Newman, A.H.3
Kulkarni, S.S.4
Kozikowski, A.P.5
Pan, S.6
Surratt, C.K.7
-
15
-
-
0028104102
-
Novel 3α-diphenylmethoxytropane analogues are potent dopamine uptake inhibitors without cocaine-like behavioral profiles
-
Newman, A. H.; Allen, A. C.; Izenwasser, S.; Katz, J. L. Novel 3α-Diphenylmethoxytropane Analogues are Potent Dopamine Uptake Inhibitors without Cocaine-like Behavioral Profiles. J. Med. Chem. 1994, 37, 2258-2261.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2258-2261
-
-
Newman, A.H.1
Allen, A.C.2
Izenwasser, S.3
Katz, J.L.4
-
16
-
-
0028804967
-
Novel 4′- and 4′,4″-substituted-3α- (diphenylmethoxy)-tropane analogues are potent and selective dopamine uptake inhibitors
-
Newman, A. H.; Kline, R. H.; Allen, A. C.; George, C.; Izenwasser, S.; Katz, J. L. Novel 4′- and 4′,4″-Substituted-3α- (diphenylmethoxy)-tropane Analogues are Potent and Selective Dopamine Uptake Inhibitors. J. Med. Chem. 1995, 38, 3933-3940.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3933-3940
-
-
Newman, A.H.1
Kline, R.H.2
Allen, A.C.3
George, C.4
Izenwasser, S.5
Katz, J.L.6
-
17
-
-
0030997211
-
3′-chloro-3α-(diphenylmethoxy)tropane but not 4′-chloro-3α-(diphenyl-methoxy)tropane produces a cocaine-like behavioral profile
-
Kline, R. H.; Izenwasser, S.; Katz, J. L.; Newman, A. H. 3′-Chloro-3α-(diphenylmethoxy)tropane But Not 4′-Chloro- 3α-(diphenyl-methoxy)tropane Produces a Cocaine-like Behavioral Profile. J. Med. Chem. 1997, 40, 851-857.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 851-857
-
-
Kline, R.H.1
Izenwasser, S.2
Katz, J.L.3
Newman, A.H.4
-
18
-
-
0031434059
-
Novel N-substituted 4′,4″-difluoro-3α-(diphenylmethoxy) -tropane analogues: Selective ligands for the dopamine transporter
-
Agoston, G. E.; Wu, J. H.; Izenwasser, S.; George, C.; Katz, J. L.; Kline, R. H.; Newman, A. H. Novel N-Substituted 4′,4″-Difluoro- 3α-(diphenylmethoxy)-tropane Analogues: Selective Ligands for the Dopamine Transporter. J. Med. Chem. 1997, 40, 4329-4339.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 4329-4339
-
-
Agoston, G.E.1
Wu, J.H.2
Izenwasser, S.3
George, C.4
Katz, J.L.5
Kline, R.H.6
Newman, A.H.7
-
19
-
-
0028133248
-
The discovery of an unusually selective and novel cocaine analog: Difluoropine. Synthesis and inhibition of binding at cocaine recognition sites
-
Meltzer, P. C.; Liang, A. Y.; Madras, B. K. The Discovery of an Unusually Selective and Novel Cocaine Analog: Difluoropine. Synthesis and Inhibition of Binding at Cocaine Recognition Sites. J. Med. Chem. 1994, 37, 2001-2010.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2001-2010
-
-
Meltzer, P.C.1
Liang, A.Y.2
Madras, B.K.3
-
20
-
-
33750098417
-
Relationship between conformational changes in the dopamine transporter and cocaine-like subjective effects of uptake inhibitors
-
submitted
-
Loland, C. J.; Desai, R. I.; Gerstbrein, K.; Sitte, H. H.; Newman, A. H.; Katz, J. L.; Gether, U. Relationship Between Conformational Changes in the Dopamine Transporter and Cocaine-like Subjective Effects of Uptake Inhibitors, J. Biol. Chem. 2006, submitted.
-
(2006)
J. Biol. Chem.
-
-
Loland, C.J.1
Desai, R.I.2
Gerstbrein, K.3
Sitte, H.H.4
Newman, A.H.5
Katz, J.L.6
Gether, U.7
-
21
-
-
0032589936
-
Novel 3α-diphenylmethoxytropane analogs: Selective dopamine uptake inhibitors with behavioral effects distinct from those of cocaine
-
Katz, J. K.; Izenwasser, S., Kline, R. H., Allen, A. C.; Newman, A. H. Novel 3α-Diphenylmethoxytropane Analogs: Selective Dopamine Uptake Inhibitors with Behavioral Effects Distinct from Those of Cocaine. J. Pharmacol. Exp. Ther. 1999, 288, 302-315.
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.288
, pp. 302-315
-
-
Katz, J.K.1
Izenwasser, S.2
Kline, R.H.3
Allen, A.C.4
Newman, A.H.5
-
22
-
-
27644516824
-
Effects of N-substituted analogues of benztropine: Diminished cocaine-like effects in dopamine transporter ligands
-
Katz, J. L.; Kopajtic, T.; Agoston, G. E.; Newman, A. H. Effects of N-Substituted Analogues of Benztropine: Diminished Cocaine-like Effects in Dopamine Transporter Ligands. J. Pharmacol. Exp. Ther. 2004, 288, 302-315.
-
(2004)
J. Pharmacol. Exp. Ther.
, vol.288
, pp. 302-315
-
-
Katz, J.L.1
Kopajtic, T.2
Agoston, G.E.3
Newman, A.H.4
-
23
-
-
0035094778
-
Further studies of the reinforcing effects of benztropine analogs in rhesus monkeys
-
Woolverton, W. L.; Hecht, G. S.; Agoston, G. E.; Katz, J. L.; Newman, A. H. Further Studies of the Reinforcing Effects of Benztropine Analogs in Rhesus Monkeys. Psychopharmacology 2001, 154, 375-382.
-
(2001)
Psychopharmacology
, vol.154
, pp. 375-382
-
-
Woolverton, W.L.1
Hecht, G.S.2
Agoston, G.E.3
Katz, J.L.4
Newman, A.H.5
-
24
-
-
19444364404
-
Place conditioning and locomotor effects of N-substituted, 4′, 4″-difluorobenztropine analogues in rats
-
Li, S.-M.; Newman, A. H.; Katz, J. L. Place Conditioning and Locomotor Effects of N-Substituted, 4′, 4″-Difluorobenztropine Analogues in Rats. J. Pharmacol. Exp. Ther. 2005, 313, 1223-1230.
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.313
, pp. 1223-1230
-
-
Li, S.-M.1
Newman, A.H.2
Katz, J.L.3
-
25
-
-
0037029801
-
Enantioselective synthesis of S-(+)-2β-carboalkoxy-3α-[bis(4- fluorophenyl)-methoxy]tropanes as novel probes for the dopamine transporter
-
Zou, M.-F.; Agoston, G. E.; Belov, Y.; Kopajtic, T.; Katz, J. L.; Newman, A. H. Enantioselective Synthesis of S-(+)-2β-Carboalkoxy-3α-[bis(4- fluorophenyl)-methoxy]tropanes as Novel Probes for the Dopamine Transporter. Bioorg. Med. Chem. Lett. 2002, 12, 1249-1252.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1249-1252
-
-
Zou, M.-F.1
Agoston, G.E.2
Belov, Y.3
Kopajtic, T.4
Katz, J.L.5
Newman, A.H.6
-
26
-
-
0038121717
-
Structure-activity relationship comparison of (S)-2β-substituted 3α-[bis(4-fluorophenyl)-methoxy]tropanes and (R)-2β-substituted 3β-(3,4-Dichlorophenyl)tropanes at the dopamine transporter
-
Zou, M.-F.; Kopajtic, T.; Katz, J. L.; Newman, A. H. Structure-Activity Relationship Comparison of (S)-2β-Substituted 3α-[bis(4-fluorophenyl) -methoxy]tropanes and (R)-2β-Substituted 3β-(3,4-Dichlorophenyl) tropanes at the Dopamine Transporter. J. Med. Chem. 2003, 46, 2908-2916.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2908-2916
-
-
Zou, M.-F.1
Kopajtic, T.2
Katz, J.L.3
Newman, A.H.4
-
27
-
-
14244260728
-
Identification of a dopamine transporter ligand that blocks the stimulant effects of cocaine
-
Desai, R. I.; Kopajtic, T.; Koffarnus, M.; Newman, A. H.; Katz, J. L. Identification of a Dopamine Transporter Ligand that Blocks the Stimulant Effects of Cocaine. J. Neurosci. 2005, 25(8), 1889-1893.
-
(2005)
J. Neurosci.
, vol.25
, Issue.8
, pp. 1889-1893
-
-
Desai, R.I.1
Kopajtic, T.2
Koffarnus, M.3
Newman, A.H.4
Katz, J.L.5
-
28
-
-
25644460008
-
Relationship between in vivo occupancy at the dopamine transporter and behavioral effects of cocaine, GBR 12909 and benztropine analogues
-
Desai, R.; Kopajtic, T.; French, D.; Newman, A. H.; Katz, J. L. Relationship Between In Vivo Occupancy at the Dopamine Transporter and Behavioral Effects of Cocaine, GBR 12909 and Benztropine Analogues. J. Pharmacol. Exp. Ther. 2005, 315, 397-404.
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.315
, pp. 397-404
-
-
Desai, R.1
Kopajtic, T.2
French, D.3
Newman, A.H.4
Katz, J.L.5
-
29
-
-
0035089185
-
Dopamine transporter binding without cocaine-like behavioral effects: Synthesis and evaluation of benztropine analogues alone and in combination with cocaine in rodents
-
Katz, J. L.; Agoston, G. E.; Ailing, K. L.; Kline, R. H.; Forster, M. J.; Woolverton, W. L.; Kopajtic, T. A.; Newman, A. H. Dopamine Transporter Binding Without Cocaine-like Behavioral Effects: Synthesis and Evaluation of Benztropine Analogues Alone and in Combination with Cocaine in Rodents. Psychopharmacology 2001, 154, 362-374.
-
(2001)
Psychopharmacology
, vol.154
, pp. 362-374
-
-
Katz, J.L.1
Agoston, G.E.2
Ailing, K.L.3
Kline, R.H.4
Forster, M.J.5
Woolverton, W.L.6
Kopajtic, T.A.7
Newman, A.H.8
-
30
-
-
2942602683
-
Structure-activity relationship at monoamine transporters for a series of N-substituted-3α-(bis[4-fluorophenyl]methoxy)tropanes: Comparative molecular field analysis, synthesis, and pharmacological evaluation
-
Kulkarni, S.; Grundt, P.; Kopajtic, T.; Katz, J. L.; Newman, A. H. Structure-Activity Relationship at Monoamine Transporters for a series of N-Substituted-3α-(bis[4-fluorophenyl]methoxy)tropanes: Comparative Molecular Field Analysis, Synthesis, and Pharmacological Evaluation. J. Med. Chem. 2004, 47, 3388-3398.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 3388-3398
-
-
Kulkarni, S.1
Grundt, P.2
Kopajtic, T.3
Katz, J.L.4
Newman, A.H.5
-
31
-
-
0020631201
-
3H]pirenzepine binding in the rat provide evidence for distinct M1 and M2 muscarinic receptor subtypes
-
3H]pirenzepine binding in the rat provide evidence for distinct M1 and M2 muscarinic receptor subtypes. Life Sci. 1983, 32, 3001-3011.
-
(1983)
Life Sci.
, vol.32
, pp. 3001-3011
-
-
Watson, M.1
Yamamura, H.I.2
Roeske, W.R.3
-
32
-
-
0037075844
-
Synthesis and biological evaluation of 2-substituted 3β-tolyltropane derivatives at dopamine, serotonin, and norepinephrine transporters
-
Xu, L.; Kelkar, S. V.; Izenwasser, S.; Kopajtic, T.; Katz, J. L.; Klein-Stevens, C.; Zhu, N.; Lomenzo, S. A.; Winfield, L.; Trudell, M. L. Synthesis and Biological Evaluation of 2-Substituted 3β-Tolyltropane Derivatives at Dopamine, Serotonin, and Norepinephrine Transporters J. Med. Chem. 2002, 45, 1203-1210.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 1203-1210
-
-
Xu, L.1
Kelkar, S.V.2
Izenwasser, S.3
Kopajtic, T.4
Katz, J.L.5
Klein-Stevens, C.6
Zhu, N.7
Lomenzo, S.A.8
Winfield, L.9
Trudell, M.L.10
-
33
-
-
0030051988
-
2-Carbomethoxy-3-(diarylmethoxy)-1αH,5αH-tropane analogues: Synthesis and inhibition of binding at the dopamine transporter and comparison with piperazines of the GBR series
-
Meltzer, P. C.; Liang, A. Y.; Madras, B. K. 2-Carbomethoxy-3- (diarylmethoxy)-1αH,5αH-tropane Analogues: Synthesis and Inhibition of Binding at the Dopamine Transporter and Comparison with Piperazines of the GBR Series. J. Med. Chem. 1996, 39, 371-379.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 371-379
-
-
Meltzer, P.C.1
Liang, A.Y.2
Madras, B.K.3
-
34
-
-
2442501261
-
The Effect of 6-substituted-4′, 4″-difluorobenztropines on monoamine transporters and the muscarinic M1 receptor
-
Grundt, P.; Kopajtic, T. A.; Katz, J. L.; Newman, A. H. The Effect of 6-substituted-4′, 4″-Difluorobenztropines on Monoamine Transporters and the Muscarinic M1 Receptor. Bioorg. Med. Chem. Lett. 2004, 14, 3295-3298.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 3295-3298
-
-
Grundt, P.1
Kopajtic, T.A.2
Katz, J.L.3
Newman, A.H.4
|