Sfoglia per Autore
Preparation and use of nucleotide bisphosphate as P2Y antagonists
1998 Boyer, J. L.; Harden, T. K.; Jacobson, K. A.; Camaioni, Emidio
Structure-activity relationships of P2 receptor agonists and antagonists
1998 K. A., Jacobson; Y. C., Kim; Camaioni, Emidio; A. M., van Rhee
Modulation of apoptosis in human lymphocytes by adenosine analogues
1998 Barbieri, D; Franceschi, C; Camaioni, Emidio; Costanzi, S; Vittori, S; Volpini, R; Cristalli, G.
Competitive and selective antagonism of P2Y(1) receptors by N-6-methyl 2 '-deoxyadenosine 3 ',5 '-bisphosphate
1998 Boyer, Jl; Mohanram, A; Camaioni, Emidio; Jacobson, Ka; Harden, Tk
Deoxyadenosine bisphosphate derivatives as potent antagonists at P2Y(1) receptors
1998 Camaioni, Emidio; Boyer, Jl; Mohanram, A; Harden, Tk; Jacobson, Ka
Human P2Y(1) receptor: Molecular modeling and site-directed mutagenesis as tools to identify agonist and antagonist recognition sites
1998 Moro, S; Guo, Dp; Camaioni, Emidio; Boyer, Jl; Harden, Tk
Some 6-phenylazopyridoxalphosphate derivatives influence P2-purinoreceptor-mediated effects
1998 A. U., Ziganshin; A. V., Rychkov; L. E., Ziganshina; Kim, Y. u. C. h.; Camaioni, Emidio; G., Burnstock; K. A., Jacobson
Synthesis of New 3′-Deoxyribonucleosides Employing the Acid-Catalyzed Fusion Method
1998 R., Volpini; Camaioni, Emidio; S., Costanzi; S., Vittori; G., Cristalli
Synthesis of New Nucleosides by coupling of chloropurines with 2- and 3-deoxy derivatives of N-methyl-D-ribofuranuronamide
1998 R., Volpini; Camaioni, Emidio; S., Vittori; L., Barboni; C., Lambertucci; G., Cristalli
New substituted 9-alkylpurines as adenosine receptor ligands
1998 Camaioni, Emidio; Costanzi, S; Vittori, S; Volpini, R; Klotz, Kn; Cristalli, G.
Characterization of potent ligands at human recombinant adenosine receptors
1998 G., Cristalli; Camaioni, Emidio; S., Costanzi; S., Vittori; R., Volpini; K. N., Klotz
Synthesis and structure-activity relationships of pyridoxal-6-arylazo-5′-phosphate and phosphonate derivatives as P2 receptor antagonists
1998 Y. C., Kim; Camaioni, Emidio; A. U., Ziganshin; X. D., Ji; B. F., King; S. S., Wildman; A., Rychkov; Yoburn, J. o.; H., Kim; A., Mohanram; T. K., Harden; J. L., Boyer; G., Burnstock; K. A., Jacobson
Molecular recognition in P2 receptors: Ligand development aided by molecular modeling and mutagenesis
1999 Jacobson, K.; Hoffmann, C.; Kim, Y.; Camaioni, Emidio; Nandanan, E.; Jang, S.; Guo, D.; Ji, X.; Von Kugelgen, I.; Moro, S.; Ziganshin, A.; Rychkov, A.; King, B.; Brown, S.; Wildman, S.; Burnstock, G.; Boyer, J.; Mohanram, A.; Harden, T.
Synthesis and Receptor Affinity of Polysubstituted Adenosines
1999 S., Vittori; Camaioni, Emidio; S., Costanzi; R., Volpini; K. N., Klotz; G., Cristalli
Structure-Activity Relationships of Adenosine Deaminase Inhibitors
1999 S., Vittori; Camaioni, Emidio; S., Costanzi; R., Volpini; G., Lupidi; G., Cristalli
Coupling of 2,6-Dichloropurine and 2,6-Dichlorodeazapurines with Ribose and Ribose Modified Sugars
1999 S., Vittori; Camaioni, Emidio; S., Costanzi; R., Volpini; G., Cristalli
2-Substituted N-ethylcarboxamidoadenosine derivatives as high-affinity agonists at human A3 adenosine receptors
1999 Klotz, K.; Camaioni, Emidio; Volpini, R.; Kachler, S.; Vittori, S.; Cristalli, G.
Synthesis of Di- And Tri-Substituted Adenosine Derivatives and Their Affinities at Human Adenosine Receptor Subtypes
1999 R., Volpini; Camaioni, Emidio; S., Costanzi; S., Vittori; K. N., Klotz; G., Cristalli
Structure-activity relationships of bisphophonate nucleotide derivatives as P2Y1 receptor antagonists and partial agonists
1999 Nandanan, E.; Camaioni, Emidio; Jang, S.; Kim, Y.; Cristalli, G.; Hederwijn, P.; Secrist, J.; Tiwari, K.; Mohanram, A.; Harden, T.; Boyer, J.; Jacobson, K.
Effects of new arylazido compounds of pyridoxal phosphate on ecto-ATPase activity of guinea pig tissues
2000 Ziganshin, A.; Zaitev, A.; Zaiteva, I.; Kim, Y.; Camaioni, Emidio; Burnstock, G.; Jacobson, K.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Preparation and use of nucleotide bisphosphate as P2Y antagonists | 1998 | Boyer, J. L.; Harden, T. K.; Jacobson, K. A.; Camaioni, Emidio | |
| Structure-activity relationships of P2 receptor agonists and antagonists | 1998 | K. A., Jacobson; Y. C., Kim; Camaioni, Emidio; A. M., van Rhee | |
| Modulation of apoptosis in human lymphocytes by adenosine analogues | 1998 | Barbieri, D; Franceschi, C; Camaioni, Emidio; Costanzi, S; Vittori, S; Volpini, R; Cristalli, G. | |
| Competitive and selective antagonism of P2Y(1) receptors by N-6-methyl 2 '-deoxyadenosine 3 ',5 '-bisphosphate | 1998 | Boyer, Jl; Mohanram, A; Camaioni, Emidio; Jacobson, Ka; Harden, Tk | |
| Deoxyadenosine bisphosphate derivatives as potent antagonists at P2Y(1) receptors | 1998 | Camaioni, Emidio; Boyer, Jl; Mohanram, A; Harden, Tk; Jacobson, Ka | |
| Human P2Y(1) receptor: Molecular modeling and site-directed mutagenesis as tools to identify agonist and antagonist recognition sites | 1998 | Moro, S; Guo, Dp; Camaioni, Emidio; Boyer, Jl; Harden, Tk | |
| Some 6-phenylazopyridoxalphosphate derivatives influence P2-purinoreceptor-mediated effects | 1998 | A. U., Ziganshin; A. V., Rychkov; L. E., Ziganshina; Kim, Y. u. C. h.; Camaioni, Emidio; G., Burnstock; K. A., Jacobson | |
| Synthesis of New 3′-Deoxyribonucleosides Employing the Acid-Catalyzed Fusion Method | 1998 | R., Volpini; Camaioni, Emidio; S., Costanzi; S., Vittori; G., Cristalli | |
| Synthesis of New Nucleosides by coupling of chloropurines with 2- and 3-deoxy derivatives of N-methyl-D-ribofuranuronamide | 1998 | R., Volpini; Camaioni, Emidio; S., Vittori; L., Barboni; C., Lambertucci; G., Cristalli | |
| New substituted 9-alkylpurines as adenosine receptor ligands | 1998 | Camaioni, Emidio; Costanzi, S; Vittori, S; Volpini, R; Klotz, Kn; Cristalli, G. | |
| Characterization of potent ligands at human recombinant adenosine receptors | 1998 | G., Cristalli; Camaioni, Emidio; S., Costanzi; S., Vittori; R., Volpini; K. N., Klotz | |
| Synthesis and structure-activity relationships of pyridoxal-6-arylazo-5′-phosphate and phosphonate derivatives as P2 receptor antagonists | 1998 | Y. C., Kim; Camaioni, Emidio; A. U., Ziganshin; X. D., Ji; B. F., King; S. S., Wildman; A., Rychkov; Yoburn, J. o.; H., Kim; A., Mohanram; T. K., Harden; J. L., Boyer; G., Burnstock; K. A., Jacobson | |
| Molecular recognition in P2 receptors: Ligand development aided by molecular modeling and mutagenesis | 1999 | Jacobson, K.; Hoffmann, C.; Kim, Y.; Camaioni, Emidio; Nandanan, E.; Jang, S.; Guo, D.; Ji, X.; Von Kugelgen, I.; Moro, S.; Ziganshin, A.; Rychkov, A.; King, B.; Brown, S.; Wildman, S.; Burnstock, G.; Boyer, J.; Mohanram, A.; Harden, T. | |
| Synthesis and Receptor Affinity of Polysubstituted Adenosines | 1999 | S., Vittori; Camaioni, Emidio; S., Costanzi; R., Volpini; K. N., Klotz; G., Cristalli | |
| Structure-Activity Relationships of Adenosine Deaminase Inhibitors | 1999 | S., Vittori; Camaioni, Emidio; S., Costanzi; R., Volpini; G., Lupidi; G., Cristalli | |
| Coupling of 2,6-Dichloropurine and 2,6-Dichlorodeazapurines with Ribose and Ribose Modified Sugars | 1999 | S., Vittori; Camaioni, Emidio; S., Costanzi; R., Volpini; G., Cristalli | |
| 2-Substituted N-ethylcarboxamidoadenosine derivatives as high-affinity agonists at human A3 adenosine receptors | 1999 | Klotz, K.; Camaioni, Emidio; Volpini, R.; Kachler, S.; Vittori, S.; Cristalli, G. | |
| Synthesis of Di- And Tri-Substituted Adenosine Derivatives and Their Affinities at Human Adenosine Receptor Subtypes | 1999 | R., Volpini; Camaioni, Emidio; S., Costanzi; S., Vittori; K. N., Klotz; G., Cristalli | |
| Structure-activity relationships of bisphophonate nucleotide derivatives as P2Y1 receptor antagonists and partial agonists | 1999 | Nandanan, E.; Camaioni, Emidio; Jang, S.; Kim, Y.; Cristalli, G.; Hederwijn, P.; Secrist, J.; Tiwari, K.; Mohanram, A.; Harden, T.; Boyer, J.; Jacobson, K. | |
| Effects of new arylazido compounds of pyridoxal phosphate on ecto-ATPase activity of guinea pig tissues | 2000 | Ziganshin, A.; Zaitev, A.; Zaiteva, I.; Kim, Y.; Camaioni, Emidio; Burnstock, G.; Jacobson, K. |
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