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Pd(0) nanocatalyst stabilized on a novel agar/pectin composite and its catalytic activity in the synthesis of biphenyl compounds by Suzuki-Miyaura cross coupling reaction and reduction of o-nitroaniline.

Carbohydrate polymers

Baran T.
PMID: 29804998
Carbohydr Polym. 2018 Sep 01;195:45-52. doi: 10.1016/j.carbpol.2018.04.064. Epub 2018 Apr 21.

The most important parameters for the fabrication of metallic nanoparticles are their synthesis method and the selection of stabilizer. These properties influence durability, shape, size, distribution, and catalytic performance of metallic nanoparticles. Therefore, a novel agar/pectin composite (APC) was...

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Baran T. Pd(0) nanocatalyst stabilized on a novel agar/pectin composite and its catalytic activity in the synthesis of biphenyl compounds by Suzuki-Miyaura cross coupling reaction and reduction of o-nitroaniline. Carbohydr Polym. 2018;195:45-52doi: 10.1016/j.carbpol.2018.04.064.
Baran, T. (2018). Pd(0) nanocatalyst stabilized on a novel agar/pectin composite and its catalytic activity in the synthesis of biphenyl compounds by Suzuki-Miyaura cross coupling reaction and reduction of o-nitroaniline. Carbohydrate polymers, 19545-52. https://doi.org/10.1016/j.carbpol.2018.04.064
Baran, Talat. "Pd(0) nanocatalyst stabilized on a novel agar/pectin composite and its catalytic activity in the synthesis of biphenyl compounds by Suzuki-Miyaura cross coupling reaction and reduction of o-nitroaniline." Carbohydrate polymers vol. 195 (2018): 45-52. doi: https://doi.org/10.1016/j.carbpol.2018.04.064
Baran T. Pd(0) nanocatalyst stabilized on a novel agar/pectin composite and its catalytic activity in the synthesis of biphenyl compounds by Suzuki-Miyaura cross coupling reaction and reduction of o-nitroaniline. Carbohydr Polym. 2018 Sep 01;195:45-52. doi: 10.1016/j.carbpol.2018.04.064. Epub 2018 Apr 21. PMID: 29804998.
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Reductive Coupling of Diynes at Rhodium Gives Fluorescent Rhodacyclopentadienes or Phosphorescent Rhodium 2,2'-Biphenyl Complexes.

Chemistry (Weinheim an der Bergstrasse, Germany)

Sieck C, Tay MG, Thibault MH, Edkins RM, Costuas K, Halet JF, Batsanov AS, Haehnel M, Edkins K, Lorbach A, Steffen A, Marder TB.
PMID: 27355689
Chemistry. 2016 Jul 18;22(30):10523-32. doi: 10.1002/chem.201601912. Epub 2016 Jun 29.

Reactions of [Rh(κ(2) -O,O-acac)(PMe3 )2 ] (acac=acetylacetonato) and α,ω-bis(arylbutadiynyl)alkanes afford two isomeric types of MC4 metallacycles with very different photophysical properties. As a result of a [2+2] reductive coupling at Rh, 2,5-bis(arylethynyl)rhodacyclopentadienes (A) are formed, which display intense fluorescence...

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Sieck C, Tay MG, Thibault MH, et al. Reductive Coupling of Diynes at Rhodium Gives Fluorescent Rhodacyclopentadienes or Phosphorescent Rhodium 2,2'-Biphenyl Complexes. Chemistry. 2016;22(30):10523-32doi: 10.1002/chem.201601912.
Sieck, C., Tay, M. G., Thibault, M. H., Edkins, R. M., Costuas, K., Halet, J. F., Batsanov, A. S., Haehnel, M., Edkins, K., Lorbach, A., Steffen, A., & Marder, T. B. (2016). Reductive Coupling of Diynes at Rhodium Gives Fluorescent Rhodacyclopentadienes or Phosphorescent Rhodium 2,2'-Biphenyl Complexes. Chemistry (Weinheim an der Bergstrasse, Germany), 22(30), 10523-32. https://doi.org/10.1002/chem.201601912
Sieck, Carolin, et al. "Reductive Coupling of Diynes at Rhodium Gives Fluorescent Rhodacyclopentadienes or Phosphorescent Rhodium 2,2'-Biphenyl Complexes." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,30 (2016): 10523-32. doi: https://doi.org/10.1002/chem.201601912
Sieck C, Tay MG, Thibault MH, Edkins RM, Costuas K, Halet JF, Batsanov AS, Haehnel M, Edkins K, Lorbach A, Steffen A, Marder TB. Reductive Coupling of Diynes at Rhodium Gives Fluorescent Rhodacyclopentadienes or Phosphorescent Rhodium 2,2'-Biphenyl Complexes. Chemistry. 2016 Jul 18;22(30):10523-32. doi: 10.1002/chem.201601912. Epub 2016 Jun 29. PMID: 27355689.
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Controlling axial conformation in 2-arylpyridines and 1-arylisoquinolines: application to the asymmetric synthesis of QUINAP by dynamic thermodynamic resolution.

Journal of the American Chemical Society

Clayden J, Fletcher SP, McDouall JJ, Rowbottom SJ.
PMID: 19309078
J Am Chem Soc. 2009 Apr 15;131(14):5331-43. doi: 10.1021/ja900722q.

Unlike related biphenyl compounds, 2-arylpyridines and 1-arylisoquinolines can be induced to adopt preferentially one of two axial conformations by the presence of a sulfinyl substituent adjacent to the Ar-Ar bond. In the case of more substituted biaryls, the compounds...

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Clayden J, Fletcher SP, McDouall JJ, et al. Controlling axial conformation in 2-arylpyridines and 1-arylisoquinolines: application to the asymmetric synthesis of QUINAP by dynamic thermodynamic resolution. J Am Chem Soc. 2009;131(14):5331-43doi: 10.1021/ja900722q.
Clayden, J., Fletcher, S. P., McDouall, J. J., & Rowbottom, S. J. (2009). Controlling axial conformation in 2-arylpyridines and 1-arylisoquinolines: application to the asymmetric synthesis of QUINAP by dynamic thermodynamic resolution. Journal of the American Chemical Society, 131(14), 5331-43. https://doi.org/10.1021/ja900722q
Clayden, Jonathan, et al. "Controlling axial conformation in 2-arylpyridines and 1-arylisoquinolines: application to the asymmetric synthesis of QUINAP by dynamic thermodynamic resolution." Journal of the American Chemical Society vol. 131,14 (2009): 5331-43. doi: https://doi.org/10.1021/ja900722q
Clayden J, Fletcher SP, McDouall JJ, Rowbottom SJ. Controlling axial conformation in 2-arylpyridines and 1-arylisoquinolines: application to the asymmetric synthesis of QUINAP by dynamic thermodynamic resolution. J Am Chem Soc. 2009 Apr 15;131(14):5331-43. doi: 10.1021/ja900722q. PMID: 19309078.
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Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions.

Accounts of chemical research

Marion N, Nolan SP.
PMID: 18774825
Acc Chem Res. 2008 Nov 18;41(11):1440-9. doi: 10.1021/ar800020y.

Metal-catalyzed cross-coupling reactions, notably those permitting C-C bond formation, have witnessed a meteoritic development and are now routinely employed as a powerful synthetic tool both in academia and in industry. In this context, palladium is arguably the most studied...

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Marion N, Nolan SP. Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions. Acc Chem Res. 2008;41(11):1440-9doi: 10.1021/ar800020y.
Marion, N., & Nolan, S. P. (2008). Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions. Accounts of chemical research, 41(11), 1440-9. https://doi.org/10.1021/ar800020y
Marion, Nicolas, and Nolan, Steven P. "Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions." Accounts of chemical research vol. 41,11 (2008): 1440-9. doi: https://doi.org/10.1021/ar800020y
Marion N, Nolan SP. Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions. Acc Chem Res. 2008 Nov 18;41(11):1440-9. doi: 10.1021/ar800020y. PMID: 18774825.
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Structural characterization, gelation ability, and energy-framework analysis of two bis(long-chain ester)-substituted 4,4'-biphenyl compounds.

Acta crystallographica. Section C, Structural chemistry

Geiger DK, Geiger HC, Moore SM, Roberts WR.
PMID: 28978785
Acta Crystallogr C Struct Chem. 2017 Oct 01;73:791-796. doi: 10.1107/S2053229617013237. Epub 2017 Sep 25.

There are few examples of single-crystal structure determinations of gelators, as gel formation requires that the dissolved gelator self-assemble into a three-dimensional network structure incorporating solvent via noncovalent interactions rather than self-assembly followed by crystallization. In the solid-state structures...

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Geiger DK, Geiger HC, Moore SM, et al. Structural characterization, gelation ability, and energy-framework analysis of two bis(long-chain ester)-substituted 4,4'-biphenyl compounds. Acta Crystallogr C Struct Chem. 2017;73:791-796doi: 10.1107/S2053229617013237.
Geiger, D. K., Geiger, H. C., Moore, S. M., & Roberts, W. R. (2017). Structural characterization, gelation ability, and energy-framework analysis of two bis(long-chain ester)-substituted 4,4'-biphenyl compounds. Acta crystallographica. Section C, Structural chemistry, 73791-796. https://doi.org/10.1107/S2053229617013237
Geiger, David K, et al. "Structural characterization, gelation ability, and energy-framework analysis of two bis(long-chain ester)-substituted 4,4'-biphenyl compounds." Acta crystallographica. Section C, Structural chemistry vol. 73 (2017): 791-796. doi: https://doi.org/10.1107/S2053229617013237
Geiger DK, Geiger HC, Moore SM, Roberts WR. Structural characterization, gelation ability, and energy-framework analysis of two bis(long-chain ester)-substituted 4,4'-biphenyl compounds. Acta Crystallogr C Struct Chem. 2017 Oct 01;73:791-796. doi: 10.1107/S2053229617013237. Epub 2017 Sep 25. PMID: 28978785.
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Charge distribution in arylhydrazine-centered mixed valence compounds with smaller bridges (five to nine bonds between closest nitrogens).

The journal of physical chemistry. A

Nelsen SF, Schultz KP.
PMID: 19354243
J Phys Chem A. 2009 May 07;113(18):5324-32. doi: 10.1021/jp810645q.

Charge distribution in six aromatic-bridged, aryldialkylhydrazine-centered mixed valence radical cations is discussed through consideration of their optical spectra. The compounds considered have two 2-phenyl-2,3-diazabicyclo-[2.2.2]octane-3-yl (HyPh) charge-bearing units linked by a 1,4-phenylene bridge and its p-methoxyphenyl (HyAn) analogue, as well...

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Nelsen SF, Schultz KP. Charge distribution in arylhydrazine-centered mixed valence compounds with smaller bridges (five to nine bonds between closest nitrogens). J Phys Chem A. 2009;113(18):5324-32doi: 10.1021/jp810645q.
Nelsen, S. F., & Schultz, K. P. (2009). Charge distribution in arylhydrazine-centered mixed valence compounds with smaller bridges (five to nine bonds between closest nitrogens). The journal of physical chemistry. A, 113(18), 5324-32. https://doi.org/10.1021/jp810645q
Nelsen, Stephen F, and Schultz, Kevin P. "Charge distribution in arylhydrazine-centered mixed valence compounds with smaller bridges (five to nine bonds between closest nitrogens)." The journal of physical chemistry. A vol. 113,18 (2009): 5324-32. doi: https://doi.org/10.1021/jp810645q
Nelsen SF, Schultz KP. Charge distribution in arylhydrazine-centered mixed valence compounds with smaller bridges (five to nine bonds between closest nitrogens). J Phys Chem A. 2009 May 07;113(18):5324-32. doi: 10.1021/jp810645q. PMID: 19354243.
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Intrauterine exposure to 2,3',4,4',5-pentachlorobiphenyl alters spermatogenesis and testicular DNA methylation levels in F1 male mice.

Ecotoxicology and environmental safety

Tao YR, Zhang YT, Han XY, Zhang L, Jiang LG, Ma Y, Meng LJ, He QL, Liu SZ.
PMID: 34461319
Ecotoxicol Environ Saf. 2021 Aug 27;224:112652. doi: 10.1016/j.ecoenv.2021.112652. Epub 2021 Aug 27.

Polychlorinated biphenyls (PCBs) are synthetic biphenyl compounds with high toxicity. There are a total of 209 homologs, among which 2,3',4,4',5-pentachlorobiphenyl (PCB118) is one of the dioxin-like PCBs. PCB118 can accumulate in pregnant mice, leading to fetus directly exposure during...

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Tao YR, Zhang YT, Han XY, et al. Intrauterine exposure to 2,3',4,4',5-pentachlorobiphenyl alters spermatogenesis and testicular DNA methylation levels in F1 male mice. Ecotoxicol Environ Saf. 2021;224:112652doi: 10.1016/j.ecoenv.2021.112652.
Tao, Y. R., Zhang, Y. T., Han, X. Y., Zhang, L., Jiang, L. G., Ma, Y., Meng, L. J., He, Q. L., & Liu, S. Z. (2021). Intrauterine exposure to 2,3',4,4',5-pentachlorobiphenyl alters spermatogenesis and testicular DNA methylation levels in F1 male mice. Ecotoxicology and environmental safety, 224112652. https://doi.org/10.1016/j.ecoenv.2021.112652
Tao, Yu-Rong, et al. "Intrauterine exposure to 2,3',4,4',5-pentachlorobiphenyl alters spermatogenesis and testicular DNA methylation levels in F1 male mice." Ecotoxicology and environmental safety vol. 224 (2021): 112652. doi: https://doi.org/10.1016/j.ecoenv.2021.112652
Tao YR, Zhang YT, Han XY, Zhang L, Jiang LG, Ma Y, Meng LJ, He QL, Liu SZ. Intrauterine exposure to 2,3',4,4',5-pentachlorobiphenyl alters spermatogenesis and testicular DNA methylation levels in F1 male mice. Ecotoxicol Environ Saf. 2021 Aug 27;224:112652. doi: 10.1016/j.ecoenv.2021.112652. Epub 2021 Aug 27. PMID: 34461319.
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CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

Gado F, Ceni C, Ferrisi R, Sbrana G, Stevenson LA, Macchia M, Pertwee RG, Bertini S, Manera C, Ortore G.
PMID: 34863873
Eur J Pharm Sci. 2021 Dec 01;169:106088. doi: 10.1016/j.ejps.2021.106088. Epub 2021 Dec 01.

The development of cannabinoid receptor type-1 (CB1R) modulators has been implicated in multiple pathophysiological events ranging from memory deficits to neurodegenerative disorders among others, even if their central psychiatric side effects such as depression, anxiety, and suicidal tendencies, have...

Cite
Gado F, Ceni C, Ferrisi R, et al. CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. Eur J Pharm Sci. 2021;169:106088doi: 10.1016/j.ejps.2021.106088.
Gado, F., Ceni, C., Ferrisi, R., Sbrana, G., Stevenson, L. A., Macchia, M., Pertwee, R. G., Bertini, S., Manera, C., & Ortore, G. (2021). CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 169106088. https://doi.org/10.1016/j.ejps.2021.106088
Gado, Francesca, et al. "CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators." European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences vol. 169 (2021): 106088. doi: https://doi.org/10.1016/j.ejps.2021.106088
Gado F, Ceni C, Ferrisi R, Sbrana G, Stevenson LA, Macchia M, Pertwee RG, Bertini S, Manera C, Ortore G. CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. Eur J Pharm Sci. 2021 Dec 01;169:106088. doi: 10.1016/j.ejps.2021.106088. Epub 2021 Dec 01. PMID: 34863873.
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CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

Gado F, Ceni C, Ferrisi R, Sbrana G, Stevenson LA, Macchia M, Pertwee RG, Bertini S, Manera C, Ortore G.
PMID: 34863873
Eur J Pharm Sci. 2021 Dec 01;169:106088. doi: 10.1016/j.ejps.2021.106088. Epub 2021 Dec 01.

The development of cannabinoid receptor type-1 (CB1R) modulators has been implicated in multiple pathophysiological events ranging from memory deficits to neurodegenerative disorders among others, even if their central psychiatric side effects such as depression, anxiety, and suicidal tendencies, have...

Cite
Gado F, Ceni C, Ferrisi R, et al. CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. Eur J Pharm Sci. 2021;169:106088doi: 10.1016/j.ejps.2021.106088.
Gado, F., Ceni, C., Ferrisi, R., Sbrana, G., Stevenson, L. A., Macchia, M., Pertwee, R. G., Bertini, S., Manera, C., & Ortore, G. (2021). CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 169106088. https://doi.org/10.1016/j.ejps.2021.106088
Gado, Francesca, et al. "CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators." European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences vol. 169 (2021): 106088. doi: https://doi.org/10.1016/j.ejps.2021.106088
Gado F, Ceni C, Ferrisi R, Sbrana G, Stevenson LA, Macchia M, Pertwee RG, Bertini S, Manera C, Ortore G. CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. Eur J Pharm Sci. 2021 Dec 01;169:106088. doi: 10.1016/j.ejps.2021.106088. Epub 2021 Dec 01. PMID: 34863873.
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Ultrasound-accelerated synthesis of biphenyl compounds using novel Pd(0) nanoparticles immobilized on bio-composite.

Ultrasonics sonochemistry

Baran T.
PMID: 29705317
Ultrason Sonochem. 2018 Jul;45:231-237. doi: 10.1016/j.ultsonch.2018.03.017. Epub 2018 Mar 31.

This study describes (i) an eco-friendly approach for design of Pd(0) nanoparticles on a natural composite, which is composed of carboxymethyl cellulose/agar polysaccharides (CMC/AG), without using any toxic reducing agents and (ii) development of ultrasound assisted simple protocol for...

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Baran T. Ultrasound-accelerated synthesis of biphenyl compounds using novel Pd(0) nanoparticles immobilized on bio-composite. Ultrason Sonochem. 2018;45:231-237doi: 10.1016/j.ultsonch.2018.03.017.
Baran, T. (2018). Ultrasound-accelerated synthesis of biphenyl compounds using novel Pd(0) nanoparticles immobilized on bio-composite. Ultrasonics sonochemistry, 45231-237. https://doi.org/10.1016/j.ultsonch.2018.03.017
Baran, Talat. "Ultrasound-accelerated synthesis of biphenyl compounds using novel Pd(0) nanoparticles immobilized on bio-composite." Ultrasonics sonochemistry vol. 45 (2018): 231-237. doi: https://doi.org/10.1016/j.ultsonch.2018.03.017
Baran T. Ultrasound-accelerated synthesis of biphenyl compounds using novel Pd(0) nanoparticles immobilized on bio-composite. Ultrason Sonochem. 2018 Jul;45:231-237. doi: 10.1016/j.ultsonch.2018.03.017. Epub 2018 Mar 31. PMID: 29705317.
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CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

Gado F, Ceni C, Ferrisi R, Sbrana G, Stevenson LA, Macchia M, Pertwee RG, Bertini S, Manera C, Ortore G.
PMID: 34863873
Eur J Pharm Sci. 2021 Dec 01;169:106088. doi: 10.1016/j.ejps.2021.106088. Epub 2021 Dec 01.

The development of cannabinoid receptor type-1 (CB1R) modulators has been implicated in multiple pathophysiological events ranging from memory deficits to neurodegenerative disorders among others, even if their central psychiatric side effects such as depression, anxiety, and suicidal tendencies, have...

Cite
Gado F, Ceni C, Ferrisi R, et al. CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. Eur J Pharm Sci. 2021;169:106088doi: 10.1016/j.ejps.2021.106088.
Gado, F., Ceni, C., Ferrisi, R., Sbrana, G., Stevenson, L. A., Macchia, M., Pertwee, R. G., Bertini, S., Manera, C., & Ortore, G. (2021). CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 169106088. https://doi.org/10.1016/j.ejps.2021.106088
Gado, Francesca, et al. "CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators." European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences vol. 169 (2021): 106088. doi: https://doi.org/10.1016/j.ejps.2021.106088
Gado F, Ceni C, Ferrisi R, Sbrana G, Stevenson LA, Macchia M, Pertwee RG, Bertini S, Manera C, Ortore G. CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. Eur J Pharm Sci. 2021 Dec 01;169:106088. doi: 10.1016/j.ejps.2021.106088. Epub 2021 Dec 01. PMID: 34863873.
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CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

Gado F, Ceni C, Ferrisi R, Sbrana G, Stevenson LA, Macchia M, Pertwee RG, Bertini S, Manera C, Ortore G.
PMID: 34863873
Eur J Pharm Sci. 2021 Dec 01;169:106088. doi: 10.1016/j.ejps.2021.106088. Epub 2021 Dec 01.

The development of cannabinoid receptor type-1 (CB1R) modulators has been implicated in multiple pathophysiological events ranging from memory deficits to neurodegenerative disorders among others, even if their central psychiatric side effects such as depression, anxiety, and suicidal tendencies, have...

Cite
Gado F, Ceni C, Ferrisi R, et al. CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. Eur J Pharm Sci. 2021;169:106088doi: 10.1016/j.ejps.2021.106088.
Gado, F., Ceni, C., Ferrisi, R., Sbrana, G., Stevenson, L. A., Macchia, M., Pertwee, R. G., Bertini, S., Manera, C., & Ortore, G. (2021). CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 169106088. https://doi.org/10.1016/j.ejps.2021.106088
Gado, Francesca, et al. "CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators." European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences vol. 169 (2021): 106088. doi: https://doi.org/10.1016/j.ejps.2021.106088
Gado F, Ceni C, Ferrisi R, Sbrana G, Stevenson LA, Macchia M, Pertwee RG, Bertini S, Manera C, Ortore G. CB1 receptor binding sites for NAM and PAM: A first approach for studying, new n‑butyl‑diphenylcarboxamides as allosteric modulators. Eur J Pharm Sci. 2021 Dec 01;169:106088. doi: 10.1016/j.ejps.2021.106088. Epub 2021 Dec 01. PMID: 34863873.
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