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1
Simplified immunosuppressive and neuroprotective agents based on gracilin A
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Simplified immunosuppressive and neuroprotective agents based on gracilin A

Abbasov, Mikail E ; Alvariño, Rebeca ; Chaheine, Christian M ; Alonso, Eva ; Sánchez, Jon A ; Conner, Michael L ; Alfonso, Amparo ; Jaspars, Marcel ; Botana, Luis M ; Romo, Daniel

Nature chemistry, 2019-04, Vol.11 (4), p.342-350 [Periódico revisado por pares]

England: Nature Publishing Group

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Treatment of multiple sclerosis - success from bench to bedside
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Treatment of multiple sclerosis - success from bench to bedside

Tintore, Mar ; Vidal-Jordana, Angela ; Sastre-Garriga, Jaume

Nature reviews. Neurology, 2019-01, Vol.15 (1), p.53-58 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Are GPCRs Still a Source of New Targets?
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Are GPCRs Still a Source of New Targets?

Garland, Stephen L.

Journal of biomolecular screening, 2013-10, Vol.18 (9), p.947-966 [Periódico revisado por pares]

Los Angeles, CA: SAGE Publications

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4
An Immunomodulatory Peptide Dendrimer Inspired from Glatiramer Acetate
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An Immunomodulatory Peptide Dendrimer Inspired from Glatiramer Acetate

Erzina, Dina ; Capecchi, Alice ; Javor, Sacha ; Reymond, Jean‐Louis

Angewandte Chemie (International ed.), 2021-12, Vol.60 (50), p.26403-26408 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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5
Total synthesis of periploside A, a unique pregnane hexasaccharide with potent immunosuppressive effects
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Total synthesis of periploside A, a unique pregnane hexasaccharide with potent immunosuppressive effects

Zhang, Xiaheng ; Zhou, Yu ; Zuo, Jianping ; Yu, Biao

Nature communications, 2015-01, Vol.6 (1), p.5879-5879, Article 5879 [Periódico revisado por pares]

England: Nature Publishing Group

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6
Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C–H Functionalization
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Scopariusicides, Novel Unsymmetrical Cyclobutanes: Structural Elucidation and Concise Synthesis by a Combination of Intermolecular [2 + 2] Cycloaddition and C–H Functionalization

Zhou, Min ; Li, Xing-Ren ; Tang, Jian-Wei ; Liu, Yang ; Li, Xiao-Nian ; Wu, Bin ; Qin, Hong-Bo ; Du, Xue ; Li, Li-Mei ; Wang, Wei-Guang ; Pu, Jian-Xin ; Sun, Han-Dong

Organic letters, 2015-12, Vol.17 (24), p.6062-6065 [Periódico revisado por pares]

United States: American Chemical Society

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7
Fingolimod (FTY720): A Recently Approved Multiple Sclerosis Drug Based on a Fungal Secondary Metabolite
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Fingolimod (FTY720): A Recently Approved Multiple Sclerosis Drug Based on a Fungal Secondary Metabolite

Strader, Cherilyn R ; Pearce, Cedric J ; Oberlies, Nicholas H

Journal of natural products (Washington, D.C.), 2011-04, Vol.74 (4), p.900-907 [Periódico revisado por pares]

Northbrook, IL: American Chemical Society and American Society of Pharmacognosy

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8
Synthesis of novel 2-(1-adamantanylcarboxamido)thiophene derivatives. Selective cannabinoid type 2 (CB2) receptor agonists as potential agents for the treatment of skin inflammatory disease
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Synthesis of novel 2-(1-adamantanylcarboxamido)thiophene derivatives. Selective cannabinoid type 2 (CB2) receptor agonists as potential agents for the treatment of skin inflammatory disease

Mugnaini, Claudia ; Rabbito, Alessandro ; Brizzi, Antonella ; Palombi, Nastasja ; Petrosino, Stefania ; Verde, Roberta ; Di Marzo, Vincenzo ; Ligresti, Alessia ; Corelli, Federico

European journal of medicinal chemistry, 2019-01, Vol.161, p.239-251 [Periódico revisado por pares]

France: Elsevier Masson SAS

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9
Pharmacological Effects of FTY720 and its Derivatives
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Pharmacological Effects of FTY720 and its Derivatives

Han, Mengyuan ; Liu, Xiangran ; Hailati, Sendaer ; Maihemuti, Nulibiya ; Nurahmat, Nurbiya ; Dilimulati, Dilihuma ; Baishan, Alhar ; Aikebaier, Alifeiye ; Zhou, Wenting ; Pan, Yan

Current topics in medicinal chemistry, 2024, Vol.24 (3), p.192-200 [Periódico revisado por pares]

United Arab Emirates: Benham Science Publishers

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10
Discovery, Total Synthesis and Key Structural Elements for the Immunosuppressive Activity of Cocosolide, a Symmetrical Glycosylated Macrolide Dimer from Marine Cyanobacteria
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Discovery, Total Synthesis and Key Structural Elements for the Immunosuppressive Activity of Cocosolide, a Symmetrical Glycosylated Macrolide Dimer from Marine Cyanobacteria

Gunasekera, Sarath P. ; Li, Yang ; Ratnayake, Ranjala ; Luo, Danmeng ; Lo, Jeannette ; Reibenspies, Joseph H. ; Xu, Zhengshuang ; Clare-Salzler, Michael J. ; Ye, Tao ; Paul, Valerie J. ; Luesch, Hendrik

Chemistry : a European journal, 2016-06, Vol.22 (24), p.8158-8166 [Periódico revisado por pares]

Germany: Blackwell Publishing Ltd

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