Synthesis and activity of endomorphin-2 and morphiceptin analogues with proline surrogates in position 2.

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The design of multitarget ligands for chronic and neuropathic pain.The cis-4-amino-L-proline residue as a scaffold for the synthesis of cyclic and linear endomorphin-2 analogues.Conformational behaviour of peptides containing a 2-pyrrolidinemethanesulfonic acid (2PyMS) residue.

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P2860

Synthesis and activity of endomorphin-2 and morphiceptin analogues with proline surrogates in position 2.

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2010 nî lūn-bûn

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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2010年论文

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2010年论文

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Synthesis and activity of endo ...... line surrogates in position 2.

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Synthesis and activity of endo ...... line surrogates in position 2.

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Synthesis and activity of endo ...... line surrogates in position 2.

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Synthesis and activity of endo ...... line surrogates in position 2.

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Synthesis and activity of endo ...... line surrogates in position 2.

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Synthesis and activity of endo ...... line surrogates in position 2.

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P1476

Synthesis and activity of endo ...... line surrogates in position 2.

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P2093

Adriano Mollica

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Anna Sansone

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Annalisa Masi

http://www.w3.org/2001/XMLSchema#string

Cesare Giordano

http://www.w3.org/2001/XMLSchema#string

Federica Feliciani

http://www.w3.org/2001/XMLSchema#string

Francesco Pinnen

http://www.w3.org/2001/XMLSchema#string

Frank Porreca

http://www.w3.org/2001/XMLSchema#string

Gino Lucente

http://www.w3.org/2001/XMLSchema#string

Ivana Cacciatore

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Josephine Lai

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P2860

Synthesis of cyclic peptidosulfonamides as scaffolds for MC4 pharmacophoric groups.

A potent and selective endogenous agonist for the mu-opiate receptor.

Novel D-amino acid tetrapeptides produce potent antinociception by selectively acting at peripheral kappa-opioid receptors.

Recent advances in design, synthesis and biological activity of aminoalkylsulfonates and sulfonamidopeptides.

Molecular diversity of peptidomimetics: approaches to the solid-phase synthesis of peptidosulfonamides.

Structural investigation of endomorphins by experimental and theoretical methods: hunting for the bioactive conformation.

Synthesis and evaluation of new endomorphin analogues modified at the Pro(2) residue.

ACTH: a short introductory review.

Morphiceptin (NH4-tyr-pro-phe-pro-COHN2): a potent and specific agonist for morphine (mu) receptors.

Biological activity of endomorphin and [Dmt1]endomorphin analogs with six-membered proline surrogates in position 2.

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4594-4600

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scholarly article

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10.1016/J.EJMECH.2010.07.022

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2010-07-21T00:00:00Z

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45537356

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20692738

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5689459

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Synthesis and activity of endomorphin-2 and morphiceptin analogues with proline surrogates in position 2.

about

P2860

P2860

Synthesis and activity of endomorphin-2 and morphiceptin analogues with proline surrogates in position 2.

description

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932