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The Cyclic Imine Core Common to the Marine Macrocyclic Toxins Is Sufficient to Dictate Nicotinic Acetylcholine Receptor Antagonism

• Authors : Bourne, Yves; Sulzenbacher, Gerlind; Chabaud, Laurent ...

Subjects: acetylcholine-binding protein; binding affinity; competitive antagonism

• Source: ISSN: 1660-3397 ; Marine drugs ; https://hal.science/hal-04542228 ; Marine drugs, 2024, Marine Biotoxins 2.0, 22 (4), pp.149. ⟨10.3390/md22040149⟩ ; MDPI.

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The Cyclic Imine Core Common to the Marine Macrocyclic Toxins Is Sufficient to Dictate Nicotinic Acetylcholine Receptor Antagonism

• Authors : Bourne, Yves; Sulzenbacher, Gerlind; Chabaud, Laurent ...

Subjects: acetylcholine-binding protein; binding affinity; competitive antagonism

• Source: ISSN: 1660-3397 ; Marine drugs ; https://hal.science/hal-04542228 ; Marine drugs, 2024, Marine Biotoxins 2.0, 22 (4), pp.149. ⟨10.3390/md22040149⟩ ; MDPI.

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Novel tetragonal boron pnictides BX (X = N, P, As, Sb, Bi) with square B2X2 motifs from crystal chemistry and first principles

• Authors : Matar, Samir; Solozhenko, Vladimir;

Subjects: boron pnictides; DFT; crystal structure

• Source: ISSN: 2073-4352 ; Crystals ; https://hal.science/hal-04543511 ; Crystals, 2024, 14 (4), pp.359. ⟨10.3390/cryst14040359⟩.

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The Cyclic Imine Core Common to the Marine Macrocyclic Toxins Is Sufficient to Dictate Nicotinic Acetylcholine Receptor Antagonism

• Authors : Bourne, Yves; Sulzenbacher, Gerlind; Chabaud, Laurent ...

Subjects: acetylcholine-binding protein; binding affinity; competitive antagonism

• Source: ISSN: 1660-3397 ; Marine drugs ; https://hal.science/hal-04542228 ; Marine drugs, 2024, Marine Biotoxins 2.0, 22 (4), pp.149. ⟨10.3390/md22040149⟩ ; MDPI.

Record details

The Cyclic Imine Core Common to the Marine Macrocyclic Toxins Is Sufficient to Dictate Nicotinic Acetylcholine Receptor Antagonism

• Authors : Bourne, Yves; Sulzenbacher, Gerlind; Chabaud, Laurent ...

Subjects: acetylcholine-binding protein; binding affinity; competitive antagonism

• Source: ISSN: 1660-3397 ; Marine drugs ; https://hal.science/hal-04542228 ; Marine drugs, 2024, Marine Biotoxins 2.0, 22 (4), pp.149. ⟨10.3390/md22040149⟩ ; MDPI.

Record details

The Cyclic Imine Core Common to the Marine Macrocyclic Toxins Is Sufficient to Dictate Nicotinic Acetylcholine Receptor Antagonism

• Authors : Bourne, Yves; Sulzenbacher, Gerlind; Chabaud, Laurent ...

Subjects: acetylcholine-binding protein; binding affinity; competitive antagonism

• Source: ISSN: 1660-3397 ; Marine drugs ; https://hal.science/hal-04542228 ; Marine drugs, 2024, Marine Biotoxins 2.0, 22 (4), pp.149. ⟨10.3390/md22040149⟩ ; MDPI.

Record details

Structural and Functional Characterization of Drosophila melanogaster α-Amylase

• Authors : Rhimi, Moez; da Lage, Jean-Luc; Haser, Richard ...

Subjects: α-amylase glycoside hydrolase family 13 (GH13) crystal structure acarbose inhibitors Drosophila melanogaster adaptation calcium binding flexible loop evolution; α-amylase; glycoside hydrolase family 13 (GH13)

• Source: ISSN: 1420-3049 ; Molecules ; https://hal.science/hal-04160596 ; Molecules, 2023, 28 (14), pp.5327. ⟨10.3390/molecules28145327⟩.

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The effect of vanadium on modified Z-phase characteristics in austenitic steels

• Authors : Vodárek, Vlastimil; Holešinský, Jan; Kuboň, Zdeněk

Subjects: AISI 316LN+Nb+V; Super 304H; modified Z-phase

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Structural Study of a New MbtI-Inhibitor Complex: Towards an Optimized Model for Structure-Based Drug Discovery

• Authors : Mori, Matteo; Villa, Stefania; Chiarelli, Laurent ...

Subjects: Mycobacterium tuberculosis; salicylate synthase; siderophore

• Source: ISSN: 1424-8247 ; Pharmaceuticals ; https://pasteur.hal.science/pasteur-04366722 ; Pharmaceuticals, 2023, 16 (11), pp.1559. ⟨10.3390/ph16111559⟩.

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Structural Study of a New MbtI-Inhibitor Complex: Towards an Optimized Model for Structure-Based Drug Discovery

• Authors : Mori, Matteo; Villa, Stefania; Chiarelli, Laurent ...

Subjects: Mycobacterium tuberculosis; salicylate synthase; siderophore

• Source: ISSN: 1424-8247 ; Pharmaceuticals ; https://pasteur.hal.science/pasteur-04366722 ; Pharmaceuticals, 2023, 16 (11), pp.1559. ⟨10.3390/ph16111559⟩.

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