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北京石油化工学院2026年研究生招生接收调剂公告
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yaoguiyang

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An essential feature of Cyp inhibitors designed to be used as
antiviral agents is that the immunosuppressive activity due to CN
inhibition is reduced or removed. This has been most effectively
achieved by modification of the side chain of the [MeLeu]4 residue,
which is involved in a tight ‘aromatic sandwich’ with CN residues
Trp352 and Phe356 (Fig. 4). Surprisingly, moving one methyl group
at the [MeLeu]4 residue to give [MeIle]4CsA (NIM-811), was found
to remove immunosuppressive activity, while retaining the same affinity for CypA as CsA itself.58 This ability to reduce
immunosuppressive activity by making small chemical changes
at [MeLeu]4 was further demonstrated by [MeVal]4CsA59 and
[40-HOMeLeu]4CsA55a,59,60 which show >2500-fold and >100-fold
loss of immunosuppressive activity, respectively.
The [BMT]1 residue characteristic of the cyclosporins is unique
in that in the cyclophilin-bound conformation, this group
extends from the cyclophilin binding interface to a region very
near the calcineurin-binding region (Figure 2). Early work had
suggested that P1-modified cyclosporins can retain cyclophilin
binding affinity without maintaining the immunosuppressive
activity of 1.73,117 In particular, the Merck group highlighted the
cyclophilin binding activity of [CH(OH)CH(CH3)-
CH2SCH3]1-CsA, which has 178% of the cyclophilin binding
activity of 1 but only 10% of the immunosuppressive potency.74
Aurinia has reported that extension of the BMT group of the
cyclosporins and addition of a D-Ala group in the P3 position
provides a series of nonimmunosuppressive cyclophilin
analogue molecules such as 14 (Figure 9).118 This molecule
has more than 14-fold greater inhibition of cyclophilin A
isomerase activity relative to 1. Furthermore, while specific
assay methodology was not provided, it was asserted that this
example has only 3% of the immunosuppressive activity of 1.
Although the structure has not been revealed, in July 2013 it
was reported that Aurinia had identified a lead candidate and
was in the process of fully evaluating the scope of the anti-HCV
activity of this analogue.

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