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1 Gly-NH(2)) and key pharmacophore elements of melanotropins.
4 timulates the synthesis and release of alpha-melanotropin (alpha-MSH) and adrenocorticotropic hormone
5 tropic cells [corticotropin (ACTH) and alpha-melanotropin (alpha-MSH)], and with somatolactin endocri
9 It has been shown by extensive studies that melanotropin bioactivities are critically dependent on t
10 ding interactions between melanoma cells and melanotropin-bound beads also could be abolished by prio
12 2), compound 1, a cyclic derivative of alpha-melanotropin, is a nonselective high affinity antagonist
13 sent the first examples of a class of cyclic melanotropin ligands with high selectivity and defined b
14 Examination of conformationally constrained melanotropin peptide (Ac-Nle4-c[Asp5-His-Phe7-Arg-Trp9-A
15 longed (residual) biological activity of the melanotropin peptides alpha-MSH (alpha-melanocyte-stimul
16 nal 16 kDa fragment, also known as pro-gamma-melanotropin (pro-gamma-MSH), is required, releasing sho
17 is-Phe7-Arg-Trp9-Ala-Lys]-NH2) on four human melanotropin receptors (hMC1R, hMC3R, hMC4R, and hMC5R)
18 and keratinocytes were also shown to express melanotropin receptors by the same criteria established
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