Design of MC1R Selective γ-MSH Analogues with Canonical Amino Acids Leads to Potency and Pigmentation.
about
Development of Novel Melanocortin Receptor Agonists Based on the Cyclic Peptide Framework of Sunflower Trypsin Inhibitor-1.Replacement of Arg with Nle and modified D-Phe in the core sequence of MSHs, Ac-His-D-Phe-Arg-Trp-NH2, leads to hMC1R selectivity and pigmentation.Development of Macrocyclic Peptidomimetics Containing Constrained α,α-Dialkylated Amino Acids with Potent and Selective Activity at Human Melanocortin Receptors.MC1R: Front and Center in the Bright Side of Dark Eumelanin and DNA Repair
P2860
Design of MC1R Selective γ-MSH Analogues with Canonical Amino Acids Leads to Potency and Pigmentation.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年學術文章
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2017年學術文章
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name
Design of MC1R Selective γ-MSH ...... s to Potency and Pigmentation.
@en
Design of MC1R Selective γ-MSH ...... s to Potency and Pigmentation.
@nl
type
label
Design of MC1R Selective γ-MSH ...... s to Potency and Pigmentation.
@en
Design of MC1R Selective γ-MSH ...... s to Potency and Pigmentation.
@nl
prefLabel
Design of MC1R Selective γ-MSH ...... s to Potency and Pigmentation.
@en
Design of MC1R Selective γ-MSH ...... s to Potency and Pigmentation.
@nl
P2093
P2860
P1476
Design of MC1R Selective γ-MSH ...... s to Potency and Pigmentation.
@en
P2093
Ioanna Zoi
Jonathon R Sawyer
Saghar Mowlazadeh Haghighi
Victor J Hruby
P2860
P304
P356
10.1021/ACS.JMEDCHEM.7B01295
P407
P577
2017-11-13T00:00:00Z