Galanin (1-13)-Neuropeptide Y (25-36) amide

Catalog No.: A62267
Galanin/Galanin Receptor Ligand
Galanin (1-13)-Neuropeptide Y (25-36) amide is a high-affinity ligand for galanin receptors, acting primarily through the modulation of galanin signaling pathways. This peptide demonstrates significant biological activity in neuropeptide signaling and is relevant for research applications focusing on neurobiology, appetite regulation, and stress response mechanisms. Its use can enhance understanding of galanin's role in various physiological and pathological processes.
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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionGalanin (1-13)-Neuropeptide Y (25-36) amide is a high-affinity ligand for galanin receptors, acting primarily through the modulation of galanin signaling pathways. This peptide demonstrates significant biological activity in neuropeptide signaling and is relevant for research applications focusing on neurobiology, appetite regulation, and stress response mechanisms. Its use can enhance understanding of galanin's role in various physiological and pathological processes.
Product Information
Catalog NumA62267
FormulaC136H209N41O34
Molecular Weight2962.37
CAS Number147138-51-0
SequenceGly-Trp-Thr-Leu-Asn-Ser-Ala-Gly-Tyr-Leu-Leu-Gly-Pro-Arg-His-Tyr-Ile-Asn-Leu-Ile-Thr-Arg-Gln-Arg-Tyr-NH2
Sequence shorteningGWTLNSAGYLLGPRHYINLITRQRY-NH2
SMILESC([C@@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(NCC(N[C@@H](CC1=CC=C(O)C=C1)C(N[C@H](C(N[C@H](C(NCC(=O)N2[C@H](C(N[C@H](C(N[C@@H](CC3=CN=CN3)C(N[C@@H](CC4=CC=C(O)C=C4)C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@@H](CC5=CC=C(O)C=C5)C(N)=O)=O)CCCNC(=N)N)=O)CCC(N)=O)=O)CCCNC(=N)N)=O)[C@@H](C)O)=O)[C@H](CC)C)=O)CC(C)C)=O)CC(N)=O)=O)[C@H](CC)C)=O)=O)=O)CCCNC(=N)N)=O)CCC2)=O)CC(C)C)=O)CC(C)C)=O)=O)=O)C)=O)CO)=O)CC(N)=O)=O)CC(C)C)=O)[C@@H](C)O)=O)NC(CN)=O)C=6C=7C(NC6)=CC=CC7
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