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Merck
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Documentos Principais

G7160

Sigma-Aldrich

Galanin Fragment 1-13-Spantide I

≥95% (HPLC)

Sinônimo(s):

C7

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About This Item

Fórmula empírica (Notação de Hill):
C138H199N35O30
Número CAS:
Peso molecular:
2828.27
Número MDL:
Código UNSPSC:
12352200

Ensaio

≥95% (HPLC)

nº de adesão UniProt

temperatura de armazenamento

−20°C

Informações sobre genes

Amino Acid Sequence

Gly-Trp-Thr-Leu-Asn-Ser-Ala-Gly-Tyr-Leu-Leu-Gly-Pro-D-Arg-Pro-Lys-Pro-Gln-Gln-D-Trp-Phe-D-Trp-Leu-Leu-NH2

Ações bioquímicas/fisiológicas

Tandem-linked peptide which acts as a potent galanin receptor antagonist

Código de classe de armazenamento

13 - Non Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


Certificados de análise (COA)

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L G Ulman et al.
Regulatory peptides, 51(1), 17-23 (1994-04-14)
Previous studies have shown that injection of galanin (GAL: 6.2 nmol/kg) causes prolonged inhibition of cardiac vagal action in anaesthetised cats. Stimulation of the cardiac sympathetic nerve (16 Hz for 5 min) also produces inhibition of cardiac vagal action, an
I Kisfalvi et al.
Journal of physiology, Paris, 94(1), 37-42 (2000-04-13)
The neuropeptide galanin has been reported to have a wide range of biological actions both in the central nervous system and in the gastrointestinal tract. Recent works led to the discovery of selective galanin receptor antagonists including M15 (galanin(1-12)-Pro-substanceP(5-11)-amide), M35
D A Mahns et al.
Regulatory peptides, 67(3), 163-168 (1996-12-17)
Galanin is a neuropeptide that causes a marked pressor response in several non-mammalian vertebrate species, and some marsupials. In this study, the effect of three galanin antagonists were tested on the pressor response to an intravenous dose (6.3 nmol/kg) of
I Kisfalvi et al.
Journal of physiology, Paris, 95(1-6), 385-389 (2001-10-12)
Galanin is a neuropeptide having a wide range of biological actions. Recently selective galanin receptor antagonists such as M35 [galanin(1-12)-Pro-bradykinin(2-9)-amide] and C7 [galanin(1-12)-Pro-spantide-amide] have been described. These antagonists have blocked the actions of galanin on flexor reflex, glucose-induced insulin secretion
R L Corwin et al.
The European journal of neuroscience, 5(11), 1528-1533 (1993-11-01)
Galanin significantly increased food intake when microinjected into the region of the central nucleus of the amygdala as well as into the paraventricular nucleus of the hypothalamus. In the amygdala this effect was specific to feeding; no change in grooming

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