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83651-90-5

83651-90-5 Structure

83651-90-5 Structure
IdentificationBack Directory
[Name]

ALPHA-CGRP (RAT)
[CAS]

83651-90-5
[Synonyms]

CGRP (RAT)
Rat α-CGRP
A-CGRP (RAT)
α-CGRP (rat)
ALPHA-CGRP (RAT)
α-CGRP (mouse, rat)
a-CGRP (Mouse, rat)
alpha-CGRP (mouse, rat)
calcitonin gene-rel. peptide
CALCITONIN GENE RELATED PEPTIDE RAT
Rat α-calcitonin gene-related peptide
ALPHA-CALCITONIN GENE RELATED PEPTIDE, RAT
α-CGRP (mouse, rat)|Calcitonin Gene Related Peptide,rat
calcitonin gene-regulated peptide, cyclic disulfide, rat
SCNTATCVTHRLAGLLSRSGGVVKDNFVPTNVGSEAF-NH2 (DISULFIDE BRIDGE: 2-7)
SER-CYS-ASN-THR-ALA-THR-CYS-VAL-THR-HIS-ARG-LEU-ALA-GLY-LEU-LEU-SER-ARG-SER-GLY-GLY-VAL-VAL-LYS-ASP-ASN-PHE-VAL-PRO-THR-ASN-VAL-GLY-SER-GLU-ALA-PHE-NH2
H-SER-CYS-ASN-THR-ALA-THR-CYS-VAL-THR-HIS-ARG-LEU-ALA-GLY-LEU-LEU-SER-ARG-SER-GLY-GLY-VAL-VAL-LYS-ASP-ASN-PHE-VAL-PRO-THR-ASN-VAL-GLY-SER-GLU-ALA-PHE-NH2
VAL-THR-HIS-ARG-LEU-ALA-GLY-LEU-LEU-SER-ARG-SER-GLY-GLY-VAL-VAL-LYS-ASP-ASN-PHE-VAL-PRO-THR-ASN-VAL-GLY-SER-GLU-ALA-PHE-NH2: VTHRLAGLLSRSGGVVKDNFVPTNVGSEAF-NH2
H-SER-CYS-ASN-THR-ALA-THR-CYS-VAL-THR-HIS-ARG-LEU-ALA-GLY-LEU-LEU-SER-ARG-SER-GLY-GLY-VAL-VAL-LYS-ASP-ASN-PHE-VAL-PRO-THR-ASN-VAL-GLY-SER-GLU-ALA-PHE-NH2 (DISULFIDE BRIDGE: 2-7)
[Molecular Formula]

C162H262N50O52S2
[MDL Number]

MFCD00081460
[MOL File]

83651-90-5.mol
[Molecular Weight]

3806.25
Chemical PropertiesBack Directory
[storage temp. ]

−20°C
[form ]

powder
[color ]

White to off-white
[Water Solubility ]

Soluble to 0.80 mg/ml in water
[Sequence]

H-Ser-Cys-Asn-Thr-Ala-Thr-Cys-Val-Thr-His-Arg-Leu-Ala-Gly-Leu-Leu-Ser-Arg-Ser-Gly-Gly-Val-Val-Lys-Asp-Asn-Phe-Val-Pro-Thr-Asn-Val-Gly-Ser-Glu-Ala-Phe-NH2 (Disulfide bridge:Cys2-Cys7)
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

α-CGRP (mouse, rat), a neuropeptide (calcitonin gene-related peptide (CGRP)) mainly expressed in neuromuscular junction, is a potent vasodilator. α-CGRP (mouse, rat) can lead to a fall in blood pressure and an increase in heart rate by peripheral administration, also relax colonie smooth muscle. α-CGRP (mouse, rat) has the potential in cardiovascular, pro-inflammatory, migraine and metabolic studies[1][2][3][4].
[in vivo]

α-CGRP (mouse, rat) (0.25, 0.5, 1 μg/kg/min, intravenous) dose-dependent decreases mean arterial blood pressure, while heart rate and systemic vascular conduction increased, while cardiac output remained unchanged[3].
α-CGRP (mouse, rat) plays an important role in the regulation of Kainic acid (KA) induced pyramid-cell death in hippocampal CA3 region[4].

[storage]

Desiccate at -20°C
[References]

[1] Whitby K, et al. Castanospermine, a potent inhibitor of dengue virus infection in vitro and in vivo. J Virol. 2005 Jul;79(14):8698-706. DOI:10.1128/JVI.79.14.8698-8706.2005
[2] Xu H, et al. Transcriptional Atlas of Intestinal Immune Cells Reveals that Neuropeptide α-CGRP Modulates Group 2 Innate Lymphoid Cell Responses. Immunity. 2019 Oct 15;51(4):696-708.e9. DOI:10.1016/j.immuni.2019.09.004
[3] Arulmani U, et al. Effects of the calcitonin gene-related peptide (CGRP) receptor antagonist BIBN4096BS on alpha-CGRP-induced regional haemodynamic changes in anaesthetised rats. Basic Clin Pharmacol Toxicol. 2004 Jun;94(6):291-7. DOI:10.1111/j.1742-7843.2004.pto940606.x
[4] Park SH, et al. Role of α-CGRP in the regulation of neurotoxic responses induced by kainic acid in mice. Peptides. 2013 Jun;44:158-62. DOI:10.1016/j.peptides.2013.04.001
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