Cortistatin 14 (mouse, rat)

Cortistatin-14 expressed in the cortex and hippocampus. Structural and functional similarities to somatostatin-14. Neuronal depressant and sleep-modulating properties in vivo. An important mediator of immunity and inflammation.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
Cortistatin 14 (mouse, rat)(CAS 186901-48-4)

CAT No: 10-101-253

CAS No:186901-48-4

Synonyms/Alias:cortistatin14;Cortistatin 14;cortistatin;193829-96-8;Cortistatin 14, human, rat;Cortistatin-14;186901-48-4;Cortistatin-14 (trifluoroacetate salt);CST-14;Corticostatin-14;CHEMBL5192321;BDBM85324;DTXSID00583202;PUBCHEM_16133803;HY-P1212;Cortistatin-14, >=97% (HPLC);AKOS024457590;NCGC00167271-01;DA-52063;DA-52064;CAS_186901-48-4;CS-0029008;

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M.F/Formula
C81H113N19O19S2
M.W/Mr.
1721
Sequence
One Letter Code:PCKNFFWKTFSSCK
Three Letter Code:H-Pro-Cys(1)-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Ser-Ser-Cys(1)-Lys-OH
Application
Cortistatin-14 may be used in competition binding assay with sst4 receptors (CHO-sst4) of CHO cells and sst1 receptors (CHO-sst1).[5]
Appearance
White or off-white lyophilized powder
Purity
≥97% (HPLC)

Cortistatin 14 (mouse, rat) is a synthetic peptide that closely mimics the endogenous neuropeptide cortistatin found in murine species. Characterized by its distinct amino acid sequence and structural similarity to somatostatin, this compound exhibits unique biological activities, particularly within the central nervous system. Researchers value Cortistatin 14 for its ability to modulate neuronal excitability, influence neurotransmitter release, and interact with various G protein-coupled receptors. Its multifaceted properties make it a powerful tool for the exploration of neurophysiological processes, as well as for advancing the understanding of peptide-receptor interactions and signaling pathways in rodent models. The stability and bioactivity of Cortistatin 14 in experimental settings support its widespread adoption in neuroscience, immunology, and endocrinology research.

Neurophysiology research: Cortistatin 14 is extensively utilized in the study of neuronal signaling and synaptic modulation, given its capacity to regulate the activity of both inhibitory and excitatory neurons. By binding to somatostatin receptors and potentially other related receptors, it enables researchers to dissect the mechanisms underlying neural oscillations, sleep regulation, and synaptic plasticity. In electrophysiological assays and brain slice preparations, the peptide allows for precise modulation of neuronal firing, contributing to a deeper understanding of cortical network dynamics and the physiological roles of neuropeptides in the mammalian brain.

Neuroinflammation studies: In experimental models of neuroinflammation, cortistatin analogs are employed to investigate their effects on glial cell activation, cytokine release, and the maintenance of blood-brain barrier integrity. The peptide's interaction with immune cells in the central nervous system provides valuable insights into neuroimmune crosstalk and the molecular pathways that govern inflammatory responses. Researchers utilize it to probe the mechanisms by which endogenous neuropeptides modulate inflammation, offering a clearer picture of homeostatic and pathological processes in the CNS.

Endocrine function analysis: The use of Cortistatin 14 extends to the examination of hormone secretion and endocrine signaling pathways in rodents. By modulating the release of growth hormone, adrenocorticotropic hormone, and other pituitary-derived peptides, cortistatin analogs help elucidate the regulatory circuits that control endocrine homeostasis. Experimental protocols involving the administration of this peptide in vitro and in vivo facilitate the mapping of hypothalamic-pituitary axis interactions and the identification of novel regulatory nodes within these systems.

Sleep and circadian rhythm research: As a neuropeptide implicated in the regulation of sleep-wake cycles, cortistatin is frequently employed in studies examining the molecular and cellular mechanisms of sleep architecture. Its administration in rodent models allows scientists to assess alterations in sleep patterns, slow-wave activity, and circadian behaviors. The peptide's influence on thalamocortical oscillations and neural synchronization provides a valuable experimental approach for unraveling the neurochemical basis of sleep regulation and the interplay between neurotransmitter systems.

Cognitive and behavioral studies: In the realm of behavioral neuroscience, Cortistatin 14 serves as a tool for investigating learning, memory, and anxiety-related behaviors in mice and rats. By modulating synaptic transmission and neuronal excitability, it enables the exploration of how neuropeptide signaling contributes to cognitive processes and emotional regulation. Researchers use it in combination with behavioral assays to link molecular mechanisms with observable phenotypes, advancing the understanding of peptide function in complex behaviors and neuropsychiatric conditions.

Peptide-receptor interaction assays: Finally, Cortistatin 14 is instrumental in the study of ligand-receptor binding characteristics and downstream signaling events. Through the use of radioligand binding assays, fluorescence-based detection, or cell-based functional assays, scientists can delineate the affinity, selectivity, and efficacy of cortistatin analogs at various receptor subtypes. These investigations shed light on receptor pharmacology, signaling bias, and the structural determinants of ligand recognition, supporting the development of targeted research tools and new hypotheses in peptide biology.

Source#
Synthetic
Long-term Storage Conditions
1% acetic acid: 1 mg/mL
InChI
InChI=1S/C81H113N19O19S2/c1-46(103)67-80(117)95-59(38-49-24-9-4-10-25-49)73(110)96-62(42-101)76(113)97-63(43-102)77(114)99-65(79(116)90-56(81(118)119)30-15-18-34-84)45-121-120-44-64(98-68(105)53-31-19-35-86-53)78(115)89-54(28-13-16-32-82)69(106)94-61(40-66(85)104)75(112)92-57(36-47-20-5-2-6-21-47)71(108)91-58(37-48-22-7-3-8-23-48)72(109)93-60(39-50-41-87-52-27-12-11-26-51(50)52)74(111)88-55(70(107)100-67)29-14-17-33-83/h2-12,20-27,41,46,53-65,67,86-87,101-103H,13-19,28-40,42-45,82-84H2,1H3,(H2,85,104)(H,88,111)(H,89,115)(H,90,116)(H,91,108)(H,92,112)(H,93,109)(H,94,106)(H,95,117)(H,96,110)(H,97,113)(H,98,105)(H,99,114)(H,100,107)(H,118,119)/t46-,53+,54+,55+,56+,57+,58+,59+,60+,61+,62+,63+,64+,65+,67+/m1/s1
InChI Key
DDRPLNQJNRBRNY-WYYADCIBSA-N
Canonical SMILES
CC(C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(CSSCC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CCCCN)CC2=CNC3=CC=CC=C32)CC4=CC=CC=C4)CC5=CC=CC=C5)CC(=O)N)CCCCN)NC(=O)C6CCCN6)C(=O)NC(CCCCN)C(=O)O)CO)CO)CC7=CC=CC=C7)O

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