Neurotensin

Neurotensin, a gut tridecapeptide, acts as a potent cellular mitogen for various colorectal and pancreatic cancers which possess high-affinity neurotensin receptors (NTR).

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: R1549

CAS No:39379-15-2

Synonyms/Alias:NEUROTENSIN;55508-42-4;39379-15-2;Neurotensin 1-13;XHB61LG5QS;CHEMBL407196;Neurotensin (ox);Neurotensin (cattle);CCRIS 3327;[3H]-Neurotensin;11-Tyr-neurotensin;(D-Tyr11)neurotensin;neurotensin (1-13);neurotensin-(1-13);UNII-XHB61LG5QS;Neurotensin, tyr(11)-;Neurotensin, tyrosine(11)-;CHEBI:7542;GTPL1574;GTPL1579;GTPL3830;Neurotensin, >=90% (HPLC);PCJGZPGTCUMMOT-ISULXFBGSA-N;H-Pyr-Leu-Tyr-Glu-Asn-Lys-Pro-Arg-Arg-Pro-Tyr-Ile-Leu-OH;[125I]NT;Neurotensin (ox), 11-D-tyrosine-;BDBM50130880;[3H]neurotensin (human, mouse, rat);[125I]neurotensin (human, mouse, rat);NCGC00167274-01;DA-66045;FN109271;NT(1-13);NS00074250;Q27087905;pGlu-Leu-Tyr-Glu-Asn-Lys-Pro-Arg-Arg-Pro-Tyr-Ile-Leu;Pyr-Leu-Tyr-Glu-Asn-Lys-Pro-Arg-Arg-Pro-Tyr-Ile-Leu;

Chemical Name:(Z)-5-(((Z)-1-((6-amino-1-(2-((Z)-(((Z)-1-((1-(2-((Z)-(((Z)-1-(((Z)-1-((1-carboxy-3-methylbutyl)imino)-1-hydroxy-3-methylpentan-2-yl)imino)-1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)imino)(hydroxy)methyl)pyrrolidin-1-yl)-5-guanidino-1-oxopentan-2-yl)imino)

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cGMP Peptide
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M.F/Formula
C78H121N21O20
M.W/Mr.
1672.9
Sequence
One Letter Code:XLYENKPRRPYIL
Three Letter Code:H-Pyr-Leu-Tyr-Glu-Asn-Lys-Pro-Arg-Arg-Pro-Tyr-Ile-Leu-OH
Application
As a biologically active neuropeptide for proteomics research
Appearance
White to off-white lyophilized solid
Purity
≥97% by HPLC

Neurotensin is a tridecapeptide neurotransmitter and neuromodulator widely recognized for its multifaceted role in the central and peripheral nervous systems. As an endogenous peptide, it exerts significant influence on dopaminergic, cholinergic, and glutamatergic signaling, making it a focal point of research in neurobiology and peptide biochemistry. Its unique ability to interact with specific G protein-coupled receptors and modulate a variety of physiological processes underscores its importance in studies of neural communication, gastrointestinal function, and peptide-receptor interactions. The well-characterized structure and bioactivity profile of neurotensin have established it as a valuable tool for investigating peptide-mediated signaling pathways, receptor pharmacology, and peptide-based functional assays.

Neuroscience research: Neurotensin serves as a powerful model compound for elucidating the mechanisms of neurotransmission and neuromodulation within the central nervous system. Researchers utilize it to study its effects on synaptic plasticity, neuronal excitability, and neurotransmitter release, particularly in relation to dopaminergic and glutamatergic pathways. Its capacity to modulate neural circuits offers insight into the molecular underpinnings of behavior, cognition, and neuropsychiatric disorders, making it indispensable for basic and translational neuroscience investigations.

Receptor pharmacology: The peptide is extensively employed in the characterization of neurotensin receptor subtypes, including NTS1 and NTS2, which are implicated in diverse physiological and pharmacological responses. By acting as a selective ligand, neurotensin enables detailed binding studies, receptor mapping, and signal transduction analyses. These applications facilitate the identification of receptor-specific agonists or antagonists and support the development of novel pharmacological probes targeting peptide receptors.

Gastrointestinal physiology: Neurotensin is a key regulator of gastrointestinal motility and secretion, and it is frequently used to explore the molecular basis of gut-brain communication. Experimental models leverage its actions to investigate peptide-mediated regulation of smooth muscle contraction, intestinal transit, and secretory processes. These studies advance understanding of the enteric nervous system and provide a foundation for dissecting the roles of neuropeptides in digestive physiology.

Peptide biochemistry and structure-function studies: As a representative neuropeptide, neurotensin is invaluable for probing the relationship between peptide structure and biological activity. Researchers employ it in synthetic modification experiments, conformational analyses, and stability testing to elucidate how sequence variations or chemical modifications impact receptor affinity and functional outcomes. Such studies inform the rational design of peptide analogs and contribute to broader efforts in peptide engineering and functional optimization.

Analytical method development: The well-defined sequence and bioactivity of neurotensin make it a reliable standard for developing and validating analytical techniques such as high-performance liquid chromatography (HPLC), mass spectrometry, and immunoassays. Its use in assay calibration, quantification, and detection underpins methodological advances in peptide analysis, supporting both qualitative and quantitative research applications across the fields of neurochemistry and peptide analytics.

Length
13
Long-term Storage Conditions
Soluble to 0.70 mg/ml in water
InChI
InChI=1S/C78H121N21O20/c1-7-43(6)63(73(115)96-57(76(118)119)37-42(4)5)97-70(112)55(39-45-21-25-47(101)26-22-45)95-72(114)59-18-13-35-99(59)75(117)52(16-11-33-86-78(83)84)90-64(106)48(15-10-32-85-77(81)82)89-71(113)58-17-12-34-98(58)74(116)51(14-8-9-31-79)91-69(111)56(40-60(80)102)94-66(108)50(28-30-62(104)105)88-68(110)54(38-44-19-23-46(100)24-20-44)93-67(109)53(36-41(2)3)92-65(107)49-27-29-61(103)87-49/h19-26,41-43,48-59,63,100-101H,7-18,27-40,79H2,1-6H3,(H2,80,102)(H,87,103)(H,88,110)(H,89,113)(H,90,106)(H,91,111)(H,92,107)(H,93,109)(H,94,108)(H,95,114)(H,96,115)(H,97,112)(H,104,105)(H,118,119)(H4,81,82,85)(H4,83,84,86)/t43-,48-,49-,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-,63-/m0/s1
InChI Key
PCJGZPGTCUMMOT-ISULXFBGSA-N
Canonical SMILES
CCC(C(/N=C(O)/C(/N=C(O)/C1CCCN1C(C(/N=C(O)/C(/N=C(O)/C2CCCN2C(C(/N=C(O)/C(/N=C(O)/C(/N=C(O)/C(/N=C(O)/C(/N=C(O)/C3CCC(O)=N3)CC(C)C)CC4=CC=C(O)C=C4)CCC(O)=O)CC(O)=N)CCCCN)=O)CCCNC(N)=N)CCCNC(N)=N)=O)CC5=CC=C(O)C=C5)/C(O)=N/C(C(O)=O)CC(C)C)C

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