Endothelin-2, human

Endothelin-2, human is a 21-amino acid vasoactive peptide that binds to G-protein-linked transmembrane receptors, ET-RA and ET-RB.

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

CAT No: R1341

CAS No:123562-20-9

Synonyms/Alias:123562-20-9;Endothelin-2 (human, canine);Human endothelin-2;Endothelin-2, human;Endothelin-2 (Human);PED-4209-S;AKOS034831531;Cys-Ser-Cys-Ser-Ser-Trp-Leu-Asp-Lys-Glu-Cys-Val-Tyr-Phe-Cys-His-Leu-Asp-Ile-Ile-Trp;L023974;Q27077186;

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cGMP Peptide
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M.F/Formula
C115H160N26O32S4
M.W/Mr.
2546.9
Sequence
One Letter Code:CSCSSWLDKECVYFCHLDXXW
Three Letter Code:H-DL-Cys(1)-DL-Ser-DL-Cys(2)-DL-Ser-DL-Ser-DL-Trp-DL-Leu-DL-Asp-DL-Lys-DL-Glu-DL-Cys(2)-DL-Val-DL-Tyr-DL-Phe-DL-Cys(1)-DL-His-DL-Leu-DL-Asp-DL-xiIle-DL-xiIle-DL-Trp-OH

Endothelin-2, human is a synthetic peptide that mirrors the endogenous human endothelin-2, one of the three principal isoforms in the endothelin peptide family. As a potent vasoactive peptide, it plays a significant role in modulating vascular tone, cellular proliferation, and hormone production, making it a valuable tool for cardiovascular and physiological research. Its sequence specificity and receptor selectivity have positioned it as an essential reagent for dissecting the functional nuances of endothelin signaling pathways. Researchers utilize human endothelin-2 to elucidate mechanisms underlying vasoconstriction, tissue remodeling, and various pathophysiological processes, contributing to the broader understanding of peptide-mediated cellular communication.

Receptor Pharmacology: In receptor binding studies, endothelin-2 serves as a key ligand for characterizing the pharmacodynamics of endothelin receptors, particularly ETA and ETB subtypes. Its ability to selectively activate these G protein-coupled receptors enables researchers to differentiate receptor-specific responses in vascular smooth muscle cells, endothelial cells, and other target tissues. This functionality aids in mapping receptor distribution, quantifying binding affinities, and evaluating the downstream signaling cascades triggered by peptide-receptor interactions.

Vascular Biology Research: The peptide is extensively employed in experimental models to investigate the mechanisms of vasoconstriction and vascular homeostasis. By applying endothelin-2 to isolated vessel preparations or cultured vascular cells, scientists can analyze contractile responses, calcium signaling dynamics, and the interplay with other vasoactive mediators. Such studies are fundamental for understanding the regulation of blood pressure, vessel tone, and the pathogenesis of hypertension or vascular dysfunction at a molecular level.

Cell Proliferation and Fibrosis Studies: Endothelin-2 is frequently used to explore its mitogenic effects on various cell types, including smooth muscle cells, fibroblasts, and epithelial cells. Its capacity to stimulate proliferation and extracellular matrix production provides a model system for interrogating fibrotic processes, tissue remodeling, and the cellular responses to injury or stress. These insights are instrumental in deciphering the cellular mechanisms that contribute to organ fibrosis and structural alterations in disease models.

Endocrine and Paracrine Signaling Analysis: The peptide is a valuable tool for examining its role as both an endocrine and paracrine mediator. Researchers utilize it to probe the regulation of hormone secretion, autocrine feedback loops, and cross-talk with other signaling molecules such as nitric oxide or angiotensin II. Investigations into these interactions enhance the understanding of peptide-mediated control of physiological functions, including fluid balance, renal function, and reproductive biology.

Peptide Structure-Function Relationship Studies: As a well-defined synthetic peptide, human endothelin-2 is integral to structure-activity relationship (SAR) investigations. By introducing specific sequence modifications or employing analogs, researchers can delineate the critical residues responsible for receptor binding, biological potency, and signaling specificity. Such studies facilitate the rational design of novel peptide ligands and contribute to the development of advanced molecular probes for endothelin research.

Length
21
InChI
InChI=1S/C115H160N26O32S4/c1-11-59(9)93(113(170)132-82(115(172)173)41-64-46-120-71-27-19-17-25-68(64)71)141-114(171)94(60(10)12-2)140-105(162)81(44-91(150)151)130-99(156)75(37-57(5)6)125-103(160)79(42-65-47-118-55-121-65)128-109(166)86-52-175-174-51-69(117)95(152)133-83(48-142)108(165)138-87-53-176-177-54-88(111(168)139-92(58(7)8)112(169)131-77(39-62-29-31-66(145)32-30-62)100(157)126-76(101(158)137-86)38-61-22-14-13-15-23-61)136-97(154)73(33-34-89(146)147)123-96(153)72(28-20-21-35-116)122-104(161)80(43-90(148)149)129-98(155)74(36-56(3)4)124-102(159)78(40-63-45-119-70-26-18-16-24-67(63)70)127-106(163)84(49-143)134-107(164)85(50-144)135-110(87)167/h13-19,22-27,29-32,45-47,55-60,69,72-88,92-94,119-120,142-145H,11-12,20-21,28,33-44,48-54,116-117H2,1-10H3,(H,118,121)(H,122,161)(H,123,153)(H,124,159)(H,125,160)(H,126,157)(H,127,163)(H,128,166)(H,129,155)(H,130,156)(H,131,169)(H,132,170)(H,133,152)(H,134,164)(H,135,167)(H,136,154)(H,137,158)(H,138,165)(H,139,168)(H,140,162)(H,141,171)(H,146,147)(H,148,149)(H,150,151)(H,172,173)
InChI Key
MLFJHYIHIKEBTQ-UHFFFAOYSA-N

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