PT-141 10 mg
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PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide derived from α-MSH (C₅₀H₆₈N₁₄O₁₀, 1025.18 Da). It is being studied as a model compound in scientific research. Intended solely for laboratory and research purposes; not for human or animal consumption. Not a medicinal product or food supplement.
€ 54,95
Dodání a platba
Doručení je možné v Evropské unii, Spojeném království a Spojených státech. Přesné služby a ceny pro danou adresu budou potvrzeny při placení.
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Dodání
Destinace: Evropská unie, Spojené království a Spojené státy.
Nastavení doručování se konfigurujeZatím nebyla povolena žádná doručovací služba. Dostupné služby a ceny se zde zobrazí po dokončení nastavení obchodu.
Platba
Platby kartou, kryptoměny, bankovní převody nebo jiné metody se zobrazí pouze tehdy, pokud budou pro tuto objednávku povoleny a dostupné.
Popis
PT-141 (Bremelanotide) is a synthetic peptide belonging to the class of melanocortin receptor ligands; chemically, it is a cyclic heptapeptide with an intramolecular lactam bridge. In scientific research, it is studied as a model compound for melanocortin receptor pharmacology and as a reference standard in analytical work. This compound is offered as a freeze-dried powder of 10 mg per vial, exclusively for laboratory and research purposes.
What is PT-141?
PT-141 is a cyclic heptapeptide with the sequence Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH, systematically designated as N-acetyl-L-norleucyl-L-α-aspartyl-L-histidyl-D-phenylalanyl-L-arginyl-L-tryptophyll-L-lysine-(2→7)-lactam. The ring is formed by the amide bond between the side chains of the aspartic acid and lysine, thereby fixing the molecule in a fixed spatial conformation; together with the D-configuration of the phenylalanine residue, this makes the peptide less susceptible to degradation by peptidases in vitro than a comparable linear motif. The compound is derived from the endogenous melanocortin peptide α-MSH and contains the conserved His-D-Phe-Arg-Trp core motif, described in the literature as the pharmacophore of this peptide family.
In research models, PT-141 is characterized as an agonist of the melanocortin receptors, a family of G-protein-coupled receptors referred to in the literature as MC1R through MC5R. In cell models expressing these subtypes, the measured response occurs via activation of adenylate cyclase and an increase in intracellular cAMP; this second-messenger response forms the basis for binding and activity determinations in vitro. Because the peptide does not target the subtypes equally, it serves as a comparison ligand in selectivity studies. Consequently, PT-141 is used as a model compound and reference substance within scientific research.
Oblasti výzkumu
In a laboratory context, PT-141 occurs in the following research areas, among others:
- Receptor research into G-protein-coupled melanocortin receptors (MC1R to MC5R) and the subtype selectivity of cyclic α-MSH analogues in vitro.
- Signal transduction study in which the cAMP response is monitored in cell lines expressing a melanocortin receptor.
- Structure-activity relationship study into the influence of the lactam bridge and D-phenylalanine substitution on receptor affinity.
- Biophysical modeling of conformation-restricted cyclic peptides and their enzymatic stability.
- Analytical method development and validation (HPLC, LC-MS) using PT-141 as the reference standard.
- Studie stability a rozpustnosti lyofilizovaných peptidů za kontrolovaných podmínek.
Každá z těchto aplikací zahrnuje kontrolovaný laboratorní nebo preklinický modelový výzkum.
PT-141 in our research range
PT-141 falls under the category of freeze-dried peptides in vial form within our range. Researchers working with this category frequently combine the compound with other peptides that possess their own biochemical target. While PT-141 focuses on the melanocortin receptor family and the associated cAMP-mediated signal transduction, other components within the same product line have been specifically chosen to cover divergent receptor systems or enzymatic targets. These compounds share the freeze-dried vial format but differ fundamentally in amino acid sequence, molecular class, and investigated mechanism.
Specifikace
| Specifikace | Hodnota |
|---|---|
| Ochutnat | PT-141 (Bremelanotide) |
| Synonyma | Bremelanotide; N-acetyl-L-norleucyl-L-α-aspartyl-L-histidyl-D-phenylalanyl-L-arginyl-L-tryptophyll-L-lysine-(2→7)-lactam; development code PT-141 |
| Sekvence | Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH |
| Číslo CAS | 189691-06-3 |
| Molekulární vzorec / hmotnost | C50H68N14O10 / 1025.2 Da |
| PubChem CID | 9941379 |
| Třída | Cyclic heptapeptide, melanocortin receptor agonist |
| Formulář | Lyofilizát (lyofilizovaný prášek) v lahvičce |
| Množství na lahvičku | 10 mg |
| Skladování | Uchovávejte v chladničce, chraňte před světlem a vlhkostí |
Tvar, manipulace a skladování
PT-141 is supplied as a freeze-dried powder with a standardized quantity of 10 mg per vial. Unlike a solid tablet form, a lyophilisate is first placed in a suitable solvent; in the dry state, the material is more stable than in dissolved form, which explains why peptides of this type are offered in a freeze-dried form.
Store the unopened vial refrigerated, protected from direct light and moisture, in the original packaging. Handle the compound with standard laboratory precautions: work in a clean environment, use appropriate personal protective equipment, and prevent cross-contamination with other research materials. Keep the packaging out of reach of unauthorized persons.
Složení a laboratorní výsledky
The lyophilisate contains PT-141 with a controlled purity of ≥ 99% (HPLC). The stated 10 mg refers to the peptide content of the vial; the volume of the freeze-dried cake may vary.
Přehled dostupné analytické dokumentace naleznete na našich stránka s výsledky laboratorních testůZprávy se shromažďují centrálně tam, abyste mohli data začlenit do vlastních výzkumných záznamů.
Často kladené otázky
To which dust class does PT-141 belong?
PT-141 is a synthetic cyclic heptapeptide belonging to the group of melanocortin receptor ligands, derived from the endogenous peptide α-MSH. It is therefore not a small organic molecule, but a peptide with a defined amino acid sequence.
What role does the lactam bridge play in research?
The amide bond between the side chains of aspartic acid and lysine closes the molecule into a ring. This cyclization fixes the conformation and increases resistance to enzymatic degradation in vitro, making the compound a widely used model in structure-activity research.
V jaké formě je dodáváno připojení?
As freeze-dried powder (lyophilisate) of 10 mg in a sealed vial, with a purity of ≥ 99% (HPLC).
Jak mám skladovat lahvičku?
Refrigerated, protected from light and moisture, and preferably in the original packaging. Avoid repeated temperature changes.



Recenze
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