Gonadorelin 2mg

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Gonadorelin – Peptide for Research Applications
Gonadorelin is a synthetic decapeptide that corresponds in structure to an endogenous hormone-related peptide. It is used in laboratories for preclinical studies focusing on receptor binding, peptide configuration, and molecular signaling pathways under controlled conditions.

€ 39,95

Proces objednávania

Doručenie a platba

Doručenie je možné v Európskej únii, Spojenom kráľovstve a Spojených štátoch. Presné služby a ceny pre danú adresu budú potvrdené pri platbe.

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Doručenie

Destinácie: Európska únia, Spojené kráľovstvo a Spojené štáty.

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Popis

Gonadorelin is a synthetic decapeptide, a chemically biterminally modified peptide with a pyroglutamyl start and a C-terminal glycinamide. In scientific research, it is studied as a model compound for receptor-linked peptide chemistry and as a reference standard in analytical work. This compound is offered as a freeze-dried powder of 2 mg per vial, exclusively for laboratory and research purposes.

What is Gonadorelin?

Gonadorelin is the synthetic form of gonadotropin-releasing hormone (GnRH, also referred to as LHRH) and consists of ten amino acids in the sequence pGlu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH2The two ends are chemically unique. At the N-terminus, there is no free amine but a pyroglutamic acid: an intramolecularly cyclized glutamine in which the amino group is incorporated into a lactam ring. At the C-terminus, there is no free carboxylate but a glycinamide. Both ends are therefore electrically neutralized, meaning the net charge is determined entirely by the side chains, in practice primarily by the arginine at position 8 and the histidine at position 2. This charge neutralization simultaneously reduces the binding sites for amino- and carboxypeptidases.

In research models, Gonadorelin is used as a reference ligand for the GnRH receptor, a class A G-protein-coupled receptor. Because this peptide is the best-characterized ligand for that receptor, it serves as a reference point in binding studies using pituitary cell culture systems and membrane preparations when comparing modified analogs. Structural research focuses on the conformation in the binding groove: the glycine at position 6 allows for a tight bend. In vitro, the peptide is also a favored substrate for enzymological work, because degradation occurs selectively between glycine-6 ​​and leucine-7 and between proline-9 and the glycinamide. Consequently, Gonadorelin is used as a model compound and reference substance within scientific research.

Oblasti výskumu

In a laboratory context, Gonadorelin occurs in the following research areas, among others:

  • Receptor research on the GnRH receptor as a class A G-protein-coupled receptor, with Gonadorelin as the reference ligand in binding assays.
  • Enzymological research into selective peptide cleavage by neutral endopeptidases and post-proline-cleaving enzymes.
  • Structure-activity relationship study on decapeptide analogs, in which positions 6 and 10 are systematically varied.
  • Biophysical conformation analysis (CD spectroscopy, NMR, molecular modeling) of the curve around the glycine at position 6.
  • Analytical method development and validation (reverse-phase HPLC, LC-MS) with Gonadorelin as the peptide reference standard.
  • Stability study of tryptophan oxidation and cyclized peptide ends.

Každá z týchto aplikácií zahŕňa kontrolovaný laboratórny alebo predklinický modelový výskum.

Gonadorelin in our research assortment

Gonadorelin falls under the category of freeze-dried investigational compounds in vial form within our product range. While Gonadorelin focuses on a G-protein-coupled receptor and the influence of terminal modifications, other components within the same product line have been specifically chosen to cover enzymatic or metal-coordinated targets. These compounds share the freeze-dried vial form but differ fundamentally in molecular class and investigated mechanism.

Špecifikácie

ŠpecifikáciaHodnota
VzorkaGonadorelin
Synonymágonadotropin-releasing hormone (GnRH); LHRH; luliberin
PostupnosťpGlu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH2
Číslo CAS33515-09-2
Molekulárny vzorec / hmotnosťC55H75N17O13 / 1182.29 Da
PubChem CID638793
TriedaDecapeptide; amidated at the C-terminus, cyclized at the N-terminus
FormulárLyofilizovaný prášok (lyofilizovaný prášok) v uzavretej liekovke
Množstvo na injekčnú liekovku2 mg
SkladovanieSkladujte na chladnom a tmavom mieste, chránené pred svetlom a vlhkosťou.

Tvar, manipulácia a skladovanie

Gonadorelin is supplied as a white freeze-dried powder of 2 mg per vial, sealed under a rubber stopper with aluminium sealing. With this small quantity, the lyophilisate is often barely visible as a thin layer at the bottom, which is normal in the milligram range. In a laboratory setting, the material is further processed according to the applicable analytical protocol.

Store the closed vial in a cool, dark place, protected from light and moisture, preferably in the original packaging. The tryptophan at position 3 is photosensitive and oxidizable, which makes protection against light and oxygen particularly relevant for this peptide. Handle the compound with standard laboratory precautions: work in a clean environment, use appropriate personal protective equipment, and prevent cross-contamination. Keep the packaging out of reach of unauthorized persons.

Zloženie a laboratórne výsledky

The lyophilisate contains 2 mg Gonadorelin per vial with a controlled purity of ≥ 99% (HPLC). No fillers or stabilizers are added, so that oxidation products can be attributed purely to the sample itself.

Prehľad dostupnej analytickej dokumentácie nájdete na našej stránka s výsledkami laboratórnych testov, kde sa centrálne zhromažďujú správy.

Často kladené otázky

To which substance class does Gonadorelin belong?
A decapeptide and the synthetic counterpart of gonadotropin-releasing hormone (GnRH), with a cyclized N-terminus and an amidated C-terminus.

Why are the two ends chemically unique?
The pyroglutamic acid and the glycinamide contain no free amino group or free carboxylate. Both ends are therefore charge-neutral, which limits the binding sites for amino- and carboxypeptidases.

V akej forme je dodávané pripojenie?
As a freeze-dried powder of 2 mg in a sealed vial, without added excipients.

Ako mám skladovať injekčnú liekovku?
Refrigerated and dark, protected from light and moisture, preferably unopened in the original packaging.

Špecifikácia

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