Moligand™ Moligand™ per flussi di lavoro cromatografici e analitici sensibili che richiedono un'interferenza minima della linea di base.
Room temperature Spedizione . Consultare il COA specifico del lotto per le specifiche esatte.
SDS, COA, scheda tecnica e scheda delle specifiche disponibili per il download. COA specifico del lotto accessibile tramite ricerca per numero di lotto.
Citato in 0 pubblicazioni peer-reviewed su cromatografia, sintesi organica e reazioni di accoppiamento incrociato.
Documento completo su pericoli, manipolazione, stoccaggio e conformità normativa.
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Visualizza scheda delle specifiche →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic Polymers |
| Classe | Polypeptides |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Polypeptides |
| Alternative Parents | Peptides Tyrosine and derivatives Phenylalanine and derivatives Arginine and derivatives Glutamine and derivatives Glutamic acid and derivatives Leucine and derivatives Isoleucine and derivatives Aspartic acid and derivatives Tetracarboxylic acids and derivatives Valine and derivatives N-acyl-alpha amino acids and derivatives Tryptamines and derivatives Alpha amino acid amides Serine and derivatives Alanine and derivatives 3-alkylindoles Amphetamines and derivatives 1-hydroxy-2-unsubstituted benzenoids Amino fatty acids Hydroxy fatty acids Substituted pyrroles N-acyl amines Heteroaromatic compounds Secondary carboxylic acid amides Guanidines Primary carboxylic acid amides Secondary alcohols Amino acids Carboxylic acids Carboximidamides Azacyclic compounds Primary alcohols Hydrocarbon derivatives Imines Monoalkylamines Organopnictogen compounds Carbonyl compounds Organic oxides |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Polypeptide - Alpha peptide - Tyrosine or derivatives - Arginine or derivatives - Phenylalanine or derivatives - Glutamine or derivatives - Glutamic acid or derivatives - Aspartic acid or derivatives - Leucine or derivatives - Isoleucine or derivatives - N-acyl-alpha amino acid or derivatives - Tetracarboxylic acid or derivatives - Valine or derivatives - Alpha-amino acid amide - Triptan - Serine or derivatives - Alanine or derivatives - Amphetamine or derivatives - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - 3-alkylindole - Indole or derivatives - Indole - 1-hydroxy-2-unsubstituted benzenoid - Amino fatty acid - Phenol - Hydroxy fatty acid - Fatty amide - Substituted pyrrole - N-acyl-amine - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Heteroaromatic compound - Pyrrole - Amino acid or derivatives - Amino acid - Carboxamide group - Guanidine - Secondary carboxylic acid amide - Secondary alcohol - Primary carboxylic acid amide - Carboxylic acid derivative - Carboximidamide - Carboxylic acid - Organoheterocyclic compound - Azacycle - Primary alcohol - Organopnictogen compound - Imine - Amine - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Primary aliphatic amine - Alcohol - Organic oxide - Organonitrogen compound - Organooxygen compound - Primary amine - Aromatic heteropolycyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as polypeptides. These are peptides containing ten or more amino acid residues. |
| External Descriptors | Not available |
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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| Reference |
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No validated, item-specific protocols are provided for this product. The following general procedures are offered as practical guidance for peptide handling (not specifications):
Documentation:
For assay‑specific parameters (concentrations, incubation times), consult your method SOPs or literature relevant to GLP‑1 fragments.
Context (literature, for background only; not a product claim):
Use in research:
Important: Functional outcomes can be assay‑dependent and sequence‑specific. Verify sequence, termini (amide vs acid), and any modifications on the CoA, and design controls accordingly.
This item is a peptide research reagent rather than a buffering compound. Nonetheless, appropriate buffers are central to successful handling and assays.
General buffer guidance (not item-specific):
Not a classical buffering agent: There is no defined pKa set or buffering range for this peptide suitable for use as a buffer. Select buffer systems based on the downstream biological or analytical protocol.
For peptide handling, the greenest choice is typically to maximize aqueous media and minimize hazardous organics.
Greener selections (general guidance):
Comparison (typical pros/cons):
| Option | Pros | Cons | |---|---|---| | Water/buffer | Non-toxic, biodegradable, assay-compatible | Limited for highly hydrophobic sequences | | DMSO | Strong solubilizer; miscible with water | High EHS burden; can affect assays | | MeCN (HPLC) | Volatile; compatible with LC | Flammable; toxicity and solvent waste |
Process considerations:
Note: These are general green-chemistry practices for peptides and are not item-specific specifications.
No therapeutic claims. This research reagent is not intended for human or veterinary use.
Relevant formulation/CMC contexts (general, non‑clinical):
Regulatory status:
Practical considerations:
Item-specific physico-chemical specifications are not provided in the product data.
General/literature expectations for GLP‑1(9–36)-type peptides (for planning only):
Important:
What this generally implies:
Practical notes for this item:
Comparison of common research grades (general guidance):
Bottom line: Treat Moligand™ as a research‑grade peptide for screening and method development. Defer to the item’s CoA for all numerical specifications.
This peptide is primarily used as a research tool in biochemistry and analytical science rather than as a substrate for classical organic reactions. Typical laboratory applications include:
Practical tips:
As a peptide reagent, typical “reactions” involve bioconjugation or analytical sample preparation rather than small‑molecule transformations. General conditions (literature guidance):
Yields: Highly sequence- and reagent-dependent; assess conversion by LC‑MS. Always verify the exact sequence/termini on the CoA before selecting conditions.
General laboratory precautions for peptides and biomolecules:
Always consult the product’s Safety Data Sheet (SDS) for authoritative hazard classifications and emergency measures.
GLP‑1‑type peptides are polar and typically dissolve in aqueous media. Optimal solvent choice depends on the specific sequence, counter‑ion, and desired application.
Small comparison (general):
Tip: Prepare a small‑volume concentrated stock in suitable solvent, then dilute into assay/buffer immediately prior to use to limit adsorption and degradation.
General best practices for peptide stability (not item-specific; defer to label if different):
Reconstitution guidance (general):
Stability notes:
Always prioritize the storage instructions on the product label/CoA for this specific item.
A peptide fragment corresponding to residues 9–36 of human GLP‑1, widely used as a biochemical research tool and peptide chemistry reference.
Structural features (general/literature):
2D description in words (literature-based):
Notes:
Although supplied as a finished peptide, GLP‑1(9–36) can serve as a versatile scaffold for chemical derivatization and method development.
Analytical method development:
Note: Exact reactive residue content is sequence‑dependent. Consult the item CoA/Spec Sheet for the definitive amino acid sequence and termini before planning site‑selective chemistry.
No target or application specificity is provided for this catalog item.
General literature context:
La nostra guida alla selezione delle qualità copre purezza, stato dello stabilizzatore e idoneità all'applicazione per tutte le varianti del nostro catalogo.
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