Catalog |
name |
Description |
price |
R-R-0762 |
[Phe13,Tyr19]-MCH (human, mouse, rat) |
(Phe13,Tyr19)-MCH (human, mouse, rat)/CAS.160201-86-5 is a potent SLC-1 and S643b receptor ligand. (Phe13,Tyr19)-MCH (human, mouse, rat) can be used as an agonist for SLC-1 and S643b receptor. |
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R-R-0763 |
[D-Phe2,6,Pro3]-LHRH |
[D-Phe2,6, Pro3]-LH-RH/CAS:67019-15-2 is a potent luteinizing hormone releasing hormone (LHRH) antagonist. |
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R-R-0764 |
Ac-[Tyr1,D-Phe2]-GRF (1-29) amide (human) |
[Ac-Tyr1,D-Phe2]GRF 1-29, amide (human), a growth hormone releasing factor (GRF) analogue, is a vasoactive intestinal peptide (VIP) antagonist. |
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R-R-0765 |
H-GLU(PHE-OH)-OH |
H-GLU(PHE-OH)-OH/CAS:7432-24-8/H-gamma-Glu-Phe-OH from ruixi. This branched dipeptide was detected in the urine of patients with phenylketonuria and later on in the urine of healthy individuals. γ-Glu-Phe and other branched dipeptides have been isolated from hard cheese, where they contribute to the typical flavor of this dairy product. |
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R-R-0766 |
H-Glu-Gly-Phe-OH |
H-Glu-Gly-Phe-OH/CAS 42155-93-1 is a labile tripeptide molecule that has been synthesized. The tripeptide is synthesized by coupling the amino acid H-Glu to Gly-Phe and then adding an amide bond to form the peptide. This study of the structure of H-Glu-Gly-Phe-OH was done using techniques such as electrospray ionization, chromatographic methods, and proton nuclear magnetic resonance spectroscopy. The compound was found to be neutral in charge and stable at room temperature, but unstable under acidic conditions. It is also soluble in any buffer with a pH range from 2.0 to 12.0 and can be purified by column chromatography or preparative HPLC. |
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R-R-0785 |
NOTA-cyclic RGDyK |
NOTA-cyclic RGDyK/Cyclic Arg-Gly-Asp-D-Tyr-Lys-NOTA from ruixi. NOTA-cyclic RGDyK is a compound composed of NOTA (nitroxide pentacyclic) and cyclic RGDyK. This compound consists of a cyclic structure NOTA with four nitrogen atoms and a cyclic peptide molecule cyclic RGDyK. NOTA has good chemical stability and ligand binding affinity. cyclic RGDyK forms a complex that binds to the αvβ3 integrin receptor by specifically binding to the receptor. |
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R-R-0786 |
Phosphorylase Kinase b-Subunit Fragment (420-436) |
Phosphorylase Kinase b-Subunit Fragment (420-436)/CAS.150829-21-3/Phosphorylase Kinase β-Subunit Fragment (420-436) is the β-Subunit fragment (peptide 430-436) of phosphorylase kinase. Phosphorylase kinase is a serine/threonine-specific protein kinase which activates glycogen phosphorylase to release glucose-1-phosphate from glycogen. |
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R-R-0787 |
[Cys0]-GTP-Binding Protein Gsa (28-42); GTP-Binding Protein Fragment, Gs alpha |
[Cys0]-GTP-Binding Protein Gsa (28-42) are important tools for researchers involved in studying intracellular signaling pathways, drug development, and the discovery of new therapeutic targets, so understanding their properties and potential applications is critical for those working in the fields of molecular biology, biochemistry, and pharmacology. |
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R-R-0788 |
[Cys0]-GTP-Binding Protein Gs alpha (28-42) |
[Cys0]-GTP-Binding Protein Gs alpha (28-42)/CAS:101038-78-2 refers to a specific peptide fragment derived from the GTP-binding protein alpha subunit, commonly known as Gs alpha. The fragment spans amino acids 28 to 42 of the Gs alpha protein. |
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R-R-0789 |
Eglin c (60-63)-methyl ester |
Eglin c (60-63)-methyl ester/CAS:131696-94-1 refers to a specific modified form of the protein Eglin c. Eglin c is a protein found in the salivary glands of the leech Hirudo medicinalis, and it is known for its potent inhibitory activity against serine proteases. |
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