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Self-assembling Peptide
QL6 peptide is a self-assembling peptide that forms β-sheets at neutral pH, creating a conducive environment for tissue engineering applications. This peptide demonstrates significant anti-inflammatory properties and reduces tissue scarring, making it valuable for regenerative medicine research. QL6 peptide is particularly useful for the development of nanofiber scaffolds in spinal cord injury (SCI) studies, facilitating cellular growth and repair within damaged tissues. -
Self-assembling Peptide Hydrogel
RAD16-I is a self-assembling peptide hydrogel that forms a three-dimensional nanofiber network under physiological conditions, closely resembling the extracellular matrix. This hydrogel exhibits high water content, biocompatibility, and degradability, making it an excellent scaffold for three-dimensional cell culture. RAD16-I supports cell adhesion, proliferation, differentiation, and insulin secretion while stabilizing islet clusters and promoting cardiac lineage differentiation. It is particularly valuable for research applications related to myocardial infarction and diabetes, providing a suitable nano-microenvironment for cell-based studies. -
Peptide
ELINLATMCR is a soybean-derived peptide that targets soybean proteins, serving as a marker for the detection of soybean allergens. This peptide is particularly useful in analytical applications employing UHPLC-MS/MS, facilitating the identification and quantification of allergenic components in food samples. Its specificity makes it a valuable tool for researchers studying food allergies and developing allergen detection methodologies. -
Kidney-targeting Carrier Peptide
(KKEEE)3K is a kidney-targeting carrier peptide designed to enhance the delivery of therapeutic agents to renal tissues. This peptide demonstrates remarkable specificity for kidney cells, making it a valuable tool for studies focused on renal delivery mechanisms and targeted therapies. Research applications include drug delivery systems aimed at improving treatment efficacy for kidney diseases. -
Egg Peptide
EALQPIHDLADEAISR is an egg peptide derived from yolk proteins, found in both hen eggs and Coturnix japonica eggs. This specific peptide serves as a valuable marker for the detection of egg allergens using ultra-high-performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS). Its application is crucial in food safety and allergy research, aiding in the identification and quantification of egg protein content in various products. -
Coumarin-labeled Amanitin Peptide
Coumarin-Phalloidin is a coumarin-labeled derivative of the Amanitin peptide targeting actin filaments. This novel actin probe is specifically designed for triple immunofluorescence microscopy, enabling detailed visualization of the cytoskeletal architecture in cells. Its strong fluorescence properties facilitate enhanced imaging and analysis in various cellular and molecular biology applications. -
Active Peptide
[Ala2] Met-Enkephalinamide is an active peptide that primarily targets opioid receptors in the central nervous system. This compound is involved in modulating pain perception and emotional responses, making it an important tool in studies related to analgesia and neurobiology. Researchers utilize [Ala2] Met-Enkephalinamide for exploring the mechanisms of opioid signaling and its potential therapeutic applications in pain management and addiction. -
Cyclic Oligopeptide
Cyclosporin E, a cyclic oligopeptide originally isolated from fungi such as Trichoderma polysporum, exhibits properties relevant to the study of the Cyclosporin family. This compound is particularly valuable for investigating the structure-activity relationships and molecular dynamics of cyclosporins. Its unique structural attributes make Cyclosporin E an essential reagent in medicinal chemistry and biophysical research. -
Polystyrene Binding Peptide
HWGMWSY is a polystyrene binding peptide that specifically interacts with polystyrene plastic surfaces. Its primary mechanism involves non-specific adhesion to various polymer substrates, facilitating studies of peptide-material interactions. This peptide is valuable in research applications focused on material science, biomaterials development, and peptide-based sensor technologies. -
Dipeptide
H-Asn-Arg-OH is a dipeptide comprised of asparagine and arginine linked by a peptide bond. This compound is useful in the synthesis of polypeptides and can serve as a building block for developing biologically active peptides. Its applications extend to studies involving peptide interactions and function in various biological systems. -
Dipeptide
Lysyllysine trihydrochloride is a dipeptide consisting of two linked L-lysine residues. This compound serves as an effective enzyme cleavage linker, facilitating the connection of bioactive peptides in various applications. Additionally, it plays a crucial role as a component in the development of complex antibacterial agents, contributing to research in peptide chemistry and antimicrobial efficacy. -
Dipeptide
Lysyllysine (L-Lysyl-L-lysine) is a dipeptide formed by the linkage of two L-lysine amino acids. This compound serves as an effective enzyme cleavage linker for conjugating bioactive peptides, and it plays a role in the synthesis of more complex antibacterial agents. Its structural properties make it valuable in peptide chemistry and antimicrobial research applications. -
Peptide Nucleic Acid Monomer
Boc-PNA-T-OH is a thymine-containing peptide nucleic acid (PNA) monomer designed for solid-phase synthesis of PNA oligomers. This reagent facilitates the incorporation of thymine into PNA constructs, enabling researchers to explore gene recognition, regulation, and molecular diagnostics. Boc-PNA-T-OH is essential for applications in antisense technology, gene silencing, and the development of novel therapeutic agents. -
Peptide
H-Arg-Ser-Arg-OH is a peptide that serves as a versatile building block for synthesizing larger peptide constructs. This sequence incorporates di-leucine and RSRR motifs, making it valuable in studies related to peptide design and functionality. Its applications extend to the exploration of peptide interactions and the development of therapeutic agents in various biological contexts. -
Peptide Nucleic Acid Monomer
Fmoc-PNA-U-OH is a peptide nucleic acid monomer designed for the synthesis of peptide nucleic acids (PNAs). This compound exhibits specific binding affinity to adenine, enhanced resistance to enzymatic degradation, and robust hybridization capabilities. Fmoc-PNA-U-OH is valuable in various research applications, including gene diagnosis, molecular biology studies, and the development of antisense therapeutic strategies. -
Tripeptide
ACV Tripeptide is a pivotal tripeptide that serves as the initial intermediate in the biosynthetic pathway for penicillin and cephalosporin classes of β-lactam antibiotics in bacteria and fungi. It is synthesized nonribosomally by the enzyme ACV synthetase (ACVS), encoded by the pchAB gene. This compound plays a crucial role in the production of β-lactam antibiotics, making it essential for research focused on antibiotic biosynthesis and the development of new antimicrobial agents. -
Peptide Nucleic Acid Monomer
Fmoc-PNA-M(Boc)-OH is a peptide nucleic acid (PNA) monomer featuring Fmoc and Boc protecting groups. This compound is utilized in the synthesis of peptide nucleic acids, which serve as powerful tools in genetic research, diagnostics, and therapeutic applications. Its structural properties enable effective binding to complementary nucleic acid sequences, making it valuable for studies involving gene regulation, antisense strategies, and the development of nucleic acid-based therapeutics. -
Peptide Nucleic Acid Monomer
Boc-PNA-C(Z)-OH is a peptide nucleic acid monomer featuring a protected cytosine. The amino group is safeguarded by a tert-butoxycarbonyl (Boc) group, while the cytosine is protected by a benzyloxycarbonyl (Z) group. This compound is essential for the synthesis of peptide nucleic acids, facilitating research in areas such as gene regulation, antisense oligonucleotide design, and studies on nucleic acid interactions. -
Fibrinopeptide B
[Glu1]-Fibrinopeptide B is a bioactive fragment derived from the first 14 amino acid residues of fibrinopeptide B. It acts as a thrombin-derived proteolytic cleavage product of the fibrinogen B beta-chain, playing a significant role in stimulating human neutrophils, monocytes, and fibroblasts. This peptide is valuable in research applications related to inflammation, wound healing, and immunological responses. -
Peptide Nucleic Acid Monomer
Fmoc-PNA-G(Bhoc)-OH is a guanine-containing peptide nucleic acid monomer featuring Bhoc and Fmoc protective groups on the nucleobase and backbone, respectively. This compound is essential for the synthesis of peptide nucleic acids, enabling the design of nucleic acid analogs with enhanced stability and versatility. Its unique properties facilitate research in areas such as gene expression regulation, antisense oligonucleotide development, and targeted therapeutic approaches. -
Insoluble Peptide
4-(Hydroxymethyl)phenylacetic acid functions primarily as a key constituent in the synthesis of insoluble polypeptides. This compound can react with DEPBT and 4-acetylaniline to yield amide intermediates, facilitating various synthetic applications. Additionally, it is a metabolite arising from the microbial metabolism of flavonoids like quercetin. Notably, 4-(Hydroxymethyl)phenylacetic acid exhibits significant inhibitory effects on the oxidation of 6-mercaptopurine (6-MP), while demonstrating minimal impact on xanthine oxidation. -
Polypeptide
Cyclo(Arg-Gly-Asp-D-Tyr-ε-azido-Nle) is a cyclic polypeptide designed to target integrins, specifically facilitating cell adhesion and migration. Its structure incorporates an azido group, enabling conjugation chemistry for imaging or therapeutic applications. This compound is valuable in research focused on tumor targeting and angiogenesis, particularly in the synthesis of radiolabeled compounds such as [18F]FPyKYNE-c(RGDyK). -
Synthetic Peptide Analogue
IRI-514 is a synthetic peptide analogue of Thymopentin, functioning primarily in the modulation of neuroendocrine and behavioral responses to stress. This compound has been studied for its potential applications in understanding stress-related disorders and their effects on the neuroendocrine system. Researchers utilize IRI-514 to explore its effects on stress resilience and related physiological responses. -
Tripeptide
Nle-Arg-Phe-NH2 acetate is a tripeptide compound that functions as a bioactive modulator in various biochemical pathways. This compound exhibits significant biological activity, including the potential to influence cell signaling and interaction. Nle-Arg-Phe-NH2 acetate is primarily utilized in research focusing on peptide synthesis, receptor studies, and investigations into the modulation of physiological responses. -
Natural Product
Cycloleonuripeptide A is a natural product derived from motherwort, exhibiting a unique mechanism as a peptide compound. It has demonstrated potential anti-inflammatory and neuroprotective activities, making it a valuable candidate for research in pain management and neurodegenerative diseases. This compound is of interest for studies exploring the therapeutic benefits of natural products in pharmacological applications. -
Cyclic Peptide
Pseudostellarin E is a cyclic peptide characterized by a proline-rich structure, derived from the roots of Pseudostellaria heterophylla. This compound can be synthesized through the overexpression of its precursor gene prePhPE in the leaves of Nicotiana benthamiana. Pseudostellarin E is of interest for its potential biological activities and applications in research focusing on cyclic peptides and their therapeutic implications. -
Peptide
Cionin is a disulfotyrosyl hybrid peptide derived from cholecystokinin and gastrin. It primarily targets cholecystokinin receptors, mediating various physiological functions such as gastric motility and enzyme secretion. This compound is utilized in research applications examining gastrointestinal physiology and the endocrine system. Its unique structure allows for the exploration of receptor interactions and signaling pathways in peptide studies. -
peptide
(β-Asp28)-Exenatide is a peptide derivative produced through the degradation of exenatide, resulting from the formation and cleavage of asparagine. This compound serves as a valuable tool for studying the stability and metabolism of exenatide in various biological settings. Its implications in pharmacological research enhance the understanding of peptide therapeutics and their potential modifications. -
Synthetic Peptide
Acetyl angiotensinogen (1-14), human is a synthetic peptide that represents the N-terminal acetylated form of human angiotensinogen (1-14). This compound serves as an important tool for studying the renin-angiotensin system and its role in hypertension and cardiovascular diseases. It is valuable in research applications involving peptide interactions and receptor signaling pathways relevant to blood pressure regulation and fluid homeostasis. -
Monocyclic Octapeptide
Lyciumin C is a monocyclic octapeptide characterized by a unique C-N linkage between the nitrogen of tryptophan and the alpha carbon of glycine. This compound exhibits significant biological activity that supports its application in various pharmacological studies. Research indicates its potential roles in cell signaling and biological modulation, making it a valuable tool for investigations in peptide chemistry and therapeutic development. -
Amelogenin-derived Peptide
QP5 is an amelogenin-derived peptide that targets hydroxyapatite and demineralized tooth enamel surfaces. It transiently stabilizes amorphous calcium phosphate (ACP), regulates hydroxyapatite crystallization, and promotes remineralization of carious lesions. In rat caries models, QP5 has demonstrated significant efficacy in enhancing remineralization, making it valuable for research in oral diseases such as dental caries. -
Peptide
hCT(18-32) is a peptide derived from human calcitonin (hCT), targeting the calcitonin receptor. This peptide exhibits significant biological activity by influencing calcium homeostasis and bone metabolism. hCT(18-32) is frequently utilized in research focused on osteoporosis, bone density regulation, and related metabolic disorders. -
Pentapeptide
Cyclo(RGDfK(Mal)) is a cyclized pentapeptide that targets integrins, enhancing cell adhesion and infiltration of human pluripotent stem cells. This compound facilitates the development of 3D stem cell cultures, promoting effective expansion and maintenance of stem cell populations for research applications in regenerative medicine and tissue engineering. -
Structural Unit of the Antitubercular Peptide
(S)-3-Aminoazepan-2-one is a key structural unit of antitubercular peptides, functioning as the core scaffold for hexapeptide antibacterial agents. This compound exhibits significant biological activity against Mycobacterium tuberculosis, making it an important focus in tuberculosis research. Its role in the synthesis of novel antimicrobial agents contributes to the ongoing search for effective treatments against this infectious disease. -
α-helical Peptide
Annulatin (3-O-Methylmyricetin) is an α-helical peptide that primarily induces histamine release from mast cells, which plays a critical role in allergic responses and immune regulation. Additionally, it exhibits low hemolytic activity, making it potentially useful for various research applications in immunology and cellular biology. Its unique properties may facilitate studies involving mast cell function and the modulation of immune responses. -
Tripeptide
Copper tripeptide acetate (GHK-Cu acetate) targets various cellular pathways involved in skin regeneration. This tripeptide functions as a potent chemoattractant during wound healing, promoting the recruitment of inflammatory and endothelial cells. Research has demonstrated that Copper tripeptide acetate enhances the expression of messenger RNA for key structural components such as collagen, elastin, proteoglycans, and glycosaminoglycans in fibroblasts, thereby supporting tissue repair and regeneration. Its role as a natural modulator makes it an important reagent for studies in dermatological research and regenerative medicine. -
Acidic Polypeptide
Poly-L-aspartic acid is an acidic polypeptide known for its pH-dependent conformational changes. This compound is of significant interest in research focusing on pH-responsive structural transitions within biological systems. Its unique properties make it suitable for various applications in biochemistry and molecular biology. -
Chromogenic Peptide Substrate
Tos-Gly-Pro-Arg-ANBA-IPA is a chromogenic peptide substrate that targets proteolytic enzymes. This compound is designed for use in luminescence assays, enabling the detection and quantification of enzyme activity. It serves as a valuable tool in biochemical research, facilitating studies in enzymology and related fields. -
Peptide Derivative
Lys-Ala-βNA is a peptide derivative specifically designed as a substrate for Dipeptidyl peptidase III (DPP III). This compound plays a vital role in biochemical studies related to proteolysis and enzymatic activity. It is particularly useful for investigating the function and inhibition of DPP III in various biological systems. -
dipeptide
H-Gly-Arg-OH is a dipeptide composed of glycine and arginine. This compound serves as a substrate for various enzymes and plays a crucial role in cellular signaling pathways. H-Gly-Arg-OH is utilized in research applications focused on peptide synthesis, proteomics, and the study of protein interactions, contributing to the understanding of biological processes and potential therapeutic targets. -
Tridecapeptide
Type A Allatostatin I is a tridecapeptide with significant inhibitory effects on juvenile hormone synthesis in insects. This neuropeptide plays a crucial role in regulating various physiological processes, making it valuable for research into insect endocrinology and pest management strategies. Its application extends to studies on the hormonal regulation of development and behavior in insect species. -
Octapeptide
Allatostatin IV is an octapeptide that functions primarily as a neuropeptide involved in the modulation of juvenile hormone synthesis in insects. This compound exhibits key biological activities, including the inhibition of hormone production, making it valuable in entomological research. Allatostatin IV is instrumental in studies exploring insect development, physiology, and the regulatory mechanisms of neuropeptides. -
TFLLR-NH2 Negative Control Peptide
RLLFT-NH2 is a reversed peptide sequence designed as a negative control for TFLLR-NH2. This compound serves as a valuable tool for researchers studying peptide functionalities and interactions, providing a baseline for comparison in experimental assays. Its application is crucial in validating results and ensuring specificity in peptide-related studies, enhancing the reliability of experimental data. -
Peptide-Linked Tracer
Bevonescein (ALM-488) is a fluorescein-conjugated peptide that serves as a targeted tracer for the delivery of fluorescent moieties to nerve tissues following intravenous administration. It specifically binds to nerve-associated connective tissue, enabling real-time fluorescence imaging of peripheral nerves in living organisms as well as human ex vivo nerve samples. Suitable for visualizing both intact and degenerated nerves, Bevonescein exhibits an excitation/emission peak at 480/530 nm, making it valuable for neurobiological research and applications in nerve injury studies. -
Natriuretic Peptide
Atrial Natriuretic Peptide (1-28), human, porcine, Biotin-labeled targets the natriuretic peptide system and is crucial for regulating fluid homeostasis and blood pressure. This biotin-labeled peptide facilitates the study of cardiovascular physiology and pathophysiology. It holds potential for applications in cardiovascular disease research and the development of therapeutic interventions. -
Peptide
Biotin-myelin basic protein (94-102) is a peptide fragment that plays a critical role in myelination within the nervous system. It facilitates the adhesion of cytosolic surfaces in multilayered compact myelin and functions as a membrane actin-binding protein, potentially linking extracellular signaling to the cytoskeleton in oligodendrocytes. This peptide is valuable for research applications focused on myelination processes and oligodendrocyte function. -
Fluorescent Peptide Substrate
Suc-Leu-Tyr-AMC is a fluorescent peptide substrate designed specifically for µ-calpain and m-calpain enzymes. It is characterized by an excitation wavelength of 360 nm and an emission wavelength of 460 nm, making it suitable for fluorescence-based assays. This reagent serves as a vital tool in studying calpain activity and related biological processes. Its application in research can aid in the understanding of proteolytic cleavage and its implications in various physiological and pathological conditions. -
Fluorescent peptide substrate
H-GLU-AMC-OH is a fluorescent peptide substrate specifically designed for the assessment of aminopeptidase A enzyme activity. This compound enables sensitive quantification and observation of enzyme kinetics in various biological samples. Its application is beneficial in studies involving peptide metabolism and enzyme regulation, providing valuable insights into aminotransferase functions. -
Dansyl-Labeled Peptide
Dansyl-Gly-Cys-Val-Leu-Ser is a dansyl-labeled peptide primarily recognized for its ability to facilitate fluorescence studies of peptide interactions and conformational dynamics. This compound serves as a valuable tool in biochemical and biophysical research, enabling researchers to investigate protein folding, binding affinities, and proteolytic activity. Its fluorescent properties make it an ideal candidate for studies involving cellular uptake and localization. -
Bioactive Peptide
Z-Gly-Gly-Arg-AFC is a bioactive peptide that serves as a substrate for plasminogen activators. This compound possesses fluorescent properties, making it a valuable tool for studying enzyme activity in various biological assays. Applications include the investigation of plasminogen activation pathways and screening for potential therapeutic agents targeting these pathways.

