Amino Acids (AA)

<p>Met-Thr-OH is a peptide binding inhibitor that is used as a research tool for determining the role of metalloproteins in vivo. Methionine aminopeptidase (MetAP) is an enzyme that cleaves methionine from protein and peptides and has been shown to play a vital role in cancer progression. MetAP has been shown to be inhibited by Met-Thr-OH, which binds to the enzyme's active site and blocks its activity. The inhibition of MetAP limits the production of proteins involved in cell growth and proliferation, leading to reductions in tumor size. This inhibition may also be due to the inhibition of other functional groups such as phosphorylation, dephosphorylation, or nitrosylation.</p>

<p>Please enquire for more information about Boc-Asn-o-nitrophenyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about DABCYL-(Asn670,Leu671)-Amyloid b/A4 Protein Precursor770 (661-675)-EDANS ammonium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (Leu31,Pro34)-Neuropeptide Y (13-36) (human, rat) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Cyclo(-D-His-Pro) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Fmoc-Ile-Ser(Psi(Me ,Me)pro)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Ala-Phe-Ala-OH is a peptidomimetic that has been shown to have hydrogen bonding interactions with caco-2 cells. It also has the ability to form micelles and x-ray diffraction data show that the molecule has a right handed helical conformation. This compound was synthesized by reacting H-Ala-Phe with H-Gly-Gly in an amino acid condensation reaction, followed by hydrolysis of the amide bonds. The bioisosteres for this compound are tripeptides, which are amino acids linked by peptide bonds. The interaction of this compound with caco-2 cells is thought to be due to the hydrogen bonding interactions between this molecule and the hydroxyl groups on the cell surface.</p>

<p>Fmoc-L-Lys(Alloc)-OH is a peptide that consists of an amino acid sequence that is a variant of the human insulin molecule. The peptide has been modified to incorporate a pegyl group, which increases the serum stability of this drug and prevents enzymatic degradation. This compound has been tested in vitro by binding to nuclear DNA and inhibiting receptor binding. Fmoc-L-Lys(Alloc)-OH has also shown anticancer effects in vivo with tumor xenografts and apoptosis protein expression in human serum, as well as an increase in serine protease activity.</p>

<p>Oxytocin is a hormone that is released from the pituitary gland. It has been shown to have a variety of biological effects, including stimulation of uterine contractions, breast milk production, and social behaviors such as bonding and sexual behavior. Oxytocin has also been shown to regulate the release of gamma-aminobutyric acid (GABA) in the brain. This effect may be due to oxytocin's ability to stimulate GABA receptors. In addition, oxytocin can inhibit lipolysis by inhibiting the release of fatty acids from adipose tissue. The effect on fatty acid release is due to an inhibition of phosphodiesterase activity. Oxytocin can also cause membrane hyperpolarization by increasing potassium ion flow through channels in the cell membrane. Oxytocin has also been shown to act as a growth factor for certain types of cells, such as smooth muscle cells and osteoblasts.</p>

<p>Please enquire for more information about H-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-Leu-Val-Ile-His-Asn-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Lys(isopropyl)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Activated Protein C (390-404) (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>The peptide Ac-Phe-Glu-Trp-Thr-Pro-Gly-Trp-Tyr-Gln-L-azetidine-2-carbonyl-Tyr-Ala-Leu-Pro-Leu (AFGP) is a small molecule that has been shown to be effective in the prophylaxis and treatment of infectious diseases. AFGP is used as an excipient in intravenous solutions, such as antibiotics, vaccines, and other injectable drugs. It also functions as a diluent for lyophilized products. In addition to its use in the pharmaceutical industry, AFGP is also used as an excipient for vaccine preparations and other injectable drugs. AFGP has been shown to reduce the symptoms of inflammatory diseases, such as asthma and rheumatoid arthritis. This peptide has also been shown to have antiinflammatory and antifibrotic properties.</p>

<p>Please enquire for more information about (Thr28, Nle 31)-Cholecystokinin-33 (25-33) (sulfated) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Nectofibrin Hexapeptide is a peptide that interacts with the antigen-binding site of an antibody. It has been shown to be able to bind to the ovary cells of rats and may have diagnostic value in autoimmune diseases such as idiopathic thrombocytopenic purpura. The sequence of this molecule is Arg-Gly-Asp, which shows complementarity with the receptor binding site on the ovary cells. This peptide could be used for immunotherapy or diagnostics in autoimmune diseases.</p>

<p>Please enquire for more information about (Ala11,D-Leu15)-Orexin B (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Hymenistatin I is a cyclic peptide that is synthesized from the natural amino acid L-proline. It has been shown to inhibit tumor growth and is used in the treatment of bladder cancer. The synthesis of Hymenistatin I begins with the protection of proline as an N-tert-butyloxycarbonyl derivative, followed by a sequence of coupling reactions. This synthetic process involves the use of a linker, such as tetrazole or succinimidyl ester, for example. The final product can then be purified by HPLC analysis. Hymenistatin I inhibits calcineurin inhibitor, which are immunosuppressive agents that are used to treat lymphocytic leukemia and other autoimmune diseases.</p>

<p>Furin inhibitor II is a small molecule that inhibits the activity of furin, which is an enzyme used in the processing of growth factor-β1. Furin inhibitor II binds to human receptors and blocks their binding to the surface glycoprotein on cancer cells. Furin inhibitor II also has physiological activities, such as reducing inflammation, inhibiting viral replication, and inhibiting the growth of bacteria. Furin inhibitor II may be useful for treating cancer or infectious diseases.</p>

<p>Please enquire for more information about FMOC-D-CYS(TRT)-WANG RESIN - 200-400 mesh including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Dnp-Pro-Leu-Gly-Leu-Trp-Ala-D-Arg-NH2 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Ac-Arg-Ser-Leu-Lys-AMC trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Suc-Ala-Gln-Pro-Phe-pNA is a peptide that is composed of 18 amino acids. This peptide has a molecular weight of 2,812. It has been shown to have biochemical activity in vitro and in vivo. Suc-Ala-Gln-Pro-Phe-pNA is an erythropoietin receptor agonist that has shown homologous sequences with tyrosine kinase receptors and collagen. This protein was expressed in the endoplasmic reticulum, cytosol, and mitochondria of cells. The enzyme phosphatase hydrolyzed the peptide during incubation with calf thymus DNA.</p>

<p>Suc-Ala-Ala-Phe-pNA is a peptide that is being studied for its potential to act as an anticancer agent. It inhibits the growth of tumor cells by binding to the neurokinin receptor and thereby blocking the production of substances such as epidermal growth factor, which promote tumor growth. Suc-Ala-Ala-Phe-pNA also has been shown to inhibit the activity of enzymes involved in glucocorticoid receptors, which are proteins that play a key role in regulating the immune response. This peptide also has been shown to be active against mouse skin cells and human prostate cancer cells. In addition, it is believed that this peptide may be useful in gene therapy because it can induce apoptosis in tumor cells without affecting normal tissue.</p>

<p>Please enquire for more information about Boc-4-phosphono-Phe(Et)2-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-D-Leu-pNA including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (1S,2R)-Fmoc-aminocyclohexane carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-Ala-Glu-OH is an amino acid with a glutamate residue. It is a synthetic amino acid that has been shown to have excitotoxic effects in the brain. The mechanism of action is thought to involve the activation of ionotropic glutamate receptors and the inhibition of voltage-gated potassium channels, leading to neuronal cell death. This compound has been found to be a sweetener in biochemical reactions. Z-Ala-Glu-OH was shown to undergo proteolytic degradation, which may be due to aminopeptidases present in the gut or enzyme preparations used during digestion. This amino acid was also shown to have neurodegenerative properties when given orally to mealworms, as well as profiles that are similar to those found in humans with neurodegenerative diseases such as Alzheimer's disease and amyotrophic lateral sclerosis.</p>

<p>Annexin A1 (1-11) is a peptide that is part of the annexin family. It is involved in the degranulation of cells and inhibits inflammation by inhibiting the production of pro-inflammatory cytokines. Annexin A1 (1-11) has been shown to be an anti-inflammatory compound as it binds to phospholipids on the surface of neutrophils, leading to inhibition of their chemotaxis and phagocytosis. This peptide also interacts with other annexins and prevents apoptosis by blocking caspase activity. Finally, it has been found that annexin A1 (1-11) can promote the healing of wounds in mice by accelerating reepithelialization and reducing scar formation. The concentration required for these effects are nanomolar concentrations.</p>

<p>Ac-Gly-Pro-AFC is a dipeptidyl peptidase inhibitor that inhibits the action of protein-degrading enzymes called peptidases. Ac-Gly-Pro-AFC has been shown to be effective in treating diabetes by inhibiting the activity of fibroblast activation protein, which is involved in the development of diabetes. Ac-Gly-Pro-AFC also has an inhibitory effect on the enzyme connect, which is involved in cellular proliferation and differentiation. Clinical trials have been conducted to evaluate the efficacy of this drug for treatment of diabetic nephropathy with promising results. Ac-Gly-Pro-AFC has also been shown to have a beneficial effect on collagen synthesis and inhibition of proinflammatory cytokine release from activated macrophages.</p>

<p>Please enquire for more information about (Des-Pyr 1,Des-Gly10,D-Leu6,Pro-NHEt 9)-LHRH trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Asp-Asp-Asp-OH is a peptide that has been shown to disrupt the cytosol and cause apoptosis. It can also induce proteolytic maturation and modulate autocatalytic functions. H-Asp-Asp-Asp-OH induces apoptosis by activating caspase 9 and caspase 3, which cleaves poly (ADP ribose) polymerase (PARP). This leads to DNA fragmentation, chromatin condensation, nuclear fragmentation, cell shrinkage, membrane blebbing, and nuclear pyknosis. H-Asp-Asp-Asp-OH binds to the regulatory domain of caspase 9 and prevents it from being activated. The peptide also activates caspase 8 by binding to its regulatory domain, which then activates caspases 3 and 7. H-Asp-Asp-Asp-OH also stimulates the release of granzyme B from cytot</p>

<p>4-Fluoro-2-methoxyaniline is an inhibitor of tyrosine kinase. It is a molecule that has been isolated from the ground leaves of erythroxylon coca and is used in the treatment of diabetes mellitus. 4-Fluoro-2-methoxyaniline inhibits the growth factor receptor, epidermal growth factor (EGF), and its receptor, EGF receptor. This inhibition leads to decreased proliferation of epidermal cells and decreased insulin production by pancreatic beta cells. 4-Fluoro-2-methoxyaniline also has antioxidant properties, which may be due to its ability to scavenge free radicals.</p>

<p>Please enquire for more information about H-Pro-Leu-Gly-Gly-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Leu-Gly-Gly-OH is a protease enzyme that belongs to the family of hydrolases. It has been shown to have proteolytic activity with casein and protein synthesis with pancreatic enzymes. The kinetic data for this enzyme were determined by measuring the rate of hydrolysis at different pH levels. The optimum pH for this enzyme is 6.0, with a maximum activity at pH 7.5 and an inhibition at pH 4.0. This enzyme can be found in either the free form or as an integral membrane protein in lysosomes, where it exhibits high affinity for hydrogen bonds and low affinity for ionic bonds. H-Leu-Gly-Gly-OH is used in analytical methods such as chromatography and spectrophotometry to identify proteins in biological samples.END&gt;</p>

<p>Please enquire for more information about [2,6-Dimethyl-4-(3-[2-(Z-amino)-ethylcarbamoyl]-propoxy)-benzenesulfonyl]-Dap (Boc)-OMe including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Bz-D-Arg-pNA·HCl is a protease inhibitor that has been shown to inhibit the proteolytic activity of soybean trypsin. It also inhibits the enzyme activities of ester hydrolysis and polymerase chain reaction, as well as being reactive to other enzymes. Bz-D-Arg-pNA·HCl has been shown to be an analog of Bz-D-Arg-pNA, which is a proteolytic inhibitor of protein synthesis in vitro. This compound has been shown to have a pH optimum for activity at around pH 7.6 and exhibits protease activity in physiological conditions. The physiological function of this molecule is not yet known.</p>

<p>H-D-Arg-Gly-Asp-Trp-OH is a cyclic peptide that has been shown to bind to staphylococcal cells, inhibiting their growth. The peptide was found to have proton binding and membrane interactions. This drug has shown efficacy in biological samples such as collagen and fibrinogen. H-D-Arg-Gly-Asp-Trp-OH also can be activated by a disulfide bond. It has been found to bind with monoclonal antibodies and model systems.</p>

<p>Please enquire for more information about H-Pro-His-Pro-Phe-His-Leu-Phe-Val-Tyr-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about N-2-Ethoxyethyl-Val-Ala-anilide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Kisspeptin-54 (27-54) (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Trifluoroacetate salt</p>

<p>Please enquire for more information about N-alpha-Boc-Nbeta-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-D-2,3-diaminopropionic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ac-Glu-Ser-Met-Asp-aldehyde is a molecule that is naturally produced by the human body. It has been shown to be an endogenous caspase activator, which may lead to apoptosis. Ac-Glu-Ser-Met-Asp-aldehyde can also bind to cholesterol and influence its synthesis, thus affecting the production of other proteins. This molecule has a protease activity and can cleave peptides at specific sites. The sequences of this molecule have been determined and it has been found that these sequences are similar to those found in other proteases such as serine proteases.</p>

<p>8-Methylnonanal is a fatty acid that has been hydrogenated and sulfonated. It is an unsaturated, straight chain, alpha-methylene-containing molecule with the chemical formula CH3(CH2)4CH=CH(CH2)3COOH. 8-Methylnonanal can be used as an additive in polyolefin production to improve processability. 8-Methylnonanal is used as a reaction system for the synthesis of monomers and polymers. In addition, it reacts with sulfuric acid to produce sulfuric acid esters and alkyl sulfonic acids. This chemical also reacts with fatty acids to form various products such as fatty acid methyl esters (FAMEs).</p>

<p>Fmoc-Gly-Thr(Psi(Me,Me)pro)-OH is a high-performance liquid chromatography (HPLC) phase. It is used for the separation of peptides and amino acids. Fmoc-Gly-Thr(Psi(Me,Me)pro)-OH is used in industrial applications to reduce pressure, as well as in the production of large quantities of liquid chromatography.</p>

<p>Cyclo(-Arg-Ala-Asp-D-Phe-Lys) trifluoroacetate salt is a peptidomimetic that inhibits the growth of tumor cells by inhibiting angiogenesis, which is the formation of new blood vessels. It has been shown to effectively inhibit the proliferation of endothelial cells and decrease tumor vasculature in human ovarian carcinoma. Cyclo(-Arg-Ala-Asp-D-Phe-Lys) trifluoroacetate salt binds to cyclic peptides in the body and prevents them from being broken down by peptidases. This increases their uptake into cancer cells and inhibits angiogenesis, leading to a decrease in tumor size and number.</p>

<p>Hippuryl-His-Leu-OH is a peptide that inhibits the activity of angiotensin converting enzyme (ACE) at a concentration of 50 μM. It has been shown to inhibit cyclase and other enzymes in vitro. The binding of this compound to ACE prevents the conversion of angiotensin I to angiotensin II, which is a potent vasoconstrictor. Hippuryl-His-Leu-OH also has inhibitory properties against atrial natriuretic peptide (ANP), and can be used as an antihypertensive agent. This drug has been shown to have growth factor β1 activities, and can be used for the treatment of cardiac diseases such as myocardial infarction. Structural analysis shows that this drug binds to the active site of ACE, inhibiting its activity by blocking access to substrate or by altering substrate specificity.</p>

<p>Please enquire for more information about Neuropeptide W-30 (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Fmoc-D-Cys(Mtt)-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Asn-bNA including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Hydroxyl-Tyr-Tyr-OH is a fatty acid that belongs to the group of dietary lipids. It has been shown to have antioxidative properties and can be used in the treatment of pancreatic cancer. Hydroxyl-Tyr-Tyr-OH has also been shown to be an important regulatory molecule that controls certain cellular processes, including cell growth and differentiation. It may be involved in some disease processes, such as cancer and vasoactive intestinal peptide secretion, as well as being a reaction product of other molecules. Hydroxyl-Tyr-Tyr-OH can be found in urine samples after oral ingestion.</p>

<p>Please enquire for more information about Ac-Ala-Gln-Ala-pNA including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Caerulein (desulfated) Pyr-Gln-Asp-Tyr-Thr-Gly-Trp-Met-Asp-Phe-NH2 is a decapeptide that is found in the Australian frog, Caerulea. It has been shown to be a potent extractant of ionic materials and can be used in the separation of proteins by ion exchange chromatography. The sequence is as follows: Caerulein (desulfated) Pyr-Gln-Asp-Tyr-Thr-Gly-Trp-Met-Asp-Phe. It has an acid composition of Cys, Asp, Tyr, Glu, Pro, Gly, Phe and Met. The amino acid composition is Pro, Ala, Gly, Val, Gln and Leu. Caerulein (desulfated) Pyr-Gln has been shown to have antihypertensive effects due to</p>

<p>Intermediate in the synthesis of lenvatinib</p>

<p>Please enquire for more information about Z-Trp-NH2 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Boc-(Dmmb(Trt))Gly-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about LQEQ-19 (mouse, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Phenyl 1H-5-(2'-hydroxyphenyl)pyrazole (1PHPP) is a fine chemical that has been used in research and as a reagent. It is also a useful building block for the synthesis of other compounds. 1PHPP can be used to prepare complex compounds with versatile building blocks or scaffolds, which can serve as reaction components in organic syntheses. This compound has been shown to react with various functional groups.</p>

<p>Growth hormone-releasing factor (GRF) is a peptide fragment of amino acids 1–2 from GHRH (growth hormone-releasing hormone). This 1-29 region is the shortest fully functional fragment of GHRH. GRF is also known as sermorelin. Sermorelin binds to the growth hormone-releasing hormone receptor (GHRH-R), and acts as a surrogate for GHRH, causing growth hormone secretion.human: H-YADAIFTNSYRKVLGQLSARKLLQDIMSR-NH2rat:        H-HADAIFTSSYRR I LGQLYARKLLHEIMNR-NH2</p>

<p>Please enquire for more information about (Phe2, Nle 4)-ACTH (1-24) (human, bovine, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Phenyl-piperidine is a nitro compound that has been shown to be toxic for the kidneys and nervous system. 4-Phenyl-piperidine has been shown to inhibit dopamine uptake in the striatum and locomotor activity in rats. It also inhibits the hydrolysis of hydrochloric acid, which produces hydrogen ion (H+) ions, resulting in an acidic environment. The chemical structures of 4-phenyl-piperidine are similar to those of tricyclic antidepressants drugs, such as amitriptyline and imipramine, with a phenyl ring attached to an amine group. This drug is used as a pharmaceutical preparation for treating depression by inhibiting the reuptake of serotonin and norepinephrine, which are neurotransmitters that affect mood.</p>

<p>Suc-Ala-Ala-Val-pNA (Suc-AAV-pNA) is a specific substrate for human and rat neutrophil elastases.</p>

<p>N-Methyl-1,2-phenylenediamine dihydrochloride (NMP) is a synthetic compound that is used as the precursor to various pharmaceuticals, such as the antihypertensive drug clonidine. NMP can be synthesized from benzene and ammonia or phenylmagnesium bromide. It is carcinogenic in animals and humans, and has been shown to cause DNA damage and cell apoptosis. The chemical has a high potential for nitrosation reactions when exposed to nitrites. This reaction produces nitric oxide, which is cytotoxic and can lead to liver cancer in rats.<br>The synthesis of NMP generates impurities such as methanol solvent, sodium sulfide, and hydrogen chloride gas. These impurities are often found in recycled NMP due to incomplete removal during processing.</p>

<p>Please enquire for more information about Stresscopin (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about PAR-2 (1-6) amide (human) (scrambled) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Fmoc-Pro-Phe-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Acetyl-ACTH (7-24) (human, bovine, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (Lauroyl-Cys-Tyr-Gly(-Glu-Glu-Asn-Val)6-OH)2 (Disulfide bond) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about GRPP (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-D-Phe-D-Phe-OH is a polypeptide that contains 24 amino acids. It is synthesized by the filamentous fungus, Aspergillus niger, and has been found to be an optimal substrate for aminopeptidase. H-D-Phe-D-Phe-OH has also been shown to be a homolog of the halophilic enzyme from Halobacterium salinarum.</p>

<p>Please enquire for more information about (D-Ala3)-Dynorphin A (1-11) amide trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Fmoc-epsilon-aminocaproic acid-Wang resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Lys-Val-OH hydrochloride salt is a polymerase chain that has been synthesized from the amino acid lysine. It is an optical sensor that can be used to detect and quantify proteins. H-Lys-Val-OH hydrochloride salt binds to DNA in the cell nucleus and is sensitive to the concentration of adenosine triphosphate (ATP) in cells. This nucleotide plays an important role in cellular energy production. The binding constants for H-Lys-Val-OH hydrochloride salt are determined from the fluorescence emission spectrum, which changes with different concentrations of ATP. The method can be used to measure glomerular filtration rates and can be used as a low energy radiation source for cervical cancer treatment.</p>

<p>Please enquire for more information about (Ala92)-Peptide 6 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>BAM-3200 is a small molecule with the chemical formula CHFOC(O)NHCHCOOH. It is a potent and selective agonist of the TrkB receptor, which binds to brain-derived neurotrophic factor (BDNF). BAM-3200 has been shown to have anti-cancer activity in mouse tumor models, as well as increased locomotor activity and improved memory retention in mice. The biological function of BAM-3200 is not yet known. Structural analysis shows that it binds to the hydroxyl group on mammalian tissue receptors, which may be due to its basic protein structure. BAM-3200 also has been shown to hydrolyze enzymes such as esterases, glucuronidases, or glutathione reductase. This agent has been shown to be selectively active against cancer cells by binding to their acidic surface structures and altering their acidity.</p>

<p>5-Amino-2-methoxyisonicotinic acid is a carboxylic acid that is used in the synthesis of aminopyridines. The compound can be synthesized from formamidine acetate and diethyl dicarbonate. This process involves lithiation, followed by addition of an amine and finally conversion to the desired product with formamidine acetate. 5-Amino-2-methoxyisonicotinic acid can also be synthesized from formamide and diethyl ether. 5-Amino-2-methoxyisonicotinic acid is an analog of 2,4,6-trimethylaniline and has been shown to have similar properties to this compound, including strong basicity.</p>

<p>Please enquire for more information about Z-Gly-Pro-Phe-Pro-Leu-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about HIV-1 rev Protein (34-50) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Ala-Ala-Pro-Ala-OH is a tetrapeptide that inhibits elastase, an enzyme that breaks down elastin. This compound has been shown to have anti-elastolytic activity in vitro and in vivo. H-Ala-Ala-Pro-Ala-OH was administered intraperitoneally to hamsters with induced emphysema, resulting in a decrease of elastin abnormalities and improvement of the ultrastructure of the lungs. It also improves pancreatic morphology and function in porcine pancreatitis models.</p>

<p>Please enquire for more information about 2-(Boc-Aminomethyl)pyrrolidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Z-Glu-Tyr-OH is a disulfide bond with a cavity. It is soluble in acidic solutions and has a cationic surface. Z-Glu-Tyr-OH is an enzyme inhibitor that blocks the activity of α subunit of protein kinase C, which is involved in intracellular signal transduction pathways. The inhibition of this enzyme may lead to apoptosis, or programmed cell death. Z-Glu-Tyr-OH also inhibits fatty acid synthesis by blocking the activity of hydroxylase enzymes, such as 3β-hydroxysteroid dehydrogenase and 17α-hydroxylase. This compound has been shown to inhibit indole-3-propionic acid production by inhibiting the kinetic and sephadex g-100 activities of the enzyme indoleamine 2,3 dioxygenase.</p>

<p>Please enquire for more information about JKC-301 Cyclo(-D-Asp-Pro-D-Ile-Leu-D-Trp) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about H-Gly-2-chlorotrityl resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Gly-Gly-NH2·HCl is a nanosized antibiotic that has been shown to have antibacterial properties. It is activated by long-chain inorganic acids, such as hydrochloric acid, and organic solvents, such as acetone. This compound has an amide group that makes it acidic. The hydrocarbon chain of this molecule may be either short or long.</p>

<p>Please enquire for more information about Boc-Glu-OFm including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Methoxy-2,3,4,9-tetrahydro-1H-beta-carbolin-1-one is a β-carboline alkaloid that is structurally related to harmaline and tetrahydroharmine. It has been shown to have antidepressant activity in animals. 6-Methoxy-2,3,4,9-tetrahydro-1H-beta-carbolin-1-one was analyzed by GC/MS and found to be present in the leaves of plants from the genus Tetraclinis. 6MHBC was also identified as a metabolite of diazepam in rat urine after administration of a single oral dose of 10 mg/kg diazepam. The observed β carboline metabolite was determined to be 6MHBC.</p>

<p>H-Trp-Ala-OH is a synthetic amino acid that has been used as an analytical reagent. The compound has shown antihypertensive activity in animal studies and can be used to prepare samples for chromatography or spectrophotometry. H-Trp-Ala-OH is soluble in water, but not in ethanol or ether. It has a neutral pH, and the carbonyl group makes it spontaneously fluorescent.</p>

<p>Please enquire for more information about Atrial Natriuretic Factor (3-28) (human, bovine, porcine) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Pyr-Trp-OH is a derivative of tryptophan. It has been found to be active in the brain and its metabolites have been shown to inhibit superoxide production by inhibiting the activity of hydroxylase and dismutase. Pyr-Trp-OH also inhibits serotonin synthesis, which may contribute to its antidepressant properties. Pyr-Trp-OH is an inhibitor of indoleamine 2,3 dioxygenase, an enzyme that converts tryptophan into kynurenine. This process generates hydrogen peroxide, which can lead to cell death. The conversion of tryptophan into serotonin also produces hydrogen peroxide, so it is possible that Pyr-Trp-OH may have antioxidant effects as well as antidepressant effects.</p>

<p>Please enquire for more information about [4-(1-Cyano-1-methylethyl)phenyl]boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>H-Glu-Glu-OH is an organic acid that has proteolytic and gene product properties. It is a hyperactive compound that can be used as a sample preparation reagent for the detection of glutamic acid in proteins. H-Glu-Glu-OH inhibits protein synthesis by binding to ribosomes, which are responsible for the production of proteins in the cell, and prevents their function. Magnetic resonance spectroscopy has been used to investigate the uptake of H-Glu-Glu-OH into mammalian cells and ovarian follicles.</p>

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