h lys trp lys oh

H-Lys-Trp-Lys-OH, a small molecule peptide, exhibits both antibacterial and antiviral activities.

H-Lys-Trp-Lys-OH acetate is a peptide with antibacterial and antiviral activities.

H-Lys-Trp-OH (KW) is an ACE inhibitory peptide with an IC50 of 7.8 μM [1].

Fmoc-Lys-OH hydrochloride is an alkyl-chain-based PROTAC linker and a non-cleavable ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs).

H-Glu(OMe)-OH, a glutamate derivative, is used in synthesizing various compounds and is associated with immune and metabolic processes in the body.

Ac-DL-Trp-OH (N-Acetyl-DL-tryptophan) was study for its possible anti- inflammatory and antinociceptive activities from the extraction of a Turkish plant, Salsola grandis.

H-Tyr(3-I)-OH (3-Iodo-L-tyrosine) is an inhibitor of tyrosine hydroxylase (Ki = 0.39 M) and an intermediate in the synthesis of thyroid hormones

Z-Lys-OH is a competitive inhibitor of papain, a lysine derivative.

H-Abu-OH (L-α-amino-n-Butyric acid) , also known as (S)-2-aminobutanoic acid, homoalanine, 2-AABA, ethylglycine, or L-butyrine, is a member of the class of compounds known as L-alpha-amino acids. H-Abu-OH is a non-proteogenic amino acid that can be found in the human kidney, in liver tissues, and in most biofluids or excreta (e.g. feces, breast milk, urine, and blood). Within the cell, H-Abu-OH is primarily located in the cytoplasm. H-Abu-OH is biosynthesized by transaminating oxobutyrate, a metabolite in isoleucine biosynthesis. As a non-proteogenic amino acid, H-Abu-OH can be used by nonribosomal peptide synthases.

Fmoc-Lys-OH (Nα-Fmoc-L-lysine) is a lysine derivative commonly utilized in the synthesis of active compounds.

H-Lys(Tfa)-OH is an inhibitor of L-lysine cyclodeaminase.

Fmoc-Lys(Boc)-OH (N-α-(Fmoc)-N-ε-(t-boc)-L-Lysine-OH) is a lysine derivative that acts as a reactive linker.

H-D-cis-Hyp-OH (D-allo-Hydroxyproline) belongs to the class of organic compounds known as proline and derivatives. Proline and derivatives are compounds containing proline or a derivative thereof resulting from a reaction of proline at the amino group or the carboxyl group, or from the replacement of any hydrogen of glycine by a heteroatom.

Lys-[Des-Arg9]Bradykinin acetate is an endogenous potent and highly selective bradykinin B1 receptor agonist (Ki values are 0.12 and > 30000 nM at human B1 and B2 receptors respectively). Hypotensive agent that reduces peripheral vascular resistance in vivo. 16-fold more potent than [Des-Arg9]-Bradykinin.

H-PRO-HIS-CYS-LYS-ARG-MET-OH acetate acts as antioxidant by reacting with active oxygen species such as superoxide and hydroxyl radicals.

Glu-urea-Lys is a molecular scaffold that targets PSMA and can be used as a prostate cancer imaging agent to study prostate-specific membrane antigens.

Leu-Tyr-Asp-Lys is a tetrapeptide compound that can be used to study metabolism-related diseases.

N-Formyl-Met-Leu-Phe-Lys (fMLFK) is a peptide that acts as a potent and selective agonist of FPR1, with EC50s of 3.5 nM for FPR1, 6.7 μM for FPR2, and 0.88 μM for FPR2-D2817.32G. This chemotactic peptide binds specifically to receptors on leukocyte membranes and its uptake can contribute to the quantitative assessment of neutrophils in localized inflammatory processes, independent of associated edema formation or microcirculatory compromise.

Lys-Bradykinin acetate is an endogenous bradykinin receptor agonist.

H-Ala-Ala-Tyr-OH acetate can be synthesized mutant peptides.

Lys-[Des-Arg9]Bradykinin,TFA is Endogenous potent and highly selective bradykinin B1 receptor agonist (Ki values are 0.12 and > 30000 nM at human B1 and B2 receptors respectively). Hypotensive agent that reduces peripheral vascular resistance in vivo. 16-fold more potent than [Des-Arg9]-Bradykinin.

H-Ile-Pro-Pro-OH acetate is a angiotensin-converting enzyme inhibitor (ACE) of milk-derived tripeptides.

N-Formyl-Nle-Leu-Phe-Nle-Tyr-Lys TFA (For-Nle-Leu-Phe-Nle-Tyr-Lys-OH (TFA)) (For-Nle-Leu-Phe-Nle-Tyr-Lys-OH TFA) is a formyl peptide receptor (FPR) agonist and a potent chemoattractant for human neutrophils, with its radioiodinated form retaining full biological activity.

Acetyl Ser-Asp-Lys-Pro is formed in bone marrow cells by enzymatic processing of thymosin β4. It inhibits the entry of pluripotent hemopoietic stem cells into S-phase of the cell cycle and protects against Ara-C lethality in mice.

H-Ser-His-OH acetate is an endogenous metabolite hydrolysis cleavage activity.

Lys-SMCC-DM1 (Lys-Nε-MCC-DM1) is an antibody-drug conjugate (ADC) targeting human epidermal growth factor receptor 2 (HER2). It contains the microtubule polymerization inhibitor DM1 as the active metabolite, which inhibits microtubule polymerization. It is commonly used in breast cancer research.

H-Phe-Phe-OH is a dipeptide composed of two phenylalanine (an essential amino acid and precursor to tyrosine) units linked together.

H-Gly-Pro-OH (Glycyl proline) is a dipeptide composed of glycine and proline, and is an end product of collagen metabolism

H-Gly-Gly-Pro-OH (Glycyl-glycyl-L-proline) is a dipeptide composed of glycine and proline, and is an end product of collagen metabolism that is further cleaved by prolidase.

Phe-Lys(Trt)-PAB is a cathepsin-cleavable linker used in the development of antibody-drug conjugates (ADCs), serving as a crucial component for releasing therapeutic agents within targeted cells.

Tyrosylalanine (H-Tyr-Ala-OH), a dipeptide comprising L-tyrosine and L-alanine, is referenced in studies [1] [2].

H-Val-Ala-OH (Valyl-alanine) is a dipeptide composed of L-Valine and L-Alanine residues, functioning as a metabolite.

H-Trp-NH2.HCl ((2S)-2-amino-3-(1H-indol-3-yl)propanamide hydrochloride) is an endogenous metabolite that has been detected in various biological fluids, e.g. Urine and blood.

H-ASP-PHE-OH (Aspartyl-phenylalanine) is used as pharmaceutical intermediates

H-Val-Pro-Pro-OH is an inhibitor of Angiotensin I converting enzyme (ACE)( IC50 : 9 μM).

H-Gly-Arg-Gly-Asp-Asn-Pro-OH (GRGDNP) is a integrin-ligand interactions inhibitor.

H-Phg(4-Cl)-OH is an amino acid derivative with extensive applications in life science research.

H-Phe(2-Me)-OH is a valuable organic compound for life sciences research, catalog number T66208.

Fmoc-Lys(Me)3-OH Chloride, with catalog number T65200 and CAS number 201004-29-7, is a valuable organic compound for life sciences research.

Lys-Phe-Glu-Arg-Gln promotes cytosolic protein degradation in serum-deprived human diploid fibroblasts [1].

Tripeptide 29 (HGly-Pro-Hyp-OH) is a bioactive peptide with oral efficacy against UVB-induced skin aging and is utilized as a cosmetic ingredient [1].

Boc-D-Trp(For)-OH, a derivative of the amino acid tryptophan with pharmacological properties including inhibition of growth hormone release, induction of sleep, and anti-inflammatory effects [1] [2], is synthesized via the ammonolysis of Boc-protected D-alanine followed by cyclization with ninhydrin to form the dipeptide.

Lys(CO-C3-p-I-Ph)-O-tBu, a pharmacokinetic modifier (PK modifier), enhances the pharmacokinetic properties of PSMA ligand molecules by increasing their residence time in plasma through improved binding to albumin and reducing absorption by the salivary glands, potentially extending the active compound's half-life. Moreover, Ac-PSMA-trillium is an effective PSMA-targeting compound for various biological applications when modified with different radioactive isotopes. When labeled with 111 In, it serves as a DOTA chelating agent and imaging agent. Alternatively, when labeled with 225 Ac, it acts as a Macropa chelator for targeted radionuclide therapy (TRT) in researching metastatic castration-resistant prostate cancer (mCRPC) [1] [2].

H-D-Thr(tBu)-OH is a useful organic compound for research in life sciences [Catalog No.: T67086, CAS No.: 201274-81-9].

Fmoc-L-Lys(Dde)-OH, with catalog number T66707 and CAS number 150629-67-7, is a valuable organic compound for life sciences research.

Fmoc-Lys(ivDde)-OH is a useful organic compound for research related to life sciences. The catalog number is T66732 and the CAS number is 204777-78-6.

H-Lys(Boc)-OH is a useful organic compound for research related to life sciences. The catalog number is T65877 and the CAS number is 2418-95-3.

Lys-Gln-Ala-Gly-Asp-Val (KQAGDV), the six carboxyl-terminal amino acids of the fibrinogen γ-chain, serves as a potent cell adhesion peptide via the α2bβ3 integrin and a strong adhesion ligand for smooth muscle cells (SMCs) [1] [2].