fmoc-tyr(tbu)-ser(psi(me,me)pro)-oh

Fmoc-Tyr(tBu)-Ser(psi(Me,Me)pro)-OH is a dipeptide.

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

Ac-Pro-Gly-Pro-OH is an acetyl-modified tripeptide compound that acts as a CXCR2 agonist.Ac-Pro-Gly-Pro-OH exhibits bactericidal and anti-inflammatory activity, inhibits apoptosis of immune cells, and suppresses the production of pro-inflammatory cytokines.Ac-Pro-Gly-Pro-OH has been used in the study of sepsis and inflammation in the lungs.

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

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

Fmoc-Gly-Ser(psi(Me,Me)pro)-OH acetate is a dipeptide.

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

NF(N-Me)GA(N-Me)IL is a biologically active peptide, representing a modified segment (amino acids 22 to 27) of the human islet amyloid polypeptide (hIAPP) sequence NFGAIL. This modification includes N-methylations at G24 and I26, transforming the amyloidogenic and cytotoxic nature of the original sequence into a non-amyloidogenic and non-cytotoxic variant. Moreover, the peptide maintains the ability to bind with high affinity to full-length hIAPP, effectively inhibiting its fibril formation.

Cys-Asp-Pro-Gly-Tyr-Ile-Gly-Ser-Arg-NH2 is a linear peptide derived from the laminin B1 chain, which disrupts tumor cell adherence and invasion into the basement membrane and exhibits anti-angiogenic properties [1].

H-Ile-Pro-Pro-OH, a milk-derived peptide, inhibits angiotensin-converting enzyme (ACE)[1] with an IC50 of 5 μM.

Fmoc-Cys(STmp)-OH is a cysteine derivative that can be used in the synthesis of bicyclic and linear peptides.

Fmoc-Arg-OH (Fmoc-L-Arginine) (Fmoc-L-Arginine) is a used in peptide synthesis.

FITC-Ahx-Gly-Arg-Gly-Asp-Ser-Pro, also known as FITC-linked GRGDSP, is a fluorescent peptide with integrin inhibitory properties. This compound impedes tumor cell adherence to endothelial blood vessel cells, potentially restricting metastasis [1].

Fmoc-N-Me-Phe-OH (Fmoc-N-methyl-L-phenylalanine) is a Malaria Parasite inhibitor.

Fmoc-Phe(4-CN)-OH is an N-Fmoc protected phenylalanine derivative and potentially useful synthetic intermediate

Fmoc-N-Me-Ala-OH is available for the peptide-coupling reaction.

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

FMoc-Arg(Tos)-OH is a synthetic amino acid used in peptide synthesis, biochemistry and molecular biology. It is a Fmoc-protected amino acid used as an intermediate in peptide and protein synthesis for solid-phase peptide synthesis.

Fmoc-N-Me-Leu-OH is available for the peptide-coupling reaction.

Ser-parafluoroPhe-Aad-Leu-Arg-Asn-Pro-NH2 is a biologically active peptide. Structure-activity studies of the thrombin receptor-tethered ligand SFLLRNP underscored the pivotal role of the Phe-2-phenyl group in receptor recognition, while substitution with para-fluorophenylalanine [(p-F)Phe] augmented its activity.

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].

Fmoc-Thr(GalNAc(Ac)3-β-D)-OH impedes the proliferation of cancer cells by selectively interacting with complex oncogenic pathways and enhancing the immune response [1].

Fmoc-Gly-Thr(psi(Me,Me)pro)-OH is a polypeptide composed of two amino acids.

SNNF(N-Me)GA(N-Me)IL is a biologically active peptide comprising double N-methylated derivatives of a partial IAPP sequence known to be amyloidogenic and cytotoxic.

SNNF(N-Me)GA(N-Me)ILSS is a biologically active peptide comprising double N-methylated derivatives of an amyloidogenic and cytotoxic partial IAPP sequence.

F(N-Me)GA(N-Me)IL is a bioactive peptide whose double N-methylated derivatives of the partial IAPP sequence lack β-sheet structure, amyloidogenicity, and cytotoxicity. These derivatives can interact with the native sequences to inhibit amyloid formation.

H-Pro-Gly-Pro-OH, a collagen-derived matrikine, traditionally acts as a neutrophil chemoattractant, guiding these cells to target locations to orchestrate localized repair responses. Additionally, this compound initiates the transcription of neurotrophins and their receptor genes following cerebral ischemia [1] [2].

H-Pro-Pro-Gln-OH is an oligopeptide that exhibits potent inhibitory activity against dipeptidyl peptidase-IV (DPP-IV) [1].

Cys-Gly-Tyr-Gly-Pro-Lys-Lys-Lys-Arg-Lys-Val-Gly-Gly is a 13-mer synthetic peptide with a sequence homologous to seven amino acids of the SV40 T antigen, known for its capability to induce nuclear transport [1].

Fmoc-B-HoPhe-OH is an amino acid derivative and has a wide range of applications in life science related research.

Fmoc-N-Me-Ser(tBu)-OH is a useful organic compound for research related to life sciences. The catalog number is T65832 and the CAS number is 197632-77-2.

H-Ser(tBu)-OH is an amino acid derivative and has a wide range of applications in life science related research.

Fmoc-Glu(OtBu)-Ser(psi(Me,Me)pro)-OH is a dipeptide.

(d(CH2)51,Tyr(Me)2, Orn8)-Oxytocin (OVT) is an antagonist of the oxytocin receptor that finds application in the study of neurological diseases [1].

Cyclo(Gly-Arg-Gly-Asp-Ser-Pro) (c(GRGDSP)) is an RGD-containing inhibitory peptide and a synthetic α5β1 integrin ligand. It competitively inhibits the binding of invasin (Inv) to α5β1 integrin on Caco-2 cells [1].

Fmoc-Lys(Ac)-OH is a useful organic compound for research related to life sciences. The catalog number is T65778 and the CAS number is 159766-56-0.

Z-N-Me-Leu-OH is a useful organic compound for research related to life sciences. The catalog number is T66764 and the CAS number is 33099-08-0.

Fmoc-Cpg-OH is an amino acid derivative and has a wide range of applications in life science related research.

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

H-Tyr(tBu)-OH is a useful organic compound for research related to life sciences. The catalog number is T65411 and the CAS number is 18822-59-8.

Fmoc-Phe(3-Cl)-OH is an amino acid derivative and has a wide range of applications in life science related research.

Fmoc-Asn(Trt)-Ser(psi(Me,Me)pro)-OH is a dipeptide.

Maculosin is a secondary metabolite of fungi and bacteria.

Fmoc-Pro-Pro-OH is an amino acid derivative and has a wide range of applications in life science related research.

Z-Tyr-OH is a useful organic compound for research related to life sciences. The catalog number is T67546 and the CAS number is 1164-16-5.

H-Arg-Gly-Tyr-Ala-Leu-Gly-OH is a competitive inhibitor of cAMP-dependent protein kinase [1].

'(D-Phe5,Cys6,11,N-Me-D-Trp8)-Somatostatin-14 (5-12) amide (Compound 4) is a somatostatin analogue exhibiting varying affinity for somatostatin receptors, with dissociation constants (Kd) of 0.61 nM for SSTR5, 11.05 nM for SSTR3, 23.5 nM for SSTR2, 1200 nM for SSTR1, and >1000 nM for SSTR4, respectively [1].'

H-Pro-Thr-Glu-Phe-p-nitro-Phe-Arg-Leu-OH is a water-soluble polypeptide capable of acting as a substrate for enzymes cathepsin D, pepsin, and pepsinogen, holding potential applications in biochemical analysis [1] [2].

Fmoc-Aib-OH is an amino acid derivative and has a wide range of applications in life science related research.