fmoc-gly-thr(psi(me,me)pro)-oh

Fmoc-Gly-Thr(psi(Me,Me)pro)-OH is a polypeptide composed of glycine and threonine containing a (psi(Me,Me)pro) modification.

Fmoc-Arg-OH [Fmoc-L-Arginine] is utilized in peptide synthesis.

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

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-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.

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

Fmoc-Cys(Acm)-OH (Fmoc-S-acetamidomethyl-L-cysteine) is a cysteine derivative.

Boc-Gly-Gly-Phe-Gly-OH acetate (GGFG acetate) is a self-assembly of N- and C-protected tetrapeptide.

Ac-Pro-Gly-Pro-OH is an acetyl-modified tripeptide compound that acts as a CXCR2 agonist, exhibiting bactericidal and anti-inflammatory activities. It inhibits apoptosis of immune cells, suppresses the production of pro-inflammatory cytokines, and has been utilized in studies of sepsis and lung inflammation.

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.

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

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.

Tyr-Gly-Gly-Phe-Met-OH (Met-Enkephalin) is a naturally occurring endogenous opioid peptide that inhibits tumor growth by binding to the opioid receptor.

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

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

His-[D-2-ME-Trp]-Ala is a peptide fragment of the growth hormone hexarelin.

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

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

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

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

Fmoc-Phe(4-F)-OH, an amino acid derivative, has a wide range of applications in life science-related research.

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, catalog number T65832 and CAS number 197632-77-2, is a valuable organic compound for life sciences research.

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

Fmoc-Lys(Ac)-OH, catalog number T65778 and CAS number 159766-56-0, is a valuable organic compound for research in life sciences.

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.

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.

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

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 that serves as a substrate for the enzymes cathepsin D, pepsin, and pepsinogen, with 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.

Boc-D-Tyr(Me)-OH, with catalog number T65034 and CAS number 68856-96-2, is a valuable organic compound for life sciences research.

Fmoc-L-HoLys(Boc)-OH is a useful organic compound for research related to life sciences. The catalog number is T65197 and the CAS number is 194718-17-7.

Fmoc-Glu(OMe)-OH (catalog number T66704, CAS number 145038-50-2) is a valuable organic compound used in life sciences research.

Fmoc-Glu(OBzl)-OH is a valuable organic compound used in life science research, catalog number T67559, CAS number 123639-61-2.

Fmoc-N-Me-Glu(OtBu)-OH is a valuable organic compound for life sciences research (catalog number: T65703; CAS number: 200616-40-6).

Fmoc-D-Cys(Trt)-OH, catalog number T65789 and CAS number 167015-11-4, is a valuable organic compound for life sciences research.

Fmoc-Glu(OAll)-OH, with catalog number T65720 and CAS number 133464-46-7, is a valuable organic compound used in life sciences research.

Fmoc-D-N-Me-Val-OH, catalog number T65652 and CAS number 103478-58-6, is a valuable organic compound for life sciences research.

Fmoc-Ile-Ser(psi(Me,Me)pro)-OH is a dipeptide characterized by the presence of an N-terminal Fmoc-protected isoleucine and a serine residue with a (psi(Me,Me)pro) modification.

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

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

(d(CH2)51,Tyr(Me)2, Orn8)-Oxytocin (OVT) is an oxytocin receptor antagonist used in neurological disease research [1].

Selective vasopressin V1A receptor antagonist. Inhibits vasopressin and oxytocin-induced increases in intracellular calcium concentrations in vitro (IC50 values are 5 and 30 nM respectively). Exhibits potent and prolonged antivasopressor activity and indu