n-formyl-met-ala-ser

N-Formyl-Met-Ala-Ser is a peptide, binds to formyl peptide receptors on neutrophils.N-Formyl-Met-Ala-Ser Peptide (fMet-Ala-Ser) binds to formyl peptide receptors on neutrophils. N-Formylmethionine-containing peptides including the most potent and known me

N-Formyl-Met-Ala-Ser TFA is a peptide, binds to formyl peptide receptors on neutrophils.N-Formyl-Met-Ala-Ser Peptide (fMet-Ala-Ser) binds to formyl peptide receptors on neutrophils. N-Formylmethionine-containing peptides including the most potent and know

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.

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[1].Potent chemoattractant for human neutrophils.Radioiodinated molecule has full biological activity.

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

N-Formyl-Met-Leu-Phe (N-Formyl-MLF) (fMLF) is a synthetic peptide that acts as an agonist at formyl peptide receptors (FPR; Ki = 0.8 pM).

Met-Arg-Phe-Ala, a peptide, serves as a potent competitive inhibitor of enkephalin-generating endopeptidase (EGE) and is utilized in neurological disease research [1].

Ser-Ala-alloresact, a sperm activating peptide (SAP), plays a pivotal role in the fertilization process through its release from the eggs of marine invertebrates, facilitating sperm activation [1] [2].

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

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.

N-Formyl-Nle-Leu-Phe-Nle-Tyr-Lys TFA is a formyl peptide receptor (FPR) agonist.

H-N-Me-Ser-OH is a useful organic compound for research related to life sciences and the catalog number is T65885.

Z-N-Me-Ala-OH is a useful organic compound for research related to life sciences. The catalog number is T65509 and the CAS number is 21691-41-8.

D-Ala-Gly-Phe-Met-NH2 monoacetate, an opioid peptide, serves as a potent agonist for the opiate δ-receptor [1].

N-Acetyl-Ser-Asp-Lys-Pro (Ac-SDKP) acetate, a specific substrate for the N-terminal active site of angiotensin-converting enzyme (ACE), functions as a natural inhibitor of pluripotent hematopoietic stem cell proliferation. Additionally, it exhibits anti-inflammatory and antifibrotic properties [1] [2].

H-N-Me-DL-Ala-OH is a useful organic compound for research related to life sciences. The catalog number is T66077 and the CAS number is 600-21-5.

Enkephalin-met, ala(2)- is a synthetic analog of methionine enkephalin.

N-Formyl-Leu-OH is a useful organic compound for research related to life sciences. The catalog number is T64888 and the CAS number is 6113-61-7.

N-Acetyl-Ser-Asp-Lys-Pro (TFA) is an endogenous tetrapeptide that is naturally produced in the bone marrow. It serves as a specific substrate for the N-terminal site of ACE, the enzyme responsible for angiotensin converting activity.

Fmoc-N-Me-D-Ala-OH is a useful organic compound for research related to life sciences and the catalog number is T65189.

Fmoc-N-Me-DL-Ala-OH is a useful organic compound for research related to life sciences. The catalog number is T67225 and the CAS number is 1362858-88-5.

H-N-Me-Ala-OH is a useful organic compound for research related to life sciences. The catalog number is T66062 and the CAS number is 3913-67-5.

D-Ala-Gly-Phe-Met-NH2, an opioid peptide, is a potent opiate δ-receptor agonist [1] .

Cys-Arg-Gly-Asp-Phe-Pro-Ala-Ser-Ser-Cys (Disulfide bridge: Cys1-Cys10), a decapeptide with a cyclic RGD active sequence, acts as an Integrin αIIbβ3 antagonist, effectively inhibiting platelet adhesion and proMMP-13 adhesion [1].

Boc-N-Me-Ala-OH is a useful organic compound for research related to life sciences. The catalog number is T67523 and the CAS number is 16948-16-6.

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