ala-ala-pro-val-chloromethylketone

Ala-Ala-Pro-Val-chloromethylketone serves as an irreversible inhibitor of human neutrophil elastase (NE), utilized in researching chronic inflammatory airway diseases.

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

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

pGlu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val is a peptides

D-{Ala-Ala-Ala-Ala-Ala}, a pentapeptide, serves as an inhibitor of immunological responses [1].

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].

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

Myristoyl tetrapeptide Ala-Ala-Pro-Val is a bioactive peptide that stimulates the expression of extracellular matrix (ECM) proteins and inhibits the expression of metalloproteinases (MMPs).

Suc-Val-Pro-Phe-SBzl (succinyl-valine-proline-phenylalanine thiobenzyl ester) acts as a CatG enzyme inhibitor, exhibiting IC50 values ranging from 111 to 225 mM.

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].

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

Argipressin, ala(10)- is a Decapeptide that differs from argipressin in the addition of an N-terminal Ala-residue.

D-Val-Leu-Lys-chloromethylketone, a tripeptide, functions as an anticoagulant [1].

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].

HS-(CH2)3CO-L-Ala-D-Ala-L-Ala-NH-CH2-S-(CH2)5-CO-DM is a peptide-cleavable agent-linker conjugate utilized in antibody-drug conjugates (ADCs), with the DM denoting the maytansinoid component [1].

Cyclo(Phe-Ala-Gly-Arg-Arg-Arg-Gly-AEEAc) is a potential nonhormonal male contraceptive that functions through the inhibition of GRTH/DDX25 phosphorylation.

FITC-β-Ala-Amyloid β-Protein (1-42) ammonium, a fluorescein isothiocyanate (FITC)-tagged monomer peptide of Aβ1-42, is instrumental in Alzheimer’s disease pathogenesis [1].

Z-Ala-Ala-Asp-chloromethylketone (Z-AAD-CMK) is a selective inhibitor of granzyme B [1].

Pam3-Cys-Ala-Gly, a synthetic bacterial lipopeptide, serves as a powerful activator of both macrophages and B cells [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].

H-Leu-Leu-Ala-OH, a tripeptide consisting of two L-leucine residues linked to L-alanine via peptide bonds, exhibits antioxidant activities [1].

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

H-Ala-OtBu.HCl 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].

H-D-Ala-D-Ala-D-Ala-D-Ala-OH is a substrate for D-aminopeptidase [1] .

Boc-3-(3-pyridyl)-D-Ala-OH is a useful organic compound for research related to life sciences. The catalog number is T65405 and the CAS number is 98266-33-2.

c(Bua-Cpa-Thi-Val-Asn-Cys)-Pro-Agm a highly efficient, selective and short-acting peptide V2 receptor agonist (V2R), with EC50s of hV2R and rV2R being 0.25 and 0.05 nM, respectively.

Fmoc-Ala-Glu-Asn-Lys-NH2 is a peptide inhibitor that selectively targets asparagine endopeptidase (AEP) and inhibits the cleavage of amyloid precursor protein (APP). AEP, a pH-controlled cysteine proteinase, plays a crucial role in the proteolytic processing of APP, and its activity is enhanced during the aging process [1].

Boc-Ala-OMe is a useful organic compound for research related to life sciences. The catalog number is T65911 and the CAS number is 28875-17-4.

Boc-Ala-Ala-OH is a useful organic compound for research related to life sciences. The catalog number is T65023 and the CAS number is 27317-69-7.

Boc-D-Ala(3,3-diphenyl)-OH is a useful organic compound for research related to life sciences. The catalog number is T66039 and the CAS number is 143060-31-5.

Boc-Val-Ala-OH is a useful organic compound for research related to life sciences. The catalog number is T66737 and the CAS number is 70396-18-8.

H-Val-Pro-Pro-OH(TFA), a proline peptide derivative from milk, is an ACE inhibitor with IC50 of 9 M.

Boc-Ala-OH is a useful organic compound for research related to life sciences. The catalog number is T65775 and the CAS number is 15761-38-3.

Z-Ala-Ala-Asn-AMC, also known as Cbz-Ala-Ala-Asn-AMC, serves as a substrate for legumain. The overexpression of legumain in 293 HEK-Leg cells results in efficient cleavage of Cbz-Ala-Ala-Asn-AMC.

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].

Lys-arg-ala-lys-ala-lys-thr-thr-lys-lys-arg is a protein kinase C substrate.

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

Z-Val-Ala-OH is a useful organic compound for research related to life sciences. The catalog number is T65515 and the CAS number is 24787-89-1.

H-D-Ala-OMe.HCl is an amino acid derivative and has a wide range of applications in life science related research.

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.

Z-Ala-OMe is a useful organic compound for research related to life sciences. The catalog number is T66749 and the CAS number is 28819-05-8.

H-Val-Ala-OH (Valyl-alanine) is a dipeptide formed from L-Valine and L-Alanine residues. It has a role as a metabolite. H-Val-Ala-OH is a dipeptide formed from L-Valine and L-Alanine residues.

Cyclo(Pro-Val) (Cyclo(prolylvalyl)) is obtained from the marine fungus and shows moderate antifungal and weak antitumor activities. Cyclo(Pro-Val) inhibits the growth of Bacillus subtilis with MIC of 0.8 g/L.

Fmoc-3-Ala(3-benzothienyl)-OH is a useful organic compound for research related to life sciences. The catalog number is T64827 and the CAS number is 177966-60-8.

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

Fmoc-Ala-Thr(psi(Me,Me)pro)-OH is a useful organic compound for research related to life sciences. The catalog number is T66617 and the CAS number is 252554-79-3.

D-Pro-Phe-Arg-Chloromethylketone, an inhibitor of coagulation factor XII and plasma kallikrein, is significant in the regulation of thrombosis and inflammation [1].

Ala-parafluoroPhe-Arg-Cha-Cit-Tyr-NH2 is a biologically active peptide functioning as a selective agonist for Protease Activated Receptor 1 (PAR-1), a subtype of G-protein coupled receptors involved in mediating thrombin's cellular effects. Exhibiting high specificity for PAR-1 over PAR-2, its selectivity was assessed via cell-based calcium signaling assays in HEK293 cells. As an agonist, it is instrumental for in vivo investigations of PAR-1 activation. PAR-1 also collaborates with PAR-4, influencing thrombin-induced hepatocellular carcinoma within 'coagulation type' tumor environments where thrombin generation occurs.