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 About 29 results found for searched term "LYP-IN-3" (0.148 seconds)

Cat.No.  Name Target
M42537 LYP-IN-3 Phosphatase
LYP-IN-3 is a selective inhibitor of Lymphoid-tyrosine phosphatase (LYP) (Ki=0.93 μM), and regulates T-cell receptor (TCR) signaling pathway in tumor progress.
M25536 Recombinant Human CXCL13/BCA-1 (E. coli) Cytokines and Growth Factors
CXC chemokine BLC; Small-inducible cytokine B13
CXCL13, also known as B-lymphocyte chemoattractant (BLC), is a CXC chemokine that is constitutively expressed in secondary lymphoid organs. Recombinant human CXCL13 is a single non-glycosylated polypeptide chain containing 87 amino acids and mature human BCA-1 shares 64 % amino acid sequence similarity with the murine protein and 23–34 % amino acid sequence identity with other known CXC chemokines. Determined by a chemotaxis bioassay using human B cells, the biological activity is in a concentration range of 1.0-10 ng/ml.
M4062 Punicalagin Anti-infection
Punicalagin is a species from Punica Granatum L. Or polyphenols isolated from the leaves of Terminalia catappa L. Punicalagin is a reversible, noncompetitive 3CLpro inhibitor that inhibits SARS-COV-2 replication in vitro. Punicalagin is an anti-hepatitis B virus (HBV) drug with antioxidant, anti-inflammatory and anticancer effects. Punicalagin has the potential to be used in COVID-19 research.
M4179 Neochlorogenic-acid NF-κB
trans-5-O-Caffeoylquinic acid
Neochlorogenic acid is a natural polyphenolic compound found in dried fruits and other plants. Neochlorogenic acid can inhibit the production of TNF-α and IL-1β. Neochlorogenic acid inhibited the expression of iNOS and COX-2 proteins. Neochlorogenic acid also inhibited the activation of phosphorylated NF-κB P65 and P38 MAPK.
M4208 (-)-Epigallocatechin gallate EGFR/HER2
EGCG; Epigallocatechol Gallate
(-)-Epigallocatechin Gallate is an antioxidant polyphenol flavonoid form green tea, and inhibits the activation of EGFR, HER2 and HER3, with antitumor activity.
M4363 Polyphyllin-VI Pyroptosis
Polyphyllin VI, an active saponin, has anticancer activity. Polyphyllin VI induces G2/M cell cycle arrest and induces apoptosis. Polyphyllin VI induces caspase-1-mediated pyroptosis by inducing ROS/NF-κB/NLRP3/GSDMD signaling axis in non-small cell lung cancer.
M9708 Chymotrypsin Enzymes & Coenzymes
α-Chymotrypsin
α-Chymotrypsin is a serine peptidase and has 241 amino acid residues contained in three polypeptide chains (A chain-13 residues, B chain-131 residues, and C chain-97 residues) linked by disulfide bridges.
M10673 Procyanidin C1 Apoptosis
PCC1
Procyanidin C1 (PCC1) is a natural polyphenol, which causes DNA damage, cell cycle arrest and induces apoptosis. Procyanidin C1 decreases the level of Bcl-2, but enhances BAX, caspase 3 and 9 expression in cancer cells.
M11215 Fibrinogen (Bovine) Others
Fibrinogen (Fg), i. e. coagulation factor I, molecular weight about 340kDa, by α, β, γ three pairs of different polypeptide chain. Polypeptide chains are linked by disulfide bonds. Protein Content: 67.30.
M13348 LyP-1 TFA Others
Lyp-1 TFA is a circular 9-amino acid tumor-targeting peptide that selectively binds its P32 receptor protein in a variety of tumor-associated cells.
M13447 Recombinant Human IGF-II (E. coli) Cytokines and Growth Factors
Insulin-like Growth Factor-II; Somatamedin A
Insulin-like Growth Factor II (IGF-II) is a 7 kDa single chain polypeptide with high homology to insulin. Protein structure:Expressed with an N-terminal Met. Igf-ii (ALA25-GLU91) , Accession # P01344-1.
M14930 Disitertide diammonium TGF-beta/Smad
P144 diammonium
Disitertide (P144) diammonium is a polypeptide inhibitor of transforming growth factor TGFβ1, specifically blocking its interaction with the receptor. Disitertide diammonium was also an inhibitor of PI3K and an inducer of apoptosis.
M17240 Methyl gallate NLR
Gallincin; NSC 363001; Methyl-3,4,5-trihydroxybenzoate
Methyl gallate is a polyphenol commonly found in the plant kingdom and is also an inhibitor of NLRP3, inhibiting the activation of NLRP3 inflammatory vesicles. In vitro, Methyl gallate is also a potent, highly specific inhibitor of herpes simplex virus (HSV) and has the ability to inhibit Treg cell migration.
M17933 Pennogenin 3-O-beta-chacotrioside Autophagy
Pennogenin 3-O-beta-chacotrioside is an active component isolated from Paris polyphylla, modulates autophagy via increasing the expressions of autophagy-related proteins LC3 and Beclin-1.
M21330 H3K4(Me3) (1-20) Peptides
H3K4(Me3) (1-20), a histone polypeptide, trimethylation of histone H3 to lysine 4 (H3K4 me3) is found in active euchromatin. Sequence: Ala-Arg-Thr-{Lys(Me3)}-Gln-Thr-Ala-Arg-Lys-Ser-Thr-Gly-Gly-Lys-Ala-Pro-Arg-Lys-Gln-Leu.
M28118 Cyclotheonamide A  Serine/Threonine Protease
Cyclotheonamide A is a serine protease inhibitor (cyclic polypeptide), which can be obtained from marine sponges of the genus Theonella. Cyclotheonamide A shows potent inhibitory activity against trypsin (Ki=0.023 µM) and streptokinase (Ki=0.035 µM) and moderate inhibitory activity against human α-thrombin (Ki=0.18 µM). Cyclotheonamide A can be used in study of antithrombotic.
M31094 Retatrutide acetate Glucagon Receptor
LY3437943 acetate
Retatrutide (LY3437943) acetate is a triple agonist peptide of the glucagon receptor (GCGR), glucosedependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R). Retatrutide acetate inhibits for human GCGR, GIPR, and GLP-1R with EC50 values of 5.79, 0.0643 and 0.775 nM, respectively.
M39159 Epitheaflagallin 3-O-gallate MMP
Epitheaflagallin 3-O-gallate is a minor polyphenol in black tea. Epitheaflagallin 3-O-gallate exhibits antioxidative activity, pancreatic lipase inhibition, and an inhibiting effect on the activity of matrix metalloprotease-1 and -3 and their synthesis by human gingival fibroblasts.
M40855 Recombinant Human Siglec-7 Protein (HEK293, C-6His) Receptor Proteins
sialic acid binding Ig-like lectin 7; CD328 antigen; p75/AIRM1; QA79
Human Siglec-7 encodes a 467 amino acid (aa) polypeptide with a hydrophobic signal peptide, an N-terminal Ig-like V-type domain, two Ig-like C2-type domains, a transmembrane region and a cytoplasmic tail. It binds equally well to both alpha 2,3- and alpha 2,6-linked sialic acid.
M42544 NC1 Phosphatase
NC1 is a noncompetitive and allosteric lymphoid-specific tyrosine phosphatase (LYP) inhibitor, with a Ki value 4.3 μM.
M42546 LYP-IN-4 Phosphatase
LYP-IN-4 is a reversible and selective inhibitor of lymphotyrosine phosphatase (LYP) (Ki=1.34 μM, IC50=3.52μM).
M43198 Tri-valine Others
Tri-valine (NSC 35938) is a polypeptide that can be separated from Creatine kinase, β-enolase, Triosephosphate isomerase and glyceraldehyde 3-phosphate dehydrogenase.
M49466 Retatrutide Glucagon Receptor
LY3437943
Retatrutide is a triple agonist peptide for glucagon receptor (GCGR), glucose-dependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R) that binds human GCGR, GIPR, and GLP-1R with EC50 values of 5.79, 0.0643, and 0.775 nM, respectively. Retatrutide can be used in studies related to obesity.
M50455 LyP-1 Others
LyP-1 is a cyclic 9‐amino‐acids tumor homing peptide and selectively bind to p32 receptors overexpressed in various tumor-associated cells.
M52697 Aminopeptidase N Ligand (CD13) NGR peptide Aminopeptidase
Aminopeptidase N Ligand (CD13) NGR peptide is a polypeptide targeting CD13 and can be used as a carrier to mediate intracellular transmission.
M53015 Pancreatic Polypeptide, bovine Neuropeptide Receptor
Pancreatic Polypeptide, bovine, a 36-amino acid, straight chain polypeptide derived primarily from the pancreas, inhibits secretin- and cholecystokinin-stimulated pancreatic secretion.
M54045 Human PD-L1 inhibitor IV PD-1/PD-L1
Human PD-L1 inhibitor IV, a polypeptide, is a competitive human PD-1 protein inhibitor with a Kd value of 1.38 μM.
M54092 Pancreatic Polypeptide, human Neuropeptide Receptor
Pancreatic Polypeptide, human is a C-terminally amidated 36 amino acid peptide, which acts as a neuropeptide Y (NPY) Y4/Y5 receptor agonist.
M58205 DDX3-IN-1 Anti-infection
DDX3 inhibitor 1
DDX3-IN-1 is a DEAD-box polypeptide 3 (DDX3) inhibitor with CC50 values of 50 and 36 μM for HIV and HCV, respectively. DDX3-IN-1 has antiviral activity.



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