| Cat.No. | Name | Information |
|---|---|---|
| M6098 | Baicalein | Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM. |
| M9325 | EGTA | EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages. |
| M9330 | Brij-35 | Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability. |
| M6154 | 2-PMPA tetrasodium | 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM. |
| M2250 | Pamidronate disodium | Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis. |
| M9916 | DPPH | DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants. |
| M9194 | Insulin (human) | Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets. |
| M3409 | Formestane | Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM. |
| M9665 | N-(2-amino-2-oxoethyl)acrylamide | N-(2-Amino-2-oxoethyl)acrylamide |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M43849 | Laminaran | Laminaran is a β-1-3-glucan from Eisenia Bicyclis, consisting of β(1→3)-glucans with β(1→6) branches, which can be catalyzed by glucoamylases such as (EC 3.2.1.6). Laminaran is also a typical ligand for Dectin-1, which has immunomodulatory, radioprotective and anticancer activities. It can be used in cancer immunity studies. |
| M43809 | α-Methyl-DL-aspartic acid | α-Methyl-DL-aspartic acid is a specific inhibitor of argininosuccinate synthase (ASS) and the rate-limiting enzyme of the 1-citrulline to 1-arginine cycle. |
| M43354 | GALA | GALA is a biological active peptide. |
| M43321 | FRETS-VWF73 | FRETS-VWF73 is a biological active peptide. |
| M43293 | Gly-d-Phe | Gly-d-Phe is an affinity ligand for Thermolysin. |
| M43224 | γ-Fibrinogen 377-395 | γ-Fibrinogen377-395 is a fibrinogen-derived inhibitory peptide, as well as fibrinogen epitope. |
| M43222 | γ-Fibrinogen 377-395 TFA | γ-Fibrinogen377-395 TFA is a fibrinogen-derived inhibitory peptide, as well as fibrinogen epitope. |
| M43197 | Fibrinogen-Binding Peptide TFA | Fibrinogen-Binding Peptide TFA (designed by anticomplementarity hypothesis) is a presumptive peptide mimic of the vitronectin binding site on the fibrinogen receptor. |
| M43191 | Hexaarginine | Hexa-arginine, consisting of six arginines, is a polycationic peptide that can penetrate cells efficiently. |
| M43172 | Bz-DTPA | Bz-DTPA is a bifunctional chelator. |
| M43129 | CDFI | CDFI is an inhibitor of the lipid II flippase MurJ. |
| M43054 | Maleimide-NOTA | Maleimide-NOTA is a chelator for the labeling of peptides and antibodies. |
| M43029 | DPyPE | DPyPE is a phosphatidylethanolamine lipid composed of polyisoprene alkyl chains. |
| M43019 | MRT-2359 | MRT-2359 is an orally active and potent degrader of GSPT1 with anti-tumor activity. |
| M42950 | Advantame | Advantame is a non-caloric artificial sweetener, analogue of aspartame, commonly used as a food additive. |
| M42901 | Alitame anhydrous | Alitame (anhydrous) is a high-intensity sweetener formed from the amino acids L-aspartic acid and D-alanine, and an amine derived from thietane. |
| M42884 | Digoxigenin NHS ester | Digoxigenin NHS ester is an activated ester which readily reacts with amino groups under mild conditions, attaching the digoxigenin moiety to proteins or amino-. |
| M42876 | ELOVL6-IN-4 | ELOVL6-IN-4 is a potent, selective, and orally active long chain fatty acid elongase 6 (ELOVL6) inhibitor with IC50s of 79 nM and 94 nM for human and mouse ELOVL6, respectively. |
| M42874 | JY-2 | JY-2 is a moderately selective and orally active Forkhead transcription factor forkhead box O1 (FoxO1) inhibitor that inhibits FoxO1 transcriptional activity with an IC50 of 22 μM. |
| M42873 | TCRS-417 | TCRS-417 (T417) is a small molecule compound capable of docking to the interface between PBX1 and its cognate DNA target sequence, effectively interfering with PBX1-DNA interaction. |
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