| 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. |
| M9579 | XMD-17-51 | XMD-17-51 is a potent and selective NUAK1 inhibitor. |
| M9574 | Ginkgetin | Ginkgetin is a natural biflavonoid isolated from leaves of Ginkgo biloba L. with effects of anti-inflammation and anticancer activity. Ginkgetin is also a potent inhibitor of Wnt signaling, with an IC50 of 5.92 μΜ. |
| M9571 | API-1 | API-1 is a Pin1 inhibitor with an IC50 of 72.3 nM. API-1 directly and specifically binds to the Pin1 peptidyl-prolyl isomerase (PPIase) domain and potently inhibits Pin1 cis-trans isomerizing activity. |
| M9568 | SC-26196 | SC-26196 is a potent, orally active D6D inhibitor (IC50 = 0.2 µM in a rat liver microsomal assay) that completely blocks the conversion of linoleic acid to arachidonic acid (AA). |
| M9567 | Leptin (116-130) mouse | Leptin (116-130) mouse is a synthetic leptin peptide fragment. |
| M9563 | 2,1,3-Benzothiadiazole-5-carbaldehyde | 2,1,3-Benzothiadiazole-5-carbaldehyde |
| M9557 | BAY-1816032 | BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazoles 1) kinase inhibitor with an IC50 of 7 nM. |
| M9543 | Dextran (Mw 40000) | Dextran (Dextran 40000) has an inhibitory effect on thrombocyte aggregation. |
| M9531 | NADP disodium salt | NADP disodium salt is a participant coenzyme in aerobic and anaerobic oxidations. |
| M9517 | Sodium hippurate | Hippuric acid is a low molecular weight phenolic carboxylic acid urinary metabolite that may be a useful urinary biomarker for certain cancers such as gastric cancer and oxidative stress. |
| M9511 | DO264 | DO264 is a potent selective, and in vivo active ABHD12 inhibitor, with an IC50 of 11 nM. |
| M9497 | ML-792 | ML-792 is a potent and selective SAE inhibitor with nanomolar potency in cellular assays. |
| M9475 | Sardomozide dihydrochloride | Sardomozide dihydrochloride (also known as SAM486A or CGP48664) is a second-generation polyamine synthesis inhibitor, which inhibits the activity of the polyamine biosynthetic enzyme S-adenosylmethionine decarboxylase (SAMDC). |
| M9448 | X-α-Gal | X-α-Gal is suitable as a substrate for α-galactosidase. |
| M9412 | IACS-10759 | Iacs-10759 is a potent inhibitor of the oxidative phosphorylation complex I (OXPHOS). |
| M9393 | PTZ-343 | PTZ-343 is a water-soluble enhancer of luminol chemiluminescent peroxidation catalyzed by horseradish peroxidase (HRP). |
| M9378 | NHS-Biotin | NHS-Biotin is an amine reactive biotinylation reagent, used in the biotinylation of proteins and peptides. |
| M9377 | Polycaprolactone (MW 80,000) | |
| M9374 | Fmoc-Trp(1-Me)-OH | Fmoc-Trp(1-Me)-OH is synthesized by N-(9-Fluorenylmethoxycarbonyloxy)succinimide (Fmoc-ONSu) and 1-Methyl-Ltrypthophan. |
| M9355 | UNC2541 | UNC2541 is a potent and Mer tyrosine kinase (MerTK)-specific inhibitor, binds in the MerTK ATP pocket, with an IC50 of 4.4 nM, more selective over Axl, Tyro3 and Flt3. UNC2541 inhibits phosphorylated MerTK (pMerTK; EC50, 510 nM). |
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